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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by first author.
Page 20: 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 |
|---|---|---|---|---|---|
| 1901 | 10 | 13 | 1114 1993 JOURNAL OF MEDICAL GENETICS 30(2):94-96 SMITS APT; DREESEN JCFM; POST JG; SMEETS DFCM; DEDIESMULDERS C; SPAANSVANDERBIJL T; GOVAERTS LCP; WARREN ST; OOSTRA BA; VANOOST BA THE FRAGILE-X SYNDROME - NO EVIDENCE FOR ANY RECENT MUTATIONS | 27 | 34 |
| 1902 | 13 | 22 | 936 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):244-254 SNOW K; DOUD L; HAGERMAN R; HULL C; HIRST MC; DAVIES KE; THIBODEAU SL ANALYSIS OF MUTATIONS AT THE FRAGILE-X LOCUS USING THE DNA PROBE OX1.9 | 14 | 16 |
| 1903 | 22 | 34 | 1058 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(6):1217-1228 SNOW K; DOUD LK; HAGERMAN R; PERGOLIZZI RG; ERSTER SH; THIBODEAU SN ANALYSIS OF A CGG SEQUENCE AT THE FMR-I LOCUS IN FRAGILE-X FAMILIES AND IN THE GENERAL-POPULATION | 84 | 136 |
| 1904 | 17 | 29 | 1221 1994 HUMAN MOLECULAR GENETICS 3(9):1543-1551 SNOW K; TESTER DJ; KRUCKEBERG KE; SCHAID DJ; THIBODEAU SN SEQUENCE-ANALYSIS OF THE FRAGILE-X TRINUCLEOTIDE REPEAT - IMPLICATIONS FOR THE ORIGIN OF THE FRAGILE-X MUTATION | 47 | 115 |
| 1905 | 0 | 0 | 198 1984 CYTOGENETICS AND CELL GENETICS 37(1-4):587-587 SNYDER FF; LIN CC; HARASYM CA; JAMRO HK; KUSHNIG ML; LOWE JK; OBRIEN SI EVIDENCE FOR CLOSE ASSOCIATION BETWEEN THE FRAGILE X(Q27-28)- CHROMOSOME SITE AND GLUCOSE-6-PHOSPHATE-DEHYDROGENASE (G6PD) BUT NOT WITH HYPOXANTHINE-GUANINE PHOSPHORIBOSYLTRANSFERASE (HPRT) | 3 | 3 |
| 1906 | 18 | 33 | 1242 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 | 17 | 32 |
| 1907 | 17 | 44 | 1167 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):378-385 SOBESKY WE; PENNINGTON BF; PORTER D; HULL CE; HAGERMAN RJ EMOTIONAL AND NEUROCOGNITIVE DEFICITS IN FRAGILE-X | 25 | 30 |
| 1908 | 19 | 37 | 1332 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):280-292 Sobesky WE; Porter D; Pennington BF; Hagerman RJ Dimensions of shyness in fragile X females | 12 | 17 |
| 1909 | 18 | 29 | 1434 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):340-345 Sobesky WE; Taylor AK; Pennington BF; Bennetto L; Porter D; Riddle J; Hagerman RJ Molecular/clinical correlations in females with fragile X | 26 | 35 |
| 1910 | 0 | 0 | 1778 1999 CYTOGENETICS AND CELL GENETICS 85(1-2):165-165 Sofocleous C; Mavrou A; Fryssira H; Kolialexi A; Tsenghi C; Metaxotou C FMRP (Fragile X Mental Retardation Protein) studies in mentally retarded children in Greece | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1911 | 0 | 0 | 2073 2001 SCIENCE 294(5548):1809-1809 Sohn E Genetics - Fragile X's missing partners identified | 0 | 1 |
