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Nodes: 2647,
Authors: 5321,
Journals: 428,
Outer References: 16458,
Words: 3536
Collection span: 1967 - 2005
View: Overview. Sorted by journal name.
Page 8: 1 2 3 4 5 6 7 8 9
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 2101 | 0 | 0 | 1554 1996 JOURNAL OF NEUROCHEMISTRY 67:S34-S34 Chen TA; Lu XF; Yi YH; Ho WKK Analysis of a CGG sequence at the FMR-1 locus in fragile X site by PCR-DGGE method. | 0 | 0 |
| 2102 | 0 | 0 | 1555 1996 JOURNAL OF NEUROCHEMISTRY 67:S36-S36 Chen TA; Lu XF; Ilo WKK; Yi YH; Chen SQ; et al. Variation of the CGG repeat in FMR-1 gene in non retarded Chinese population and fragile X syndrome patients | 0 | 0 |
| 2103 | 0 | 0 | 2449 2003 JOURNAL OF NEUROCHEMISTRY 85:1-1 Huber KM Recent progress in understanding the neural mechanisms of Fragile X Syndrome | 0 | 0 |
| 2104 | 7 | 15 | 302 1985 JOURNAL OF NEUROGENETICS 2(3):231-237 FORSTERGIBSON CJ; MULLIGAN LM; PARTINGTON MW; SIMPSON NE; HOLDEN JJA; et al. THE GENETIC-DISTANCE BETWEEN THE COAGULATION FACTOR-IX GENE AND THE LOCUS FOR THE FRAGILE-X SYNDROME - CLINICAL IMPLICATIONS | 13 | 23 |
| 2105 | 19 | 35 | 2450 2003 JOURNAL OF NEUROGENETICS 17(2-3):223-230 Major T; Culjkovic B; Stojkovic O; Gucscekic M; Lakic A; et al. Prevalence of the fragile X syndrome in Yugoslav patients with non-specific mental retardation | 0 | 0 |
| 2106 | 1 | 4 | 720 1990 JOURNAL OF NEUROLOGY 237(1):65-66 MUSUMECI SA; FERRI R; BERGONZI P THE SPECIFICITY OF THE CHARACTERISTIC SLEEP EEG PATTERN IN THE FRAGILE-X SYNDROME | 1 | 1 |
| 2107 | 6 | 25 | 303 1985 JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY 48(2):150-153 FINELLI PF; PUESCHEL SM; PADREMENDOZA T; OBRIEN MM NEUROLOGICAL FINDINGS IN PATIENTS WITH THE FRAGILE-X SYNDROME | 20 | 29 |
| 2108 | 0 | 0 | 2640 2005 JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY 76(1):151-151 Ealing J; Mavrogiannis LA; Kingston H; Cockburn DJ; Taylor GR; et al. An atypical tetra nucleotide expansion in DM2 (PROMM) | 0 | 0 |
| 2109 | 0 | 0 | 2303 2002 JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY 61(5):450-450 Greco CM; Hagerman RJ; Tassone F; Chudley AE; Del Bigio MR; et al. Neuronal and astrocytic intranuclear inclusions in Fragile X carriers with cerebellar tremor/ataxia and cognitive changes. | 0 | 0 |
| 2110 | 23 | 59 | 1689 1997 JOURNAL OF NEUROSCIENCE 17(5):1539-1547 Feng Y; Gutekunst CA; Eberhart DE; Yi H; Warren ST; et al. Fragile X mental retardation protein: Nucleocytoplasmic shuttling and association with somatodendritic ribosomes | 85 | 145 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2111 | 12 | 37 | 2559 2004 JOURNAL OF NEUROSCIENCE 24(11):2648-2655 Antar LN; Afroz R; Dictenberg JB; Carroll RC; Bassell GJ Metabotropic glutamate receptor activation regulates Fragile X mental retardation protein and Fmr1 mRNA localization differentially in dendrites and at synapses | 10 | 15 |
| 2112 | 40 | 97 | 2560 2004 JOURNAL OF NEUROSCIENCE 24(25):5798-5809 Michel CI; Kraft R; Restifo LL Defective neuronal development in the mushroom bodies of Drosophila Fragile X Mental Retardation 1 Mutants | 6 | 7 |
| 2113 | 23 | 34 | 2561 2004 JOURNAL OF NEUROSCIENCE 24(33):7272-7276 Stefani G; Fraser CE; Darnell JC; Darnell RB Fragile X mental retardation protein is associated with translating polyribosomes in neuronal cells | 2 | 3 |
| 2114 | 16 | 25 | 2562 2004 JOURNAL OF NEUROSCIENCE 24(47):10579-10583 Gabel LA; Won S; Kawai H; McKinney M; Tartakoff AM; et al. Visual experience regulates transient expression and dendritic localization of Fragile X mental retardation protein | 1 | 1 |
| 2115 | 1 | 1 | 2563 2004 JOURNAL OF NEUROSCIENCE 24(50):CP3-CP4 Gabel LA; Won S; Kawai H; McKinney M; Tartakoff AM; et al. Visual experience regulates transient expression and dendritic localization of fragile X mental retardation protein (vol 24, pg 10579, 2004) | 0 | 0 |
| 2116 | 17 | 40 | 1784 1998 JOURNAL OF NEUROSCIENCE RESEARCH 51(1):41-48 Berry-Kravis E; Ciurlionis R Overexpression of fragile X gene (FMR-1) transcripts increases cAMP production in neural cells | 1 | 1 |
| 2117 | 67 | 98 | 2304 2002 JOURNAL OF NEUROSCIENCE RESEARCH 70(5):623-630 Todd PK; Malter JS Fragile X mental retardation protein in plasticity and disease | 1 | 4 |
| 2118 | 14 | 52 | 402 1986 JOURNAL OF PEDIATRIC PSYCHOLOGY 11(1):91-102 MADISON LS; MOSHER GA; GEORGE CH FRAGILE-X SYNDROME - DIAGNOSIS AND RESEARCH | 0 | 12 |
| 2119 | 32 | 85 | 482 1987 JOURNAL OF PEDIATRICS 110(6):821-831 CHUDLEY AE; HAGERMAN RJ FRAGILE-X SYNDROME | 53 | 80 |
| 2120 | 19 | 25 | 1005 1992 JOURNAL OF PEDIATRICS 121(3):385-390 POTTER NT; LOZZIO CB; ANDERSON IJ; BOWLIN ES; MATTESON KJ USE OF A MOLECULAR GENETIC APPROACH TO DIAGNOSING THE FRAGILE-X GENOTYPE | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2121 | 22 | 51 | 1138 1993 JOURNAL OF PEDIATRICS 122(2):169-185 TARLETON JC; SAUL RA MOLECULAR GENETIC ADVANCES IN FRAGILE X-SYNDROME | 14 | 28 |
| 2122 | 12 | 14 | 1556 1996 JOURNAL OF PEDIATRICS 129(4):611-614 Giangreco CA; Steele MW; Aston CE; Cummins JH; Wenger SL A simplified six-item checklist for screening for fragile X syndrome in the pediatric population | 11 | 22 |
| 2123 | 20 | 36 | 1785 1998 JOURNAL OF PEDIATRICS 133(3):363-365 Meyer GA; Blum NJ; Hitchcock W; Fortina P Absence of the fragile X CGG trinucleotide repeat expansion in girls diagnosed with a pervasive developmental disorder | 0 | 3 |
| 2124 | 4 | 15 | 2066 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 |
| 2125 | 0 | 0 | 2451 2003 JOURNAL OF PSYCHOSOMATIC RESEARCH 55(2):156-156 Mirzaei M; Karam GA; Mahmoudi M Evaluation of prevalence the fragile X syndrome in 52 patients with moderate mental retardation with cytogenetic methods. | 0 | 0 |
| 2126 | 2 | 8 | 882 1991 JOURNAL OF REPRODUCTION AND FERTILITY 91(1):203-206 TEWARI R; RAO SRV REPLICATION STATUS OF THE FRAGILE X-CHROMOSOME AND ITS IMPLICATIONS FOR REPRODUCTIVE-PERFORMANCE IN THE INDIAN MOLE RAT (NESOKIA-INDICA) | 0 | 0 |
| 2127 | 1 | 4 | 1557 1996 JOURNAL OF SLEEP RESEARCH 5(4):272-272 Musumeci SA; Ferri R; Elia M; DelGracco S; Scuderi C; et al. Normal respiratory pattern during sleep in young fragile X-syndrome patients | 1 | 1 |
| 2128 | 5 | 12 | 1690 1997 JOURNAL OF SPECIAL EDUCATION 31(3):362-376 Powell L; Houghton S; Douglas G Comparison of etiology-specific cognitive functioning profiles for individuals with fragile X and individuals with Down syndrome | 2 | 4 |
