| Missing Links? Citation Matrix | Graphs | Glossary HistCite Guide About |
Nodes: 2647,
Authors: 5321,
Journals: 428,
Outer References: 16458,
Words: 3536
Collection span: 1967 - 2005
View: Overview. Sorted by journal name.
Page 4: 1 2 3 4 5 6 7 8 9
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 901 | 0 | 0 | 626 1989 AMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY 78(2):200-200 BUTLER MG; HAYNES JL; ALLEN GA; SINGH DN ANTHROPOMETRIC COMPARISON OF MENTALLY-RETARDED MALES WITH AND WITHOUT FRAGILE X-SYNDROME | 0 | 0 |
| 902 | 4 | 10 | 255 1985 AMERICAN JOURNAL OF PSYCHIATRY 142(1):108-110 GOLDFINE PE; MCPHERSON PM; HEATH GA; HARDESTY VA; BEAUREGARD LJ; et al. ASSOCIATION OF FRAGILE-X SYNDROME WITH AUTISM | 36 | 53 |
| 903 | 12 | 24 | 360 1986 AMERICAN JOURNAL OF PSYCHIATRY 143(1):71-73 FISCH GS; COHEN IL; WOLF EG; BROWN WT; JENKINS EC; et al. AUTISM AND THE FRAGILE X-SYNDROME | 19 | 28 |
| 904 | 17 | 54 | 2120 2001 AMERICAN JOURNAL OF PSYCHIATRY 158(7):1040-1051 Kwon H; Menon V; Eliez S; Warsofsky IS; White CD; et al. Functional neuroanatomy of visuospatial working memory in fragile X syndrome: Relation to behavioral and molecular measures | 11 | 24 |
| 905 | 1 | 5 | 256 1985 AMERICAN JOURNAL OF PUBLIC HEALTH 75(7):715-716 MILUNSKY A AN IMPORTANT CLINICAL APPROACH IN DETECTING THE FRAGILE X-SYNDROME | 0 | 1 |
| 906 | 3 | 19 | 257 1985 AMERICAN JOURNAL OF PUBLIC HEALTH 75(7):771-772 TRUSLER S; BEATTYDESANA J FRAGILE X-SYNDROME - A PUBLIC-HEALTH CONCERN | 5 | 6 |
| 907 | 17 | 42 | 2246 2002 AMERICAN JOURNAL OF SPEECH-LANGUAGE PATHOLOGY 11(4):295-304 Roberts JE; Mirrett P; Anderson K; Burchinal M; Neebe E Early communication, symbolic behavior, and social profiles of young males with fragile X syndrome | 0 | 0 |
| 908 | 5 | 42 | 426 1987 AMERICAN JOURNAL ON MENTAL RETARDATION 92(3):272-278 LACHIEWICZ AM; GULLION CM; SPIRIDIGLIOZZI GA; AYLSWORTH AS DECLINING IQS OF YOUNG MALES WITH THE FRAGILE X-SYNDROME | 48 | 64 |
| 909 | 12 | 32 | 563 1988 AMERICAN JOURNAL ON MENTAL RETARDATION 92(5):436-446 COHEN IL; FISCH GS; SUDHALTER V; WOLFSCHEIN EG; HANSON D; et al. SOCIAL GAZE, SOCIAL AVOIDANCE, AND REPETITIVE BEHAVIOR IN FRAGILE X-MALES - A CONTROLLED-STUDY | 51 | 74 |
| 910 | 11 | 24 | 627 1989 AMERICAN JOURNAL ON MENTAL RETARDATION 93(4):406-411 WOLFF PH; GARDNER J; PACCIA J; LAPPEN J THE GREETING BEHAVIOR OF FRAGILE X-MALES | 26 | 39 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 911 | 11 | 23 | 690 1990 AMERICAN JOURNAL ON MENTAL RETARDATION 94(4):431-441 SUDHALTER V; COHEN IL; SILVERMAN W; WOLFSCHEIN EG CONVERSATIONAL ANALYSES OF MALES WITH FRAGILE-X, DOWN SYNDROME, AND AUTISM - COMPARISON OF THE EMERGENCE OF DEVIANT LANGUAGE | 56 | 70 |
| 912 | 9 | 32 | 691 1990 AMERICAN JOURNAL ON MENTAL RETARDATION 94(4):442-447 CANTU ES; STONE JW; WING AA; LANGEE HR; WILLIAMS CA CYTOGENETIC SURVEY FOR AUTISTIC FRAGILE-X CARRIERS IN A MENTAL-RETARDATION CENTER | 5 | 16 |
| 913 | 4 | 14 | 966 1992 AMERICAN JOURNAL ON MENTAL RETARDATION 96(5):528-535 MERYASH DL CHARACTERISTICS OF FRAGILE-X RELATIVES WITH DIFFERENT ATTITUDES TOWARD TERMINATING AN AFFECTED PREGNANCY | 4 | 5 |
| 914 | 1 | 22 | 967 1992 AMERICAN JOURNAL ON MENTAL RETARDATION 97(1):39-46 HODAPP RM; LECKMAN JF; DYKENS EM; SPARROW SS; ZELINSKY DG; et al. K-ABC PROFILES IN CHILDREN WITH FRAGILE-X SYNDROME, DOWN-SYNDROME, AND NONSPECIFIC MENTAL-RETARDATION | 18 | 40 |
| 915 | 2 | 3 | 1081 1993 AMERICAN JOURNAL ON MENTAL RETARDATION 97(4):477-479 SIMENSEN RJ FRAGILE X-SYNDROME - DIAGNOSIS, TREATMENT, AND RESEARCH - HAGERMAN,RJ, SILVERMAN,AC | 0 | 0 |
| 916 | 16 | 33 | 1220 1994 AMERICAN JOURNAL ON MENTAL RETARDATION 98(4):455-462 KERBY DS; DAWSON BL AUTISTIC FEATURES, PERSONALITY, AND ADAPTIVE-BEHAVIOR IN MALES WITH THE FRAGILE-X SYNDROME AND NO AUTISM | 14 | 23 |
| 917 | 19 | 41 | 1221 1994 AMERICAN JOURNAL ON MENTAL RETARDATION 98(5):567-579 LACHIEWICZ AM; SPIRIDIGLIOZZI GA; GULLION CM; RANSFORD SN; RAO K ABERRANT BEHAVIORS OF YOUNG BOYS WITH FRAGILE X-SYNDROME | 28 | 33 |
| 918 | 13 | 23 | 1719 1998 AMERICAN JOURNAL ON MENTAL RETARDATION 103(1):29-39 Bailey DB; Hatton DD; Skinner M Early developmental trajectories of males with fragile X syndrome | 30 | 32 |
| 919 | 14 | 37 | 1982 2000 AMERICAN JOURNAL ON MENTAL RETARDATION 105(4):286-299 Kau ASM; Reider EE; Payne L; Meyer WA; Freund L Early behavior signs of psychiatric phenotypes in fragile X syndrome | 2 | 4 |
| 920 | 17 | 37 | 2121 2001 AMERICAN JOURNAL ON MENTAL RETARDATION 106(1):16-27 Bailey DB; Hatton DD; Tassone F; Skinner M; Taylor AK Variability in FMRP and early development in males with fragile X syndrome | 16 | 15 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 921 | 13 | 43 | 2122 2001 AMERICAN JOURNAL ON MENTAL RETARDATION 106(1):28-38 Belser RC; Sudhalter V Conversational characteristics of children with fragile X syndrome: Repetitive speech | 9 | 12 |
| 922 | 23 | 55 | 2123 2001 AMERICAN JOURNAL ON MENTAL RETARDATION 106(3):216-230 Roberts JE; Mirrett P; Burchinal M Receptive and expressive communication development of young males with fragile X syndrome | 6 | 10 |
| 923 | 16 | 58 | 2124 2001 AMERICAN JOURNAL ON MENTAL RETARDATION 106(5):389-400 Sudhalter V; Belser RC Conversational characteristics of children with fragile x syndrome: Tangential language | 5 | 8 |
| 924 | 15 | 39 | 2385 2003 AMERICAN JOURNAL ON MENTAL RETARDATION 108(3):149-160 Abbeduto L; Murphy MM; Cawthon SW; Richmond EK; Weissman MD; et al. Receptive language skills of adolescents and young adults with Down or fragile X syndrome | 2 | 5 |
| 925 | 29 | 60 | 2386 2003 AMERICAN JOURNAL ON MENTAL RETARDATION 108(5):314-326 Demark JL; Feldman MA; Holden JJA Behavioral relationship between autism and fragile X syndrome | 1 | 2 |
| 926 | 22 | 50 | 2387 2003 AMERICAN JOURNAL ON MENTAL RETARDATION 108(6):373-390 Hatton DD; Wheeler AC; Skinner ML; Bailey DB; Sullivan KM; et al. Adaptive behavior in children with fragile X syndrome | 0 | 1 |
| 927 | 17 | 51 | 2495 2004 AMERICAN JOURNAL ON MENTAL RETARDATION 109(3):208-218 Philofsky A; Hepburn SL; Hayes A; Hagerman R; Rogers SJ Linguistic and cognitive functioning and autism symptoms in young children with fragile X syndrome | 0 | 1 |
| 928 | 14 | 79 | 2496 2004 AMERICAN JOURNAL ON MENTAL RETARDATION 109(3):237-254 Abbeduto L; Seltzer MM; Shattuck P; Krauss MW; Orsmond G; et al. Psychological well-being and coping in mothers of youths with autism, Down syndrome, or fragile X syndrome | 0 | 1 |
| 929 | 4 | 53 | 628 1989 AMERICAN ZOOLOGIST 29(2):569-591 LAIRD CD FROM POLYTENE CHROMOSOMES TO HUMAN EMBRYOLOGY - CONNECTIONS VIA THE HUMAN FRAGILE-X SYNDROME | 1 | 3 |
| 930 | 0 | 0 | 13 1981 ANGLO-WELSH REVIEW (68):6-9 WESTLEY M 'FRAGILE-X' | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 931 | 0 | 2 | 52 1982 ANNALES DE GENETIQUE 25(3):149-151 LEJEUNE J; LEGRAND N; LAFOURCADE J; RETHORE MO; RAOUL O; et al. THE FRAGILE X - EFFECT OF TRIMETHOPRIME TREATMENT | 15 | 24 |
| 932 | 2 | 4 | 114 1983 ANNALES DE GENETIQUE 26(3):147-149 CALVAMERCADO MP; MAUNOURY C; RETHORE MO; LEJEUNE J FRAGILE-X AND INHIBITION OF DIHYDROFOLATE-REDUCTASE - COMPARED EFFECTS OF 2 ANTIBIOTICS - TRIMETHOPRIME AND PYRIMETHAMINE | 6 | 13 |
| 933 | 2 | 15 | 115 1983 ANNALES DE GENETIQUE 26(3):171-173 JACKY PB; DILL FJ FRAGILE-X CHROMOSOME AND CHROMOSOME CONDENSATION | 1 | 4 |
