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Nodes: 2647,
Authors: 5321,
Journals: 428,
Outer References: 16458,
Words: 3536
Collection span: 1967 - 2005
View: Overview. Sorted by LCS.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 301 | 24 | 40 | 2011 2000 EXPERIMENTAL CELL RESEARCH 258(1):162-170 Bakker CE; Otero YD; Bontekoe C; Raghoe P; Luteijn T; et al. Immunocytochemical and biochemical characterization of FMRP, FXR1P, and FXR2P in the mouse | 22 | 31 |
| 302 | 31 | 40 | 2288 2002 HUMAN MOLECULAR GENETICS 11(4):371-378 Dombrowski C; Levesque S; Morel ML; Rouillard P; Morgan K; et al. Premutation and intermediate-size FMR1 alleles in 10,572 males from the general population: Loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles | 22 | 34 |
| 303 | 0 | 3 | 22 1981 HUMAN GENETICS 59(2):186-186 FONATSCH C A SIMPLE METHOD TO DEMONSTRATE THE FRAGILE X-CHROMOSOME IN FIBROBLASTS | 21 | 38 |
| 304 | 3 | 15 | 299 1985 JOURNAL OF MEDICAL GENETICS 22(2):85-91 TUCKERMAN E; WEBB T; BUNDEY SE FREQUENCY AND REPLICATION STATUS OF THE FRAGILE-X, FRA(X)(Q27-28), IN A PAIR OF MONOZYGOTIC TWINS OF MARKEDLY DIFFERING INTELLIGENCE | 21 | 36 |
| 305 | 6 | 10 | 486 1987 LANCET 1(8527):280-280 BROWN WT; WU Y; GROSS AC; CHAN CB; DOBKIN CS; et al. RFLP FOR LINKAGE ANALYSIS OF FRAGILE-X SYNDROME | 21 | 35 |
| 306 | 10 | 22 | 746 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(3):656-661 KREMER EJ; YU S; PRITCHARD M; NAGARAJA R; HEITZ D; et al. ISOLATION OF A HUMAN DNA-SEQUENCE WHICH SPANS THE FRAGILE-X | 21 | 32 |
| 307 | 7 | 12 | 830 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):505-508 BRAINARD SS; SCHREINER RA; HAGERMAN RJ COGNITIVE PROFILES OF THE CARRIER FRAGILE-X WOMAN | 21 | 25 |
| 308 | 3 | 10 | 832 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):511-513 MUSUMECI SA; FERRI R; ELIA M; COLOGNOLA RM; BERGONZI P; et al. EPILEPSY AND FRAGILE-X SYNDROME - A FOLLOW-UP-STUDY | 21 | 36 |
| 309 | 12 | 47 | 864 1991 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 33(9):776-788 FERRIER LJ; BASHIR AS; MERYASH DL; JOHNSTON J; WOLFF P CONVERSATIONAL SKILLS OF INDIVIDUALS WITH FRAGILE-X SYNDROME - A COMPARISON WITH AUTISM AND DOWN-SYNDROME | 21 | 25 |
| 310 | 20 | 27 | 1032 1993 AMERICAN JOURNAL OF DISEASES OF CHILDREN 147(7):723-726 STALEY LW; HULL CE; MAZZOCCO MMM; THIBODEAU SN; SNOW K; et al. MOLECULAR-CLINICAL CORRELATIONS IN CHILDREN AND ADULTS WITH FRAGILE X-SYNDROME | 21 | 24 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 311 | 60 | 138 | 1080 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 48(2):112-121 FISCH GS WHAT IS ASSOCIATED WITH THE FRAGILE-X SYNDROME | 21 | 34 |
| 312 | 18 | 33 | 1266 1994 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 33(2):247-255 SOBESKY WE; HULL CE; HAGERMAN RJ SYMPTOMS OF SCHIZOTYPAL PERSONALITY-DISORDER IN FRAGILE-X WOMEN | 21 | 36 |
| 313 | 28 | 92 | 1332 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 60(6):480-493 Schapiro MB; Murphy DGM; Hagerman RJ; Azari NP; Alexander GE; et al. Adult fragile X syndrome: Neuropsychology, brain anatomy, and metabolism | 21 | 31 |
| 314 | 15 | 38 | 1366 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):270-279 Belser RC; Sudhalter V Arousal difficulties in males with fragile X syndrome: A preliminary report | 21 | 26 |
| 315 | 2 | 5 | 1422 1995 LANCET 346(8970):309-310 CONWAY GS; HETTIARACHCHI S; MURRAY A; JACOBS PA FRAGILE-X PREMUTATIONS IN FAMILIAL PREMATURE OVARIAN FAILURE | 21 | 43 |
| 316 | 18 | 63 | 1789 1998 NEUROLOGY 50(1):121-130 Mostofsky SH; Mazzocco MMM; Aakalu G; Warsofsky IS; Denckla MB; et al. Decreased cerebellar posterior vermis size in fragile X syndrome - Correlation with neurocognitive performance | 21 | 48 |
| 317 | 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 |
| 318 | 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 |
| 319 | 15 | 43 | 2189 2001 NEUROSCIENCE 103(4):1043-1050 Chen L; Toth M Fragile X mice develop sensory hyperreactivity to auditory stimuli | 21 | 34 |
| 320 | 0 | 23 | 24 1981 JOURNAL OF MEDICAL GENETICS 18(5):366-373 PROOPS R; WEBB T THE FRAGILE X-CHROMOSOME IN THE MARTIN-BELL-RENPENNING SYNDROME AND IN MALES WITH OTHER FORMS OF FAMILIAL MENTAL-RETARDATION | 20 | 32 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 321 | 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 |
| 322 | 4 | 19 | 171 1984 AMERICAN JOURNAL OF HUMAN GENETICS 36(3):640-645 KNOLL JH; CHUDLEY AE; GERRARD JW FRAGILE (X) X-LINKED MENTAL-RETARDATION .2. FREQUENCY AND REPLICATION PATTERN OF FRAGILE (X) (Q28) IN HETEROZYGOTES | 20 | 31 |
| 323 | 6 | 13 | 185 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):289-297 BROWN WT; JENKINS EC; FRIEDMAN E; BROOKS J; COHEN IL; et al. FOLIC-ACID THERAPY IN THE FRAGILE-X SYNDROME | 20 | 28 |
| 324 | 1 | 15 | 284 1985 HUMAN GENETICS 69(1):44-46 WARREN ST; GLOVER TW; DAVIDSON RL; JAGADEESWARAN P LINKAGE AND RECOMBINATION BETWEEN FRAGILE X-LINKED MENTAL-RETARDATION AND THE FACTOR-IX GENE | 20 | 37 |
| 325 | 5 | 19 | 286 1985 HUMAN GENETICS 69(3):209-211 KRAWCZUN MS; JENKINS EC; BROWN WT ANALYSIS OF THE FRAGILE-X CHROMOSOME - LOCALIZATION AND DETECTION OF THE FRAGILE SITE IN HIGH-RESOLUTION PREPARATIONS | 20 | 33 |
| 326 | 6 | 25 | 303 1985 JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY 48(2):150-153 FINELLI PF; PUESCHEL SM; PADREMENDOZA T; OBRIEN MM NEUROLOGICAL FINDINGS IN PATIENTS WITH THE FRAGILE-X SYNDROME | 20 | 29 |
| 327 | 2 | 7 | 307 1985 LANCET 1(8433):870-870 TOMMERUP N; SONDERGAARD F; TONNESEN T; KRISTENSEN M; ARVEILER B; et al. 1ST TRIMESTER PRENATAL-DIAGNOSIS OF A MALE FETUS WITH FRAGILE-X | 20 | 31 |
| 328 | 11 | 41 | 471 1987 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 17(4):457-468 PAUL R; DYKENS E; LECKMAN JF; WATSON M; BREG WR; et al. A COMPARISON OF LANGUAGE CHARACTERISTICS OF MENTALLY-RETARDED ADULTS WITH FRAGILE-X SYNDROME AND THOSE WITH NONSPECIFIC MENTAL-RETARDATION AND AUTISM | 20 | 27 |
| 329 | 30 | 56 | 917 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):47-55 FISCH GS IS AUTISM ASSOCIATED WITH THE FRAGILE-X SYNDROME | 20 | 36 |
| 330 | 11 | 18 | 921 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):72-77 LACHIEWICZ AM ABNORMAL BEHAVIORS OF YOUNG GIRLS WITH FRAGILE-X SYNDROME | 20 | 27 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 331 | 20 | 36 | 991 1992 HUMAN GENETICS 90(1-2):55-61 ERSTER SH; BROWN WT; GOONEWARDENA P; DOBKIN CS; JENKINS EC; et al. POLYMERASE CHAIN-REACTION ANALYSIS OF FRAGILE X-MUTATIONS | 20 | 31 |
| 332 | 13 | 28 | 1219 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 54(4):378-383 THOMPSON NM; GULLEY ML; ROGENESS GA; CLAYTON RJ; JOHNSON C; et al. NEUROBEHAVIORAL CHARACTERISTICS OF CGG AMPLIFICATION STATUS IN FRAGILE-X FEMALES | 20 | 28 |
| 333 | 15 | 25 | 1398 1995 HUMAN MOLECULAR GENETICS 4(12):2199-2208 EICHLER EE; HAMMOND HA; MACPHERSON JN; WARD PA; NELSON DL POPULATION SURVEY OF THE HUMAN FMR1 CGG REPEAT SUBSTRUCTURE SUGGESTS BIASED POLARITY FOR THE LOSS OF AGG INTERRUPTIONS | 20 | 35 |
| 334 | 16 | 24 | 1460 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):191-195 Brown WT; Nolin S; Houck G; Ding XH; Glicksman A; et al. Prenatal diagnosis and carrier screening for fragile X by PCR | 20 | 28 |
| 335 | 24 | 61 | 1671 1997 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 27(4):415-435 Mazzocco MMM; Kates WR; Baumgardner TL; Freund LS; Reiss AL Autistic behaviors among girls with fragile X syndrome | 20 | 25 |
| 336 | 2 | 54 | 1707 1997 PSYCHIATRY RESEARCH-NEUROIMAGING 75(1):31-48 Kates WR; Abrams MT; Kaufmann WE; Breiter SN; Reiss AL Reliability and validity of MRI measurement of the amygdala and hippocampus in children with fragile X syndrome | 20 | 63 |
| 337 | 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 |
