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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by first author.
Page 18: 1 (Abbeduto L) 2 (BELGHITI D) 3 (Brown WT) 4 (Chen X) 5 (DAKER MG) 6 (DYKENS E) 7 (FITCHETT M) 8 (GLOVER TW) 9 (HAGERMAN RJ) 10 (HOFFMAN M) 11 (JANCAR J) 12 (KIMCHISARFATY C) 13 (LEE JT) 14 (MAES B) 15 (MIGEON BR) 16 (Myers GF) 17 (Patsalis PC) 18 (REISS AL) 19 (Schenck A) 20 (SMITS APT) 21 (SZABO P) 22 (TURNER G) 23 (Wang YC) 24 (WOHRLE D)
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1701 | 4 | 12 | 336 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):393-401 REISS AL; FEINSTEIN C; TOOMEY KE; GOLDSMITH B; ROSENBAUM K; CARUSO MA PSYCHIATRIC DISABILITY ASSOCIATED WITH THE FRAGILE-X CHROMOSOME | 29 | 44 |
| 1702 | 28 | 73 | 690 1990 BIOLOGICAL PSYCHIATRY 27(2):223-240 REISS AL; FREUND L FRAGILE X-SYNDROME | 22 | 28 |
| 1703 | 11 | 26 | 716 1990 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 29(6):885-891 REISS AL; FREUND L FRAGILE X SYNDROME, DSM-III-R, AND AUTISM | 40 | 59 |
| 1704 | 12 | 22 | 908 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):35-46 REISS AL; FREUND L BEHAVIORAL-PHENOTYPE OF FRAGILE-X SYNDROME - DSM-III-R AUTISTIC BEHAVIOR IN MALE-CHILDREN | 52 | 71 |
| 1705 | 23 | 47 | 1026 1993 AMERICAN JOURNAL OF HUMAN GENETICS 52(5):884-894 REISS AL; FREUND L; ABRAMS MT; BOEHM C; KAZAZIAN H NEUROBEHAVIORAL EFFECTS OF THE FRAGILE-X PREMUTATION IN ADULT WOMEN - A CONTROLLED-STUDY | 70 | 95 |
| 1706 | 17 | 34 | 738 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(2):279-288 REISS AL; FREUND L; TSENG JE; JOSHI PK NEUROANATOMY IN FRAGILE-X FEMALES - THE POSTERIOR-FOSSA | 43 | 64 |
| 1707 | 9 | 24 | 613 1989 AMERICAN JOURNAL OF HUMAN GENETICS 45(5):697-705 REISS AL; FREUND L; VINOGRADOV S; HAGERMAN R; CRONISTER A PARENTAL INHERITANCE AND PSYCHOLOGICAL DISABILITY IN FRAGILE-X FEMALES | 26 | 31 |
| 1708 | 7 | 32 | 560 1988 ARCHIVES OF GENERAL PSYCHIATRY 45(1):25-30 REISS AL; HAGERMAN RJ; VINOGRADOV S; ABRAMS M; KING RJ PSYCHIATRIC DISABILITY IN FEMALE CARRIERS OF THE FRAGILE X-CHROMOSOME | 56 | 91 |
| 1709 | 23 | 31 | 1218 1994 HUMAN MOLECULAR GENETICS 3(3):393-398 REISS AL; KAZAZIAN HH; KREBS CM; MCAUGHAN A; BOEHM CD; ABRAMS MT; NELSON DL FREQUENCY AND STABILITY OF THE FRAGILE-X PREMUTATION | 29 | 61 |
| 1710 | 22 | 61 | 1251 1994 NEUROLOGY 44(7):1317-1324 REISS AL; LEE J; FREUND L NEUROANATOMY OF FRAGILE-X SYNDROME - THE TEMPORAL-LOBE | 49 | 83 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1711 | 2 | 17 | 552 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 |
| 1712 | 0 | 1 | 589 1988 HUMAN GENETICS 80(2):193-193 REKILA AM; VAISANEN ML; KAHKONEN M; LEISTI J; WINQVIST R A NEW RFLP WITH STUI AND PROBE CX55.7 (DXS105) AND ITS USEFULNESS IN CARRIER ANALYSIS OF FRAGILE X-SYNDROME | 2 | 6 |