| 934 | 9 | 17 | 116 1983 ANNALES DE GENETIQUE 26(4):247-250 TEJADA I; BOUE J; GILGENKRANTZ S PRENATAL-DIAGNOSIS OF FRAGILE X-CHROMOSOME ON AMNIOTIC-FLUID CELLS | 6 | 9 |
| 935 | 1 | 13 | 117 1983 ANNALES DE GENETIQUE 26(4):251-253 FRYNS JP; KLECZKOWSKA A; KUBIEN E; PETIT P; HASPESLAGH M; et al. XY XXY MOSAICISM AND FRAGILE X-SYNDROME | 12 | 17 |
| 936 | 4 | 11 | 192 1984 ANNALES DE GENETIQUE 27(4):230-232 LEJEUNE J; RETHORE MO; DEBLOIS MC; RAVEL A ASSAY OF FOLIC-ACID TREATMENT IN FRAGILE-X SYNDROME | 8 | 13 |
| 937 | 0 | 10 | 361 1986 ANNALES DE GENETIQUE 29(4):261-263 BELGHITI D; RAZAVIENCHA F; RAOUL O; HIRBEC G; GUILLOT F; et al. COINCIDENCE OF FAMILIAL SYSTEMIC LUPUS-ERYTHEMATOSUS AND THE FRAGILE-X SYNDROME | 0 | 3 |
| 938 | 8 | 13 | 692 1990 ANNALES DE GENETIQUE 33(2):109-110 LUCOTTE G A NEW DNA PROBE OF POTENTIAL USE FOR DIAGNOSIS OF THE FRAGILE-X SYNDROME | 0 | 0 |
| 939 | 1 | 15 | 839 1991 ANNALES DE GENETIQUE 34(2):111-114 BARLETTA C; RAGUSA RM; GAROFALO G; SCILLATO F; RUGGERI M SEGREGATION ANALYSIS OF AUTOSOMAL FRAGILE SITES IN 3 FAMILIES WITH THE FRAGILE X-CHROMOSOME | 0 | 5 |
| 940 | 22 | 32 | 1630 1997 ANNALES DE GENETIQUE 40(3):139-144 Gerard B; LeHeuzey MF; Brunie G; Lewine P; Saiag MC; et al. Systematic screening for fragile X syndrome in a cohort of 574 mentally retarded children | 4 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 941 | 22 | 38 | 1871 1999 ANNALES DE GENETIQUE 42(4):197-201 Arrieta I; Criado B; Martinez B; Telez M; Nunez T; et al. A survey of fragile X syndrome in a sample from Spanish Basque country | 4 | 4 |
| 942 | 22 | 37 | 1983 2000 ANNALES DE GENETIQUE 43(1):29-34 Gonzalez-del Angel A; Vidal S; Saldana Y; del Castillo V; Alcantara MA; et al. Molecular diagnosis of the fragile X and FRAXE syndromes in patients with mental retardation of unknown cause in Mexico | 2 | 4 |
| 943 | 10 | 21 | 2388 2003 ANNALES DE GENETIQUE 46(1):53-55 Santos CB; Hjalgrim H; Carneiro FRG; Ribeiro M; Boy RT; et al. Concurrence of fragile X and Klinefelter syndromes: report of a new case of paternal nondisjunction | 0 | 0 |
| 944 | 0 | 0 | 1082 1993 ANNALES DE PEDIATRIE 40(9):565-572 BLANC DS; DANGELO J; ETANGS NLD AUTISM AND THE FRAGILE X-SYNDROME | 1 | 1 |
| 945 | 2 | 15 | 1631 1997 ANNALES MEDICO-PSYCHOLOGIQUES 155(7):457-460 BillonGalland IO The fragile X syndrome and its clinical psychotic expression | 0 | 0 |
| 946 | 0 | 0 | 1632 1997 ANNALES MEDICO-PSYCHOLOGIQUES 155(7):460-460 Koupernik; Doutheau; Rapporteur The fragile X syndrome and its clinical psychotic expression - Discussion | 0 | 0 |
| 947 | 10 | 25 | 1505 1996 ANNALS OF CLINICAL AND LABORATORY SCIENCE 26(4):323-328 Mark HFL; Bier JAB; Scola P The frequency of chromosomal abnormalities in patients referred for fragile X analysis | 1 | 4 |
| 948 | 6 | 10 | 1633 1997 ANNALS OF CLINICAL BIOCHEMISTRY 34:517-520 Chen TA; Lu XF; Che PK; Ho WKK Variation of the CGG repeat in FMR-1 gene in normal and fragile X Chinese subjects | 6 | 7 |
| 949 | 27 | 32 | 2125 2001 ANNALS OF CLINICAL BIOCHEMISTRY 38:264-271 Saha S; Karmakar P; Chatterjee C; Banerjee D; Das S; et al. Fragile X syndrome in Calcutta, India | 2 | 4 |
| 950 | 9 | 31 | 362 1986 ANNALS OF HUMAN GENETICS 50:385-398 LOESCH DZ DERMATOGLYPHIC FINDINGS IN FRAGILE X-SYNDROME - A CAUSAL HYPOTHESIS POINTS TO X-Y INTERCHANGE | 9 | 14 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 951 | 17 | 36 | 427 1987 ANNALS OF HUMAN GENETICS 51:107-124 GIANNELLI F; MORRIS AH; GARRETT C; DAKER M; THURSTON C; et al. GENETIC-HETEROGENEITY OF X-LINKED MENTAL-RETARDATION WITH FRAGILE-X - ASSOCIATION OF TIGHT LINKAGE TO FACTOR-IX AND INCOMPLETE PENETRANCE IN MALES | 7 | 16 |
| 952 | 20 | 30 | 1720 1998 ANNALS OF HUMAN GENETICS 62:337-347 Huggins RM; Loesch DZ; Sherman SL A branching non-linear autoregressive model for the transmission of the fragile X dynamic repeat mutation | 1 | 2 |
| 953 | 25 | 37 | 968 1992 ANNALS OF MEDICINE 24(6):453-456 POUSTKA A FRAGILE-X SYNDROME - MOLECULAR ANALYSIS REVEALS A NEW MECHANISM OF MUTATION IN HUMAN GENETIC-DISEASES | 0 | 0 |
| 954 | 28 | 43 | 1634 1997 ANNALS OF MEDICINE 29(6):563-567 Oostra BA; Hoogeveen AT Animal model for fragile X syndrome | 3 | 8 |
| 955 | 9 | 47 | 258 1985 ANNALS OF NEUROLOGY 18(6):665-669 WISNIEWSKI KE; FRENCH JH; FERNANDO S; BROWN WT; JENKINS EC; et al. FRAGILE X-SYNDROME - ASSOCIATED NEUROLOGICAL ABNORMALITIES AND DEVELOPMENTAL-DISABILITIES | 27 | 43 |
| 956 | 0 | 0 | 363 1986 ANNALS OF NEUROLOGY 20(3):417-417 PAYTON JB; STEELE MW; WENGER SL; MINSHEW NJ ASSOCIATION OF THE FRAGILE-X CHROMOSOME ABNORMALITY WITH INFANTILE-AUTISM | 4 | 4 |
| 957 | 0 | 0 | 693 1990 ANNALS OF NEUROLOGY 28(3):440-440 BERRYKRAVIS E; HUTTENLOCHER PR CYCLIC-AMP METABOLISM IN FRAGILE X-SYNDROME | 0 | 0 |
| 958 | 4 | 31 | 840 1991 ANNALS OF NEUROLOGY 29(1):26-32 REISS AL; AYLWARD E; FREUND LS; JOSHI PK; BRYAN RN NEUROANATOMY OF FRAGILE-X-SYNDROME - THE POSTERIOR-FOSSA | 60 | 114 |
| 959 | 0 | 0 | 841 1991 ANNALS OF NEUROLOGY 30(3):450-450 BERRYKRAVIS E; HODGES C DEMONSTRATION OF ABNORMAL CYCLIC ADENOSINE-MONOPHOSPHATE PRODUCTION IN MULTIPLE TISSUES FROM INDIVIDUALS WITH FRAGILE X-SYNDROME | 0 | 0 |
| 960 | 5 | 22 | 969 1992 ANNALS OF NEUROLOGY 31(1):22-26 BERRYKRAVIS E; HUTTENLOCHER PR CYCLIC-AMP METABOLISM IN FRAGILE-X SYNDROME | 14 | 19 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 961 | 0 | 0 | 1222 1994 ANNALS OF NEUROLOGY 36(3):544-544 GUERREIRO M; MOURARIBEIRO MV; KATO M; CAMARGO E; DEFARIA APM BRAIN SINGLE-PHOTON EMISSION COMPUTED-TOMOGRAPHY IMAGING IN FRAGILE-X SYNDROME | 0 | 0 |
| 962 | 0 | 0 | 1334 1995 ANNALS OF NEUROLOGY 38(3):499-499 BERRYKRAVIS E; CIURLIONIS R OVEREXPRESSION OF FRAGILE-X GENE (FMR-1) TRANSCRIPTS IN NEURAL CELLS RESULTS IN INCREASED LEVELS OF CYCLIC ADENOSINE-MONOPHOSPHATE PRODUCTION | 0 | 0 |
| 963 | 0 | 0 | 2126 2001 ANNALS OF NEUROLOGY 50(3):S108-S108 Berry-Kravis E Characterization of epilepsy in fragile X syndrome | 0 | 0 |
| 964 | 0 | 0 | 2247 2002 ANNALS OF NEUROLOGY 52(3):S86-S86 Berry-Kravis E; Lewin F; Wuu J; Leehey M; Hagerman R; et al. Tremor and ataxia in adult fragile X premutation carriers: Blinded videotape evaluation | 0 | 0 |
| 965 | 15 | 31 | 2389 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 | 11 | 14 |
| 966 | 0 | 0 | 2390 2003 ANNALS OF NEUROLOGY 54:S105-S106 Kaufmann WE; Danko CG; Kau ASM; Thevarajah S; Bukelis I; et al. Increased protein acetylation in lymphocytes predicts autistic behavior in Fragile X syndrome | 1 | 1 |
| 967 | 0 | 0 | 2391 2003 ANNALS OF NEUROLOGY 54:S144-S144 Berry-Kravis E; Potanos K Clinical response to psychopharmacology for behavior in Fragile X syndrome | 0 | 0 |
| 968 | 0 | 0 | 2392 2003 ANNALS OF NEUROLOGY 54:S150-S150 Berry-Kravis E; Potanos K Stimulant therapy in fragile X syndrome | 0 | 0 |
| 969 | 0 | 0 | 2497 2004 ANNALS OF NEUROLOGY 56:S104-S104 Cortell R; Bukelis I; Gray RM; Cox C; Tierney E; et al. Autism spectrum disorder in boys with Fragile X: Serial evaluation | 0 | 0 |
| 970 | 16 | 20 | 2623 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 971 | 5 | 19 | 1984 2000 ANNALS OF SAUDI MEDICINE 20(1):16-19 Al Husain M; Salih MAM; Zaki OK; Al Othman L; Al Nasser MN A clinical study of mentally retarded children with fragile X syndrome in Saudi Arabia | 0 | 0 |
| 972 | 21 | 41 | 1985 2000 ANNALS OF SAUDI MEDICINE 20(3-4):214-217 Iqbal MA; Sakati N; Nester M; Ozand P Cytogenetic diagnosis of fragile X syndrome: Study of 305 suspected cases in Saudi Arabia | 0 | 0 |
