| Missing Links? Citation Matrix | Graphs | Glossary HistCite Guide About |
|
A HIGH-RESOLUTION RECOMBINATION MAP OF THE HUMAN GENOME KONG A; GUDBJARTSSON DF; SAINZ J; JONSDOTTIR GM; GUDJONSSON SA; RICHARDSSON B; SIGURDARDOTTIR S; BARNARD J; HALLBECK B; MASSON G; SHLIEN A; PALSSON ST; FRIGGE ML; THORGEIRSSON TE; GULCHER JR; STEFANSSON K NATURE GENETICS 31: (3) 241-247 JUL 2002 and the citing papers |
Nodes: 264,
Authors: 2298,
Journals: 82,
Outer References: 8062,
Words: 1014
Collection span: 2002 - 2005
View: Overview. Sorted by journal name.
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1 | 1 | 48 | 1 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(3):483-491 Hakonarson H; Bjornsdottir US; Halapi E; Palsson S; Adalsteinsdottir E; et al. A major susceptibility gene for asthma maps to chromosome 14q24 | 1 | 24 |
| 2 | 1 | 57 | 2 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):877-892 Stefansson H; Sigurdsson E; Steinthorsdottir V; Bjornsdottir S; Sigmundsson T; et al. Neuregulin 1 and susceptibility to schizophrenia | 12 | 161 |
| 3 | 1 | 26 | 3 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(5):1161-1167 Otto E; Hoefele J; Ruf R; Mueller AM; Hiller KS; et al. A gene mutated in nephronophthisis and retinitis pigmentosa encodes a novel protein, nephroretinin, conserved in evolution | 0 | 22 |
| 4 | 1 | 59 | 4 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(6):1353-1368 Froenicke L; Anderson LK; Wienberg J; Ashley T Male mouse recombination maps for each autosome identified by chromosome painting | 5 | 21 |
| 5 | 1 | 27 | 5 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(6):1395-1412 Foulkes WD; Thiffault I; Gruber SB; Horwitz M; Hamel N; et al. The founder mutation MSH2*1906G -> C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population | 1 | 17 |
| 6 | 1 | 60 | 13 2003 AMERICAN JOURNAL OF HUMAN GENETICS 72(1):88-100 Borrego S; Wright FA; Fernandez RM; Williams N; Lopez-Alonso M; et al. A founding locus within the RET proto-oncogene may account for a large proportion of apparently sporadic Hirschsprung disease and a subset of cases of sporadic medullary thyroid carcinoma | 1 | 14 |
| 7 | 1 | 64 | 14 2003 AMERICAN JOURNAL OF HUMAN GENETICS 72(1):125-131 Karason A; Gudjonsson JE; Upmanyu R; Antonsdottir AA; Hauksson VB; et al. A susceptibility gene for psoriatic arthritis maps to chromosome 16q: Evidence for imprinting | 3 | 19 |
| 8 | 1 | 38 | 15 2003 AMERICAN JOURNAL OF HUMAN GENETICS 72(1):168-177 Laivuori H; Lahermo P; Ollikainen V; Widen E; Haiva-Mallinen L; et al. Susceptibility loci for preeclampsia on chromosomes 2p25 and 9p13 in Finnish families | 1 | 7 |
| 9 | 1 | 37 | 16 2003 AMERICAN JOURNAL OF HUMAN GENETICS 72(2):364-374 Omi K; Ohashi J; Patarapotikul J; Hananantachai H; Naka I; et al. CD36 polymorphism is associated with protection from cerebral malaria | 0 | 7 |
| 10 | 1 | 26 | 17 2003 AMERICAN JOURNAL OF HUMAN GENETICS 72(4):850-868 Fan RZ; Knapp M Genome association studies of complex diseases by case-control designs | 0 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 11 | 1 | 21 | 18 2003 AMERICAN JOURNAL OF HUMAN GENETICS 72(4):1053-1057 Pankratz N; Nichols WC; Uniacke SK; Halter C; Rudolph A; et al. Significant linkage of Parkinson disease to chromosome 2q36-37 | 1 | 13 |
| 12 | 2 | 14 | 19 2003 AMERICAN JOURNAL OF HUMAN GENETICS 72(5):1213-1220 Service SK; Sandkuijl LA; Freimer NB Cost-effective designs for linkage disequilibrium mapping of complex traits | 0 | 5 |
| 13 | 1 | 50 | 20 2003 AMERICAN JOURNAL OF HUMAN GENETICS 72(5):1221-1230 Thorgeirsson TE; Oskarsson H; Desnica N; Kostic JP; Stefansson JG; et al. Anxiety with panic disorder linked to chromosome 9q in Iceland | 2 | 9 |
| 14 | 1 | 68 | 21 2003 AMERICAN JOURNAL OF HUMAN GENETICS 72(5):1251-1260 Bakker SC; van der Meulen EM; Buitelaar JK; Sandkuijl LA; Pauls DL; et al. A whole-genome scan in 164 Dutch sib pairs with attention-deficit/hyperactivity disorder: Suggestive evidence for linkage on chromosomes 7p and 15q | 2 | 15 |
| 15 | 1 | 33 | 22 2003 AMERICAN JOURNAL OF HUMAN GENETICS 72(6):1370-1388 Helgason A; Hrafnkelsson B; Gulcher JR; Ward R; Stefansson K A populationwide coalescent analysis of Icelandic matrilineal and patrilineal genealogies: Evidence for a faster evolutionary rate of mtDNA lineages than Y chromosomes | 1 | 5 |
| 16 | 2 | 44 | 23 2003 AMERICAN JOURNAL OF HUMAN GENETICS 72(6):1448-1459 Stefansson SE; Jonsson H; Ingvarsson T; Manolescu I; Jonsson HH; et al. Genomewide scan for hand osteoarthritis: A novel mutation in matrilin-3 | 2 | 14 |
| 17 | 4 | 43 | 24 2003 AMERICAN JOURNAL OF HUMAN GENETICS 72(6):1527-1535 Hellmann I; Ebersberger I; Ptak SE; Paabo S; Przeworski M A neutral explanation for the correlation of diversity with recombination rates in humans | 13 | 26 |
| 18 | 3 | 100 | 25 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(1):5-16 Arnheim N; Calabrese P; Nordborg M Hot and cold spots of recombination in the human genome: The reason we should find them and how this can be achieved | 9 | 17 |
| 19 | 1 | 21 | 26 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(1):17-33 Levinson DF; Levinson MD; Segurado R; Lewis CM Genome scan meta-analysis of schizophrenia and bipolar disorder, part I: Methods and power analysis | 2 | 21 |
| 20 | 1 | 46 | 27 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(2):271-284 Matise TC; Sachidanandam R; Clark AG; Kruglyak L; Wijsman E; et al. A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set | 6 | 14 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 21 | 2 | 70 | 28 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(2):323-335 Reynisdottir I; Thorleifsson G; Benediktsson R; Sigurdsson G; Emilsson V; et al. Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2 | 1 | 5 |
| 22 | 4 | 41 | 29 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(3):502-515 Wall JD; Pritchard JK Assessing the performance of the haplotype block model of linkage disequilibrium | 5 | 24 |
| 23 | 1 | 31 | 30 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(3):580-590 Walsh EC; Mather KA; Schaffner SF; Farwell L; Daly MJ; et al. An integrated haplotype map of the human major histocompatibility complex | 3 | 17 |
| 24 | 3 | 66 | 31 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(3):601-611 Fallin MD; Lasseter VK; Wolyniec PS; McGrath JA; Nestadt G; et al. Genomewide linkage scan for schizophrenia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 10q22 | 0 | 3 |
| 25 | 2 | 54 | 32 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(4):835-848 Bachinski LL; Udd B; Meola G; Sansone V; Bassez G; et al. Confirmation of the type 2 myotonic dystrophy (CCTG)(n) expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins: A single shared haplotype indicates an ancestral founder effect | 0 | 6 |
| 26 | 1 | 28 | 33 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(4):957-966 Dowling O; Difeo A; Ramirez MC; Tukel T; Narla G; et al. Mutations in capillary morphogenesis gene-2 result in the allelic disorders juvenile hyaline fibromatosis and infantile systemic hyalinosis | 0 | 4 |
| 27 | 1 | 50 | 34 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):986-993 Bjornsson A; Gudmundsson G; Gudfinnsson E; Hrafnsdottir M; Benedikz J; et al. Localization of a gene for migraine without aura to chromosome 4q21 | 1 | 3 |
