HistCite - index: Fragile X

Tue Aug 24 10:42:22 2004

All papers with "Fragile X" in the title.

Nodes: 2369
Authors: 4634, Journals: 373, Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by GCS.
Page 14: 1 (1246) 2 (77) 3 (47) 4 (34) 5 (25) 6 (19) 7 (14) 8 (11) 9 (9) 10 (7) 11 (5) 12 (4) 13 (3) 14 (2) 15 (1) 16 (1) 17 (0) 18 (0) 19 (0) 20 (0) 21 (0) 22 (0) 23 (0) 24 (0)

# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1301 1 4 298 1985 JOURNAL OF MEDICAL GENETICS 22(5):397-397
WINTER RM; PEMBREY ME; DAVIES KE
ANALYSIS OF LINKAGE DATA WITH FACTOR-IX CORROBORATES THE HYPOTHESIS THAT A PREMUTATION, FOLLOWED BY A RECOMBINATION EVENT, GENERATES THE FULL MUTATION IN FRAGILE X-LINKED MENTAL-RETARDATION
2 2
1302 1 4 313 1986 AMERICAN JOURNAL OF DISEASES OF CHILDREN 140(4):327-327
BOWERS EJ
FRAGILE-X SYNDROME AND LEARNING-DISABILITIES
1 2
1303 3 5 373 1986 CLINICAL GENETICS 29(2):95-95
DEARCE MA; HECHT F; SUTHERLAND GR; WEBB GC
GUIDELINES FOR THE DIAGNOSIS OF FRAGILE X
0 2
1304 0 0 405 1986 PEDIATRIC RESEARCH 20(4):A269-A269
MURPHY PD; WATSON MS; KIDD KK; BREG WR
MOLECULAR APPROACHES TO CARRIER DETECTION AND PRENATAL-DIAGNOSIS OF THE FRAGILE-X SYNDROME (MCKUSICK NUMBER 30920)
1 2
1305 1 4 412 1987 AMERICAN JOURNAL OF DISEASES OF CHILDREN 141(6):601-601
BARTOLUCCI G; SZATMARI P
POSSIBLE SIMILARITIES BETWEEN THE FRAGILE-X AND ASPERGERS SYNDROMES
1 2
1306 17 31 431 1987 BRITISH MEDICAL JOURNAL 295(6598):564-565
KINNELL HG
FRAGILE X-SYNDROME - AN IMPORTANT PREVENTABLE CAUSE OF MENTAL HANDICAP
2 2
1307 1 22 438 1987 COLLEGIUM ANTROPOLOGICUM 11(2):305-316
LOESCH DZ
FACTOR-ANALYSIS OF RIDGE-PATTERNS AND HAND MEASUREMENTS IN NORMAL AND FRAGILE-X MALES
0 2
1308 0 0 442 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):598-598
CONNOR JM; OSMAN H; STEFANI L; NEVIN NC; HOFKER M
LINKAGE ANALYSIS IN FAMILIES WITH THE FRAGILE-X SYNDROME USING CX55-7 (DXS105)
0 2
1309 0 0 444 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):688-689
SCHWARTZ C; PATTERSON M; DAVIES K; TRUNCA C; TRASK B; PHELAN MC
THE USE OF DISTAL DELETIONS OF XQ TO ORDER LOCI BETWEEN FACTOR-IX AND THE FRAGILE-X SITE (XQ27.3)
1 2
1310 0 0 494 1987 TERATOLOGY 36(3):453-453
SUZUKI Y; CHYO H; MATSUI A; SHIMOMURA C; FUNAHASI M
CLINICAL-DIAGNOSIS OF FRAGILE-X SYNDROME
1 2
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1311 6 11 518 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):177-183
MILONE G; CONTI L; RIZZO R; SANFILIPPO S; SAMMITO V; ROMANO C
A DERMATOGLYPHIC STUDY OF A GROUP OF SICILIAN CHILDREN WITH FRAGILE-X SYNDROME
1 2
1312 2 8 523 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):231-236
SUTHERS GK; TURNER G; MULLEY JC
CASE-REPORT - FRAGILE-X SYNDROME AND NEPHROGENIC DIABETES-INSIPIDUS
1 2
1313 1 7 535 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):443-450
NOLIN SL; JENKINS EC; BROWN WT; DOBKIN CS
INSITU NICK TRANSLATION OF THE FRAGILE-X REGION
1 2
1314 2 13 579 1988 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 30(5):646-649
CAMMARATA S; ARCHIDIACONO N; ROMEO G; BENASSI G; GUARINO M; DALESSANDRO R
PREVALENCE OF MENTAL-RETARDATION RELATED TO FRAGILE X SYNDROME AND OTHER CHROMOSOMAL-ABNORMALITIES IN THE REPUBLIC OF SAN MARINO
0 2
1315 3 5 584 1988 HUMAN GENETICS 78(4):383-383
BUTLER MG; JOSEPH GM; RAMES LJ; CACHEIRO N; LOZZIO CB
CHROMOSOME BREAKAGE IN CONTROL AND FRAGILE-X SUBJECTS USING FOLATE-DEFICIENT CULTURE CONDITIONS
2 2
1316 0 1 638 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):1100-1101
WAHLSTROM J; WITTENGERSTROM I; ANVRET M; ODEN A; JOHANNESSON T; HOLMQUIST D
RETT SYNDROME RELATED TO FRAGILE X(P22) IN CAFFEINE-INDUCED LYMPHOCYTES CULTURES
0 2
1317 10 17 642 1989 HUMAN GENETICS 82(1):79-81
SCHAAP T
THE ROLE OF RECOMBINATION IN THE EVOLVEMENT OF THE FRAGILE X-MUTATION
2 2
1318 3 4 653 1989 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 28(6):966-966
PAYTON JB; STEELE MW; WENGER SL; MINSHEW NJ
FRAGILE-X AND AUTISM
2 2
1319 0 0 655 1989 M S-MEDECINE SCIENCES 5(7):450-458
JORDAN BR; MATTEI JF
FRAGILE X-LINKED MENTAL-RETARDATION, 1989
2 2
1320 29 39 666 1989 ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 17(2):91-97
VONGONTARD A
PSYCHOPATHOLOGY ASSOCIATED WITH THE FRAGILE-X SYNDROME
1 2
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1321 0 0 667 1989 ZHURNAL NEVROPATOLOGII I PSIKHIATRII IMENI S S KORSAKOVA 89(8):101-105
BLYUMINA MG
CLINICAL SIGNS OF OLIGOPHRENIA WITH FRAGILE X-CHROMOSOME IN PREPUBERTY AND POSTPUBERTY MALES
1 2
1322 12 20 676 1990 AMERICAN JOURNAL OF HUMAN GENETICS 47(6):988-993
OHASHI H; KUWANO A; TSUKAHARA M; ARINAMI T; KAJII T
REPLICATION PATTERNS OF THE FRAGILE-X IN HETEROZYGOUS CARRIERS - ANALYSIS BY A BRDURD ANTIBODY METHOD
1 2
1323 2 4 689 1990 ARCHIVES OF DISEASE IN CHILDHOOD 65(3):335-335
REDINGTON A; BUSH A
FRAGILE-X MENTAL-RETARDATION
2 2
1324 0 2 724 1990 NUCLEIC ACIDS RESEARCH 18(3):692-692
HUPKES PE; VANBENNEKOM CA; VANOOST BA; OOSTRA BA
RN1, A NEW POLYMORPHIC MARKER NEAR THE FRAGILE-X LOCUS - (HGM10 ASSIGNMENT DXS-369)
1 2
1325 0 1 736 1991 AMERICAN JOURNAL OF HUMAN GENETICS 48(4):815-815