| 973 | 43 | 97 | 364 1986 ANNALS OF THE NEW YORK ACADEMY OF SCIENCES 477:129-150 BROWN WT; JENKINS EC; KRAWCZUN MS; WISNIEWSKI K; RUDELLI R; et al. THE FRAGILE-X SYNDROME | 10 | 13 |
| 974 | 38 | 118 | 365 1986 ANNUAL REVIEW OF GENETICS 20:109-145 NUSSBAUM RL; LEDBETTER DH FRAGILE-X SYNDROME - A UNIQUE MUTATION IN MAN | 65 | 112 |
| 975 | 71 | 125 | 1335 1995 ANNUAL REVIEW OF NEUROSCIENCE 18:77-99 WARREN ST; ASHLEY CT TRIPLET REPEAT EXPANSION MUTATIONS - THE EXAMPLE OF FRAGILE-X SYNDROME | 26 | 58 |
| 976 | 99 | 179 | 2248 2002 ANNUAL REVIEW OF NEUROSCIENCE 25:315-338 O'Donnell WT; Warren ST A decade of molecular studies of fragile X syndrome | 0 | 63 |
| 977 | 10 | 98 | 2624 2005 APPLIED PSYCHOLINGUISTICS 26(1):7-27 Rice ML; Warren SF; Betz SK Language symptoms of developmental language disorders: An overview of autism, Down syndrome, fragile X, specific language impairment, and Williams syndrome | 0 | 1 |
| 978 | 20 | 37 | 1506 1996 ARCHIVES DE PEDIATRIE 3(8):814-821 Mornet E; SimonBouy B Molecular biology of fragile X syndrome: Applications to genetic counselling and molecular diagnosis | 3 | 4 |
| 979 | 0 | 0 | 1635 1997 ARCHIVES DE PEDIATRIE 4(2):195-195 Mornet E Fragile X syndrome - Response | 0 | 0 |
| 980 | 1 | 1 | 1636 1997 ARCHIVES DE PEDIATRIE 4(2):195-195 Beauvais P Fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 981 | 17 | 20 | 1637 1997 ARCHIVES DE PEDIATRIE 4(3):227-236 Cossee M; Moutou C; Biancalana V; Bouix JC; Plessis G; et al. The fragile X syndrome is still underdiagnosed: Efficacy of molecular testing in mentally retarded probands | 3 | 3 |
| 982 | 11 | 15 | 2393 2003 ARCHIVES DE PEDIATRIE 10(5):401-402 Ramos FJ; Willemsen R Diagnosis of the Fragile X Syndrome by the analysis of FMRP expression in blood and hair roots | 0 | 0 |
| 983 | 5 | 13 | 2625 2005 ARCHIVES DE PEDIATRIE 12(2):176-179 Vantalon V; Briard-Luginbuhl V; Mouren MC Fragile X syndrome and very early onset schizophrenia: a female case study | 0 | 0 |
| 984 | 16 | 81 | 53 1982 ARCHIVES FRANCAISES DE PEDIATRIE 39(8):633-639 MATTEI JF FRAGILE X-LINKED MENTAL-RETARDATION | 3 | 3 |
| 985 | 38 | 83 | 629 1989 ARCHIVES FRANCAISES DE PEDIATRIE 46(3):211-216 LELOUARN P; MORAINE C; PERROT A; BARTHELEMY C; GARREAU B; et al. AUTISM AND FRAGILE X-SYNDROME | 3 | 5 |
| 986 | 1 | 40 | 694 1990 ARCHIVES FRANCAISES DE PEDIATRIE 47(10):701-703 PIUSSAN C X-LINKED MENTAL-RETARDATION WITHOUT FRAGILE X-CHROMOSOME | 0 | 0 |
| 987 | 27 | 41 | 970 1992 ARCHIVES FRANCAISES DE PEDIATRIE 49(2):99-103 BURSZTEJN C; ALEMBIK Y; STOLL C; POUPIER G; FELLER L; et al. FRAGILE-X SYNDROME ASSOCIATED WITH INFANTILE-AUTISM AND PSYCHOTIC DISORDERS | 0 | 2 |
| 988 | 3 | 4 | 971 1992 ARCHIVES FRANCAISES DE PEDIATRIE 49(5):477-477 DROUIN V; VANNIER JP; MOIROT H; MITROFANOFF P; TRON P WILMS-TUMOR AND FRAGILE-X SYNDROME | 1 | 1 |
| 989 | 0 | 0 | 1872 1999 ARCHIVES OF CLINICAL NEUROPSYCHOLOGY 14(8):767-767 Lesniak-Karpiak K; Mazzocco MM; Lanham DC; Denckla MB Behavioral assessment of social skills in children with Turner syndrome or Fragile X. | 0 | 0 |
| 990 | 0 | 0 | 1873 1999 ARCHIVES OF CLINICAL NEUROPSYCHOLOGY 14(8):767-768 Lanham DC; Mazzocco MM; Denckla MB Depression and anxiety in girls with Fragile X or Turner Syndrome. | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 991 | 7 | 26 | 259 1985 ARCHIVES OF DISEASE IN CHILDHOOD 60(11):1001-1007 THAKE A; TODD J; BUNDEY S; WEBB T IS IT POSSIBLE TO MAKE A CLINICAL-DIAGNOSIS OF THE FRAGILE X-SYNDROME IN A BOY | 22 | 28 |
| 992 | 6 | 8 | 630 1989 ARCHIVES OF DISEASE IN CHILDHOOD 64(9):1223-1224 WINTER RM FRAGILE-X MENTAL-RETARDATION | 1 | 3 |
| 993 | 2 | 4 | 695 1990 ARCHIVES OF DISEASE IN CHILDHOOD 65(3):335-335 REDINGTON A; BUSH A FRAGILE-X MENTAL-RETARDATION | 2 | 2 |
| 994 | 1 | 1 | 972 1992 ARCHIVES OF DISEASE IN CHILDHOOD 67(11):1337-1337 [Anon] SISTERS OF FRAGILE-X BOYS | 0 | 0 |
| 995 | 27 | 43 | 1336 1995 ARCHIVES OF DISEASE IN CHILDHOOD 72(1):3-5 TURK J FRAGILE-X SYNDROME | 2 | 4 |
| 996 | 16 | 30 | 1337 1995 ARCHIVES OF DISEASE IN CHILDHOOD 72(1):33-37 SLANEY SF; WILKIE AOM; HIRST MC; CHARLTON R; MCKINLEY M; et al. DNA TESTING FOR FRAGILE-X SYNDROME IN SCHOOLS FOR LEARNING-DIFFICULTIES | 13 | 21 |
| 997 | 2 | 5 | 1338 1995 ARCHIVES OF DISEASE IN CHILDHOOD 72(6):544-544 TURK J TREATMENT OF FRAGILE-X SYNDROME | 0 | 0 |
| 998 | 1 | 1 | 1507 1996 ARCHIVES OF DISEASE IN CHILDHOOD 74(1):88-88 Magnay D; Morritt J; Waterston T Fragile X syndrome | 0 | 0 |
| 999 | 2 | 23 | 1638 1997 ARCHIVES OF DISEASE IN CHILDHOOD 76(3):264-267 Corrigan N; Stewart M; Scott M; Fee F Fragile X, iron, and neurodevelopmental screening in 8 year old children with mild to moderate learning difficulties | 0 | 4 |
| 1000 | 7 | 32 | 564 1988 ARCHIVES OF GENERAL PSYCHIATRY 45(1):25-30 REISS AL; HAGERMAN RJ; VINOGRADOV S; ABRAMS M; KING RJ PSYCHIATRIC DISABILITY IN FEMALE CARRIERS OF THE FRAGILE X-CHROMOSOME | 59 | 93 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1001 | 15 | 30 | 973 1992 ARCHIVES OF GENERAL PSYCHIATRY 49(1):54-60 FREUND LS; REISS AL; HAGERMAN R; VINOGRADOV S CHROMOSOME FRAGILITY AND PSYCHOPATHOLOGY IN OBLIGATE FEMALE CARRIERS OF THE FRAGILE X-CHROMOSOME | 27 | 47 |
| 1002 | 14 | 50 | 2498 2004 ARCHIVES OF GENERAL PSYCHIATRY 61(3):281-288 Garrett AS; Menon V; MacKenzie K; Reiss AL Here's looking at you, kid - Neural systems underlying face and gaze processing in fragile X syndrome | 0 | 1 |
| 1003 | 11 | 19 | 1339 1995 ARCHIVES OF MEDICAL RESEARCH 26:S77-S83 DiazGallardo MY; BarrosNunez P; Diaz CA; Hernandez A; GomezEspinel I; et al. Molecular characterization of the fragile-X syndrome in the Mexican population | 2 | 4 |
| 1004 | 0 | 1 | 1508 1996 ARCHIVES OF MEDICAL RESEARCH 27(3):427-427 DiazGallardo Molecular characterization of the fragile-x syndrome in the Mexican population (vol 26, pg S77, 1995) | 0 | 0 |
| 1005 | 4 | 13 | 1509 1996 ARCHIVES OF MEDICAL RESEARCH 27(4):587-588 Rivera H Fragile X studies and authorship | 1 | 5 |
| 1006 | 1 | 1 | 1639 1997 ARCHIVES OF MEDICAL RESEARCH 28(1):149-149 Rivera H Fragile X studies and authorship (vol 27, pg 587, 1996) | 0 | 0 |
| 1007 | 13 | 35 | 2249 2002 ARCHIVES OF MEDICAL RESEARCH 33(2):128-135 Wang TS; Hsieh LJ; Hsu TY; Chung CH; Li SY DNA damage and repair in lymphoblastoid cell lines from normal donors and fragile X syndrome patients | 0 | 1 |
| 1008 | 2 | 17 | 631 1989 ARCHIVES OF NEUROLOGY 46(12):1269-1270 GRIGSBY J; HAGERMAN R FRAGILE-X SYNDROME - A GENETIC ETIOLOGY FOR DEVELOPMENTAL GERSTMANN SYNDROME | 0 | 0 |
| 1009 | 13 | 30 | 2394 2003 ARCHIVES OF NEUROLOGY 60(1):117-121 Leehey MA; Munhoz RP; Lang AE; Brunberg JA; Grigsby J; et al. The fragile X premutation presenting as essential tremor | 12 | 23 |
| 1010 | 2 | 12 | 2395 2003 ARCHIVES OF NEUROLOGY 60(9):1197-1200 Kalidas S; Smith DP Functional genomics, fragile X syndrome, and RNA interference | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1011 | 13 | 30 | 428 1987 ARCHIVES OF OPHTHALMOLOGY 105(8):1099-1102 STORM RL; PEBENITO R; FERRETTI C OPHTHALMOLOGIC FINDINGS IN THE FRAGILE X-SYNDROME | 5 | 7 |
| 1012 | 42 | 66 | 1083 1993 ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE 117(11):1121-1125 TSONGALIS GJ; SILVERMAN LM MOLECULAR PATHOLOGY OF THE FRAGILE-X SYNDROME | 0 | 2 |
| 1013 | 10 | 11 | 1223 1994 ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE 148(1):63-64 LEUNG AKC; MCLEOD DR; ROBSON WLM; FAGAN JE PICTURE OF THE MONTH - FRAGILE-X SYNDROME | 0 | 1 |