| 2129 | 15 | 47 | 2179 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 |
| 2130 | 3 | 44 | 223 1984 JOURNAL OF SPEECH AND HEARING DISORDERS 49(3):328-332 PAUL R; COHEN DJ; BREG WR; WATSON M; HERMAN S FRAGILE-X SYNDROME - ITS RELATIONS TO SPEECH AND LANGUAGE DISORDERS | 13 | 17 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2131 | 1 | 6 | 304 1985 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 24(2):239-240 HAGERMAN RJ; JACKSON AW AUTISM OR FRAGILE-X SYNDROME | 0 | 1 |
| 2132 | 1 | 1 | 305 1985 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 24(2):240-240 SHELL J; CAMPBELL M AUTISM OR FRAGILE-X SYNDROME - REPLY | 0 | 0 |
| 2133 | 0 | 1 | 306 1985 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 24(5):673-674 SZYMANSKI LS THE FRAGILE-X SYNDROME - DIAGNOSIS, BIOCHEMISTRY AND INTERVENTION - HAGERMAN,RJ, MCBOGG,PM | 0 | 0 |
| 2134 | 11 | 36 | 403 1986 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 25(5):641-644 WRIGHT HH; YOUNG SR; EDWARDS JG; ABRAMSON RK; DUNCAN J FRAGILE X-SYNDROME IN A POPULATION OF AUTISTIC-CHILDREN | 16 | 21 |
| 2135 | 56 | 112 | 483 1987 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 26(4):463-471 BREGMAN JD; DYKENS E; WATSON M; ORT SI; LECKMAN JF FRAGILE-X SYNDROME - VARIABILITY OF PHENOTYPIC-EXPRESSION | 24 | 41 |
| 2136 | 11 | 25 | 484 1987 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 26(4):589-592 GOLDFINE PE; MCPHERSON PM; HARDESTY VA; HEATH GA; BEAUREGARD LJ; et al. FRAGILE-X CHROMOSOME ASSOCIATED WITH PRIMARY LEARNING-DISABILITY | 12 | 15 |
| 2137 | 4 | 5 | 485 1987 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 26(6):938-938 HAGERMAN RJ FRAGILE-X CHROMOSOME AND LEARNING-DISABILITY | 0 | 0 |
| 2138 | 10 | 16 | 654 1989 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 28(3):417-421 PAYTON JB; STEELE MW; WENGER SL; MINSHEW NJ THE FRAGILE-X MARKER AND AUTISM IN PERSPECTIVE | 19 | 37 |
| 2139 | 5 | 34 | 655 1989 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 28(3):422-426 DYKENS EM; HODAPP RM; ORT S; FINUCANE B; SHAPIRO LR; et al. THE TRAJECTORY OF DEVELOPMENT IN MALES WITH FRAGILE-X SYNDROME | 33 | 52 |
| 2140 | 9 | 27 | 656 1989 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 28(3):427-430 DYKENS EM; HODAPP RM; LECKMAN JF ADAPTIVE AND MALADAPTIVE FUNCTIONING OF INSTITUTIONALIZED AND NONINSTITUTIONALIZED FRAGILE-X MALES | 17 | 28 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2141 | 4 | 4 | 657 1989 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 28(6):965-966 FISCH GS FRAGILE-X AND AUTISM | 3 | 4 |
| 2142 | 3 | 4 | 658 1989 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 28(6):966-966 PAYTON JB; STEELE MW; WENGER SL; MINSHEW NJ FRAGILE-X AND AUTISM | 2 | 2 |
| 2143 | 6 | 24 | 721 1990 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 29(2):214-219 HODAPP RM; DYKENS EM; HAGERMAN RJ; SCHREINER R; LACHIEWICZ AM; et al. DEVELOPMENTAL IMPLICATIONS OF CHANGING TRAJECTORIES OF IQ IN MALES WITH FRAGILE-X SYNDROME | 32 | 45 |
| 2144 | 11 | 26 | 722 1990 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 29(6):885-891 REISS AL; FREUND L FRAGILE X SYNDROME, DSM-III-R, AND AUTISM | 42 | 60 |
| 2145 | 24 | 53 | 883 1991 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 30(5):825-830 PIVEN J; GAYLE J; LANDA R; WZOREK M; FOLSTEIN S THE PREVALENCE OF FRAGILE-X IN A SAMPLE OF AUTISTIC INDIVIDUALS DIAGNOSED USING A STANDARDIZED INTERVIEW | 7 | 26 |
| 2146 | 9 | 18 | 884 1991 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 30(5):831-834 HILTON DK; MARTIN CA; HEFFRON WM; HALL BD; JOHNSON GL IMIPRAMINE TREATMENT OF ADHD IN A FRAGILE-X CHILD | 5 | 10 |
| 2147 | 10 | 30 | 1006 1992 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 31(6):1141-1148 MAZZOCCO MMM; HAGERMAN RJ; CRONISTERSILVERMAN A; PENNINGTON BF SPECIFIC FRONTAL-LOBE DEFICITS AMONG WOMEN WITH THE FRAGILE-X GENE | 47 | 62 |
| 2148 | 18 | 33 | 1266 1994 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 33(2):247-255 SOBESKY WE; HULL CE; HAGERMAN RJ SYMPTOMS OF SCHIZOTYPAL PERSONALITY-DISORDER IN FRAGILE-X WOMEN | 21 | 36 |
| 2149 | 11 | 37 | 1267 1994 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 33(2):256-264 DORN MB; MAZZOCCO MMM; HAGERMAN RJ BEHAVIORAL AND PSYCHIATRIC-DISORDERS IN ADULT MALE CARRIERS OF FRAGILE-X | 25 | 33 |
| 2150 | 15 | 18 | 1268 1994 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 33(9):1316-1321 MERENSTEIN SA; SHYU V; SOBESKY WE; STALEY L; BERRYKRAVIS E; et al. FRAGILE-X SYNDROME IN A NORMAL IQ MALE WITH LEARNING AND EMOTIONAL-PROBLEMS | 18 | 22 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2151 | 20 | 43 | 1922 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 |
| 2152 | 3 | 5 | 2067 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 |
| 2153 | 1 | 5 | 2068 2000 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 39(4):398-398 Levitas A Fragile X syndrome | 0 | 0 |
| 2154 | 0 | 5 | 2069 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 |
| 2155 | 13 | 25 | 2305 2002 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 41(3):237-244 Dyer-Friedman J; Glaser B; Hessl D; Johnston C; Huffman LC; et al. Genetic and environmental influences on the cognitive outcomes of children with fragile X syndrome | 6 | 6 |
| 2156 | 8 | 10 | 2452 2003 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 42(3):372-375 Lombroso PJ Genetics of childhood disorders: XLVIII. Learning and memory, part 1: Fragile X syndrome update | 0 | 0 |
| 2157 | 2 | 5 | 2453 2003 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 42(5):516-517 Lung FW; Chen PJ Fragile X syndrome in adolescent prostitutes in southern Taiwan | 0 | 1 |
| 2158 | 0 | 0 | 2306 2002 JOURNAL OF THE AMERICAN GERIATRICS SOCIETY 50(4):S48-S48 Grigsby J; Leehey M; Hagerman RJ; Epstein J; Wilson R; et al. Dementia and a tremor-ataxia disorder among older male carriers of the fragile X premutation. | 0 | 1 |
| 2159 | 11 | 17 | 2070 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 |
