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Nodes: 1364,
Authors: 3358,
Journals: 307,
Outer References: 11901,
Words: 2507
Collection span: 1995 - 2005
View: Overview. Sorted by year, source, volume, issue, page.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 601 | 0 | 0 | 601 1999 CYTOGENETICS AND CELL GENETICS 85(1-2):165-165 Sofocleous C; Mavrou A; Fryssira H; Kolialexi A; Tsenghi C; et al. FMRP (Fragile X Mental Retardation Protein) studies in mentally retarded children in Greece | 0 | 0 |
| 602 | 0 | 0 | 602 1999 CYTOGENETICS AND CELL GENETICS 85(1-2):167-167 Tayel SM; Al-Naggar RL; Ali FE; Al-Awadi SA Two-step fragile X screening program in mentally retarded males | 0 | 0 |
| 603 | 8 | 65 | 603 1999 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 41(9):625-632 Hatton DD; Bailey DB; Hargett-Beck MQ; Skinner M; Clark RD Behavioral style of young boys with fragile X syndrome | 9 | 13 |
| 604 | 4 | 23 | 604 1999 DIAGNOSTIC MOLECULAR PATHOLOGY 8(3):152-156 Tzeng CC; Cho WC; Kuo PL; Chen RM Pilot fragile X screening in normal population of Taiwan | 7 | 10 |
| 605 | 4 | 54 | 605 1999 EPILEPSIA 40(8):1092-1099 Musumeci SA; Hagerman RJ; Ferri R; Bosco P; Dalla Bernardina B; et al. Epilepsy and EEG findings in males with fragile X syndrome | 10 | 19 |
| 606 | 5 | 23 | 606 1999 EUROPEAN JOURNAL OF HUMAN GENETICS 7(2):212-216 Ryynanen M; Heinonen S; Makkonen M; Kajanoja E; Mannermaa A; et al. Feasibility and acceptance of screening for fragile X mutations in low-risk pregnancies | 13 | 18 |
| 607 | 7 | 33 | 607 1999 EUROPEAN JOURNAL OF HUMAN GENETICS 7(5):526-532 Kooy RF; Reyniers E; Verhoye M; Sijbers J; Bakker CE; et al. Neuroanatomy of the fragile X knockout mouse brain studied using in vivo high resolution magnetic resonance imaging | 9 | 21 |
| 608 | 10 | 34 | 608 1999 EUROPEAN JOURNAL OF HUMAN GENETICS 7(7):771-777 Larsen LA; Armstrong JSM; Gronskov K; Hjalgrim H; Brondum-Nielsen K; et al. Analysis of FMR1 (CGG)(n) alleles and FRAXA microsatellite haplotypes in the population of Greenland: implications for the population of the New World from Asia | 3 | 5 |
| 609 | 0 | 28 | 609 1999 EXPERIMENTAL CELL RESEARCH 251(2):388-400 Yano H; Wang BE; Ahmad I; Zhang JZ; Abo T; et al. Identification of (CAG)(n) and (CGG)(n) repeat-binding proteins, CAGERs expressed in mature neurons of the mouse brain | 0 | 5 |
| 610 | 0 | 0 | 610 1999 FASEB JOURNAL 13(5):A703-A703 Greenough WT; Weiler IJ; Angenstein F; Klintsova A; Bauchwitz R Synthesis of the fragile X mental retardation protein at synapses: Possible role in synaptic development and plasticity | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 611 | 2 | 21 | 611 1999 GENETIC TESTING 3(3):301-304 Melis MA; Addis M; Lepiani C; Congeddu E; Cossu P; et al. A strategy for fragile-X carrier screening | 0 | 2 |
| 612 | 3 | 8 | 612 1999 GENETICS AND MOLECULAR BIOLOGY 22(2):169-172 Pena SDJ; Sturzeneker R Diagnosis of the fragile X syndrome in males using methylation-specific PCR of the FMR1 locus | 0 | 2 |
| 613 | 1 | 14 | 613 1999 GENETICS AND MOLECULAR BIOLOGY 22(4):471-474 Vianna-Morgante AM; Costa SS; Pavanello RDM; Otto PA; Mingroni-Netto RC Premature ovarian failure (POF) in Brazilian fragile X carriers | 1 | 4 |
| 614 | 2 | 10 | 614 1999 HEREDITAS 130(2):189-190 Sucharov CC; Silva R; Rondinelli E; Moura-Neto RS Fragile X trinucleotide repeats from a normal population in Rio de Janeiro, Brazil | 0 | 1 |
| 615 | 11 | 57 | 615 1999 HUMAN BIOLOGY 71(1):55-68 Arrieta I; Gil A; Nunez T; Telez M; Martinez B; et al. Stability of the FMRI CGG repeat in a Basque sample | 4 | 5 |
| 616 | 12 | 50 | 616 1999 HUMAN MOLECULAR GENETICS 8(5):863-869 Tamanini F; Bontekoe C; Bakker CE; van Unen L; Anar B; et al. Different targets for the fragile X-related proteins revealed by their distinct nuclear localizations | 30 | 39 |
| 617 | 13 | 67 | 617 1999 HUMAN MOLECULAR GENETICS 8(12):2293-2302 Burman RW; Popovich BW; Jacky PB; Turker MS Fully expanded FMR1 CGG repeats exhibit a length-and differentiation-dependent instability in cell hybrids that is independent of DNA methylation | 9 | 12 |
| 618 | 11 | 39 | 618 1999 HUMAN MOLECULAR GENETICS 8(13):2557-2566 Bardoni B; Schenck A; Mandel JL A novel RNA-binding nuclear protein that interacts with the fragile X mental retardation (FMR1) protein | 34 | 47 |
| 619 | 3 | 32 | 619 1999 HUMAN MUTATION 14(1):71-79 Panagopoulos I; Lassen C; Kristoffersson U; Aman P A methylation PCR approach for detection of fragile X syndrome | 3 | 4 |
| 620 | 0 | 0 | 620 1999 HUMAN REPRODUCTION 14:235-235 Sermon K; Seneca S; Lissens W; De Vos A; Vandervorst M; et al. Preimplantation genetic diagnosis for fragile-X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 621 | 0 | 0 | 621 1999 HUMAN REPRODUCTION 14:354-355 Gersak K; Kregar-Velikonja N; Meden-Vrtovec H; Peterlin B Fragile X premutation screening in women with premature menopause | 1 | 1 |
| 622 | 0 | 29 | 622 1999 INTERNATIONAL JOURNAL OF BEHAVIORAL DEVELOPMENT 23(2):519-531 Burack JA; Shulman C; Katzir E; Schaap T; Brennan JM; et al. Cognitive and behavioural development of Israeli males with fragile X and Down Syndrome | 1 | 1 |
| 623 | 26 | 96 | 623 1999 INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE 3(6):639-645 Pimentel MMG Fragile X syndrome | 0 | 5 |
| 624 | 6 | 41 | 624 1999 JOURNAL OF BIOLOGICAL CHEMISTRY 274(18):12797-12802 Fry M; Loeb LA Human Werner syndrome DNA helicase unwinds tetrahelical structures of the fragile X syndrome repeat sequence d(CGG)(n) | 11 | 104 |
| 625 | 0 | 18 | 625 1999 JOURNAL OF CHILD NEUROLOGY 14(2):108-112 Singh R; Sutherland GR; Manson J Partial seizures with focal epileptogenic electroencephalographic patterns in three related female patients with fragile-X syndrome | 1 | 1 |
| 626 | 0 | 45 | 626 1999 JOURNAL OF EARLY INTERVENTION 22(2):137-151 Jackson SC; Roberts JE Family and professional congruence in communication assessments of preschool boys with fragile X syndrome | 0 | 0 |
| 627 | 1 | 10 | 627 1999 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 43:47-53 Carmichael B; Pembrey M; Turner G; Barnicoat A Diagnosis of fragile-X syndrome: the experiences of parents | 9 | 11 |
| 628 | 2 | 34 | 628 1999 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 43:314-324 York A; von Fraunhofer N; Turk J; Sedgwick P Fragile-X syndrome, Down's syndrome and autism: awareness and knowledge amongst special educators | 2 | 4 |
| 629 | 2 | 42 | 629 1999 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 43:466-474 Garner C; Callias M; Turk J Executive function and theory of mind performance of boys with fragile-X syndrome | 3 | 4 |
| 630 | 0 | 0 | 630 1999 JOURNAL OF MEDICAL GENETICS 36:S64-S64 Lazarau L; Warburton SA; Roberts CE; Hughes HE; Bartlett S; et al. Fragile X syndrome carrier females with full mutations inherited from a normal transmitting male | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 631 | 0 | 0 | 631 1999 JOURNAL OF MEDICAL GENETICS 36:S65-S65 Chotai K; Payne SJ A fragile-X male mosaic for normal, premutation and full mutation FMR-1 alleles | 0 | 0 |
| 632 | 1 | 21 | 632 1999 JOURNAL OF MEDICAL GENETICS 36(2):167-170 de Vries BBA; van den Boer-van den Berg HMA; Niermeijer MF; Tibben A Dilemmas in Counselling females with the fragile X syndrome | 0 | 1 |
| 633 | 2 | 5 | 633 1999 JOURNAL OF MEDICAL GENETICS 36(2):171-171 Macpherson J; Murray A; Webb J; Jacobs P Fragile X syndrome: of POF and premutations | 1 | 2 |
| 634 | 0 | 0 | 634 1999 JOURNAL OF MEDICAL GENETICS 36(2):171-172 De Vries BBA; Halley DJJ; Oostra BA; Niermeijer MF Fragile X syndrome: of POF and premutations | 0 | 0 |
| 635 | 6 | 18 | 635 1999 JOURNAL OF MEDICAL GENETICS 36(3):253-257 Helderman-van den Enden ATJM; Maaswinkel-Mooij PD; Hoogendoorn E; Willemsen R; Maat-Kievit JA; et al. Monozygotic twin brothers with the fragile X syndrome: different CGG repeats and different mental capacities | 3 | 9 |
| 636 | 6 | 22 | 636 1999 JOURNAL OF MEDICAL GENETICS 36(6):467-470 de Vries BBA; Mohkamsing S; van den Ouweland AMW; Mol E; Gelsema K; et al. Screening for the fragile X syndrome among the mentally retarded: a clinical study | 4 | 12 |
| 637 | 3 | 6 | 637 1999 JOURNAL OF MEDICAL GENETICS 36(7):565-566 Moore SJ; Strain L; Cole GF; Miedzybrodzka Z; Kelly KF; et al. Fragile X syndrome with FMR1 and FMR2 deletion | 1 | 3 |
| 638 | 2 | 28 | 638 1999 JOURNAL OF MEDICAL SCREENING 6(2):70-76 Wildhagen MF; van Os TAM; Polder JJ; ten Kate LP; Habbema JDF Efficacy of cascade testing for fragile X syndrome | 3 | 5 |
