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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by NCR.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 701 | 13 | 28 | 1663 1998 HUMAN MOLECULAR GENETICS 7(1):109-113 Chiurazzi P; Pomponi MG; Willemsen R; Oostra BA; Neri G In vitro reactivation of the FMR1 gene involved in fragile X syndrome | 21 | 47 |
| 702 | 17 | 28 | 1673 1998 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 28(6):499-508 Bailey DB; Mesibov GB; Hatton DD; Clark RD; Roberts JE; Mayhew L Autistic behavior in young boys with fragile X syndrome | 29 | 36 |
| 703 | 4 | 28 | 1731 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):298-301 Kotilainen J; Pirinen S Dental maturity is advanced in fragile X syndrome | 2 | 2 |
| 704 | 18 | 28 | 1811 1999 JOURNAL OF MEDICAL SCREENING 6(2):70-76 Wildhagen MF; van Os TAM; Polder JJ; ten Kate LP; Habbema JDF Efficacy of cascade testing for fragile X syndrome | 3 | 5 |
| 705 | 9 | 28 | 1825 2000 AMERICAN JOURNAL OF HUMAN GENETICS 66(2):413-418 Hundscheid RDL; Sistermans EA; Thomas CMG; Braat DDM; Straatman H; Kiemeney LALM; Oostra BA; Smits APT Imprinting effect in premature ovarian failure confined to paternally inherited fragile X premutations | 14 | 29 |
| 706 | 8 | 28 | 2028 2001 JOURNAL OF BIOLOGICAL CHEMISTRY 276(6):4357-4364 Kumari D; Usdin K Interaction of the transcription factors USF1, USF2, and alpha-Pal/Nrf-1 with the FMR1 promoter - Implications for Fragile X mental retardation syndrome | 12 | 20 |
| 707 | 16 | 28 | 2077 2002 ACTA PAEDIATRICA 91(5):535-539 Hecimovic S; Tarnik IP; Baric I; Cakarun Z; Pavelic K Screening for fragile X syndrome: results from a school for mentally retarded children | 0 | 0 |
| 708 | 12 | 28 | 2099 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 111(2):140-146 Irwin SA; Idupulapati M; Gilbert ME; Harris JB; Chakravarti AB; Rogers EJ; Crisostomo RA; Larsen BP; Mehta A; Alcantara CJ; Patel B; Swain RA; Weiler IJ; Oostra BA; Greenough WT Dendritic spine and dendritic field characteristics of layer V pyramidal neurons in the visual cortex of fragile-X knockout mice | 7 | 10 |
| 709 | 15 | 28 | 2225 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 117A(1):21-29 Glaser B; Hessl D; Dyer-Friedman J; Johnston C; Wisbeck J; Taylor A; Reiss A Biological and environmental contributions to adaptive behavior in fragile X syndrome | 0 | 4 |
| 710 | 20 | 28 | 2290 2003 JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION 102(1):12-16 Chi J; Chen DJ; Lin CN; Chiu CY; Huang CB; Chiu PC; Lin CH; Lin SJ; Tzeng CC 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 |
| 711 | 7 | 27 | 259 1985 CLINICAL GENETICS 27(2):113-117 BLOMQUIST HK; BOHMAN M; EDVINSSON SO; GILLBERG C; GUSTAVSON KH; HOLMGREN G; WAHLSTROM J FREQUENCY OF THE FRAGILE X-SYNDROME IN INFANTILE-AUTISM - A SWEDISH MULTICENTER STUDY | 50 | 84 |