| 2160 | 21 | 28 | 2454 2003 JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION 102(1):12-16 Chi J; Chen DJ; Lin CN; Chiu CY; Huang CB; et al. Feasibility of blood spot PCR in large-scale screening of fragile X syndrome in southern Taiwan | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2161 | 7 | 21 | 2564 2004 JOURNAL OF THE NEUROLOGICAL SCIENCES 227(1):115-118 Garland EM; Vnencak-Jones CL; Biaggioni I; Davis TL; Montine TJ; et al. Fragile X gene premutation in multiple system atrophy | 0 | 0 |
| 2162 | 5 | 11 | 723 1990 JOURNAL OF THE ROYAL SOCIETY OF MEDICINE 83(1):1-2 GOODYEAR HM; SONKSON PM FRAGILE X-SYNDROME - AN IMPORTANT CAUSE OF MENTAL-RETARDATION | 0 | 0 |
| 2163 | 0 | 1 | 724 1990 JOURNAL OF THE ROYAL SOCIETY OF MEDICINE 83(6):415-415 HALSTEAD S FRAGILE X-SYNDROME | 0 | 0 |
| 2164 | 0 | 0 | 725 1990 JOURNAL OF THE ROYAL SOCIETY OF MEDICINE 83(6):415-415 GOODYEAR HM; SONKSON PM FRAGILE X-SYNDROME - REPLY | 0 | 0 |
| 2165 | 8 | 35 | 1691 1997 JOURNAL OF THEORETICAL BIOLOGY 188(1):53-67 Bat O; Kimmel M; Axelrod DE Computer simulation of expansions of DNA triplet repeats in the fragile X syndrome and Huntington's disease | 2 | 4 |
| 2166 | 1 | 6 | 1269 1994 KLINISCHE PADIATRIE 206(5):410-411 FEHLOW P; MIOSGE W; WALTHER F ASSOCIATION OF SAETHRE-CHOTZEN-SYNDROME AND FRAGILE-X-SYNDROME | 0 | 0 |
| 2167 | 9 | 33 | 1558 1996 KOREAN JOURNAL OF GENETICS 18(3):199-210 Choi SK; Kim HY; Paik YK Cytogenetic analysis of a Korean family with fragile X syndrome | 0 | 1 |
| 2168 | 0 | 9 | 26 1981 LANCET 1(8219):556-557 SOUDEK D; MCGREGOR T SOURCES OF ERROR IN FRAGILE-X DETERMINATION | 6 | 9 |
| 2169 | 0 | 9 | 27 1981 LANCET 1(8219):557-557 EBERLE G; ZANKL H; ZANKL M SOURCES OF ERROR IN FRAGILE-X DETERMINATION | 4 | 8 |
| 2170 | 0 | 0 | 28 1981 LANCET 1(8223):780-780 DAKER MG; CHIDIAC P; FEAR CN; BERRY AC FRAGILE X IN A NORMAL-MALE - A CAUTIONARY TALE | 52 | 84 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2171 | 0 | 4 | 29 1981 LANCET 2(8254):1055-1055 BROWN WT; MEZZACAPPA PM; JENKINS EC SCREENING FOR FRAGILE X SYNDROME BY TESTICULAR SIZE MEASUREMENT | 16 | 23 |
| 2172 | 1 | 1 | 30 1981 LANCET 2(8257):1231-1232 WEBB GC; ROGERS JG; PITT DB; HALLIDAY J; THEOBALD T TRANSMISSION OF FRAGILE (X) (Q27) SITE FROM A MALE | 40 | 66 |
| 2173 | 1 | 4 | 31 1981 LANCET 2(8258):1292-1292 JENKINS EC; BROWN WT; DUNCAN CJ; BROOKS J; BENYISHAY M; et al. FEASIBILITY OF FRAGILE X-CHROMOSOME PRENATAL-DIAGNOSIS DEMONSTRATED | 56 | 77 |
| 2174 | 1 | 3 | 76 1982 LANCET 1(8263):99-100 SHAPIRO LR; WILMOT PL; BRENHOLZ P; LEFF A; MARTINO M; et al. PRENATAL-DIAGNOSIS OF FRAGILE-X CHROMOSOME | 38 | 59 |
| 2175 | 2 | 8 | 77 1982 LANCET 1(8263):100-100 BROWN WT; FRIEDMAN E; JENKINS EC; BROOKS J; WISNIEWSKI K; et al. ASSOCIATION OF FRAGILE-X SYNDROME WITH AUTISM | 50 | 77 |
| 2176 | 2 | 8 | 78 1982 LANCET 1(8263):100-100 SUTHERLAND GR; JACKY PB PRENATAL-DIAGNOSIS OF FRAGILE-X CHROMOSOME | 6 | 13 |
| 2177 | 0 | 4 | 79 1982 LANCET 1(8263):101-101 GARDNER AP; HOWELL RT; MCDERMOTT A FRAGILE-X CHROMOSOME - CONSISTENT DEMONSTRATION OF FRAGILE SITE IN FIBROBLAST-CULTURES | 10 | 14 |
| 2178 | 4 | 9 | 80 1982 LANCET 1(8266):273-274 LEJEUNE J IS THE FRAGILE-X SYNDROME AMENABLE TO TREATMENT | 47 | 62 |
| 2179 | 0 | 0 | 81 1982 LANCET 2(8307):1104-1104 KINNELL HG FRAGILE-X DISORDER ASSOCIATED WITH ANTISOCIAL PERSONALITY | 3 | 5 |
| 2180 | 1 | 9 | 153 1983 LANCET 1(8335):1221-1222 RUDELLI RD; JENKINS EC; WISNIEWSKI K; MORETZ R; BYRNE J; et al. TESTICULAR SIZE IN FETAL FRAGILE X SYNDROME | 14 | 19 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2181 | 0 | 4 | 154 1983 LANCET 2(8364):1427-1427 KINNELL HG; BANU SP INSTITUTIONAL PREVALENCE OF FRAGILE X-SYNDROME | 5 | 8 |
| 2182 | 1 | 4 | 224 1984 LANCET 1(8370):220-220 WEBB T; THAKE A; TODD J; BUNDEY S PREVALENCE OF FRAGILE X-CHROMOSOME | 2 | 4 |
| 2183 | 2 | 4 | 225 1984 LANCET 1(8370):220-220 JANCAR J PREVALENCE OF FRAGILE X-CHROMOSOME | 1 | 3 |
| 2184 | 0 | 4 | 226 1984 LANCET 1(8370):220-221 LINNA SL; SIMILA S; HARO E; HERVA R PREVALENCE OF FRAGILE X-CHROMOSOME | 2 | 4 |
| 2185 | 1 | 2 | 227 1984 LANCET 2(8398):349-349 CHOO KH; GEORGE D; FILBY G; HALLIDAY JL; LEVERSHA M; et al. LINKAGE ANALYSIS OF X-LINKED MENTAL-RETARDATION WITH AND WITHOUT FRAGILE-X USING FACTOR-IX GENE PROBE | 22 | 44 |
| 2186 | 2 | 7 | 307 1985 LANCET 1(8433):870-870 TOMMERUP N; SONDERGAARD F; TONNESEN T; KRISTENSEN M; ARVEILER B; et al. 1ST TRIMESTER PRENATAL-DIAGNOSIS OF A MALE FETUS WITH FRAGILE-X | 20 | 31 |
| 2187 | 2 | 10 | 308 1985 LANCET 1(8433):871-871 OBERLE I; MANDEL JL; BOUE J; MATTEI MG; MATTEI JF POLYMORPHIC DNA MARKERS IN PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME | 14 | 27 |
| 2188 | 5 | 12 | 404 1986 LANCET 2(8517):1191-1192 [Anon] PREVENTIVE SCREENING FOR FRAGILE-X SYNDROME | 3 | 0 |
| 2189 | 6 | 10 | 486 1987 LANCET 1(8527):280-280 BROWN WT; WU Y; GROSS AC; CHAN CB; DOBKIN CS; et al. RFLP FOR LINKAGE ANALYSIS OF FRAGILE-X SYNDROME | 21 | 35 |
| 2190 | 1 | 2 | 487 1987 LANCET 2(8554):329-329 VERLOES A; SACRE JP; GEUBELLE F SOTOS SYNDROME AND FRAGILE-X CHROMOSOMES | 1 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2191 | 1 | 5 | 659 1989 LANCET 2(8657):279-279 SCHEPIS C; PALAZZO R; RAGUSA RM; SPINA E; BARLETTA C ASSOCIATION OF CUTIS VERTICIS GYRATA WITH FRAGILE-X SYNDROME AND FRAGILITY OF CHROMOSOME-12 | 0 | 11 |
| 2192 | 0 | 1 | 726 1990 LANCET 336(8723):1131-1131 TEMPLE IK; BARAITSER M; PEMBREY ME; BUTLER L; JACOBS P; et al. UNUSUAL PRESENTATION OF FRAGILE-X SYNDROME | 2 | 3 |
| 2193 | 5 | 9 | 885 1991 LANCET 338(8772):956-957 HIRST M; KNIGHT S; DAVIES K; CROSS G; OCRAFT K; et al. PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME | 29 | 35 |
| 2194 | 4 | 6 | 886 1991 LANCET 338(8772):957-958 DOBKIN CS; DING XH; JENKINS EC; KRAWCZUN MS; BROWN WT; et al. PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME | 22 | 24 |
| 2195 | 8 | 10 | 1007 1992 LANCET 339(8788):271-272 PERGOLIZZI RG; ERSTER SH; GOONEWARDENA P; BROWN WT DETECTION OF FULL FRAGILE-X MUTATION | 48 | 69 |
| 2196 | 6 | 22 | 1008 1992 LANCET 339(8803):1210-1213 TURNER G; ROBINSON H; LAING S; VANDENBERK M; COLLEY A; et al. POPULATION SCREENING FOR FRAGILE-X | 22 | 39 |
| 2197 | 6 | 7 | 1139 1993 LANCET 341(8841):373-374 PALOMAKI GE; HADDOW JE IS IT TIME FOR POPULATION-BASED PRENATAL SCREENING FOR FRAGILE-X | 10 | 13 |
| 2198 | 2 | 3 | 1140 1993 LANCET 341(8847):769-770 BONTHRON D; STRAIN L POPULATION SCREENING FOR FRAGILE-X SYNDROME | 10 | 11 |