| 28 | 1 | 70 | 35 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):994-1015 Zietkiewicz E; Yotova V; Gehl D; Wambach T; Arrieta I; et al. Haplotypes in the dystrophin DNA segment point to a mosaic origin of modern human diversity | 1 | 8 |
| 29 | 1 | 53 | 36 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(6):1330-1340 Wall JD; Frisse LA; Hudson RR; Di Rienzo A Comparative linkage-disequilibrium analysis of the beta-globin hotspot in primates | 10 | 15 |
| 30 | 3 | 70 | 37 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(6):1355-1367 Williams NM; Norton N; Williams H; Ekholm B; Hamshere ML; et al. A systematic genomewide linkage study in 353 sib pairs with schizophrenia | 0 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 31 | 2 | 21 | 116 2004 AMERICAN JOURNAL OF HUMAN GENETICS 74(1):40-49 Anderson EC; Slatkin M Population-genetic basis of haplotype blocks in the 5q31 region | 1 | 6 |
| 32 | 1 | 33 | 117 2004 AMERICAN JOURNAL OF HUMAN GENETICS 74(1):62-72 Zollner S; Wen XQ; Hanchard NA; Herbert MA; Ober C; et al. Evidence for extensive transmission distortion in the human genome | 0 | 5 |
| 33 | 1 | 26 | 118 2004 AMERICAN JOURNAL OF HUMAN GENETICS 74(1):188-191 Spritz RA; Gowan K; Bennett DC; Fain PR Novel vitiligo susceptibility loci on chromosomes 7 (AIS2) and 8 (AIS3), confirmation of SLEV1 on chromosome 17, and their roles in an autoimmune diathesis | 0 | 0 |
| 34 | 1 | 52 | 119 2004 AMERICAN JOURNAL OF HUMAN GENETICS 74(3):444-453 van Asselt KM; Kok HS; Putter H; Wijmenga C; Peeters PHM; et al. Linkage analysis of extremely discordant and concordant sibling pairs identifies quantitative trait loci influencing variation in human menopausal age | 0 | 1 |
| 35 | 2 | 28 | 120 2004 AMERICAN JOURNAL OF HUMAN GENETICS 74(3):521-531 Sun F; Oliver-Bonet M; Liehr T; Starke H; Ko E; et al. Human male recombination maps for individual chromosomes | 2 | 4 |
| 36 | 2 | 32 | 121 2004 AMERICAN JOURNAL OF HUMAN GENETICS 74(5):846-855 Maniatis N; Collins A; Gibson J; Zhang WH; Tapper W; et al. Positional cloning by linkage disequilibrium | 1 | 3 |
| 37 | 1 | 59 | 122 2004 AMERICAN JOURNAL OF HUMAN GENETICS 74(5):931-944 Wang E; Ding YC; Flodman P; Kidd JR; Kidd KK; et al. The genetic architecture of selection at the human dopamine receptor D4 (DRD4) gene locus | 0 | 2 |
| 38 | 2 | 52 | 123 2004 AMERICAN JOURNAL OF HUMAN GENETICS 74(5):1001-1013 Smith MW; Patterson N; Lautenberger JA; Truelove AL; McDonald GJ; et al. A high-density admixture map for disease gene discovery in African Americans | 0 | 7 |
| 39 | 1 | 36 | 124 2004 AMERICAN JOURNAL OF HUMAN GENETICS 74(5):1064-1073 Lafreniere RG; MacDonald MLE; Dube MP; MacFarlane J; O'Driscoll M; et al. Identification of a novel gene (HSN2) causing hereditary sensory and autonomic neuropathy type II through the study of Canadian genetic isolates | 0 | 2 |
| 40 | 1 | 40 | 125 2004 AMERICAN JOURNAL OF HUMAN GENETICS 74(6):1111-1120 Bersaglieri T; Sabeti PC; Patterson N; Vanderploeg T; Schaffner SF; et al. Genetic signatures of strong recent positive selection at the lactase gene | 1 | 7 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 41 | 2 | 96 | 126 2004 AMERICAN JOURNAL OF HUMAN GENETICS 74(6):1154-1167 Holmans P; Zubenko GS; Crowe RR; DePaulo JR; Scheftner WA; et al. Genomewide significant linkage to recurrent, early-onset major depressive disorder on chromosome 15q | 0 | 0 |
| 42 | 1 | 56 | 127 2004 AMERICAN JOURNAL OF HUMAN GENETICS 74(6):1225-1238 Newbury DF; Cleak JD; Banfield E; Marlow AJ; Fisher SE; et al. Highly significant linkage to the SLI1 locus in an expanded sample of individuals affected by specific language impairment | 0 | 0 |
| 43 | 1 | 29 | 128 2004 AMERICAN JOURNAL OF HUMAN GENETICS 74(6):1314-1320 Wiggs JL; Lynch S; Ynagi G; Maselli M; Auguste J; et al. A genomewide scan identifies novel early-onset primary open-angle glaucoma loci on 9q22 and 20p12 | 0 | 0 |
| 44 | 3 | 29 | 129 2004 AMERICAN JOURNAL OF HUMAN GENETICS 75(1):54-64 John S; Shephard N; Liu GY; Zeggini E; Cao MQ; et al. Whole-genome scan, in a complex disease, using 11,245 single-nucleotide polymorphisms: Comparison with microsatellites | 4 | 8 |
| 45 | 1 | 24 | 130 2004 AMERICAN JOURNAL OF HUMAN GENETICS 75(3):508-513 Willour VL; Shugart YY; Samuels J; Grados M; Cullen B; et al. Replication study supports evidence for linkage to 9p24 in obsessive-compulsive disorder | 0 | 0 |
| 46 | 1 | 64 | 131 2004 AMERICAN JOURNAL OF HUMAN GENETICS 75(4):596-609 Morar B; Gresham D; Angelicheva D; Tournev I; Gooding R; et al. Mutation history of the Roma/Gypsies | 0 | 0 |
| 47 | 5 | 32 | 132 2004 AMERICAN JOURNAL OF HUMAN GENETICS 75(4):647-653 Furman I; Rieder MJ; da Ponte S; Carrington DP; Nickerson DA; et al. Sequence-based linkage analysis | 0 | 0 |
| 48 | 2 | 47 | 133 2004 AMERICAN JOURNAL OF HUMAN GENETICS 75(4):661-668 Ogdie MN; Fisher SE; Yang M; Ishii J; Francks C; et al. Attention deficit hyperactivity disorder: Fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11 | 0 | 2 |
| 49 | 5 | 27 | 134 2004 AMERICAN JOURNAL OF HUMAN GENETICS 75(4):687-692 Evans DM; Cardon LR Guidelines for genotyping in genomewide linkage studies: Single-nucleotide-polymorphism maps versus microsatellite maps | 1 | 1 |
| 50 | 3 | 34 | 135 2004 AMERICAN JOURNAL OF HUMAN GENETICS 75(6):948-965 Schaid DJ; Guenther JC; Christensen GB; Hebbring S; Rosenow C; et al. Comparison of microsatellites versus single-nucleotide polymorphisms in a genome linkage screen for prostate cancer-susceptibility loci | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 51 | 1 | 72 | 136 2004 AMERICAN JOURNAL OF HUMAN GENETICS 75(6):1015-1031 Falchi M; Forabosco P; Mocci E; Borlino CC; Picciau A; et al. A genomewide search using an original pairwise sampling approach for large genealogies identifies a new locus for total and low-density lipoprotein cholesterol in two genetically differentiated isolates of Sardinia | 0 | 0 |
| 52 | 1 | 44 | 137 2004 AMERICAN JOURNAL OF HUMAN GENETICS 75(6):1046-1058 Francks C; Paracchini S; Smith SD; Richardson AJ; Scerri TS; et al. A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States | 0 | 0 |
| 53 | 1 | 24 | 138 2004 AMERICAN JOURNAL OF HUMAN GENETICS 75(6):1094-1105 Monks SA; Leonardson A; Zhu H; Cundiff P; Pietrusiak P; et al. Genetic inheritance of gene expression in human cell lines | 0 | 0 |
| 54 | 4 | 16 | 139 2004 AMERICAN JOURNAL OF HUMAN GENETICS 75(6):1143-1148 Kong X; Murphy K; Raj T; He C; White PS; et al. A combined linkage-physical map of the human genome | 0 | 0 |
| 55 | 1 | 51 | 263 2005 AMERICAN JOURNAL OF HUMAN GENETICS 76(1):100-111 de Geus EJC; Posthuma D; Kupper N; van den Berg M; Willemsen G; et al. A whole-genome scan for 24-hour respiration rate: A major locus at 10q26 influences respiration during sleep | 0 | 0 |
| 56 | 1 | 4 | 38 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 120A(1):1-4 Kurpinski KT; Magyari PA; Gorlin RJ; Ng D; Biesecker LG Designation of the TARP syndrome and linkage to Xp11.23-q13.3 without samples from affected patients | 0 | 0 |
| 57 | 1 | 23 | 140 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 131A(2):209-212 Probst FJ; Hedera P; Sclafani AM; Martin DM; Martin DM; et al. Skewed X-inactivation in carriers establishes linkage in an X-linked deafness-mental retardation syndrome | 0 | 0 |