FINUCANE B; SCOTT CI; KURTZ MB
CONCURRENCE OF DOMINANT PIEBALD TRAIT AND FRAGILE X-SYNDROME
0 2
1326 16 47 789 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):298-304
GLASS IA; PIRRIT LA; WHITE EM; BELL MV; DAVIES KE; COCKBURN F; CONNOR JM
LINKAGE ANALYSIS IN THE FRAGILE-X SYNDROME USING MULTIPLE DISTAL XQ POLYMORPHIC DNA MARKERS
2 2
1327 2 9 790 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):305-310
MURPHY PD; WATSON MS; SHAPIRO LR; WILMOT PL; BREG WR
DNA-BASED GENETIC TESTING IN 50 FRAGILE-X FAMILIES
2 2
1328 3 20 795 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):343-346
BROWN WT; GROSS AC; GOONEWARDENA P; FERRANDO C; DOBKIN C; JENKINS EC
LINKAGE IN FRAGILE-X FAMILIES OF 3 DISTAL FLANKING MARKERS - ST14, DX13, AND F8
1 2
1329 7 11 798 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):363-366
DRUGGE U; BLOMQUIST HK; GUSTAVSON KH; HOLMGREN G
FRAGILE-X FAMILIES IN A NORTHERN SWEDISH COUNTY - A GENEALOGICAL STUDY OF POSSIBLY AFFECTED INDIVIDUALS IN THE 19TH-CENTURY
2 2
1330 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
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1331 4 7 805 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):396-399
SHERMAN SL
COLLABORATIVE PROSPECTIVE-STUDY OF THE FRAGILE-X SYNDROME - REQUEST FOR PARTICIPATION
2 2
1332 0 0 844 1991 CLINICAL RESEARCH 39(1):A1-A1
GOLDSON E; HAGERMAN RJ
TEMPERAMENT AND THE FRAGILE-X SYNDROME
2 2
1333 1 3 856 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2085-2085
RIGGINS GJ; SHERMAN SL; OOSTRA BA; FEITELL D; SUTCLIFFE JS; NELSON DL; VANOOST BA; SMITS AP; KUHL D; CASKEY CT; WARREN ST
A HIGHLY POLYMORPHIC DINUCLEOTIDE REPEAT, DXS 548, IS TIGHTLY LINKED TO THE FRAGILE-X SITE
1 2
1334 2 8 860 1991 HUMAN GENETICS 87(1):95-96
KAHKONEN M; HAATAJA R; LEISTI J
URIDINE ENHANCES EXPRESSION OF THE FRAGILE-X CHROMOSOME IN HUMAN-LYMPHOCYTES
2 2
1335 5 10 863 1991 HUMAN GENETICS 87(4):503-505
STEEN AM; MARCUS S; SAHLEN S; NIELSEN KB; LAMBERT B
THE FRAGILE-X MUTATION DOES NOT HAVE ANY MAJOR EFFECT ON THE EXPRESSION OF THE HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE (HPRT) LOCUS IN HUMAN FIBROBLASTS
0 2
1336 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
1337 27 41 961 1992 ARCHIVES FRANCAISES DE PEDIATRIE 49(2):99-103
BURSZTEJN C; ALEMBIK Y; STOLL C; POUPIER G; FELLER L; HAMON J; TRIBOUT JL; GARDONE MC; DANIONGRILLIAT A
FRAGILE-X SYNDROME ASSOCIATED WITH INFANTILE-AUTISM AND PSYCHOTIC DISORDERS
0 2
1338 15 22 968 1992 CLINICAL GENETICS 42(1):22-26
MARTINEZ F; BADIA L; PRIETO F
A FRAGILE-X FAMILY WITH HIGH PENETRANCE IN FEMALES - RISK HETEROGENEITY
0 2
1339 8 9 995 1992 JOURNAL OF MEDICAL GENETICS 29(12):919-920
TARLETON J; WONG S; SCHWARTZ C
DIRECT ANALYSIS OF THE FMR-1 GENE PROVIDES AN EXPLANATION FOR AN EXCEPTIONAL CASE OF A FRAGILE-X NEGATIVE, MENTALLY-RETARDED MALE IN A FRAGILE-X FAMILY
1 2
1340 12 17 1004 1992 MENTAL RETARDATION 30(6):355-361
KEENAN J; KASTNER T; NATHANSON R; RICHARDSON N; HINTON J; CRESS DA
A STATEWIDE PUBLIC AND PROFESSIONAL-EDUCATION PROGRAM ON FRAGILE X SYNDROME
0 2
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1341 16 34 1016 1992 REMEDIAL AND SPECIAL EDUCATION 13(2):32-39
SANTOS KE
FRAGILE X-SYNDROME - AN EDUCATORS ROLE IN IDENTIFICATION, PREVENTION, AND INTERVENTION
0 2
1342 23 29 1023 1993 AMERICAN JOURNAL OF DISEASES OF CHILDREN 147(11):1231-1235
RAMOS FJ; EUNPU DL; FINUCANE B; PFENDNER EG
DIRECT DNA TESTING FOR FRAGILE-X SYNDROME
1 2
1343 0 0 1027 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):3-3
ROUSSEAU F; REHEL R; ROUILLARD P; DEGRANDPRE P; MORGAN K; KHANDIJIAN EW
MUTATIONAL PREVALENCE OF FRAGILE X-PREMUTATIONS IN 10,624 FEMALES FROM THE GENERAL-POPULATION BY SOUTHERN BLOTTING
0 2
1344 0 0 1037 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):465-465
KRUYER H; MILA M; GLOVER G; CASTELLVBEL S; CARBONELL P; VOLPINI V; ESTIVILL X
MONOZYGOTIC TWINS DISCORDANT FOR THE FRAGILE-X SYNDROME (FXS)
0 2
1345 0 0 1039 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):678-678
EBERHART DE; WARREN ST
ABNORMAL CHROMATIN STRUCTURE ASSOCIATED WITH THE FULL FRAGILE-X MUTATION
1 2
1346 0 0 1047 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1208-1208
NOLIN SL; HOUCK GE; LI SY; DING XH; BROWN WT; DOBKIN CS
MOSAICISM IN FRAGILE-X AFFECTED MALES
0 2
1347 0 0 1050 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1241-1241
TORRES W; SAHOTA A; BOYADJIEV S; VANCE GH; WEAVER DD
FRAGILE-X FULL MUTATION IN 2 CLINICALLY UNAFFECTED BROTHERS
1 2
1348 42 66 1068 1993 ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE 117(11):1121-1125
TSONGALIS GJ; SILVERMAN LM
MOLECULAR PATHOLOGY OF THE FRAGILE-X SYNDROME
0 2
1349 13 23 1091 1993 GENETIKA 29(6):1026-1034
BARANOV VS; ASEEV MV; RAKISHEVA ZB; KULESHOV NP; MARINICHEVA GS; BYCHKOVA AM; ZUKIN VD; LEDASCHEVA EA; AMOASHYI DS; KUZNETZOVA TV; VAHARLOVSKY VG
MOLECULAR DIAGNOSIS OF FRAGILE X-SYNDROME (SYN MARTIN-BELL) IN THE PATIENTS OF NATIVE POPULATIONS
0 2
1350 8 14 1092 1993 HUMAN GENETICS 91(1):80-82