| 1713 | 20 | 37 | 1753 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):245-249 Reyniers E; Martin JJ; Cras P; Van Marck E; Handig I; Jorens HZJ; Oostra BA; Kooy RF; Willems PJ Postmortem examination of two fragile X brothers with an FMR1 full mutation | 14 | 19 |
| 1714 | 28 | 44 | 1137 1993 NATURE GENETICS 4(2):143-146 REYNIERS E; VITS L; DEBOULLE K; VANROY B; VANVELZEN D; DEGRAAFF E; VERKERK AJMH; JORENS HZJ; DARBY JK; OOSTRA B; WILLEMS PJ THE FULL MUTATION IN THE FMR-1 GENE OF MALE FRAGILE-X PATIENTS IS ABSENT IN THEIR SPERM | 82 | 167 |
| 1715 | 0 | 0 | 1535 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A110-A110 Rhee LE; Hatcher SL; Robb KM; Towner DR Fragile X syndrome associated with birth defects. | 0 | 0 |
| 1716 | 1 | 7 | 81 1982 PEDIATRICS 69(5):668-669 RHOADS FA X-LINKED MENTAL-RETARDATION AND FRAGILE-X OR MARKER-X SYNDROME | 11 | 12 |
| 1717 | 0 | 4 | 175 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):209-214 RHOADS FA FRAGILE-X SYNDROME IN HAWAII - A SUMMARY OF CLINICAL-EXPERIENCE | 10 | 21 |
| 1718 | 1 | 7 | 22 1981 JOURNAL OF MENTAL DEFICIENCY RESEARCH 25(DEC):253-& RICHARDS BW; SYLVESTER PE; BROOKER C FRAGILE X-LINKED MENTAL-RETARDATION - THE MARTIN-BELL SYNDROME | 36 | 55 |
| 1719 | 8 | 20 | 1008 1992 NATURE GENETICS 1(4):257-260 RICHARDS RI; HOLMAN K; FRIEND K; KREMER E; HILLEN D; STAPLES A; BROWN WT; GOONEWARDENA P; TARLETON J; SCHWARTZ C; SUTHERLAND GR EVIDENCE OF FOUNDER CHROMOSOMES IN FRAGILE-X SYNDROME | 69 | 158 |
| 1720 | 5 | 10 | 871 1991 JOURNAL OF MEDICAL GENETICS 28(12):818-823 RICHARDS RI; HOLMAN K; KOZMAN H; KREMER E; LYNCH M; PRITCHARD M; YU S; MULLEY J; SUTHERLAND GR FRAGILE-X SYNDROME - GENETIC LOCALIZATION BY LINKAGE MAPPING OF 2 MICROSATELLITE REPEATS FRAXAC1 AND FRAXAC2 WHICH IMMEDIATELY FLANK THE FRAGILE SITE | 52 | 100 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1721 | 10 | 29 | 1100 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 | 11 | 80 |
| 1722 | 6 | 17 | 737 1991 AMERICAN JOURNAL OF HUMAN GENETICS 48(6):1051-1057 RICHARDS RI; SHEN Y; HOLMAN K; KOZMAN H; HYLAND VJ; MULLEY JC; SUTHERLAND GR FRAGILE-X SYNDROME - DIAGNOSIS USING HIGHLY POLYMORPHIC MICROSATELLITE MARKERS | 14 | 40 |
| 1723 | 26 | 44 | 1017 1992 TRENDS IN GENETICS 8(7):249-255 RICHARDS RI; SUTHERLAND GR FRAGILE X-SYNDROME - THE MOLECULAR PICTURE COMES INTO FOCUS | 13 | 39 |
| 1724 | 7 | 32 | 2279 2003 JOURNAL OF INTELLECTUAL & DEVELOPMENTAL DISABILITY 28(2):135-144 Richdale AL A descriptive analysis of sleep behaviour in children with Fragile X | 0 | 0 |
| 1725 | 19 | 29 | 2266 2003 GENETIC TESTING 7(4):339-343 Rife M; Badenas C; Mallolas J; Jimenez L; Cervera R; Maya A; Glover G; Rivera F; Mila M Incidence of Fragile X in 5,000 consecutive newborn males | 0 | 0 |
