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Nodes: 37,
Authors: 175,
Journals: 26,
Outer References: 1801,
Words: 183
Collection span: 1994 - 2005
View: Overview. Sorted by NCR.
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
|---|---|---|---|---|---|
| 1 | 0 | 449 | 34 2005 MOLECULAR PSYCHIATRY 10 (2): 160-184 Geuze E; Vermetten E; Bremner JD MR-based in vivo hippocampal volumetrics: 2. Findings in neuropsychiatric disorders | 0 | 1 |
| 2 | 0 | 175 | 1 1994 JOURNAL OF THE NEUROLOGICAL SCIENCES 124 (2): 119-140 MULLER U; GRAEBER MB; HABERHAUSEN G; KOHLER A MOLECULAR-BASIS AND DIAGNOSIS OF NEUROGENETIC DISORDERS | 0 | 14 |
| 3 | 0 | 144 | 8 2000 ANNUAL REVIEW OF NEUROSCIENCE 23: 343-391 Cowan WM; Harter DH; Kandel ER The emergence of modern neuroscience: Some implications for neurology and psychiatry | 0 | 14 |
| 4 | 0 | 138 | 4 1996 MEDICAL HYPOTHESES 47 (4): 289-298 Fischer KM Genes for Prader Willi Syndrome Angelman syndrome and fragile X syndrome are homologous, with genetic imprinting and unstable trinucleotide repeats causing mental retardation, autism and aggression | 1 | 4 |
| 5 | 0 | 129 | 10 2002 DEVELOPMENT AND PSYCHOPATHOLOGY 14 (3): 437-461 Kopnisky KL; Cowan WM; Hyman SE Levels of analysis in psychiatric research | 0 | 0 |
| 6 | 3 | 128 | 25 2004 LANCET NEUROLOGY 3 (11): 652-662 Healy DG; Abou-Sleiman PM; Wood NW PINK, PANK, or PARK? A clinicians' guide to familial parkinsonism | 0 | 2 |
| 7 | 1 | 127 | 6 1997 MEDICAL HYPOTHESES 49 (4): 337-345 Fischer KM Parkinson's disease, amyotrophic lateral sclerosis and spinal muscular atrophy are caused by an unstable (CAG)(n) trinucleotide repeat microsatellite | 0 | 1 |
| 8 | 0 | 82 | 3 1996 HUMAN MOLECULAR GENETICS 5 (5): 607-616 Margolis RL; Stine OC; McInnis MG; Ranen NG; Rubinsztein DC; et al. cDNA cloning of a human homologue of the Caenorhabditis elegans cell fate-determining gene mab-21: Expression, chromosomal localization and analysis of a highly polymorphic (CAG)(n) trinucleotide repeat | 1 | 32 |
| 9 | 1 | 80 | 5 1997 HUMAN GENETICS 100 (1): 114-122 Margolis RL; Abraham MR; Gatchell SB; Li SH; Kidwai AS; et al. cDNAs with long CAG trinucleotide repeats from human brain | 0 | 56 |
| 10 | 6 | 80 | 20 2004 AMERICAN JOURNAL OF HUMAN GENETICS 74 (5): 805-816 Hagerman PJ; Hagerman RJ The fragile-X premutation: A maturing perspective | 4 | 17 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 11 | 0 | 60 | 18 2003 NEUROBIOLOGY OF AGING 24 (8): 1105-1111 Glanzer JG; Eberwine JH Mechanisms of translational control in dendrites | 0 | 1 |
| 12 | 3 | 55 | 23 2004 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 291 (4): 460-469 Jacquemont S; Hagerman RJ; Leehey MA; Hall DA; Levine RA; et al. Penetrance of the fragile X - Associated tremor/ataxia syndrome in a premutation carrier population | 8 | 17 |
| 13 | 4 | 55 | 26 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10 (1): 25-30 Hagerman PJ; Hagerman RJ Fragile X-associated tremor/ataxia syndrome (FXTAS) | 0 | 2 |
| 14 | 1 | 51 | 22 2004 CIRCULATING NUCLEIC ACIDS IN PLASMA/SERUM III AND SERUM PROTEOMICS 1022: 163-184 Wissler JH Extracellular and circulating redox-and metalloregulated eRNA and eRNP - Copper ion-structured RNA cytokines (angiotropin ribokines) and bioaptamer targets imparting RNA chaperone and novel biofunctions to S100-EF-hand and disease-associated proteins | 0 | 0 |
| 15 | 5 | 46 | 37 2005 REVISTA DE NEUROLOGIA 40 (7): 431-437 Castro-Volio I; Cuenca-Berger P Neurodevelopmental (fragile X syndrome) and neurodegenerative (tremoriataxia syndrome) disorders associated to the 'growth' of a gene | 0 | 0 |
| 16 | 3 | 41 | 21 2004 AMERICAN JOURNAL ON MENTAL RETARDATION 109 (2): 154-164 Jacquemont S; Farzin F; Hall D; Leehey M; Tassone F; et al. Aging in individuals with the FMR1 mutation | 1 | 7 |
| 17 | 1 | 36 | 14 2003 AMERICAN JOURNAL OF HUMAN GENETICS 72 (4): 869-878 Jacquemont S; Hagerman RJ; Leehey M; Grigsby J; Zhang L; et al. Fragile X premutation tremor/ataxia syndrome: Molecular, clinical, and neuroimaging correlates | 13 | 47 |