| 2199 | 1 | 3 | 1141 1993 LANCET 341(8847):770-770 HOWARDPEEBLES PN; MADDALENA A; BLACK SH; SCHULMAN JD POPULATION SCREENING FOR FRAGILE-X SYNDROME | 9 | 10 |
| 2200 | 3 | 4 | 1142 1993 LANCET 341(8847):770-770 BUNDEY S; NORMAN E POPULATION SCREENING FOR FRAGILE-X SYNDROME | 8 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2201 | 6 | 7 | 1143 1993 LANCET 342(8878):1004-1005 YOUNG ID DIAGNOSING FRAGILE-X SYNDROME | 1 | 1 |
| 2202 | 6 | 9 | 1144 1993 LANCET 342(8878):1025-1026 WANG Q; GREEN E; BARNICOAT A; GARRETT D; MULLARKEY M; et al. CYTOGENETIC VERSUS DNA DIAGNOSIS IN ROUTINE REFERRALS FOR FRAGILE-X SYNDROME | 15 | 22 |
| 2203 | 3 | 4 | 1145 1993 LANCET 342(8886-7):1563-1564 MOORE DY DIAGNOSING FRAGILE X-SYNDROME | 0 | 0 |
| 2204 | 2 | 5 | 1270 1994 LANCET 344(8935):1500-1500 TURNER G; ROBINSON H; WAKE S; MARTIN N DIZYGOUS TWINNING AND PREMATURE MENOPAUSE IN FRAGILE-X SYNDROME | 33 | 52 |
| 2205 | 8 | 9 | 1421 1995 LANCET 345(8958):1147-1148 WILLEMSEN R; MOHKAMSING S; DEVRIES B; DEVYS D; VANDENOUWELAND A; et al. RAPID ANTIBODY-TEST FOR FRAGILE-X SYNDROME | 81 | 101 |
| 2206 | 2 | 5 | 1422 1995 LANCET 346(8970):309-310 CONWAY GS; HETTIARACHCHI S; MURRAY A; JACOBS PA FRAGILE-X PREMUTATIONS IN FAMILIAL PREMATURE OVARIAN FAILURE | 21 | 43 |
| 2207 | 3 | 4 | 1559 1996 LANCET 348(9032):967-968 Willemsen R; Oosterwijk JC; Los FJ; Galjaard H; Oostra BA Prenatal diagnosis of fragile X syndrome | 11 | 16 |
| 2208 | 4 | 4 | 1923 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 |
| 2209 | 0 | 0 | 2307 2002 LANCET NEUROLOGY 1(3):141-141 May TS Evidence of altered synaptic plasticity found in fragile X syndrome | 0 | 0 |
| 2210 | 0 | 0 | 2565 2004 LANCET NEUROLOGY 3(12):701-701 Nelson R Drosophila model increases understanding of fragile-X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2211 | 23 | 69 | 2455 2003 LANGUAGE SPEECH AND HEARING SERVICES IN SCHOOLS 34(4):320-331 Mirrett PL; Roberts JE Early intervention practices and communication intervention strategies for young males with fragile X syndrome | 0 | 0 |
| 2212 | 0 | 1 | 2071 2000 LIBRARY JOURNAL 125(11):105-105 Griffin KH Children with Fragile X Syndrome: A parents' guide. | 0 | 0 |
| 2213 | 1 | 7 | 32 1981 LYON MEDICAL 246(20):428-429 [Anon] MENTAL-RETARDATION DUE TO A FRAGILE X-CHROMOSOME | 0 | 0 |
| 2214 | 0 | 0 | 660 1989 M S-MEDECINE SCIENCES 5(7):450-458 JORDAN BR; MATTEI JF FRAGILE X-LINKED MENTAL-RETARDATION, 1989 | 2 | 2 |
| 2215 | 0 | 0 | 887 1991 M S-MEDECINE SCIENCES 7(4):378-379 OBERLE I; MANDEL JL FRAGILE-X MENTAL-RETARDATION - VERY LOCALIZED GENOMIC IMPRINTING CLOSELY LINKED TO CLINICAL EXPRESSION | 0 | 0 |
| 2216 | 0 | 0 | 888 1991 M S-MEDECINE SCIENCES 7(6):637-639 ROUSSEAU F; HEITZ D; OBERLE I; MANDEL JL; KRETZ C THE FRAGILE X-SYNDROME - NEW SURPRISES | 0 | 0 |
| 2217 | 0 | 0 | 1009 1992 M S-MEDECINE SCIENCES 8(3):252-254 GILGENKRANTZ H FRAGILE-X - WHATS NEW | 0 | 0 |
| 2218 | 0 | 0 | 1010 1992 M S-MEDECINE SCIENCES 8(8):878-878 DREYFUSS JC CLINICAL FRAGILE-X SYNDROME DUE TO TOTAL OR PARTIAL GENE DELETION | 0 | 0 |
| 2219 | 0 | 10 | 2180 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 |
| 2220 | 3 | 45 | 1560 1996 MEDICAL ANTHROPOLOGY QUARTERLY 10(4):537-550 Nelkin D The social dynamics of genetic testing: The case of Fragile-X | 1 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2221 | 4 | 138 | 1561 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 |
| 2222 | 2 | 88 | 1786 1998 MEDICAL HYPOTHESES 51(3):223-233 Fischer KM Expanded (CAG)(n), (CGG)(n) and (GAA)(n) trinucleotide repeat microsatellites, and mutant purine synthesis and pigmentation genes cause schizophrenia and autism | 0 | 2 |
| 2223 | 17 | 34 | 1146 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 |
| 2224 | 4 | 5 | 1924 1999 MEDICAL JOURNAL OF AUSTRALIA 170(12):624-624 Cohen J; Loesch DZ Fragile X syndrome: do professionals know about it? | 0 | 0 |
| 2225 | 11 | 17 | 2181 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 |
| 2226 | 17 | 25 | 1011 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 |
| 2227 | 8 | 19 | 1012 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 |
| 2228 | 0 | 0 | 155 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 |
| 2229 | 36 | 59 | 1423 1995 MEDICINA-BUENOS AIRES 55(5):457-466 BANARES VG UPDATING THE FRAGILE-X SYNDROME | 0 | 0 |
| 2230 | 12 | 17 | 1013 1992 MENTAL RETARDATION 30(6):355-361 KEENAN J; KASTNER T; NATHANSON R; RICHARDSON N; HINTON J; et al. A STATEWIDE PUBLIC AND PROFESSIONAL-EDUCATION PROGRAM ON FRAGILE X SYNDROME | 0 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2231 | 9 | 24 | 1147 1993 MENTAL RETARDATION 31(4):221-227 WILSON PG; MAZZOCCO MMM AWARENESS AND KNOWLEDGE OF FRAGILE-X SYNDROME AMONG SPECIAL EDUCATORS | 2 | 3 |
| 2232 | 18 | 21 | 1148 1993 MENTAL RETARDATION 31(5):279-283 SMITH SE COGNITIVE DEFICITS ASSOCIATED WITH FRAGILE-X SYNDROME | 2 | 3 |
| 2233 | 2 | 2 | 1271 1994 MENTAL RETARDATION 32(2):156-156 SPITZ HH FRAGILE-X SYNDROME IS NOT THE 2ND LEADING CAUSE OF MENTAL-RETARDATION | 0 | 1 |
| 2234 | 22 | 29 | 2072 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 |
| 2235 | 42 | 92 | 1692 1997 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 3(4):313-322 Abbeduto L; Hagerman RJ Language and communication in fragile X syndrome | 10 | 17 |
| 2236 | 7 | 113 | 1925 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 |
| 2237 | 60 | 117 | 2073 2000 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 6(2):96-106 Mazzocco MMM Advances in research on the fragile X syndrome | 20 | 24 |
| 2238 | 0 | 0 | 2566 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 |
| 2239 | 16 | 48 | 2567 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):3-10 Bailey DB Newborn screening for fragile X syndrome | 0 | 1 |
| 2240 | 34 | 67 | 2568 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):11-16 Cornish K; Sudhalter V; Turk J Attention and language in fragile X | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2241 | 39 | 74 | 2569 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 | 1 | 2 |
| 2242 | 29 | 55 | 2570 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):25-30 Hagerman PJ; Hagerman RJ Fragile X-associated tremor/ataxia syndrome (FXTAS) | 0 | 1 |
| 2243 | 39 | 66 | 2571 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 | 1 | 1 |
| 2244 | 15 | 45 | 2572 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 |