| 1726 | 18 | 22 | 2192 2002 PRENATAL DIAGNOSIS 22(6):459-462 Rife M; Mallolas J; Badenas C; Tazon B; Miguelez MR; Pampols T; Sanchez A; Mila M Pilot study for the neonatal screening of fragile X syndrome | 3 | 3 |
| 1727 | 1 | 1 | 2305 2003 PRENATAL DIAGNOSIS 23(9):771-771 Rife M; Mallolas J; Badenas C; Tazon B; Miguelez MR; Pampols T; Sanchez A; Mila M Pilot study for the neonatal screening of fragile X syndrome (vol 22, pg 459, 2002) | 0 | 0 |
| 1728 | 0 | 0 | 2214 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):383-383 Rigby AS; Turk J; Mills AC; James N; Hollis C; Cornish K; Dalton A; Manly T Social functioning in male premutation carriers of Fragile X (FRAX) syndrome | 0 | 0 |
| 1729 | 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 |
| 1730 | 0 | 0 | 775 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):357-357 RIGGINS GJ; SHERMAN SL; OOSTRA BA; FEITELL D; SUTCLIFFE JS; NELSON DL; VANOOST BA; SMITS APT; KUHL D; CASKEY CT; WARREN ST A FREQUENT DINUCLEOTIDE POLYMORPHISM OF THE FRAGILE-X BREAKPOINT CLUSTER REGION IS TIGHTLY LINKED TO THE FRAGILE-X SYNDROME LOCUS | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1731 | 14 | 25 | 935 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):237-243 RIGGINS GJ; SHERMAN SL; OOSTRA BA; SUTCLIFFE JS; FEITELL D; NELSON DL; VANOOST BA; SMITS APT; RAMOS FJ; PFENDNER E; KUHL DPA; CASKEY CT; WARREN ST CHARACTERIZATION OF A HIGHLY POLYMORPHIC DINUCLEOTIDE REPEAT 150-KB PROXIMAL TO THE FRAGILE-X SITE | 35 | 57 |
| 1732 | 0 | 0 | 761 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):273-273 RISCILE GR FRAGILE-X PATIENTS WITH ATYPICAL PHENOTYPES | 0 | 0 |
| 1733 | 4 | 13 | 1458 1996 ARCHIVES OF MEDICAL RESEARCH 27(4):587-588 Rivera H Fragile X studies and authorship | 1 | 5 |
| 1734 | 1 | 1 | 1570 1997 ARCHIVES OF MEDICAL RESEARCH 28(1):149-149 Rivera H Fragile X studies and authorship (vol 27, pg 587, 1996) | 0 | 0 |
| 1735 | 15 | 44 | 2143 2002 HUMAN BRAIN MAPPING 16(4):206-218 Rivera SM; Menon V; White CD; Glaser B; Reiss AL Functional brain activation during arithmetic processing in females with fragile X Syndrome is related to FMRI protein expression | 7 | 13 |
| 1736 | 16 | 86 | 2014 2001 DEVELOPMENTAL PSYCHOBIOLOGY 39(2):107-123 Roberts JE; Boccia ML; Bailey DB; Hatton DD; Skinner M Cardiovascular indices of physiological arousal in boys with fragile X syndrome | 7 | 7 |
| 1737 | 17 | 42 | 2104 2002 AMERICAN JOURNAL OF SPEECH-LANGUAGE PATHOLOGY 11(4):295-304 Roberts JE; Mirrett P; Anderson K; Burchinal M; Neebe E Early communication, symbolic behavior, and social profiles of young males with fragile X syndrome | 0 | 0 |
| 1738 | 23 | 55 | 1994 2001 AMERICAN JOURNAL ON MENTAL RETARDATION 106(3):216-230 Roberts JE; Mirrett P; Burchinal M Receptive and expressive communication development of young males with fragile X syndrome | 5 | 8 |