| 58 | 2 | 74 | 141 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS 124B(1):101-112 Stassen HH; Bridler R; Hell D; Weisbrod M; Scharfetter C Ethnicity-independent genetic basis of functional psychoses: A genotype-to-phenotype approach | 0 | 0 |
| 59 | 1 | 14 | 142 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS 125B(1):83-86 Hong KS; McInnes LA; Service SK; Song T; Lucas J; et al. Genetic mapping using haplotype and model-free linkage analysis supports previous evidence for a locus predisposing to severe bipolar disorder at 5q31-33 | 0 | 0 |
| 60 | 1 | 43 | 143 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS 127B(1):104-112 McCauley JL; Olson LM; Dowd M; Amin T; Steele A; et al. Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism | 0 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 61 | 2 | 35 | 144 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS 128B(1):94-101 Gelernter J; Liu XX; Hesselbrock V; Page GP; Goddard A; et al. Results of a genomewide linkage scan: Support for chromosomes 9 and 11 loci increasing risk for cigarette smoking | 0 | 0 |
| 62 | 1 | 52 | 145 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS 131B(1):51-59 McCauley JL; Olson LM; Delahanty R; Amin T; Nurmi EL; et al. A linkage disequilibrium map of the 1-Mb 15q12 GABA(A) receptor subunit cluster and association to autism | 0 | 0 |
| 63 | 2 | 45 | 146 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS 131B(1):67-75 Chapman NH; Igo RP; Thomson JB; Matsushita M; Brkanac Z; et al. Linkage analyses of four regions previously implicated in dyslexia: Confirmation of a locus on chromosome 15q | 0 | 0 |
| 64 | 1 | 115 | 39 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS 123C(1):36-47 Schulze TG; McMahon FJ Genetic linkage and association studies in bipolar affective disorder: A time for optimism | 0 | 2 |
| 65 | 1 | 33 | 147 2004 AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE 169(9):1007-1013 Birkisson IF; Halapi E; Bjornsdottir US; Shkolny DL; Adalsteinsdottir E; et al. Genetic approaches to assessing evidence for a T helper type 1 cytokine defect in adult asthma | 0 | 0 |
| 66 | 1 | 50 | 148 2004 AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE 169(11):1217-1223 Gohlke H; Illig T; Bahnweg M; Klopp N; Andre E; et al. Association of the interleukin-1 receptor antagonist gene with asthma | 0 | 1 |
| 67 | 1 | 33 | 40 2003 ANNALS OF HUMAN GENETICS 67:487-494 Tapper WJ; Maniatis N; Morton NE; Collins A A metric linkage disequilibrium map of a human chromosome | 1 | 4 |
| 68 | 1 | 32 | 149 2004 ANNALS OF HUMAN GENETICS 68:313-323 Alves S; Rocha J; Amorim A; Prata MJ Tracing the origin of the most common thiopurine methyltransferase (TPMT) variants: Preliminary data from the patterns of haplotypic association with two CA repeats | 0 | 0 |
| 69 | 1 | 42 | 150 2004 ANNALS OF HUMAN GENETICS 68:428-437 Alonso S; Armour JAL Compound haplotypes at Xp11.23 and human population growth in Eurasia | 0 | 0 |
| 70 | 2 | 37 | 151 2004 ANNALS OF HUMAN GENETICS 68:563-573 Wang H; Hao B; Zhou K; Chen X; Wu S; et al. Linkage disequilibrium and haplotype architecture for two ABC transporter genes (ABCC1 and ABCG2) in Chinese population: Implications for pharmacogenomic association studies | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 71 | 1 | 26 | 41 2003 ANNALS OF NEUROLOGY 53(3):376-381 Marconi R; De Fusco M; Aridon P; Plewnia K; Rossi M; et al. Familial hemiplegic migraine type 2 is linked to 0.9Mb region on chromosome 1q23 | 0 | 7 |
| 72 | 1 | 59 | 42 2003 ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS 4:437-457 Leppert MF; Singh NA Nonsyndromic seizure disorders: Epilepsy and the use of the Internet to advance research | 0 | 0 |
| 73 | 5 | 139 | 152 2004 ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS 5:317-349 Lynn A; Ashley T; Hassold T Variation inhuman meiotic recombination | 0 | 1 |
| 74 | 9 | 153 | 153 2004 ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS 5:351-378 Enard W; Paabo S Comparative primate genomics | 0 | 0 |
| 75 | 1 | 28 | 154 2004 ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY 130(3):281-288 Kemperman MH; De Leenheer EMR; Huygen PLM; van Wijk E; van Duijnhoven G; et al. A Dutch family with hearing loss linked to the DFNA20/26 locus - Longitudinal analysis of hearing impairment | 0 | 0 |
| 76 | 1 | 38 | 43 2003 ARTHRITIS AND RHEUMATISM 48(1):90-96 Newton J; Brown MA; Milicic A; Ackerman H; Darke C; et al. The effect of HLA-DR on susceptibility to rheumatoid arthritis is influenced by the associated lymphotoxin alpha-tumor necrosis factor haplotype | 0 | 14 |
| 77 | 1 | 13 | 155 2004 ARTHRITIS AND RHEUMATISM 50(1):98-102 Forster T; Chapman K; Marcelline L; Mustafa Z; Southam L; et al. Finer linkage mapping of primary osteoarthritis susceptibility loci on chromosomes 4 and 16 in families with affected women | 0 | 1 |
| 78 | 2 | 10 | 156 2004 BIOINFORMATICS 20(17):3280-3283 Bahlo M; Xing L; Wilkinson CR HumanMSD and MouseMSD: generating genetic maps for human and murine microsatellite markers | 0 | 0 |
| 79 | 1 | 71 | 44 2003 BIOLOGICAL PSYCHIATRY 54(11):1265-1273 McInnis MG; Dick DM; Willour VL; Avramopoulos D; MacKinnon DF; et al. Genome-wide scan and conditional analysis in bipolar disorder: Evidence for genomic interaction in the National Institute of Mental Health Genetics Initiative bipolar pedigrees | 0 | 4 |
| 80 | 1 | 31 | 45 2003 BIOTECHNOLOGY AND BIOENGINEERING 84(1):96-102 Nakayama H; Arakaki A; Maruyama K; Takeyama H; Matsunaga T Single-nucleotide polymorphism analysis using fluorescence resonance energy transfer between DNA-labeling fluorophore, fluorescein isothiocyanate, and DNA intercalator, POPO-3, on bacterial magnetic particles | 0 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 81 | 2 | 36 | 46 2003 BMC GENOMICS 4 Ghebranious N; Vaske D; Yu AD; Zhao CF; Marth G; et al. STRP Screening Sets for the human genome at 5 cM density | 0 | 2 |
| 82 | 1 | 19 | 47 2003 CLINICAL GENETICS 63(1):39-45 DeWan AT; Parrado AR; Leal SM A second kindred linked to DFNA20 (17q25.3) reduces the genetic interval | 0 | 2 |
| 83 | 1 | 21 | 157 2004 CLINICAL GENETICS 66(1):73-78 Rafiq MA; Ansar M; Pham T; Amin-ud-din M; Anwar M; et al. Localization of a novel locus for hereditary nail dysplasia to chromosome 17q25.1-17q25.3 | 0 | 0 |
| 84 | 1 | 24 | 158 2004 CLINICAL GENETICS 66(4):341-348 Kumar A; Blanton SH; Babu M; Markandaya M; Girimaji SC Genetic analysis of primary microcephaly in Indian families: novel ASPM mutations | 0 | 0 |
| 85 | 5 | 50 | 48 2003 COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY 68:79-88 Bertranpetit J; Calafell F; Comas D; Gonzalez-Neira A; Navarro A Structure of linkage disequilibrium in humans: Genome factors and population stratification | 0 | 0 |
| 86 | 1 | 26 | 49 2003 COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY 68:471-477 Clark AG; Glanowski S; Nielsen R; Thomas P; Kejariwal A; et al. Positive selection in the human genome inferred from human-chimp-mouse orthologous gene alignments | 0 | 0 |
| 87 | 1 | 22 | 159 2004 COLLEGIUM ANTROPOLOGICUM 28(1):403-421 Rudan I; Stevanovic R; Vitart V; Vuletic G; Sibbett L; et al. Lost in transition - The island of Susak (1951-2001) | 0 | 0 |