| 639 | 4 | 43 | 639 1999 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 38(10):1294-1301 Murphy DGM; Mentis MJ; Pietrini P; Grady CL; Moore CJ; et al. Premutation female carriers of fragile X syndrome: A pilot study on brain anatomy and metabolism | 8 | 9 |
| 640 | 2 | 4 | 640 1999 LANCET 353(9159):1153-1154 Hong CJ; Song HL; Lai HC; Tsai SJ; Hsiao KJ Methanol/acetone treatment helps the amplification of FMR1 CGG repeat fragment in dried blood spots from Guthrie cards | 1 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 641 | 3 | 5 | 641 1999 MEDICAL JOURNAL OF AUSTRALIA 170(12):624-624 Cohen J; Loesch DZ Fragile X syndrome: do professionals know about it? | 0 | 0 |
| 642 | 3 | 113 | 642 1999 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 5(4):305-313 Hagerman RJ Psychopharmacological interventions in fragile X syndrome, fetal alcohol syndrome, Prader-Willi syndrome, Angelman syndrome, Smith-Magenis syndrome, and velocardiofacial syndrome | 0 | 2 |
| 643 | 11 | 74 | 643 1999 MOLECULAR AND CELLULAR BIOLOGY 19(8):5675-5684 White PJ; Borts RH; Hirst MC Stability of the human fragile X (CGG)(n) triplet repeat array in Saccharomyces cerevisiae deficient in aspects of DNA metabolism | 12 | 45 |
| 644 | 11 | 46 | 644 1999 MOLECULAR AND CELLULAR BIOLOGY 19(12):7925-7932 Ceman S; Brown V; Warren ST Isolation of an FMRP-associated messenger ribonucleoprotein particle and identification of nucleolin and the fragile X-related proteins as components of the complex | 50 | 76 |
| 645 | 0 | 0 | 645 1999 MOLECULAR PSYCHIATRY 4:S56-S56 Fisch GS; Carpenter N; Holden JA; Pandya A; Howard-Peebles PN; et al. Psychopathology in genetic disorders producing cognitive deficits: Adaptive and maladative behavior in the fragile X syndrome, Williams syndrome and neurofibromatosis type 1. | 0 | 0 |
| 646 | 2 | 30 | 646 1999 NATURE GENETICS 22(1):98-101 Coffee B; Zhang FP; Warren ST; Reines D Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells | 27 | 102 |
| 647 | 1 | 1 | 647 1999 NATURE GENETICS 22(2):209-209 Coffee B Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells (vol 22, pg 98, 1999) | 2 | 5 |
| 648 | 11 | 53 | 648 1999 NEUROSCIENCE 94(1):185-192 Paradee W; Melikian HE; Rasmussen DL; Kenneson A; Conn PJ; et al. Fragile X mouse: Strain effects of knockout phenotype and evidence suggesting deficient amygdala function | 23 | 42 |
| 649 | 6 | 23 | 649 1999 PRENATAL DIAGNOSIS 19(13):1223-1230 Sermon K; Seneca S; Vanderfaeillie A; Lissens W; Joris H; et al. Preimplantation diagnosis for fragile X syndrome based on the detection of the non-expanded paternal and maternal CGG | 2 | 26 |
| 650 | 10 | 43 | 650 1999 RNA-A PUBLICATION OF THE RNA SOCIETY 5(9):1248-1258 Adinolfi S; Bagni C; Musco G; Gibson T; Mazzarella L; et al. Dissecting FMR1, the protein responsible for fragile X syndrome, in its structural and functional domains | 22 | 29 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 651 | 3 | 20 | 651 1999 ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 27(3):175-181 Sarimski K Play and communicative behaviour in young boys with fragile-X syndrome. | 0 | 1 |
| 652 | 7 | 40 | 652 2000 AMERICAN JOURNAL OF HUMAN GENETICS 66(1):6-15 Tassone F; Hagerman RJ; Taylor AK; Gane LW; Godfrey TE; et al. Elevated levels of FMR1 mRNA in carrier males: A new mechanism of involvement in the fragile-X syndrome | 62 | 96 |
| 653 | 6 | 28 | 653 2000 AMERICAN JOURNAL OF HUMAN GENETICS 66(2):413-418 Hundscheid RDL; Sistermans EA; Thomas CMG; Braat DDM; Straatman H; et al. Imprinting effect in premature ovarian failure confined to paternally inherited fragile X premutations | 15 | 31 |
| 654 | 16 | 52 | 654 2000 AMERICAN JOURNAL OF HUMAN GENETICS 66(2):480-493 Crawford DC; Schwartz CE; Meadows KL; Newman JL; Taft LF; et al. Survey of the fragile X syndrome CGG repeat and the short-tendem-repeat and single-nucleotide-polymorphism haplotypes in an African American population | 9 | 18 |
| 655 | 6 | 8 | 655 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(1):11-13 Sherman SL Premature ovarian failure among fragile X premutation carriers: Parent-of-origin effect? | 4 | 8 |
| 656 | 1 | 4 | 656 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(1):253-254 Murray A; Ennis S; Morton N No evidence for parent of origin influencing premature ovarian failure in fragile X premutation carriers | 9 | 17 |
| 657 | 4 | 8 | 657 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(1):254-255 Vianna-Morgante AM; Costa SS Premature ovarian failure is associated with maternally and paternally inherited premutation in Brazilian families with fragile X | 8 | 16 |
| 658 | 3 | 3 | 658 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(1):256-258 Hundscheid RDL; Thomas CMG; Braat DDM; Oostra BA; Smits APT Premature ovarian failure is associated with maternally and paternally inherited premutation in Brazilian families with fragile X - Reply | 2 | 5 |
| 659 | 0 | 0 | 659 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):18-18 Brown V; Ceman S; Jin P; Jin C; Wilkinson KD; et al. Messenger RNAs associated with the fragile X mental retardation protein in mouse brain. | 1 | 1 |
| 660 | 0 | 0 | 660 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):18-18 Jin P; Feng Y; Brown V; Warren ST Identification of polyribosomes-associated mRNAs regulated by fragile X mental retardation protein (FMRP) using oligonucleotide microarrays. | 1 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 661 | 0 | 0 | 661 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):25-25 Crawford DC; Wilson B; Sherman SL Factors involved in the initial mutation of the fragile X CGG repeat as determined by sperm small pool-PCR. | 0 | 0 |
| 662 | 0 | 0 | 662 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):26-26 Hagerman RJ; Tassone F; Leehey M; Hills J; Wilson R; et al. Cerebellar tremor and cerebellar cortical atrophy in older males with the fragile X premutation. | 0 | 0 |
| 663 | 0 | 0 | 663 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):50-50 Neri G; Pomponi MG; Pietrobono R; Chiurazzi P; Oostra BA Differential reactivation of the FMR1 gene in fragile X patients cell lines. | 0 | 0 |
| 664 | 0 | 0 | 664 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):50-50 Kenneson A; Zhang F; Warren ST Fragile X premutation alleles are associated with reduced FMRP levels due to a reduction of message translatability. | 0 | 0 |
| 665 | 0 | 0 | 665 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):57-57 Li MM; Nelson L; Bamshad M; Ward K Fragile X mosaics in a family with multiple mildly affected individuals. | 0 | 0 |
| 666 | 0 | 0 | 666 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):130-130 Khalifa M; Struthers J High frequency of Klinefelter syndrome among a large population of patients referred for Fragile X syndrome testing due to undiagnosed mental retardation. | 0 | 0 |
| 667 | 0 | 0 | 667 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):135-135 Harris SW; Brown KE; Hills JL; Tassone F; Hagerman PJ; et al. Adaptive functioning and molecular relationships in individuals with fragile X syndrome. | 0 | 0 |
| 668 | 0 | 0 | 668 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):184-184 Tassone F; Hagerman RJ; Taylor AK; Hagerman PJ Clinical and molecular correlations in individuals with a fragile X full mutation. | 0 | 0 |
| 669 | 0 | 0 | 669 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):200-200 Ceman SS; Kenneson A; Nelson R; Jin C; Lakkis L; et al. Development and characterization of a unique set of anti-FMRP antibodies using a novel strategy. | 0 | 0 |
| 670 | 0 | 0 | 670 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):236-236 Mathews DJ; Hudson R; Eichier E; Chakravarti A Sequence variation and linkage disequilibrium at the fragile X syndrome locus. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 671 | 0 | 0 | 671 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):238-238 Sullivan AK; Crawford DC; Meadows KL; Wilson B; Sherman SL Parent-child transmission of intermediate FMR1 CGG repeat alleles: Examination of factors associated with repeat instability. | 0 | 0 |
| 672 | 0 | 0 | 672 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):247-247 Brown NM; Friez MJ; Longshore JW; Stenzel TT Evaluation of an automated commercially available PCR kit for determination of Fragile X (FRAXA) normal, gray-zone and premutation allele sizes. | 0 | 0 |
| 673 | 0 | 0 | 673 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):248-248 Murphy KM; Nunes ME Comparison of child-only versus mother/child sample collection in Fragile X testing. | 0 | 0 |
