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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by journal name.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 2001 | 3 | 45 | 1500 1996 MEDICAL ANTHROPOLOGY QUARTERLY 10(4):537-550 Nelkin D The social dynamics of genetic testing: The case of Fragile-X | 1 | 6 |
| 2002 | 4 | 138 | 1501 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 | 0 | 4 |
| 2003 | 17 | 34 | 1129 1993 MEDICAL JOURNAL OF AUSTRALIA 158(7):482-485 SUTHERLAND GR; MULLEY JC; RICHARDS RI FRAGILE-X SYNDROME - THE MOST COMMON CAUSE OF FAMILIAL INTELLECTUAL HANDICAP | 1 | 5 |
| 2004 | 4 | 5 | 1813 1999 MEDICAL JOURNAL OF AUSTRALIA 170(12):624-624 Cohen J; Loesch DZ Fragile X syndrome: do professionals know about it? | 0 | 0 |
| 2005 | 11 | 17 | 2042 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 |
| 2006 | 17 | 25 | 1002 1992 MEDICINA CLINICA 98(4):121-124 GINE R; ESPINAS ML; ANTICH J; CARBALLO M MOLECULAR-GENETICS OF THE FRAGILE-X SYNDROME - MOLECULAR DIAGNOSIS BY DNA PROBES | 1 | 1 |
| 2007 | 8 | 19 | 1003 1992 MEDICINA CLINICA 98(4):131-133 PRIETO F; MARTINEZCASTELLANO F THE FRAGILE-X SYNDROME AND ITS RELATION WITH OTHER SYNDROMES LINKED TO CHROMOSOME-X ASSOCIATED WITH MENTAL-RETARDATION | 0 | 0 |
| 2008 | 0 | 0 | 152 1983 MEDICINA-BUENOS AIRES 43(6):756-756 DELREY G; COCO R INVESTIGATION OF FRAGILE X-CHROMOSOMES IN MEN WITH MENTAL-RETARDATION (RM) OF UNKNOWN CAUSE | 0 | 0 |
| 2009 | 35 | 59 | 1379 1995 MEDICINA-BUENOS AIRES 55(5):457-466 BANARES VG UPDATING THE FRAGILE-X SYNDROME | 0 | 0 |
| 2010 | 12 | 17 | 1004 1992 MENTAL RETARDATION 30(6):355-361 KEENAN J; KASTNER T; NATHANSON R; RICHARDSON N; HINTON J; CRESS DA A STATEWIDE PUBLIC AND PROFESSIONAL-EDUCATION PROGRAM ON FRAGILE X SYNDROME | 0 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2011 | 9 | 24 | 1130 1993 MENTAL RETARDATION 31(4):221-227 WILSON PG; MAZZOCCO MMM AWARENESS AND KNOWLEDGE OF FRAGILE-X SYNDROME AMONG SPECIAL EDUCATORS | 2 | 3 |
| 2012 | 18 | 21 | 1131 1993 MENTAL RETARDATION 31(5):279-283 SMITH SE COGNITIVE DEFICITS ASSOCIATED WITH FRAGILE-X SYNDROME | 2 | 3 |
| 2013 | 2 | 2 | 1247 1994 MENTAL RETARDATION 32(2):156-156 SPITZ HH FRAGILE-X SYNDROME IS NOT THE 2ND LEADING CAUSE OF MENTAL-RETARDATION | 0 | 1 |
| 2014 | 22 | 29 | 1944 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 |
| 2015 | 42 | 92 | 1616 1997 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 3(4):313-322 Abbeduto L; Hagerman RJ Language and communication in fragile X syndrome | 10 | 14 |
| 2016 | 7 | 113 | 1814 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 |
| 2017 | 57 | 117 | 1945 2000 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 6(2):96-106 Mazzocco MMM Advances in research on the fragile X syndrome | 18 | 20 |
| 2018 | 0 | 0 | 2342 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):1-2 Crnic LS; Hagerman R Preface: Fragile X syndrome: Frontiers of understanding gene-brain-behavior relationships | 0 | 0 |
| 2019 | 16 | 48 | 2343 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):3-10 Bailey DB Newborn screening for fragile X syndrome | 0 | 0 |