| 1739 | 4 | 11 | 1413 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):198-202 Robinson H; Wake S; Wright F; Laing S; Turner G Informed choice in fragile X syndrome and its effects on prevalence | 9 | 11 |
| 1740 | 12 | 33 | 670 1990 AMERICAN JOURNAL OF HUMAN GENETICS 46(4):738-743 ROCCHI M; ARCHIDIACONO N; RINALDI A; FILIPPI G; BARTOLUCCI G; FANCELLO GS; SINISCALCO M MENTAL-RETARDATION IN HETEROZYGOTES FOR THE FRAGILE-X MUTATION - EVIDENCE IN FAVOR OF AN X INACTIVATION-DEPENDENT EFFECT | 11 | 13 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1741 | 0 | 0 | 746 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):103-103 ROCCHI M; MORABITO E; DINATALE P IDURONATE SULFATASE ACTIVITY ON LYMPHOBLASTOID CELL-LINES FROM SUBJECTS AFFECTED BY FRAGILE-X SYNDROME | 0 | 0 |
| 1742 | 2 | 7 | 308 1985 PRENATAL DIAGNOSIS 5(3):229-231 ROCCHI M; PECILE V; ARCHIDIACONO N; MONNI G; DUMEZ Y; FILIPPI G PRENATAL-DIAGNOSIS OF THE FRAGILE-X IN MALE MONOZYGOTIC TWINS - DISCORDANT EXPRESSION OF THE FRAGILE SITE IN AMNIOCYTES | 5 | 10 |
| 1743 | 0 | 0 | 1965 2001 ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY 221:U3-U3 Rodesittisuk P; Romero RM; Haworth IS Conformation of fragile X-associated triplet repeat DNA containing C-C mismatch pairs. | 0 | 0 |
| 1744 | 3 | 10 | 1524 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):227-231 Roge B Fragile X syndrome. Special education: the French context | 0 | 0 |
| 1745 | 4 | 6 | 2254 2003 CLINICAL GENETICS 64(1):54-56 Rogers C; Partington MW; Turner GM Tremor, ataxia and dementia in older men may indicate a carrier of the fragile X syndrome | 3 | 3 |
| 1746 | 10 | 20 | 420 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 |
| 1747 | 18 | 34 | 2033 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 | 9 | 15 |
| 1748 | 8 | 20 | 2049 2001 NEUROREPORT 12(11):2573-2576 Rojas DC; Benkers TL; Rogers SJ; Teale PD; Reite ML; Hagerman RJ Auditory evoked magnetic fields in adults with fragile X syndrome | 2 | 3 |
| 1749 | 4 | 4 | 796 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):347-348 ROMANO V; MASCALI G; CHIAVETTA V; RAGUSA RM; BARLETTA C; ROMANO C; MOLLICA F; MATTINA T; GROSS A; BROWN WT; DOBKIN CS; FERRANDO C RFLP ANALYSIS IN 5 SICILIAN FAMILIES WITH THE FRAGILE-X SYNDROME | 0 | 0 |
| 1750 | 12 | 22 | 811 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):421-424 ROSENBERG C; VIANNAMORGANTE AM; OTTO PA; NAVAJAS L EFFECT OF X-INACTIVATION ON FRAGILE-X FREQUENCY AND MENTAL-RETARDATION | 3 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1751 | 0 | 0 | 79 1982 NEUROLOGY 32(4):A190-A190 ROSENBERGER PB; WILSONCIAMBRONE S; MILUNSKY A SPEECH FLUENCY DISORDER IN THE FRAGILE-X SYNDROME | 2 | 2 |