| 712 | 4 | 27 | 323 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):195-206 HANSON DM; JACKSON AW; HAGERMAN RJ SPEECH DISTURBANCES (CLUTTERING) IN MILDLY IMPAIRED MALES WITH THE MARTIN-BELL FRAGILE-X SYNDROME | 39 | 45 |
| 713 | 9 | 27 | 328 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):273-289 FROSTERISKENIUS U; BODEKER K; OEPEN T; MATTHES R; PIPER U; SCHWINGER E FOLIC-ACID TREATMENT IN MALES AND FEMALES WITH FRAGILE-(X)- SYNDROME | 10 | 15 |
| 714 | 9 | 27 | 446 1987 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 29(6):711-719 THAKE A; TODD J; WEBB T; BUNDEY S CHILDREN WITH THE FRAGILE X-CHROMOSOME AT SCHOOLS FOR THE MILDLY MENTALLY-RETARDED | 11 | 15 |
| 715 | 8 | 27 | 457 1987 HUMAN GENETICS 77(1):60-65 OBERLE I; CAMERINO G; WROGEMANN K; ARVEILER B; HANAUER A; RAIMONDI E; MANDEL JL MULTIPOINT GENETIC-MAPPING OF THE XQ26-Q28 REGION IN FAMILIES WITH FRAGILE-X MENTAL-RETARDATION AND IN NORMAL-FAMILIES REVEALS TIGHT LINKAGE OF MARKERS IN Q26-Q27 | 17 | 60 |
| 716 | 13 | 27 | 519 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):191-200 KEMPER MB; HAGERMAN RJ; ALTSHULSTARK D COGNITIVE PROFILES OF BOYS WITH THE FRAGILE-X SYNDROME | 55 | 73 |
| 717 | 14 | 27 | 538 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):531-542 SCHWARTZ CE; PHELAN MC; BRIGHTHARP C; PANCOAST I; HOWARDPEEBLES PN; THIBODEAU S; BROWN WT; JENKINS EC FRAGILE-X SYNDROME - LINKAGE ANALYSIS IN BLACK AND WHITE-POPULATIONS | 4 | 4 |
| 718 | 9 | 27 | 651 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 | 16 | 27 |
| 719 | 13 | 27 | 696 1990 CLINICAL GENETICS 37(5):341-346 BORGHGRAEF M; FRYNS JP; VANDENBERGHE H THE FEMALE AND THE FRAGILE X-SYNDROME - DATA ON CLINICAL AND PSYCHOLOGICAL FINDINGS IN 7 FRA(X) CARRIERS | 16 | 20 |
| 720 | 10 | 27 | 699 1990 EUROPEAN NEUROLOGY 30(1):32-37 RAIMONDI E; LENTI C; ROMAGNONI M; NEGRI R; GAMBINI E; MUSETTI L; DECARLI L FRAGILE-X MENTAL-RETARDATION IN A LARGE 5-GENERATION FAMILY - A CLINICAL AND CYTOGENETIC STUDY | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 721 | 9 | 27 | 907 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):28-34 FISCH GS; SHAPIRO LR; SIMENSEN R; SCHWARTZ CE; FRYNS JP; BORGHGRAEF M; CURFS LM; HOWARDPEEBLES PN; ARINAMI T; MAVROU A LONGITUDINAL CHANGES IN IQ AMONG FRAGILE-X MALES - CLINICAL-EVIDENCE OF MORE THAN ONE MUTATION | 12 | 12 |
| 722 | 20 | 27 | 1022 1993 AMERICAN JOURNAL OF DISEASES OF CHILDREN 147(7):723-726 STALEY LW; HULL CE; MAZZOCCO MMM; THIBODEAU SN; SNOW K; WILSON VL; TAYLOR A; MCGAVRAN L; WEINER D; RIDDLE J; OCONNOR R; HAGERMAN RJ MOLECULAR-CLINICAL CORRELATIONS IN CHILDREN AND ADULTS WITH FRAGILE X-SYNDROME | 21 | 24 |
| 723 | 16 | 27 | 1094 1993 HUMAN GENETICS 92(3):269-272 BUYLE S; REYNIERS E; VITS L; DEBOULLE K; HANDIG I; WUYTS FLE; DEELEN W; HALLEY DJJ; OOSTRA BA; WILLEMS PJ FOUNDER EFFECT IN A BELGIAN-DUTCH FRAGILE-X POPULATION | 19 | 29 |
