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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by first author.
Page 8: 1 (Abbeduto L) 2 (BELGHITI D) 3 (Brown WT) 4 (Chen X) 5 (DAKER MG) 6 (DYKENS E) 7 (FITCHETT M) 8 (GLOVER TW) 9 (HAGERMAN RJ) 10 (HOFFMAN M) 11 (JANCAR J) 12 (KIMCHISARFATY C) 13 (LEE JT) 14 (MAES B) 15 (MIGEON BR) 16 (Myers GF) 17 (Patsalis PC) 18 (REISS AL) 19 (Schenck A) 20 (SMITS APT) 21 (SZABO P) 22 (TURNER G) 23 (Wang YC) 24 (WOHRLE D)
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 701 | 5 | 24 | 315 1986 AMERICAN JOURNAL OF HUMAN GENETICS 38(3):309-318 GLOVER TW; COYLEMORRIS J; PEARCEBIRGE L; BERGER C; GEMMILL RM DNA DEMETHYLATION INDUCED BY 5-AZACYTIDINE DOES NOT AFFECT FRAGILE-X EXPRESSION | 3 | 6 |
| 702 | 11 | 50 | 1489 1996 JOURNAL OF BIOLOGICAL CHEMISTRY 271(40):24325-24328 Godde JS; Kass SU; Hirst MC; Wolffe AP Nucleosome assembly on methylated CGG triplet repeats in the Fragile X Mental Retardation gene 1 promoter | 2 | 38 |
| 703 | 13 | 37 | 1419 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):246-251 Godfraind JM; Reyniers E; DeBoulle K; DHooge R; DeDeyn PP; Bakker CE; Oostra BA; Kooy RF; Willems PJ Long-term potentiation in the hippocampus of fragile X knockout mice | 22 | 31 |
| 704 | 26 | 43 | 1950 2000 MOLECULAR DIAGNOSIS 5(3):169-178 Gold B; Radu D; Balanko A; Chiang CS Diagnosis of Fragile X syndrome by Southern blot hybridization using a chemiluminescent probe: A laboratory protocol | 0 | 1 |
| 705 | 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 |
| 706 | 4 | 10 | 252 1985 AMERICAN JOURNAL OF PSYCHIATRY 142(1):108-110 GOLDFINE PE; MCPHERSON PM; HEATH GA; HARDESTY VA; BEAUREGARD LJ; GORDON B ASSOCIATION OF FRAGILE-X SYNDROME WITH AUTISM | 35 | 52 |
| 707 | 4 | 10 | 1630 1997 SOUTH AFRICAN MEDICAL JOURNAL 87(4):418-420 Goldman A; Krause A; Jenkins T Fragile X syndrome occurs in the South African black population | 2 | 4 |
| 708 | 3 | 19 | 2063 2001 REVISTA DE NEUROLOGIA 33:S32-S36 Goldson E Sensory integration and fragile X syndrome | 0 | 0 |
| 709 | 0 | 0 | 844 1991 CLINICAL RESEARCH 39(1):A1-A1 GOLDSON E; HAGERMAN RJ TEMPERAMENT AND THE FRAGILE-X SYNDROME | 2 | 2 |
| 710 | 23 | 48 | 973 1992 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 34(9):826-832 GOLDSON E; HAGERMAN RJ THE FRAGILE-X SYNDROME | 3 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 711 | 8 | 14 | 1021 1993 AMERICAN JOURNAL OF DISEASES OF CHILDREN 147(6):605-606 GOLDSON E; HAGERMAN RJ FRAGILE-X SYNDROME AND FAILURE-TO-THRIVE | 4 | 4 |
| 712 | 20 | 37 | 1867 2000 ANNALES DE GENETIQUE 43(1):29-34 Gonzalez-del Angel A; Vidal S; Saldana Y; del Castillo V; Alcantara MA; Macias M; Luna JP; Orozco L Molecular diagnosis of the fragile X and FRAXE syndromes in patients with mental retardation of unknown cause in Mexico | 2 | 3 |
| 713 | 5 | 11 | 717 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 |
| 714 | 0 | 0 | 718 1990 JOURNAL OF THE ROYAL SOCIETY OF MEDICINE 83(6):415-415 GOODYEAR HM; SONKSON PM FRAGILE X-SYNDROME - REPLY | 0 | 0 |