| 2020 | 34 | 67 | 2344 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):11-16 Cornish K; Sudhalter V; Turk J Attention and language in fragile X | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2021 | 39 | 74 | 2345 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):17-24 Hessl D; Rivera SM; Reiss AL The neuroanatomy and neuroendocrinotogy of fragile X syndrome | 0 | 0 |
| 2022 | 28 | 55 | 2346 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):25-30 Hagerman PJ; Hagerman RJ Fragile X-associated tremor/ataxia syndrome (FXTAS) | 0 | 0 |
| 2023 | 38 | 66 | 2347 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):31-41 Loesch DZ; Huggins RM; Hagerman RJ Phenotypic variation and FMRP levels in fragile X | 0 | 0 |
| 2024 | 15 | 45 | 2348 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):42-48 Berry-Kravis E; Potanos K Psychopharmacology in fragile X syndrome - Present and future | 0 | 0 |
| 2025 | 18 | 32 | 2349 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):49-52 Darnell JC; Warren ST; Darnell RB The fragile X mental retardation protein, FMRP, recognizes G-quartets | 0 | 0 |
| 2026 | 23 | 54 | 2350 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):53-59 Beckel-Mitchener A; Greenough WT Correlates across the structural, functional, and molecular phenotypes of fragile X syndrome | 0 | 0 |
| 2027 | 38 | 102 | 2351 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):60-67 Willemsen R; Oostra BA; Bassell GJ; Dictenberg J The fragile X syndrome: From molecular genetics to neurobiology | 0 | 0 |
| 2028 | 7 | 66 | 2352 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):75-81 Rattazzi MC; LaFauci G; Brown WT Prospects for gene therapy in the fragile X syndrome | 0 | 0 |
| 2029 | 9 | 13 | 2161 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):131-134 Kaufmann WE Neurobiology of fragile X syndrome: From molecular genetics to neurobehavioral phenotype | 0 | 2 |
| 2030 | 49 | 82 | 2162 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):135-144 Kaufmann WE; Cohen S; Sun HT; Ho G Molecular phenotype of fragile X syndrome: FMRP, FXRPs, and protein targets | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2031 | 15 | 20 | 2163 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):145-147 Feng Y Fragile X mental retardation: Misregulation of protein synthesis in the developing brain? | 1 | 2 |
| 2032 | 39 | 64 | 2164 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):148-155 Hoogeveen AT; Willemsen R; Oostra BA Fragile X syndrome, the fragile X related proteins, and animal models | 1 | 3 |
| 2033 | 10 | 14 | 2165 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):156-158 Churchill JD; Beckel-Mitchener A; Weiler IJ; Greenough WT Effects of fragile X syndrome and an FMR1 knockout mouse model on forebrain neuronal cell biology | 0 | 0 |
| 2034 | 20 | 42 | 2166 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):159-167 Kates WR; Folley BS; Lanham DC; Capone GT; Kaufmann WE Cerebral growth in fragile X syndrome: Review and comparison with Down syndrome | 2 | 5 |
| 2035 | 16 | 35 | 2167 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):168-173 Hagerman RJ; Miller LJ; McGrath-Clarke J; Riley K; Goldson E; Harris SW; Simon J; Church K; Bonnell J; Ognibene TC; McIntosh DN Influence of stimulants on electrodermal studies in fragile X syndrome | 1 | 1 |