DREESEN JCFM; VANDENHURK JAJM; SMITS APT; VANDENOUWELAND AMW; MARKSLAG PWB; VANOOST BA
DXS539, A POLYMORPHIC DNA MARKER PROXIMAL OF THE FRAGILE-X GENE
0 2
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1351 4 7 1171 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):403-404
SCHAAP C; FRYNS JP
SEVERE PROGRESSIVE NEUROLOGICAL DISORDER ASSOCIATED WITH HYDROCEPHALUS IN A MAN WITH FRAGILE-X-SYNDROME
1 2
1352 14 17 1194 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 53(4):370-373
PUISSANT H; MALINGE MC; LARGETPIET A; MARTIN D; CHAUVEAU P; ODENT S; PLESSIS G; PARENT P; LEMAREC B; LARGETPIET L
MOLECULAR ANALYSIS OF 53 FRAGILE-X FAMILIES WITH THE PROBE-STB12.3
1 2
1353 13 16 1228 1994 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 271(7):552-553
CASKEY CT
FRAGILE-X SYNDROME - IMPROVING UNDERSTANDING AND DIAGNOSIS
2 2
1354 9 20 1232 1994 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 38:1-8
DEVRIES LBA; HALLEY DJJ; OOSTRA BA; NIERMEIJER MF
THE FRAGILE-X SYNDROME - A GROWING GENE CAUSING FAMILIAL INTELLECTUAL DISABILITY
1 2
1355 2 11 1257 1994 THERIOGENOLOGY 42(5):789-794
LLAMBI S; POSTIGLIONI A
LOCALIZATION OF THE FRAGILE-X CHROMOSOME BREAK POINTS IN HOLSTEIN-FRIESIAN CATTLE (BOS-TAURUS)
0 2
1356 0 0 1281 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1395-1395
HART PS; OLSON SM; CRANDALL K; TARLETON J
FRAGILE-X SYNDROME RESULTING FROM A 400 BASEPAIR DELETION WITHIN THE FMR1 GENE
0 2
1357 43 78 1320 1995 CLINICS IN LABORATORY MEDICINE 15(4):859-&
Brown WT
Perspectives and molecular diagnosis of the fragile X syndrome
2 2
1358 5 9 1343 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):408-410
HowardPeebles PN; Maddalena A; Black SH; Levinson G; Bick DP; Schulman JD
Fragile X screening in pediatric and obstetrical patients
2 2
1359 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
1360 0 0 1367 1995 JOURNAL OF MEDICAL GENETICS 32(2):144-145
MORTON JE; RINDL PM; BULLOCK S; BUNDEY S; WEBB T
FRAGILE-X SYNDROME IS LESS COMMON THAN PREVIOUSLY ESTIMATED
1 2
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1361 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
1362 27 77 1514 1996 SCREENING 4(4):175-192
Meadows KL; Sherman SL
Fragile X syndrome: Examination of issues pertaining to population-based screening
2 2
1363 17 20 1568 1997 ARCHIVES DE PEDIATRIE 4(3):227-236
Cossee M; Moutou C; Biancalana V; Bouix JC; Plessis G; Delobel B; Croquette MF; Gilgenkrantz S; Lambert JC; Malpuech G; Stoll C; Lanoe JL; Pechevis M; Mandel JL
The fragile X syndrome is still underdiagnosed: Efficacy of molecular testing in mentally retarded probands
2 2
1364 25 35 1571 1997 BRAZILIAN JOURNAL OF GENETICS 20(4):731-739
Mingroni-Netto RC; Pavanello RCM; Otto PA; Vianna-Morgante AM
Experience with molecular and cytogenetic diagnosis of fragile X syndrome in Brazilian families
2 2
1365 10 16 1582 1997 DIAGNOSTIC MOLECULAR PATHOLOGY 6(3):161-166
Marini T; Pflueger S; Jackson A; Naber S; Karpells S; Naeem R
A five-year experience with fragile X testing - Setting laboratory standards of practice and a cost-effective protocol
1 2
1366 23 44 1627 1997 PSYCHIATRIC GENETICS 7(3):115-119
ODwyer J; Holmes J; Mueller R; Taylor G
The prevalence of Fragile-X syndrome in an institution for people with learning disability
1 2
1367 20 33 1633 1998 AMERICAN JOURNAL OF MEDICAL GENETICS 79(3):200-204
Bonaventure G; Torrado M; Barreiro C; Chertkoff L
Fragile X founder effects in Argentina
0 2
1368 19 30 1638 1998 ANNALS OF HUMAN GENETICS 62:337-347
Huggins RM; Loesch DZ; Sherman SL
A branching non-linear autoregressive model for the transmission of the fragile X dynamic repeat mutation
1 2
1369 4 9 1728 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):281-285
Teisl JT; Reiss AL; Mazzocco MMM
Maximizing the sensitivity of a screening questionnaire for determining fragile X at-risk status
2 2
1370 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
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1371 7 14 1741 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):342-346
Jenkins EC; Wen GY; Kim KS; Zhong N; Sapienza VJ; Hong H; Chen J; Li SY; Houck GE; Ding XH; Nolin SL; Dobkin CS; Brown WT
Prenatal fragile X detection using cytoplasmic and nuclear-specific monoclonal antibodies
2 2
1372 35 50 1776 1999 CURRENT OPINION IN PSYCHIATRY 12(5):573-578
Harris SW; Hagerman RJ
Fragile X syndrome: new developments
2 2
1373 13 21 1786 1999 GENETIC TESTING 3(3):301-304
Melis MA; Addis M; Lepiani C; Congeddu E; Cossu P; Cao A
A strategy for fragile-X carrier screening
0 2
1374 3 8 1787 1999 GENETICS AND MOLECULAR BIOLOGY 22(2):169-172
Pena SDJ; Sturzeneker R
Diagnosis of the fragile X syndrome in males using methylation-specific PCR of the FMR1 locus
0 2
1375 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
1376 0 0 1831 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):18-18
Jin P; Feng Y; Brown V; Warren ST
Identification of polyribosomes-associated mRNAs regulated by fragile X mental retardation protein (FMRP) using oligonucleotide microarrays.