| 1014 | 2 | 5 | 1721 1998 ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE 152(1):89-90 Tsuchiya KD; Forsythe M; Robin NH; Tunnessen WW Picture of the month - Fragile X syndrome | 0 | 0 |
| 1015 | 0 | 0 | 366 1986 ARCHIVOS DE BIOLOGIA Y MEDICINA EXPERIMENTALES 19(1):R133-R133 LACASSIE Y; MORENO R; ALLIENDE MA; DELABARRA F; BARAHONA G; et al. LACK OF EFFECT OF FOLIC-ACID THERAPY ON MENTAL RETARDED PATIENTS WITH FRAGILE-X OR OTHER AUTOSOMAL FRAGILITIES IN A DOUBLE-BLIND-STUDY | 0 | 0 |
| 1016 | 0 | 0 | 7 1980 ARIZONA MEDICINE 37(11):764-766 HECHT F; KAISERMCCAW B; MOORE BC; CADIEN J; GLOVER TW THE FRAGILE X-CHROMOSOME MENTAL-RETARDATION AND LARGE TESTES | 2 | 2 |
| 1017 | 14 | 24 | 1722 1998 ARQUIVOS DE NEURO-PSIQUIATRIA 56(1):9-17 Felix TM; De Pina-Neto JM Fragile X syndrome - Clinical and cytogenetic studies | 0 | 0 |
| 1018 | 12 | 30 | 1723 1998 ARQUIVOS DE NEURO-PSIQUIATRIA 56(1):18-23 Guerreiro MM; Camargo EE; Kato M; Marques-De-Faria AP; Ciasca SM; et al. Fragile X syndrome - Clinical, electroencephalographic and neuroimaging characteristics | 8 | 14 |
| 1019 | 15 | 30 | 2127 2001 ARQUIVOS DE NEURO-PSIQUIATRIA 59(1):83-88 Boy R; Correia PS; Llerena JC; Machado-Ferreira MD; Pimentel MMG Fragile X syndrome confirmed by molecular analysis: a case-control study with pre and post-puberal patients | 0 | 0 |
| 1020 | 17 | 30 | 2250 2002 ARQUIVOS DE NEURO-PSIQUIATRIA 60(4):981-985 Yonamine SM; da Silva AA Characteristics of the communication in individuals with fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1021 | 5 | 8 | 1986 2000 AUSTRALIAN AND NEW ZEALAND JOURNAL OF MEDICINE 30(1):86-88 Driscoll G; Clark J; Elakis G; Turner G Early menopause in a family carrying a fragile X premutation | 1 | 3 |
| 1022 | 10 | 18 | 1874 1999 AUSTRALIAN AND NEW ZEALAND JOURNAL OF PSYCHIATRY 33(3):436-440 Al-Semaan Y; Malla AK; Lazosky A Schizoaffective disorder in a fragile-X carrier | 0 | 0 |
| 1023 | 0 | 0 | 2128 2001 AUSTRALIAN JOURNAL OF PSYCHOLOGY 53(1):58-58 Gould E Melatonin profiles and sleep characteristics in boys with fragile X Syndrome: A preliminary study | 0 | 0 |
| 1024 | 0 | 0 | 367 1986 AUSTRALIAN PAEDIATRIC JOURNAL 22(3):237-237 TURNER G; LAING S; ROBINSON H; PURVISSMITH S A PROGRAM FOR PRIMARY PREVENTION OF INTELLECTUAL HANDICAP - FRAGILE (X) SCREENING | 0 | 0 |
| 1025 | 0 | 0 | 368 1986 AUSTRALIAN PAEDIATRIC JOURNAL 22(4):350-350 LOESCH DZ; HAY D PHENOTYPIC DIVERSITY OF FRAGILE-X FEMALES AND ITS GENETIC-IMPLICATIONS | 0 | 0 |
| 1026 | 0 | 0 | 369 1986 AUSTRALIAN PAEDIATRIC JOURNAL 22(4):352-352 MULLEY JC; THORN K; SUTHERLAND GR LINKAGE RELATIONSHIPS OF THE FRAGILE-X | 0 | 0 |
| 1027 | 0 | 0 | 370 1986 AUSTRALIAN PAEDIATRIC JOURNAL 22(4):356-356 SUTHERLAND GR; BAKER E INDUCTION OF THE FRAGILE-X IN FIBROBLASTS BY THYMIDINE | 0 | 0 |
| 1028 | 0 | 0 | 429 1987 AUSTRALIAN PAEDIATRIC JOURNAL 23(1):75-75 LOESCH DZ DERMATOGLYPHIC ABNORMALITY IN FRAGILE X-SYNDROME - A NEW CAUSAL HYPOTHESIS | 0 | 0 |
| 1029 | 0 | 0 | 430 1987 AUSTRALIAN PAEDIATRIC JOURNAL 23(1):79-79 GEDEON AK; MULLEY JC; SUTHERLAND GR LINKAGE ANALYSIS AND CARRIER DETECTION OF THE FRAGILE-X | 0 | 0 |
| 1030 | 0 | 0 | 431 1987 AUSTRALIAN PAEDIATRIC JOURNAL 23(1):81-81 SUTHERLAND GR; BAKER E; HOCKEY A; PURVISSMITH S THE USE OF THYMIDINE INDUCTION OF THE FRAGILE X-CHROMOSOME IN PRENATAL-DIAGNOSIS | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1031 | 0 | 0 | 565 1988 AUSTRALIAN PAEDIATRIC JOURNAL 24(1):91-91 TURNER G ISSUES ARISING FROM FRAGILE-X PREVENTIVE SCREENING | 0 | 0 |
| 1032 | 0 | 0 | 566 1988 AUSTRALIAN PAEDIATRIC JOURNAL 24(1):91-91 LAING S; LATHAM M; KENNY J; PURVISSMITH S; TURNER G CYTOGENETIC ANOMALIES IN A POPULATION SELECTED FOR FRAGILE-X SCREENING | 0 | 0 |
| 1033 | 0 | 0 | 567 1988 AUSTRALIAN PAEDIATRIC JOURNAL 24(1):93-94 GARRY MB; MACFARLANE SC; PULLON DHH FRAGILE-X POSITIVE TURNERS MOSAIC | 0 | 0 |
| 1034 | 0 | 0 | 568 1988 AUSTRALIAN PAEDIATRIC JOURNAL 24(1):96-96 PURVISSMITH S; LAING S; STEWART L; TURNER G; WASS D; et al. PRENATAL-DIAGNOSIS OF FRAGILE-X | 0 | 0 |
| 1035 | 0 | 2 | 569 1988 AUSTRALIAN PAEDIATRIC JOURNAL 24(1):97-97 SUTHERS GK; THODE A; TURNER GL CASE-REPORT - FRAGILE-X SYNDROME AND NEPHROGENIC DIABETES-INSIPIDUS | 0 | 0 |
| 1036 | 0 | 0 | 54 1982 BEHAVIOR GENETICS 12(6):599-599 THEOBALD TM; HAY DA BEHAVIORAL-CORRELATES OF THE FRAGILE X-SYNDROME | 0 | 0 |
| 1037 | 0 | 0 | 432 1987 BEHAVIOR GENETICS 17(6):642-642 VANDENBERG SG A STATUS-REPORT ON THE FRAGILE X-SYNDROME | 0 | 0 |
| 1038 | 0 | 0 | 1084 1993 BEHAVIOR GENETICS 23(6):555-555 HUGGINS RM THE USE OF ROBUST STATISTICAL-METHODS TO DETERMINE THE EFFECT OF GENOTYPE ON PHENOTYPE IN FRAGILE-X | 0 | 0 |
| 1039 | 0 | 0 | 1085 1993 BEHAVIOR GENETICS 23(6):557-557 LOESCH DZ; HUGGINS R; HAY DA; GODEON; AK; et al. GENOTYPE-PHENOTYPE RELATIONSHIPS IN FRAGILE-X - A FAMILY STUDY | 0 | 0 |
| 1040 | 0 | 0 | 1086 1993 BEHAVIOR GENETICS 23(6):569-569 WARD M; HAY DA COGNITION AND READING-ABILITY IN FRAGILE-X MALES - IS THERE A RELATIONSHIP | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1041 | 0 | 0 | 2499 2004 BEHAVIOR GENETICS 34(6):638-638 Fisch GS; Simensen RJ; Schroer RJ Longitudinal assessment of cognitive-behavioral features of children and adolescents with either autism or the fragile X mutation | 0 | 0 |
| 1042 | 2 | 29 | 1987 2000 BEHAVIOR RESEARCH METHODS INSTRUMENTS & COMPUTERS 32(1):5-10 Boccia ML; Roberts JE Behavior and autonomic nervous system function assessed via heart period measures: The case of hyperarousal in boys with fragile X syndrome | 8 | 11 |
| 1043 | 3 | 42 | 1340 1995 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 217(3):1015-1025 Xing GQ; Zhang LX; Zhang L; Heynen T; Yoshikawa T; et al. Rat PPAR delta contains a CGG triplet repeat and is prominently expressed in the thalamic nuclei | 0 | 54 |
| 1044 | 13 | 24 | 1510 1996 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 225(1):27-33 Willemsen R; Bontekoe C; Tamanini F; Galjaard H; Hoogeveen A; et al. Association of FMRP with ribosomal precursor particles in the nucleolus | 25 | 30 |
| 1045 | 9 | 19 | 1988 2000 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 275(2):608-610 Beaulieu MA A distinct FMRP polysomal population at an advanced stage of mammalian erythropoiesis | 2 | 2 |
| 1046 | 11 | 33 | 1989 2000 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 275(3):973-980 Sung YJ; Conti J; Currie JR; Brown WT; Denman RB RNAs that interact with the Fragile X syndrome RNA binding protein FMRP | 27 | 35 |
| 1047 | 4 | 46 | 1990 2000 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 278(3):833-838 Patel PK; Bhavesh NS; Hosur RV Cation-dependent conformational switches in d-TGGCGGC containing two triplet repeats of Fragile X Syndrome: NMR observations | 4 | 9 |
| 1048 | 11 | 38 | 1991 2000 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 279(3):904-908 Ceman S; Nelson R; Warren ST Identification of mouse YB1/p50 as a component of the FMRP-associated mRNP particle | 21 | 29 |
| 1049 | 12 | 24 | 2251 2002 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 292(4):1063-1069 Denman RB; Sung YJ Species-specific and isoform-specific RNA binding of human and mouse fragile X mental retardation proteins | 6 | 6 |