| 2036 | 25 | 35 | 2168 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):174-178 Kau ASM; Meyer WA; Kaufmann WE Early development in males with fragile X syndrome: A review of the literature | 2 | 3 |
| 2037 | 33 | 52 | 2169 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):179-186 Keysor CS; Mazzocco MMM A developmental approach to understanding fragile X syndrome in females | 5 | 5 |
| 2038 | 16 | 57 | 1502 1996 MOLECULAR AND CELLULAR BIOLOGY 16(7):3825-3832 Siomi MC; Zhang Y; Siomi H; Dreyfuss G Specific sequences in the fragile X syndrome protein FMR1 and the FXR proteins mediate their binding to 60S ribosomal subunits and the interactions among them | 48 | 98 |
| 2039 | 19 | 74 | 1815 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 | 9 | 39 |
| 2040 | 14 | 46 | 1816 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 | 35 | 64 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2041 | 30 | 74 | 1946 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 | 33 | 42 |
| 2042 | 15 | 43 | 2170 2002 MOLECULAR AND CELLULAR BIOLOGY 22(23):8332-8341 Otero YD; Severijnen LA; van Cappellen G; Schrier M; Oostra B; Willemsen R Transport of fragile X mental retardation protein via granules in neurites of PC12 cells | 6 | 15 |
| 2043 | 23 | 53 | 2171 2002 MOLECULAR AND CELLULAR BIOLOGY 22(24):8438-8447 Siomi MC; Higashijima K; Ishizuka A; Siomi H Casein kinase II phosphorylates the fragile X mental retardation protein and modulates its biological properties | 5 | 11 |
| 2044 | 2 | 13 | 2043 2001 MOLECULAR AND CELLULAR ENDOCRINOLOGY 183:S77-S85 Sermon K; Seneca S; De Rycke M; Goossens V; Van de Velde H; De Vos A; Platteau P; Lissens W; Van Steirteghem A; Liebaers I PGD in the lab for triplet repeat diseases - myotonic dystrophy, Huntington's disease and Fragile-X syndrome | 0 | 9 |
| 2045 | 22 | 75 | 2172 2002 MOLECULAR AND CELLULAR NEUROSCIENCE 19(2):138-151 Li JX; Pelletier MR; Velazquez JLP; Carlen PL Reduced cortical synaptic plasticity and GluR1 expression associated with fragile X mental retardation protein deficiency | 9 | 13 |
| 2046 | 4 | 8 | 1248 1994 MOLECULAR AND CELLULAR PROBES 8(2):177-180 CAO J; TARLETON J; BARBERIO D; DAVIDOW LS A SIMPLE FRAGILE-X PCR ASSAY WITH 7-DEAZAGUANINE-SUBSTITUTED DNA VISUALIZED BY ETHIDIUM-BROMIDE | 2 | 5 |
| 2047 | 8 | 10 | 1249 1994 MOLECULAR AND CELLULAR PROBES 8(3):241-244 DAVIDOW LS; BARBERIO D; CAO J; MCCORMICK I AN IMPROVED FRAGILE-X SOUTHERN BLOT PROBE WITHOUT THE CGGS ELIMINATES BACKGROUND BANDS | 0 | 0 |
| 2048 | 12 | 20 | 1947 2000 MOLECULAR AND CELLULAR PROBES 14(2):115-119 Mila M; Castellvi-Bel S; Sanchez A; Barcelo A; Badenas C; Mallolas J; Estivill X Rare variants in the promoter of the fragile X syndrome gene (FMR1) | 3 | 4 |
| 2049 | 0 | 0 | 1380 1995 MOLECULAR BIOLOGY OF THE CELL 6:1801-1801 TANEJA KL; NELSON D; SINGER RH SPATIAL-DISTRIBUTION OF CGG REPEAT SEQUENCES IN NUCLEI OF FRAGILE-X PATIENT CELLS | 0 | 0 |
| 2050 | 0 | 0 | 1691 1998 MOLECULAR BIOLOGY OF THE CELL 9:185A-185A Lichtenstein H; Tartakoff A Nuclear export of the Fragile X gene product, FMRP | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2051 | 8 | 32 | 1948 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 | 6 | 9 |