| 674 | 0 | 0 | 674 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):254-254 Weinhaeusel A; Skarits C; Haas OA Methylation-sensitive PCR (MS-PCR) analysis of the fragile X (FRAXA) syndrome. | 0 | 0 |
| 675 | 0 | 0 | 675 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):348-348 Dyack S; Steele L; Koultchitski G; Yang Y; Weksberg R; et al. AGG interruptions in the CGG trinucleotide repeat tract of the FMR1 gene may contribute to stability of Fragile X premutations. | 0 | 0 |
| 676 | 0 | 0 | 676 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):360-360 Ramos FJ; Mila M; Ortilles M; Rife M; Tazon B; et al. Validity of the analysis of the FMRP expression in bloodsmears as a screening method for the Fragile X Syndrome. | 1 | 1 |
| 677 | 0 | 0 | 677 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):364-364 Chen SH; Xu B; Shoof JM; Buroker NE; Scott CR Evidence for a stepwise expansion of the CGG repeats within the FMR1 gene. | 0 | 0 |
| 678 | 0 | 0 | 678 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):365-365 O'Donnell WT; Warren ST Investigating the cause of macroorchidism in fragile X syndrome using oligonucleotide microarrays. | 0 | 0 |
| 679 | 0 | 0 | 679 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):365-365 Nolin SL; Rousseau F; Houck GE; Gargano AD; Biancalana V; et al. FMR1 CGG expansion to full mutation: What is the lower limit in premutation females? | 0 | 0 |
| 680 | 0 | 0 | 680 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):366-366 Raca G; Siyanova E; Mirkin S Janus effects of premutation size CGG repeats on gene expression. | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 681 | 0 | 0 | 681 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):366-366 Parades WJ; Warren ST Meiotic stability of a fragile X premutation CGG trinucleotide repeat in a mouse model. | 0 | 0 |
| 682 | 0 | 0 | 682 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):415-415 Najmabadi H; Taghizadeh F; Teimourian SH; Karimi-Nejad R; Shafeghati Y; et al. Molecular analysis of Fragile X syndrome in Iranian population. | 0 | 0 |
| 683 | 0 | 0 | 683 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):428-428 Brown WT; Ding X; Idrissi AE; Scalia J; Glicksman A; et al. Fragile X transgene and embryonic lethality in mice. | 0 | 0 |
| 684 | 1 | 42 | 684 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 92(4):229-236 Lachiewicz AM; Dawson DV; Spiridigliozzi GA Physical characteristics of young boys with fragile X syndrome: Reasons for difficulties in making a diagnosis in young males | 12 | 13 |
| 685 | 3 | 22 | 685 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 92(5):336-342 McConkie-Rosell A; Spiridigliozzi GA; Sullivan JA; Dawson DV; Lachiewicz AM Carrier testing in fragile X syndrome: Effect on self-concept | 2 | 4 |
| 686 | 8 | 33 | 686 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 93(2):99-106 Larsen LA; Armstrong JSM; Gronskov K; Hjalgrim H; Macpherson JN; et al. Haplotype and AGG-interspersion analysis of FMR1 (CGG)(n) alleles in the Danish population: Implications for multiple mutational pathways towards fragile X alleles | 4 | 6 |
| 687 | 10 | 35 | 687 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 94(3):232-236 Tassone F; Hagerman RJ; Loesch DZ; Lachiewicz A; Taylor AK; et al. Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA | 20 | 26 |
| 688 | 3 | 24 | 688 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 94(5):345-360 Fryns JP; Borghgraef M; Brown TW; Chelly J; Fisch GS; et al. 9th international workshop on fragile X syndrome and X-linked mental retardation | 0 | 3 |
| 689 | 5 | 14 | 689 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(2):105-107 Tuncbilek E; Alikasifoglu M; Aktas D; Duman F; Yanik H; et al. Screening for the fragile X syndrome among mentally retarded males by hair root analysis | 6 | 6 |
| 690 | 6 | 33 | 690 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(2):123-129 Hjalgrim H; Hansen BF; Brondum-Nielsen K; Nolting D; Kjaer I Aspects of skeletal development in fragile X syndrome fetuses | 2 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 691 | 10 | 59 | 691 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(2):150-156 Backes M; Genc B; Schreck J; Doerfler W; Lehmkuhl G; et al. Cognitive and behavioral profile of fragile X boys: Correlations to molecular data | 8 | 12 |
| 692 | 8 | 46 | 692 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(4):307-315 Gould EL; Loesch DZ; Martin MJ; Hagerman RJ; Armstrong SM; et al. Melatonin profiles and sleep characteristics in boys with fragile X syndrome: A preliminary study | 13 | 19 |
| 693 | 2 | 11 | 693 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(4):358-360 Missirian C; Moncla A; Voelckel MA; Ravix V; Philip N Fragile X syndrome and 22q11.2 microdeletion in the same sibship | 0 | 0 |
| 694 | 1 | 9 | 694 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(5):516-517 Limprasert P; Jaruratanasirikul S; Vasiknanonte P Unilateral macroorchidism in fragile X syndrome | 2 | 2 |
| 695 | 54 | 116 | 695 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 97(2):153-163 Bardoni B; Mandel JL; Fisch GS FMR1 gene and fragile X syndrome | 12 | 21 |
| 696 | 20 | 48 | 696 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 97(3):183-188 Willemsen R; Oostra BA FMRP detection assay for the diagnosis of the fragile X syndrome | 2 | 4 |
| 697 | 16 | 33 | 697 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 97(3):189-194 Sherman SL Premature ovarian failure in the fragile X syndrome | 15 | 30 |
| 698 | 12 | 40 | 698 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 97(3):195-203 Tassone F; Hagerman RJ; Chamberlain WD; Hagerman PJ Transcription of the FMR1 gene in individuals with fragile X syndrome | 29 | 34 |
| 699 | 3 | 37 | 699 2000 AMERICAN JOURNAL ON MENTAL RETARDATION 105(4):286-299 Kau ASM; Reider EE; Payne L; Meyer WA; Freund L Early behavior signs of psychiatric phenotypes in fragile X syndrome | 2 | 4 |
| 700 | 11 | 37 | 700 2000 ANNALES DE GENETIQUE 43(1):29-34 Gonzalez-del Angel A; Vidal S; Saldana Y; del Castillo V; Alcantara MA; et al. Molecular diagnosis of the fragile X and FRAXE syndromes in patients with mental retardation of unknown cause in Mexico | 2 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 701 | 0 | 19 | 701 2000 ANNALS OF SAUDI MEDICINE 20(1):16-19 Al Husain M; Salih MAM; Zaki OK; Al Othman L; Al Nasser MN A clinical study of mentally retarded children with fragile X syndrome in Saudi Arabia | 0 | 0 |
| 702 | 3 | 41 | 702 2000 ANNALS OF SAUDI MEDICINE 20(3-4):214-217 Iqbal MA; Sakati N; Nester M; Ozand P Cytogenetic diagnosis of fragile X syndrome: Study of 305 suspected cases in Saudi Arabia | 0 | 0 |
| 703 | 3 | 8 | 703 2000 AUSTRALIAN AND NEW ZEALAND JOURNAL OF MEDICINE 30(1):86-88 Driscoll G; Clark J; Elakis G; Turner G Early menopause in a family carrying a fragile X premutation | 1 | 3 |
| 704 | 2 | 29 | 704 2000 BEHAVIOR RESEARCH METHODS INSTRUMENTS & COMPUTERS 32(1):5-10 Boccia ML; Roberts JE Behavior and autonomic nervous system function assessed via heart period measures: The case of hyperarousal in boys with fragile X syndrome | 8 | 11 |
| 705 | 6 | 19 | 705 2000 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 275(2):608-610 Beaulieu MA A distinct FMRP polysomal population at an advanced stage of mammalian erythropoiesis | 2 | 2 |
| 706 | 6 | 33 | 706 2000 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 275(3):973-980 Sung YJ; Conti J; Currie JR; Brown WT; Denman RB RNAs that interact with the Fragile X syndrome RNA binding protein FMRP | 27 | 35 |
| 707 | 3 | 46 | 707 2000 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 278(3):833-838 Patel PK; Bhavesh NS; Hosur RV Cation-dependent conformational switches in d-TGGCGGC containing two triplet repeats of Fragile X Syndrome: NMR observations | 4 | 9 |
| 708 | 9 | 38 | 708 2000 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 279(3):904-908 Ceman S; Nelson R; Warren ST Identification of mouse YB1/p50 as a component of the FMRP-associated mRNP particle | 21 | 29 |
| 709 | 4 | 52 | 709 2000 BRAIN AND COGNITION 44(3):387-401 Munir F; Cornish KM; Wilding J Nature of the working memory deficit in Fragile-X syndrome | 8 | 9 |
| 710 | 6 | 14 | 710 2000 BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY 107(8):969-972 Kallinen J; Korhonen K; Kortelainen S; Heinonen S; Ryynanen M Pregnancy outcome in carriers of fragile X | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 711 | 4 | 59 | 711 2000 CELL 100(3):323-332 Lewis HA; Musunuru K; Jensen KB; Edo C; Chen H; et al. Sequence-specific RNA binding by a Nova KH domain: Implications for paraneoplastic disease and the fragile X syndrome | 9 | 97 |