1 2
1377 3 24 1855 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 94(5):345-360
Fryns JP; Borghgraef M; Brown TW; Chelly J; Fisch GS; Hamel B; Hanauer A; Lacombe D; Luo L; MacPherson JN; Mandel JL; Moraine C; Mulley J; Nelson D; Oostra B; Partington M; Ramakers GJA; Ropers HH; Rousseau F; Schwartz C; Steinbach P; Stoll C; Tranebjaerg L; Turner G; Van Bokhoven H; Vianna-Morgante A; Villard L; Warren ST
9th international workshop on fragile X syndrome and X-linked mental retardation
0 2
1378 4 9 1861 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(5):516-517
Limprasert P; Jaruratanasirikul S; Vasiknanonte P
Unilateral macroorchidism in fragile X syndrome
2 2
1379 23 46 1882 2000 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 42(11):768-774
Sheldon L; Turk J
Monozygotic boys with fragile X syndrome
1 2
1380 27 44 1891 2000 GENETICS IN MEDICINE 2(4):242-248
Burman RW; Anoe KS; Popovich BW
Fragile X full mutations ave more similar in siblings than in unrelated patients: further evidence for a familial factor in CGG repeat dynamics
1 2
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1381 3 6 1893 2000 HUMAN GENETICS 107(2):195-196
Castellvi-Bel S; Fernandez-Burriel M; Rife M; Jimenez D; Mallolas J; Sanchez A; Ramos F; Mila M
Detection of the fragile X syndrome protein for the evaluation of FMR1 intermediate alleles
1 2
1382 6 14 1953 2000 NEUROBIOLOGY OF LEARNING AND MEMORY 74(1):80-93
Irwin SA; Swain RA; Christmon CA; Chakravarti A; Weiler IJ; Greenough WT
Evidence for altered fragile-x mental retardation protein expression in response to behavioral stimulation (vol 73, pg 87, 2000)
2 2
1383 15 32 1987 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 103(3):226-230
Schultz-Pedersen S; Hasle H; Olsen JH; Friedrich U
Evidence of decreased risk of cancer in individuals with fragile X
0 2
1384 21 34 2008 2001 CELLULAR AND MOLECULAR NEUROBIOLOGY 21(1):29-38
Castren M; Haapasalo A; Oostra BA; Castren E
Subcellular localization of fragile X mental retardation protein with the I304N mutation in the RNA-binding domain in cultured hippocampal neurons
2 2
1385 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
1386 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
1387 13 31 2032 2001 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 22(6):353-359
Myers GF; Mazzocco MMM; Maddalena A; Reiss AL
No widespread psychological effect of the fragile X premutation in childhood: Evidence from a preliminary controlled study
2 2
1388 0 0 2079 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):185-185
Jacquemont S; Hagerman RJ; Leehey M; Greco C; Brunberg J; Tassone F; Gane LW; Jardini T; Harris SW; Zhang L; Grigsby J; Des Portes V; Berry-Kravis E; Brown WT; Hagerman PJ
Characterization of a progressive neurological condition in older adult male carriers of the fragile X premutation.
2 2
1389 5 9 2110 2002 BRAIN & DEVELOPMENT 24(8):766-769
Incorpora G; Sorge G; Sorge A; Pavone L
Epilepsy in fragile X syndrome
2 2
1390 17 39 2147 2002 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 32(2):107-114
Fisch GS; Simensen RJ; Schroer RJ
Longitudinal changes in cognitive and adaptive Behavior scores in children and adolescents with the fragile X mutation or autism
2 2
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1391 9 13 2161 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):131-134
Kaufmann WE
Neurobiology of fragile X syndrome: From molecular genetics to neurobehavioral phenotype
0 2
1392 15 20 2163 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):145-147
Feng Y
Fragile X mental retardation: Misregulation of protein synthesis in the developing brain?