| 2052 | 20 | 37 | 1949 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 | 15 | 17 |
| 2053 | 24 | 47 | 1617 1997 MOLECULAR CELL 1(1):109-118 Feng Y; Absher D; Eberhart DE; Brown V; Malter HE; Warren ST FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association | 65 | 114 |
| 2054 | 7 | 20 | 1618 1997 MOLECULAR DIAGNOSIS 2(4):259-269 Hamdan H; Tynan JA; Fenwick RA; Leon JA Automated detection of trinucleotide repeats in fragile X syndrome | 4 | 6 |
| 2055 | 1 | 1 | 1692 1998 MOLECULAR DIAGNOSIS 3(4):249-249 Hamdan H; Tynan JA; Fenwick RA; Leon JA Automated detection of trinucleotide repeats in Fragile X syndrome (vol 2, pg 259, 1997) | 0 | 0 |
| 2056 | 26 | 43 | 1950 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 |
| 2057 | 63 | 108 | 2044 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 | 1 |
| 2058 | 30 | 45 | 1951 2000 MOLECULAR MEDICINE TODAY 6(5):193-198 Kooy RF; Willemsen R; Oostra BA Fragile X syndrome at the turn of the century | 12 | 18 |
| 2059 | 0 | 0 | 1817 1999 MOLECULAR PSYCHIATRY 4:S56-S56 Fisch GS; Carpenter N; Holden JA; Pandya A; Howard-Peebles PN; Tarleton J Psychopathology in genetic disorders producing cognitive deficits: Adaptive and maladative behavior in the fragile X syndrome, Williams syndrome and neurofibromatosis type 1. | 0 | 0 |
| 2060 | 11 | 41 | 2353 2004 MOLECULAR PSYCHIATRY 9(4):417-425 Frankland PW; Wang Y; Rosner B; Shimizu T; Balleine BW; Dykens EM; Ornitz EM; Silva AJ Sensorimotor gating abnormalities in young males with fragile X syndrome and Fmr1-knockout mice | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2061 | 0 | 0 | 1005 1992 MONATSSCHRIFT KINDERHEILKUNDE 140(7):404-404 KRUSE K GIRLS WITH FRAGILE-X SYNDROME (MARTIN-BELL SYNDROME) | 0 | 0 |
| 2062 | 0 | 2 | 2045 2001 MONATSSCHRIFT KINDERHEILKUNDE 149(3):264-264 Gladtke E Trimethoprim in the fragile X syndrome? | 0 | 0 |
| 2063 | 35 | 66 | 2173 2002 MONATSSCHRIFT KINDERHEILKUNDE 150(12):1486-+ Backes M; von Gontard A Behavioural phenotype of fragile X syndrome | 0 | 0 |
| 2064 | 0 | 0 | 2174 2002 MOVEMENT DISORDERS 17:S351-S351 Leehey MA; Grigsby J; Rubinstein D; Jacquemont S; Greco C; Zhang L Parkinsonism, tremor and ataxia in a female fragile X carrier | 1 | 1 |
| 2065 | 0 | 0 | 2292 2003 MOVEMENT DISORDERS 18(9):1091-1091 Kraft S; Parboosingh J; Suchowersky O Absence of fragile X premutation alleles in patients referred with spinocerebellar ataxia | 0 | 0 |
| 2066 | 0 | 0 | 2354 2004 MOVEMENT DISORDERS 19:S20-S20 Zhao Y; Puong K; Law H; Wong M; Ng I; Tan E Fragile X premutation alleles in patients with sporadic cerebellar ataxia | 0 | 0 |
| 2067 | 0 | 0 | 2355 2004 MOVEMENT DISORDERS 19:S21-S21 Hall DA; Pelak VS; Hagerman RJ; Hagerman PJ; Leehey MA Ocular motility in Fragile X premutation carriers and Fragile X associated tremor/ataxia syndrome (FXTAS) | 0 | 0 |
| 2068 | 0 | 0 | 2356 2004 MOVEMENT DISORDERS 19:S338-S338 Leehey MA; Berry-Kravis E; Jacquemont S; Zhang L; Hagerman R; Hagerman PJ Misdiagnosis of fragile X associated tremor/ataxia syndrome (FXTAS) | 0 | 0 |