| 712 | 17 | 79 | 712 2000 CEREBRAL CORTEX 10(10):1038-1044 Irwin SA; Galvez R; Greenough WT Dendritic spine structural anomalies in fragile-X mental retardation syndrome | 35 | 55 |
| 713 | 14 | 38 | 713 2000 CEREBRAL CORTEX 10(10):1045-1052 Braun K; Segal M FMRP involvement in formation of synapses among cultured hippocampal neurons | 21 | 23 |
| 714 | 3 | 18 | 714 2000 CHINESE SCIENCE BULLETIN 45(6):516-520 Chen YT; Bardoni B; Yu M; Zhu N; Wu GY; et al. Fragile X mental retardation protein interacts with TDG | 0 | 0 |
| 715 | 0 | 0 | 715 2000 CLINICAL CHEMISTRY 46(6):A206-A206 Boday A; Prusa R; Matoska V Radioactive PCR for the screening and diagnostics of fragile X chromosome syndrome - FRAXA. | 0 | 0 |
| 716 | 1 | 12 | 716 2000 CLINICAL CHEMISTRY AND LABORATORY MEDICINE 38(9):935-938 Poon PMK; Zhao Z; Wu XQ; Ni YX; Pang CP Rapid analysis of CGG repeat length in the FMR1 gene | 0 | 0 |
| 717 | 1 | 13 | 717 2000 CLINICAL GENETICS 57(6):456-458 Lisik M The comparison of anthropometric variables in mentally retarded boys with and without fragile X syndrome | 0 | 0 |
| 718 | 11 | 33 | 718 2000 CLINICAL GENETICS 58(2):111-115 Kallinen J; Heinonen S; Mannermaa A; Ryynanen M Prenatal diagnosis of fragile X syndrome and the risk of expansion of a premutation | 3 | 5 |
| 719 | 0 | 13 | 719 2000 CLINICAL RHEUMATOLOGY 19(4):262-264 Granel B; Ravix V; Pedeillier K; Serratrice J; Disdier P; et al. A first molecular approach towards CGG repeat expansion in FMR1 gene in systemic lupus erythematosus and in Sjogren's syndrome: A preliminary report | 0 | 0 |
| 720 | 1 | 6 | 720 2000 CYTOGENETICS AND CELL GENETICS 89(1-2):11-13 Bardoni B; Giglio S; Schenck A; Rocchi M; Mandel JL Assignment of NUFIP1 (Nuclear FMRP Interacting Protein 1) gene to chromosome 13q14 and assignment of a pseudogene to chromosome 6q12 | 2 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 721 | 2 | 46 | 721 2000 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 42(11):768-774 Sheldon L; Turk J Monozygotic boys with fragile X syndrome | 1 | 2 |
| 722 | 0 | 43 | 722 2000 EMBO JOURNAL 19(17):4745-4758 Yaremchuk A; Cusack S; Tukalo M Crystal structure of a eukaryote/archaeon-like prolyl-tRNA synthetase and its complex with tRNA(Pro)(CGG) | 0 | 31 |
| 723 | 7 | 32 | 723 2000 EPILEPSIA 41(1):19-23 Musumeci SA; Bosco P; Calabrese G; Bakker C; De Sarro GB; et al. Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome | 26 | 35 |
| 724 | 5 | 21 | 724 2000 EUROPEAN JOURNAL OF HUMAN GENETICS 8(4):247-252 Murray A; Ennis S; MacSwiney F; Webb J; Morton NE Reproductive and menstrual history of females with fragile X expansions | 11 | 15 |
| 725 | 0 | 0 | 725 2000 EUROPEAN JOURNAL OF NEUROSCIENCE 12:104-104 Braun K; Segal M FMRP involvement in the formation of functional synaptic connections among cultured hippocampal neurons | 0 | 0 |
| 726 | 0 | 0 | 726 2000 EUROPEAN JOURNAL OF NEUROSCIENCE 12:305-305 Beckel-Mitchener AC; Weiler IJ; Klintsova AY; Harms L; Belt B; et al. Analysis of protein synthesis in Fragile X knockout mice | 0 | 0 |
| 727 | 0 | 18 | 727 2000 EUROPEAN JOURNAL OF NEUROSCIENCE 12(1):381-384 Miller WJ; Skinner JA; Foss GS; Davies KE Localization of the fragile X mental retardation 2 (FMR2) protein in mammalian brain | 0 | 7 |
| 728 | 16 | 40 | 728 2000 EXPERIMENTAL CELL RESEARCH 258(1):162-170 Bakker CE; Otero YD; Bontekoe C; Raghoe P; Luteijn T; et al. Immunocytochemical and biochemical characterization of FMRP, FXR1P, and FXR2P in the mouse | 22 | 31 |
| 729 | 0 | 0 | 729 2000 GENETIC COUNSELING 11(3):281-311 [Anon] ACTS: Of the 9th International Workshop on Fragile X Syndrome and X Linked Mental Retardation August 23-25, 1999, Le Bischenberg, Strasbourg, France - Abstracts | 0 | 0 |
| 730 | 2 | 16 | 730 2000 GENETIC TESTING 4(3):235-239 Tzountzouris J; Kennedy D; Skuterud M; Connolly-Wilson M; Holden JJA; et al. Apparently unstable normal FMR1 alleles in nine developmentally delayed patients: Implications for molecular diagnosis of the Fragile X syndrome | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 731 | 4 | 10 | 731 2000 GENETIC TESTING 4(3):241-242 Brown WT; Nolin SL Apparent FMR1 allele instability in non-Fragile X males - Invited commentary | 0 | 1 |
| 732 | 5 | 20 | 732 2000 GENETIC TESTING 4(3):289-292 Geva E; Yaron Y; Shomrat R; Ben-Yehuda A; Zabari S; et al. The risk of Fragile X premutation expansion is lower in carriers detected by general prenatal screening than in carriers from known Fragile X families | 3 | 4 |
| 733 | 12 | 44 | 733 2000 GENETICS IN MEDICINE 2(4):242-248 Burman RW; Anoe KS; Popovich BW Fragile X full mutations ave more similar in siblings than in unrelated patients: further evidence for a familial factor in CGG repeat dynamics | 1 | 2 |
| 734 | 8 | 12 | 734 2000 HUMAN GENETICS 106(3):366-369 Arocena DG; de Diego Y; Oostra BA; Willemsen R; Rodriguez MM A fragile X case with an amplification/deletion mosaic pattern | 0 | 0 |
| 735 | 3 | 6 | 735 2000 HUMAN GENETICS 107(2):195-196 Castellvi-Bel S; Fernandez-Burriel M; Rife M; Jimenez D; Mallolas J; et al. Detection of the fragile X syndrome protein for the evaluation of FMR1 intermediate alleles | 1 | 3 |
| 736 | 8 | 62 | 736 2000 HUMAN MOLECULAR GENETICS 9(1):93-100 Balakumaran BS; Freudenreich CH; Zakian VA CGG/CCG repeats exhibit orientation-dependent instability and orientation-independent fragility in Saccharomyces cerevisiae | 0 | 20 |
| 737 | 32 | 82 | 737 2000 HUMAN MOLECULAR GENETICS 9(6):901-908 Jin P; Warren ST Understanding the molecular basis of fragile X syndrome | 44 | 82 |
| 738 | 19 | 55 | 738 2000 HUMAN MOLECULAR GENETICS 9(10):1487-1493 Tamanini F; Kirkpatrick LL; Schonkeren J; van Unen L; Bontekoe C; et al. The fragile X-related proteins FXR1P and FXR2P contain a functional nucleolar-targeting signal equivalent to the HIV-1 regulatory proteins | 9 | 14 |
| 739 | 27 | 62 | 739 2000 HUMAN MOLECULAR GENETICS 9(12):1759-1769 Crawford DC; Zhang FP; Wilson B; Warren ST; Sherman SL Fragile X CGG repeat structures among African-Americans: identification of a novel factor responsible for repeat instability | 7 | 11 |
| 740 | 21 | 55 | 740 2000 HUMAN MOLECULAR GENETICS 9(19):2909-2918 Crawford DC; Wilson B; Sherman SL Factors involved in the initial mutation of the fragile X CGG repeat as determined by sperm small pool PCR | 3 | 11 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 741 | 0 | 0 | 741 2000 HUMAN REPRODUCTION 15:12-12 Apessos A; Harper J; Delhanty JDA Preimplantation genetic diagnosis of the fragile X syndrome by use of linked polymorphic markers | 0 | 0 |
| 742 | 0 | 0 | 742 2000 HUMAN REPRODUCTION 15:47-48 Hundscheid RDL; Sistermans EA; Thomas CMG; Straatman H; Kiemeney LALM; et al. Shorter reproductive life and a high risk for premature ovarian failure (POF) in women who have inherited fragile X premutations from their fathers | 0 | 0 |
| 743 | 10 | 41 | 743 2000 HUMAN REPRODUCTION 15(1):197-202 Marozzi A; Vegetti W; Manfredini E; Tibiletti MG; Testa G; et al. Association between idiopathic premature ovarian failure and fragile X premutation | 10 | 30 |
| 744 | 1 | 2 | 744 2000 HUMAN REPRODUCTION 15(8):1874-1874 Rychlik DF Regarding recall bias in the association between idiopathic premature ovarian failure and fragile X premutation | 0 | 0 |
| 745 | 1 | 2 | 745 2000 HUMAN REPRODUCTION 15(8):1874-1875 Marozzi A Regarding recall bias in the association between idiopathic premature ovarian failure and fragile X premutation | 1 | 1 |
| 746 | 0 | 0 | 746 2000 INFANT MENTAL HEALTH JOURNAL 21(4-5):243-243 Lis A; Zennaro A; Pinto M; Peroni S; Snaidero R Paternal styles identified with the self reflective scale and the CGG | 0 | 0 |
| 747 | 0 | 0 | 747 2000 INFANT MENTAL HEALTH JOURNAL 21(4-5):330-330 Ghuman JK; Tierney E; Kau A; Reider E Social interaction problems in infants and preschool children with fragile-X syndrome, Smith-Lemli-Opitz syndrome and other developmental disorders | 0 | 0 |
| 748 | 4 | 41 | 748 2000 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 30(1):49-59 Bailey DB; Hatton DD; Mesibov G; Ament N; Skinner M Early development, temperament, and functional impairment in autism and fragile X syndrome | 16 | 19 |
| 749 | 12 | 50 | 749 2000 JOURNAL OF BIOLOGICAL CHEMISTRY 275(3):2231-2238 Weisman-Shomer P; Naot Y; Fry M Tetrahelical forms of the fragile X syndrome expanded sequence d(CGG)(n) are destabilized by two heterogeneous nuclear ribonucleoprotein-related telomeric DNA-binding proteins | 7 | 10 |