1 2
1393 7 58 2188 2002 NUCLEIC ACIDS RESEARCH 30(17):3672-3681
Weisman-Shomer P; Cohen E; Fry M
Distinct domains in the CArG-box binding factor A destabilize tetraplex forms of the fragile X expanded sequence d(CGG)(n)
1 2
1394 30 44 2221 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 116A(1):44-51
Steyaert J; Legius E; Borghgraef M; Fryns JP
A distinct neurocognitive phenotype in female fragile-X premutation carriers assessed with visual attention tasks
0 2
1395 18 62 2249 2003 BMC MOLECULAR BIOLOGY 4
Chandler SP; Kansagra P; Hirst MC
Fragile X (CGG)(n) repeats induce a transcriptional repression in cis upon a linked promoter: Evidence for a chromatin mediated effect
0 2
1396 38 52 2272 2003 HUMAN MOLECULAR GENETICS 12(23):3087-3096
Mazroui R; Huot ME; Tremblay S; Boilard N; Labelle Y; Khandjian EW
Fragile X Mental Retardation protein determinants required for its association with polyribosomal mRNPs
2 2
1397 7 23 2302 2003 NUCLEIC ACIDS RESEARCH 31(21):6243-6248
Handa V; Saha T; Usdin K
The fragile X syndrome repeats form RNA hairpins that do not activate the interferon-inducible protein kinase, PKR, but are cut by Dicer
0 2
1398 20 45 2306 2003 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 100(24):14374-14378
Todd PK; Mack KJ; Malter JS
The fragile X mental retardation protein is required for type-I metabotropic glutamate receptor-dependent translation of PSD-95
1 2
1399 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
1400 0 0 7 1981 AMERICAN JOURNAL OF HUMAN GENETICS 33(6):A100-A100
CARPENTER NJ; LEICHTMAN LG; LOGAN A; SAY B
FRAGILE X-LINKED MENTAL-RETARDATION
1 1

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1301	1	4	298 1985 JOURNAL OF MEDICAL GENETICS 22(5):397-397 WINTER RM; PEMBREY ME; DAVIES KE ANALYSIS OF LINKAGE DATA WITH FACTOR-IX CORROBORATES THE HYPOTHESIS THAT A PREMUTATION, FOLLOWED BY A RECOMBINATION EVENT, GENERATES THE FULL MUTATION IN FRAGILE X-LINKED MENTAL-RETARDATION	2	2
1302	1	4	313 1986 AMERICAN JOURNAL OF DISEASES OF CHILDREN 140(4):327-327 BOWERS EJ FRAGILE-X SYNDROME AND LEARNING-DISABILITIES	1	2
1303	3	5	373 1986 CLINICAL GENETICS 29(2):95-95 DEARCE MA; HECHT F; SUTHERLAND GR; WEBB GC GUIDELINES FOR THE DIAGNOSIS OF FRAGILE X	0	2
1304	0	0	405 1986 PEDIATRIC RESEARCH 20(4):A269-A269 MURPHY PD; WATSON MS; KIDD KK; BREG WR MOLECULAR APPROACHES TO CARRIER DETECTION AND PRENATAL-DIAGNOSIS OF THE FRAGILE-X SYNDROME (MCKUSICK NUMBER 30920)	1	2
1305	1	4	412 1987 AMERICAN JOURNAL OF DISEASES OF CHILDREN 141(6):601-601 BARTOLUCCI G; SZATMARI P POSSIBLE SIMILARITIES BETWEEN THE FRAGILE-X AND ASPERGERS SYNDROMES	1	2
1306	17	31	431 1987 BRITISH MEDICAL JOURNAL 295(6598):564-565 KINNELL HG FRAGILE X-SYNDROME - AN IMPORTANT PREVENTABLE CAUSE OF MENTAL HANDICAP	2	2
1307	1	22	438 1987 COLLEGIUM ANTROPOLOGICUM 11(2):305-316 LOESCH DZ FACTOR-ANALYSIS OF RIDGE-PATTERNS AND HAND MEASUREMENTS IN NORMAL AND FRAGILE-X MALES	0	2
1308	0	0	442 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):598-598 CONNOR JM; OSMAN H; STEFANI L; NEVIN NC; HOFKER M LINKAGE ANALYSIS IN FAMILIES WITH THE FRAGILE-X SYNDROME USING CX55-7 (DXS105)	0	2
1309	0	0	444 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):688-689 SCHWARTZ C; PATTERSON M; DAVIES K; TRUNCA C; TRASK B; PHELAN MC THE USE OF DISTAL DELETIONS OF XQ TO ORDER LOCI BETWEEN FACTOR-IX AND THE FRAGILE-X SITE (XQ27.3)	1	2
1310	0	0	494 1987 TERATOLOGY 36(3):453-453 SUZUKI Y; CHYO H; MATSUI A; SHIMOMURA C; FUNAHASI M CLINICAL-DIAGNOSIS OF FRAGILE-X SYNDROME	1	2
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1311	6	11	518 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):177-183 MILONE G; CONTI L; RIZZO R; SANFILIPPO S; SAMMITO V; ROMANO C A DERMATOGLYPHIC STUDY OF A GROUP OF SICILIAN CHILDREN WITH FRAGILE-X SYNDROME	1	2
1312	2	8	523 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):231-236 SUTHERS GK; TURNER G; MULLEY JC CASE-REPORT - FRAGILE-X SYNDROME AND NEPHROGENIC DIABETES-INSIPIDUS	1	2
1313	1	7	535 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):443-450 NOLIN SL; JENKINS EC; BROWN WT; DOBKIN CS INSITU NICK TRANSLATION OF THE FRAGILE-X REGION	1	2
1314	2	13	579 1988 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 30(5):646-649 CAMMARATA S; ARCHIDIACONO N; ROMEO G; BENASSI G; GUARINO M; DALESSANDRO R PREVALENCE OF MENTAL-RETARDATION RELATED TO FRAGILE X SYNDROME AND OTHER CHROMOSOMAL-ABNORMALITIES IN THE REPUBLIC OF SAN MARINO	0	2
1315	3	5	584 1988 HUMAN GENETICS 78(4):383-383 BUTLER MG; JOSEPH GM; RAMES LJ; CACHEIRO N; LOZZIO CB CHROMOSOME BREAKAGE IN CONTROL AND FRAGILE-X SUBJECTS USING FOLATE-DEFICIENT CULTURE CONDITIONS	2	2
1316	0	1	638 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):1100-1101 WAHLSTROM J; WITTENGERSTROM I; ANVRET M; ODEN A; JOHANNESSON T; HOLMQUIST D RETT SYNDROME RELATED TO FRAGILE X(P22) IN CAFFEINE-INDUCED LYMPHOCYTES CULTURES	0	2
1317	10	17	642 1989 HUMAN GENETICS 82(1):79-81 SCHAAP T THE ROLE OF RECOMBINATION IN THE EVOLVEMENT OF THE FRAGILE X-MUTATION	2	2
1318	3	4	653 1989 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 28(6):966-966 PAYTON JB; STEELE MW; WENGER SL; MINSHEW NJ FRAGILE-X AND AUTISM	2	2
1319	0	0	655 1989 M S-MEDECINE SCIENCES 5(7):450-458 JORDAN BR; MATTEI JF FRAGILE X-LINKED MENTAL-RETARDATION, 1989	2	2
1320	29	39	666 1989 ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 17(2):91-97 VONGONTARD A PSYCHOPATHOLOGY ASSOCIATED WITH THE FRAGILE-X SYNDROME	1	2