| 724 | 10 | 27 | 1119 1993 JOURNAL OF MEDICAL GENETICS 30(9):761-766 DEVRIES BBA; FRYNS JP; BUTLER MG; CANZIANI F; WESBYVANSWAAY E; VANHEMEL JO; OOSTRA BA; HALLEY DJJ; NIERMEIJER MF CLINICAL AND MOLECULAR STUDIES IN FRAGILE-X PATIENTS WITH A PRADER-WILLI-LIKE PHENOTYPE | 18 | 33 |
| 725 | 16 | 27 | 1133 1993 NATURE GENETICS 3(1):31-35 DEBOULLE K; VERKERK AJMH; REYNIERS E; VITS L; HENDRICKX J; VANROY B; VANDENBOS F; DEGRAAFF E; OOSTRA BA; WILLEMS PJ A POINT MUTATION IN THE FMR-1 GENE ASSOCIATED WITH FRAGILE-X MENTAL-RETARDATION | 131 | 262 |
| 726 | 11 | 27 | 1147 1993 SOMATIC CELL AND MOLECULAR GENETICS 19(4):393-404 LUO SY; ROBINSON JC; REISS AL; MIGEON BR DNA METHYLATION OF THE FRAGILE-X LOCUS IN SOMATIC AND GERM-CELLS DURING FETAL DEVELOPMENT - RELEVANCE TO THE FRAGILE-X SYNDROME AND X-INACTIVATION | 6 | 19 |
| 727 | 9 | 27 | 1148 1993 TRENDS IN BIOCHEMICAL SCIENCES 18(9):331-333 GIBSON TJ; RICE PM; THOMPSON JD; HERINGA J KH DOMAINS WITHIN THE FMR1 SEQUENCE SUGGEST THAT FRAGILE-X SYNDROME STEMS FROM A DEFECT IN RNA-METABOLISM | 21 | 59 |
| 728 | 16 | 27 | 1233 1994 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 38:27-35 SABARATNAM M; LAVER S; BUTLER L; PEMBREY M FRAGILE-X SYNDROME IN NORTH-EAST ESSEX - TOWARDS SYSTEMATIC SCREENING - CLINICAL-SELECTION | 6 | 8 |
| 729 | 20 | 27 | 1292 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(6):1408-1413 LOESCH DZ; HUGGINS R; PETROVIC V; SLATER H EXPANSION OF THE CGG REPEAT IN FRAGILE-X IN THE FMR1 GENE DEPENDS ON THE SEX OF THE OFFSPRING | 5 | 12 |
| 730 | 16 | 27 | 1372 1995 JOURNAL OF MEDICAL GENETICS 32(3):236-239 MACPHERSON JN; CURTIS G; CROLLA JA; DENNIS N; MIGEON B; GREWAL PK; HIRST MC; DAVIES KE; JACOBS PA UNUSUAL (CGG)(N) EXPANSION AND RECOMBINATION IN A FAMILY WITH FRAGILE-X AND DIGEORGE-SYNDROME | 3 | 11 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 731 | 19 | 27 | 1474 1996 EUROPEAN JOURNAL OF HUMAN GENETICS 4(1):8-12 Malzac P; Biancalana V; Voelckel MA; Moncla A; Pellissier MC; Boccaccio I; Mattei JF Unexpected inheritance of the (CGG)(n) trinucleotide expansion in a fragile X syndrome family | 4 | 6 |
| 732 | 5 | 27 | 1505 1996 NUCLEIC ACIDS RESEARCH 24(4):784-792 Mariappan SVS; Catasti P; Chen X; Ratliff R; Moyzis RK; Bradbury EM; Gupta G Solution structures of the individual single strands of the fragile X DNA triplets (GCC)(n)center dot(GGC)(n) | 10 | 48 |
| 733 | 8 | 27 | 1512 1996 PSYCHIATRY RESEARCH 64(2):97-104 Thompson NM; Rogeness GA; McClure E; Clayton R; Johnson C Influence of depression on cognitive functioning in Fragile X females | 1 | 5 |
| 734 | 13 | 27 | 1525 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):232-238 Turk J Treatments and services for individuals with fragile X syndrome and their families | 0 | 0 |