| 715 | 14 | 31 | 793 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):322-327 GOONEWARDENA P; BROWN WT; GROSS AC; FERRANDO C; DOBKIN C; ROMANO V; BOSCO P; CERATTO N; PETTERSSON U; DAHL N LINKAGE ANALYSIS OF THE FRAGILE-X SYNDROME USING A NEW DNA MARKER U6.2 DEFINING LOCUS DXS304 | 1 | 1 |
| 716 | 0 | 0 | 773 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):341-341 GOONEWARDENA P; GLICKSMAN A; BROWN WT LINKAGE ANALYSIS OF PROXIMAL DNA MARKERS RN1 AND VK23 USED IN THE DIAGNOSIS OF FRAGILE-X SYNDROME | 0 | 0 |
| 717 | 0 | 0 | 634 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):1007-1007 GOONEWARDENA P; GROSS AC; FERRANDO CJ; BROWN T; DAHL N; PETTERSSON U ANONYMOUS DNA PROBE U6.2 (DXS304) FROM XQ MAPS DISTAL TO THE DXS98 LOCUS AND SHOWS CLOSE LINKAGE TO THE FRAGILE-X SYNDROME | 0 | 1 |
| 718 | 0 | 0 | 375 1986 CLINICAL GENETICS 29(5):462-462 GOONEWARDENA P; GUSTAVSON KH; HOLMGREN G; TOLUN A; CHOTAI J; JOHNSEN E; PETTERSSON U STUDIES ON FRAGILE X-MENTAL RETARDATION BY THE USE OF DNA PROBES | 1 | 1 |
| 719 | 7 | 12 | 377 1986 CLINICAL GENETICS 30(4):249-254 GOONEWARDENA P; GUSTAVSON KH; HOLMGREN G; TOLUN A; CHOTAI J; JOHNSEN E; PETTERSSON U ANALYSIS OF FRAGILE X-MENTAL RETARDATION FAMILIES USING FLANKING POLYMORPHIC DNA PROBES | 7 | 13 |
| 720 | 0 | 0 | 272 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):645-645 GOONEWARDENA P; TOLUN A; GUSTAVSON KH; HOLMGREN G; LINDSTEN J; PETTERSSON U STUDIES ON THE FRAGILE-X MENTAL-RETARDATION SYNDROME, DUCHENNE MUSCULAR-DYSTROPHY AND X-LINKED RETINITIS PIGMENTOSA IN SWEDISH FAMILIES, BY THE USE OF DNA PROBES | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 721 | 1 | 1 | 1287 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1914-1914 GOONEWARDENA P; ZHANG J A SINGLE TUBE NONRADIOACTIVE PCR ASSAY FOR THE DETECTION OF THE FULL SPECTRUM OR FMR1 CGG REPEATS SEEN IN THE NORMAL, CARRIER AND FRAGILE-X SYNDROME INDIVIDUALS | 0 | 0 |
| 722 | 8 | 22 | 1632 1997 ZHURNAL NEVROPATOLOGII I PSIKHIATRII IMENI S S KORSAKOVA 97(8):33-37 Gorbachevskaya NL; Denisova LV Bioelectric brain activity in patients with syndrome of fragile X-chromosome and in their mothers | 0 | 1 |
| 723 | 0 | 0 | 443 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):622-622 GOSDEN C; BUCHANAN J; NEWTON M; KESTON M; WRIGHT AF; PRIMROSE D; CLAYTON JF; CHRISTIE S; HASTIE N; EVANS HJ FRAGILE-X SYNDROME - NEW LINKAGE DATA IN 10 FAMILIES | 0 | 0 |
| 724 | 0 | 0 | 1999 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 |
| 725 | 12 | 46 | 1859 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(4):307-315 Gould EL; Loesch DZ; Martin MJ; Hagerman RJ; Armstrong SM; Huggins RM Melatonin profiles and sleep characteristics in boys with fragile X syndrome: A preliminary study | 10 | 15 |
| 726 | 28 | 88 | 2001 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 |
| 727 | 2 | 5 | 852 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2065-2065 GRAHAM CA; GRIER DG; CLARKSON M; STEWART FJ; NEVIN NC LINKAGE ANALYSIS IN FRAGILE-X SYNDROME | 0 | 0 |
| 728 | 0 | 0 | 306 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 |