| 2245 | 19 | 32 | 2573 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 | 1 |
| 2246 | 24 | 54 | 2574 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 | 2 |
| 2247 | 42 | 102 | 2575 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 | 2 | 5 |
| 2248 | 21 | 82 | 2576 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):68-74 Siomi H; Ishizuka A; Siomi MC RNA interference: A new mechanism by which FMRP acts in the normal brain? What can drosophila teach us? | 1 | 4 |
| 2249 | 7 | 66 | 2577 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 |
| 2250 | 0 | 1 | 1562 1996 MICHIGAN LAW REVIEW 94(6):1810-1838 Friedman RD Statistics and the evaluation of evidence for forensic scientists - Aitken,CGG | 0 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2251 | 10 | 13 | 2308 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):131-134 Kaufmann WE Neurobiology of fragile X syndrome: From molecular genetics to neurobehavioral phenotype | 0 | 2 |
| 2252 | 55 | 82 | 2309 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 |
| 2253 | 15 | 20 | 2310 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):145-147 Feng Y Fragile X mental retardation: Misregulation of protein synthesis in the developing brain? | 2 | 2 |
| 2254 | 43 | 64 | 2311 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 | 4 |
| 2255 | 10 | 14 | 2312 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 |
| 2256 | 20 | 42 | 2313 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 | 6 |
| 2257 | 16 | 35 | 2314 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):168-173 Hagerman RJ; Miller LJ; McGrath-Clarke J; Riley K; Goldson E; et al. Influence of stimulants on electrodermal studies in fragile X syndrome | 3 | 3 |
| 2258 | 25 | 35 | 2315 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 |
| 2259 | 33 | 52 | 2316 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):179-186 Keysor CS; Mazzocco MMM A developmental approach to understanding fragile X syndrome in females | 8 | 9 |
| 2260 | 25 | 61 | 2641 2005 MOLECULAR & CELLULAR PROTEOMICS 4(3):278-290 Zhang YQ; Friedman DB; Wang Z; Woodruff E; Pan LY; et al. Protein expression profiling of the Drosophila fragile X mutant brain reveals up-regulation of monoamine synthesis | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2261 | 17 | 57 | 1563 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 | 58 | 109 |
| 2262 | 24 | 74 | 1926 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 |
| 2263 | 17 | 46 | 1927 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 |
| 2264 | 31 | 74 | 2074 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 |
| 2265 | 17 | 43 | 2317 2002 MOLECULAR AND CELLULAR BIOLOGY 22(23):8332-8341 Otero YD; Severijnen LA; van Cappellen G; Schrier M; Oostra B; et al. Transport of fragile X mental retardation protein via granules in neurites of PC12 cells | 17 | 24 |
| 2266 | 23 | 53 | 2318 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 | 14 | 16 |
| 2267 | 2 | 13 | 2182 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 |
| 2268 | 23 | 75 | 2319 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 | 18 | 20 |
| 2269 | 4 | 8 | 1272 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 |
| 2270 | 8 | 10 | 1273 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2271 | 12 | 20 | 2075 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 |
| 2272 | 0 | 0 | 1424 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 |
| 2273 | 0 | 0 | 1787 1998 MOLECULAR BIOLOGY OF THE CELL 9:185A-185A Lichtenstein H; Tartakoff A Nuclear export of the Fragile X gene product, FMRP | 0 | 0 |
| 2274 | 8 | 32 | 2076 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 |
| 2275 | 21 | 37 | 2077 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 |
| 2276 | 27 | 61 | 2456 2003 MOLECULAR BRAIN RESEARCH 110(2):267-278 Todd PK; Malter JS; Mack KJ Whisker stimulation-dependent translation of FMRP in the barrel cortex requires activation of type I metabotropic glutamate receptors | 4 | 3 |
| 2277 | 15 | 36 | 2578 2004 MOLECULAR BRAIN RESEARCH 131(1-2):101-109 Lauterborn JC Stress induced changes in cortical and hypothalamic c-fos expression are altered in fragile X mutant mice | 0 | 0 |
| 2278 | 26 | 47 | 1693 1997 MOLECULAR CELL 1(1):109-118 Feng Y; Absher D; Eberhart DE; Brown V; Malter HE; et al. FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association | 89 | 134 |
| 2279 | 7 | 20 | 1694 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 |
| 2280 | 1 | 1 | 1788 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2281 | 28 | 43 | 2078 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 |
| 2282 | 65 | 108 | 2183 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 |
| 2283 | 11 | 11 | 2579 2004 MOLECULAR HUMAN REPRODUCTION 10(10):773-776 Rife M; Badenas C; Quinto L; Puigoriol E; Tazon B; et al. Analysis of CGG variation through 642 meioses in Fragile X families | 1 | 1 |
| 2284 | 32 | 45 | 2079 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 |
| 2285 | 1 | 50 | 2580 2004 MOLECULAR MICROBIOLOGY 54(3):742-754 Blaha B; Semsey S; Ferenczi S; Csiszovszki Z; Papp PP; et al. A proline tRNA(CGG) gene encompassing the attachment site of temperate phage 16-3 is functional and convertible to suppressor tRNA | 0 | 0 |
| 2286 | 0 | 0 | 1928 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 |
| 2287 | 11 | 41 | 2581 2004 MOLECULAR PSYCHIATRY 9(4):417-425 Frankland PW; Wang Y; Rosner B; Shimizu T; Balleine BW; et al. Sensorimotor gating abnormalities in young males with fragile X syndrome and Fmr1-knockout mice | 0 | 1 |
| 2288 | 0 | 0 | 1014 1992 MONATSSCHRIFT KINDERHEILKUNDE 140(7):404-404 KRUSE K GIRLS WITH FRAGILE-X SYNDROME (MARTIN-BELL SYNDROME) | 0 | 0 |
| 2289 | 0 | 2 | 2184 2001 MONATSSCHRIFT KINDERHEILKUNDE 149(3):264-264 Gladtke E Trimethoprim in the fragile X syndrome? | 0 | 0 |
| 2290 | 35 | 66 | 2320 2002 MONATSSCHRIFT KINDERHEILKUNDE 150(12):1486-+ Backes M; von Gontard A Behavioural phenotype of fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2291 | 0 | 0 | 2321 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 | 1 | 1 |
| 2292 | 0 | 0 | 2457 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 |
| 2293 | 0 | 0 | 2582 2004 MOVEMENT DISORDERS 19:S20-S20 Zhao Y; Puong K; Law H; Wong M; Ng I; et al. Fragile X premutation alleles in patients with sporadic cerebellar ataxia | 0 | 0 |