| 735 | 11 | 27 | 1757 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):300-303 Uzielli MLG; Guarducci S; Lapi E; Cecconi A; Ricci U; Ricotti G; Biondi C; Scarselli B; Vieri F; Scarnato P; Gori F; Sereni A Premature ovarian failure (POF) and fragile X premutation females: From POF to fragile X carrier identification, from fragile X carrier diagnosis to POF association data | 11 | 24 |
| 736 | 11 | 27 | 2015 2001 DIAGNOSTIC MOLECULAR PATHOLOGY 10(1):34-40 Tzeng CC; Lin SJ; Chen YJ; Kuo PL; Jong YJ; Tsai LP; Chen RM An effective strategy of using molecular testing to screen mentally retarded individuals for fragile X syndrome | 1 | 2 |
| 737 | 13 | 27 | 2075 2001 SEIZURE-EUROPEAN JOURNAL OF EPILEPSY 10(1):60-63 Sabaratnam M; Vroegop PG; Gangadharan SK Epilepsy and EEG findings in 18 males with fragile X syndrome | 4 | 5 |
| 738 | 8 | 27 | 2177 2002 NEUROBIOLOGY OF DISEASE 10(3):211-218 D'Agata V; Warren ST; Zhao WQ; Torre ER; Alkon DL; Cavallaro S Gene expression profiles in a transgenic animal model of fragile X syndrome | 0 | 10 |
| 739 | 13 | 27 | 2191 2002 PEDIATRICS 109(1) Flynn BJ; Myers SM; Cera PJ; Mowad JJ Testicular torsion in an adolescent with fragile X syndrome | 0 | 0 |
| 740 | 5 | 26 | 87 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(5):869-878 POPOVICH BW; ROSENBLATT DS; COOPER BA; VEKEMANS M INTRACELLULAR FOLATE DISTRIBUTION IN CULTURED FIBROBLASTS FROM PATIENTS WITH THE FRAGILE-X SYNDROME | 8 | 12 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 741 | 6 | 26 | 136 1983 HUMAN GENETICS 64(3):240-245 NIELSEN KB; TOMMERUP N; POULSEN H; JACOBSEN P; BECK B; MIKKELSEN M CARRIER DETECTION AND X-INACTIVATION STUDIES IN THE FRAGILE-X SYNDROME - CYTOGENETIC STUDIES IN 63 OBLIGATE AND POTENTIAL CARRIERS OF THE FRAGILE-X | 23 | 35 |
| 742 | 6 | 26 | 160 1983 REVISTA MEDICA DE CHILE 111(6):597-600 SANTOS M; MORIZON G THE FRAGILE X SYNDROME - A CHROMOSOMAL DEFECT ASSOCIATED WITH MENTAL-RETARDATION | 0 | 0 |
| 743 | 1 | 26 | 237 1985 AMERICAN JOURNAL OF DANCE THERAPY 8:67-80 WOLFSCHEIN EG; FISCH GS; COHEN IL A STUDY OF THE USE OF NONVERBAL SYSTEMS IN THE DIFFERENTIAL-DIAGNOSIS OF AUTISTIC, MENTALLY-RETARDED AND FRAGILE X-INDIVIDUALS | 0 | 0 |
| 744 | 7 | 26 | 256 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 |
| 745 | 5 | 26 | 319 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):157-169 FRYNS JP THE FEMALE AND THE FRAGILE-X - A STUDY OF 144 OBLIGATE FEMALE CARRIERS | 76 | 101 |
| 746 | 21 | 26 | 331 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):313-324 TOMMERUP N; AULA P; GUSTAVII B; HEIBERG A; HOLMGREN G; VONKOSKULL H; LEISTI J; MIKKELSEN M; MITELMAN F; NIELSEN KB; STEINBACH P; STENGELRUTKOWSKI S; WAHLSTROM J; ZANG K; ZANKL M 2ND TRIMESTER PRENATAL-DIAGNOSIS OF THE FRAGILE-X | 7 | 14 |
| 747 | 12 | 26 | 409 1986 SOUTHERN MEDICAL JOURNAL 79(4):405-409 YOUNG RS; JARAMILLO C; MCCOMBS JL; MOORE CM; JORGENSON RJ FRAGILE-X MENTAL-RETARDATION SYNDROME TRANSMITTED THROUGH INTELLECTUALLY NORMAL MALES - IMPLICATIONS FOR GENETIC-COUNSELING | 3 | 6 |