| 750 | 5 | 29 | 750 2000 JOURNAL OF BIOLOGICAL CHEMISTRY 275(9):6447-6452 Muller-Hartmann H; Deissler H; Naumann F; Schmitz B; Schroer J; et al. The human 20-kDa 5 '-(CGG)(n)-3 '-binding protein is targeted to the nucleus and affects the activity of the FMR1 promoter | 11 | 16 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 751 | 15 | 59 | 751 2000 JOURNAL OF BIOLOGICAL CHEMISTRY 275(42):33134-33141 Uliel L; Weisman-Shomer P; Oren-Jazans H; Newcomb T; Loeb LA; et al. Human Ku antigen tightly binds and stabilizes a tetrahelical form of the fragile X syndrome d(CGG)(n) expanded sequence | 1 | 7 |
| 752 | 0 | 0 | 752 2000 JOURNAL OF COGNITIVE NEUROSCIENCE :57-57 Merin NM; Menon V; White CD; Glover GH; Reiss AL Gaze processing deficits in fragile X syndrome investigated using fMRI | 0 | 0 |
| 753 | 0 | 0 | 753 2000 JOURNAL OF COGNITIVE NEUROSCIENCE :98-98 White CD; Menon V; Eliez S; Reiss AL An fMRI study of brain activation in Fragile X Syndrome during a go-nogo task | 0 | 0 |
| 754 | 0 | 0 | 754 2000 JOURNAL OF COGNITIVE NEUROSCIENCE :146-146 Kwon H; Menon V; Eliez S; Dyer-Friedman J; Glover GH; et al. Functional neuroanatomy of visuospatial working memory in fragile X syndrome: Relation to behavior and FMR-1 protein expression | 0 | 0 |
| 755 | 5 | 39 | 755 2000 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 21(4):278-282 Wisbeck JM; Huffman LC; Freund L; Gunnar MR; Davis EP; et al. Cortisol and social stressors in children with fragile X: A pilot study | 9 | 11 |
| 756 | 4 | 32 | 756 2000 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 21(5):315-321 Bailey DB; Skinner D; Hatton D; Roberts J Family experiences and factors associated with the diagnosis of fragile X syndrome | 12 | 15 |
| 757 | 2 | 16 | 757 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:81-85 Sabaratnam M Pathological and neuropathological findings in two males with fragile-X syndrome | 2 | 4 |
| 758 | 0 | 0 | 758 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:189-189 Abbeduto L; Kesin E; Pavetto M; Weissman M; O'Brien A; et al. Theory of mind deficits in mental retardation: a comparison of Down syndrome and fragile-X syndrome | 0 | 0 |
| 759 | 0 | 0 | 759 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:222-222 Brown WT; Nolin S; Houck G; Ding X; Glicksman A; et al. Progress fragile-X syndrome analysis | 0 | 0 |
| 760 | 0 | 0 | 760 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:247-247 Cornish KM; Munir F Profile of memory and attention problems in adults with fragile-X syndrome: Clinical and educational implications | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 761 | 0 | 0 | 761 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:273-273 Einfeld SL; Tonge B; Turner G; Parmenter T; Smith A Longitudinal course of behavioural and emotional problems of young persons with Prader-Willi, fragile-X, Williams and Down syndromes | 0 | 0 |
| 762 | 0 | 0 | 762 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:305-305 Hagerman RJ; Miller LJ; McGrath-Clarke J; Riley K; Goldson E; et al. Influence of stimulants on electrodermal studies in fragile-X syndrome | 0 | 0 |
| 763 | 0 | 0 | 763 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:317-317 Karrer JH; Hagerman RJ; Karrer RS; Fitzpatrick D; Vavold J; et al. Genotypic-specific event-related brain potentials among infants and toddlers with fragile-X syndrome and Down syndrome | 1 | 1 |
| 764 | 0 | 0 | 764 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:318-318 Hills JL; Wilson R; Sobesky W; Harris SW; Grigsby J; et al. Executive functioning deficits in adult males with the fragile-X premutation: an emerging phenotype | 0 | 0 |
| 765 | 0 | 0 | 765 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:374-374 Lung FW; Shu BC Fragile-X syndrome in adolescent prostitutes | 0 | 0 |
| 766 | 0 | 0 | 766 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:380-380 Manjunatha KR; Chettn GK; Arathi R; Bhaskar RG; Nandini PM; et al. Fragile-X syndrome: Cytogenetics and molecular analysis of subjects from Indian population | 0 | 0 |
| 767 | 0 | 0 | 767 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:405-405 Munir F; Comish KM; Wilding J A neuropsychological profile of attention and hyperactivity in boys with fragile-X syndrome: Implications for clinical intervention | 0 | 0 |
| 768 | 0 | 0 | 768 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:419-419 Orsmond G; Abbeduto L; Pavetto M; O'Brien A; Kesin E; et al. Stress and coping in parents of adolescents and young adults with fragile-X syndrome or Down syndrome | 0 | 0 |
| 769 | 0 | 0 | 769 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:449-449 Sabaratnam M; Murthy V; Wijeratne A Fragile-X syndrome: A 10-year follow-up | 0 | 0 |
| 770 | 0 | 0 | 770 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:483-483 Tassone F; Hagerman RJ; Loesch DZ; Lachiewicz A; Taylor AK; et al. FMRI messenger RNA levels in male subjects with fragile-X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 771 | 0 | 0 | 771 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:496-497 Tzeng CC; Lin SJ; Chen YY; Chen RM An effective strategy of using a molecular test to screen individuals with mental retardation for fragile-X syndrome | 0 | 0 |
| 772 | 0 | 0 | 772 2000 JOURNAL OF INVESTIGATIVE MEDICINE 48(1):11A-11A Peterson TL; Hagerman RJ; Tassone F Genotype-phenotype relationships in fragile X families. | 0 | 0 |
| 773 | 0 | 0 | 773 2000 JOURNAL OF MEDICAL GENETICS 37:S18-S18 Mandel JL The fragile X syndrome: from families to CGG expansions and FMR1 gene function | 0 | 0 |
| 774 | 0 | 0 | 774 2000 JOURNAL OF MEDICAL GENETICS 37:S20-S20 Fisher A; Macpherson JN; Dennis NR; Barber JCK Targeted testing for fragile X: an audit of the first year. | 0 | 0 |
| 775 | 0 | 0 | 775 2000 JOURNAL OF MEDICAL GENETICS 37:S44-S44 James T; Trigg A; Lindley VH; Fews GA; Roberts E; et al. An unexpected finding of fragile X (FRAXA) syndrome in a fetal blood sample referred for abnormalities on ultrasound scan | 0 | 0 |
| 776 | 0 | 0 | 776 2000 JOURNAL OF MEDICAL GENETICS 37:S66-S66 Lazarou LP; Myring J; Knight SJL; Gardner AP; Clarke A Fragile X (E) syndrome. How common is it? | 0 | 0 |
| 777 | 0 | 0 | 777 2000 JOURNAL OF MEDICAL GENETICS 37:S75-S75 Fratter C; Morsman A; Seller A Genetic analysis for Fragile X syndrome by fluorescent PCR | 0 | 0 |
| 778 | 0 | 0 | 778 2000 JOURNAL OF MEDICAL GENETICS 37:S78-S78 Chotai K; Buckingham AE; Bentley CM; Wycherley RJ; Payne SJ Fragile-X intermediate alleles - A clinical dilemma | 0 | 0 |
| 779 | 5 | 36 | 779 2000 JOURNAL OF MEDICAL GENETICS 37(1):77-79 Beresford RG; Tatlidil C; Riddell DC; Welch JP; Ludman MD; et al. Absence of fragile X syndrome in Nova Scotia | 4 | 5 |
| 780 | 5 | 16 | 780 2000 JOURNAL OF MEDICAL GENETICS 37(8):603-604 Willemsen R; Olmer R; Otero YD; Oostra BA Twin sisters, monozygotic with the fragile X mutation, but with a different phenotype | 8 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 781 | 20 | 66 | 781 2000 JOURNAL OF MEDICAL GENETICS 37(11):842-850 Salat U; Bardoni B; Wohrle D; Steinbach P Increase of FMRP expression, raised levels of FMR1 mRNA, and clonal selection in proliferating cells with unmethylated fragile X repeat expansions: a clue to the sex bias in the transmission of full mutations? | 4 | 6 |
| 782 | 3 | 6 | 782 2000 JOURNAL OF MOLECULAR DIAGNOSTICS 2(3):128-131 Daly TM; Rafii A; Martin RA; Zehnbauer BA Novel polymorphism in the FMR1 gene resulting in a "pseudodeletion" of FMR1 in a commonly used fragile X assay | 0 | 0 |
| 783 | 2 | 15 | 783 2000 JOURNAL OF PSYCHOEDUCATIONAL ASSESSMENT 18(3):255-267 Hooper SR; Hatton DD; Baranek GT; Roberts JP; Bailey DB Nonverbal assessment of IQ, attention, and memory abilities in children with fragile-X syndrome using the Leiter-R | 1 | 1 |
| 784 | 2 | 5 | 784 2000 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 39(2):264-266 Eliez S; Reiss AL Generics of childhood disorders: XI. Fragile X syndrome | 0 | 0 |
| 785 | 1 | 5 | 785 2000 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 39(4):398-398 Levitas A Fragile X syndrome | 0 | 0 |
| 786 | 0 | 5 | 786 2000 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 39(4):398-399 Lombroso PJ Fragile X syndrome - Dr. Lombroso replies | 0 | 0 |
| 787 | 2 | 17 | 787 2000 JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION 99(5):402-407 Wang YC; Li C; Lin ML; Lin WH; Li SY Molecular diagnosis of fragile X syndrome and distribution of CGG repeats in the FMR-1 gene in Taiwanese | 0 | 0 |