| 729 | 10 | 14 | 1761 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 85(3):311-316 Grasso M; Faravelli F; Lo Nigro C; Chiurazzi P; Sperandeo MP; Argusti A; Pomponi MG; Lecora M; Sebastio GF; Perroni L; Andria G; Neri G; Bricarelli FD Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patients | 1 | 1 |
| 730 | 9 | 10 | 1410 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):187-190 Grasso M; Perroni L; Colella S; Piombo G; Argusti A; Lituania M; Buscaglia M; Giussani U; Grimoldi MG; Bricarelli FD Prenatal diagnosis of 30 fetuses at risk for fragile X syndrome | 1 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 731 | 0 | 0 | 2156 2002 JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY 61(5):450-450 Greco CM; Hagerman RJ; Tassone F; Chudley AE; Del Bigio MR; Jacquemont S; Leehey M; Hagerman PJ Neuronal and astrocytic intranuclear inclusions in Fragile X carriers with cerebellar tremor/ataxia and cognitive changes. | 0 | 0 |
| 732 | 0 | 0 | 2219 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):586-586 Greco CM; Tassone F; Jaquemont S; Hagerman RJ; Sahota PK; Delacourte A; Maurage CA; Hagerman PJ Intranuclear neuronal inclusions in two female carriers of the fragile X premutation | 0 | 0 |
| 733 | 37 | 136 | 2257 2003 CYTOGENETIC AND GENOME RESEARCH 100(1-4):65-76 Greene E; Handa V; Kumari D; Usdin K Transcription defects induced by repeat expansion: fragile X syndrome, FRAXE mental retardation, progressive myoclonus epilepsy type 1, and Friedreich ataxia | 0 | 0 |
| 734 | 10 | 36 | 2055 2001 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 98(13):7101-7106 Greenough WT; Klintsova AY; Irwin SA; Galvez R; Bates KE; Weiler IJ Synaptic regulation of protein synthesis and the fragile X protein | 30 | 49 |
| 735 | 0 | 0 | 1785 1999 FASEB JOURNAL 13(5):A703-A703 Greenough WT; Weiler IJ; Angenstein F; Klintsova A; Bauchwitz R Synthesis of the fragile X mental retardation protein at synapses: Possible role in synaptic development and plasticity | 0 | 0 |
| 736 | 0 | 1 | 1943 2000 LIBRARY JOURNAL 125(11):105-105 Griffin KH Children with Fragile X Syndrome: A parents' guide. | 0 | 0 |
| 737 | 0 | 0 | 2081 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):270-270 Griffin KJ; Bei T; Meck J; Wong LJ; Bondy C; Stratakis CA Gender ambiguity and fragile X: a new syndrome. | 0 | 0 |
| 738 | 1 | 6 | 874 1991 JOURNAL OF MEDICAL GENETICS 28(12):837-839 GRIFFITHS MJ; STRACHAN MC A SINGLE LYMPHOCYTE CULTURE FOR FRAGILE-X INDUCTION AND PROMETAPHASE CHROMOSOME ANALYSIS | 0 | 0 |
| 739 | 2 | 17 | 627 1989 ARCHIVES OF NEUROLOGY 46(12):1269-1270 GRIGSBY J; HAGERMAN R FRAGILE-X SYNDROME - A GENETIC ETIOLOGY FOR DEVELOPMENTAL GERSTMANN SYNDROME | 0 | 0 |
| 740 | 0 | 0 | 1315 1995 BRAIN AND COGNITION 28(1):111-111 GRIGSBY J; KAYE K VARIABLE EXPRESSION OF DEVELOPMENTAL GERSTMANN SIGNS IN FRAGILE-X SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 741 | 0 | 0 | 1316 1995 BRAIN AND COGNITION 28(1):111-112 GRIGSBY J; KAYE K DISSOCIATIONS IN DEVELOPMENTAL DYSCALCULIA SECONDARY TO FRAGILE-X SYNDROME | 0 | 0 |
| 742 | 11 | 29 | 917 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):111-115 GRIGSBY J; KEMPER MB; HAGERMAN RJ VERBAL-LEARNING AND MEMORY AMONG HETEROZYGOUS FRAGILE-X FEMALES | 7 | 7 |