| 1912 | 19 | 35 | 675 1990 AMERICAN JOURNAL OF HUMAN GENETICS 47(3):395-402 SOOD R; MULLIGAN LM; POON R; WHITE BN; HOLDEN JJA GENETIC-MAPPING OF 2 NEW DNA MARKERS IN XQ26-Q28 RELATIVE TO THE FRAGILE-X SYNDROME LOCUS | 3 | 7 |
| 1913 | 0 | 3 | 257 1985 CANADIAN MEDICAL ASSOCIATION JOURNAL 133(5):358-& SOUDEK D FRAGILE-X - A SYMPTOM OF THE DISEASE | 2 | 4 |
| 1914 | 3 | 6 | 267 1985 CLINICAL GENETICS 28(5):399-400 SOUDEK D DECREASE OF FRAGILE X-FREQUENCY IN STORED-BLOOD SAMPLES - INDIVIDUAL VARIABILITY | 1 | 1 |
| 1915 | 4 | 5 | 378 1986 CLINICAL GENETICS 30(4):346-347 SOUDEK D FRAGILE-X - EXPERIENCE OF A LABORATORY | 3 | 3 |
| 1916 | 3 | 9 | 137 1983 HUMAN GENETICS 65(1):88-89 SOUDEK D; EMANUEL M A FRAGILE X SUPPRESSOR IN THE NORMAL HUMAN-BLOOD | 3 | 4 |
| 1917 | 0 | 2 | 14 1981 CLINICAL GENETICS 19(2):140-141 SOUDEK D; GORZNY N NO FRAGILE X-CHROMOSOME IN NORMAL MEN | 1 | 3 |
| 1918 | 0 | 9 | 23 1981 LANCET 1(8219):556-557 SOUDEK D; MCGREGOR T SOURCES OF ERROR IN FRAGILE-X DETERMINATION | 6 | 9 |
| 1919 | 4 | 16 | 177 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):241-252 SOUDEK D; PARTINGTON MW; LAWSON JS THE FRAGILE-X SYNDROME .1. FAMILIAL VARIATION IN THE PROPORTION OF LYMPHOCYTES WITH THE FRAGILE SITE IN MALES | 24 | 29 |
| 1920 | 195 | 429 | 509 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):31-60 SPANO LM; OPITZ JM BIBLIOGRAPHY ON X-LINKED MENTAL-RETARDATION, THE FRAGILE-X AND RELATED SUBJECTS-IV (1988) | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1921 | 0 | 0 | 781 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):173-185 SPANO LM; OPITZ JM BIBLIOGRAPHY ON X-LINKED MENTAL-RETARDATION, THE FRAGILE-X, AND RELATED SUBJECTS .5. (1991) | 0 | 1 |
| 1922 | 10 | 12 | 1409 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):181-183 Spence WC; Black SH; Fallon L; Maddalena A; Cummings E; MenapaceDrew G; Bick DP; Levinson G; Schulman JD; HowardPeebles PN Molecular fragile X screening in normal populations | 13 | 17 |
| 1923 | 9 | 28 | 1299 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 60(1):39-43 SPINELLI M; ROCHA ACD; GIACHETI CM; RICHIERICOSTA A WORD-FINDING DIFFICULTIES, VERBAL PARAPHASIAS, AND VERBAL DYSPRAXIA IN 10 INDIVIDUALS WITH FRAGILE-X-SYNDROME | 5 | 5 |
| 1924 | 2 | 2 | 1247 1994 MENTAL RETARDATION 32(2):156-156 SPITZ HH FRAGILE-X SYNDROME IS NOT THE 2ND LEADING CAUSE OF MENTAL-RETARDATION | 0 | 1 |
| 1925 | 4 | 9 | 628 1989 BRITISH HEART JOURNAL 61(3):289-291 SREERAM N; WREN C; BHATE M; ROBERTSON P; HUNTER S CARDIAC ABNORMALITIES IN THE FRAGILE X-SYNDROME | 6 | 9 |
| 1926 | 20 | 27 | 1022 1993 AMERICAN JOURNAL OF DISEASES OF CHILDREN 147(7):723-726 STALEY LW; HULL CE; MAZZOCCO MMM; THIBODEAU SN; SNOW K; WILSON VL; TAYLOR A; MCGAVRAN L; WEINER D; RIDDLE J; OCONNOR R; HAGERMAN RJ MOLECULAR-CLINICAL CORRELATIONS IN CHILDREN AND ADULTS WITH FRAGILE X-SYNDROME | 21 | 24 |