| 338 | 27 | 35 | 1970 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 94(3):232-236 Tassone F; Hagerman RJ; Loesch DZ; Lachiewicz A; Taylor AK; et al. Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA | 20 | 26 |
| 339 | 60 | 117 | 2073 2000 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 6(2):96-106 Mazzocco MMM Advances in research on the fragile X syndrome | 20 | 24 |
| 340 | 0 | 15 | 73 1982 JOURNAL OF MEDICAL GENETICS 19(1):44-48 WEBB GC; HALLIDAY JL; PITT DB; JUDGE CG; LEVERSHA M FRAGILE (X)(Q27) SITES IN A PEDIGREE WITH FEMALE CARRIERS SHOWING MILD TO SEVERE MENTAL-RETARDATION | 19 | 36 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 341 | 0 | 0 | 86 1982 PEDIATRICS 69(5):670-670 HARPEY JP TREATMENT OF FRAGILE-X | 19 | 24 |
| 342 | 2 | 28 | 111 1983 AMERICAN JOURNAL OF MEDICAL GENETICS 15(1):113-119 FILIPPI G; RINALDI A; ARCHIDIACONO N; ROCCHI M; BALAZS I; et al. LINKAGE BETWEEN G6PD AND FRAGILE-X SYNDROME | 19 | 43 |
| 343 | 3 | 18 | 325 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):189-194 LOEHR JP; SYNHORST DP; WOLFE RR; HAGERMAN RJ AORTIC ROOT DILATATION AND MITRAL-VALVE PROLAPSE IN THE FRAGILE-X SYNDROME | 19 | 28 |
| 344 | 11 | 38 | 329 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):241-262 HAGERMAN RJ; JACKSON AW; LEVITAS A; BRADEN M; MCBOGG P; et al. ORAL FOLIC-ACID VERSUS PLACEBO IN THE TREATMENT OF MALES WITH THE FRAGILE-X SYNDROME | 19 | 27 |
| 345 | 8 | 25 | 336 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 |
| 346 | 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 |
| 347 | 14 | 29 | 616 1989 AMERICAN JOURNAL OF HUMAN GENETICS 45(2):304-309 DAHL N; GOONEWARDENA P; MALMGREN H; GUSTAVSON KH; HOLMGREN G; et al. LINKAGE ANALYSIS OF FAMILIES WITH FRAGILE-X MENTAL-RETARDATION, USING A NOVEL RFLP MARKER (DXS 304) | 19 | 40 |
| 348 | 10 | 16 | 654 1989 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 28(3):417-421 PAYTON JB; STEELE MW; WENGER SL; MINSHEW NJ THE FRAGILE-X MARKER AND AUTISM IN PERSPECTIVE | 19 | 37 |
| 349 | 4 | 12 | 920 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):65-71 SUDHALTER V; MARANION M; BROOKS P EXPRESSIVE SEMANTIC DEFICIT IN THE PRODUCTIVE LANGUAGE OF MALES WITH FRAGILE-X SYNDROME | 19 | 21 |
| 350 | 10 | 27 | 1136 1993 JOURNAL OF MEDICAL GENETICS 30(9):761-766 DEVRIES BBA; FRYNS JP; BUTLER MG; CANZIANI F; WESBYVANSWAAY E; et al. CLINICAL AND MOLECULAR STUDIES IN FRAGILE-X PATIENTS WITH A PRADER-WILLI-LIKE PHENOTYPE | 19 | 33 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 351 | 20 | 37 | 1285 1995 AMERICAN JOURNAL OF HUMAN GENETICS 56(5):1042-1051 QUAN F; ZONANA J; GUNTER K; PETERSON KL; MAGENIS RE; et al. AN ATYPICAL CASE OF FRAGILE-X SYNDROME CAUSED BY A DELETION THAT INCLUDES THE FMRI GENE | 19 | 30 |
| 352 | 6 | 29 | 1545 1996 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 26(3):287-301 Dykens E; Ort S; Cohen I; Finucane B; Spiridigliozzi G; et al. Trajectories and profiles of adaptive behavior in males with fragile X syndrome: Multicenter studies | 19 | 23 |
| 353 | 27 | 51 | 1778 1998 JOURNAL OF MEDICAL GENETICS 35(2):103-111 Wohrle D; Salat U; Glaser D; Mucke J; Meisel-Stosiek M; et al. Unusual mutations in high functioning fragile X males: apparent instability of expanded unmethylated CGG repeats | 19 | 32 |
| 354 | 20 | 37 | 1857 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):245-249 Reyniers E; Martin JJ; Cras P; Van Marck E; Handig I; et al. Postmortem examination of two fragile X brothers with an FMR1 full mutation | 19 | 23 |
| 355 | 5 | 17 | 138 1983 HUMAN GENETICS 64(2):148-150 NUSSBAUM RL; AIRHART SD; LEDBETTER DH EXPRESSION OF THE FRAGILE (X)CHROMOSOME IN AN INTERSPECIFIC SOMATIC-CELL HYBRID | 18 | 58 |
| 356 | 8 | 17 | 152 1983 JOURNAL OF MENTAL DEFICIENCY RESEARCH 27(SEP):211-226 NIELSEN KB DIAGNOSIS OF THE FRAGILE-X SYNDROME (MARTIN-BELL SYNDROME) - CLINICAL FINDINGS IN 27 MALES WITH THE FRAGILE SITE AT XQ28 | 18 | 26 |
| 357 | 0 | 9 | 204 1984 HUMAN GENETICS 65(4):400-401 FRYNS JP; KLECZKOWSKA A; KUBIEN E; PETIT P; VANDENBERGHE H INACTIVATION PATTERN OF THE FRAGILE-X IN HETEROZYGOUS CARRIERS | 18 | 27 |
| 358 | 32 | 50 | 550 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):655-663 FISCH GS; COHEN IL; JENKINS EC; BROWN WT SCREENING DEVELOPMENTALLY DISABLED MALE POPULATIONS FOR FRAGILE-X - THE EFFECT OF SAMPLE-SIZE | 18 | 22 |
| 359 | 12 | 19 | 789 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):251-255 NOLIN SL; SNIDER DA; JENKINS EC; BROWN WT; KRAWCZUN M; et al. FRAGILE-X SCREENING-PROGRAM IN NEW-YORK-STATE | 18 | 24 |
| 360 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 361 | 7 | 9 | 1016 1992 NATURE GENETICS 1(4):237-238 CHAKRAVARTI A FRAGILE-X FOUNDER EFFECT | 18 | 32 |
| 362 | 12 | 25 | 1191 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 | 18 | 29 |
| 363 | 12 | 21 | 1213 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):527-534 LEVINSON G; MADDALENA A; PALMER FT; HARTON GL; BICK DP; et al. IMPROVED SIZING OF FRAGILE-X CCG REPEATS BY NESTED POLYMERASE CHAIN-REACTION | 18 | 29 |
| 364 | 15 | 18 | 1268 1994 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 33(9):1316-1321 MERENSTEIN SA; SHYU V; SOBESKY WE; STALEY L; BERRYKRAVIS E; et al. FRAGILE-X SYNDROME IN A NORMAL IQ MALE WITH LEARNING AND EMOTIONAL-PROBLEMS | 18 | 22 |
| 365 | 27 | 42 | 1324 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(6):1414-1425 ASHLEY AE; SHERMAN SL POPULATION-DYNAMICS OF A MEIOTIC MITOTIC EXPANSION MODEL FOR THE FRAGILE-X SYNDROME | 18 | 20 |
| 366 | 33 | 50 | 1463 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):203-208 Chiurazzi P; Macpherson J; Sherman S; Neri G Significance of linkage disequilibrium between the fragile X locus and its flanking markers | 18 | 25 |
| 367 | 53 | 104 | 1761 1998 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 28(5):393-405 Feinstein C; Reiss AL Autism: The point of view from fragile X studies | 18 | 45 |
| 368 | 14 | 54 | 2294 2002 JOURNAL OF BIOLOGICAL CHEMISTRY 277(40):37804-37810 Ohashi S; Koike K; Omori A; Ichinose S; Ohara S; et al. Identification of mRNA/protein (mRNP) complexes containing Pur alpha, mStaufen, Fragile X Protein, and myosin Va and their association with rough endoplasmic reticulum equipped with a kinesin motor | 18 | 48 |
| 369 | 23 | 75 | 2319 2002 MOLECULAR AND CELLULAR NEUROSCIENCE 19(2):138-151 Li JX; Pelletier MR; Velazquez JLP; Carlen PL Reduced cortical synaptic plasticity and GluR1 expression associated with fragile X mental retardation protein deficiency | 18 | 20 |
| 370 | 37 | 55 | 2476 2003 TRENDS IN BIOCHEMICAL SCIENCES 28(3):152-158 Jin P; Warren ST New insights into fragile X syndrome: from molecules to neurobehaviors | 18 | 34 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 371 | 2 | 6 | 64 1982 HUMAN GENETICS 61(2):160-162 STEINBACH P; BARBI G; BOLLER T ON THE FREQUENCY OF TELOMERIC CHROMOSOMAL CHANGES INDUCED BY CULTURE CONDITIONS SUITABLE FOR FRAGILE-X EXPRESSION | 17 | 31 |
| 372 | 1 | 6 | 83 1982 NEW ENGLAND JOURNAL OF MEDICINE 306(25):1551-1552 POPOVICH B; VEKEMANS M; ROSENBLATT D; MONROE P FRAGILE-X | 17 | 21 |
| 373 | 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 |
| 374 | 3 | 35 | 236 1984 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES 81(24):7855-7859 SZABO P; PURRELLO M; ROCCHI M; ARCHIDIACONO N; ALHADEFF B; et al. CYTOLOGICAL MAPPING OF THE HUMAN GLUCOSE-6-PHOSPHATE-DEHYDROGENASE GENE DISTAL TO THE FRAGILE-X SITE SUGGESTS A HIGH-RATE OF MEIOTIC RECOMBINATION ACROSS THIS SITE | 17 | 71 |
| 375 | 17 | 42 | 333 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):297-311 JENKINS EC; BROWN WT; WILSON MG; LIN MS; ALFI OS; et al. THE PRENATAL DETECTION OF THE FRAGILE-X CHROMOSOME - REVIEW OF RECENT EXPERIENCE | 17 | 27 |