| 743 | 0 | 0 | 2159 2002 JOURNAL OF THE AMERICAN GERIATRICS SOCIETY 50(4):S48-S48 Grigsby J; Leehey M; Hagerman RJ; Epstein J; Wilson R; Jacquemont S; Greco C; Brunberg J; Tassone F; Hagerman P Dementia and a tremor-ataxia disorder among older male carriers of the fragile X premutation. | 0 | 1 |
| 744 | 3 | 36 | 484 1987 NEUROPSYCHOLOGIA 25(6):881-891 GRIGSBY JP; KEMPER MB; HAGERMAN RJ DEVELOPMENTAL GERSTMANN SYNDROME WITHOUT APHASIA IN FRAGILE-X SYNDROME | 16 | 27 |
| 745 | 7 | 30 | 678 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 35(1):28-35 GRIGSBY JP; KEMPER MB; HAGERMAN RJ; MYERS CS NEUROPSYCHOLOGICAL DYSFUNCTION AMONG AFFECTED HETEROZYGOUS FRAGILE-X FEMALES | 22 | 28 |
| 746 | 12 | 14 | 1648 1998 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 40(1):62-64 Gringras P; Barnicoat A Retesting for fragile X syndrome in cytogenetically normal males | 1 | 3 |
| 747 | 0 | 0 | 1661 1998 HUMAN GENETICS 103(3):366-366 Gronskov K; Brondum-Nielsen K Regarding the letter from Dr. Stephen T. Warren of the Emory University School of Medicine concerning our article "Mutational analysis of the FMR1 gene in 118 mentally retarded males suspected of fragile X syndrome: absence of prevalent mutations" | 0 | 0 |
| 748 | 21 | 41 | 1660 1998 HUMAN GENETICS 102(4):440-445 Gronskov K; Hallberg A; Brondum-Nielsen K Mutational analysis of the FMR1 gene in 118 mentally retarded males suspected of fragile X syndrome: absence of prevalent mutations | 3 | 8 |
| 749 | 0 | 0 | 635 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):1009-1009 GROSS AC; FERRANDO CJ; BROWN WT LINKAGE DATA FOR FRAGILE-X AND 3 DISTAL MARKERS | 0 | 1 |
| 750 | 0 | 0 | 2130 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:229-229 Gryschenko NV; Malarchuk SG; Livshits LA CGG-repeat expansion and metilation status of the promotor region of FMR1 gene analysis in the Fragile-X sindrome patients from Ukraine | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 751 | 0 | 0 | 1201 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 |
| 752 | 0 | 0 | 1250 1994 NEUROLOGY 44(4):A400-A400 GUERREIRO M; MOURARIBEIRO MVL; CAMARGO EE; KATO M; MENEZES JR; GUERREIRO CAM NEUROBIOLOGY OF FRAGILE-X-SYNDROME (FXS) | 0 | 0 |
| 753 | 12 | 30 | 1641 1998 ARQUIVOS DE NEURO-PSIQUIATRIA 56(1):18-23 Guerreiro MM; Camargo EE; Kato M; Marques-De-Faria AP; Ciasca SM; Guerreiro CAM; Netto JRM; Moura-Ribeiro MVL Fragile X syndrome - Clinical, electroencephalographic and neuroimaging characteristics | 7 | 13 |
| 754 | 4 | 22 | 1593 1997 HUMAN HEREDITY 47(5):254-262 Gurling HMD; Bolton PF; Vincent J; Melmer G; Rutter M Molecular and cytogenetic investigations of the fragile X region including the Frax A and Frax E CGG trinucleotide repeat sequences in families multiplex for autism and related phenotypes | 0 | 7 |
| 755 | 1 | 10 | 348 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):581-587 GUSTAVSON KH; BLOMQUIST H; HOLMGREN G PREVALENCE OF THE FRAGILE-X SYNDROME IN MENTALLY-RETARDED BOYS IN A SWEDISH COUNTY | 52 | 74 |
| 756 | 6 | 18 | 263 1985 CLINICAL GENETICS 27(5):463-467 GUSTAVSON KH; DAHLBOM K; FLOOD A; HOLMGREN G; BLOMQUIST HK; SANNER G EFFECT OF FOLIC-ACID TREATMENT IN THE FRAGILE X-SYNDROME | 10 | 14 |