| 18 | 0 | 31 | 2 1996 AMERICAN JOURNAL OF HUMAN GENETICS 58 (6): 1120-1126 Lindsay S; Splitt M; Edney S; Berney TP; Knight SJL; et al. PPM-X: A new X-linked mental retardation syndrome with psychosis, pyramidal signs, and macroorchidism maps to Xq28 | 0 | 14 |
| 19 | 1 | 31 | 15 2003 ANNALS OF NEUROLOGY 53 (5): 616-623 Berry-Kravis E; Lewin F; Wuu J; Leehey M; Hagerman R; et al. Tremor and ataxia in fragile X premutation carriers: Blinded videotape study | 7 | 16 |
| 20 | 4 | 31 | 31 2005 CLINICAL GENETICS 67 (5): 412-417 Loesch DZ; Churchyard A; Brotchie P; Marot M; Tassone F Evidence for, and a spectrum of, neurological involvement in carriers of the fragile X pre-mutation: FXTAS and beyond | 0 | 0 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 21 | 0 | 28 | 17 2003 CURRENT OPINION IN NEUROLOGY 16 (4): 481-485 Sethi KD Tremor | 0 | 2 |
| 22 | 0 | 26 | 7 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 88 (1): 25-28 Schuback DE; Mulligan EL; Sims KB; Tivol EA; Greenberg BD; et al. Screen for MAOA mutations in target human groups | 0 | 10 |
| 23 | 0 | 25 | 19 2003 PARKINSON'S DISEASE: THE LIFE CYCLE OF THE DOPAMINE NEURON 991: 333-338 Wissler JH Redox-and metalloregulated RNA bioaptamer targets of proteins associated with Parkinson's and other neurodegenerative diseases - Factors of relevance in the life cycle of cells | 1 | 1 |
| 24 | 4 | 23 | 27 2004 MOVEMENT DISORDERS 19 (8): 930-933 Arocena DG; Louis ED; Tassone F; Gilliam TC; Ottman R; et al. Screen for expanded FMR1 alleles in patients with essential tremor | 2 | 2 |
| 25 | 4 | 20 | 30 2005 ANNALS OF NEUROLOGY 57 (1): 144-147 Berry-Kravis E; Potanos K; Weinberg D; Zhou LL; Goetz CG Fragile X-associated tremor/ataxia syndrome in sisters related to X-inactivation | 0 | 1 |
| 26 | 5 | 20 | 35 2005 MOVEMENT DISORDERS 20 (2): 230-233 Toft M; Aasly J; Bisceglio G; Adler CH; Uitti RJ; et al. Parkinsonism, FXTAS, and FMR1 premutations | 0 | 0 |
| 27 | 1 | 19 | 29 2004 NEUROSCIENCE LETTERS 368 (1): 21-24 Annesi G; Nicoletti G; Tarantino P; Cutuli N; Annesi F; et al. FRAXE intermediate alleles are associated with Parkinson's disease | 0 | 0 |
| 28 | 6 | 15 | 32 2005 EUROPEAN JOURNAL OF HUMAN GENETICS 13 (1): 2-3 Jacquemont S Screening for FXTAS | 0 | 0 |
| 29 | 0 | 10 | 9 2001 NEUROLOGY 57 (1): 127-130 Hagerman RJ; Leehey M; Heinrichs W; Tassone F; Wilson R; et al. Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X | 19 | 80 |
| 30 | 2 | 10 | 28 2004 NEUROLOGY 63 (2): 362-363 Tan EK; Zhao Y; Puong KY; Law HY; Chan LL; et al. Fragile X premutation alleles in SCA, ET, and parkinsonism in an Asian cohort | 4 | 4 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 31 | 3 | 9 | 24 2004 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 292 (14): 1685-1686 Deng H; Le WD; Jankovic J Premutation Alleles associated with Parkinson disease and essential tremor | 0 | 1 |
| 32 | 2 | 8 | 33 2005 JOURNAL OF CLINICAL NEUROSCIENCE 12 (1): 42-43 Storey E; Billimoria P Increased T-2 signal in the middle cerebellar peduncles on MRI is not specific for fragile X premutation syndrome | 0 | 0 |
| 33 | 1 | 6 | 16 2003 CLINICAL GENETICS 64 (1): 54-56 Rogers C; Partington MW; Turner GM Tremor, ataxia and dementia in older men may indicate a carrier of the fragile X syndrome | 3 | 4 |
| 34 | 3 | 6 | 36 2005 NEUROGENETICS 6 (1): 51-52 Tan EK; Zhao Y; Puong KY; Law HY; Chan LL; et al. Expanded FMR1 alleles are rare in idiopathic Parkinson's disease | 0 | 0 |
| 35 | 0 | 0 | 11 2002 MOVEMENT DISORDERS 17: S351-S351 Leehey MA; Grigsby J; Rubinstein D; Jacquemont S; Greco C; et al. Parkinsonism, tremor and ataxia in a female fragile X carrier | 0 | 1 |
| 36 | 0 | 0 | 12 2002 NEUROLOGY 58 (6): 987-987 Munoz DG Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X | 0 | 0 |
| 37 | 0 | 0 | 13 2002 NEUROLOGY 58 (6): 987-988 Hagerman RJ; Greco C; Jacquemont S; Leehy M; Hagerman P Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X - Reply | 0 | 0 |
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