| 1927 | 0 | 0 | 1541 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A192-A192 Staley-Gane L; Holloway SL; Flynn L; Logan L; Hageman RJ Assessment of patient agenda prior to genetic counseling for fragile X syndrome. | 0 | 0 |
| 1928 | 0 | 0 | 1264 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):135-135 STALEYGANE L; FLYNN L; CRONISTERSILVERMAN A; HAGERMAN RJ EXPANDING THE ROLE OF THE GENETIC COUNSELOR WORKING WITH FRAGILE-X FAMILIES | 0 | 0 |
| 1929 | 11 | 18 | 2223 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 116A(2):176-178 Stalker HJ; Keller KL; Gray BA; Zori RT Concurrence of fragile X syndrome and 47, XYY in an individual with a Prader-Willi-Like phenotype | 0 | 0 |
| 1930 | 6 | 34 | 429 1987 BIOLOGICAL PSYCHIATRY 22(3):303-312 STCLAIR DM; BLACKWOOD DHR; OLIVER CJ; DICKENS P P3 ABNORMALITY IN FRAGILE-X SYNDROME | 5 | 16 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1931 | 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 |
| 1932 | 0 | 1 | 226 1984 NEW ENGLAND JOURNAL OF MEDICINE 310(22):1471-1471 STEIN M THE FRAGILE X SYNDROME - DIAGNOSIS, BIOCHEMISTRY, AND INTERVENTION - HAGERMAN,RJ, MCBOGG,PM | 0 | 0 |
| 1933 | 2 | 6 | 61 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 |
| 1934 | 0 | 0 | 2126 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:227-227 Steinbach P; Jakubiczka S; Bettecken T X inactivation and fragile X methylation in human placentas | 0 | 0 |
| 1935 | 35 | 45 | 1097 1993 HUMAN GENETICS 92(5):491-498 STEINBACH P; WOHRLE D; TARIVERDIAN G; KENNERKNECHT I; BARBI G; EDLINGER H; ENDERS H; GOTZSOTHMANN M; HEILBRONNER H; HOSENFELD D; KIRCHEISEN R; MAJEWSKI F; MEINECKE P; PASSARGE E; SCHMIDT A; SEIDEL H; WOLFF G; ZANKL M MOLECULAR ANALYSIS OF MUTATIONS IN THE GENE FMR-1 SEGREGATING IN FRAGILE X-FAMILIES | 7 | 11 |
| 1936 | 0 | 0 | 610 1988 ZEITSCHRIFT FUR KLINISCHE MEDIZIN-ZKM 43(6):451-454 STEINBICKER V; SEEMANOVA E; MISSBACH D THE SYNDROME OF THE FRAGILE X (MARTIN-BELL-SYNDROME MBS) | 0 | 1 |
| 1937 | 3 | 36 | 2100 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 111(4):381-387 Steinhausen HC; von Gontard A; Spohr HL; Hauffa BP; Eiholzer U; Backes M; Willms J; Malin Z Behavioral phenotypes in four mental retardation syndromes: Fetal alcohol syndrome, Prader-Willi syndrome, fragile X syndrome, and tuberosis sclerosis | 0 | 0 |
| 1938 | 6 | 11 | 1696 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 | 10 | 16 |
| 1939 | 3 | 6 | 1166 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):374-377 STEYAERT J; BORGHGRAEF M; FRYNS JP APPARENTLY ENHANCED VISUAL INFORMATION-PROCESSING IN FEMALE FRAGILE-X CARRIERS - PRELIMINARY FINDINGS | 1 | 1 |
| 1940 | 0 | 0 | 2101 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 114(7):833-833 Steyaert J; Borghgraef M; Fryns JP A distinct neurocognitive phenotype in female fragile X premutation carriers | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1941 | 0 | 3 | 918 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):116-119 STEYAERT J; BORGHGRAEF M; GAULTHIER C; FRYNS JP; VANDENBERGHE H COGNITIVE PROFILE IN ADULT, NORMAL INTELLIGENT FEMALE FRAGILE-X CARRIERS | 6 | 9 |