| 376 | 7 | 20 | 421 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 27(2):435-448 MULLEY JC; GEDEON AK; THORN KA; BATES LJ; SUTHERLAND GR LINKAGE AND GENETIC-COUNSELING FOR THE FRAGILE-X USING DNA PROBE-52A, PROBE-F9, PROBE-DX13, AND PROBE-ST14 | 17 | 43 |
| 377 | 8 | 27 | 461 1987 HUMAN GENETICS 77(1):60-65 OBERLE I; CAMERINO G; WROGEMANN K; ARVEILER B; HANAUER A; et al. 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 |
| 378 | 13 | 33 | 476 1987 JOURNAL OF MEDICAL GENETICS 24(7):413-421 VEENEMA H; CARPENTER NJ; BAKKER E; HOFKER MH; WARD AM; et al. THE FRAGILE-X SYNDROME IN A LARGE FAMILY .3. INVESTIGATIONS ON LINKAGE OF FLANKING DNA MARKERS WITH THE FRAGILE SITE-XQ27 | 17 | 38 |
| 379 | 9 | 28 | 584 1988 EPILEPSIA 29(1):41-47 MUSUMECI SA; COLOGNOLA RM; FERRI R; GIGLI GL; PETRELLA MA; et al. FRAGILE-X SYNDROME - A PARTICULAR EPILEPTOGENIC EEG PATTERN | 17 | 38 |
| 380 | 0 | 0 | 644 1989 GENOMICS 4(4):570-578 PATTERSON MN; BELL MV; BLOOMFIELD J; FLINT T; DORKINS H; et al. GENETIC AND PHYSICAL MAPPING OF A NOVEL REGION CLOSE TO THE FRAGILE X-SITE ON THE HUMAN X-CHROMOSOME | 17 | 43 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 381 | 7 | 16 | 648 1989 HUMAN GENETICS 82(3):216-218 DAHL N; HAMMARSTROMHEEROMA K; GOONEWARDENA P; WADELIUS C; GUSTAVSON KH; et al. ISOLATION OF A DNA PROBE OF POTENTIAL USE FOR DIAGNOSIS OF THE FRAGILE-X SYNDROME | 17 | 32 |
| 382 | 9 | 27 | 656 1989 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 28(3):427-430 DYKENS EM; HODAPP RM; LECKMAN JF ADAPTIVE AND MALADAPTIVE FUNCTIONING OF INSTITUTIONALIZED AND NONINSTITUTIONALIZED FRAGILE-X MALES | 17 | 28 |
| 383 | 13 | 27 | 702 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 | 17 | 20 |
| 384 | 10 | 29 | 1116 1993 HUMAN MOLECULAR GENETICS 2(9):1429-1435 RICHARDS RI; HOLMAN K; YU S; SUTHERLAND GR FRAGILE-X SYNDROME UNSTABLE ELEMENT, P(CCG)N, AND OTHER SIMPLE TANDEM REPEAT SEQUENCES ARE BINDING-SITES FOR SPECIFIC NUCLEAR PROTEINS | 17 | 80 |
| 385 | 28 | 64 | 1171 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 50(2):190-200 MAES B; FRYNS JP; VANWALLEGHEM M; VANDENBERGHE H COGNITIVE-FUNCTIONING AND INFORMATION-PROCESSING OF ADULT MENTALLY-RETARDED MEN WITH FRAGILE-X SYNDROME | 17 | 24 |
| 386 | 15 | 17 | 1192 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):428-435 KOLEHMAINEN K POPULATION-GENETICS OF FRAGILE-X - A MULTIPLE ALLELE MODEL WITH VARIABLE RISK OF CGG REPEAT EXPANSION | 17 | 22 |
| 387 | 12 | 16 | 1198 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):454-457 TROTTIER Y; IMBERT G; POUSTKA A; FRYNS JP; MANDEL JL MALE WITH TYPICAL FRAGILE-X PHENOTYPE IS DELETED FOR PART OF THE FMR1 GENE AND FOR ABOUT 100 KB OF UPSTREAM REGION | 17 | 27 |
| 388 | 27 | 37 | 1203 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):474-481 HAGERMAN RJ; WILSON P; STALEY LW; LANG KA; FAN T; et al. EVALUATION OF SCHOOL-CHILDREN AT HIGH-RISK FOR FRAGILE-X-SYNDROME UTILIZING BUCCAL CELL FMR-1 TESTING | 17 | 36 |
| 389 | 1 | 2 | 1216 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 53(4):380-381 PARK V; HOWARDPEEBLES P; SHERMAN S; TAYLOR A; WULFSBERG E POLICY STATEMENT - AMERICAN-COLLEGE-OF-MEDICAL-GENETICS - FRAGILE-X-SYNDROME - DIAGNOSTIC AND CARRIER TESTING | 17 | 28 |
| 390 | 19 | 64 | 1232 1994 DEVELOPMENTAL BRAIN DYSFUNCTION 7(2-3):155-164 HAGERMAN RJ; FULTON MJ; LEAMAN A; RIDDLE J; HAGERMAN K; et al. A SURVEY OF FLUOXETINE THERAPY IN FRAGILE-X SYNDROME | 17 | 19 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 391 | 17 | 33 | 1364 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):242-251 Freund LS; Peebles CD; Aylward E; Reiss AL Preliminary report on cognitive and adaptive behaviors of preschool-aged males with fragile X | 17 | 22 |
| 392 | 15 | 46 | 1404 1995 JOURNAL OF BIOLOGICAL CHEMISTRY 270(48):28970-28977 NADEL Y; WEISMANSHOMER P; FRY M THE FRAGILE-X SYNDROME SINGLE-STRAND D(CGG)(N) NUCLEOTIDE REPEATS READILY FOLD BACK TO FORM UNIMOLECULAR HAIRPIN STRUCTURES | 17 | 50 |
| 393 | 10 | 20 | 1415 1995 JOURNAL OF MEDICAL GENETICS 32(3):170-173 WANG Q; GREEN E; BOBROW M; MATHEW CG A RAPID, NONRADIOACTIVE SCREENING-TEST FOR FRAGILE-X MUTATIONS AT THE FRAXA AND FRAXE LOCI | 17 | 28 |
| 394 | 26 | 59 | 1464 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):209-215 Chiurazzi P; Genuardi M; Kozak L; GiovannucciUzielli ML; Bussani C; et al. Fragile X founder chromosomes in Italy: A few initial events and possible explanation for their heterogeneity | 17 | 26 |
| 395 | 15 | 21 | 1551 1996 JOURNAL OF MEDICAL GENETICS 33(5):376-378 Wang ZM; Taylor AK; Bridge JA FMR1 fully expanded mutation with minimal methylation in a high functioning fragile X male | 17 | 22 |
| 396 | 26 | 41 | 1587 1997 AMERICAN JOURNAL OF HUMAN GENETICS 60(1):103-112 FalikZaccai TC; Shachak E; Yalon M; Lis Z; Borochowitz Z; et al. Predisposition to the fragile X syndrome in Jews of Tunisian descent is due to the absence of AGG interruptions on a rare Mediterranean haplotype | 17 | 27 |
| 397 | 23 | 62 | 1746 1998 GENOMICS 50(2):229-240 Lavedan C; Grabczyk E; Usdin K; Nussbaum RL Long uninterrupted CGG repeats within the first exon of the human FMR1 gene are not intrinsically unstable in transgenic mice | 17 | 21 |
| 398 | 33 | 40 | 1856 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):233-239 Taylor AK; Tassone F; Dyer PN; Hersch SM; Harris JB; et al. Tissue heterogeneity of the FMR1 mutation in a high-functioning male with fragile X syndrome | 17 | 24 |
| 399 | 21 | 37 | 2077 2000 MOLECULAR BRAIN RESEARCH 80(1):17-25 Todd PK; Mack KJ Sensory stimulation increases cortical expression of the fragile X mental retardation protein in vivo | 17 | 17 |
| 400 | 13 | 47 | 2082 2000 NEUROPSYCHOLOGIA 38(9):1261-1270 Munir F; Cornish KM; Wilding J A neuropsychological profile of attention deficits in young males with fragile X syndrome | 17 | 21 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 401 | 108 | 154 | 2153 2001 GENETICS IN MEDICINE 3(5):359-371 Crawford DC; Acuna JM; Sherman SL FMR1 and the fragile X syndrome: Human genome epidemiology review | 17 | 25 |
| 402 | 14 | 47 | 2244 2002 AMERICAN JOURNAL OF NEURORADIOLOGY 23(10):1757-1766 Brunberg JA; Jacquemont S; Hagerman RJ; Berry-Kravis EM; Grigsby J; et al. Fragile X premutation carriers: Characteristic MR imaging findings of adult male patients with progressive cerebellar and cognitive dysfunction | 17 | 27 |
| 403 | 17 | 43 | 2317 2002 MOLECULAR AND CELLULAR BIOLOGY 22(23):8332-8341 Otero YD; Severijnen LA; van Cappellen G; Schrier M; Oostra B; et al. Transport of fragile X mental retardation protein via granules in neurites of PC12 cells | 17 | 24 |
| 404 | 0 | 4 | 29 1981 LANCET 2(8254):1055-1055 BROWN WT; MEZZACAPPA PM; JENKINS EC SCREENING FOR FRAGILE X SYNDROME BY TESTICULAR SIZE MEASUREMENT | 16 | 23 |
| 405 | 0 | 0 | 50 1982 AMERICAN JOURNAL OF MEDICAL GENETICS 11(4):489-495 HECHT F; JACKY PB; SUTHERLAND GR THE FRAGILE X-CHROMOSOME - CURRENT METHODS | 16 | 35 |
| 406 | 1 | 14 | 112 1983 AMERICAN JOURNAL OF MEDICAL GENETICS 15(4):631-635 HOWARDPEEBLES PN; FINLEY WH SCREENING OF MENTALLY-RETARDED MALES FOR MACRO-ORCHIDISM AND THE FRAGILE-X CHROMOSOME | 16 | 22 |
| 407 | 7 | 21 | 161 1983 PRENATAL DIAGNOSIS 3(2):131-137 WEBB T; GOSDEN CM; RODECK CH; HAMILL MA; EASON PE PRENATAL-DIAGNOSIS OF X-LINKED MENTAL-RETARDATION WITH FRAGILE (X) USING FETOSCOPY AND FETAL BLOOD-SAMPLING | 16 | 32 |
| 408 | 5 | 29 | 300 1985 JOURNAL OF MEDICAL GENETICS 22(4):258-266 BUNDEY S; WEBB TP; THAKE A; TODD J A COMMUNITY STUDY OF SEVERE MENTAL-RETARDATION IN THE WEST MIDLANDS AND THE IMPORTANCE OF THE FRAGILE X-CHROMOSOME IN ITS ETIOLOGY | 16 | 32 |
| 409 | 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 |