| 748 | 14 | 26 | 456 1987 HUMAN GENETICS 76(4):344-347 ARINAMI T; KONDO I; NAKAJIMA S; HAMAGUCHI H FREQUENCY OF THE FRAGILE X-SYNDROME IN INSTITUTIONALIZED MENTALLY-RETARDED FEMALES IN JAPAN | 7 | 9 |
| 749 | 11 | 26 | 716 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 | 40 | 59 |
| 750 | 11 | 26 | 941 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):307-311 VAISANEN ML; KAHKONEN M; LEISTI J CARRIER DETECTION OF THE FRAGILE-X SYNDROME WITH FLANKING RFLP MARKERS AND LINKAGE ANALYSIS | 2 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 751 | 19 | 26 | 1018 1992 ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 20(2):113-120 VONGONTARD A; HILLIG U; HEROLD D CLINICAL AND CYTOGENETIC PROBLEMS IN THE DIAGNOSIS OF THE FRAGILE-X SYNDROME | 1 | 1 |
| 752 | 6 | 26 | 1061 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 46(4):415-422 LOESCH DZ; HUGGINS RM; CHIN WF EFFECT OF FRAGILE-X ON PHYSICAL AND INTELLECTUAL TRAITS ESTIMATED BY PEDIGREE ANALYSIS | 7 | 9 |
| 753 | 20 | 26 | 1077 1993 CLINICAL GENETICS 43(1):34-38 HORI T; YAMAUCHI M; SEKI N; TSUJI S; IKUKO K HERITABLE UNSTABLE DNA-SEQUENCES AND HYPERMETHYLATION ASSOCIATED WITH FRAGILE-X SYNDROME IN JAPANESE FAMILIES | 9 | 13 |
| 754 | 7 | 26 | 1106 1993 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 23(1):135-145 DYKENS EM; HODAPP RM; ORT SI; LECKMAN JF TRAJECTORY OF ADAPTIVE-BEHAVIOR IN MALES WITH FRAGILE X-SYNDROME | 27 | 37 |
| 755 | 13 | 26 | 1164 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):364-369 LACHIEWICZ AM; DAWSON DV BEHAVIOR PROBLEMS OF YOUNG GIRLS WITH FRAGILE-X-SYNDROME - FACTOR SCORES ON THE CONNERS PARENTS QUESTIONNAIRE | 11 | 18 |
| 756 | 12 | 26 | 1354 1995 GENETIC EPIDEMIOLOGY 12(3):279-290 HUGGINS RM; LOESCH DZ USE OF ROBUST STATISTICAL-METHODS TO DETERMINE THE EFFECT OF FRAGILE-X ON MEANS AND VARIANCE-COMPONENTS OF A QUANTITATIVE TRAIT | 1 | 2 |
| 757 | 15 | 26 | 1366 1995 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 39:544-553 Butler MG; Pratesi R; VnencakJones CL Molecular genetic analysis of mentally retarded males with features of the fragile-X syndrome | 0 | 1 |
| 758 | 17 | 26 | 1481 1996 HUMAN GENETICS 97(4):512-515 Mornet E; Chateau C; Taillandier A; SimonBouy B; Serre JL Recurrent and unexpected segregation of the FMR1 CGG repeat in a family with fragile X syndrome | 4 | 8 |
| 759 | 15 | 26 | 1482 1996 HUMAN GENETICS 97(6):808-812 Haddad LA; MingroniNetto RC; ViannaMorgante AM; Pena SDJ A PCR-based test suitable for screening for fragile X syndrome among mentally retarded males | 7 | 16 |
| 760 | 18 | 26 | 1575 1997 CLINICAL GENETICS 51(1):1-6 Loesch DZ; Petrovic V; Francis DI; Oertel R; Slater H ''Reduction'' of CGG trinucleotide expansion from mother to offspring in seven fragile-X families | 4 | 7 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 761 | 8 | 26 | 1649 1998 EPIGENETICS 214:280-290 Laird; Pillus; Hirst; Bestor; Jaenisch; Wilkins; Gasser; Wolffe; Francke; Bird; Riggs; Horz Rules of DNA methylation in humans inferred from the fragile X gene, FMR1 - Final general discussion | 0 | 0 |