| 1942 | 7 | 13 | 1423 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 |
| 1943 | 4 | 7 | 1165 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):370-373 STEYAERT J; DECRUYENAERE M; BORGHGRAEF M; FRYNS JP PERSONALITY PROFILE IN ADULT FEMALE FRAGILE-X CARRIERS - ASSESSED WITH THE MINNESOTA MULTIPHASIC PERSONALITY PROFILE (MMPI) | 3 | 8 |
| 1944 | 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 |
| 1945 | 18 | 64 | 1596 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 | 36 |
| 1946 | 7 | 18 | 1984 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 100(2):110-115 Stoll C Problems in the diagnosis of fragile X syndrome in young children are still present | 3 | 3 |
| 1947 | 4 | 7 | 1659 1998 HUMAN GENETICS 102(1):54-56 Storm K; Handig I; Reyniers E; Oostra BA; Kooy RF; Willems PJ Incomplete EcoRI digestion may lead to false diagnosis of fragile X syndrome | 0 | 1 |
| 1948 | 13 | 30 | 424 1987 ARCHIVES OF OPHTHALMOLOGY 105(8):1099-1102 STORM RL; PEBENITO R; FERRETTI C OPHTHALMOLOGIC FINDINGS IN THE FRAGILE X-SYNDROME | 5 | 7 |
| 1949 | 0 | 0 | 1235 1994 JOURNAL OF MEDICAL GENETICS 31(2):170-170 STRAIN L; PORTEOUS MEM; BONTHRON DT PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME - MANAGEMENT OF THE MALE FETUS WITH A PREMUTATION | 0 | 0 |
| 1950 | 16 | 21 | 1255 1994 PRENATAL DIAGNOSIS 14(6):469-474 STRAIN L; PORTEOUS MEM; GOSDEN CM; ELLIS PM; NEILSON JP; BONTHRON DT PRENATAL-DIAGNOSIS OF FRAGILE-X-SYNDROME - MANAGEMENT OF THE MALE FETUS WITH A PREMUTATION | 3 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1951 | 0 | 0 | 1655 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6:159-159 Strelnikov V; Nemstova M; Demina N; Galkina V; Kuleshov N; Zaletayev D DNA testing for fragile X syndrome | 0 | 0 |
| 1952 | 12 | 25 | 954 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 44(5):676-682 STROM CM; BRUSCA RM; PIZZI WJ DOUBLE-BLIND, PLACEBO-CONTROLLED CROSSOVER STUDY OF FOLINIC ACID (LEUCOVORIN(R)) FOR THE TREATMENT OF FRAGILE-X SYNDROME | 1 | 3 |
| 1953 | 1 | 42 | 2019 2001 GENETICS 157(2):717-725 Su MA; Wisotzkey RG; Newfeld SJ A screen for modifiers of decapentaplegic mutant phenotypes identifies lilliputian, the only member of the Fragile-X/Burkitt's lymphoma family of transcription factors in Drosophila melanogaster | 0 | 6 |
| 1954 | 1 | 2 | 581 1988 HUMAN GENETICS 78(2):196-197 SUBRT I; STIRSKA K FREQUENCY OF TRIRADIAL AND MULTIRADIAL CONFIGURATIONS IN FRAGILE X-CHROMOSOMES | 0 | 0 |
| 1955 | 5 | 10 | 1789 1999 HEREDITAS 130(2):189-190 Sucharov CC; Silva R; Rondinelli E; Moura-Neto RS Fragile X trinucleotide repeats from a normal population in Rio de Janeiro, Brazil | 0 | 0 |