| 410 | 14 | 23 | 387 1986 EXPERIMENTAL CELL BIOLOGY 54(1):40-48 JENKINS EC; BROWN WT; BROOKS J; DUNCAN CJ; SANZ MM; et al. LOW-FREQUENCIES OF APPARENTLY FRAGILE X-CHROMOSOMES IN NORMAL CONTROL CULTURES - A POSSIBLE EXPLANATION | 16 | 20 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 411 | 11 | 36 | 403 1986 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 25(5):641-644 WRIGHT HH; YOUNG SR; EDWARDS JG; ABRAMSON RK; DUNCAN J FRAGILE X-SYNDROME IN A POPULATION OF AUTISTIC-CHILDREN | 16 | 21 |
| 412 | 3 | 36 | 488 1987 NEUROPSYCHOLOGIA 25(6):881-891 GRIGSBY JP; KEMPER MB; HAGERMAN RJ DEVELOPMENTAL GERSTMANN SYNDROME WITHOUT APHASIA IN FRAGILE-X SYNDROME | 16 | 27 |
| 413 | 2 | 17 | 556 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(2):407-414 REISS AL; PATEL S; KUMAR AJ; FREUND L PRELIMINARY COMMUNICATION - NEUROANATOMICAL VARIATIONS OF THE POSTERIOR-FOSSA IN MEN WITH THE FRAGILE-X (MARTIN-BELL) SYNDROME | 16 | 38 |
| 414 | 7 | 32 | 791 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):260-268 BUTLER MG; ALLEN GA; HAYNES JL; SINGH DN; WATSON MS; et al. ANTHROPOMETRIC COMPARISON OF MENTALLY-RETARDED MALES WITH AND WITHOUT THE FRAGILE-X SYNDROME | 16 | 22 |
| 415 | 14 | 31 | 834 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 40(2):234-243 CIANCHETTI C; SANNIOFANCELLO G; FRATTA AL; MANCONI F; ORANO A; et al. NEUROPSYCHOLOGICAL, PSYCHIATRIC, AND PHYSICAL MANIFESTATIONS IN 149 MEMBERS FROM 18 FRAGILE-X FAMILIES | 16 | 19 |
| 416 | 9 | 25 | 896 1991 NUCLEIC ACIDS RESEARCH 19(12):3283-3288 HIRST MC; RACK K; NAKAHORI Y; ROCHE A; BELL MV; et al. A YAC CONTIG ACROSS THE FRAGILE X SITE DEFINES THE REGION OF FRAGILITY | 16 | 42 |
| 417 | 18 | 25 | 1240 1994 HUMAN GENETICS 94(5):523-526 VITS L; DEBOULLE K; REYNIERS E; HANDIG I; DARBY JK; et al. APPARENT REGRESSION OF THE CGG REPEAT IN FMR1 TO AN ALLELE OF NORMAL SIZE | 16 | 20 |
| 418 | 3 | 44 | 1403 1995 JOURNAL OF BIOLOGICAL CHEMISTRY 270(45):27014-27021 KANG SM; OHSHIMA K; SHIMIZU M; AMIRHAERI S; WELLS RD PAUSING OF DNA-SYNTHESIS IN-VITRO AT SPECIFIC LOCI IN CTG AND CGG TRIPLET REPEATS FROM HUMAN HEREDITARY-DISEASE GENES | 16 | 96 |
| 419 | 21 | 33 | 1654 1997 EUROPEAN JOURNAL OF HUMAN GENETICS 5(5):293-298 Bontekoe CJM; deGraaff E; Nieuwenhuizen IM; Willemsen R; Oostra BA FMR1 premutation allele (CGG)(81) is stable in mice | 16 | 18 |
| 420 | 89 | 136 | 1869 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 88(1):11-24 Kaufmann WE; Reiss AL Molecular and cellular genetics of fragile X syndrome | 16 | 28 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 421 | 10 | 41 | 2031 2000 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 30(1):49-59 Bailey DB; Hatton DD; Mesibov G; Ament N; Skinner M Early development, temperament, and functional impairment in autism and fragile X syndrome | 16 | 19 |
| 422 | 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 |
| 423 | 16 | 33 | 2163 2001 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 31(2):165-174 Bailey DB; Hatton DD; Skinner M; Mesibov G Autistic behavior, FMR1 protein, and developmental trajectories in young males with fragile X syndrome | 16 | 22 |
| 424 | 14 | 19 | 2178 2001 JOURNAL OF MEDICAL GENETICS 38(7):453-456 Tassone F; Hagerman RJ; Taylor AK; Hagerman PJ A majority of fragile X males with methylated, full mutation alleles have significant levels of FMR1 messenger RNA | 16 | 22 |
| 425 | 22 | 39 | 2591 2004 NATURE NEUROSCIENCE 7(2):113-117 Jin P; Zarnescu DC; Ceman S; Nakamoto M; Mowrey J; et al. Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway | 16 | 38 |
| 426 | 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 |
| 427 | 2 | 11 | 187 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):303-310 WANG JCC; ERBE RW FOLATE METABOLISM IN CELLS FROM FRAGILE-X SYNDROME PATIENTS AND CARRIERS | 15 | 22 |
| 428 | 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 |
| 429 | 5 | 17 | 295 1985 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 15(3):335-338 PUESCHEL SM; HERMAN R; GRODEN G SCREENING-CHILDREN WITH AUTISM FOR FRAGILE-X SYNDROME AND PHENYLKETONURIA | 15 | 25 |
| 430 | 4 | 11 | 352 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):589-595 SANFILIPPO S; RAGUSA RM; MUSUMECI S; NERI G FRAGILE-X MENTAL-RETARDATION - PREVALENCE IN A GROUP OF INSTITUTIONALIZED PATIENTS IN ITALY AND DESCRIPTION OF A NOVEL EEG PATTERN | 15 | 22 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 431 | 6 | 17 | 744 1991 AMERICAN JOURNAL OF HUMAN GENETICS 48(6):1051-1057 RICHARDS RI; SHEN Y; HOLMAN K; KOZMAN H; HYLAND VJ; et al. FRAGILE-X SYNDROME - DIAGNOSIS USING HIGHLY POLYMORPHIC MICROSATELLITE MARKERS | 15 | 40 |
| 432 | 6 | 9 | 1144 1993 LANCET 342(8878):1025-1026 WANG Q; GREEN E; BARNICOAT A; GARRETT D; MULLARKEY M; et al. CYTOGENETIC VERSUS DNA DIAGNOSIS IN ROUTINE REFERRALS FOR FRAGILE-X SYNDROME | 15 | 22 |
| 433 | 15 | 21 | 1201 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):466-470 HOFSTEE Y; ARINAMI T; HAMAGUCHI H COMPARISON BETWEEN THE CYTOGENETIC TEST FOR FRAGILE-X AND THE MOLECULAR ANALYSIS OF THE FMR-1 GENE IN JAPANESE MENTALLY-RETARDED INDIVIDUALS | 15 | 20 |
| 434 | 21 | 34 | 1238 1994 HUMAN GENETICS 94(4):395-400 MILA M; KRUYER H; GLOVER G; SANCHEZ A; CARBONELL P; et al. MOLECULAR ANALYSIS OF THE (CGG)(N) EXPANSION IN THE FMR-1 GENE IN 59 SPANISH FRAGILE-X SYNDROME FAMILIES | 15 | 16 |
| 435 | 13 | 19 | 1239 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 | 15 | 20 |
| 436 | 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 |
| 437 | 11 | 67 | 1420 1995 JOURNAL OF MOLECULAR BIOLOGY 254(4):638-656 KETTANI A; KUMAR RA; PATEL DJ SOLUTION STRUCTURE OF A DNA QUADRUPLEX CONTAINING THE FRAGILE-X SYNDROME TRIPLET REPEAT | 15 | 98 |
| 438 | 19 | 28 | 1471 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):261-265 Zhong N; Ju WN; Pietrofesa J; Wang DW; Dobkin C; et al. Fragile X ''gray zone'' alleles: AGG patterns, expansion risks, and associated haplotypes | 15 | 27 |
| 439 | 7 | 13 | 1474 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):274-277 Steyaert J; Borghgraef M; Legius E; Fryns JP Molecular-intelligence correlations in young fragile X males with a mild CGG repeat expansion in the FMR1 gene | 15 | 19 |
| 440 | 16 | 21 | 1489 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):365-369 Cohen IL; Nolin SL; Sudhalter V; Ding XH; Dobkin CS; et al. Mosaicism for the FMR1 gene influences adaptive skills development in fragile X-affected males | 15 | 16 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 441 | 22 | 25 | 1625 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 | 15 | 22 |
| 442 | 28 | 42 | 1712 1998 AMERICAN JOURNAL OF HUMAN GENETICS 63(3):776-785 Ashley-Koch AE; Robinson H; Glicksman AE; Nolin SL; Schwartz CE; et al. Examination of factors associated with instability of the FMR1 CGG repeat | 15 | 22 |
| 443 | 9 | 28 | 1936 2000 AMERICAN JOURNAL OF HUMAN GENETICS 66(2):413-418 Hundscheid RDL; Sistermans EA; Thomas CMG; Braat DDM; Straatman H; et al. Imprinting effect in premature ovarian failure confined to paternally inherited fragile X premutations | 15 | 31 |
| 444 | 22 | 33 | 1980 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 97(3):189-194 Sherman SL Premature ovarian failure in the fragile X syndrome | 15 | 30 |
| 445 | 32 | 45 | 2079 2000 MOLECULAR MEDICINE TODAY 6(5):193-198 Kooy RF; Willemsen R; Oostra BA Fragile X syndrome at the turn of the century | 15 | 21 |
| 446 | 10 | 28 | 2164 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 | 15 | 23 |
| 447 | 38 | 51 | 2258 2002 CURRENT OPINION IN GENETICS & DEVELOPMENT 12(3):278-283 Hagerman RJ; Hagerman PJ The fragile X premutation: into the phenotypic fold | 15 | 25 |
| 448 | 0 | 6 | 6 1980 AMERICAN JOURNAL OF MEDICAL GENETICS 7(4):503-505 KAISERMCCAW B; HECHT F; CADIEN JD; MOORE BC FRAGILE X-LINKED MENTAL-RETARDATION | 14 | 22 |