| 1752 | 11 | 29 | 241 1985 AMERICAN JOURNAL OF HUMAN GENETICS 37(3):543-552 ROSENBLATT DS; DUSCHENES EA; HELLSTROM FV; GOLICK MS; VEKEMANS MJJ; ZEESMAN SF; ANDERMANN E FOLIC-ACID BLINDED TRIAL IN IDENTICAL-TWINS WITH FRAGILE-X SYNDROME | 9 | 13 |
| 1753 | 0 | 0 | 307 1985 PEDIATRIC RESEARCH 19(4):A253-A253 ROSENBLATT DS; ZEESMAN SF; VEKEMANS MJJ; DUSCHENES EA; HELLSTROM FV; GOLICK MS; ANDERMANN E FOLIC-ACID BLINDED TRIAL IN IDENTICAL-TWINS WITH FRAGILE X-SYNDROME | 0 | 0 |
| 1754 | 57 | 91 | 1212 1994 EUROPEAN JOURNAL OF CLINICAL INVESTIGATION 24(1):1-10 ROUSSEAU F THE FRAGILE-X SYNDROME - IMPLICATIONS OF MOLECULAR-GENETICS FOR THE CLINICAL SYNDROME | 7 | 10 |
| 1755 | 15 | 28 | 885 1991 NEW ENGLAND JOURNAL OF MEDICINE 325(24):1673-1681 ROUSSEAU F; HEITZ D; BIANCALANA V; BLUMENFELD S; KRETZ C; BOUE J; TOMMERUP N; VANDERHAGEN C; DELOZIERBLANCHET C; CROQUETTE MF; GILGENKRANTZ S; JALBERT P; VOELCKEL MA; OBERLE I; MANDEL JL DIRECT DIAGNOSIS BY DNA ANALYSIS OF THE FRAGILE X-SYNDROME OF MENTAL-RETARDATION | 268 | 438 |
| 1756 | 16 | 19 | 932 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):197-207 ROUSSEAU F; HEITZ D; BIANCALANA V; OBERLE I; MANDEL JL ON SOME TECHNICAL ASPECTS OF DIRECT DNA DIAGNOSIS OF THE FRAGILE-X SYNDROME | 27 | 46 |
| 1757 | 11 | 20 | 873 1991 JOURNAL OF MEDICAL GENETICS 28(12):830-836 ROUSSEAU F; HEITZ D; OBERLE I; MANDEL JL SELECTION IN BLOOD-CELLS FROM FEMALE CARRIERS OF THE FRAGILE-X SYNDROME - INVERSE CORRELATION BETWEEN AGE AND PROPORTION OF ACTIVE X-CHROMOSOMES CARRYING THE FULL MUTATION | 62 | 84 |
| 1758 | 0 | 0 | 881 1991 M S-MEDECINE SCIENCES 7(6):637-639 ROUSSEAU F; HEITZ D; OBERLE I; MANDEL JL; KRETZ C THE FRAGILE X-SYNDROME - NEW SURPRISES | 0 | 0 |
| 1759 | 30 | 38 | 1151 1994 AMERICAN JOURNAL OF HUMAN GENETICS 55(2):225-237 ROUSSEAU F; HEITZ D; TARLETON J; MACPHERSON J; MALMGREN H; DAHL N; BARNICOAT A; MATHEW C; MORNET E; TEJADA I; MADDALENA A; SPIEGEL R; SCHINZEL A; MARCOS JAG; SCHORDERET DF; SCHAAP T; MACCIONI L; RUSSO S; JACOBS PA; SCHWARTZ C; MANDEL JL A MULTICENTER STUDY ON GENOTYPE-PHENOTYPE CORRELATIONS IN THE FRAGILE-X-SYNDROME, USING DIRECT DIAGNOSIS WITH PROBE STB-12.3 - THE FIRST 2,253 CASES | 119 | 165 |
| 1760 | 0 | 0 | 1030 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):78-78 ROUSSEAU F; HEITZ D; TARLETON J; MACPHERSON J; PETTERSON U; MATHEW C; MORNET E; MADDALENA A; SCHINZEL A; MARCOS JAG; SCHORDERET DF; SCHAAP T; MACCIONI L; RUSSO S; JACOBS PA; SCHWARTZ C; MANDEL JL A COLLABORATIVE MULTICENTER STUDY OF DIRECT DIAGNOSIS OF THE FRAGILE-X SYNDROME WITH PROBE STB12.3 - THE 1ST 2253 CASES | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1761 | 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 |
| 1762 | 0 | 0 | 1048 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1222-1222 ROUSSEAU F; ROBB L; DERKALOUSTIAN V A MENTALLY NORMAL-MALE CARRIER OF A FRAGILE-X FULL MUTATION GAVE BIRTH TO A PREMUTATED DAUGHTER | 0 | 0 |