| 1956 | 0 | 0 | 1550 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A407-A407 Sucharov CC; Varandas FR; Rondinelli E; Carakushansky G; Moura-Neto RS Establishment of a differential diagnostic of patients with Mental Retardation based on Southern-blot and PCR considering the frequency of Fragile X trinucleotide repeats from normal population in Rio de Janeiro, Brazil. | 0 | 0 |
| 1957 | 16 | 58 | 1995 2001 AMERICAN JOURNAL ON MENTAL RETARDATION 106(5):389-400 Sudhalter V; Belser RC Conversational characteristics of children with fragile x syndrome: Tangential language | 3 | 5 |
| 1958 | 11 | 23 | 684 1990 AMERICAN JOURNAL ON MENTAL RETARDATION 94(4):431-441 SUDHALTER V; COHEN IL; SILVERMAN W; WOLFSCHEIN EG CONVERSATIONAL ANALYSES OF MALES WITH FRAGILE-X, DOWN SYNDROME, AND AUTISM - COMPARISON OF THE EMERGENCE OF DEVIANT LANGUAGE | 51 | 64 |
| 1959 | 4 | 12 | 912 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 | 18 | 20 |
| 1960 | 3 | 21 | 820 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):493-497 SUDHALTER V; SCARBOROUGH HS; COHEN IL SYNTACTIC DELAY AND PRAGMATIC DEVIANCE IN THE LANGUAGE OF FRAGILE-X MALES | 21 | 29 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1961 | 0 | 0 | 463 1987 JAPANESE JOURNAL OF HUMAN GENETICS 32(2):122-123 SUGIO Y FRAGILE-X SYNDROME - COLLABORATIVE STUDIES OF JAPANESE PATIENTS | 0 | 0 |
| 1962 | 6 | 9 | 448 1987 GENETIKA 23(3):504-509 SULEIMANOVA DG; KULESHOV NP SPONTANEOUS AND INDUCED CHROMOSOMAL INSTABILITY IN PATIENTS WITH FRAGILE X-CHROMOSOME, SUFFERING FROM X-LINKED MENTAL-RETARDATION | 1 | 3 |
| 1963 | 19 | 55 | 1986 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 103(1):81-90 Sun HT; Cohen S; Kaufmann WE Annexin-1 is abnormally expressed in fragile X syndrome: Two-dimensional electrophoresis study in lymphocytes | 3 | 8 |
| 1964 | 7 | 12 | 1762 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 86(2):162-164 Sun YJ; Baumer A Nonrandom X inactivation and selection of fragile X full mutation in fetal fibroblasts | 1 | 3 |
| 1965 | 4 | 10 | 2310 2004 ACTA PHARMACOLOGICA SINICA 25(7):973-976 Sun YJ; Han X Dynamic behavior of fragile X full mutations in cultured female fetal fibroblasts | 0 | 0 |
| 1966 | 3 | 21 | 2016 2001 ELECTROPHORESIS 22(6):1188-1193 Sung WC; Lee GB; Tzeng CC; Chen SH Plastic microchip electrophoresis for genetic screening: The analysis of polymerase chain reactions products of fragile X (CGG)n alleles | 0 | 10 |
| 1967 | 10 | 33 | 1872 2000 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 275(3):973-980 Sung YJ; Conti J; Currie JR; Brown WT; Denman RB RNAs that interact with the Fragile X syndrome RNA binding protein FMRP | 23 | 30 |