| 449 | 13 | 68 | 144 1983 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 4(2):122-130 HAGERMAN RJ; MCBOGG P; HAGERMAN PJ THE FRAGILE-X SYNDROME - HISTORY, DIAGNOSIS, AND TREATMENT | 14 | 18 |
| 450 | 8 | 31 | 146 1983 JOURNAL OF MEDICAL GENETICS 20(3):169-178 MCDERMOTT A; WALTERS R; HOWELL RT; GARDNER A FRAGILE X-CHROMOSOME - CLINICAL AND CYTOGENETIC STUDIES ON CASES FROM 7 FAMILIES | 14 | 18 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 451 | 1 | 9 | 153 1983 LANCET 1(8335):1221-1222 RUDELLI RD; JENKINS EC; WISNIEWSKI K; MORETZ R; BYRNE J; et al. TESTICULAR SIZE IN FETAL FRAGILE X SYNDROME | 14 | 19 |
| 452 | 6 | 24 | 237 1984 SOMATIC CELL AND MOLECULAR GENETICS 10(4):409-413 WARREN ST; DAVIDSON RL EXPRESSION OF FRAGILE X-CHROMOSOME IN HUMAN RODENT SOMATIC-CELL HYBRIDS | 14 | 19 |
| 453 | 9 | 23 | 246 1985 AMERICAN JOURNAL OF HUMAN GENETICS 37(5):956-964 HOWARDPEEBLES PN; FRIEDMAN JM UNAFFECTED CARRIER MALES IN FAMILIES WITH FRAGILE-X SYNDROME | 14 | 19 |
| 454 | 2 | 10 | 308 1985 LANCET 1(8433):871-871 OBERLE I; MANDEL JL; BOUE J; MATTEI MG; MATTEI JF POLYMORPHIC DNA MARKERS IN PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME | 14 | 27 |
| 455 | 2 | 6 | 353 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):611-617 JACOBS PA; SHERMAN S; TURNER G; WEBB T THE FRAGILE(X) SYNDROME - THE MUTATION PROBLEM | 14 | 19 |
| 456 | 6 | 21 | 400 1986 JOURNAL OF MENTAL DEFICIENCY RESEARCH 30:27-39 GILLBERG C; PERSSON E; WAHLSTROM J THE AUTISM-FRAGILE-X SYNDROME (AFRAX) - A POPULATION-BASED STUDY OF 10 BOYS | 14 | 25 |
| 457 | 17 | 38 | 473 1987 JOURNAL OF MEDICAL GENETICS 24(1):23-31 VEENEMA H; GERAEDTS JPM; BEVERSTOCK GC; PEARSON PL THE FRAGILE X-SYNDROME IN A LARGE FAMILY .1. CYTOGENETIC AND CLINICAL INVESTIGATIONS | 14 | 21 |
| 458 | 4 | 9 | 517 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):109-113 FRYNS JP; VANDENBERGHE H THE CONCURRENCE OF KLINEFELTER SYNDROME AND FRAGILE-X SYNDROME | 14 | 17 |
| 459 | 24 | 44 | 700 1990 CLINICAL GENETICS 37(1):2-11 SUTHERLAND GR; MULLEY JC DIAGNOSTIC MOLECULAR-GENETICS OF THE FRAGILE-X | 14 | 16 |
| 460 | 7 | 15 | 829 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):503-504 CRONISTER A; HAGERMAN RJ; WITTENBERGER M; AMIRI K MENTAL IMPAIRMENT IN CYTOGENETICALLY POSITIVE FRAGILE-X FEMALES | 14 | 15 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 461 | 13 | 22 | 944 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):244-254 SNOW K; DOUD L; HAGERMAN R; HULL C; HIRST MC; et al. ANALYSIS OF MUTATIONS AT THE FRAGILE-X LOCUS USING THE DNA PROBE OX1.9 | 14 | 16 |
| 462 | 15 | 17 | 946 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):268-278 MALMGREN H; STEENBONDESON ML; GUSTAVSON KH; SEEMANOVA E; HOLMGREN G; et al. METHYLATION AND MUTATION PATTERNS IN THE FRAGILE-X SYNDROME | 14 | 17 |
| 463 | 5 | 22 | 969 1992 ANNALS OF NEUROLOGY 31(1):22-26 BERRYKRAVIS E; HUTTENLOCHER PR CYCLIC-AMP METABOLISM IN FRAGILE-X SYNDROME | 14 | 19 |
| 464 | 22 | 51 | 1138 1993 JOURNAL OF PEDIATRICS 122(2):169-185 TARLETON JC; SAUL RA MOLECULAR GENETIC ADVANCES IN FRAGILE X-SYNDROME | 14 | 28 |
| 465 | 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 |
| 466 | 19 | 37 | 1367 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):280-292 Sobesky WE; Porter D; Pennington BF; Hagerman RJ Dimensions of shyness in fragile X females | 14 | 19 |
| 467 | 23 | 45 | 1465 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):220-225 Eichler EE; Nelson DL Genetic variation and evolutionary stability of the FMR1 CGG repeat in six closed human populations | 14 | 18 |
| 468 | 29 | 43 | 1466 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):226-233 Zhong N; Kajanoja E; Smits B; Pietrofesa J; Curley D; et al. Fragile X founder effects and new mutations in Finland | 14 | 26 |
| 469 | 22 | 31 | 1486 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):350-355 WrightTalamante C; Cheema A; Riddle JE; Luckey DW; Taylor AK; et al. A controlled study of longitudinal IQ changes in females and males with fragile X syndrome | 14 | 16 |
| 470 | 19 | 44 | 1553 1996 JOURNAL OF MOLECULAR BIOLOGY 258(4):614-626 Shimizu M; Gellibolian R; Oostra BA; Wells RD Cloning, characterization and properties of plasmids containing CGG triplet repeats from the FMR-1 gene | 14 | 49 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 471 | 17 | 64 | 1661 1997 HUMAN GENETICS 100(3-4):407-414 Lavedan CN; Garrett L; Nussbaum RL Trinucleotide repeats (CGG)(22)TGG(CGG)(43)TGG(CGG)(21) from the fragile X gene remain stable in transgenic mice | 14 | 19 |
| 472 | 20 | 35 | 1752 1998 HUMAN MOLECULAR GENETICS 7(12):1935-1946 Gunter C; Paradee W; Crawford DC; Meadows KA; Newman J; et al. Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1 | 14 | 26 |
| 473 | 11 | 27 | 1861 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):300-303 Uzielli MLG; Guarducci S; Lapi E; Cecconi A; Ricci U; et al. 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 | 14 | 26 |
| 474 | 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 |
| 475 | 15 | 30 | 1881 1999 CORTEX 35(2):263-271 Cornish KM; Munir F; Cross G Spatial cognition in males with Fragile-X syndrome: Evidence for a neuropsychological phenotype | 14 | 16 |
| 476 | 23 | 53 | 2318 2002 MOLECULAR AND CELLULAR BIOLOGY 22(24):8438-8447 Siomi MC; Higashijima K; Ishizuka A; Siomi H Casein kinase II phosphorylates the fragile X mental retardation protein and modulates its biological properties | 14 | 16 |
| 477 | 3 | 44 | 223 1984 JOURNAL OF SPEECH AND HEARING DISORDERS 49(3):328-332 PAUL R; COHEN DJ; BREG WR; WATSON M; HERMAN S FRAGILE-X SYNDROME - ITS RELATIONS TO SPEECH AND LANGUAGE DISORDERS | 13 | 17 |
| 478 | 7 | 15 | 302 1985 JOURNAL OF NEUROGENETICS 2(3):231-237 FORSTERGIBSON CJ; MULLIGAN LM; PARTINGTON MW; SIMPSON NE; HOLDEN JJA; et al. THE GENETIC-DISTANCE BETWEEN THE COAGULATION FACTOR-IX GENE AND THE LOCUS FOR THE FRAGILE-X SYNDROME - CLINICAL IMPLICATIONS | 13 | 23 |
| 479 | 1 | 3 | 350 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):567-572 JACOBS PA; MAYER M; ABRUZZO MA STUDIES OF THE FRAGILE (X) SYNDROME IN POPULATIONS OF MENTALLY-RETARDED INDIVIDUALS IN HAWAII | 13 | 16 |
| 480 | 9 | 16 | 391 1986 HUMAN GENETICS 74(1):93-97 WINTER RM; PEMBREY ME ANALYSIS OF LINKAGE RELATIONSHIPS BETWEEN GENETIC-MARKERS AROUND THE FRAGILE X LOCUS WITH SPECIAL REFERENCE TO THE DAUGHTERS OF NORMAL TRANSMITTING MALES | 13 | 17 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 481 | 10 | 20 | 424 1987 AMERICAN JOURNAL OF MENTAL DEFICIENCY 91(5):445-449 ROGERS RC; SIMENSEN RJ FRAGILE-X SYNDROME - A COMMON ETIOLOGY OF MENTAL-RETARDATION | 13 | 19 |
| 482 | 17 | 44 | 499 1988 AMERICAN JOURNAL OF DISEASES OF CHILDREN 142(11):1216-1221 HAGERMAN R; BERRY R; JACKSON AW; CAMPBELL J; SMITH ACM; et al. INSTITUTIONAL SCREENING FOR THE FRAGILE-X SYNDROME | 13 | 22 |
| 483 | 5 | 13 | 545 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):567-580 MULLEY J; TURNER G; BAIN S; SUTHERLAND GR LINKAGE BETWEEN THE FRAGILE-X AND F9, DXS52 (ST14), DXS98 (4D-8) AND DXS105 (CX55.7) | 13 | 20 |
| 484 | 2 | 10 | 562 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):779-781 BUTLER MG; NAJJAR JL DO SOME PATIENTS WITH FRAGILE-X SYNDROME HAVE PRECOCIOUS PUBERTY | 13 | 15 |
| 485 | 19 | 40 | 589 1988 HUMAN GENETICS 79(3):219-227 THIBODEAU SN; DORKINS HR; FAULK KR; BERRY R; SMITH ACM; et al. LINKAGE ANALYSIS USING MULTIPLE DNA POLYMORPHIC MARKERS IN NORMAL-FAMILIES AND IN FAMILIES WITH FRAGILE-X SYNDROME | 13 | 23 |
| 486 | 10 | 14 | 624 1989 AMERICAN JOURNAL OF MEDICAL GENETICS 34(2):302-303 COHEN IL; BROWN WT; JENKINS EC; KRAWCZUN MS; FRENCH JH; et al. FRAGILE-X SYNDROME IN FEMALES WITH AUTISM | 13 | 16 |
| 487 | 0 | 0 | 645 1989 GENOMICS 5(4):797-801 VINCENT A; DAHL N; OBERLE I; HANAUER A; MANDEL JL; et al. THE POLYMORPHIC MARKER DXS304 IS WITHIN 5-CENTIMORGANS OF THE FRAGILE-X LOCUS | 13 | 23 |