| 1050 | 1 | 26 | 2396 2003 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 303(1):81-90 Monleon D; Esteve V; Celda B NMR study of hexanucleotide d(CCGCGG)(2) containing two triplet repeats of fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1051 | 9 | 26 | 2397 2003 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 305(2):434-441 Dolzhanskaya N; Sung YJ; Conti J; Currie JR; Denman RB The fragile X mental retardation protein interacts with U-rich RNAs in a yeast three-hybrid system | 5 | 7 |
| 1052 | 14 | 43 | 2398 2003 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 310(1):1-7 Denman RB Deja vu all over again: FMRP binds U-rich target mRNAs | 2 | 4 |
| 1053 | 20 | 36 | 1875 1999 BIOCHEMICAL JOURNAL 343:517-523 Tamanini F; van Unen L; Bakker C; Sacchi N; Galjaard H; et al. Oligomerization properties of fragile-X mental-retardation protein (FMRP) and the fragile-X-related proteins FXR1P and FXR2P | 20 | 23 |
| 1054 | 10 | 47 | 2626 2005 BIOCHEMICAL JOURNAL 386:297-303 Kumari D; Gabrielian A; Wheeler D; Usdin K The roles of Sp1, Sp3, USF1/USF2 and NRF-1 in the regulation and three-dimensional structure of the Fragile X mental retardation gene promoter | 0 | 0 |
| 1055 | 2 | 32 | 1341 1995 BIOCHEMISTRY 34(39):12803-12811 MITAS M; YU A; DILL J; HAWORTH IS THE TRINUCLEOTIDE REPEAT SEQUENCE D(CGG)(15) FORMS A HEAT-STABLE HAIRPIN CONTAINING G(SYN)CENTER-DOT-G(ANTI) BASE-PAIRS | 15 | 63 |
| 1056 | 12 | 81 | 1511 1996 BIOCHEMISTRY 35(15):5041-5053 Pearson CE; Sinden RR Alternative structures in duplex DNA formed within the trinucleotide repeats of the myotonic dystrophy and fragile X loci | 4 | 91 |
| 1057 | 27 | 40 | 2399 2003 BIOCHEMISTRY 42(35):10437-10444 Adinolfi S; Ramos A; Martin SR; Dal Piaz F; Pucci P; et al. The N-terminus of the fragile X mental retardation protein contains a novel domain involved in dimerization and RNA binding | 6 | 7 |
| 1058 | 52 | 98 | 1876 1999 BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE 77(4):331-342 Khandjian EW Biology of the fragile X mental retardation protein, an RNA-binding protein | 14 | 22 |
| 1059 | 40 | 112 | 1342 1995 BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE 1271(2-3):293-303 FLANNERY AV; HIRST MC; KNIGHT SJL; RITCHIE RJ; DAVIES KE THE FRAGILE-X SYNDROME | 2 | 5 |
| 1060 | 16 | 38 | 842 1991 BIOESSAYS 13(5):243-251 JORDAN BR FRAGILE X-LINKED MENTAL-RETARDATION AND THE DIFFICULTIES OF REVERSE GENETICS | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1061 | 4 | 6 | 2400 2003 BIOFUTUR (229):36-37 Nourrit F Fragile X and interference. | 0 | 0 |
| 1062 | 6 | 34 | 433 1987 BIOLOGICAL PSYCHIATRY 22(3):303-312 STCLAIR DM; BLACKWOOD DHR; OLIVER CJ; DICKENS P P3 ABNORMALITY IN FRAGILE-X SYNDROME | 5 | 16 |
| 1063 | 28 | 73 | 696 1990 BIOLOGICAL PSYCHIATRY 27(2):223-240 REISS AL; FREUND L FRAGILE X-SYNDROME | 22 | 28 |
| 1064 | 5 | 13 | 843 1991 BIOLOGICAL PSYCHIATRY 29(3):298-299 MENDLEWICZ J; HIRSCH D BIPOLAR MANIC-DEPRESSIVE ILLNESS AND THE FRAGILE-X SYNDROME | 0 | 1 |
| 1065 | 5 | 17 | 1087 1993 BIOLOGICAL PSYCHIATRY 33(3):213-216 JEFFRIES FM; REISS AL; BROWN WT; MEYERS DA; GLICKSMAN AC; et al. BIPOLAR SPECTRUM DISORDER AND FRAGILE-X SYNDROME - A FAMILY STUDY | 4 | 13 |
| 1066 | 0 | 0 | 1088 1993 BIOLOGICAL PSYCHIATRY 33(6A):A161-A161 ABRAMS M; FREUND L; REISS AL MOLECULAR PREDICTORS OF COGNITIVE FUNCTION IN FRAGILE X-SYNDROME | 0 | 0 |
| 1067 | 0 | 0 | 1343 1995 BIOLOGICAL PSYCHIATRY 37(9):629-629 REISS AL FRAGILE-X SYNDROME | 0 | 0 |
| 1068 | 0 | 0 | 2401 2003 BIOLOGICAL PSYCHIATRY 53(8):49S-49S Daly EM; Moore CJ; Schmitz N; Morris R; Murphy KC; et al. Expansion of CGG trinucleotide repeats: Effect on neuropsychology of male premutation carriers of Fragile X syndrome | 0 | 0 |
| 1069 | 0 | 0 | 2402 2003 BIOLOGICAL PSYCHIATRY 53(8):152S-152S Moore CJ; Daly EM; Tassone F; Tysoe C; Schmitz N; et al. The effect of premutation CGG trinucleotide repeat expansion, and %FMRP(+) lymphocytes reduction, on brain anatomy | 0 | 0 |
| 1070 | 0 | 0 | 2500 2004 BIOLOGICAL PSYCHIATRY 55:159S-159S Daly EM; Moore CJ; Simmons A; Tassone F; Tysoe C; et al. A H-1 magnetic resonance spectroscopy study of males with premutation expansion of CGG trinucleoticle repeats | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1071 | 0 | 0 | 1512 1996 BIOLOGICALS 24(3):210-210 Chehab FF; Wall J; Cai SP Lessons derived from the clinical molecular diagnosis of cystic fibrosis, thalassaemia, Fragile X and Huntington's disease | 0 | 0 |
| 1072 | 0 | 1 | 118 1983 BIOLOGY OF THE CELL 48(2-3):A92-A92 LENOARD C; SCHOEVAERT D; SELVA J APPLICATION OF THE AUTOMATIC-ANALYSIS OF METAPHASES TO THE DIAGNOSIS OF THE FRAGILE-X IN MAN | 0 | 0 |
| 1073 | 38 | 53 | 2403 2003 BIOLOGY OF THE CELL 95(3-4):221-228 Schaeffer C; Beaulande M; Ehresmann C; Ehresmann B; Moine H The RNA binding protein FMRP: new connections and missing links | 3 | 8 |
| 1074 | 0 | 0 | 371 1986 BIOPHYSICAL JOURNAL 49(2):A18-A18 STUTZIN A; POLLARD HB SYNEXIN-INDUCED FUSION OF CHROMAFFIN GRANULE GHOSTS (CGG) STUDIED BY A NOVEL FLUORESCENCE ASSAY | 0 | 0 |
| 1075 | 0 | 24 | 1344 1995 BIOPHYSICAL JOURNAL 69(2):553-558 RAMAKRISHNAN B; SUNDARALINGAM M CRYSTAL-STRUCTURE OF THE A-DNA DECAMER D(CCIGGCCM(5)CGG) AT 1.6-ANGSTROM SHOWING THE UNEXPECTED WOBBLE I-CENTER-DOT-M(5)C BASE-PAIR | 0 | 7 |
| 1076 | 0 | 0 | 1513 1996 BIOPHYSICAL JOURNAL 70(2):SU496-SU496 Chen X; Mariappan SVS; Ratliff R; Moyzis RK; Smith SS; et al. The formation and methylation of the ''slippage structures'' in vitro: The molecular basis of the fragile-X syndrome | 0 | 0 |
| 1077 | 0 | 0 | 1724 1998 BIOPHYSICAL JOURNAL 74(2):A333-A333 Sinden RR; Pearson CE; Chastain PD; Potaman VN; Levene SD Unusual helical properties and alternative structures of CTG and CGG repeats. | 0 | 0 |
| 1078 | 0 | 28 | 2129 2001 BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY 65(7):1568-1574 Tani S; Itoh T; Kato M; Kobayashi T; Tsukagoshi N In vivo and in vitro analyses of the AmyR binding site of the Aspergillus nidulans agdA promoter; Requirement of the CGG direct repeat for induction and high affinity binding of AmyR | 0 | 4 |
| 1079 | 0 | 30 | 1345 1995 BIOSPECTROSCOPY 1(4):235-245 CARMONA P; MOLINA M; LASAGABASTER A; ESCOBAR R DETERMINATION OF THE HYDROGEN-BONDED STRUCTURE OF CGG TRIMERS IN CHLOROFORM SOLUTION BY VIBRATIONAL SPECTROSCOPY | 0 | 2 |
| 1080 | 0 | 29 | 632 1989 BLOOD 74(2):828-832 MORLE L; MORLE F; ROUX AF; GODET J; FORGET BG; et al. SPECTRIN TUNIS (SP-ALPHA-I/78), AN ELLIPTOCYTOGENIC VARIANT, IS DUE TO THE CGG -] TGG CODON CHANGE (ARG -] TRP) AT POSITION-35 OF THE ALPHA-I DOMAIN | 0 | 33 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1081 | 0 | 0 | 1877 1999 BLOOD 94(10):94A-94A Warren TL; Dahle CE; Buikema BS; Weiner GJ Immunotherapy of lymphoma using CgG oligodeoxynucleotides. | 0 | 0 |
| 1082 | 23 | 62 | 2404 2003 BMC MOLECULAR BIOLOGY 4 Chandler SP; Kansagra P; Hirst MC Fragile X (CGG)(n) repeats induce a transcriptional repression in cis upon a linked promoter: Evidence for a chromatin mediated effect | 0 | 3 |
| 1083 | 2 | 6 | 1346 1995 BONE MARROW TRANSPLANTATION 16(4):625-626 MORTON J; ARNOLD L; FLETCHER B; MCCARTHY C; ROWELL J; et al. ALLOGENEIC BMT FROM A DONOR WITH FRAGILE-X SYNDROME - CYTOGENETIC AND MOLECULAR EVALUATION | 0 | 0 |
| 1084 | 34 | 53 | 2130 2001 BRAIN 124:1610-1618 Eliez S; Blasey CM; Freund LS; Hastie T; Reiss AL Brain anatomy, gender and IQ in children and adolescents with fragile X syndrome | 9 | 15 |