| 762 | 14 | 26 | 1669 1998 INDIAN JOURNAL OF MEDICAL RESEARCH 108:12-16 Jain U; Verma IC; Kapoor AK Prevalence of fragile X(A) syndrome in mentally retarded children at a genetics referral centre in Delhi, India | 2 | 3 |
| 763 | 13 | 26 | 1726 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):257-263 Fisch GS; Carpenter NJ; Holden JJA; Simensen R; Howard-Peebles PN; Maddalena A; Pandya A; Nance W Longitudinal assessment of adaptive and maladaptive behaviors in fragile X males: Growth, development, and profiles | 7 | 7 |
| 764 | 20 | 26 | 1747 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):204-207 Mingroni-Netto RC; Costa SS; Angeli CB; Vianna-Morgante AM DXS548/FRAXAC1 haplotypes in fragile X chromosomes in the Brazilian population | 0 | 3 |
| 765 | 6 | 26 | 1982 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 98(1):37-45 McConkie-Rosell A; Spiridigliozzi GA; Sullivan JA; Dawson DV; Lachiewicz AM Longitudinal study of the carrier testing process for fragile X syndrome: Perceptions and coping | 2 | 3 |
| 766 | 1 | 26 | 2244 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 |
| 767 | 9 | 26 | 2245 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 | 2 | 3 |
| 768 | 14 | 26 | 2299 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 | 1 |
| 769 | 14 | 26 | 2312 2004 AMERICAN JOURNAL OF HUMAN GENETICS 74(5):1051-1056 Hagerman RJ; Leavitt BR; Farzin F; Jacquemont S; Greco CM; Brunberg JA; Tassone F; Hessl D; Harris SW; Zhang L; Jardini T; Gane LW; Ferranti J; Ruiz L; Leehey MA; Grigsby J; Hagerman PJ Fragile-X-associated tremor/ataxia syndrome (FXTAS) in females with the FMR1 premutation | 1 | 1 |
| 770 | 5 | 25 | 147 1983 JOURNAL OF MEDICAL GENETICS 20(6):404-407 VEKEMANS M; POPOVICH B; ROSENBLATT D; MONROE P CHROMOSOMAL BREAKAGE IN NORMAL AND FRAGILE-X SUBJECTS USING LOW FOLATE CULTURE CONDITIONS | 12 | 21 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 771 | 3 | 25 | 174 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):195-207 SIMPSON NE; NEWMAN BJ; PARTINGTON MW FRAGILE-X SYNDROME .3. DERMATOGLYPHIC STUDIES IN MALES | 10 | 16 |
| 772 | 5 | 25 | 210 1984 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 14(2):197-204 AUGUST GJ; LOCKHART LH FAMILIAL AUTISM AND THE FRAGILE-X-CHROMOSOME | 10 | 21 |
| 773 | 6 | 25 | 300 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 | 19 | 28 |
| 774 | 8 | 25 | 333 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):353-358 MCGILLIVRAY BC; HERBST DS; DILL FJ; SANDERCOCK HJ; TISCHLER B INFANTILE-AUTISM - AN OCCASIONAL MANIFESTATION OF FRAGILE-(X) MENTAL-RETARDATION | 19 | 28 |