| 757 | 0 | 19 | 13 1981 CLINICAL GENETICS 19(2):101-110 GUSTAVSON KH; HOLMGREN G; BLOMQUIST HK; MIKKELSEN M; NORDENSON I; POULSEN H; TOMMERUP N FAMILIAL X-LINKED MENTAL-RETARDATION AND FRAGILE X-CHROMOSOMES IN 2 SWEDISH FAMILIES | 28 | 42 |
| 758 | 13 | 19 | 1217 1994 HUMAN GENETICS 94(5):479-483 HAATAJA R; VAISANEN ML; LI MY; RYYNANEN M; LEISTI J THE FRAGILE-X SYNDROME IN FINLAND - DEMONSTRATION OF A FOUNDER EFFECT BY ANALYSIS OF MICROSATELLITE HAPLOTYPES | 11 | 19 |
| 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 | 33 | 2260 2003 CYTOGENETIC AND GENOME RESEARCH 100(1-4):206-212 Hagerman PJ; Greco CM; Hagerman RJ A cerebellar tremor/ataxia syndrome among fragile X premutation carriers | 2 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 761 | 0 | 0 | 2080 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):259-259 Hagerman PJ; Greco CM; Hagerman RJ; Tassone F; Chudley AE; Del Bigio R; Jacquement S; Gane L; Leehey M Neuronal intranuclear inclusions in a tremor/ataxia syndrome among fragile X premutation carriers. | 0 | 0 |
| 762 | 0 | 0 | 2123 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:63-63 Hagerman PJ; Greco CM; Tassone F; Chudley A; Del Bigio MR; Jacquemont S; Leehey M; Hagerman RJ Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers | 0 | 0 |
| 763 | 37 | 80 | 2311 2004 AMERICAN JOURNAL OF HUMAN GENETICS 74(5):805-816 Hagerman PJ; Hagerman RJ The fragile-X premutation: A maturing perspective | 2 | 2 |
| 764 | 28 | 55 | 2346 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):25-30 Hagerman PJ; Hagerman RJ Fragile X-associated tremor/ataxia syndrome (FXTAS) | 0 | 0 |
| 765 | 2 | 6 | 2334 2004 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 291(24):2945-2946 Hagerman PJ; Hagerman RJ; Gane LW Genetic counseling for families of patients with fragile X syndrome - In reply | 0 | 0 |
| 766 | 0 | 0 | 2362 2004 NEUROLOGY 62(7):A48-A48 Hagerman PJ; Jacquemont S; Hagerman RJ; Leehey MA; Hall DA; Levine RA; Brunberg JA; Zhang L; Jardini T; Gane LW; Harris SW; Herman K; Grigsby J; Greco CM; Berry-Kravis E; Tassone F 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 |
| 767 | 11 | 16 | 1006 1992 NATURE GENETICS 1(3):157-158 HAGERMAN R CLINICAL CONUNDRUMS IN FRAGILE-X SYNDROME | 7 | 8 |
| 768 | 3 | 10 | 1623 1997 PEDIATRICS 99(5):753-753 Hagerman R Fragile X: Treatment of hyperactivity | 0 | 1 |
| 769 | 0 | 0 | 697 1990 CLINICAL RESEARCH 38(1):A164-A164 HAGERMAN R; AMIRI K; CRONISTER A; WITTENBERGER M; SCHREINER R; SOBESKY W FRAGILE-X GIRLS - PHYSICAL AND NEUROCOGNITIVE STATUS AND OUTCOME | 0 | 0 |
| 770 | 17 | 44 | 495 1988 AMERICAN JOURNAL OF DISEASES OF CHILDREN 142(11):1216-1221 HAGERMAN R; BERRY R; JACKSON AW; CAMPBELL J; SMITH ACM; MCGAVRAN L INSTITUTIONAL SCREENING FOR THE FRAGILE-X SYNDROME | 12 | 21 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 771 | 0 | 0 | 2082 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):287-287 Hagerman R; Goodlin-Jones BL; Spence S; Albrect L; Bacalman S; Tassone F; Gane LW; Harris SW; Hagerman PJ The fragile X premutation and autistic spectrum disorders. | 0 | 0 |