| 88 | 1 | 51 | 160 2004 COMPUTATIONAL METHODS FOR SNPS AND HAPLOTYPE INFERENCE 2983:26-47 Halldorsson BV; Bafna V; Edwards N; Lippert R; Yooseph S; et al. A survey of computational methods for determining haplotypes | 0 | 0 |
| 89 | 2 | 11 | 50 2003 CURRENT BIOLOGY 13(16):R641-R643 Marais G; Galtier N Sex chromosomes: how X-Y recombination stops | 0 | 2 |
| 90 | 2 | 59 | 161 2004 CURRENT BIOLOGY 14(17):1531-1539 Rockman MV; Hahn MW; Soranzo N; Loisel DA; Goldstein DB; et al. Positive selection on MMP3 regulation has shaped heart disease risk | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 91 | 1 | 61 | 51 2003 CURRENT OPINION IN CLINICAL NUTRITION AND METABOLIC CARE 6(4):369-375 Swarbrick MM; Vaisse C Emerging trends in the search for genetic variants predisposing to human obesity | 0 | 1 |
| 92 | 2 | 38 | 52 2003 CURRENT OPINION IN DRUG DISCOVERY & DEVELOPMENT 6(3):304-309 Freudenberg J Genome-wide prediction of disease-relevant genes and variants | 0 | 0 |
| 93 | 1 | 55 | 6 2002 CURRENT OPINION IN GENETICS & DEVELOPMENT 12(6):657-663 Nachman MW Variation in recombination rate across the genome: evidence and implications | 8 | 12 |
| 94 | 1 | 42 | 53 2003 CURRENT OPINION IN ONCOLOGY 15(1):50-54 Zhou W Mapping genetic alterations in tumors with single nucleotide polymorphisms | 0 | 3 |
| 95 | 6 | 139 | 162 2004 CYTOGENETIC AND GENOME RESEARCH 105(2-4):385-394 Galtier N; Bonhomme F; Moulia C; Belkhir K; Caminade P; et al. Mouse biodiversity in the genomic era | 0 | 0 |
| 96 | 3 | 15 | 163 2004 CYTOGENETIC AND GENOME RESEARCH 106(1):39-42 Sun F; Trpkov K; Rademaker A; Ko E; Barclay L; et al. The effect of cold storage on recombination frequencies in human male testicular cells | 0 | 0 |
| 97 | 3 | 36 | 164 2004 CYTOGENETIC AND GENOME RESEARCH 107(3-4):208-215 Tease C; Hulten MA Inter-sex variation in synaptonemal complex lengths largely determine the different recombination rates in male and female germ cells | 0 | 0 |
| 98 | 1 | 23 | 165 2004 CYTOGENETIC AND GENOME RESEARCH 107(3-4):249-255 Hassold T; Judis L; Chan ER; Schwartz S; Seftel A; et al. Cytological studies of meiotic recombination in human males | 0 | 1 |
| 99 | 1 | 53 | 166 2004 DIABETES 53(2):492-499 Das SK; Hasstedt SJ; Zhang ZX; Elbein SC Linkage and association mapping of a chromosome 1q21-q24 type 2 diabetes susceptibility locus in Northern European Caucasians | 0 | 4 |
| 100 | 1 | 55 | 167 2004 DIABETES 53(5):1375-1384 Kim SH; Ma XW; Weremowicz S; Ercolino T; Powers C; et al. Identification of a locus for maturity-onset diabetes of the young on chromosome 8p23 | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 101 | 1 | 25 | 168 2004 DIABETES 53(7):1876-1883 Senee V; Vattem KM; Delepine M; Rainbow LA; Haton C; et al. Wolcott-Rallison syndrome - Clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneity | 0 | 1 |
| 102 | 1 | 59 | 54 2003 DISCRETE MATHEMATICS AND THEORETICAL COMPUTER SCIENCE, PROCEEDINGS 2731:26-47 Halldorsson BV; Bafna V; Edwards N; Lippert R; Yooseph S; et al. Combinatorial problems arising in SNP and haplotype analysis | 0 | 1 |
| 103 | 4 | 85 | 169 2004 DRUG DEVELOPMENT RESEARCH 62(2):86-96 Hakonarsson H; Stefansson K Role of pharmacogenomics in drug development | 0 | 0 |
| 104 | 1 | 35 | 170 2004 EMBO JOURNAL 23(8):1815-1824 Kee K; Protacio RU; Arora C; Keeney S Spatial organization and dynamics of the association of Rec102 and Rec104 with meiotic chromosomes | 0 | 1 |
| 105 | 1 | 38 | 171 2004 ENDOCRINE-RELATED CANCER 11(2):365-376 Trovato M; Ulivieri A; Dominici R; Ruggeri RM; Vitarelli E; et al. Clinico-pathological significance of cell-type-specific loss of heterozygosity on chromosome 7q21: analysis of 318 microdissected thyroid lesions | 0 | 0 |
| 106 | 5 | 115 | 172 2004 ENDOCRINOLOGIST 14(6):346-352 Nathan BM; Hirschhorn JN; Palmert MR Strategies for studying complex genetic traits | 0 | 0 |
| 107 | 1 | 36 | 55 2003 ENVIRONMENTAL HEALTH PERSPECTIVES 111(11):1421-1427 Yu LZ; Kalla K; Guthrie E; Vidrine A; Klimecki WT Genetic variation in genes associated with arsenic metabolism: Glutathione S-transferase omega 1-1 and purine nucleoside phosphorylase polymorphisms in European and indigenous Americans | 0 | 2 |
| 108 | 1 | 41 | 173 2004 EUROPEAN JOURNAL OF ENDOCRINOLOGY 150(5):643-648 Luccio-Camelo DC; Une KN; Ferreira RES; Khoo SK; Nickolov R; et al. A meiotic recombination in a new isolated familial somatotropinoma kindred | 0 | 1 |
| 109 | 1 | 20 | 56 2003 EUROPEAN JOURNAL OF HUMAN GENETICS 11(5):420-423 Keen TJ; Mohamed MD; McKibbin M; Rashid Y; Jafri H; et al. Identification of a locus (LCA9) for Leber's congenital amaurosis on chromosome 1p36 | 0 | 3 |
| 110 | 1 | 10 | 57 2003 EUROPEAN JOURNAL OF HUMAN GENETICS 11(10):812-815 Wajid M; Abbasi AA; Ansar M; Pham TL; Yan K; et al. DFNB39, a recessive form of sensorineural hearing impairment, maps to chromosome 7q11.22-q21.12 | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 111 | 1 | 30 | 174 2004 EUROPEAN JOURNAL OF HUMAN GENETICS 12(6):489-494 Koskenmies S; Widen E; Onkamo P; Sevon P; Julkunen H; et al. Haplotype associations define target regions for susceptibility loci in systemic lupus erythematosus | 0 | 0 |
| 112 | 1 | 19 | 175 2004 EUROPEAN JOURNAL OF HUMAN GENETICS 12(8):633-638 Franke L; van Bakel H; Diosdado BA; van Belzen M; Wapenaar M; et al. TEAM: a tool for the integration of expression, and linkage and association maps | 0 | 0 |
| 113 | 1 | 36 | 176 2004 EUROPEAN JOURNAL OF HUMAN GENETICS 12(10):820-828 Willemsen G; Boomsma DI; Beem AL; Vink JM; Slagboom PE; et al. QTLs for height: results of a full genome scan in Dutch sibling pairs | 0 | 0 |
| 114 | 4 | 75 | 177 2004 FLUCTUATION AND NOISE LETTERS 4(3):L453-L464 Li WT; Holste D Spectral analysis of guanine and cytosine fluctuations of mouse genomic DNA | 0 | 0 |
| 115 | 1 | 79 | 58 2003 GENE 317(1-2):67-77 Filatov DA; Gerrard DT High mutation rates in human and ape pseudoautosomal genes | 2 | 3 |
| 116 | 1 | 22 | 59 2003 GENES AND IMMUNITY 4(8):559-563 Giedraitis V; Modin H; Callander M; Landtblom AM; Fossdal R; et al. Genome-wide TDT analysis in a localized population with a high prevalence of multiple sclerosis indicates the importance of a region on chromosome 14q | 0 | 1 |
| 117 | 1 | 73 | 60 2003 GENETIC EPIDEMIOLOGY 24(4):243-252 Leal SM Genetic maps of microsatellite and single-nucleotide polymorphism markers: Are the distances accurate? | 3 | 4 |
| 118 | 3 | 53 | 178 2004 GENETICA 122(3):245-252 Boyle AS; Noor MAF Variation in recombination rate may bias human genetic disease mapping studies | 0 | 0 |
| 119 | 1 | 68 | 7 2002 GENETICS 162(4):1849-1861 Saunders MA; Hammer MF; Nachman MW Nucleotide variability at G6pd and the signature of malarial selection in humans | 5 | 15 |
| 120 | 2 | 60 | 61 2003 GENETICS 164(3):1043-1053 Wakeley J; Lessard S Theory of the effects of population structure and sampling on patterns of linkage disequilibrium applied to genomic data from humans | 0 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 121 | 1 | 43 | 62 2003 GENETICS 164(4):1567-1587 Falush D; Stephens M; Pritchard JK Inference of population structure using multilocus genotype data: Linked loci and correlated allele frequencies | 1 | 31 |
| 122 | 1 | 50 | 63 2003 GENETICS 164(4):1667-1676 Przeworski M Estimating the time since the fixation of a beneficial allele | 1 | 6 |
| 123 | 1 | 9 | 64 2003 GENETICS 165(3):1629-1632 Lercher MJ; Hurst LD Imprinted chromosomal regions of the human genome have unusually high recombination rates | 0 | 1 |