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1321	0	0	667 1989 ZHURNAL NEVROPATOLOGII I PSIKHIATRII IMENI S S KORSAKOVA 89(8):101-105 BLYUMINA MG CLINICAL SIGNS OF OLIGOPHRENIA WITH FRAGILE X-CHROMOSOME IN PREPUBERTY AND POSTPUBERTY MALES	1	2
1322	12	20	676 1990 AMERICAN JOURNAL OF HUMAN GENETICS 47(6):988-993 OHASHI H; KUWANO A; TSUKAHARA M; ARINAMI T; KAJII T REPLICATION PATTERNS OF THE FRAGILE-X IN HETEROZYGOUS CARRIERS - ANALYSIS BY A BRDURD ANTIBODY METHOD	1	2
1323	2	4	689 1990 ARCHIVES OF DISEASE IN CHILDHOOD 65(3):335-335 REDINGTON A; BUSH A FRAGILE-X MENTAL-RETARDATION	2	2
1324	0	2	724 1990 NUCLEIC ACIDS RESEARCH 18(3):692-692 HUPKES PE; VANBENNEKOM CA; VANOOST BA; OOSTRA BA RN1, A NEW POLYMORPHIC MARKER NEAR THE FRAGILE-X LOCUS - (HGM10 ASSIGNMENT DXS-369)	1	2
1325	0	1	736 1991 AMERICAN JOURNAL OF HUMAN GENETICS 48(4):815-815 FINUCANE B; SCOTT CI; KURTZ MB CONCURRENCE OF DOMINANT PIEBALD TRAIT AND FRAGILE X-SYNDROME	0	2
1326	16	47	789 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):298-304 GLASS IA; PIRRIT LA; WHITE EM; BELL MV; DAVIES KE; COCKBURN F; CONNOR JM LINKAGE ANALYSIS IN THE FRAGILE-X SYNDROME USING MULTIPLE DISTAL XQ POLYMORPHIC DNA MARKERS	2	2
1327	2	9	790 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):305-310 MURPHY PD; WATSON MS; SHAPIRO LR; WILMOT PL; BREG WR DNA-BASED GENETIC TESTING IN 50 FRAGILE-X FAMILIES	2	2
1328	3	20	795 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):343-346 BROWN WT; GROSS AC; GOONEWARDENA P; FERRANDO C; DOBKIN C; JENKINS EC LINKAGE IN FRAGILE-X FAMILIES OF 3 DISTAL FLANKING MARKERS - ST14, DX13, AND F8	1	2
1329	7	11	798 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):363-366 DRUGGE U; BLOMQUIST HK; GUSTAVSON KH; HOLMGREN G FRAGILE-X FAMILIES IN A NORTHERN SWEDISH COUNTY - A GENEALOGICAL STUDY OF POSSIBLY AFFECTED INDIVIDUALS IN THE 19TH-CENTURY	2	2
1330	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
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1331	4	7	805 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):396-399 SHERMAN SL COLLABORATIVE PROSPECTIVE-STUDY OF THE FRAGILE-X SYNDROME - REQUEST FOR PARTICIPATION	2	2
1332	0	0	844 1991 CLINICAL RESEARCH 39(1):A1-A1 GOLDSON E; HAGERMAN RJ TEMPERAMENT AND THE FRAGILE-X SYNDROME	2	2
1333	1	3	856 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2085-2085 RIGGINS GJ; SHERMAN SL; OOSTRA BA; FEITELL D; SUTCLIFFE JS; NELSON DL; VANOOST BA; SMITS AP; KUHL D; CASKEY CT; WARREN ST A HIGHLY POLYMORPHIC DINUCLEOTIDE REPEAT, DXS 548, IS TIGHTLY LINKED TO THE FRAGILE-X SITE	1	2
1334	2	8	860 1991 HUMAN GENETICS 87(1):95-96 KAHKONEN M; HAATAJA R; LEISTI J URIDINE ENHANCES EXPRESSION OF THE FRAGILE-X CHROMOSOME IN HUMAN-LYMPHOCYTES	2	2
1335	5	10	863 1991 HUMAN GENETICS 87(4):503-505 STEEN AM; MARCUS S; SAHLEN S; NIELSEN KB; LAMBERT B THE FRAGILE-X MUTATION DOES NOT HAVE ANY MAJOR EFFECT ON THE EXPRESSION OF THE HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE (HPRT) LOCUS IN HUMAN FIBROBLASTS	0	2
1336	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
1337	27	41	961 1992 ARCHIVES FRANCAISES DE PEDIATRIE 49(2):99-103 BURSZTEJN C; ALEMBIK Y; STOLL C; POUPIER G; FELLER L; HAMON J; TRIBOUT JL; GARDONE MC; DANIONGRILLIAT A FRAGILE-X SYNDROME ASSOCIATED WITH INFANTILE-AUTISM AND PSYCHOTIC DISORDERS	0	2
1338	15	22	968 1992 CLINICAL GENETICS 42(1):22-26 MARTINEZ F; BADIA L; PRIETO F A FRAGILE-X FAMILY WITH HIGH PENETRANCE IN FEMALES - RISK HETEROGENEITY	0	2
1339	8	9	995 1992 JOURNAL OF MEDICAL GENETICS 29(12):919-920 TARLETON J; WONG S; SCHWARTZ C DIRECT ANALYSIS OF THE FMR-1 GENE PROVIDES AN EXPLANATION FOR AN EXCEPTIONAL CASE OF A FRAGILE-X NEGATIVE, MENTALLY-RETARDED MALE IN A FRAGILE-X FAMILY	1	2
1340	12	17	1004 1992 MENTAL RETARDATION 30(6):355-361 KEENAN J; KASTNER T; NATHANSON R; RICHARDSON N; HINTON J; CRESS DA A STATEWIDE PUBLIC AND PROFESSIONAL-EDUCATION PROGRAM ON FRAGILE X SYNDROME	0	2
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1341	16	34	1016 1992 REMEDIAL AND SPECIAL EDUCATION 13(2):32-39 SANTOS KE FRAGILE X-SYNDROME - AN EDUCATORS ROLE IN IDENTIFICATION, PREVENTION, AND INTERVENTION	0	2
1342	23	29	1023 1993 AMERICAN JOURNAL OF DISEASES OF CHILDREN 147(11):1231-1235 RAMOS FJ; EUNPU DL; FINUCANE B; PFENDNER EG DIRECT DNA TESTING FOR FRAGILE-X SYNDROME	1	2
1343	0	0	1027 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):3-3 ROUSSEAU F; REHEL R; ROUILLARD P; DEGRANDPRE P; MORGAN K; KHANDIJIAN EW MUTATIONAL PREVALENCE OF FRAGILE X-PREMUTATIONS IN 10,624 FEMALES FROM THE GENERAL-POPULATION BY SOUTHERN BLOTTING	0	2
1344	0	0	1037 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):465-465 KRUYER H; MILA M; GLOVER G; CASTELLVBEL S; CARBONELL P; VOLPINI V; ESTIVILL X MONOZYGOTIC TWINS DISCORDANT FOR THE FRAGILE-X SYNDROME (FXS)	0	2
1345	0	0	1039 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):678-678 EBERHART DE; WARREN ST ABNORMAL CHROMATIN STRUCTURE ASSOCIATED WITH THE FULL FRAGILE-X MUTATION	1	2
1346	0	0	1047 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1208-1208 NOLIN SL; HOUCK GE; LI SY; DING XH; BROWN WT; DOBKIN CS MOSAICISM IN FRAGILE-X AFFECTED MALES	0	2
1347	0	0	1050 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1241-1241 TORRES W; SAHOTA A; BOYADJIEV S; VANCE GH; WEAVER DD FRAGILE-X FULL MUTATION IN 2 CLINICALLY UNAFFECTED BROTHERS	1	2