| 788 | 0 | 1 | 788 2000 LIBRARY JOURNAL 125(11):105-105 Griffin KH Children with Fragile X Syndrome: A parents' guide. | 0 | 0 |
| 789 | 2 | 29 | 789 2000 MENTAL RETARDATION 38(3):207-215 Maes B; Fryns JP; Ghesquiere P; Borghgraef M Phenotypic checklist to screen for fragile X syndrome in people with mental retardation | 2 | 5 |
| 790 | 34 | 117 | 790 2000 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 6(2):96-106 Mazzocco MMM Advances in research on the fragile X syndrome | 20 | 24 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 791 | 14 | 74 | 791 2000 MOLECULAR AND CELLULAR BIOLOGY 20(22):8536-8547 Wan LL; Dockendorff TC; Jongens TA; Dreyfuss G Characterization of dFMR1, a Drosophila melanogaster homolog of the fragile X mental retardation protein | 44 | 57 |
| 792 | 6 | 20 | 792 2000 MOLECULAR AND CELLULAR PROBES 14(2):115-119 Mila M; Castellvi-Bel S; Sanchez A; Barcelo A; Badenas C; et al. Rare variants in the promoter of the fragile X syndrome gene (FMR1) | 5 | 5 |
| 793 | 6 | 32 | 793 2000 MOLECULAR BRAIN RESEARCH 75(2):337-341 Valentine G; Chakravarty S; Sarvey J; Bramham C; Herkenham M Fragile X (fmr1) mRNA expression is differentially regulated in two adult models of activity-dependent gene expression | 7 | 9 |
| 794 | 12 | 37 | 794 2000 MOLECULAR BRAIN RESEARCH 80(1):17-25 Todd PK; Mack KJ Sensory stimulation increases cortical expression of the fragile X mental retardation protein in vivo | 17 | 17 |
| 795 | 15 | 43 | 795 2000 MOLECULAR DIAGNOSIS 5(3):169-178 Gold B; Radu D; Balanko A; Chiang CS Diagnosis of Fragile X syndrome by Southern blot hybridization using a chemiluminescent probe: A laboratory protocol | 0 | 1 |
| 796 | 24 | 45 | 796 2000 MOLECULAR MEDICINE TODAY 6(5):193-198 Kooy RF; Willemsen R; Oostra BA Fragile X syndrome at the turn of the century | 15 | 21 |
| 797 | 3 | 13 | 797 2000 NEUROBIOLOGY OF LEARNING AND MEMORY 73(1):87-93 Irwin SA; Swain RA; Christmon CA; Chakravarti A; Weiler IJ; et al. Evidence for altered Fragile-X mental retardation protein expression in response to behavioral stimulation | 23 | 27 |
| 798 | 4 | 14 | 798 2000 NEUROBIOLOGY OF LEARNING AND MEMORY 74(1):80-93 Irwin SA; Swain RA; Christmon CA; Chakravarti A; Weiler IJ; et al. Evidence for altered fragile-x mental retardation protein expression in response to behavioral stimulation (vol 73, pg 87, 2000) | 2 | 2 |
| 799 | 3 | 47 | 799 2000 NEUROPSYCHOLOGIA 38(9):1261-1270 Munir F; Cornish KM; Wilding J A neuropsychological profile of attention deficits in young males with fragile X syndrome | 17 | 21 |
| 800 | 10 | 53 | 800 2000 NEUROSCIENCE RESEARCH COMMUNICATIONS 26(3):255-263 de Vries BBA; Oostra BA The fragile X syndrome: A model for mental retardation | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 801 | 3 | 18 | 801 2000 NEUROSCIENCE RESEARCH COMMUNICATIONS 26(3):265-277 Bakker CE; Kooy RF; D'Hooge R; Tamanini F; Willemsen R; et al. Introduction of a FMR1 transgene in the fragile X knockout mouse. | 3 | 3 |
| 802 | 14 | 45 | 802 2000 NUCLEIC ACIDS RESEARCH 28(7):1535-1541 Weisman-Shomer P; Cohen E; Fry M Interruption of the fragile X syndrome expanded sequence d(CGG)(n) by interspersed d(AGG) trinucleotides diminishes the formation and stability of d(CGG)(n) tetrahelical structures | 6 | 11 |
| 803 | 4 | 42 | 803 2000 NUCLEIC ACIDS RESEARCH 28(10):2141-2152 Genc B; Muller-Hartmann H; Zeschnigk M; Deissler H; Schmitz B; et al. Methylation mosaicism of 5 '-(CGG)(n)-3 ' repeats in fragile X, premutation and normal individuals | 3 | 6 |
| 804 | 10 | 54 | 804 2000 OPTOMETRY AND VISION SCIENCE 77(11):592-599 Block SS; Brusca-Vega R; Pizzi WJ; Berry-Kravis E; Maino DM; et al. Cognitive and visual processing skills and their relationship to mutation size in full and premutation female fragile X carriers | 0 | 0 |
| 805 | 1 | 10 | 805 2000 PEDIATRIC HEMATOLOGY AND ONCOLOGY 17(7):597-600 Ferrari A; Meazza C; Casanova M Nasopharyngeal carcinoma in a boy with fragile X syndrome | 0 | 0 |
| 806 | 7 | 17 | 806 2000 PRENATAL DIAGNOSIS 20(8):611-614 Pesso R; Berkenstadt H; Cuckle H; Gak E; Peleg L; et al. Screening for fragile X syndrome in women of reproductive age | 13 | 17 |
| 807 | 1 | 6 | 807 2000 PRENATAL DIAGNOSIS 20(10):854-855 Wilkin H; Tuohy J; Theewis W Prenatal diagnosis of fragile X and Turner mosaicism in a 12-week fetus | 1 | 1 |
| 808 | 0 | 5 | 808 2000 REVISTA DE NEUROLOGIA 30(10):996-997 Serrano-Castro PJ; Serrano-Castillo P A historical description of the association of macro-orchidea, mental retardation and cranial dysmorphia in males (fragile X chromosome syndrome) by A.B Richerand | 0 | 0 |
| 809 | 0 | 10 | 809 2000 VETERINARNI MEDICINA 45(10-11):308-310 Slota E; Danielak-Czech B; Pietraszewska J; Kozubska-Sobocinska A Preliminary identification of the fragile X in two crossbred cows | 0 | 1 |
| 810 | 0 | 0 | 810 2001 ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY 221:U3-U3 Rodesittisuk P; Romero RM; Haworth IS Conformation of fragile X-associated triplet repeat DNA containing C-C mismatch pairs. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 811 | 12 | 40 | 811 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(2):351-360 Toledano-Alhadef H; Basel-Vanagaite L; Magal N; Davidov B; Ehrlich S; et al. Fragile-X carrier screening and the prevalence of premutation and full-mutation carriers in Israel | 13 | 22 |
| 812 | 11 | 34 | 812 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(3):504-515 Wohrle D; Salat U; Hameister H; Vogel W; Steinbach P Demethylation, reactivation, and destabilization of human fragile X full-mutation alleles in mouse embryocarcinoma cells | 4 | 10 |
| 813 | 0 | 0 | 813 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):177-177 Hagerman RJ; Greco C; Chudley A; Leehey M; Tassone F; et al. Neuropathology and neurodegenerative features in some older male premutation carriers of fragile X syndrome. | 3 | 4 |
| 814 | 0 | 0 | 814 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):291-291 Thiele H; Peters H; Bahrke D; Hansmann I Homozygosity for a premutation of the FMR1 gene and normal phenotype in two sisters from a family with fragile X syndrome. | 0 | 0 |
| 815 | 0 | 0 | 815 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):352-352 Gantois I; Reyniers E; Kooy RF Identification of genes differentially expressed in the fragile X syndrome. | 0 | 0 |
| 816 | 0 | 0 | 816 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):372-372 Naumann F; Muller-Hartmann H; Deissler H; Doerfler W Functional studies on the human 5 '-CGG-3 '-binding protein CGGBP1 (p20). | 0 | 0 |
| 817 | 0 | 0 | 817 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):372-372 Neri G; Pomponi MG; Pietrobono R; Chiurazzi P Pharmacological reactivation of the FMR1 gene of the fragile X syndrome. | 0 | 0 |
| 818 | 0 | 0 | 818 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):430-430 Jakupciak JP; O'Connell CD; Atha DA; Richie KL Standardization of PCR amplification for fragile X trinucleotide repeat measurements. | 0 | 0 |
| 819 | 0 | 0 | 819 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):431-431 Jenkins EC; Li SY; Yao XL; Lanter S; Sudhalter V; et al. Detecting mosaic FMR-1 (fragile X) mutations: Southern blotting versus monoclonal antibody analysis. | 0 | 0 |
| 820 | 0 | 0 | 820 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):436-436 Patel ZM; Menon SR; D'souza AK; Adhia RA; Sanghavi DA; et al. Validity of the analysis of FMRP expression in blood smears as a screening method for the fragile X syndrome in Indian population. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 821 | 0 | 0 | 821 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):438-438 Zhou Y; Chong SS Simplified molecular diagnostic testing for fragile X syndrome using methylation-specific PCR (ms-PCR). | 0 | 0 |
| 822 | 0 | 0 | 822 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):554-554 Heine-Sur D; Pico G; Torres-Juan L; Bernues M; Iglesias J; et al. A female with Fragile-X shows an affected male-like phenotype and skewed inactivation of the functional chromosome. | 0 | 0 |
| 823 | 0 | 0 | 823 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):585-585 Essop FB; Greenberg J; Basel D; Krause A Molecular analysis of a fragile X family with two females homozygous for a premutation. | 0 | 0 |
| 824 | 0 | 0 | 824 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):586-586 Nolin SL; Houck GE; Gargano AD; Brown WT Large fragile X premutatin alleles may often contain two AGG Interruptions. | 0 | 0 |