| 124 | 1 | 42 | 65 2003 GENETICS 165(4):2063-2070 Zhang JZ Evolution of the human ASPM gene, a major determinant of brain size | 0 | 12 |
| 125 | 1 | 126 | 179 2004 GENETICS 166(1):307-329 Samollow PB; Kammerer CM; Mahaney SM; Schneider JL; Westenberger SJ; et al. First-generation linkage map of the gray, short-tailed opossum, Monodelphis domestica, reveals genome-wide reduction in female recombination rates | 0 | 0 |
| 126 | 6 | 44 | 180 2004 GENETICS 167(1):387-397 Ptak SE; Voelpel K; Przeworski M Insights into recombination from patterns of linkage disequilibrium in humans | 1 | 3 |
| 127 | 5 | 79 | 181 2004 GENETICS 167(1):423-437 Nachman MW; D'Agostino SL; Tillquist CR; Mobasher Z; Hammer MF Nucleotide variation at Msn and Alas2, two genes flanking the centromere of the X chromosome in humans | 1 | 1 |
| 128 | 3 | 44 | 182 2004 GENETICS 167(3):1461-1473 Jeffrey DW Estimating recombination rates using three-site likelihoods | 0 | 0 |
| 129 | 6 | 72 | 183 2004 GENETICS 167(4):1841-1853 Hammer MF; Garrigan D; Wood E; Wilder JA; Mobasher Z; et al. Heterogeneous patterns of variation among multiple human x-linked loci: The possible role of diversity-reducing selection in non-Africans | 0 | 0 |
| 130 | 4 | 49 | 184 2004 GENETICS 167(4):2067-2081 Fearnhead P; Harding RM; Schneider JA; Myers S; Donnelly P Application of coalescent mediods to reveal fine-scale rate vairiation and recombination hotspots | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 131 | 2 | 87 | 66 2003 GENOME RESEARCH 13(1):13-26 Hardison RC; Roskin KM; Yang S; Diekhans M; Kent WJ; et al. Covariation in frequencies of substitution, deletion, transposition, and recombination during eutherian evolution | 10 | 54 |
| 132 | 3 | 34 | 67 2003 GENOME RESEARCH 13(4):732-741 Giardine B; Elnitski L; Riemer C; Makalowska L; Schwartz S; et al. GALA, a database for genomic sequence alignments and annotations | 0 | 8 |
| 133 | 1 | 40 | 68 2003 GENOME RESEARCH 13(6):1158-1168 Innan H; Padhukasahasram B; Nordborg M The pattern of polymorphism on human chromosome 21 | 3 | 10 |
| 134 | 1 | 56 | 69 2003 GENOME RESEARCH 13(9):2059-2068 Ventura M; Mudge JM; Palumbo V; Burn S; Blennow E; et al. Neocentromeres in 15q24-26 map to duplicons which flanked an ancestral centromere in 15q25 | 0 | 12 |
| 135 | 2 | 35 | 70 2003 GENOME RESEARCH 13(10):2260-2264 Urrutia AO; Hurst LD The signature of selection mediated by expression on human genes | 2 | 11 |
| 136 | 1 | 30 | 185 2004 GENOME RESEARCH 14(3):414-425 Matsuzaki H; Loi H; Dong S; Tsai YY; Fang J; et al. Parallel genotyping of over 10,000 SNPs using a one-primer assay on a high-density oligonucleotide array | 4 | 23 |
| 137 | 8 | 70 | 186 2004 GENOME RESEARCH 14(4):528-538 Jensen-Seaman MI; Furey TS; Payseur BA; Lu YT; Roskin KM; et al. Comparative recombination rates in the rat, mouse, and human genomes | 0 | 3 |
| 138 | 3 | 44 | 187 2004 GENOME RESEARCH 14(4):567-573 Makova KD; Yang S; Chiaromonte F Insertions and deletions are male biased too: A whole-genome analysis in rodents | 0 | 2 |
| 139 | 5 | 70 | 188 2004 GENOME RESEARCH 14(6):1002-1013 Lercher MJ; Chamary JV; Hurst LD Genomic regionality in rates of evolution is not explained by clustering of genes of comparable expression profile | 0 | 0 |
| 140 | 1 | 22 | 189 2004 GENOME RESEARCH 14(6):1199-1205 Nievergelt CM; Smith DW; Kohlenberg JB; Schork NJ Large-scale integration of human genetic and physical maps | 2 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 141 | 2 | 35 | 190 2004 GENOME RESEARCH 14(7):1221-1231 Boissinot S; Entezam A; Young L; Munson PJ; Furano AV The Insertional history of an active family of L1 retrotransposons in humans | 0 | 0 |
| 142 | 1 | 17 | 191 2004 GENOME RESEARCH 14(7):1358-1361 Greenwood TA; Rana BK; Schork NJ Human haplotype block sizes are negatively correlated with recombination rates | 0 | 0 |
| 143 | 2 | 30 | 192 2004 GENOME RESEARCH 14(8):1633-1640 Halldorsson BV; Bafna V; Lippert R; Schwartz R; De La Vega FM; et al. Optimal haplotype block-free selection of tagging SNPs for genome-wide association studies | 0 | 1 |
| 144 | 1 | 21 | 193 2004 GENOME RESEARCH 14(10A):1987-1998 Ihara N; Takasuga A; Mizoshita K; Takeda H; Sugimoto M; et al. A comprehensive genetic map of the cattle genome based on 3802 microsatellites | 0 | 0 |
| 145 | 2 | 27 | 194 2004 GENOME RESEARCH 14(10B):2034-2040 Furey TS; Diekhans M; Lu YT; Graves TA; Oddy L; et al. Analysis of human mRNAs with the reference genome sequence reveals potent errors, polymorphisms, and RNA editing | 0 | 0 |
| 146 | 1 | 36 | 195 2004 GENOMICS 83(2):335-345 Smirnov D; Bruzel A; Morley M; Cheung VG Direct IBD mapping: identical-by-descent mapping without genotyping | 0 | 0 |
| 147 | 2 | 23 | 196 2004 GENOMICS 84(4):623-630 Hao K; Li C; Rosenow C; Wong WH Estimation of genotype error rate using samples with pedigree information - an application on the GeneChip Mapping 10K array | 0 | 0 |
| 148 | 1 | 27 | 71 2003 GUT 52:II1-II5 Thomas G; Cann H Irruption of genomics in the search for disease related genes | 0 | 0 |
| 149 | 1 | 58 | 197 2004 HUMAN GENETICS 114(4):366-376 Frisch A; Colombo R; Michaelovsky E; Karpati M; Goldman B; et al. Origin and spread of the 1278insTATC mutation causing Tay-Sachs disease in Ashkenazi Jews: genetic drift as a robust and parsimonious hypothesis | 0 | 1 |
| 150 | 1 | 24 | 198 2004 HUMAN GENETICS 114(5):510-516 Peyrard-Janvid M; Anthoni H; Onkamo P; Lahermo P; Zucchelli M; et al. Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 151 | 1 | 25 | 199 2004 HUMAN GENETICS 114(6):588-593 Sivagnanasundaram S; Broman KW; Liu M; Petronis A Quasi-linkage: a confounding factor in linkage analysis of complex diseases? | 0 | 0 |
| 152 | 1 | 43 | 200 2004 HUMAN GENETICS 115(2):149-156 Luijendijk MWJ; van Wijk E; Bischoff AMLC; Krieger E; Huygen PLM; et al. Identification and molecular modelling of a mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11) | 0 | 1 |
| 153 | 1 | 75 | 8 2002 HUMAN HEREDITY 54(4):199-209 Brzustowicz LM; Hayter JE; Hodgkinson KA; Chow EWC; Bassett AS Fine mapping of the schizophrenia susceptibility locus on chromosome 1q22 | 0 | 3 |
| 154 | 1 | 14 | 72 2003 HUMAN HEREDITY 55(1):71-74 Ansar M; Ramzan M; Pham TL; Yan K; Jamal SM; et al. Localization of a novel autosomal recessive non-syndromic hearing impairment locus (DFNB38) to 6q26-q27 in a consanguineous kindred from Pakistan | 0 | 0 |
| 155 | 1 | 54 | 73 2003 HUMAN HEREDITY 56(4):166-187 Fan RZ; Jung JS High-resolution joint linkage disequilibrium and linkage mapping of quantitative trait loci based on sibship data | 0 | 0 |
| 156 | 2 | 27 | 201 2004 HUMAN HEREDITY 57(2):100-108 Feenstra B; Greenberg DA; Hodge SE Using Lod scores to detect sex differences in male-female recombination fractions | 0 | 0 |
| 157 | 1 | 25 | 74 2003 HUMAN MOLECULAR GENETICS 12(1):51-59 Varilo T; Paunio T; Parker A; Perola M; Meyer J; et al. The interval of linkage disequilibrium (LD) detected with microsatellite and SNP markers in chromosomes of Finnish populations with different histories | 3 | 17 |
| 158 | 1 | 21 | 75 2003 HUMAN MOLECULAR GENETICS 12(7):771-776 Shifman S; Kuypers J; Kokoris M; Yakir B; Darvasi A Linkage disequilibrium patterns of the human genome across populations | 0 | 12 |