| 1085 | 28 | 62 | 2501 2004 BRAIN 127:591-601 Kogan CS; Boutet I; Cornish K; Zangenehpour S; Mullen KT; et al. Differential impact of the FMR1 gene on visual processing in fragile X syndrome | 2 | 2 |
| 1086 | 23 | 40 | 2502 2004 BRAIN 127:2672-2681 Moore CJ; Daly EM; Tassone F; Tysoe C; Schmitz N; et al. The effect of pre-mutation of X chromosome CGG trinucleotide repeats on brain anatomy | 0 | 0 |
| 1087 | 1 | 14 | 697 1990 BRAIN & DEVELOPMENT 12(1):128-130 WAHLSTROM J; WITTENGERSTROM I; MELLQUIST L; ANVRET M; ODEN A THE RETT SYNDROME RELATED TO FRAGILE-X(P22) IN CAFFEINE-INDUCED LYMPHOCYTE CULTURE | 0 | 13 |
| 1088 | 26 | 39 | 1347 1995 BRAIN & DEVELOPMENT 17(5):317-321 NANBA E; KOHNO Y; MATSUDA A; YANO M; SATO C; et al. NONRADIOACTIVE DNA DIAGNOSIS FOR THE FRAGILE-X SYNDROME IN MENTALLY-RETARDED JAPANESE MALES | 8 | 17 |
| 1089 | 4 | 5 | 1348 1995 BRAIN & DEVELOPMENT 17(5):322-322 NAKAHORI Y THE INCIDENCE OF THE FRAGILE-X SYNDROME IN JAPANESE - COMMENTARY ON NANBAS PAPER | 0 | 0 |
| 1090 | 4 | 7 | 1349 1995 BRAIN & DEVELOPMENT 17(5):323-323 KONDO I NONRADIOACTIVE DNA DIAGNOSIS FOR THE FRAGILE-X SYNDROME IN JAPANESE MENTALLY-RETARDED MALES - COMMENT | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1091 | 5 | 9 | 2252 2002 BRAIN & DEVELOPMENT 24(8):766-769 Incorpora G; Sorge G; Sorge A; Pavone L Epilepsy in fragile X syndrome | 2 | 3 |
| 1092 | 12 | 21 | 2503 2004 BRAIN & DEVELOPMENT 26(6):380-383 Suwa K; Momoi MY Non-invasive screening of fragile X syndrome A using urine and hair roots | 0 | 0 |
| 1093 | 0 | 0 | 1350 1995 BRAIN AND COGNITION 28(1):111-111 GRIGSBY J; KAYE K VARIABLE EXPRESSION OF DEVELOPMENTAL GERSTMANN SIGNS IN FRAGILE-X SYNDROME | 0 | 0 |
| 1094 | 0 | 0 | 1351 1995 BRAIN AND COGNITION 28(1):111-112 GRIGSBY J; KAYE K DISSOCIATIONS IN DEVELOPMENTAL DYSCALCULIA SECONDARY TO FRAGILE-X SYNDROME | 0 | 0 |
| 1095 | 11 | 52 | 1992 2000 BRAIN AND COGNITION 44(3):387-401 Munir F; Cornish KM; Wilding J Nature of the working memory deficit in Fragile-X syndrome | 8 | 9 |
| 1096 | 3 | 6 | 2504 2004 BRAIN AND COGNITION 54(3):235-239 Cornish K; Swainson R; Cunnington R; Wilding J; Morris P; et al. Do women with fragile X syndrome have problems in switching attention: Preliminary findings from ERP and fMRI | 0 | 0 |
| 1097 | 0 | 0 | 2505 2004 BRAIN AND COGNITION 56(1):121-121 Kogan C; Boutet I; Cornish K; Andermann E; DerKaloustian V; et al. Evidence for a transient channel visual deficit in Fragile X Syndrome | 0 | 0 |
| 1098 | 29 | 49 | 2627 2005 BRAIN AND COGNITION 57(1):53-60 Cornish K; Kogan C; Turk J; Manly T; James N; et al. The emerging fragile X premutation phenotype: Evidence from the domain of social cognition | 0 | 0 |
| 1099 | 4 | 44 | 570 1988 BRAIN AND LANGUAGE 34(2):203-221 VILKMAN E; NIEMI J; IKONEN U FRAGILE-X SPEECH PHONOLOGY IN FINNISH | 5 | 6 |
| 1100 | 14 | 46 | 2253 2002 BRAIN RESEARCH 927(1):8-17 Nielsen DM; Derber WJ; McClellan DA; Crnic LS Alterations in the auditory startle response in Fmr1 targeted mutant mouse models of fragile X syndrome | 11 | 15 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1101 | 13 | 41 | 2405 2003 BRAIN RESEARCH 971(1):83-89 Galvez R; Gopal AR; Greenough WT Somatosensory cortical barrel dendritic abnormalities in a mouse model of the fragile X mental retardation syndrome | 4 | 6 |
| 1102 | 26 | 36 | 2406 2003 BRAIN RESEARCH 972(1-2):9-15 Segal M; Kreher U; Greenberger V; Braun K Is fragile X mental retardation protein involved in activity-induced plasticity of dendritic spines? | 0 | 1 |
| 1103 | 34 | 88 | 2131 2001 BRAIN RESEARCH BULLETIN 56(3-4):367-373 Grabczyk E; Kumari D; Usdin K Fragile X syndrome and Friedreich's ataxia: Two different paradigms for repeat induced transcript insufficiency | 0 | 4 |
| 1104 | 45 | 85 | 2132 2001 BRAIN RESEARCH BULLETIN 56(3-4):375-382 Bardoni B; Schenck A; Mandel JL The Fragile X mental retardation protein | 6 | 9 |
| 1105 | 35 | 62 | 2133 2001 BRAIN RESEARCH BULLETIN 56(3-4):383-387 Chiurazzi P; Neri G Pharmacological reactivation of inactive genes: The fragile X experience | 0 | 1 |
| 1106 | 20 | 38 | 2407 2003 BRAIN TOPOGRAPHY 15(3):165-171 Castren M; Paakkonen A; Tarkka IM; Ryynanen M; Partanen J Augmentation of auditory N1 in children with fragile X syndrome | 2 | 2 |
| 1107 | 27 | 35 | 1640 1997 BRAZILIAN JOURNAL OF GENETICS 20(4):731-739 Mingroni-Netto RC; Pavanello RCM; Otto PA; Vianna-Morgante AM Experience with molecular and cytogenetic diagnosis of fragile X syndrome in Brazilian families | 2 | 2 |
| 1108 | 2 | 14 | 698 1990 BRITISH DENTAL JOURNAL 168(4):160-162 NUNN JH; DURNING P FRAGILE-X (MARTIN BELL) SYNDROME AND DENTAL-CARE | 0 | 0 |
| 1109 | 4 | 9 | 633 1989 BRITISH HEART JOURNAL 61(3):289-291 SREERAM N; WREN C; BHATE M; ROBERTSON P; HUNTER S CARDIAC ABNORMALITIES IN THE FRAGILE X-SYNDROME | 6 | 9 |
| 1110 | 14 | 28 | 1224 1994 BRITISH JOURNAL OF CLINICAL PRACTICE 48(1):42-44 PATEL BD THE FRAGILE-X SYNDROME | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1111 | 0 | 1 | 1514 1996 BRITISH JOURNAL OF DEVELOPMENTAL PSYCHOLOGY 14:247-248 Happe F Behavior and development in fragile X syndrome - Dykens,EM, Hodapp,RM, Leckman,JF | 0 | 0 |
| 1112 | 1 | 8 | 1089 1993 BRITISH JOURNAL OF HAEMATOLOGY 85(2):415-416 VORST EJ; LEVENE NA; NISANI R; BERREBI A FRAGILE-X SYNDROME AND MYELODYSPLASIA DISCOVERED DURING PREGNANCY | 3 | 5 |
| 1113 | 0 | 12 | 1515 1996 BRITISH JOURNAL OF HAEMATOLOGY 93(4):841-844 Arjona SN; EloyGarcia J; Gu LH; Smetanina NS; Huisman THJ The dominant beta-thalassaemia in a Spanish family is due to a frameshift that introduces an extra CGG codon (=arginine) at the 5' end of the second exon | 0 | 5 |
| 1114 | 6 | 13 | 699 1990 BRITISH JOURNAL OF HOSPITAL MEDICINE 43(1):17-17 BUNDEY S FRAGILE-X SYNDROME | 1 | 1 |
| 1115 | 11 | 14 | 1993 2000 BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY 107(8):969-972 Kallinen J; Korhonen K; Kortelainen S; Heinonen S; Ryynanen M Pregnancy outcome in carriers of fragile X | 0 | 0 |
| 1116 | 2 | 11 | 119 1983 BRITISH JOURNAL OF PSYCHIATRY 143(SEP):256-260 GILLBERG C IDENTICAL TRIPLETS WITH INFANTILE-AUTISM AND THE FRAGILE-X SYNDROME | 20 | 38 |
| 1117 | 3 | 11 | 372 1986 BRITISH JOURNAL OF PSYCHIATRY 148:655-657 PRIMROSE DA; ELMATMATI R; BOYD E; GOSDEN C; NEWTON M PREVALENCE OF THE FRAGILE-X SYNDROME IN AN INSTITUTION FOR THE MENTALLY-HANDICAPPED | 16 | 22 |
| 1118 | 2 | 4 | 434 1987 BRITISH JOURNAL OF PSYCHIATRY 150:700-702 DEB S; COWIE VA; TIMBERLAKE C A CASE OF MOSAICISM WITH FRAGILE-X AND FRAGILE-XXY COMPONENTS | 5 | 5 |
| 1119 | 83 | 119 | 974 1992 BRITISH JOURNAL OF PSYCHIATRY 160:24-35 TURK J THE FRAGILE-X SYNDROME - ON THE WAY TO A BEHAVIORAL-PHENOTYPE | 25 | 46 |
| 1120 | 0 | 1 | 1352 1995 BRITISH JOURNAL OF PSYCHIATRY 166:688-688 COOKE LB BEHAVIOR AND DEVELOPMENT IN FRAGILE-X SYNDROME - DYKENS,E | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1121 | 17 | 31 | 435 1987 BRITISH MEDICAL JOURNAL 295(6598):564-565 KINNELL HG FRAGILE X-SYNDROME - AN IMPORTANT PREVENTABLE CAUSE OF MENTAL HANDICAP | 2 | 2 |
| 1122 | 1 | 4 | 436 1987 BRITISH MEDICAL JOURNAL 295(6603):922-922 MCKINLEY MJ; NICOLAIDES KH; KEARNEY LU; HERON O FRAGILE-X SYNDROME | 1 | 3 |
| 1123 | 1 | 2 | 844 1991 BRITISH MEDICAL JOURNAL 302(6789):1359-1359 CHARATAN F GENE FOR FRAGILE-X SYNDROME DISCOVERED | 0 | 0 |
| 1124 | 5 | 11 | 975 1992 BRITISH MEDICAL JOURNAL 305(6847):208-208 MOORE DWY NEW DEVELOPMENTS IN THE FRAGILE-X SYNDROME | 1 | 1 |