| 772 | 0 | 0 | 1033 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):144-144 HAGERMAN R; HULL C; CARPENTER I; STALEY L; OCONNOR R; SEYDEL C; MAZZOCCO M; TAYLOR A HIGH-FUNCTIONING FRAGILE X MALES | 1 | 1 |
| 773 | 9 | 24 | 238 1985 AMERICAN JOURNAL OF DISEASES OF CHILDREN 139(7):674-678 HAGERMAN R; KEMPER M; HUDSON M LEARNING-DISABILITIES AND ATTENTIONAL PROBLEMS IN BOYS WITH THE FRAGILE X-SYNDROME | 54 | 71 |
| 774 | 0 | 0 | 90 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A92-A92 HAGERMAN R; MCBOGG P; LEVITUS A; MCGAVRAN L; SMITH A; BERRY B; BRADEN M; VANHOUSEN K; NEWALL K; MATUS I FOLIC-ACID TREATMENT OF THE FRAGILE-X SYNDROME | 3 | 4 |
| 775 | 9 | 23 | 1322 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):167-184 Hagerman R; Staley L; Brown WT; Taylor A; Meadow K; Dorn M; Stoorman S; Neri G; Chiurazzi P; Levitas A; Spiridigliozzi GA; OConnor R; Weber JD; Braden M; Sudhalter V Conference summary: Fourth International Conference on Fragile X and X-linked Mental Retardation sponsored by the National Fragile X Foundation | 0 | 0 |
| 776 | 1 | 7 | 314 1986 AMERICAN JOURNAL OF DISEASES OF CHILDREN 140(4):327-328 HAGERMAN RJ FRAGILE-X SYNDROME AND LEARNING-DISABILITIES - REPLY | 1 | 1 |
| 777 | 1 | 1 | 413 1987 AMERICAN JOURNAL OF DISEASES OF CHILDREN 141(6):601-602 HAGERMAN RJ POSSIBLE SIMILARITIES BETWEEN THE FRAGILE-X AND ASPERGERS SYNDROMES - REPLY | 1 | 1 |
| 778 | 4 | 5 | 481 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 |
| 779 | 49 | 76 | 988 1992 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 33(7):1127-1139 HAGERMAN RJ FRAGILE-X SYNDROME - ADVANCES AND CONTROVERSY | 3 | 7 |
| 780 | 64 | 95 | 1464 1996 CHILD AND ADOLESCENT PSYCHIATRIC CLINICS OF NORTH AMERICA 5(4):895-& Hagerman RJ Fragile X syndrome | 1 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 781 | 60 | 94 | 1472 1996 DEVELOPMENTAL PSYCHOLOGY 32(3):416-424 Hagerman RJ Biomedical advances in developmental psychology: The case of fragile X syndrome | 3 | 8 |
| 782 | 13 | 24 | 1520 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):202-208 Hagerman RJ Fragile X syndrome: meeting the challenges of diagnosis and care | 0 | 0 |
| 783 | 76 | 123 | 1631 1997 WESTERN JOURNAL OF MEDICINE 166(2):129-137 Hagerman RJ Fragile X syndrome - Molecular and clinical insights and treatment issues | 5 | 8 |
| 784 | 7 | 113 | 1814 1999 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 5(4):305-313 Hagerman RJ Psychopharmacological interventions in fragile X syndrome, fetal alcohol syndrome, Prader-Willi syndrome, Angelman syndrome, Smith-Magenis syndrome, and velocardiofacial syndrome | 0 | 2 |
| 785 | 5 | 36 | 411 1987 AMERICAN JOURNAL OF DISEASES OF CHILDREN 141(2):184-187 HAGERMAN RJ; ALTSHULSTARK D; MCBOGG P RECURRENT OTITIS-MEDIA IN THE FRAGILE X-SYNDROME | 9 | 14 |
| 786 | 12 | 21 | 786 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):283-287 HAGERMAN RJ; AMIRI K; CRONISTER A FRAGILE-X CHECKLIST | 45 | 60 |
| 787 | 0 | 0 | 747 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):139-139 HAGERMAN RJ; BRUNSCHWIG A; MILLER L; BUTLER MG SELECTED STANDARDS FOR ANTHROPOMETRIC MEASUREMENTS IN FRAGILE X-SYNDROME | 0 | 0 |