| 1763 | 33 | 42 | 1291 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(5):1006-1018 ROUSSEAU F; ROUILLARD P; MOREL ML; KHANDJIAN EW; MORGAN K PREVALENCE OF CARRIERS OF PREMUTATION-SIZE ALLELES OF THE FMRI GENE AND IMPLICATIONS FOR THE POPULATION-GENETICS OF THE FRAGILE-X SYNDROME | 78 | 105 |
| 1764 | 5 | 14 | 701 1990 HUMAN GENETICS 84(3):263-266 ROUSSEAU F; VINCENT A; OBERLE I; MANDEL JL NEW INFORMATIVE POLYMORPHISM AT THE DXS304 LOCUS, A CLOSE DISTAL MARKER FOR THE FRAGILE X-LOCUS | 4 | 19 |
| 1765 | 7 | 17 | 733 1991 AMERICAN JOURNAL OF HUMAN GENETICS 48(1):108-116 ROUSSEAU F; VINCENT A; RIVELLA S; HEITZ D; TRIBOLI C; MAESTRINI E; WARREN ST; SUTHERS GK; GOODFELLOW P; MANDEL JL; TONIOLO D; OBERLE I 4 CHROMOSOMAL BREAKPOINTS AND 4 NEW PROBES MARK OUT A 10-CM REGION ENCOMPASSING THE FRAGILE-X LOCUS (FRAXA) | 25 | 48 |
| 1766 | 10 | 25 | 1335 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):327-335 Roy JC; Johnsen J; Breese K; Hagerman R Fragile X syndrome: What is the impact of diagnosis on families? | 3 | 6 |
| 1767 | 0 | 0 | 505 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):23-24 RUDELLI R; MADRID R; BROWN WT FURTHER NEUROPATHOLOGICAL OBSERVATIONS IN ADULT FRAGILE-X | 0 | 0 |
| 1768 | 7 | 52 | 235 1985 ACTA NEUROPATHOLOGICA 67(3-4):289-295 RUDELLI RD; BROWN WT; WISNIEWSKI K; JENKINS EC; LAUREKAMIONOWSKA M; CONNELL F; WISNIEWSKI HM ADULT FRAGILE X-SYNDROME - CLINICO-NEUROPATHOLOGIC FINDINGS | 71 | 110 |
| 1769 | 1 | 9 | 150 1983 LANCET 1(8335):1221-1222 RUDELLI RD; JENKINS EC; WISNIEWSKI K; MORETZ R; BYRNE J; BROWN WT TESTICULAR SIZE IN FETAL FRAGILE X SYNDROME | 14 | 19 |
| 1770 | 18 | 30 | 1644 1998 CLINICAL GENETICS 54(4):309-314 Russo S; Briscioli V; Cogliati F; Macchi M; Lalatta F; Larizza L An unusual fragile X sibship: female compound heterozygote and male with a partially methylated full mutation | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1771 | 1 | 2 | 1901 2000 HUMAN REPRODUCTION 15(8):1874-1874 Rychlik DF Regarding recall bias in the association between idiopathic premature ovarian failure and fragile X premutation | 0 | 0 |
| 1772 | 14 | 23 | 1783 1999 EUROPEAN JOURNAL OF HUMAN GENETICS 7(2):212-216 Ryynanen M; Heinonen S; Makkonen M; Kajanoja E; Mannermaa A; Pertti K Feasibility and acceptance of screening for fragile X mutations in low-risk pregnancies | 12 | 16 |
| 1773 | 12 | 24 | 1302 1995 AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY 172(4):1236-1239 RYYNANEN M; KIRKINEN P; MANNERMAA A; SAARIKOSKI S CARRIER DIAGNOSIS OF THE FRAGILE-X SYNDROME - A CHALLENGE IN ANTENATAL CLINICS | 6 | 8 |
| 1774 | 7 | 10 | 1180 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):463-465 RYYNANEN M; PULKKINEN L; KIRKINEN P; SAARIKOSKI S FRAGILE-X SYNDROME IN EAST FINLAND - MOLECULAR APPROACH TO GENETIC AND PRENATAL-DIAGNOSIS | 3 | 4 |