| 488 | 9 | 34 | 825 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):481-487 FISCH GS; ARINAMI T; FROSTERISKENIUS U; FRYNS JP; CURFS LM; et al. RELATIONSHIP BETWEEN AGE AND IQ AMONG FRAGILE-X MALES - A MULTICENTER STUDY | 13 | 14 |
| 489 | 26 | 44 | 1027 1992 TRENDS IN GENETICS 8(7):249-255 RICHARDS RI; SUTHERLAND GR FRAGILE X-SYNDROME - THE MOLECULAR PICTURE COMES INTO FOCUS | 13 | 39 |
| 490 | 14 | 36 | 1182 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):358-363 HAY DA DOES IQ DECLINE WITH AGE IN FRAGILE-X A METHODOLOGICAL CRITIQUE | 13 | 14 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 491 | 13 | 26 | 1183 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 | 13 | 20 |
| 492 | 12 | 13 | 1207 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):497-500 SMITS A; SMEETS D; HAMEL B; DREESEN J; DEHAAN A; et al. PREDICTION OF MENTAL STATUS IN CARRIERS OF THE FRAGILE-X MUTATION USING CGG REPEAT LENGTH | 13 | 16 |
| 493 | 14 | 31 | 1280 1994 PEDIATRICS 93(6):992-995 LACHIEWICZ AM; DAWSON DV DO YOUNG BOYS WITH FRAGILE-X-SYNDROME HAVE MACROORCHIDISM | 13 | 17 |
| 494 | 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 |
| 495 | 10 | 12 | 1458 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):181-183 Spence WC; Black SH; Fallon L; Maddalena A; Cummings E; et al. Molecular fragile X screening in normal populations | 13 | 18 |
| 496 | 18 | 21 | 1470 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):256-260 Sherman SL; Meadows KL; Ashley AE Examination of factors that influence the expansion of the fragile X mutation in a sample of conceptuses from known carrier females | 13 | 16 |
| 497 | 18 | 21 | 1480 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):309-312 Maddalena A; Yadvish KN; Spence WC; HowardPeebles PN A fragile X mosaic male with a cryptic full mutation detected in epithelium but not in blood | 13 | 16 |
| 498 | 16 | 25 | 1497 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):428-433 Meadows KL; Pettay D; Newman J; Hersey J; Ashley AE; et al. Survey of the fragile X syndrome and the fragile X E syndrome in a special education needs population | 13 | 27 |
| 499 | 30 | 43 | 1620 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(6):1362-1369 Kenneson A; Cramer DW; Warren ST Fragile X premutations are not a major cause of early menopause | 13 | 22 |
| 500 | 21 | 51 | 1674 1997 JOURNAL OF CLINICAL INVESTIGATION 100(2):331-338 Jakala P; Hanninen T; Ryynanen M; Laakso M; Partanen K; et al. Fragile-X: Neuropsychological test performance, CGG triplet repeat lengths, and hippocampal volumes | 13 | 21 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 501 | 14 | 23 | 1889 1999 EUROPEAN JOURNAL OF HUMAN GENETICS 7(2):212-216 Ryynanen M; Heinonen S; Makkonen M; Kajanoja E; Mannermaa A; et al. Feasibility and acceptance of screening for fragile X mutations in low-risk pregnancies | 13 | 18 |
| 502 | 12 | 46 | 1975 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(4):307-315 Gould EL; Loesch DZ; Martin MJ; Hagerman RJ; Armstrong SM; et al. Melatonin profiles and sleep characteristics in boys with fragile X syndrome: A preliminary study | 13 | 19 |
| 503 | 10 | 17 | 2089 2000 PRENATAL DIAGNOSIS 20(8):611-614 Pesso R; Berkenstadt H; Cuckle H; Gak E; Peleg L; et al. Screening for fragile X syndrome in women of reproductive age | 13 | 17 |
| 504 | 29 | 40 | 2094 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(2):351-360 Toledano-Alhadef H; Basel-Vanagaite L; Magal N; Davidov B; Ehrlich S; et al. Fragile-X carrier screening and the prevalence of premutation and full-mutation carriers in Israel | 13 | 22 |
| 505 | 18 | 34 | 2171 2001 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 22(6):409-417 Rogers SJ; Wehner EA; Hagerman R The behavioral phenotype in fragile X: Symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders | 13 | 24 |
| 506 | 5 | 37 | 2256 2002 CURRENT BIOLOGY 12(15):1331-1335 Inoue SB; Shimoda M; Nishinokubi I; Siomi MC; Okamura M; et al. A role for the Drosophila fragile X-related gene in circadian output | 13 | 17 |
| 507 | 32 | 39 | 2348 2003 AMERICAN JOURNAL OF HUMAN GENETICS 72(2):454-464 Nolin SL; Brown WT; Glicksman A; Houck GE; Gargano AD; et al. Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles | 13 | 21 |
| 508 | 4 | 23 | 63 1982 HUMAN GENETICS 61(2):113-117 NIELSEN KB; TOMMERUP N; DYGGVE HV; SCHOU C MACRO-ORCHIDISM AND FRAGILE-X IN MENTALLY-RETARDED MALES - CLINICAL, CYTOGENETIC, AND SOME HORMONAL INVESTIGATIONS IN MENTALLY-RETARDED MALES, INCLUDING 2 WITH THE FRAGILE SITE AT XQ28, FRA(X)(Q28) | 12 | 22 |
| 509 | 2 | 5 | 66 1982 HUMAN GENETICS 61(3):254-255 EBERLE G; ZANKL M; ZANKL H THE EXPRESSION OF FRAGILE X-CHROMOSOMES IN MEMBERS OF THE SAME FAMILY AT DIFFERENT TIMES OF EXAMINATION | 12 | 14 |
| 510 | 5 | 13 | 69 1982 HUMAN GENETICS 62(3):285-286 SCHMIDT A; PASSARGE E; SEEMANOVA E; MACEK M PRENATAL DETECTION OF A FETUS HEMIZYGOUS FOR THE FRAGILE X-CHROMOSOME | 12 | 18 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 511 | 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 |
| 512 | 5 | 25 | 150 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 |
| 513 | 5 | 19 | 166 1984 ACTA PSYCHIATRICA SCANDINAVICA 70(5):510-514 JORGENSEN OS; NIELSEN KB; ISAGER T; MOURIDSEN SE FRAGILE X-CHROMOSOME AMONG CHILD PSYCHIATRIC-PATIENTS WITH DISTURBANCES OF LANGUAGE AND SOCIAL RELATIONSHIPS - A PILOT-STUDY | 12 | 21 |
| 514 | 0 | 4 | 178 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):209-214 RHOADS FA FRAGILE-X SYNDROME IN HAWAII - A SUMMARY OF CLINICAL-EXPERIENCE | 12 | 21 |
| 515 | 4 | 13 | 190 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 18(3):483-491 DANIEL A; EKBLOM L; PHILLIPS S CONSTITUTIVE FRAGILE SITES 1P31, 3P14, 6Q26, AND 16Q23 AND THEIR USE AS CONTROLS FOR FALSE-NEGATIVE RESULTS WITH THE FRAGILE(X) | 12 | 50 |
| 516 | 6 | 13 | 399 1986 JOURNAL OF MEDICAL GENETICS 23(5):407-410 TUCKERMAN E; WEBB T; THAKE A REPLICATION STATUS OF FRAGILE X(Q27.3) IN 13 FEMALE HETEROZYGOTES | 12 | 16 |
| 517 | 11 | 25 | 484 1987 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 26(4):589-592 GOLDFINE PE; MCPHERSON PM; HARDESTY VA; HEATH GA; BEAUREGARD LJ; et al. FRAGILE-X CHROMOSOME ASSOCIATED WITH PRIMARY LEARNING-DISABILITY | 12 | 15 |
| 518 | 2 | 8 | 530 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):347-354 SHAPIRO LR; WILMOT PL; MURPHY PD; BREG WR EXPERIENCE WITH MULTIPLE APPROACHES TO THE PRENATAL-DIAGNOSIS OF THE FRAGILE-X SYNDROME - AMNIOTIC-FLUID, CHORIONIC VILLI, FETAL BLOOD AND MOLECULAR METHODS | 12 | 19 |
| 519 | 7 | 16 | 549 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):641-654 SCHWARTZ CE; PHELAN MC; PULLIAM LH; WILKES G; VANNER LV; et al. FRAGILE-X SYNDROME - INCIDENCE, CLINICAL AND CYTOGENETIC FINDINGS IN THE BLACK AND WHITE-POPULATIONS OF SOUTH-CAROLINA | 12 | 15 |
| 520 | 5 | 14 | 674 1990 AMERICAN JOURNAL OF HUMAN GENETICS 46(3):443-451 SVED JA; LAIRD CD POPULATION GENETIC CONSEQUENCES OF THE FRAGILE-X SYNDROME, BASED ON THE X-INACTIVATION IMPRINTING MODEL | 12 | 22 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 521 | 9 | 23 | 871 1991 JOURNAL OF ABNORMAL CHILD PSYCHOLOGY 19(3):253-262 EINFELD S; HALL W; LEVY F HYPERACTIVITY AND THE FRAGILE X SYNDROME | 12 | 13 |
| 522 | 9 | 27 | 915 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):28-34 FISCH GS; SHAPIRO LR; SIMENSEN R; SCHWARTZ CE; FRYNS JP; et al. LONGITUDINAL CHANGES IN IQ AMONG FRAGILE-X MALES - CLINICAL-EVIDENCE OF MORE THAN ONE MUTATION | 12 | 12 |
| 523 | 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 |
| 524 | 9 | 30 | 1187 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):386-391 EINFELD SL; TONGE BJ; FLORIO T BEHAVIORAL AND EMOTIONAL DISTURBANCE IN FRAGILE-X-SYNDROME | 12 | 23 |