| 788 | 15 | 32 | 335 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):375-380 HAGERMAN RJ; CHUDLEY AE; KNOLL JH; JACKSON AW; KEMPER M; AHMAD R AUTISM IN FRAGILE-X FEMALES | 32 | 46 |
| 789 | 19 | 64 | 1211 1994 DEVELOPMENTAL BRAIN DYSFUNCTION 7(2-3):155-164 HAGERMAN RJ; FULTON MJ; LEAMAN A; RIDDLE J; HAGERMAN K; SOBESKY W A SURVEY OF FLUOXETINE THERAPY IN FRAGILE-X SYNDROME | 16 | 18 |
| 790 | 0 | 0 | 1968 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):177-177 Hagerman RJ; Greco C; Chudley A; Leehey M; Tassone F; Grigsby J; Hills J; Wilson R; Harris SW; Hagerman PJ Neuropathology and neurodegenerative features in some older male premutation carriers of fragile X syndrome. | 3 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 791 | 0 | 0 | 2181 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 |
| 792 | 63 | 108 | 2044 2001 MOLECULAR GENETICS AND METABOLISM 74(1-2):89-97 Hagerman RJ; Hagerman PJ Fragile X syndrome: A model of gene-brain-behavior relationships | 1 | 1 |
| 793 | 61 | 105 | 2066 2001 REVISTA DE NEUROLOGIA 33:S51-S57 Hagerman RJ; Hagerman PJ Fragile X syndrome: A model of gene-brain-behaviour relationships | 0 | 0 |
| 794 | 35 | 51 | 2116 2002 CURRENT OPINION IN GENETICS & DEVELOPMENT 12(3):278-283 Hagerman RJ; Hagerman PJ The fragile X premutation: into the phenotypic fold | 6 | 17 |
| 795 | 13 | 41 | 1734 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):313-317 Hagerman RJ; Hills J; Scharfenaker S; Lewis H Fragile X syndrome and selective mutism | 11 | 18 |
| 796 | 38 | 61 | 1155 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):298-308 HAGERMAN RJ; HULL CE; SAFANDA JF; CARPENTER I; STALEY LW; OCONNOR RA; SEYDEL C; MAZZOCCO MMM; SNOW K; THIBODEAU SN; KUHL D; NELSON DL; CASKEY CT; TAYLOR AK HIGH FUNCTIONING FRAGILE-X MALES - DEMONSTRATION OF AN UNMETHYLATED FULLY EXPANDED FMR-1 MUTATION ASSOCIATED WITH PROTEIN EXPRESSION | 67 | 95 |
| 797 | 1 | 6 | 301 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 |
| 798 | 0 | 0 | 437 1987 CLINICAL RESEARCH 35(1):A211-A211 HAGERMAN RJ; JACKSON AW; BERRY R; CAMPBELL J; STILLMAN E; SMITH ACM; MCGAVRAN L PREDICTORS OF THE FRAGILE-X SYNDROME | 0 | 0 |
| 799 | 11 | 38 | 326 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):241-262 HAGERMAN RJ; JACKSON AW; LEVITAS A; BRADEN M; MCBOGG P; KEMPER M; MCGAVRAN L; BERRY R; MATUS I; HAGERMAN PJ ORAL FOLIC-ACID VERSUS PLACEBO IN THE TREATMENT OF MALES WITH THE FRAGILE-X SYNDROME | 18 | 26 |
| 800 | 13 | 42 | 334 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):359-374 HAGERMAN RJ; JACKSON AW; LEVITAS A; RIMLAND B; BRADEN M AN ANALYSIS OF AUTISM IN 50 MALES WITH THE FRAGILE-X SYNDROME | 74 | 104 |
Page 8: 1 (Abbeduto L) 2 (BELGHITI D) 3 (Brown WT) 4 (Chen X) 5 (DAKER MG) 6 (DYKENS E) 7 (FITCHETT M) 8 (GLOVER TW) 9 (HAGERMAN RJ) 10 (HOFFMAN M) 11 (JANCAR J) 12 (KIMCHISARFATY C) 13 (LEE JT) 14 (MAES B) 15 (MIGEON BR) 16 (Myers GF) 17 (Patsalis PC) 18 (REISS AL) 19 (Schenck A) 20 (SMITS APT) 21 (SZABO P) 22 (TURNER G) 23 (Wang YC) 24 (WOHRLE D)
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