| 1775 | 8 | 16 | 1912 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:81-85 Sabaratnam M Pathological and neuropathological findings in two males with fragile-X syndrome | 2 | 4 |
| 1776 | 16 | 27 | 1233 1994 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 38:27-35 SABARATNAM M; LAVER S; BUTLER L; PEMBREY M FRAGILE-X SYNDROME IN NORTH-EAST ESSEX - TOWARDS SYSTEMATIC SCREENING - CLINICAL-SELECTION | 6 | 8 |
| 1777 | 14 | 24 | 2264 2003 EUROPEAN CHILD & ADOLESCENT PSYCHIATRY 12(4):172-177 Sabaratnam M; Murthy NV; Wijeratne A; Buckingham A; Payne S Autistic-like behaviour profile and psychiatric morbidity in Fragile X Syndrome - A prospective ten-year follow-up study | 0 | 0 |
| 1778 | 0 | 0 | 1924 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:449-449 Sabaratnam M; Murthy V; Wijeratne A Fragile-X syndrome: A 10-year follow-up | 0 | 0 |
| 1779 | 13 | 27 | 2075 2001 SEIZURE-EUROPEAN JOURNAL OF EPILEPSY 10(1):60-63 Sabaratnam M; Vroegop PG; Gangadharan SK Epilepsy and EEG findings in 18 males with fragile X syndrome | 4 | 5 |
| 1780 | 0 | 0 | 2030 2001 JOURNAL OF DENTAL RESEARCH 80(4):1133-1133 Sabbagh A Clinical and panoramic radiographic considerations of oral conditions in Fragile X Syndrome (Martin-Bell Syndrome) | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1781 | 0 | 7 | 2070 2001 REVISTA DE NEUROLOGIA 33:S77-S81 Safont-Tria NB Psychomotricity and fragile X syndrome | 0 | 0 |
| 1782 | 26 | 32 | 1996 2001 ANNALS OF CLINICAL BIOCHEMISTRY 38:264-271 Saha S; Karmakar P; Chatterjee C; Banerjee D; Das S; Dasgupta UB Fragile X syndrome in Calcutta, India | 1 | 3 |
| 1783 | 36 | 66 | 1936 2000 JOURNAL OF MEDICAL GENETICS 37(11):842-850 Salat U; Bardoni B; Wohrle D; Steinbach P Increase of FMRP expression, raised levels of FMR1 mRNA, and clonal selection in proliferating cells with unmethylated fragile X repeat expansions: a clue to the sex bias in the transmission of full mutations? | 2 | 5 |
| 1784 | 4 | 11 | 349 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 |
| 1785 | 3 | 4 | 528 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):369-376 SANFILIPPO S; RAGUSA RM; SCILLATO F; RUGGERI M; NERI G FRAGILE-X EXPRESSION IN NORMAL AND MENTALLY-RETARDED SUBJECTS - EFFECT OF TREATMENT WITH AN ANTIFOLIC AGENT | 0 | 3 |
| 1786 | 9 | 21 | 2236 2003 ANNALES DE GENETIQUE 46(1):53-55 Santos CB; Hjalgrim H; Carneiro FRG; Ribeiro M; Boy RT; Pimentel MMG Concurrence of fragile X and Klinefelter syndromes: report of a new case of paternal nondisjunction | 0 | 0 |
| 1787 | 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 |
| 1788 | 6 | 26 | 160 1983 REVISTA MEDICA DE CHILE 111(6):597-600 SANTOS M; MORIZON G THE FRAGILE X SYNDROME - A CHROMOSOMAL DEFECT ASSOCIATED WITH MENTAL-RETARDATION | 0 | 0 |