| 525 | 2 | 44 | 1265 1994 JOURNAL OF MOLECULAR BIOLOGY 243(2):143-151 SMITH SS; LAAYOUN A; LINGEMAN RG; BAKER DJ; RILEY J HYPERMETHYLATION OF TELOMERE-LIKE FOLDBACKS AT CODON-12 OF THE HUMAN C-HA-RAS GENE AND THE TRINUCLEOTIDE REPEAT OF THE FMR-1 GENE OF FRAGILE-X | 12 | 55 |
| 526 | 16 | 33 | 1327 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 58(3):249-256 LOESCH DZ; HUGGINS RM; HOANG NH GROWTH IN STATURE IN FRAGILE-X FAMILIES - A MIXED LONGITUDINAL-STUDY | 12 | 14 |
| 527 | 40 | 75 | 1365 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):252-269 Cohen IL Behavioral profiles of autistic and nonautistic fragile X males | 12 | 13 |
| 528 | 8 | 35 | 1372 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):336-344 Hagerman RJ; Riddle JE; Roberts LS; Breese K; Fulton M Survey of the efficacy of clonidine in fragile X syndrome | 12 | 12 |
| 529 | 4 | 21 | 1443 1996 AMERICAN JOURNAL OF HUMAN GENETICS 58(5):906-913 Knight SJL; Ritchie RJ; Chakrabarti L; Cross G; Taylor GR; et al. A study of FRAXE in mentally retarded individuals referred for fragile X syndrome (FRAXA) testing in the United Kingdom | 12 | 41 |
| 530 | 29 | 43 | 1479 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):302-308 deGraaff E; deVries BBA; Willemsen R; vanHemel JO; Mohkamsing S; et al. The fragile X phenotype in a mosaic male with a deletion showing expression of the FMR1 protein in 28% of the cells | 12 | 13 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 531 | 5 | 27 | 1566 1996 NUCLEIC ACIDS RESEARCH 24(4):784-792 Mariappan SVS; Catasti P; Chen X; Ratliff R; Moyzis RK; et al. Solution structures of the individual single strands of the fragile X DNA triplets (GCC)(n)center dot(GGC)(n) | 12 | 49 |
| 532 | 18 | 64 | 1668 1997 HUMAN MOLECULAR GENETICS 6(11):1791-1801 Stoger R; Kajimura TM; Brown WT; Laird CD Epigenetic variation illustrated by DNA methylation patterns of the fragile-X gene FMR1 | 12 | 38 |
| 533 | 13 | 42 | 1759 1998 JOURNAL OF APPLIED RESEARCH IN INTELLECTUAL DISABILITIES 11(3):175-191 Turk J Fragile X syndrome and attentional deficits | 12 | 17 |
| 534 | 17 | 41 | 1774 1998 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 42:490-499 Turk J; Cornish K Face recognition and emotion perception in boys with fragile-X syndrome | 12 | 18 |
| 535 | 17 | 36 | 1791 1998 NEUROPSYCHOLOGIA 36(11):1239-1246 Cornish KM; Munir F; Cross G The nature of the spatial deficit in young females with Fragile-X syndrome: A neuropsychological and molecular perspective | 12 | 16 |
| 536 | 6 | 11 | 1792 1998 NEUROREPORT 9(3):477-481 Steward O; Bakker CE; Willems PJ; Oostra BA No evidence for disruption of normal patterns of mRNA localization in dendrites or dendritic transport of recently synthesized mRNA in FMR1 knockout mice, a model for human fragile-X mental retardation syndrome | 12 | 18 |
| 537 | 13 | 41 | 1835 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):313-317 Hagerman RJ; Hills J; Scharfenaker S; Lewis H Fragile X syndrome and selective mutism | 12 | 19 |
| 538 | 24 | 74 | 1926 1999 MOLECULAR AND CELLULAR BIOLOGY 19(8):5675-5684 White PJ; Borts RH; Hirst MC Stability of the human fragile X (CGG)(n) triplet repeat array in Saccharomyces cerevisiae deficient in aspects of DNA metabolism | 12 | 45 |
| 539 | 27 | 42 | 1967 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 92(4):229-236 Lachiewicz AM; Dawson DV; Spiridigliozzi GA Physical characteristics of young boys with fragile X syndrome: Reasons for difficulties in making a diagnosis in young males | 12 | 13 |
| 540 | 76 | 116 | 1978 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 97(2):153-163 Bardoni B; Mandel JL; Fisch GS FMR1 gene and fragile X syndrome | 12 | 21 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 541 | 6 | 32 | 2039 2000 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 21(5):315-321 Bailey DB; Skinner D; Hatton D; Roberts J Family experiences and factors associated with the diagnosis of fragile X syndrome | 12 | 15 |
| 542 | 29 | 45 | 2158 2001 HUMAN MOLECULAR GENETICS 10(16):1693-1699 Bontekoe CJM; Bakker CE; Nieuwenhuizen IM; van der Linde H; Lans H; et al. Instability of a (CGG)(98) repeat in the Fmr1 promoter | 12 | 15 |
| 543 | 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 |
| 544 | 21 | 53 | 2432 2003 HUMAN MOLECULAR GENETICS 12(24):3295-3305 Ceman S; O'Donnell WT; Reed M; Patton S; Pohl J; et al. Phosphorylation influences the translation state of FMRP-associated polyribosomes | 12 | 15 |
| 545 | 1 | 7 | 84 1982 PEDIATRICS 69(5):668-669 RHOADS FA X-LINKED MENTAL-RETARDATION AND FRAGILE-X OR MARKER-X SYNDROME | 11 | 12 |
| 546 | 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 |
| 547 | 9 | 27 | 450 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 |
| 548 | 4 | 7 | 455 1987 HUMAN GENETICS 75(3):269-271 WINTER RM POPULATION-GENETICS IMPLICATIONS OF THE PREMUTATION HYPOTHESIS FOR THE GENERATION OF THE FRAGILE X-MENTAL RETARDATION GENE | 11 | 12 |
| 549 | 8 | 22 | 543 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):543-550 HEILIG R; OBERLE I; ARVEILER B; HANAUER A; VIDAUD M; et al. IMPROVED DNA MARKERS FOR EFFICIENT ANALYSIS OF FRAGILE-X FAMILIES | 11 | 33 |
| 550 | 5 | 12 | 559 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):753-765 SHERMAN SL; ROGATKO A; TURNER G RECURRENCE RISKS FOR RELATIVES IN FAMILIES WITH AN ISOLATED CASE OF THE FRAGILE X SYNDROME | 11 | 15 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 551 | 12 | 33 | 676 1990 AMERICAN JOURNAL OF HUMAN GENETICS 46(4):738-743 ROCCHI M; ARCHIDIACONO N; RINALDI A; FILIPPI G; BARTOLUCCI G; et al. MENTAL-RETARDATION IN HETEROZYGOTES FOR THE FRAGILE-X MUTATION - EVIDENCE IN FAVOR OF AN X INACTIVATION-DEPENDENT EFFECT | 11 | 13 |
| 552 | 5 | 23 | 1074 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 45(1):81-87 BERRYKRAVIS E; SKLENA P DEMONSTRATION OF ABNORMAL CYCLIC-AMP PRODUCTION IN PLATELETS FROM PATIENTS WITH FRAGILE-X SYNDROME | 11 | 14 |
| 553 | 20 | 26 | 1092 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 | 11 | 13 |
| 554 | 25 | 50 | 1125 1993 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 34(5):673-688 BAILEY A; BOLTON P; BUTLER L; LECOUTEUR A; MURPHY M; et al. PREVALENCE OF THE FRAGILE-X ANOMALY AMONGST AUTISTIC TWINS AND SINGLETONS | 11 | 50 |
| 555 | 16 | 34 | 1180 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):346-352 FISCH GS; HOLDEN JJA; SIMENSEN R; CARPENTER N; HOWARDPEEBLES PN; et al. FRAGILE-X-SYNDROME A PERVASIVE DEVELOPMENTAL DISABILITY - COGNITIVE-ABILITY AND ADAPTIVE-BEHAVIOR IN MATES WITH THE FULL MUTATION | 11 | 12 |
| 556 | 9 | 21 | 1210 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):513-516 DEELEN W; BAKKER C; HALLEY DJJ; OOSTRA BA CONSERVATION OF CGG REGION IN FMR1 GENE IN MAMMALS | 11 | 16 |
| 557 | 15 | 40 | 1426 1995 NATURE GENETICS 11(3):301-308 EICHLER EE; KUNST CB; LUGENBEEL KA; RYDER OA; DAVISON D; et al. EVOLUTION OF THE CRYPTIC FMR1 CGG REPEAT | 11 | 18 |
| 558 | 5 | 21 | 1472 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):266-267 Wohrle D; Schwemmle S; Steinbach P DNA methylation and triplet repeat stability: New proposals addressing actual questions on the CGG repeat of fragile X syndrome | 11 | 18 |
| 559 | 23 | 35 | 1476 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):287-292 Brown WT; Houck GE; Ding XH; Zhong N; Nolin S; et al. Reverse mutations in the fragile X syndrome | 11 | 18 |
| 560 | 8 | 43 | 1546 1996 JOURNAL OF BIOLOGICAL CHEMISTRY 271(8):4327-4334 Deissler H; BehnKrappa A; Doerfler W Purification of nuclear proteins from human HeLa cells that bind specifically to the unstable tandem repeat (CGG), in the human FMR1 gene | 11 | 24 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 561 | 10 | 13 | 1550 1996 JOURNAL OF MEDICAL GENETICS 33(4):338-340 Mila M; CastellviBel S; Sanchez A; Lazaro C; Villa M; et al. Mosaicism for the fragile X syndrome full mutation and deletions within the CGG repeat of the FMR1 gene | 11 | 16 |