| 775 | 11 | 25 | 480 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; BAKER AA FRAGILE-X CHROMOSOME ASSOCIATED WITH PRIMARY LEARNING-DISABILITY | 12 | 15 |
| 776 | 13 | 25 | 801 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):374-377 VOELCKEL MA; PELLISSIER MC; PIQUET C; NGUYEN C; BOCCACCIO I; PHILIP N; MATTEI JF FRAGILE-X SYNDROME IN AN EXTENDED FAMILY WITH SPECIAL REFERENCE TO AN AFFECTED MALE WITH KLINEFELTER SYNDROME | 2 | 2 |
| 777 | 11 | 25 | 804 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):391-395 LAIRD CD POSSIBLE ERASURE OF THE IMPRINT ON A FRAGILE-X CHROMOSOME WHEN TRANSMITTED BY A MALE | 8 | 15 |
| 778 | 10 | 25 | 888 1991 NUCLEIC ACIDS RESEARCH 19(10):2567-2572 DIETRICH A; KIOSCHIS P; MONACO AP; GROSS B; KORN B; WILLIAMS SV; SHEER D; HEITZ D; OBERLE I; TONIOLO D; WARREN ST; LEHRACH H; POUSTKA A MOLECULAR-CLONING AND ANALYSIS OF THE FRAGILE X-REGION IN MAN | 23 | 45 |
| 779 | 9 | 25 | 889 1991 NUCLEIC ACIDS RESEARCH 19(12):3283-3288 HIRST MC; RACK K; NAKAHORI Y; ROCHE A; BELL MV; FLYNN G; CHRISTADOULOU Z; MACKINNON RN; FRANCIS M; LITTLER AJ; ANAND R; POUSTKA AM; LEHRACH H; SCHLESSINGER D; DURSO M; BUCKLE VJ; DAVIES KE A YAC CONTIG ACROSS THE FRAGILE X SITE DEFINES THE REGION OF FRAGILITY | 16 | 42 |
| 780 | 12 | 25 | 928 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):174-180 VONKOSKULL H; NORDSTROM AM; SALONEN R; PELTONEN L PRENATAL-DIAGNOSIS AND CARRIER DETECTION IN FRAGILE-X | 3 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 781 | 14 | 25 | 935 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):237-243 RIGGINS GJ; SHERMAN SL; OOSTRA BA; SUTCLIFFE JS; FEITELL D; NELSON DL; VANOOST BA; SMITS APT; RAMOS FJ; PFENDNER E; KUHL DPA; CASKEY CT; WARREN ST CHARACTERIZATION OF A HIGHLY POLYMORPHIC DINUCLEOTIDE REPEAT 150-KB PROXIMAL TO THE FRAGILE-X SITE | 35 | 57 |
| 782 | 5 | 25 | 953 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 44(5):543-550 LOESCH DZ; HAY DA; SHEFFIELD LJ FRAGILE-X FAMILY WITH UNUSUAL DIGITAL AND FACIAL ABNORMALITIES, CLEFT-LIP AND PALATE, AND EPILEPSY | 8 | 12 |
| 783 | 12 | 25 | 954 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 44(5):676-682 STROM CM; BRUSCA RM; PIZZI WJ DOUBLE-BLIND, PLACEBO-CONTROLLED CROSSOVER STUDY OF FOLINIC ACID (LEUCOVORIN(R)) FOR THE TREATMENT OF FRAGILE-X SYNDROME | 1 | 3 |
| 784 | 6 | 25 | 979 1992 GENOMICS 12(4):818-821 LAVAL SH; BLAIR HJ; HIRST MC; DAVIES KE; BOYD Y MAPPING OF FMR1, THE GENE IMPLICATED IN FRAGILE X-LINKED MENTAL-RETARDATION, ON THE MOUSE X-CHROMOSOME | 0 | 9 |
| 785 | 19 | 25 | 996 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 |
| 786 | 17 | 25 | 1002 1992 MEDICINA CLINICA 98(4):121-124 GINE R; ESPINAS ML; ANTICH J; CARBALLO M MOLECULAR-GENETICS OF THE FRAGILE-X SYNDROME - MOLECULAR DIAGNOSIS BY DNA PROBES | 1 | 1 |