| 1125 | 0 | 1 | 1353 1995 BRITISH MEDICAL JOURNAL 310(6973):148-148 CRAFT N STUDY SUPPORTS SCREENING FOR THE FRAGILE-X-SYNDROME | 2 | 3 |
| 1126 | 0 | 0 | 1641 1997 BRITISH MEDICAL JOURNAL 315(7102):208-208 White C Screening for fragile X is cost effective and accurate | 0 | 0 |
| 1127 | 4 | 11 | 1642 1997 BRITISH MEDICAL JOURNAL 315(7117):1174-1175 Barnicoat A Screening for fragile X syndrome: a model for genetic disorders? | 1 | 4 |
| 1128 | 8 | 10 | 1643 1997 BRITISH MEDICAL JOURNAL 315(7117):1223-1226 Turner G; Robinson H; Wake S; Laing S; Partington M Case finding for the fragile X syndrome and its consequences | 5 | 9 |
| 1129 | 0 | 0 | 14 1981 BULLETIN DE L ACADEMIE NATIONALE DE MEDECINE 165(9):1197-1206 LEJEUNE J MONOCARBONS METABOLISM AND FRAGILE-X SYNDROME | 22 | 30 |
| 1130 | 2 | 6 | 373 1986 BULLETIN OF EXPERIMENTAL BIOLOGY AND MEDICINE 102(12):1742-1745 ZAKHAROV AF; BEDELBAEVA KA; BARANOVSKAYA LI VARIABILITY OF FRAGILE X-CHROMOSOME EXPRESSION IN CONSECUTIVE CELL GENERATIONS | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1131 | 0 | 0 | 1225 1994 CANADIAN FAMILY PHYSICIAN 40:290-295 WIEBE E; WIEBE A FRAGILE-X SYNDROME | 0 | 1 |
| 1132 | 0 | 0 | 15 1981 CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES 8(2):191-191 SERGOVICH F; POZSONYI J; HINTON G RECENT ADVANCES IN MENTAL-RETARDATION THE FRAGILE X-CHROMOSOME | 1 | 0 |
| 1133 | 0 | 32 | 55 1982 CANADIAN MEDICAL ASSOCIATION JOURNAL 127(2):123-126 LARBRISSEAU A; JEAN P; MESSIER B; RICHER CL FRAGILE X-CHROMOSOME AND X-LINKED MENTAL-RETARDATION | 6 | 9 |
| 1134 | 0 | 3 | 260 1985 CANADIAN MEDICAL ASSOCIATION JOURNAL 133(5):358-& SOUDEK D FRAGILE-X - A SYMPTOM OF THE DISEASE | 2 | 4 |
| 1135 | 5 | 31 | 571 1988 CANCER 62(11):2383-2386 CUNNINGHAM M; DICKERMAN JD FRAGILE-X SYNDROME AND ACUTE LYMPHOBLASTIC-LEUKEMIA | 3 | 3 |
| 1136 | 1 | 16 | 1226 1994 CANCER RESEARCH 54(19):5212-5216 LEE ST; MCGLENNEN RC; LITZ CE CLONAL DETERMINATION BY THE FRAGILE-X (FMR1) AND PHOSPHOGLYCERATE KINASE (PGK) GENES IN HEMATOLOGICAL MALIGNANCIES | 1 | 12 |
| 1137 | 9 | 34 | 845 1991 CELL 64(4):861-866 BELL MV; HIRST MC; NAKAHORI Y; MACKINNON RN; ROCHE A; et al. PHYSICAL MAPPING ACROSS THE FRAGILE-X - HYPERMETHYLATION AND CLINICAL EXPRESSION OF THE FRAGILE-X SYNDROME | 127 | 224 |
| 1138 | 11 | 40 | 846 1991 CELL 65(5):905-914 VERKERK AJMH; PIERETTI M; SUTCLIFFE JS; FU YH; KUHL DPA; et al. IDENTIFICATION OF A GENE (FMR-1) CONTAINING A CGG REPEAT COINCIDENT WITH A BREAKPOINT CLUSTER REGION EXHIBITING LENGTH VARIATION IN FRAGILE-X SYNDROME | 576 | 1282 |
| 1139 | 10 | 15 | 847 1991 CELL 66(4):817-822 PIERETTI M; ZHANG FP; FU YH; WARREN ST; OOSTRA BA; et al. ABSENCE OF EXPRESSION OF THE FMR-1 GENE IN FRAGILE-X SYNDROME | 333 | 598 |
| 1140 | 12 | 23 | 848 1991 CELL 67(6):1047-1058 FU YH; KUHL DPA; PIZZUTI A; PIERETTI M; SUTCLIFFE JS; et al. VARIATION OF THE CGG REPEAT AT THE FRAGILE-X SITE RESULTS IN GENETIC INSTABILITY - RESOLUTION OF THE SHERMAN PARADOX | 432 | 957 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1141 | 18 | 52 | 1090 1993 CELL 73(7):1403-1409 HANSEN RS; CANFIELD TK; LAMB MM; GARTLER SM; LAIRD CD ASSOCIATION OF FRAGILE-X SYNDROME WITH DELAYED REPLICATION OF THE FMR1 GENE | 28 | 127 |
| 1142 | 15 | 56 | 1091 1993 CELL 74(2):291-298 SIOMI H; SIOMI MC; NUSSBAUM RL; DREYFUSS G THE PROTEIN PRODUCT OF THE FRAGILE-X GENE, FMR1, HAS CHARACTERISTICS OF AN RNA-BINDING PROTEIN | 141 | 334 |
| 1143 | 16 | 39 | 1227 1994 CELL 77(1):33-39 SIOMI H; CHOI MY; SIOMI MC; NUSSBAUM RL; DREYFUSS G ESSENTIAL ROLE FOR KH DOMAINS IN RNA-BINDING - IMPAIRED RNA-BINDING BY A MUTATION IN THE KH DOMAIN OF FMR1 THAT CAUSES FRAGILE-X SYNDROME | 74 | 266 |
| 1144 | 21 | 53 | 1228 1994 CELL 77(6):853-861 KUNST CB; WARREN ST CRYPTIC AND POLAR VARIATION OF THE FRAGILE-X REPEAT COULD RESULT IN PREDISPOSING NORMAL ALLELES | 101 | 244 |
| 1145 | 23 | 52 | 1229 1994 CELL 78(1):23-33 BAKKER CE; VERHEIJ C; WILLEMSEN R; VANDERHELM R; OERLEMANS F; et al. FMR1 KNOCKOUT MICE - A MODEL TO STUDY FRAGILE-X MENTAL-RETARDATION | 96 | 163 |
| 1146 | 9 | 43 | 1516 1996 CELL 85(2):237-245 Musco G; Stier G; Joseph C; Morelli MAC; Nilges M; et al. Three-dimensional structure and stability of the KH domain: Molecular insights into the fragile X syndrome | 22 | 178 |
| 1147 | 11 | 59 | 1994 2000 CELL 100(3):323-332 Lewis HA; Musunuru K; Jensen KB; Edo C; Chen H; et al. Sequence-specific RNA binding by a Nova KH domain: Implications for paraneoplastic disease and the fragile X syndrome | 9 | 97 |
| 1148 | 25 | 47 | 2134 2001 CELL 107(4):477-487 Brown V; Jin P; Ceman S; Darnell JC; O'Donnell WT; et al. Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome | 80 | 162 |
| 1149 | 17 | 85 | 2135 2001 CELL 107(4):489-499 Darnell JC; Jensen KB; Jin P; Brown V; Warren ST; et al. Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function | 74 | 149 |
| 1150 | 16 | 17 | 2136 2001 CELL 107(5):555-557 Kaytor MD; Orr HT RNA targets of the fragile X protein | 6 | 15 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1151 | 20 | 37 | 2137 2001 CELL 107(5):591-603 Zhang YQ; Bailey AM; Matthies HJG; Renden RB; Smith MA; et al. Drosophila fragile X-related gene regulates the MAP1B homolog Futsch to control synaptic structure and function | 57 | 98 |
| 1152 | 36 | 62 | 2408 2003 CELL 112(3):317-327 Zalfa F; Giorgi M; Primerano B; Moro A; Di Penta A; et al. The fragile X syndrome protein FMRP associates with BC1 RNA and regulates the translation of specific mRNAs at Synapses | 37 | 69 |
| 1153 | 7 | 21 | 2254 2002 CELLULAR & MOLECULAR BIOLOGY LETTERS 7(3):877-883 Denman RB Methylation of the arginine-glycine-rich region in the fragile X mental retardation protein FMRP differentially affects RNA binding | 2 | 6 |
| 1154 | 60 | 135 | 2506 2004 CELLULAR AND MOLECULAR LIFE SCIENCES 61(14):1714-1728 Denman RB; Dolzhanskaya N; Sung YJ Regulating a translational regulator: mechanisms cells use to control the activity of the fragile X mental retardation protein | 1 | 2 |
| 1155 | 17 | 20 | 2628 2005 CELLULAR AND MOLECULAR LIFE SCIENCES 62(2):251-252 Zalfa F; Bagni C Another view of the role of FMRP in translational regulation | 0 | 0 |
| 1156 | 23 | 34 | 2138 2001 CELLULAR AND MOLECULAR NEUROBIOLOGY 21(1):29-38 Castren M; Haapasalo A; Oostra BA; Castren E Subcellular localization of fragile X mental retardation protein with the I304N mutation in the RNA-binding domain in cultured hippocampal neurons | 3 | 3 |
| 1157 | 24 | 79 | 1995 2000 CEREBRAL CORTEX 10(10):1038-1044 Irwin SA; Galvez R; Greenough WT Dendritic spine structural anomalies in fragile-X mental retardation syndrome | 35 | 55 |
| 1158 | 23 | 38 | 1996 2000 CEREBRAL CORTEX 10(10):1045-1052 Braun K; Segal M FMRP involvement in formation of synapses among cultured hippocampal neurons | 21 | 23 |
| 1159 | 64 | 95 | 1517 1996 CHILD AND ADOLESCENT PSYCHIATRIC CLINICS OF NORTH AMERICA 5(4):895-& Hagerman RJ Fragile X syndrome | 1 | 9 |
| 1160 | 16 | 37 | 374 1986 CHILD STUDY JOURNAL 16(4):285-296 BURD L; KERBESHIAN J FRAGILE X-SYNDROME - DEVELOPMENTAL ASPECTS | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1161 | 1 | 6 | 193 1984 CHINESE MEDICAL JOURNAL 97(11):861-864 XU BZ; REN S; XIAO GF; ZHOU XT A FRAGILE X SYNDROME FAMILY | 0 | 1 |
| 1162 | 1 | 3 | 1518 1996 CHINESE SCIENCE BULLETIN 41(5):436-437 Huang T; Shen Y; Fan Y; Wu GY Expression of two alternative splicing isoforms of fragile X gene in human placenta | 0 | 0 |