| 2294 | 0 | 0 | 2583 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 |
| 2295 | 0 | 0 | 2584 2004 MOVEMENT DISORDERS 19:S338-S338 Leehey MA; Berry-Kravis E; Jacquemont S; Zhang L; Hagerman R; et al. Misdiagnosis of fragile X associated tremor/ataxia syndrome (FXTAS) | 0 | 0 |
| 2296 | 0 | 0 | 2585 2004 MOVEMENT DISORDERS 19:S339-S339 Leehey MA; Zhang L; Wheelock V; Tassone F; Hagerman R; et al. A preliminary observation: Increased frequency of fragile X expanded alleles in patients that meet diagnostic criteria for MSA | 0 | 0 |
| 2297 | 0 | 0 | 2586 2004 MOVEMENT DISORDERS 19:S359-S360 Di Maria E; Grasso M; Abbruzzese G; Mandich P; Ratto S; et al. The role for Fragile X premutation in essential tremor and spinocerebellar ataxia: Findings from two cohorts of Italian patients | 0 | 0 |
| 2298 | 0 | 0 | 2587 2004 MOVEMENT DISORDERS 19:S444-S444 Puong K; Zhao Y; Law H; Wong M; Ng I; et al. Screening for Fragile X premutation alleles in patients with essential tremor | 0 | 0 |
| 2299 | 0 | 0 | 2588 2004 MOVEMENT DISORDERS 19(9):1122-1122 Leehey MA; Hall D; Rice C; Jacquemont S; Zhang L; et al. The clinical course of fragile X-associated tremor/ataxia syndrome (FXTAS). | 0 | 0 |
| 2300 | 0 | 0 | 2589 2004 MOVEMENT DISORDERS 19(9):1127-1127 Hall DA; Rice CD; Hagerman RR; Hagerman PR; Berry-Kravis E; et al. Medical treatment for the fragile x-associated tremor/ataxia syndrome. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2301 | 6 | 19 | 405 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 |
| 2302 | 8 | 33 | 156 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 |
| 2303 | 12 | 23 | 406 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 |
| 2304 | 0 | 1 | 661 1989 NATURE 341(6243):580-580 HARRIS A; BOBROW M THE FRAGILE-X SYNDROME - DAVIES,KE | 0 | 0 |
| 2305 | 11 | 14 | 889 1991 NATURE 349(6310):624-626 VINCENT A; HEITZ D; PETIT C; KRETZ C; OBERLE I; et al. ABNORMAL PATTERN DETECTED IN FRAGILE-X PATIENTS BY PULSED-FIELD GEL-ELECTROPHORESIS | 112 | 165 |
| 2306 | 3 | 12 | 890 1991 NATURE 349(6312):742-743 CRAIG I HUMAN-GENETICS - METHYLATION AND THE FRAGILE-X | 1 | 5 |
| 2307 | 7 | 11 | 891 1991 NATURE 351(6326):439-440 DAVIES K HUMAN-GENETICS - BREAKING THE FRAGILE-X | 2 | 7 |
| 2308 | 8 | 17 | 1149 1993 NATURE 363(6431):722-724 VERHEIJ C; BAKKER CE; DEGRAAFF E; KEULEMANS J; WILLEMSEN R; et al. CHARACTERIZATION AND LOCALIZATION OF THE FMR-1 GENE-PRODUCT ASSOCIATED WITH FRAGILE-X SYNDROME | 114 | 187 |
| 2309 | 47 | 73 | 2590 2004 NATURE CELL BIOLOGY 6(11):1048-1053 Jin P; Alisch RS; Warren ST RNA and microRNAs in fragile X mental retardation | 2 | 3 |
| 2310 | 11 | 16 | 1015 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 |
| 2311 | 7 | 9 | 1016 1992 NATURE GENETICS 1(4):237-238 CHAKRAVARTI A FRAGILE-X FOUNDER EFFECT | 18 | 32 |
| 2312 | 8 | 20 | 1017 1992 NATURE GENETICS 1(4):257-260 RICHARDS RI; HOLMAN K; FRIEND K; KREMER E; HILLEN D; et al. EVIDENCE OF FOUNDER CHROMOSOMES IN FRAGILE-X SYNDROME | 78 | 158 |
| 2313 | 10 | 23 | 1018 1992 NATURE GENETICS 1(5):341-344 GEDEON AK; BAKER E; ROBINSON H; PARTINGTON MW; GROSS B; et al. FRAGILE-X SYNDROME WITHOUT CCG AMPLIFICATION HAS AN FMR1 DELETION | 87 | 138 |
| 2314 | 16 | 27 | 1150 1993 NATURE GENETICS 3(1):31-35 DEBOULLE K; VERKERK AJMH; REYNIERS E; VITS L; HENDRICKX J; et al. A POINT MUTATION IN THE FMR-1 GENE ASSOCIATED WITH FRAGILE-X MENTAL-RETARDATION | 145 | 270 |
| 2315 | 20 | 33 | 1151 1993 NATURE GENETICS 3(1):36-43 HINDS HL; ASHLEY CT; SUTCLIFFE JS; NELSON DL; WARREN ST; et al. TISSUE SPECIFIC EXPRESSION OF FMR-1 PROVIDES EVIDENCE FOR A FUNCTIONAL-ROLE IN FRAGILE-X SYNDROME | 104 | 160 |
| 2316 | 3 | 25 | 1152 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 |
| 2317 | 19 | 23 | 1153 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 | 64 | 122 |
| 2318 | 28 | 44 | 1154 1993 NATURE GENETICS 4(2):143-146 REYNIERS E; VITS L; DEBOULLE K; VANROY B; VANVELZEN D; et al. THE FULL MUTATION IN THE FMR-1 GENE OF MALE FRAGILE-X PATIENTS IS ABSENT IN THEIR SPERM | 96 | 170 |
| 2319 | 10 | 32 | 1155 1993 NATURE GENETICS 4(3):244-251 ASHLEY CT; SUTCLIFFE JS; KUNST CB; LEINER HA; EICHLER EE; et al. HUMAN AND MURINE FMR-1 - ALTERNATIVE SPLICING AND TRANSLATIONAL INITIATION DOWNSTREAM OF THE CGG-REPEAT | 74 | 120 |
| 2320 | 20 | 36 | 1156 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 | 201 | 294 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2321 | 7 | 31 | 1157 1993 NATURE GENETICS 5(3):248-253 ZHONG N; DOBKIN C; BROWN WT A COMPLEX MUTABLE POLYMORPHISM LOCATED WITHIN THE FRAGILE X-GENE | 33 | 58 |
| 2322 | 1 | 1 | 1158 1993 NATURE GENETICS 5(3):312-312 HINDS HL; ASHLEY CT; SUTCLIFFE JS; NELSON DL; WARREN ST; et al. TISSUE-SPECIFIC EXPRESSION OF FMR-1 PROVIDES EVIDENCE FOR A FUNCTIONAL-ROLE IN FRAGILE X-SYNDROME (VOL 3, PG 36, 1993) | 6 | 7 |
| 2323 | 23 | 41 | 1274 1994 NATURE GENETICS 8(1):88-94 EICHLER EE; HOLDEN JJA; POPOVICH BW; REISS AL; SNOW K; et al. LENGTH OF UNINTERRUPTED CGG REPEATS DETERMINES INSTABILITY IN THE FMR1 GENE | 92 | 243 |
| 2324 | 15 | 24 | 1425 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 | 34 | 50 |
| 2325 | 15 | 40 | 1426 1995 NATURE GENETICS 11(3):301-308 EICHLER EE; KUNST CB; LUGENBEEL KA; RYDER OA; DAVISON D; et al. EVOLUTION OF THE CRYPTIC FMR1 CGG REPEAT | 11 | 18 |
| 2326 | 10 | 31 | 1564 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 | 70 | 101 |
| 2327 | 22 | 42 | 1695 1997 NATURE GENETICS 15(2):165-169 Malter HE; Iber JC; Willemsen R; deGraaff E; Tarleton JC; et al. Characterization of the full fragile X syndrome mutation in fetal gametes | 58 | 89 |
| 2328 | 6 | 30 | 1929 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 |
| 2329 | 1 | 1 | 1930 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 |
| 2330 | 8 | 16 | 2322 2002 NATURE MEDICINE 8(11):1204-1205 Hansen RS; Laird CD A new regulatory pathway for fragile X syndrome? | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2331 | 22 | 39 | 2591 2004 NATURE NEUROSCIENCE 7(2):113-117 Jin P; Zarnescu DC; Ceman S; Nakamoto M; Mowrey J; et al. Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway | 16 | 38 |
| 2332 | 2 | 3 | 2323 2002 NATURE REVIEWS GENETICS 3(1):4-5 Patterson M Twin-track approach to fragile X | 0 | 0 |