| 825 | 0 | 0 | 825 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):635-635 Dobkin CS; Ding X; Brown WT; El Idrissi A Reduced hippocampal GABAa receptors and increased kainic acid seizure susceptibility in the fragile X mouse. | 0 | 0 |
| 826 | 0 | 0 | 826 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):667-667 Brown WT; Nolin S; Houck GE; Ding XH; Glicksman A; et al. The Fragile X Syndrome: Screening and prenatal diagnosis. | 0 | 0 |
| 827 | 0 | 0 | 827 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):669-669 Mallolas J; Badenas C; Rite M; Soler A; Borrell A; et al. Prospective study of molecular fragile X syndrome prenatal diagnosis. | 0 | 0 |
| 828 | 2 | 26 | 828 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 98(1):37-45 McConkie-Rosell A; Spiridigliozzi GA; Sullivan JA; Dawson DV; Lachiewicz AM Longitudinal study of the carrier testing process for fragile X syndrome: Perceptions and coping | 2 | 3 |
| 829 | 6 | 42 | 829 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 98(2):161-167 Irwin SA; Patel B; Idupulapati M; Harris JB; Crisostomo RA; et al. Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: A quantitative examination | 48 | 75 |
| 830 | 3 | 18 | 830 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 100(2):110-115 Stoll C Problems in the diagnosis of fragile X syndrome in young children are still present | 3 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 831 | 2 | 7 | 831 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 100(2):156-161 Kjaer I; Hjalgrim H; Russell BG Cranial and hand skeleton in fragile X syndrome | 0 | 1 |
| 832 | 15 | 55 | 832 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 103(1):81-90 Sun HT; Cohen S; Kaufmann WE Annexin-1 is abnormally expressed in fragile X syndrome: Two-dimensional electrophoresis study in lymphocytes | 4 | 9 |
| 833 | 5 | 32 | 833 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 103(3):226-230 Schultz-Pedersen S; Hasle H; Olsen JH; Friedrich U Evidence of decreased risk of cancer in individuals with fragile X | 0 | 2 |
| 834 | 4 | 39 | 834 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 103(4):314-319 Johnston C; Eliez S; Dyer-Friedman J; Hessl D; Glaser B; et al. Neurobehavioral phenotype in carriers of the fragile X premutation | 8 | 9 |
| 835 | 0 | 0 | 835 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 105(7):585-585 Daly E; Moore CJ; Schmitz N; Jacobs PA; Davis KE; et al. Premutation expansion of CGG triplet repeats affects brain; A study of male carriers of Fragile X syndrome | 0 | 0 |
| 836 | 1 | 1 | 836 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 105(7):585-585 Moore CJ; Daly E; Tassone F; Jacobs PA; Davies KE; et al. Neuroanatomical effect of FMR1 gene mRNA in premutation carriers of Fragile X syndrome | 0 | 0 |
| 837 | 8 | 54 | 837 2001 AMERICAN JOURNAL OF PSYCHIATRY 158(7):1040-1051 Kwon H; Menon V; Eliez S; Warsofsky IS; White CD; et al. Functional neuroanatomy of visuospatial working memory in fragile X syndrome: Relation to behavioral and molecular measures | 11 | 24 |
| 838 | 12 | 37 | 838 2001 AMERICAN JOURNAL ON MENTAL RETARDATION 106(1):16-27 Bailey DB; Hatton DD; Tassone F; Skinner M; Taylor AK Variability in FMRP and early development in males with fragile X syndrome | 16 | 15 |
| 839 | 5 | 43 | 839 2001 AMERICAN JOURNAL ON MENTAL RETARDATION 106(1):28-38 Belser RC; Sudhalter V Conversational characteristics of children with fragile X syndrome: Repetitive speech | 9 | 12 |
| 840 | 12 | 55 | 840 2001 AMERICAN JOURNAL ON MENTAL RETARDATION 106(3):216-230 Roberts JE; Mirrett P; Burchinal M Receptive and expressive communication development of young males with fragile X syndrome | 6 | 10 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 841 | 4 | 58 | 841 2001 AMERICAN JOURNAL ON MENTAL RETARDATION 106(5):389-400 Sudhalter V; Belser RC Conversational characteristics of children with fragile x syndrome: Tangential language | 5 | 8 |
| 842 | 11 | 32 | 842 2001 ANNALS OF CLINICAL BIOCHEMISTRY 38:264-271 Saha S; Karmakar P; Chatterjee C; Banerjee D; Das S; et al. Fragile X syndrome in Calcutta, India | 2 | 4 |
| 843 | 0 | 0 | 843 2001 ANNALS OF NEUROLOGY 50(3):S108-S108 Berry-Kravis E Characterization of epilepsy in fragile X syndrome | 0 | 0 |
| 844 | 5 | 30 | 844 2001 ARQUIVOS DE NEURO-PSIQUIATRIA 59(1):83-88 Boy R; Correia PS; Llerena JC; Machado-Ferreira MD; Pimentel MMG Fragile X syndrome confirmed by molecular analysis: a case-control study with pre and post-puberal patients | 0 | 0 |
| 845 | 0 | 0 | 845 2001 AUSTRALIAN JOURNAL OF PSYCHOLOGY 53(1):58-58 Gould E Melatonin profiles and sleep characteristics in boys with fragile X Syndrome: A preliminary study | 0 | 0 |
| 846 | 0 | 28 | 846 2001 BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY 65(7):1568-1574 Tani S; Itoh T; Kato M; Kobayashi T; Tsukagoshi N In vivo and in vitro analyses of the AmyR binding site of the Aspergillus nidulans agdA promoter; Requirement of the CGG direct repeat for induction and high affinity binding of AmyR | 0 | 4 |
| 847 | 15 | 53 | 847 2001 BRAIN 124:1610-1618 Eliez S; Blasey CM; Freund LS; Hastie T; Reiss AL Brain anatomy, gender and IQ in children and adolescents with fragile X syndrome | 9 | 15 |
| 848 | 23 | 88 | 848 2001 BRAIN RESEARCH BULLETIN 56(3-4):367-373 Grabczyk E; Kumari D; Usdin K Fragile X syndrome and Friedreich's ataxia: Two different paradigms for repeat induced transcript insufficiency | 0 | 4 |
| 849 | 34 | 85 | 849 2001 BRAIN RESEARCH BULLETIN 56(3-4):375-382 Bardoni B; Schenck A; Mandel JL The Fragile X mental retardation protein | 6 | 9 |
| 850 | 18 | 62 | 850 2001 BRAIN RESEARCH BULLETIN 56(3-4):383-387 Chiurazzi P; Neri G Pharmacological reactivation of inactive genes: The fragile X experience | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 851 | 18 | 47 | 851 2001 CELL 107(4):477-487 Brown V; Jin P; Ceman S; Darnell JC; O'Donnell WT; et al. Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome | 80 | 162 |
| 852 | 11 | 85 | 852 2001 CELL 107(4):489-499 Darnell JC; Jensen KB; Jin P; Brown V; Warren ST; et al. Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function | 74 | 149 |
| 853 | 12 | 17 | 853 2001 CELL 107(5):555-557 Kaytor MD; Orr HT RNA targets of the fragile X protein | 6 | 15 |
| 854 | 14 | 37 | 854 2001 CELL 107(5):591-603 Zhang YQ; Bailey AM; Matthies HJG; Renden RB; Smith MA; et al. Drosophila fragile X-related gene regulates the MAP1B homolog Futsch to control synaptic structure and function | 57 | 98 |
| 855 | 15 | 34 | 855 2001 CELLULAR AND MOLECULAR NEUROBIOLOGY 21(1):29-38 Castren M; Haapasalo A; Oostra BA; Castren E Subcellular localization of fragile X mental retardation protein with the I304N mutation in the RNA-binding domain in cultured hippocampal neurons | 3 | 3 |
| 856 | 45 | 100 | 856 2001 CLINICAL GENETICS 60(6):399-408 Oostra BA; Chiurazzi P The fragile X gene and its function | 5 | 11 |
| 857 | 9 | 73 | 857 2001 COGNITIVE NEUROPSYCHOLOGY 18(1):1-18 Simon JA; Keenan JM; Pennington BF; Taylor AK; Hagerman RJ Discourse processing in women with fragile X syndrome: Evidence for a deficit establishing coherence | 8 | 10 |
| 858 | 7 | 25 | 858 2001 COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING 4(3):265-272 Murray J; Cuckle H Cystic fibrosis and fragile X syndrome: The arguments for antenatal screening | 1 | 2 |
| 859 | 36 | 94 | 859 2001 CURRENT OPINION IN PSYCHIATRY 14(5):443-449 Eliez S; Feinstein C The fragile X syndrome: bridging the gap from gene to behavior | 0 | 1 |
| 860 | 0 | 1 | 860 2001 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 43(2):142-142 [Anon] Monozygotic boys with fragile X syndrome (vol 42, pg 768, 2000) | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 861 | 11 | 86 | 861 2001 DEVELOPMENTAL PSYCHOBIOLOGY 39(2):107-123 Roberts JE; Boccia ML; Bailey DB; Hatton DD; Skinner M Cardiovascular indices of physiological arousal in boys with fragile X syndrome | 7 | 7 |
| 862 | 8 | 27 | 862 2001 DIAGNOSTIC MOLECULAR PATHOLOGY 10(1):34-40 Tzeng CC; Lin SJ; Chen YJ; Kuo PL; Jong YJ; et al. An effective strategy of using molecular testing to screen mentally retarded individuals for fragile X syndrome | 1 | 3 |
| 863 | 3 | 21 | 863 2001 ELECTROPHORESIS 22(6):1188-1193 Sung WC; Lee GB; Tzeng CC; Chen SH Plastic microchip electrophoresis for genetic screening: The analysis of polymerase chain reactions products of fragile X (CGG)n alleles | 0 | 12 |
| 864 | 17 | 62 | 864 2001 EMBO JOURNAL 20(17):4803-4813 Schaeffer C; Bardoni B; Mandel JL; Ehresmann B; Ehresmann C; et al. The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif | 66 | 97 |