| 2069 | 0 | 0 | 2357 2004 MOVEMENT DISORDERS 19:S339-S339 Leehey MA; Zhang L; Wheelock V; Tassone F; Hagerman R; Hagerman P A preliminary observation: Increased frequency of fragile X expanded alleles in patients that meet diagnostic criteria for MSA | 0 | 0 |
| 2070 | 0 | 0 | 2358 2004 MOVEMENT DISORDERS 19:S359-S360 Di Maria E; Grasso M; Abbruzzese G; Mandich P; Ratto S; Sciolla R The role for Fragile X premutation in essential tremor and spinocerebellar ataxia: Findings from two cohorts of Italian patients | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2071 | 0 | 0 | 2359 2004 MOVEMENT DISORDERS 19:S444-S444 Puong K; Zhao Y; Law H; Wong M; Ng I; Tan E Screening for Fragile X premutation alleles in patients with essential tremor | 0 | 0 |
| 2072 | 6 | 19 | 401 1986 MUTATION RESEARCH 173(3):201-205 DUNCAN AMV ENHANCED SENSITIVITY OF LYMPHOBLASTOID-CELLS FROM INDIVIDUALS CARRYING THE MUTATION FOR THE FRAGILE X-SYNDROME TO THE CLASTOGENIC EFFECTS OF FUDR | 2 | 3 |
| 2073 | 8 | 33 | 153 1983 NATURE 306(5944):701-704 CAMERINO G; MATTEI MG; MATTEI JF; JAYE M; MANDEL JL CLOSE LINKAGE OF FRAGILE X MENTAL-RETARDATION SYNDROME TO HEMOPHILIA-B AND TRANSMISSION THROUGH A NORMAL-MALE | 78 | 171 |
| 2074 | 12 | 23 | 402 1986 NATURE 324(6093):161-163 LEDBETTER DH; LEDBETTER SA; NUSSBAUM RL IMPLICATIONS OF FRAGILE-X EXPRESSION IN NORMAL MALES FOR THE NATURE OF THE MUTATION | 31 | 56 |
| 2075 | 0 | 1 | 656 1989 NATURE 341(6243):580-580 HARRIS A; BOBROW M THE FRAGILE-X SYNDROME - DAVIES,KE | 0 | 0 |
| 2076 | 11 | 14 | 882 1991 NATURE 349(6310):624-626 VINCENT A; HEITZ D; PETIT C; KRETZ C; OBERLE I; MANDEL JL ABNORMAL PATTERN DETECTED IN FRAGILE-X PATIENTS BY PULSED-FIELD GEL-ELECTROPHORESIS | 105 | 164 |
| 2077 | 3 | 12 | 883 1991 NATURE 349(6312):742-743 CRAIG I HUMAN-GENETICS - METHYLATION AND THE FRAGILE-X | 1 | 5 |
| 2078 | 7 | 11 | 884 1991 NATURE 351(6326):439-440 DAVIES K HUMAN-GENETICS - BREAKING THE FRAGILE-X | 2 | 7 |
| 2079 | 8 | 17 | 1132 1993 NATURE 363(6431):722-724 VERHEIJ C; BAKKER CE; DEGRAAFF E; KEULEMANS J; WILLEMSEN R; VERKERK AJMH; GALJAARD H; REUSER AJJ; HOOGEVEEN AT; OOSTRA BA CHARACTERIZATION AND LOCALIZATION OF THE FMR-1 GENE-PRODUCT ASSOCIATED WITH FRAGILE-X SYNDROME | 103 | 182 |
| 2080 | 11 | 16 | 1006 1992 NATURE GENETICS 1(3):157-158 HAGERMAN R CLINICAL CONUNDRUMS IN FRAGILE-X SYNDROME | 7 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2081 | 7 | 9 | 1007 1992 NATURE GENETICS 1(4):237-238 CHAKRAVARTI A FRAGILE-X FOUNDER EFFECT | 15 | 32 |
| 2082 | 8 | 20 | 1008 1992 NATURE GENETICS 1(4):257-260 RICHARDS RI; HOLMAN K; FRIEND K; KREMER E; HILLEN D; STAPLES A; BROWN WT; GOONEWARDENA P; TARLETON J; SCHWARTZ C; SUTHERLAND GR EVIDENCE OF FOUNDER CHROMOSOMES IN FRAGILE-X SYNDROME | 69 | 158 |
| 2083 | 10 | 23 | 1009 1992 NATURE GENETICS 1(5):341-344 GEDEON AK; BAKER E; ROBINSON H; PARTINGTON MW; GROSS B; MANCA A; KORN B; POUSTKA A; YU S; SUTHERLAND GR; MULLEY JC FRAGILE-X SYNDROME WITHOUT CCG AMPLIFICATION HAS AN FMR1 DELETION | 82 | 137 |
| 2084 | 16 | 27 | 1133 1993 NATURE GENETICS 3(1):31-35 DEBOULLE K; VERKERK AJMH; REYNIERS E; VITS L; HENDRICKX J; VANROY B; VANDENBOS F; DEGRAAFF E; OOSTRA BA; WILLEMS PJ A POINT MUTATION IN THE FMR-1 GENE ASSOCIATED WITH FRAGILE-X MENTAL-RETARDATION | 131 | 262 |