| 2333 | 1 | 1 | 2458 2003 NATURE REVIEWS GENETICS 4(10):758-758 Casci T Fragile X: a class of its own | 0 | 0 |
| 2334 | 1 | 3 | 2459 2003 NATURE REVIEWS NEUROSCIENCE 4(4):245-245 Jones R Cell biology or the neuron - FMRP and its many partners | 0 | 0 |
| 2335 | 1 | 1 | 2460 2003 NATURE REVIEWS NEUROSCIENCE 4(10):776-777 Casci T Neurological disorders - Fragile X: a class of its own | 0 | 0 |
| 2336 | 1 | 2 | 2592 2004 NATURE REVIEWS NEUROSCIENCE 5(1):4-4 Jones R Neurological disorders: Fragile X functions | 0 | 0 |
| 2337 | 7 | 34 | 1696 1997 NATURE STRUCTURAL BIOLOGY 4(9):712-716 Musco G; Kharrat A; Stier G; Fraternali F; Gibson TJ; et al. The solution structure of the first KH domain of FMR1, the protein responsible for the fragile X syndrome | 7 | 46 |
| 2338 | 1 | 1 | 1697 1997 NATURE STRUCTURAL BIOLOGY 4(10):840-840 Musco G; Kharrat A; Stier G; Fraternali F; Gibson TJ; et al. The solution structure of the first KH domain of FMR1, the protein responsible for the fragile X syndrome (vol 4, pg 712, 1997) | 1 | 2 |
| 2339 | 4 | 13 | 1159 1993 NERVENHEILKUNDE 12(2):84-86 FROSTER UG CLINICAL AND MOLECULAR ASPECTS OF THE FRAGILE-X FORM OF MENTAL-RETARDATION (MARTIN-BELL SYNDROME) | 0 | 0 |
| 2340 | 0 | 0 | 2593 2004 NEUROBIOLOGY OF AGING 25:S434-S434 Westmark CJ; Malter JS FMRP mediates mGluR1-activated translation of APP | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2341 | 15 | 33 | 1698 1997 NEUROBIOLOGY OF DISEASE 4(5):329-336 Bardoni B; Sittler A; Shen Y; Mandel JL Analysis of domains affecting intracellular localization of the FMRP protein | 22 | 28 |
| 2342 | 8 | 27 | 2324 2002 NEUROBIOLOGY OF DISEASE 10(3):211-218 D'Agata V; Warren ST; Zhao WQ; Torre ER; Alkon DL; et al. Gene expression profiles in a transgenic animal model of fragile X syndrome | 0 | 14 |
| 2343 | 18 | 39 | 2325 2002 NEUROBIOLOGY OF DISEASE 11(1):53-63 Schenck A; Van de Bor V; Bardoni B; Giangrande A Novel features of dFMR1, the Drosophila orthologue of the fragile X mental retardation protein | 4 | 5 |
| 2344 | 24 | 59 | 2326 2002 NEUROBIOLOGY OF DISEASE 11(1):221-229 Castren M; Lampinen KE; Miettinen R; Koponen E; Sipola I; et al. BDNF regulates the expression of fragile X mental retardation protein mRNA in the hippocampus | 2 | 4 |
| 2345 | 4 | 13 | 2080 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 |
| 2346 | 6 | 14 | 2081 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 |
| 2347 | 0 | 0 | 2185 2001 NEUROIMAGE 13(6):S1076-S1076 Moore CJ; Daly EM; Schmitz N; Murphy KC; Murphy DGM Premutation expansion of CGG triplet repeats affects brain; a study of male carriers of Fragile X syndrome | 0 | 0 |
| 2348 | 0 | 0 | 662 1989 NEUROLOGIC CLINICS 7(1):107-121 BROWN WT THE FRAGILE-X SYNDROME | 1 | 1 |
| 2349 | 0 | 0 | 82 1982 NEUROLOGY 32(4):A190-A190 ROSENBERGER PB; WILSONCIAMBRONE S; MILUNSKY A SPEECH FLUENCY DISORDER IN THE FRAGILE-X SYNDROME | 2 | 2 |
| 2350 | 3 | 10 | 727 1990 NEUROLOGY 40(2):378-380 DESAI HB; DONAT J; SHOKEIR MHK; MUNOZ DG AMYOTROPHIC LATERAL SCLEROSIS IN A PATIENT WITH FRAGILE X-SYNDROME | 5 | 7 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2351 | 0 | 0 | 1275 1994 NEUROLOGY 44(4):A400-A400 GUERREIRO M; MOURARIBEIRO MVL; CAMARGO EE; KATO M; MENEZES JR; et al. NEUROBIOLOGY OF FRAGILE-X-SYNDROME (FXS) | 0 | 0 |
| 2352 | 22 | 61 | 1276 1994 NEUROLOGY 44(7):1317-1324 REISS AL; LEE J; FREUND L NEUROANATOMY OF FRAGILE-X SYNDROME - THE TEMPORAL-LOBE | 54 | 89 |
| 2353 | 0 | 0 | 1699 1997 NEUROLOGY 48(3):5062-5062 Mostofsky SH; Mazzocco MM; Aakalu G; Warsofsky IS; Denckla MB; et al. Aberrant posterior vermis size in fragile X syndrome: Correlation with neurocognitive performance | 0 | 0 |
| 2354 | 18 | 63 | 1789 1998 NEUROLOGY 50(1):121-130 Mostofsky SH; Mazzocco MMM; Aakalu G; Warsofsky IS; Denckla MB; et al. Decreased cerebellar posterior vermis size in fragile X syndrome - Correlation with neurocognitive performance | 21 | 48 |
| 2355 | 0 | 0 | 1790 1998 NEUROLOGY 50(4):A86-A86 Mostofsky SH; Reiss AL; Freund L Examination of posterior vermis size in young males with fragile X syndrome | 0 | 0 |
| 2356 | 3 | 10 | 2186 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 | 45 | 74 |
| 2357 | 0 | 0 | 2327 2002 NEUROLOGY 58(6):987-987 Munoz DG Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X | 0 | 0 |
| 2358 | 0 | 0 | 2328 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 |
| 2359 | 0 | 0 | 2329 2002 NEUROLOGY 58(7):A481-A482 Leehey MA; Brunberg JA; Lang AE; Jacquemont S; Rubinstein D; et al. MRI increased T2 signal intensity in the cerebellar peduncles: Specific for the fragile X premutation tremor/ataxia syndrome? | 0 | 0 |
| 2360 | 0 | 0 | 2330 2002 NEUROLOGY 58(7):A482-A482 Munhoz RP; Lozano AM; Lang AE Fragile X syndrome premutation mistaken as essential tremor: An unrecognized source of diagnostic confusion | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2361 | 0 | 0 | 2594 2004 NEUROLOGY 62(7):A48-A48 Hagerman PJ; Jacquemont S; Hagerman RJ; Leehey MA; Hall DA; et al. Penetrance of the Fragile X-associated Tremor/Ataxia Syndrome (FXTAS) in a premutation carrier population: Initial results from a California family-based study | 0 | 0 |
| 2362 | 7 | 10 | 2595 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 | 0 | 4 |
| 2363 | 8 | 37 | 2596 2004 NEUROLOGY 63(9):1634-1639 Kogan CS; Bertone A; Cornish K; Boutet I; Kaloustian VMD; et al. Integrative cortical dysfunction and pervasive motion perception deficit in fragile X syndrome | 0 | 0 |
| 2364 | 5 | 7 | 2597 2004 NEUROLOGY 63(11):2188-2189 Pugliese P; Annesi G; Cutuli N; Arabia G; Nicoletti G; et al. The fragile X premutation presenting as postprandial hypotension | 0 | 0 |
| 2365 | 51 | 75 | 2598 2004 NEUROLOGY INDIA 52(1):36-42 Pandey UB; Phadke SR; Mittal B Molecular diagnosis and genetic counseling for fragile X mental retardation | 0 | 0 |
| 2366 | 9 | 20 | 2331 2002 NEURON 34(6):859-862 Gao FB Understanding fragile X syndrome: Insights from retarded flies | 6 | 8 |
| 2367 | 20 | 52 | 2332 2002 NEURON 34(6):961-972 Morales J; Hiesinger PR; Schroeder AJ; Kume K; Verstreken P; et al. Drosophila fragile X protein, DFXR, regulates neuronal morphology and function in the brain | 28 | 37 |
| 2368 | 13 | 26 | 2461 2003 NEURON 37(4):555-558 Antar LN; Bassell GJ Sunrise at the synapse: The FMRP mRNP shaping the synaptic interface | 11 | 25 |