| 865 | 11 | 17 | 865 2001 EUROPEAN JOURNAL OF HUMAN GENETICS 9(9):724-727 Larsen LA; Vuust J; Nystad M; Evseeva I; Van Ghelue M; et al. Analysis of FMR1 (CGG)(n) alleles and DXS548-FRAXAC1 haplotypes in three European circumpolar populations: traces of genetic relationship with Asia | 1 | 3 |
| 866 | 0 | 0 | 866 2001 FASEB JOURNAL 15(4):A710-A710 Lenert P; Stunz LL; Krieg AM; Ashman RF Down-regulation of CgG-induced B cell NF-kappa B, AP-1 and NF-IL-6 inhibitory oligonucleotides (ODN) | 0 | 0 |
| 867 | 14 | 49 | 867 2001 GENETIC EPIDEMIOLOGY 20(1):129-144 Sharma D; Gupta M; Thelma BK Expansion mutation frequency and CGG/GCC repeat polymorphism in FMR1 and FMR2 genes in an Indian population | 4 | 6 |
| 868 | 2 | 6 | 868 2001 GENETIC TESTING 5(2):139-140 Gilbert F Comment: How many are too many when discussing triplet repeats in the FMR1 gene and the fragile X syndrome? | 0 | 1 |
| 869 | 1 | 42 | 869 2001 GENETICS 157(2):717-725 Su MA; Wisotzkey RG; Newfeld SJ A screen for modifiers of decapentaplegic mutant phenotypes identifies lilliputian, the only member of the Fragile-X/Burkitt's lymphoma family of transcription factors in Drosophila melanogaster | 0 | 6 |
| 870 | 82 | 154 | 870 2001 GENETICS IN MEDICINE 3(5):359-371 Crawford DC; Acuna JM; Sherman SL FMR1 and the fragile X syndrome: Human genome epidemiology review | 17 | 25 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 871 | 3 | 48 | 871 2001 GENOME RESEARCH 11(8):1382-1391 Mathews DJ; Kashuk C; Brightwell G; Eichler EE; Chakravarti A Sequence variation within the fragile x locus | 0 | 3 |
| 872 | 28 | 47 | 872 2001 HUMAN GENETICS 108(6):450-458 Weinhausel A; Haas OA Evaluation of the fragile X (FRAXA) syndrome with methylation-sensitive PCR | 2 | 6 |
| 873 | 16 | 31 | 873 2001 HUMAN MOLECULAR GENETICS 10(4):329-338 Laggerbauer B; Ostareck D; Keidel EM; Ostareck-Lederer A; Fischer U Evidence that fragile X mental retardation protein is a negative regulator of translation | 84 | 106 |
| 874 | 14 | 47 | 874 2001 HUMAN MOLECULAR GENETICS 10(14):1449-1454 Kenneson A; Zhang FP; Hagedorn CH; Warren ST Reduced FMRP and increased FMR1 transcription is proportionally associated with CGG repeat number in intermediate-length and premutation carriers | 36 | 46 |
| 875 | 15 | 45 | 875 2001 HUMAN MOLECULAR GENETICS 10(16):1693-1699 Bontekoe CJM; Bakker CE; Nieuwenhuizen IM; van der Linde H; Lans H; et al. Instability of a (CGG)(98) repeat in the Fmr1 promoter | 12 | 15 |
| 876 | 20 | 64 | 876 2001 HUMAN MOLECULAR GENETICS 10(24):2803-2811 Huot ME; Mazroui R; Leclerc P; Khandjian EW Developmental expression of the fragile X-related 1 proteins in mouse testis: association with microtubule elements | 5 | 7 |
| 877 | 6 | 25 | 877 2001 HUMAN REPRODUCTION 16(3):457-462 Hundscheid RDL; Braat DDM; Kiemeney LALM; Smits APT; Thomas CMG Increased serum FSH in female fragile X premutation carriers with either regular menstrual cycles or on oral contraceptives | 8 | 13 |
| 878 | 0 | 22 | 878 2001 IN VIVO 15(1):105-108 Kotsinas A; Gorgoulis VG; Zacharatos P; Liloglou T; Leonardou P; et al. A new rare allele at the CGG repeat polymorphism in the first intron of human c-H-ras gene | 0 | 0 |
| 879 | 13 | 31 | 879 2001 INFANTS AND YOUNG CHILDREN 14(1):24-33 Bailey DB; Roberts JE; Mirrett P; Hatton DD Identifying infants and toddlers with fragile X syndrome: Issues and recommendations | 6 | 6 |
| 880 | 10 | 33 | 880 2001 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 31(2):165-174 Bailey DB; Hatton DD; Skinner M; Mesibov G Autistic behavior, FMR1 protein, and developmental trajectories in young males with fragile X syndrome | 16 | 22 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 881 | 4 | 28 | 881 2001 JOURNAL OF BIOLOGICAL CHEMISTRY 276(6):4357-4364 Kumari D; Usdin K Interaction of the transcription factors USF1, USF2, and alpha-Pal/Nrf-1 with the FMR1 promoter - Implications for Fragile X mental retardation syndrome | 15 | 23 |
| 882 | 10 | 58 | 882 2001 JOURNAL OF BIOLOGICAL CHEMISTRY 276(19):16439-16446 Kamath-Loeb AS; Loeb LA; Johansson E; Burgers PMJ; Fry M Interactions between the Werner syndrome helicase and DNA polymerase delta specifically facilitate copying of tetraplex and hairpin structures of the d(CGG)(n) trinucleotide repeat sequence | 4 | 44 |
| 883 | 6 | 71 | 883 2001 JOURNAL OF BIOLOGICAL CHEMISTRY 276(21):18605-18613 Bacolla A; Pradhan S; Larson JE; Roberts RJ; Wells RD Recombinant human DNA (cytosine-5) methyltransferase - III. Allosteric control, reaction order, and influence of plasmid topology and triplet repeat length on methylation of the fragile X CGG center dot CCG sequence | 0 | 15 |
| 884 | 0 | 14 | 884 2001 JOURNAL OF CRYSTAL GROWTH 226(1):101-106 Jung IH; Yoshikawa A; Lebbou K; Fukuda T; Auh KH Crystal growth by micro-pulling-down of Ca3Ga2Ge4O14 (CGG) type-Sr3Nb1-xGa3 (+) (5/3)xSi2O14 compounds | 0 | 8 |
| 885 | 0 | 0 | 885 2001 JOURNAL OF DENTAL RESEARCH 80(4):1133-1133 Sabbagh A Clinical and panoramic radiographic considerations of oral conditions in Fragile X Syndrome (Martin-Bell Syndrome) | 0 | 0 |
| 886 | 0 | 1 | 886 2001 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 22(5):337-337 Floet AW Children with fragile X syndrome: A parents' guide | 0 | 0 |
| 887 | 6 | 31 | 887 2001 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 22(6):353-359 Myers GF; Mazzocco MMM; Maddalena A; Reiss AL No widespread psychological effect of the fragile X premutation in childhood: Evidence from a preliminary controlled study | 3 | 3 |
| 888 | 10 | 34 | 888 2001 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 22(6):409-417 Rogers SJ; Wehner EA; Hagerman R The behavioral phenotype in fragile X: Symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders | 13 | 24 |
| 889 | 6 | 24 | 889 2001 JOURNAL OF KOREAN MEDICAL SCIENCE 16(3):271-275 Kwon SH; Lee KS; Hyun MC; Song KE; Kim JK Molecular screening for Fragile X syndrome in mentally handicapped children in Korea | 0 | 0 |
| 890 | 5 | 91 | 890 2001 JOURNAL OF LEARNING DISABILITIES 34(6):520-533 Mazzocco MMM Math learning disability and math LD subtypes: Evidence from studies of Turner syndrome, fragile X syndrome, and neurofibromatosis type 1 | 2 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 891 | 0 | 0 | 891 2001 JOURNAL OF MEDICAL GENETICS 38:S39-S39 Moore C; Daly EM; Tassone F; Schmitz N; Hagerman P; et al. Neuroanatomical effect of FMR1 gene mRNA in premutation carriers of Fragile X syndrome | 0 | 0 |
| 892 | 0 | 0 | 892 2001 JOURNAL OF MEDICAL GENETICS 38:S40-S40 Daly E; Moore CJ; Schmitz N; Jacobs P; Davies K; et al. Premutation expansion of CGG triplet repeats affects brain; a study of Male Carriers of Fragile X Syndrome | 0 | 0 |
| 893 | 0 | 0 | 893 2001 JOURNAL OF MEDICAL GENETICS 38:S63-S63 Warburton S; Waters J; Davison V Targeted diagnostic testing for fragile X syndrome | 0 | 0 |
| 894 | 0 | 0 | 894 2001 JOURNAL OF MEDICAL GENETICS 38:S64-S64 Wakeling W; King W; Taylor R Chemiluminescence detection offers a safe, effective and convenient alternative to radioisotopic labelling of probes for detection of Fragile X syndrome and other single gene disorders | 0 | 0 |
| 895 | 8 | 19 | 895 2001 JOURNAL OF MEDICAL GENETICS 38(7):453-456 Tassone F; Hagerman RJ; Taylor AK; Hagerman PJ A majority of fragile X males with methylated, full mutation alleles have significant levels of FMR1 messenger RNA | 16 | 22 |
| 896 | 4 | 47 | 896 2001 JOURNAL OF SPECIAL EDUCATION 34(4):194-202 Symons FJ; Clark RD; Roberts JP; Bailey DB Classroom behavior of elementary school-age boys with fragile X syndrome | 2 | 3 |
| 897 | 0 | 10 | 897 2001 MATERIALS LETTERS 51(2):129-134 Jung IH; Kang YH; Joo K; Yoshikawa A; Fukuda T; et al. Ca3Ga2Ge4O14 (CGG)-type Sr3Nb0.95Ga3.083Si2O14 single crystal grown by the Czochralski method for piezoelectric applications | 0 | 4 |
| 898 | 4 | 17 | 898 2001 MEDICAL PRINCIPLES AND PRACTICE 10(2):73-78 Alkhalaf M; Verghese L; Mushtaq SK Cytogenetic and immunohistochemical characterization of fragile X syndrome in a Kuwaiti family: Rapid antibody test for the diagnosis of mental retardation patients | 0 | 0 |
| 899 | 1 | 13 | 899 2001 MOLECULAR AND CELLULAR ENDOCRINOLOGY 183:S77-S85 Sermon K; Seneca S; De Rycke M; Goossens V; Van de Velde H; et al. PGD in the lab for triplet repeat diseases - myotonic dystrophy, Huntington's disease and Fragile-X syndrome | 0 | 10 |
| 900 | 43 | 108 | 900 2001 MOLECULAR GENETICS AND METABOLISM 74(1-2):89-97 Hagerman RJ; Hagerman PJ Fragile X syndrome: A model of gene-brain-behavior relationships | 1 | 2 |