| 1163 | 4 | 18 | 1997 2000 CHINESE SCIENCE BULLETIN 45(6):516-520 Chen YT; Bardoni B; Yu M; Zhu N; Wu GY; et al. Fragile X mental retardation protein interacts with TDG | 0 | 0 |
| 1164 | 2 | 19 | 572 1988 CHROMOSOMA 96(5):391-396 SAVAGE JRK; FITCHETT M THE BEHAVIOR OF FRAGILE-X AND OTHER ABERRATIONS DURING RECOVERY FROM LOW FOLATE CONDITIONS | 0 | 3 |
| 1165 | 2 | 29 | 573 1988 CHROMOSOMA 97(1):6-10 KEREM B; GOITEIN R; SCHAAP T CYTOLOGICAL EVIDENCE OF DEFECTIVE TEMPLATE IN THE FRAGILE X-CHROMOSOME | 2 | 5 |
| 1166 | 33 | 48 | 976 1992 CHROMOSOMA 101(7):381-387 OOSTRA BA; VERKERK AJMH THE FRAGILE X-SYNDROME - ISOLATION OF THE FMR-1 GENE AND CHARACTERIZATION OF THE FRAGILE-X MUTATION | 12 | 26 |
| 1167 | 0 | 0 | 1519 1996 CIRCULATION 94(8):534-534 Helbecque N; Dallongeville J; Arveiler D; Cambou JP; Evans A; et al. Relationship between VLDL receptor gene (CGG) repeat polymorphism and plasma apo E containing lipoparticles levels in a sample of European Caucasian men | 0 | 0 |
| 1168 | 0 | 0 | 261 1985 CLINICAL CHEMISTRY 31(6):1008-1009 THIBODEAU SN; FAULK KR; SMITH AC; BERRY R; HAGERMAN R THE USE OF RECOMBINANT DNA TECHNIQUES TO DOCUMENT THE TRANSMISSION OF FRAGILE-X SYNDROME THROUGH AN UNAFFECTED MALE CARRIER | 0 | 0 |
| 1169 | 0 | 0 | 375 1986 CLINICAL CHEMISTRY 32(6):1215-1215 THIBODEAU SN THE USE OF RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISMS (RFLP) TO DETERMINE THE CARRIER STATUS OF FRAGILE-X-SYNDROME | 0 | 0 |
| 1170 | 10 | 29 | 437 1987 CLINICAL CHEMISTRY 33(10):1726-1730 THIBODEAU SN USE OF RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM ANALYSIS FOR DETECTING CARRIERS OF FRAGILE-X SYNDROME | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1171 | 0 | 0 | 1354 1995 CLINICAL CHEMISTRY 41(11):30-30 RADU DN; CHIANG CS RAPID, NONRADIOACTIVE SOUTHERN BLOT METHOD FOR DETECTING FRAGILE-X MUTATIONS | 0 | 0 |
| 1172 | 0 | 0 | 1520 1996 CLINICAL CHEMISTRY 42(6):441-441 Tsongalis GJ; Hodges KA; Adkins S; Silverman LM Chemiluminescent detection of the CGG trinucleotide repeat expansion in fragile X syndrome. | 0 | 0 |
| 1173 | 0 | 0 | 1521 1996 CLINICAL CHEMISTRY 42(11):7-7 Hamdan H; Bailey A; Martinez JJ; Fenwick R; Leon JA Improved amplification and automated detection of trinucleotide repeats in the diagnosis of fragile X syndrome. | 0 | 0 |
| 1174 | 0 | 0 | 1998 2000 CLINICAL CHEMISTRY 46(6):A206-A206 Boday A; Prusa R; Matoska V Radioactive PCR for the screening and diagnostics of fragile X chromosome syndrome - FRAXA. | 0 | 0 |
| 1175 | 15 | 21 | 1725 1998 CLINICAL CHEMISTRY AND LABORATORY MEDICINE 36(8):649-653 Poon PMK; Chen QL; Lai KYC; Wong CK; Pang CP CGG repeat interruptions in the FMR1 gene in patients with infantile autism | 0 | 2 |
| 1176 | 15 | 19 | 1878 1999 CLINICAL CHEMISTRY AND LABORATORY MEDICINE 37(4):397-401 Houdayer C; Lemonnier A; Gerard M; Chauve C; Tredano M; et al. Improved fluorescent PCR-based assay for sizing CGG repeats at the FRAXA locus | 1 | 6 |
| 1177 | 7 | 12 | 1999 2000 CLINICAL CHEMISTRY AND LABORATORY MEDICINE 38(9):935-938 Poon PMK; Zhao Z; Wu XQ; Ni YX; Pang CP Rapid analysis of CGG repeat length in the FMR1 gene | 0 | 0 |
| 1178 | 0 | 18 | 376 1986 CLINICAL ENDOCRINOLOGY 24(3):327-333 OHARE JP; OBRIEN IAD; ARENDT J; ASTLEY P; RATCLIFFE W; et al. DOES MELATONIN DEFICIENCY CAUSE THE ENLARGED GENITALIA OF THE FRAGILE-X SYNDROME | 9 | 11 |
| 1179 | 0 | 19 | 16 1981 CLINICAL GENETICS 19(2):101-110 GUSTAVSON KH; HOLMGREN G; BLOMQUIST HK; MIKKELSEN M; NORDENSON I; et al. FAMILIAL X-LINKED MENTAL-RETARDATION AND FRAGILE X-CHROMOSOMES IN 2 SWEDISH FAMILIES | 28 | 42 |
| 1180 | 0 | 2 | 17 1981 CLINICAL GENETICS 19(2):140-141 SOUDEK D; GORZNY N NO FRAGILE X-CHROMOSOME IN NORMAL MEN | 1 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1181 | 0 | 0 | 18 1981 CLINICAL GENETICS 19(6):493-493 NIELSEN KB; TOMMERUP N; POULSEN H; MIKKELSEN M DANISH FAMILIES WITH X-LINKED MENTAL-RETARDATION AND FRAGILE X-CHROMOSOME | 1 | 1 |
| 1182 | 2 | 4 | 19 1981 CLINICAL GENETICS 20(1):78-78 HOWARDPEEBLES PN FRAGILE-X CHROMOSOME IN NORMAL MALES | 4 | 7 |
| 1183 | 0 | 0 | 120 1983 CLINICAL GENETICS 23(3):216-216 MCDERMOTT A MORE ON THE FRAGILE-X, WITH PARTICULAR REFERENCE TO FIBROBLAST AND AMNIOTIC-FLUID CULTURE, AND X-INACTIVATION | 0 | 0 |
| 1184 | 1 | 1 | 121 1983 CLINICAL GENETICS 23(3):229-229 FONATSCH C FRAGILE X-CHROMOSOME IN FIBROBLASTS - LONGITUDINAL-STUDY ON TECHNICAL VARIATIONS | 3 | 3 |
| 1185 | 0 | 0 | 122 1983 CLINICAL GENETICS 23(3):232-232 VANDERHAGEN CB; ORSTAVIK KH; BAKKE J; BERG K MONOZYGOUS MALE TRIPLETS WITH MENTAL-RETARDATION AND A FRAGILE X-CHROMOSOME | 2 | 2 |
| 1186 | 0 | 0 | 123 1983 CLINICAL GENETICS 23(3):236-236 PAJARES IL; DELICADO A; GALLEGO A; CASTROVIEJO IP FAMILIAL X-LINKED MENTAL-RETARDATION AND FRAGILE X-CHROMOSOMES IN 6 SPANISH FAMILIES | 1 | 1 |
| 1187 | 0 | 0 | 124 1983 CLINICAL GENETICS 23(3):241-241 NIELSEN KB; TOMMERUP N; MIKKELSEN M CLINICAL AND CYTOGENETIC FINDINGS IN 26 MENTALLY-RETARDED MALES WITH THE FRAGILE-X | 1 | 1 |
| 1188 | 0 | 0 | 125 1983 CLINICAL GENETICS 23(3):250-251 TEJADA I; NICOLAS H; CHERUY C; BOUE J STUDY OF A LARGE SIBSHIP WITH MENTALLY-RETARDED MALES AND FEMALES CARRYING FRAGILE-X | 1 | 1 |
| 1189 | 0 | 0 | 126 1983 CLINICAL GENETICS 23(3):254-254 VEENEMA H; GERAEDTS JPM THE FRAGILE-X CHROMOSOME SEGREGATING IN A LARGE PEDIGREE | 2 | 2 |
| 1190 | 0 | 0 | 127 1983 CLINICAL GENETICS 23(3):255-255 VERSCHRAEGENSPAE MR; VANDENBOSSCHE H; MATTON MT APPROACH TO RELATIVES IN FRAGILE X-LINKED MENTAL-RETARDATION | 0 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1191 | 5 | 14 | 128 1983 CLINICAL GENETICS 23(4):311-317 GARDNER RJM; SMART RD; CORNELL JM; MERCKEL LM; BEIGHTON P THE FRAGILE X-CHROMOSOME IN A LARGE INDIAN KINDRED | 17 | 20 |
| 1192 | 8 | 23 | 129 1983 CLINICAL GENETICS 23(6):436-440 SILVERMAN W; LUBIN R; JENKINS EC; BROWN WT THE STRENGTH OF ASSOCIATION BETWEEN FRAGILE(X) CHROMOSOME PRESENCE AND MENTAL-RETARDATION | 8 | 11 |
| 1193 | 3 | 11 | 130 1983 CLINICAL GENETICS 24(3):153-155 NIELSEN KB; TOMMERUP N; FRIIS B; HJELT K; HIPPE E FOLIC-ACID METABOLISM IN A PATIENT WITH FRAGILE-X | 0 | 9 |
| 1194 | 1 | 4 | 131 1983 CLINICAL GENETICS 24(5):320-323 DEARCE MA TABLES FOR THE CYTOGENETIC STUDY OF FRAGILE X-CHROMOSOMES FOR DIAGNOSTIC PURPOSES | 11 | 17 |
| 1195 | 3 | 15 | 132 1983 CLINICAL GENETICS 24(6):393-398 BLOMQUIST HK; GUSTAVSON KH; HOLMGREN G; NORDENSON I; PALSSONSTRAE U FRAGILE X-SYNDROME IN MILDLY MENTALLY-RETARDED CHILDREN IN A NORTHERN SWEDISH COUNTY - A PREVALENCE STUDY | 43 | 68 |
| 1196 | 0 | 3 | 194 1984 CLINICAL GENETICS 25(2):131-134 FRYNS JP; JACOBS J; KLECZKOWSKA A; VANDENBERGHE H THE PSYCHOLOGICAL PROFILE OF THE FRAGILE X-SYNDROME | 57 | 75 |
| 1197 | 1 | 9 | 195 1984 CLINICAL GENETICS 25(2):135-139 GARDINER GB; WENGER SL; STEELE MW INVITRO REVERSAL OF FRAGILE-X EXPRESSION BY EXOGENOUS THYMIDINE | 5 | 7 |
| 1198 | 2 | 11 | 196 1984 CLINICAL GENETICS 26(5):445-447 FRYNS JP; KLECZKOWSKA A; WOLFS I; VANDENBERGHE H KLINEFELTER SYNDROME AND 2 FRAGILE X-CHROMOSOMES | 15 | 21 |
| 1199 | 21 | 64 | 197 1984 CLINICAL GENETICS 26(6):497-528 FRYNS JP THE FRAGILE X-SYNDROME - A STUDY OF 83 FAMILIES | 45 | 78 |
| 1200 | 7 | 27 | 262 1985 CLINICAL GENETICS 27(2):113-117 BLOMQUIST HK; BOHMAN M; EDVINSSON SO; GILLBERG C; GUSTAVSON KH; et al. FREQUENCY OF THE FRAGILE X-SYNDROME IN INFANTILE-AUTISM - A SWEDISH MULTICENTER STUDY | 51 | 85 |