| 1789 | 10 | 20 | 1823 1999 ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 27(3):175-181 Sarimski K Play and communicative behaviour in young boys with fragile-X syndrome. | 0 | 1 |
| 1790 | 2 | 10 | 632 1989 CYTOGENETICS AND CELL GENETICS 50(2-3):172-173 SAUER SM; PHELAN MC; RICHER CL; SCHWARTZ CE PHYSICAL MAPPING OF PROBES PROXIMAL TO THE FRAGILE-X LOCUS (FRAX) CONFIRMS THE ORDER F9-DXS105 (CX55.7)-DXS98 (4D8)-FRAXA | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1791 | 2 | 19 | 568 1988 CHROMOSOMA 96(5):391-396 SAVAGE JRK; FITCHETT M THE BEHAVIOR OF FRAGILE-X AND OTHER ABERRATIONS DURING RECOVERY FROM LOW FOLATE CONDITIONS | 0 | 3 |
| 1792 | 15 | 52 | 164 1984 ALABAMA JOURNAL OF MEDICAL SCIENCES 21(1):68-72 SCARBROUGH PR; COSPER P; FINLEY SC; SMITH NB FRAGILE-X SYNDROME - AN OVERVIEW | 0 | 3 |
| 1793 | 5 | 41 | 2326 2004 DEVELOPMENTAL SCIENCE 7(1):116-130 Scerif G; Cornish K; Wilding J; Driver J; Karmiloff-Smith A Visual search in typically developing toddlers and toddlers with Fragile X or Williams syndrome | 0 | 0 |
| 1794 | 0 | 0 | 2150 2002 JOURNAL OF COGNITIVE NEUROSCIENCE :50-51 Scerif G; Wilding J; Cornish K; Driver J; Humphreys K; Karmiloff-Smith A Executive control in visual search for multiple targets in toddlers with Fragile X Syndrome | 0 | 0 |
| 1795 | 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 |
| 1796 | 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 |
| 1797 | 21 | 62 | 2017 2001 EMBO JOURNAL 20(17):4803-4813 Schaeffer C; Bardoni B; Mandel JL; Ehresmann B; Ehresmann C; Moine H The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif | 42 | 75 |
| 1798 | 28 | 92 | 1301 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 60(6):480-493 Schapiro MB; Murphy DGM; Hagerman RJ; Azari NP; Alexander GE; Miezejeski CM; Hinton VJ; Horwitz B; Haxby JV; Kumar A; White B; Grady CL Adult fragile X syndrome: Neuropsychology, brain anatomy, and metabolism | 19 | 29 |
| 1799 | 21 | 64 | 2296 2003 NEURON 38(6):887-898 Schenck A; Bardoni B; Langmann C; Harden N; Mandel JL; Giangrande A CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein | 5 | 9 |
| 1800 | 18 | 36 | 2056 2001 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 98(15):8844-8849 Schenck A; Bardoni B; Moro A; Bagni C; Mandel JL A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P | 20 | 38 |
Page 18: 1 (Abbeduto L) 2 (BELGHITI D) 3 (Brown WT) 4 (Chen X) 5 (DAKER MG) 6 (DYKENS E) 7 (FITCHETT M) 8 (GLOVER TW) 9 (HAGERMAN RJ) 10 (HOFFMAN M) 11 (JANCAR J) 12 (KIMCHISARFATY C) 13 (LEE JT) 14 (MAES B) 15 (MIGEON BR) 16 (Myers GF) 17 (Patsalis PC) 18 (REISS AL) 19 (Schenck A) 20 (SMITS APT) 21 (SZABO P) 22 (TURNER G) 23 (Wang YC) 24 (WOHRLE D)
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