1348	42	66	1068 1993 ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE 117(11):1121-1125 TSONGALIS GJ; SILVERMAN LM MOLECULAR PATHOLOGY OF THE FRAGILE-X SYNDROME	0	2
1349	13	23	1091 1993 GENETIKA 29(6):1026-1034 BARANOV VS; ASEEV MV; RAKISHEVA ZB; KULESHOV NP; MARINICHEVA GS; BYCHKOVA AM; ZUKIN VD; LEDASCHEVA EA; AMOASHYI DS; KUZNETZOVA TV; VAHARLOVSKY VG MOLECULAR DIAGNOSIS OF FRAGILE X-SYNDROME (SYN MARTIN-BELL) IN THE PATIENTS OF NATIVE POPULATIONS	0	2
1350	8	14	1092 1993 HUMAN GENETICS 91(1):80-82 DREESEN JCFM; VANDENHURK JAJM; SMITS APT; VANDENOUWELAND AMW; MARKSLAG PWB; VANOOST BA DXS539, A POLYMORPHIC DNA MARKER PROXIMAL OF THE FRAGILE-X GENE	0	2
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1351	4	7	1171 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):403-404 SCHAAP C; FRYNS JP SEVERE PROGRESSIVE NEUROLOGICAL DISORDER ASSOCIATED WITH HYDROCEPHALUS IN A MAN WITH FRAGILE-X-SYNDROME	1	2
1352	14	17	1194 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 53(4):370-373 PUISSANT H; MALINGE MC; LARGETPIET A; MARTIN D; CHAUVEAU P; ODENT S; PLESSIS G; PARENT P; LEMAREC B; LARGETPIET L MOLECULAR ANALYSIS OF 53 FRAGILE-X FAMILIES WITH THE PROBE-STB12.3	1	2
1353	13	16	1228 1994 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 271(7):552-553 CASKEY CT FRAGILE-X SYNDROME - IMPROVING UNDERSTANDING AND DIAGNOSIS	2	2
1354	9	20	1232 1994 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 38:1-8 DEVRIES LBA; HALLEY DJJ; OOSTRA BA; NIERMEIJER MF THE FRAGILE-X SYNDROME - A GROWING GENE CAUSING FAMILIAL INTELLECTUAL DISABILITY	1	2
1355	2	11	1257 1994 THERIOGENOLOGY 42(5):789-794 LLAMBI S; POSTIGLIONI A LOCALIZATION OF THE FRAGILE-X CHROMOSOME BREAK POINTS IN HOLSTEIN-FRIESIAN CATTLE (BOS-TAURUS)	0	2
1356	0	0	1281 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1395-1395 HART PS; OLSON SM; CRANDALL K; TARLETON J FRAGILE-X SYNDROME RESULTING FROM A 400 BASEPAIR DELETION WITHIN THE FMR1 GENE	0	2
1357	43	78	1320 1995 CLINICS IN LABORATORY MEDICINE 15(4):859-& Brown WT Perspectives and molecular diagnosis of the fragile X syndrome	2	2
1358	5	9	1343 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):408-410 HowardPeebles PN; Maddalena A; Black SH; Levinson G; Bick DP; Schulman JD Fragile X screening in pediatric and obstetrical patients	2	2
1359	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
1360	0	0	1367 1995 JOURNAL OF MEDICAL GENETICS 32(2):144-145 MORTON JE; RINDL PM; BULLOCK S; BUNDEY S; WEBB T FRAGILE-X SYNDROME IS LESS COMMON THAN PREVIOUSLY ESTIMATED	1	2
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1361	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
1362	27	77	1514 1996 SCREENING 4(4):175-192 Meadows KL; Sherman SL Fragile X syndrome: Examination of issues pertaining to population-based screening	2	2
1363	17	20	1568 1997 ARCHIVES DE PEDIATRIE 4(3):227-236 Cossee M; Moutou C; Biancalana V; Bouix JC; Plessis G; Delobel B; Croquette MF; Gilgenkrantz S; Lambert JC; Malpuech G; Stoll C; Lanoe JL; Pechevis M; Mandel JL The fragile X syndrome is still underdiagnosed: Efficacy of molecular testing in mentally retarded probands	2	2
1364	25	35	1571 1997 BRAZILIAN JOURNAL OF GENETICS 20(4):731-739 Mingroni-Netto RC; Pavanello RCM; Otto PA; Vianna-Morgante AM Experience with molecular and cytogenetic diagnosis of fragile X syndrome in Brazilian families	2	2
1365	10	16	1582 1997 DIAGNOSTIC MOLECULAR PATHOLOGY 6(3):161-166 Marini T; Pflueger S; Jackson A; Naber S; Karpells S; Naeem R A five-year experience with fragile X testing - Setting laboratory standards of practice and a cost-effective protocol	1	2
1366	23	44	1627 1997 PSYCHIATRIC GENETICS 7(3):115-119 ODwyer J; Holmes J; Mueller R; Taylor G The prevalence of Fragile-X syndrome in an institution for people with learning disability	1	2
1367	20	33	1633 1998 AMERICAN JOURNAL OF MEDICAL GENETICS 79(3):200-204 Bonaventure G; Torrado M; Barreiro C; Chertkoff L Fragile X founder effects in Argentina	0	2
1368	19	30	1638 1998 ANNALS OF HUMAN GENETICS 62:337-347 Huggins RM; Loesch DZ; Sherman SL A branching non-linear autoregressive model for the transmission of the fragile X dynamic repeat mutation	1	2
1369	4	9	1728 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):281-285 Teisl JT; Reiss AL; Mazzocco MMM Maximizing the sensitivity of a screening questionnaire for determining fragile X at-risk status	2	2
1370	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
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1371	7	14	1741 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):342-346 Jenkins EC; Wen GY; Kim KS; Zhong N; Sapienza VJ; Hong H; Chen J; Li SY; Houck GE; Ding XH; Nolin SL; Dobkin CS; Brown WT Prenatal fragile X detection using cytoplasmic and nuclear-specific monoclonal antibodies	2	2
1372	35	50	1776 1999 CURRENT OPINION IN PSYCHIATRY 12(5):573-578 Harris SW; Hagerman RJ Fragile X syndrome: new developments	2	2
1373	13	21	1786 1999 GENETIC TESTING 3(3):301-304 Melis MA; Addis M; Lepiani C; Congeddu E; Cossu P; Cao A A strategy for fragile-X carrier screening	0	2
1374	3	8	1787 1999 GENETICS AND MOLECULAR BIOLOGY 22(2):169-172 Pena SDJ; Sturzeneker R Diagnosis of the fragile X syndrome in males using methylation-specific PCR of the FMR1 locus	0	2
1375	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
1376	0	0	1831 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):18-18 Jin P; Feng Y; Brown V; Warren ST Identification of polyribosomes-associated mRNAs regulated by fragile X mental retardation protein (FMRP) using oligonucleotide microarrays.	1	2