| 562 | 12 | 14 | 1556 1996 JOURNAL OF PEDIATRICS 129(4):611-614 Giangreco CA; Steele MW; Aston CE; Cummins JH; Wenger SL A simplified six-item checklist for screening for fragile X syndrome in the pediatric population | 11 | 22 |
| 563 | 3 | 4 | 1559 1996 LANCET 348(9032):967-968 Willemsen R; Oosterwijk JC; Los FJ; Galjaard H; Oostra BA Prenatal diagnosis of fragile X syndrome | 11 | 16 |
| 564 | 12 | 36 | 1763 1998 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 28(6):509-517 Mazzocco MMM; Baumgardner T; Freund LS; Reiss AL Social functioning among girls with fragile X or Turner syndrome and their sisters | 11 | 15 |
| 565 | 3 | 6 | 1837 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):322-325 Allingham-Hawkins SJ; Babul-Hirji R; Chitayat D; Holden JJA; Yang KT; et al. Fragile X premutation is a significant risk factor for premature ovarian failure: The international collaborative POF in fragile X study - Preliminary data | 11 | 19 |
| 566 | 11 | 41 | 1907 1999 JOURNAL OF BIOLOGICAL CHEMISTRY 274(18):12797-12802 Fry M; Loeb LA Human Werner syndrome DNA helicase unwinds tetrahelical structures of the fragile X syndrome repeat sequence d(CGG)(n) | 11 | 104 |
| 567 | 9 | 21 | 2007 2000 EUROPEAN JOURNAL OF HUMAN GENETICS 8(4):247-252 Murray A; Ennis S; MacSwiney F; Webb J; Morton NE Reproductive and menstrual history of females with fragile X expansions | 11 | 15 |
| 568 | 9 | 29 | 2033 2000 JOURNAL OF BIOLOGICAL CHEMISTRY 275(9):6447-6452 Muller-Hartmann H; Deissler H; Naumann F; Schmitz B; Schroer J; et al. The human 20-kDa 5 '-(CGG)(n)-3 '-binding protein is targeted to the nucleus and affects the activity of the FMR1 promoter | 11 | 16 |
| 569 | 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 |
| 570 | 13 | 28 | 2239 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 111(2):140-146 Irwin SA; Idupulapati M; Gilbert ME; Harris JB; Chakravarti AB; et al. Dendritic spine and dendritic field characteristics of layer V pyramidal neurons in the visual cortex of fragile-X knockout mice | 11 | 14 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 571 | 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 |
| 572 | 28 | 41 | 2344 2002 RNA-A PUBLICATION OF THE RNA SOCIETY 8(12):1482-1488 Primerano B; Tassone F; Hagerman RJ; Hagerman P; Amaldi F; et al. Reduced FMR1 mRNA translation efficiency in Fragile X patients with premutations | 11 | 14 |
| 573 | 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 |
| 574 | 20 | 56 | 2428 2003 HUMAN MOLECULAR GENETICS 12(9):949-959 Willemsen R; Hoogeveen-Westerveld M; Reis S; Holstege J; Severijnen LAWFM; et al. The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome | 11 | 19 |
| 575 | 13 | 26 | 2461 2003 NEURON 37(4):555-558 Antar LN; Bassell GJ Sunrise at the synapse: The FMRP mRNP shaping the synaptic interface | 11 | 25 |
| 576 | 22 | 64 | 2463 2003 NEURON 38(6):887-898 Schenck A; Bardoni B; Langmann C; Harden N; Mandel JL; et al. CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein | 11 | 23 |
| 577 | 0 | 4 | 79 1982 LANCET 1(8263):101-101 GARDNER AP; HOWELL RT; MCDERMOTT A FRAGILE-X CHROMOSOME - CONSISTENT DEMONSTRATION OF FRAGILE SITE IN FIBROBLAST-CULTURES | 10 | 14 |
| 578 | 3 | 25 | 177 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 |
| 579 | 5 | 25 | 213 1984 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 14(2):197-204 AUGUST GJ; LOCKHART LH FAMILIAL AUTISM AND THE FRAGILE-X-CHROMOSOME | 10 | 21 |
| 580 | 0 | 4 | 221 1984 JOURNAL OF MEDICAL GENETICS 21(5):373-373 FITCHETT M; SEABRIGHT M DELETED X-CHROMOSOMES IN PATIENTS WITH THE FRAGILE X-SYNDROME | 10 | 14 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 581 | 14 | 34 | 254 1985 AMERICAN JOURNAL OF MENTAL DEFICIENCY 90(2):119-123 DELACRUZ FF FRAGILE-X SYNDROME | 10 | 13 |
| 582 | 6 | 18 | 266 1985 CLINICAL GENETICS 27(5):463-467 GUSTAVSON KH; DAHLBOM K; FLOOD A; HOLMGREN G; BLOMQUIST HK; et al. EFFECT OF FOLIC-ACID TREATMENT IN THE FRAGILE X-SYNDROME | 10 | 14 |
| 583 | 6 | 28 | 296 1985 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 6(2):87-90 VARLEY CK; HOLM VA; EREN MO COGNITIVE AND PSYCHIATRIC VARIABILITY IN 3 BROTHERS WITH FRAGILE X-SYNDROME | 10 | 13 |
| 584 | 2 | 17 | 328 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):227-239 BERKOVITZ GD; WILSON DP; CARPENTER NJ; BROWN TR; MIGEON CJ GONADAL-FUNCTION IN MEN WITH THE MARTIN-BELL (FRAGILE-X) SYNDROME | 10 | 14 |
| 585 | 9 | 27 | 331 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):273-289 FROSTERISKENIUS U; BODEKER K; OEPEN T; MATTHES R; PIPER U; et al. FOLIC-ACID TREATMENT IN MALES AND FEMALES WITH FRAGILE-(X)-SYNDROME | 10 | 15 |
| 586 | 7 | 13 | 341 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):429-443 LEDBETTER DH; AIRHART SD; NUSSBAUM RL SOMATIC-CELL HYBRID STUDIES OF FRAGILE-(X) EXPRESSION IN A CARRIER FEMALE AND TRANSMITTING MALE | 10 | 18 |
| 587 | 3 | 23 | 355 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):685-699 HOEGERMAN SF; RARY JM SPECULATION ON THE ROLE OF TRANSPOSABLE ELEMENTS IN HUMAN GENETIC-DISEASE WITH PARTICULAR ATTENTION TO ACHONDROPLASIA AND THE FRAGILE-X SYNDROME | 10 | 19 |
| 588 | 11 | 29 | 356 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):701-713 FRIEDMAN JM; HOWARDPEEBLES PN INHERITANCE OF FRAGILE-X SYNDROME - AN HYPOTHESIS | 10 | 16 |
| 589 | 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 |
| 590 | 8 | 31 | 502 1988 AMERICAN JOURNAL OF HUMAN GENETICS 43(5):684-688 PATTERSON M; BELL M; KRESS W; DAVIES KE; FROSTERISKENIUS U LINKAGE STUDIES IN A LARGE FRAGILE X-FAMILY | 10 | 23 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 591 | 6 | 10 | 551 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):665-672 NERI G; SANFILIPPO S; PAVONE L; MOLLICA F; BARBERI I; et al. THE FRAGILE-X IN SICILY - AN EPIDEMIOLOGICAL SURVEY | 10 | 16 |
| 592 | 8 | 12 | 552 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):673-679 HOLMGREN G; BLOMQUIST HK; DRUGGE U; GUSTAVSON KH FRAGILE-X FAMILIES IN A NORTHERN SWEDISH COUNTY - A GENEALOGICAL STUDY DEMONSTRATING APPARENT PATERNAL TRANSMISSION FROM THE 18TH-CENTURY | 10 | 10 |
| 593 | 9 | 19 | 649 1989 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 19(2):343-347 HO HH; KALOUSEK DK BRIEF REPORT - FRAGILE X-SYNDROME IN AUTISTIC BOYS | 10 | 14 |
| 594 | 6 | 17 | 686 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 37(2):265-267 MOORE PSJ; CHUDLEY AE; WINTER JSD TRUE PRECOCIOUS PUBERTY IN A GIRL WITH THE FRAGILE X-SYNDROME | 10 | 13 |
| 595 | 13 | 21 | 942 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):217-223 KNIGHT SJL; HIRST MC; ROCHE A; CHRISTODOULOU Z; HUSON SM; et al. MOLECULAR STUDIES OF THE FRAGILE-X SYNDROME | 10 | 19 |
| 596 | 6 | 7 | 1139 1993 LANCET 341(8841):373-374 PALOMAKI GE; HADDOW JE IS IT TIME FOR POPULATION-BASED PRENATAL SCREENING FOR FRAGILE-X | 10 | 13 |
| 597 | 2 | 3 | 1140 1993 LANCET 341(8847):769-770 BONTHRON D; STRAIN L POPULATION SCREENING FOR FRAGILE-X SYNDROME | 10 | 11 |
| 598 | 8 | 22 | 1173 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):294-297 ALBRIGHT SG; LACHIEWICZ AM; TARLETON JC; RAO KW; SCHWARTZ CE; et al. FRAGILE-X PHENOTYPE IN A PATIENT WITH A LARGE DE-NOVO DELETION IN XQ27-Q28 | 10 | 17 |
| 599 | 19 | 28 | 1237 1994 HUMAN GENETICS 93(2):143-147 VAISANEN ML; KAHKONEN M; LEISTI J DIAGNOSIS OF FRAGILE-X SYNDROME BY DIRECT MUTATION ANALYSIS | 10 | 12 |
| 600 | 2 | 43 | 1402 1995 JOURNAL OF BIOLOGICAL CHEMISTRY 270(39):23090-23096 CHEN FM ACID-FACILITATED SUPRAMOLECULAR ASSEMBLY OF G-QUADRUPLEXES IN D(CGG)(4) | 10 | 37 |