| 159 | 1 | 38 | 76 2003 HUMAN MOLECULAR GENETICS 12(16):1973-1979 Raby BA; Silverman EK; Lazarus R; Lange C; Kwiatkowski DJ; et al. Chromosome 12q harbors multiple genetic loci related to asthma and asthma-related phenotypes | 0 | 3 |
| 160 | 1 | 44 | 77 2003 HUMAN MOLECULAR GENETICS 12(17):2229-2239 Laurent AM; Li MZ; Sherman S; Roizes G; Buard J Recombination across the centromere of disjoined and non-disjoined chromosome 21 | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 161 | 1 | 30 | 78 2003 HUMAN MOLECULAR GENETICS 12(19):2411-2415 Lercher MJ; Urrutia AO; Pavlicek A; Hurst LD A unification of mosaic structures in the human genome | 2 | 7 |
| 162 | 1 | 48 | 79 2003 HUMAN MOLECULAR GENETICS 12(20):2569-2575 van Heel DA; Dechairo BM; McGovern DPB; Negoro K; Carey AH; et al. The IBD6 Crohn's disease locus demonstrates complex interactions with CARD15 and IBD5 disease-associated variants | 0 | 3 |
| 163 | 1 | 32 | 80 2003 HUMAN MOLECULAR GENETICS 12(20):2657-2667 Hayward C; Shu XH; Lennon A; Barran P; Zareparsi S; et al. Mutation in a short-chain collagen gene, CTRP5, results in extracellular deposit formation in late-onset retinal degeneration: a genetic model for age-related macular degeneration | 0 | 7 |
| 164 | 1 | 37 | 81 2003 HUMAN MOLECULAR GENETICS 12(24):3225-3230 Francks C; DeLisi LE; Shaw SH; Fisher SE; Richardson AJ; et al. Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11 | 1 | 1 |
| 165 | 1 | 29 | 202 2004 HUMAN MOLECULAR GENETICS 13(9):975-981 Fossdal R; Jonasson F; Kristjansdottir GT; Kong A; Stefansson H; et al. A novel TEAD1 mutation is the causative allele in Sveinsson's chorioretinal atrophy (helicoid peripapillary chorioretinal degeneration) | 0 | 0 |
| 166 | 3 | 45 | 203 2004 HUMAN MOLECULAR GENETICS 13(15):1623-1632 Tsunoda T; Lathrop GM; Sekine A; Yamada R; Takahashi A; et al. Variation of gene-based SNPs and linkage disequilibrium patterns in the human genome | 0 | 0 |
| 167 | 2 | 30 | 204 2004 HUMAN MOLECULAR GENETICS 13(17):1943-1949 Sawcer SJ; Maranian M; Singlehurst S; Yeo TW; Compston A; et al. Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping | 0 | 0 |
| 168 | 2 | 61 | 205 2004 HUMAN MOLECULAR GENETICS 13(17):1951-1958 Engelmark M; Beskow A; Magnusson J; Erlich H; Gyllensten U Affected sib-pair analysis of the contribution of HLA class I and class II loci to development of cervical cancer | 0 | 0 |
| 169 | 6 | 26 | 206 2004 HUMAN MOLECULAR GENETICS 13(22):2823-2828 Zhang J; Li F; Li J; Zhang MQ; Zhang XG Evidence and characteristics of putative human alpha recombination hotspots | 0 | 0 |
| 170 | 1 | 21 | 82 2003 HUMAN MUTATION 22(1):35-42 Sharp JD; Wheeler RB; Parker KA; Gardiner RM; Williams RE; et al. Spectrum of CLN6 mutations in variant late infantile neuronal cerolid lipofuscinosis | 0 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 171 | 1 | 35 | 83 2003 HYPERTENSION 41(1):69-74 Kuznetsova T; Staessen JA; Olszanecka A; Ryabikov A; Stolarz K; et al. Maternal and paternal influences on left ventricular mass of offspring | 0 | 2 |
| 172 | 1 | 56 | 84 2003 JOURNAL OF BIOLOGICAL CHEMISTRY 278(15):13133-13142 Sadek CM; Jimenez A; Damdimopoulos AE; Kieselbach T; Nord M; et al. Characterization of human thioredoxin-like 2 - A novel microtubule-binding thioredoxin expressed predominantly in the cilia of lung airway epithelium and spermatid manchette and axoneme | 2 | 13 |
| 173 | 2 | 76 | 85 2003 JOURNAL OF BIOLOGICAL CHEMISTRY 278(45):44874-44885 Miranda-Vizuete A; Tsang K; Yu Y; Jimenez A; Pelto-Huikko M; et al. Cloning and developmental analysis of murid spermatid-specific thioredoxin-2 (SPTRX-2), a novel sperm fibrous sheath protein and autoantigen | 1 | 8 |
| 174 | 3 | 64 | 207 2004 JOURNAL OF BIOLOGICAL CHEMISTRY 279(33):34971-34982 Jimenez A; Zu W; Rawe VY; Pelto-Huikko M; Flickinger CJ; et al. Spermatocyte/spermatid-specific thioredoxin-3, a novel Golgi apparatus-associated thioredoxin, is a specific marker of aberrant spermatogenesis | 0 | 0 |
| 175 | 1 | 55 | 208 2004 JOURNAL OF HEREDITY 95(5):406-420 Kidd KK; Pakstis AJ; Speed WC; Kidd JR Understanding human DNA sequence variation | 0 | 1 |
| 176 | 1 | 67 | 86 2003 JOURNAL OF INVESTIGATIVE DERMATOLOGY SYMPOSIUM PROCEEDINGS 8(2):199-203 Martinez-Mir A; Zlotogorski A; Ott J; Gordon D; Christiano AM Genetic linkage studies in alopecia areata | 0 | 1 |
| 177 | 1 | 53 | 209 2004 JOURNAL OF LIPID RESEARCH 45(10):1876-1884 Lilja HE; Suviolahti E; Soro-Paavonen A; Hiekkalinna T; Day A; et al. Locus for quantitative HDL-cholesterol on chromosome 10q in Finnish families with dyslipidemia | 0 | 0 |
| 178 | 1 | 26 | 87 2003 JOURNAL OF MEDICAL GENETICS 40(6):431-435 Morgan NV; Bacchelli C; Gissen P; Morton J; Ferrero GB; et al. A locus for asphyxiating thoracic dystrophy, ATD, maps to chromosome 15q13 | 2 | 5 |
| 179 | 1 | 20 | 88 2003 JOURNAL OF MEDICAL GENETICS 40(7):543-546 Mubaidin A; Roberts E; Hampshire D; Dehyyat M; Shurbaji A; et al. Karak syndrome: a novel degenerative disorder of the basal ganglia and cerebellum | 0 | 0 |
| 180 | 1 | 36 | 89 2003 JOURNAL OF MEDICAL GENETICS 40(9):657-663 Howell VM; Haven CJ; Kahnoski K; Khoo SK; Petillo D; et al. HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours | 0 | 14 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 181 | 1 | 55 | 90 2003 JOURNAL OF MEDICAL GENETICS 40(12):872-878 Martinez-Mir A; Zlotogorski A; Londono D; Gordon D; Grunn A; et al. Identification of a locus for type I punctate palmoplantar keratoderma on chromosome 15q22-q24 | 0 | 0 |
| 182 | 1 | 9 | 210 2004 JOURNAL OF MEDICAL GENETICS 41(1) Ohno K; Engel AG Lack of founder haplotype for the rapsyn N88K mutation: N88K is an ancient founder mutation or arises from multiple founders | 0 | 2 |
| 183 | 1 | 64 | 211 2004 JOURNAL OF MEDICAL GENETICS 41(3):233-239 Jeganathan D; Chodhari R; Meeks M; Faeroe O; Smyth D; et al. Loci for primary ciliary dyskinesia map to chromosome 16p12.1-12.2 and 15q13.1-15.1 in Faroe Islands and Israeli Druze genetic isolates | 0 | 0 |
| 184 | 1 | 8 | 212 2004 JOURNAL OF MEDICAL GENETICS 41(8) Woods CG; Valente EM; Bond J; Roberts E A new method for autozygosity mapping using single nucleotide polymorphisms (SNPs) and EXCLUDEAR | 0 | 0 |
| 185 | 1 | 39 | 213 2004 JOURNAL OF MEDICAL GENETICS 41(10):772-777 Pal B; Mohamed MD; Keen TJ; Williams GA; Bradbury JA; et al. A new phenotype of recessively inherited foveal hypoplasia and anterior segment dysgenesis maps to a locus on chromosome 16q23.2-24.2. | 0 | 0 |
| 186 | 1 | 23 | 214 2004 JOURNAL OF MEDICAL GENETICS 41(11):849-852 Aslam M; Chahrour MH; Razzaq A; Haque S; Yan K; et al. A novel locus for autosomal recessive form of hypotrichosis maps to chromosome 3q26.33-q27.3 | 0 | 0 |
| 187 | 2 | 9 | 215 2004 JOURNAL OF MEDICAL GENETICS 41(12) Forshew T; Johnson CA SCAMP: a spreadsheet to collate autozygosity mapping projects | 0 | 0 |
| 188 | 1 | 21 | 216 2004 JOURNAL OF MEDICAL GENETICS 41(12):941-944 Ausseil J; Loredo-Osti JC; Verner A; Darmond-Zwaig C; Maire I; et al. Localisation of a gene for mucopolysaccharidosis IIIC to the pericentromeric region of chromosome 8 | 0 | 0 |
| 189 | 1 | 31 | 217 2004 JOURNAL OF MOLECULAR EVOLUTION 58(6):653-660 Belle EMS; Duret L; Galtier N; Eyre-Walker A The decline of isochores in mammals: An assessment of the GC content variation along the mammalian phylogeny | 0 | 0 |