| 787 | 13 | 25 | 1060 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 45(5):589-593 MILUNSKY A; HUANG XL; AMOS JA; HERSKOWITZ J; FARRER LA; WYANDT HE 46,XY/47,XYY MALE WITH THE FRAGILE X-SYNDROME - CYTOGENETIC AND MOLECULAR STUDIES | 3 | 4 |
| 788 | 22 | 25 | 1116 1993 JOURNAL OF MEDICAL GENETICS 30(5):410-413 OOSTRA BA; JACKY PB; BROWN WT; ROUSSEAU F GUIDELINES FOR THE DIAGNOSIS OF FRAGILE-X SYNDROME | 45 | 60 |
| 789 | 3 | 25 | 1135 1993 NATURE GENETICS 3(1):44-48 HANZLIK AJ; OSEMLAKHANZLIK MM; HAUSER MA; KURNIT DM A RECOMBINATION-BASED ASSAY DEMONSTRATES THAT THE FRAGILE-X SEQUENCE IS TRANSCRIBED WIDELY DURING DEVELOPMENT | 9 | 14 |
| 790 | 11 | 25 | 1172 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):405-411 ZHONG N; YE LL; DOBKIN C; BROWN WT FRAGILE-X FOUNDER CHROMOSOME EFFECTS - LINKAGE DISEQUILIBRIUM OR MICROSATELLITE HETEROGENEITY | 17 | 29 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 791 | 10 | 25 | 1335 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):327-335 Roy JC; Johnsen J; Breese K; Hagerman R Fragile X syndrome: What is the impact of diagnosis on families? | 3 | 6 |
| 792 | 15 | 25 | 1446 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):428-433 Meadows KL; Pettay D; Newman J; Hersey J; Ashley AE; Sherman SL Survey of the fragile X syndrome and the fragile X E syndrome in a special education needs population | 9 | 25 |
| 793 | 10 | 25 | 1454 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 |
| 794 | 13 | 25 | 1519 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):195-201 Mandel JL The fragile X mental retardation syndrome: the FMR1 gene and its mutations | 0 | 0 |
| 795 | 21 | 25 | 1557 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 72(4):430-434 Hammond LS; Macias MM; Tarleton JC; Pai GS Fragile X syndrome and deletions in FMR1: New case and review of the literature | 13 | 21 |
| 796 | 9 | 25 | 1699 1998 REVISTA MEDICA DE CHILE 126(12):1447-1454 Aspillaga M; Jara L; Avendano I; Lopez M Fragile X syndrome. Clinical analysis of 300 Chilean patients with unspecific mental retardation | 1 | 1 |
| 797 | 19 | 25 | 1749 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):221-225 Schmucker B; Seidel J Mosaicism for a full mutation and a normal size allele in two fragile X males | 4 | 6 |
| 798 | 9 | 25 | 2011 2001 COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING 4(3):265-272 Murray J; Cuckle H Cystic fibrosis and fragile X syndrome: The arguments for antenatal screening | 1 | 2 |
| 799 | 7 | 25 | 2025 2001 HUMAN REPRODUCTION 16(3):457-462 Hundscheid RDL; Braat DDM; Kiemeney LALM; Smits APT; Thomas CMG Increased serum FSH in female fragile X premutation carriers with either regular menstrual cycles or on oral contraceptives | 6 | 10 |
| 800 | 8 | 25 | 2060 2001 REVISTA DE NEUROLOGIA 33:S20-S23 Mila M; Mallolas J Fragile X syndrome: Premature ovarian failure. Preimplantation and preconception genetic diagnosis | 0 | 0 |
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