| 2369 | 7 | 10 | 2462 2003 NEURON 38(6):843-845 Billuart P; Chelly J From fragile X mental retardation protein to Rac1 GTPase: New insights from fly CYFIP | 1 | 2 |
| 2370 | 22 | 64 | 2463 2003 NEURON 38(6):887-898 Schenck A; Bardoni B; Langmann C; Harden N; Mandel JL; et al. CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein | 11 | 23 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2371 | 7 | 35 | 2464 2003 NEURON 39(5):739-747 Jin P; Zarnescu DC; Zhang FP; Pearson CE; Lucchesi JC; et al. RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in Drosophila | 10 | 23 |
| 2372 | 4 | 10 | 2642 2005 NEURON 45(5):642-644 Dolen G; Bear MF Courting a cure for Fragile X | 0 | 0 |
| 2373 | 11 | 56 | 2643 2005 NEURON 45(5):753-764 McBride SMJ; Choi CH; Wang Y; Liebelt D; Braunstein E; et al. Pharmacological rescue of synaptic plasticity, courtship behavior, and mushroom body defects in a Drosophila model of fragile X syndrome | 1 | 1 |
| 2374 | 0 | 0 | 309 1985 NEUROPEDIATRICS 16(3):171-172 GRANSTROM ML; SIMOLA KOJ; YLINEN A; RINTAHAKA P THE FRAGILE-X SYNDROME IN CHILDHOOD - A THERAPEUTIC TRIAL WITH FOLIC-ACID | 0 | 0 |
| 2375 | 3 | 12 | 1160 1993 NEUROPEDIATRICS 24(4):211-213 REES M; DIEBOLD U; PARKER K; DOOSE H; GARDINER RM; et al. BENIGN CHILDHOOD EPILEPSY WITH CENTROTEMPORAL SPIKES AND THE FOCAL SHARP WAVE TRAIT IS NOT LINKED TO THE FRAGILE-X REGION | 6 | 23 |
| 2376 | 7 | 41 | 1277 1994 NEUROPHYSIOLOGIE CLINIQUE-CLINICAL NEUROPHYSIOLOGY 24(6):413-426 FERRI R; MUSUMECI SA; ELIA M; DELGRACCO S; SCUDERI C; et al. BIT-MAPPED SOMATOSENSORY-EVOKED POTENTIALS IN THE FRAGILE-X SYNDROME | 7 | 15 |
| 2377 | 4 | 16 | 407 1986 NEUROPSYCHOLOGIA 24(3):405-409 MIEZEJESKI CM; JENKINS EC; HILL AL; WISNIEWSKI K; FRENCH JH; et al. A PROFILE OF COGNITIVE DEFICIT IN FEMALES FROM FRAGILE-X FAMILIES | 47 | 60 |
| 2378 | 3 | 36 | 488 1987 NEUROPSYCHOLOGIA 25(6):881-891 GRIGSBY JP; KEMPER MB; HAGERMAN RJ DEVELOPMENTAL GERSTMANN SYNDROME WITHOUT APHASIA IN FRAGILE-X SYNDROME | 16 | 27 |
| 2379 | 10 | 29 | 728 1990 NEUROPSYCHOLOGIA 28(1):9-16 CROWE SF; HAY DA NEUROPSYCHOLOGICAL DIMENSIONS OF THE FRAGILE X-SYNDROME - SUPPORT FOR A NONDOMINANT HEMISPHERE DYSFUNCTION HYPOTHESIS | 38 | 54 |
| 2380 | 17 | 36 | 1791 1998 NEUROPSYCHOLOGIA 36(11):1239-1246 Cornish KM; Munir F; Cross G The nature of the spatial deficit in young females with Fragile-X syndrome: A neuropsychological and molecular perspective | 12 | 16 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2381 | 13 | 47 | 2082 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 |
| 2382 | 15 | 32 | 2333 2002 NEUROPSYCHOLOGIA 40(8):1343-1349 Wilding J; Cornish K; Munir F Further delineation of the executive deficit in males with fragile-X syndrome | 7 | 8 |
| 2383 | 52 | 101 | 2599 2004 NEUROPSYCHOLOGIA 42(14):1934-1947 Moore CJ; Daly EM; Schmitz N; Tassone F; Tysoe C; et al. A neuropsychological investigation of male premutation carriers of fragile X syndrome | 0 | 0 |
| 2384 | 27 | 61 | 1427 1995 NEUROPSYCHOLOGY 9(4):470-480 MAZZOCCO MMM; FREUND LS; BAUMGARDNER TL; FORMAN L; REISS AL NEUROPSYCHOLOGICAL AND PSYCHOSOCIAL EFFECTS OF THE FMR-1 FULL MUTATION - CASE-REPORT OF MONOZYGOTIC TWINS DISCORDANT FOR THE FRAGILE-X SYNDROME | 5 | 6 |
| 2385 | 26 | 47 | 2187 2001 NEUROPSYCHOLOGY 15(2):290-299 Bennetto L; Pennington BF; Porter D; Taylor AK; Hagerman RJ Profile of cognitive functioning in women with the fragile X mutation | 10 | 13 |
| 2386 | 41 | 101 | 2465 2003 NEUROPSYCHOLOGY 17(4):646-657 Loesch DZ; Bui QM; Grigsby J; Butler E; Epstein J; et al. Effect of the fragile X status categories and the fragile X mental retardation protein levels on executive functioning in males and females with fragile X | 1 | 1 |
| 2387 | 6 | 11 | 1792 1998 NEUROREPORT 9(3):477-481 Steward O; Bakker CE; Willems PJ; Oostra BA No evidence for disruption of normal patterns of mRNA localization in dendrites or dendritic transport of recently synthesized mRNA in FMR1 knockout mice, a model for human fragile-X mental retardation syndrome | 12 | 18 |
| 2388 | 8 | 20 | 2188 2001 NEUROREPORT 12(11):2573-2576 Rojas DC; Benkers TL; Rogers SJ; Teale PD; Reite ML; et al. Auditory evoked magnetic fields in adults with fragile X syndrome | 3 | 4 |
| 2389 | 6 | 23 | 2600 2004 NEUROREPORT 15(10):1579-1583 Greicius MD; Boyett-Anderson JM; Menon V; Reiss AL Reduced basal forebrain and hippocampal activation during memory encoding in girls with fragile X syndrome | 0 | 0 |
| 2390 | 24 | 42 | 2601 2004 NEUROREPORT 15(16):2447-2450 Veneri M; Zalfa F; Bagni C FMRP and its target RNAs: fishing for the specificity | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2391 | 19 | 53 | 1931 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 |
| 2392 | 15 | 43 | 2189 2001 NEUROSCIENCE 103(4):1043-1050 Chen L; Toth M Fragile X mice develop sensory hyperreactivity to auditory stimuli | 21 | 34 |
| 2393 | 14 | 26 | 2466 2003 NEUROSCIENCE 119(1):9-13 D'Antuono M; Merlo D; Avoli M Involvement of cholinergic and GABAergic systems in the fragile X knockout mice | 0 | 2 |
| 2394 | 22 | 39 | 2467 2003 NEUROSCIENCE 120(4):1005-1017 Chen L; Yun SW; Seto J; Liu W; Toth M The fragile X mental retardation protein binds and regulates a novel class of mRNAs containing U rich target sequences | 10 | 11 |
| 2395 | 19 | 34 | 2644 2005 NEUROSCIENCE LETTERS 377(3):141-146 El Idrissi A; Ding XH; Scalia J; Trenkner E; Brown WT; et al. Decreased GABA(A) receptor expression in the seizure-prone fragile X mouse | 0 | 0 |
| 2396 | 28 | 53 | 2083 2000 NEUROSCIENCE RESEARCH COMMUNICATIONS 26(3):255-263 de Vries BBA; Oostra BA The fragile X syndrome: A model for mental retardation | 0 | 0 |
| 2397 | 8 | 18 | 2084 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 |
| 2398 | 0 | 0 | 610 1988 NEUROTOXICOLOGY 9(1):139-140 EDWARDS DR; KEPPEN LD; GOLLIN SM AUTISM AND FRAGILE-X SYNDROME | 0 | 0 |
| 2399 | 5 | 9 | 611 1988 NEUROTOXICOLOGY 9(3):359-365 EDWARDS DR; KEPPEN LD; RANELLS JD; GOLLIN SM AUTISM IN ASSOCIATION WITH FRAGILE X-SYNDROME IN FEMALES - IMPLICATIONS FOR DIAGNOSIS AND TREATMENT IN CHILDREN | 4 | 7 |
| 2400 | 1 | 7 | 33 1981 NEW ENGLAND JOURNAL OF MEDICINE 305(22):1348-1348 NIELSEN KB; TOMMERUP N; DYGGVE H; SCHOU C MACROORCHIDISM, MENTAL-RETARDATION, AND THE FRAGILE-X | 8 | 12 |