| 190 | 1 | 26 | 218 2004 JOURNAL OF THEORETICAL BIOLOGY 228(2):185-194 Lai YL; Sun FZ Sampling distribution for microsatellites amplified by PCR: mean field approximation and its applications to genotyping | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 191 | 1 | 146 | 91 2003 LANCET 361(9369):1629-1641 Staessen JA; Wang JG; Bianchi G; Birkenhager WH Essential hypertension | 0 | 22 |
| 192 | 2 | 29 | 92 2003 MOLECULAR BIOLOGY AND EVOLUTION 20(4):579-590 Kendal WS An exponential dispersion model for the distribution of human single nucleotide polymorphisms | 0 | 0 |
| 193 | 1 | 28 | 93 2003 MOLECULAR BIOLOGY AND EVOLUTION 20(9):1506-1512 Eder V; Ventura M; Ianigro M; Teti M; Rocchi M; et al. Chromosome 6 phylogeny in primates and centromere repositioning | 0 | 12 |
| 194 | 1 | 33 | 94 2003 MOLECULAR BIOLOGY AND EVOLUTION 20(12):2123-2131 Lai YL; Sun FZ The relationship between microsatellite slippage mutation rate and the number of repeat units | 0 | 5 |
| 195 | 5 | 54 | 219 2004 MOLECULAR BIOLOGY AND EVOLUTION 21(2):410-417 Filatov DA A gradient of silent substitution rate in the human pseudoautosomal region | 0 | 1 |
| 196 | 2 | 65 | 220 2004 MOLECULAR BIOLOGY AND EVOLUTION 21(4):760-769 Le Jossec M; Wambach T; Labuda D; Sinnett D; Levy E Genetic diversity patterns in the SR-BI/II locus can be explained by a recent selective sweep | 0 | 0 |
| 197 | 2 | 77 | 221 2004 MOLECULAR BIOLOGY AND EVOLUTION 21(5):799-808 Fischer A; Wiebe V; Paabo S; Przeworski M Evidence for a complex demographic history of chimpanzees | 1 | 6 |
| 198 | 7 | 47 | 222 2004 MOLECULAR BIOLOGY AND EVOLUTION 21(6):984-990 Meunier J; Duret L Recombination drives the evolution of GC-content in the human genome | 2 | 6 |
| 199 | 2 | 76 | 223 2004 MOLECULAR BIOLOGY AND EVOLUTION 21(9):1800-1811 Storz JF; Payseur BA; Nachman MW Genome scans of DNA variability in humans reveal evidence for selective sweeps outside of Africa | 1 | 1 |
| 200 | 8 | 47 | 224 2004 MOLECULAR BIOLOGY AND EVOLUTION 21(10):1820-1830 Webster MT; Smith NGC; Lercher MJ; Ellegren H Gene expression, synteny, and local similarity in human noncoding mutation rates | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 201 | 4 | 89 | 264 2005 MOLECULAR BIOLOGY AND EVOLUTION 22(1):63-73 Stajich JE; Hahn MW Disentangling the effects of demography and selection in human history | 0 | 0 |
| 202 | 1 | 115 | 95 2003 MOLECULAR GENETICS AND METABOLISM 80(1-2):1-10 Palmert MR; Hirschhorn JN Genetic approaches to stature, pubertal timing, and other complex traits | 1 | 2 |
| 203 | 3 | 57 | 225 2004 MOLECULAR HUMAN REPRODUCTION 10(8):589-598 Oudejans CBM; Mulders J; Lachmeijer AMA; van Dijk M; Konst AAM; et al. The parent-of-origin effect of 10q22 in pre-eclamptic females coincides with two regions clustered for genes with down-regulated expression in androgenetic placentas | 0 | 2 |
| 204 | 1 | 28 | 226 2004 MOLECULAR PSYCHIATRY 9(1):93-98 Als TD; Dahl HA; Flint TJ; Wang AG; Vang M; et al. Possible evidence for a common risk locus for bipolar affective disorder and schizophrenia on chromosome 4p16 in patients from the Faroe Islands | 0 | 1 |
| 205 | 1 | 44 | 227 2004 MOLECULAR PSYCHIATRY 9(2):191-196 Avramopoulos D; Willour VL; Zandi PP; Huo Y; MacKinnon DF; et al. Linkage of bipolar affective disorder on chromosome 8q24: follow-up and parametric analysis | 0 | 0 |
| 206 | 3 | 29 | 228 2004 MOLECULAR PSYCHIATRY 9(3):312-319 Lappalainen J; Kranzler HR; Petrakis I; Somberg LK; Page G; et al. Confirmation and fine mapping of the chromosome 1 alcohol dependence risk locus | 0 | 1 |
| 207 | 2 | 81 | 229 2004 MOLECULAR PSYCHIATRY 9(8):784-795 Mowry BJ; Holmans PA; Pulver AE; Gejman PV; Riley B; et al. Multicenter linkage study of schizophrenia loci on chromosome 22q | 0 | 0 |
| 208 | 1 | 47 | 230 2004 MOLECULAR VISION 10(4-5):37-42 Toomes C; Downey L; Bottomley H; Scott S; Woodruff G; et al. Identification of a fourth locus (EVR4) for familial exudative vitreoretinopathy (FEVR) | 0 | 2 |
| 209 | 1 | 67 | 231 2004 MOLECULAR VISION 10(47):376-382 Bennett TM; Mackay DS; Knopf HLS; Shiels A A novel missense mutation in the gene for gap-junction protein alpha 3 (GJA3) associated with autosomal dominant "nuclear punctate" cataracts linked to chromosome 13q | 0 | 1 |
| 210 | 2 | 51 | 96 2003 MOVEMENT DISORDERS 18(11):1240-1249 Bertoli-Avella AM; Giroud-Benitez JL; Bonifati V; Alvarez-Gonzalez E; Heredero-Baute L; et al. Suggestive linkage to chromosome 19 in a large Cuban family with late-onset Parkinson's disease | 0 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 211 | 1 | 29 | 97 2003 MULTIPLE SCLEROSIS 9(2):128-134 Modin H; Masterman T; Thorlacius T; Stefansson M; Jonasdottir A; et al. Genome-wide linkage screen of a consanguineous multiple sclerosis kinship | 0 | 1 |
| 212 | 1 | 331 | 9 2002 NATURE 420(6915):520-562 Waterston RH; Lindblad-Toh K; Birney E; Rogers J; Abril JF; et al. Initial sequencing and comparative analysis of the mouse genome | 24 | 844 |
| 213 | 1 | 39 | 98 2003 NATURE 421(6923):601-U1 Heilig R; Eckenberg R; Petit JL; Fonknechten NR; Da Silva C; et al. The DNA sequence and analysis of human chromosome 14 | 3 | 29 |
| 214 | 2 | 49 | 99 2003 NATURE 425(6960):805-U1 Mungall AJ; Palmer SA; Sims SK; Edwards CA; Ashurst JL; et al. The DNA sequence and analysis of human chromosome 6 | 5 | 29 |
| 215 | 3 | 50 | 232 2004 NATURE 428(6982):522-528 Dunham A; Matthews LH; Burton J; Ashurst JL; Howe KL; et al. The DNA sequence and analysis of human chromosome 13 | 0 | 6 |
| 216 | 3 | 48 | 233 2004 NATURE 428(6982):529-535 Grimwood J; Gordon LA; Olsen A; Terry A; Schmutz J; et al. The DNA sequence and biology of human chromosome 19 | 2 | 8 |
| 217 | 2 | 50 | 234 2004 NATURE 429(6990):369-374 Humphray SJ; Oliver K; Hunt AR; Plumb RW; Loveland JE; et al. DNA sequence and analysis of human chromosome 9 | 0 | 1 |
| 218 | 2 | 41 | 235 2004 NATURE 429(6990):375-381 Deloukas P; Earthrowl ME; Grafham DV; Rubenfield M; French L; et al. The DNA sequence and comparative analysis of human chromosome 10 | 0 | 1 |
| 219 | 5 | 44 | 236 2004 NATURE 431(7006):268-274 Schmutz J; Martin J; Terry A; Couronne O; Grimwood J; et al. The DNA sequence and comparative analysis of human chromosome 5 | 1 | 2 |
| 220 | 4 | 48 | 237 2004 NATURE 432(7020):988-994 Martin J; Han C; Gordon LA; Terry A; Prabhakar S; et al. The sequence and analysis of duplication-rich human chromosome 16 | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 221 | 0 | 26 | 10 2002 NATURE GENETICS 31(3):241-247 Kong A; Gudbjartsson DF; Sainz J; Jonsdottir GM; Gudjonsson SA; et al. A high-resolution recombination map of the human genome | 263 | 263 |
| 222 | 1 | 46 | 11 2002 NATURE GENETICS 32(1):135-142 Reich DE; Schaffner SF; Daly MJ; McVean G; Mullikin JC; et al. Human genome sequence variation and the influence of gene history, mutation and recombination | 14 | 60 |
| 223 | 3 | 13 | 238 2004 NATURE GENETICS 36(2):114-115 Wall JD Close look at gene conversion hot spots | 0 | 2 |
| 224 | 1 | 50 | 239 2004 NATURE GENETICS 36(3):233-239 Helgadottir A; Manolescu A; Thorleifsson G; Gretarsdottir S; Jonsdottir H; et al. The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke | 3 | 34 |
| 225 | 5 | 30 | 240 2004 NATURE GENETICS 36(7):700-706 Crawford DC; Bhangale T; Li N; Hellenthal G; Rieder MJ; et al. Evidence for substantial fine-scale variation in recombination rates across the human genome | 1 | 6 |