1377	3	24	1855 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 94(5):345-360 Fryns JP; Borghgraef M; Brown TW; Chelly J; Fisch GS; Hamel B; Hanauer A; Lacombe D; Luo L; MacPherson JN; Mandel JL; Moraine C; Mulley J; Nelson D; Oostra B; Partington M; Ramakers GJA; Ropers HH; Rousseau F; Schwartz C; Steinbach P; Stoll C; Tranebjaerg L; Turner G; Van Bokhoven H; Vianna-Morgante A; Villard L; Warren ST 9th international workshop on fragile X syndrome and X-linked mental retardation	0	2
1378	4	9	1861 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(5):516-517 Limprasert P; Jaruratanasirikul S; Vasiknanonte P Unilateral macroorchidism in fragile X syndrome	2	2
1379	23	46	1882 2000 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 42(11):768-774 Sheldon L; Turk J Monozygotic boys with fragile X syndrome	1	2
1380	27	44	1891 2000 GENETICS IN MEDICINE 2(4):242-248 Burman RW; Anoe KS; Popovich BW Fragile X full mutations ave more similar in siblings than in unrelated patients: further evidence for a familial factor in CGG repeat dynamics	1	2
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1381	3	6	1893 2000 HUMAN GENETICS 107(2):195-196 Castellvi-Bel S; Fernandez-Burriel M; Rife M; Jimenez D; Mallolas J; Sanchez A; Ramos F; Mila M Detection of the fragile X syndrome protein for the evaluation of FMR1 intermediate alleles	1	2
1382	6	14	1953 2000 NEUROBIOLOGY OF LEARNING AND MEMORY 74(1):80-93 Irwin SA; Swain RA; Christmon CA; Chakravarti A; Weiler IJ; Greenough WT Evidence for altered fragile-x mental retardation protein expression in response to behavioral stimulation (vol 73, pg 87, 2000)	2	2
1383	15	32	1987 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 103(3):226-230 Schultz-Pedersen S; Hasle H; Olsen JH; Friedrich U Evidence of decreased risk of cancer in individuals with fragile X	0	2
1384	21	34	2008 2001 CELLULAR AND MOLECULAR NEUROBIOLOGY 21(1):29-38 Castren M; Haapasalo A; Oostra BA; Castren E Subcellular localization of fragile X mental retardation protein with the I304N mutation in the RNA-binding domain in cultured hippocampal neurons	2	2
1385	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
1386	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
1387	13	31	2032 2001 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 22(6):353-359 Myers GF; Mazzocco MMM; Maddalena A; Reiss AL No widespread psychological effect of the fragile X premutation in childhood: Evidence from a preliminary controlled study	2	2
1388	0	0	2079 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):185-185 Jacquemont S; Hagerman RJ; Leehey M; Greco C; Brunberg J; Tassone F; Gane LW; Jardini T; Harris SW; Zhang L; Grigsby J; Des Portes V; Berry-Kravis E; Brown WT; Hagerman PJ Characterization of a progressive neurological condition in older adult male carriers of the fragile X premutation.	2	2
1389	5	9	2110 2002 BRAIN & DEVELOPMENT 24(8):766-769 Incorpora G; Sorge G; Sorge A; Pavone L Epilepsy in fragile X syndrome	2	2
1390	17	39	2147 2002 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 32(2):107-114 Fisch GS; Simensen RJ; Schroer RJ Longitudinal changes in cognitive and adaptive Behavior scores in children and adolescents with the fragile X mutation or autism	2	2
#	LCR	NCR	Nodes / Date / Journal / Authors	LCS	GCS
1391	9	13	2161 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):131-134 Kaufmann WE Neurobiology of fragile X syndrome: From molecular genetics to neurobehavioral phenotype	0	2
1392	15	20	2163 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):145-147 Feng Y Fragile X mental retardation: Misregulation of protein synthesis in the developing brain?	1	2
1393	7	58	2188 2002 NUCLEIC ACIDS RESEARCH 30(17):3672-3681 Weisman-Shomer P; Cohen E; Fry M Distinct domains in the CArG-box binding factor A destabilize tetraplex forms of the fragile X expanded sequence d(CGG)(n)	1	2
1394	30	44	2221 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 116A(1):44-51 Steyaert J; Legius E; Borghgraef M; Fryns JP A distinct neurocognitive phenotype in female fragile-X premutation carriers assessed with visual attention tasks	0	2
1395	18	62	2249 2003 BMC MOLECULAR BIOLOGY 4 Chandler SP; Kansagra P; Hirst MC Fragile X (CGG)(n) repeats induce a transcriptional repression in cis upon a linked promoter: Evidence for a chromatin mediated effect	0	2
1396	38	52	2272 2003 HUMAN MOLECULAR GENETICS 12(23):3087-3096 Mazroui R; Huot ME; Tremblay S; Boilard N; Labelle Y; Khandjian EW Fragile X Mental Retardation protein determinants required for its association with polyribosomal mRNPs	2	2
1397	7	23	2302 2003 NUCLEIC ACIDS RESEARCH 31(21):6243-6248 Handa V; Saha T; Usdin K The fragile X syndrome repeats form RNA hairpins that do not activate the interferon-inducible protein kinase, PKR, but are cut by Dicer	0	2
1398	20	45	2306 2003 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 100(24):14374-14378 Todd PK; Mack KJ; Malter JS The fragile X mental retardation protein is required for type-I metabotropic glutamate receptor-dependent translation of PSD-95	1	2
1399	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
1400	0	0	7 1981 AMERICAN JOURNAL OF HUMAN GENETICS 33(6):A100-A100 CARPENTER NJ; LEICHTMAN LG; LOGAN A; SAY B FRAGILE X-LINKED MENTAL-RETARDATION	1	1

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