| 2085 | 20 | 33 | 1134 1993 NATURE GENETICS 3(1):36-43 HINDS HL; ASHLEY CT; SUTCLIFFE JS; NELSON DL; WARREN ST; HOUSMAN DE; SCHALLING M TISSUE SPECIFIC EXPRESSION OF FMR-1 PROVIDES EVIDENCE FOR A FUNCTIONAL-ROLE IN FRAGILE-X SYNDROME | 91 | 154 |
| 2086 | 3 | 25 | 1135 1993 NATURE GENETICS 3(1):44-48 HANZLIK AJ; OSEMLAKHANZLIK MM; HAUSER MA; KURNIT DM A RECOMBINATION-BASED ASSAY DEMONSTRATES THAT THE FRAGILE-X SEQUENCE IS TRANSCRIBED WIDELY DURING DEVELOPMENT | 9 | 14 |
| 2087 | 19 | 23 | 1136 1993 NATURE GENETICS 4(2):140-142 WOHRLE D; HENNIG I; VOGEL W; STEINBACH P MITOTIC STABILITY OF FRAGILE-X MUTATIONS IN DIFFERENTIATED CELLS INDICATES EARLY POSTCONCEPTIONAL TRINUCLEOTIDE REPEAT EXPANSION | 58 | 120 |
| 2088 | 28 | 44 | 1137 1993 NATURE GENETICS 4(2):143-146 REYNIERS E; VITS L; DEBOULLE K; VANROY B; VANVELZEN D; DEGRAAFF E; VERKERK AJMH; JORENS HZJ; DARBY JK; OOSTRA B; WILLEMS PJ THE FULL MUTATION IN THE FMR-1 GENE OF MALE FRAGILE-X PATIENTS IS ABSENT IN THEIR SPERM | 82 | 167 |
| 2089 | 19 | 36 | 1138 1993 NATURE GENETICS 4(4):335-340 DEVYS D; LUTZ Y; ROUYER N; BELLOCQ JP; MANDEL JL THE FMR-1 PROTEIN IS CYTOPLASMIC, MOST ABUNDANT IN NEURONS AND APPEARS NORMAL IN CARRIERS OF A FRAGILE X PREMUTATION | 169 | 277 |
| 2090 | 7 | 31 | 1139 1993 NATURE GENETICS 5(3):248-253 ZHONG N; DOBKIN C; BROWN WT A COMPLEX MUTABLE POLYMORPHISM LOCATED WITHIN THE FRAGILE X-GENE | 29 | 58 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2091 | 1 | 1 | 1140 1993 NATURE GENETICS 5(3):312-312 HINDS HL; ASHLEY CT; SUTCLIFFE JS; NELSON DL; WARREN ST; HOUSMAN DE; SCHALLING M TISSUE-SPECIFIC EXPRESSION OF FMR-1 PROVIDES EVIDENCE FOR A FUNCTIONAL-ROLE IN FRAGILE X-SYNDROME (VOL 3, PG 36, 1993) | 6 | 7 |
| 2092 | 15 | 24 | 1381 1995 NATURE GENETICS 10(4):483-485 LUGENBEEL KA; PEIER AM; CARSON NL; CHUDLEY AE; NELSON DL INTRAGENIC LOSS OF FUNCTION MUTATIONS DEMONSTRATE THE PRIMARY ROLE OF FMR1 IN FRAGILE-X SYNDROME | 30 | 49 |
| 2093 | 10 | 31 | 1503 1996 NATURE GENETICS 12(1):91-93 Khandjian EW; Corbin F; Woerly S; Rousseau F The fragile X mental retardation protein is associated with ribosomes | 58 | 93 |
| 2094 | 22 | 42 | 1619 1997 NATURE GENETICS 15(2):165-169 Malter HE; Iber JC; Willemsen R; deGraaff E; Tarleton JC; Leisti J; Warren ST; Oostra BA Characterization of the full fragile X syndrome mutation in fetal gametes | 45 | 84 |
| 2095 | 6 | 30 | 1818 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 | 25 | 92 |
| 2096 | 1 | 1 | 1819 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 |
| 2097 | 8 | 16 | 2175 2002 NATURE MEDICINE 8(11):1204-1205 Hansen RS; Laird CD A new regulatory pathway for fragile X syndrome? | 0 | 0 |
| 2098 | 20 | 39 | 2360 2004 NATURE NEUROSCIENCE 7(2):113-117 Jin P; Zarnescu DC; Ceman S; Nakamoto M; Mowrey J; Jongens TA; Nelson DL; Moses K; Warren ST Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway | 2 | 6 |
| 2099 | 2 | 3 | 2176 2002 NATURE REVIEWS GENETICS 3(1):4-5 Patterson M Twin-track approach to fragile X | 0 | 0 |
| 2100 | 1 | 1 | 2293 2003 NATURE REVIEWS GENETICS 4(10):758-758 Casci T Fragile X: a class of its own | 0 | 0 |
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