| 226 | 10 | 100 | 241 2004 NATURE GENETICS 36(10):1045-1051 Freimer N; Sabatti C The use of pedigree, sib-pair and association studies of common diseases for genetic mapping and epidemiology | 0 | 0 |
| 227 | 1 | 27 | 242 2004 NATURE GENETICS 36(11):1203-1206 Kong A; Barnard J; Gudbjartsson DF; Thorleifsson G; Jonsdottir G; et al. Recombination rate and reproductive success in humans | 0 | 1 |
| 228 | 1 | 2 | 12 2002 NATURE REVIEWS GENETICS 3(8):571-571 Alfred J Recharting the human genome | 0 | 0 |
| 229 | 2 | 100 | 100 2003 NATURE REVIEWS GENETICS 4(4):315-322 Muller M; Kersten S Nutrigenomics: goals and strategies | 0 | 40 |
| 230 | 5 | 98 | 101 2003 NATURE REVIEWS GENETICS 4(8):587-597 Wall JD; Pritchard JK Haplotype blocks and linkage disequilibrium in the human genome | 11 | 70 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 231 | 3 | 62 | 243 2004 NATURE REVIEWS GENETICS 5(1):43-51 Schaffner SF The X chromosome in population genetics | 0 | 1 |
| 232 | 2 | 86 | 244 2004 NATURE REVIEWS GENETICS 5(1):63-69 Schlotterer C The evolution of molecular markers - just a matter of fashion? | 1 | 3 |
| 233 | 8 | 134 | 245 2004 NATURE REVIEWS GENETICS 5(6):413-424 Kauppi L; Jeffreys AJ; Keeney S Where the crossovers are: Recombination distributions in mammals | 1 | 5 |
| 234 | 2 | 104 | 246 2004 NATURE REVIEWS GENETICS 5(6):446-455 Fazzari MJ; Greally JM Epigenomics: Beyond CpG islands | 0 | 1 |
| 235 | 2 | 99 | 247 2004 NATURE REVIEWS GENETICS 5(10):725-738 Antonarakis SE; Lyle R; Dermitzakis ET; Reymond A; Deutsch S Chromosome 21 and Down syndrome: From genomics to pathophysiology | 0 | 0 |
| 236 | 1 | 36 | 248 2004 NEUROGENETICS 5(1):35-40 Karpati M; Gazit E; Goldman B; Frisch A; Colombo R; et al. Specific mutations in the HEXA gene among Iraqi Jewish Tay-Sachs disease carriers: dating of founder ancestor | 0 | 0 |
| 237 | 1 | 21 | 102 2003 NEUROLOGY 60(10):1664-1667 Rajab A; Mochida GH; Hill A; Ganesh V; Bodell A; et al. A novel form of pontocerebellar hypoplasia maps to chromosome 7q11-21 | 0 | 1 |
| 238 | 1 | 82 | 249 2004 NEUROLOGY PSYCHIATRY AND BRAIN RESEARCH 11(1):13-22 Stassen H; Begleiter H; Beirut L; Culverhouse R; Hinrichs T; et al. Oligogenic approaches to the predisposition of alcohol dependence - A genome-wide search on 255 families | 0 | 0 |
| 239 | 1 | 40 | 250 2004 NEW ENGLAND JOURNAL OF MEDICINE 351(5):460-469 Veugelers M; Bressan M; McDermott DA; Weremowicz S; Morton CC; et al. Mutation of perinatal myosin heavy chain associated with a Carney complex variant | 0 | 2 |
| 240 | 1 | 67 | 103 2003 NUCLEIC ACIDS RESEARCH 31(17):5212-5220 Vinogradov AE Isochores and tissue-specificity | 1 | 9 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 241 | 1 | 60 | 104 2003 PEDIATRIC RESEARCH 53(1):4-9 Boright AP; Kere J; Scherer SW Genomics and pediatric research | 0 | 0 |
| 242 | 2 | 59 | 105 2003 PHARMACOGENOMICS 4(2):171-178 Zhao HY; Pfeiffer R; Gail MH Haplotype analysis in population genetics and association studies | 1 | 7 |
| 243 | 2 | 7 | 106 2003 PHARMACOGENOMICS 4(2):209-215 Hakonarson H; Gulcher JR; Stefansson K deCODE genetics, Inc. | 1 | 4 |
| 244 | 5 | 106 | 107 2003 PHARMACOGENOMICS 4(5):547-570 Hoehe MR Haplotypes and the systematic analysis of genetic variation in genes and genomes | 0 | 5 |
| 245 | 1 | 43 | 251 2004 PHARMACOGENOMICS JOURNAL 4(4):274-282 Vink JM; Beem AL; Posthuma D; Neale MC; Willemsen G; et al. Linkage analysis of smoking initiation and quantity in Dutch sibling pairs | 0 | 1 |
| 246 | 1 | 56 | 252 2004 PHYSIOLOGICAL GENOMICS 18(1):119-127 Greenwood TA; Cadman PE; Stridsberg M; Nguyen S; Taupenot L; et al. Genome-wide linkage analysis of chromogranin B expression in the CEPH pedigrees: implications for exocytotic sympathochromaffin secretion in humans | 0 | 1 |
| 247 | 2 | 54 | 108 2003 PLOS BIOLOGY 1(3):351-360 Styrkarsdottir U; Cazier JB; Kong A; Rolfsson O; Larsen H; et al. Linkage of osteoporosis to chromosome 20p12 and association to BMP2 | 0 | 1 |
| 248 | 2 | 35 | 253 2004 PLOS BIOLOGY 2(6):730-733 Hey J What's so hot about recombination hotspots? | 0 | 0 |
| 249 | 7 | 48 | 254 2004 PLOS BIOLOGY 2(6):849-855 Ptak SE; Roeder AD; Stephens M; Gilad Y; Paabo S; et al. Absence of the TAP2 human recombination hotspot in chimpanzees | 0 | 1 |
| 250 | 2 | 35 | 255 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(26):9757-9762 Loughlin J; Dowling B; Chapman K; Marcelline L; Mustafa Z; et al. Functional variants within the secreted frizzled-related protein 3 gene are associated with hip osteoarthritis in females | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 251 | 1 | 39 | 109 2003 SCIENCE 300(5617):321-324 Navarro A; Barton NH Chromosomal speciation and molecular divergence - Accelerated evolution in rearranged chromosomes | 2 | 34 |
| 252 | 1 | 23 | 110 2003 SCIENCE 302(5652):1960-1963 Clark AG; Glanowski S; Nielsen R; Thomas PD; Kejariwal A; et al. Inferring nonneutral evolution from human-chimp-mouse orthologous gene trios | 2 | 37 |
| 253 | 2 | 35 | 256 2004 SCIENCE 303(5657):537-540 Emerson JJ; Kaessmann H; Betran E; Long MY Extensive gene traffic on the mammalian X chromosome | 0 | 6 |
| 254 | 5 | 39 | 257 2004 SCIENCE 304(5670):581-584 McVean GAT; Myers SR; Hunt S; Deloukas P; Bentley DR; et al. The fine-scale structure of recombination rate variation in the human genome | 4 | 14 |
| 255 | 1 | 104 | 111 2003 SEMINARS IN RESPIRATORY AND CRITICAL CARE MEDICINE 24(2):137-149 Rybicki BA Genetic epidemiological approaches to the study of lung disease | 0 | 0 |
| 256 | 1 | 37 | 112 2003 THEORETICAL POPULATION BIOLOGY 64(4):451-471 Baird SJE; Barton NH; Etheridge AM The distribution of surviving blocks of an ancestral genome | 0 | 0 |
| 257 | 1 | 40 | 258 2004 TRANSFUSION 44(5):707-715 Roubinet F; Despiau S; Calafell F; Jin F; Bertanpetit J; et al. Evolution of the O alleles of the human ABO blood group gene | 0 | 1 |
| 258 | 3 | 79 | 113 2003 TRENDS IN GENETICS 19(6):330-338 Marais G Biased gene conversion: implications for genome and sex evolution | 7 | 17 |
| 259 | 1 | 83 | 114 2003 TRENDS IN GENETICS 19(9):514-522 de Massy B Distribution of meiotic recombination sites | 6 | 11 |
| 260 | 2 | 31 | 259 2004 TRENDS IN GENETICS 20(3):122-126 Webster MT; Smith NGC Fixation biases affecting human SNPs | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 261 | 6 | 100 | 260 2004 TRENDS IN GENETICS 20(4):196-205 Carrington M; Cullen M Justified chauvinism: advances in defining meiotic recombination through sperm typing | 0 | 0 |
| 262 | 1 | 41 | 115 2003 TWIN RESEARCH 6(2):162-169 Iliadou A; Lichtenstein P; Ahlberg S; Hoffstedt J; Arner P; et al. No linkage to obesity in candidate regions of chromosome 2 and 10 in a selected sample of Swedish twins | 0 | 2 |
| 263 | 1 | 32 | 261 2004 TWIN RESEARCH 7(2):192-196 Heijmans BT; Beem AL; Willemsen G; Posthuma D; Slagboom PE; et al. Further evidence for a QTL influencing body mass index on chromosome 7p from a genome-wide scan in Dutch families | 0 | 0 |
| 264 | 2 | 69 | 262 2004 TWIN RESEARCH 7(2):197-210 Zhu G; Evans DM; Duffy DL; Montgomery GW; Medland SE; et al. A genome scan for eye color in 502 twin families: Most variation is due to a QTL on chromosome 15q | 0 | 5 |
Generated by: HistCite 2004.12.21