| 1968 | 28 | 56 | 2276 2003 JOURNAL OF BIOLOGICAL CHEMISTRY 278(18):15669-15678 Sung YJ; Dolzhanskaya N; Nolin SL; Brown T; Currie JR; Denman RB The fragile X mental retardation protein FMRP binds elongation factor 1A mRNA and negatively regulates its translation in vivo | 5 | 9 |
| 1969 | 13 | 45 | 1504 1996 NIMHANS JOURNAL 14(3):201-207 Suresh KP; Girimaji SR; Manjunatha KR Newer genetics in mental retardation .1. Fragile X syndrome and triplet repeat mutations | 0 | 1 |
| 1970 | 24 | 128 | 138 1983 INTERNATIONAL REVIEW OF CYTOLOGY-A SURVEY OF CELL BIOLOGY 81:107-143 SUTHERLAND GR THE FRAGILE X-CHROMOSOME | 39 | 131 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1971 | 1 | 3 | 214 1984 JOURNAL OF MEDICAL GENETICS 21(1):74-75 SUTHERLAND GR ROUTINE DIAGNOSTIC-DETECTION OF THE FRAGILE X | 1 | 4 |
| 1972 | 0 | 0 | 229 1984 PATHOLOGY 16(1):108-108 SUTHERLAND GR THE FRAGILE X-CHROMOSOME | 0 | 0 |
| 1973 | 5 | 17 | 311 1985 TRENDS IN GENETICS 1(4):108-112 SUTHERLAND GR THE ENIGMA OF THE FRAGILE-X CHROMOSOME | 26 | 43 |
| 1974 | 0 | 0 | 367 1986 AUSTRALIAN PAEDIATRIC JOURNAL 22(4):356-356 SUTHERLAND GR; BAKER E INDUCTION OF THE FRAGILE-X IN FIBROBLASTS BY THYMIDINE | 0 | 0 |
| 1975 | 0 | 0 | 636 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):1086-1087 SUTHERLAND GR; BAKER E THE COMMON FRAGILE SITE (FRAXD) IS AT XQ27.2 AND CAN BE DISTINGUISHED FROM THE FRAGILE-X (FRAXA) AT XQ27.3 | 2 | 8 |
| 1976 | 5 | 23 | 695 1990 CLINICAL GENETICS 37(3):167-172 SUTHERLAND GR; BAKER E THE COMMON FRAGILE SITE IN BAND Q27 OF THE HUMAN X-CHROMOSOME IS NOT COINCIDENT WITH THE FRAGILE-X | 29 | 43 |
| 1977 | 0 | 0 | 427 1987 AUSTRALIAN PAEDIATRIC JOURNAL 23(1):81-81 SUTHERLAND GR; BAKER E; HOCKEY A; PURVISSMITH S THE USE OF THYMIDINE INDUCTION OF THE FRAGILE X-CHROMOSOME IN PRENATAL-DIAGNOSIS | 0 | 0 |
| 1978 | 4 | 7 | 491 1987 PRENATAL DIAGNOSIS 7(3):197-202 SUTHERLAND GR; BAKER E; PURVISSMITH S; HOCKEY A; KRUMINS E; EICHENBAUM SZ PRENATAL-DIAGNOSIS OF THE FRAGILE-X USING THYMIDINE INDUCTION | 5 | 13 |
| 1979 | 19 | 24 | 1153 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):281-293 SUTHERLAND GR; BROWN WT; HAGERMAN R; JENKINS E; LUBS H; MANDEL JL; NELSON D; NERI G; PARTINGTON MW; RICHARDS RI; STEVENSON R; TURNER G SIXTH INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND X-LINKED MENTAL-RETARDATION | 3 | 4 |
| 1980 | 6 | 11 | 886 1991 NEW ENGLAND JOURNAL OF MEDICINE 325(24):1720-1722 SUTHERLAND GR; GEDEON A; KORNMAN L; DONNELLY A; BYARD RW; MULLEY JC; KREMER E; LYNCH M; PRITCHARD M; YU S; RICHARDS RI PRENATAL-DIAGNOSIS OF FRAGILE X-SYNDROME BY DIRECT DETECTION OF THE UNSTABLE DNA-SEQUENCE | 61 | 86 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1981 | 2 | 8 | 75 1982 LANCET 1(8263):100-100 SUTHERLAND GR; JACKY PB PRENATAL-DIAGNOSIS OF FRAGILE-X CHROMOSOME | 6 | 13 |
| 1982 | 24 | 44 | 694 1990 CLINICAL GENETICS 37(1):2-11 SUTHERLAND GR; MULLEY JC DIAGNOSTIC MOLECULAR-GENETICS OF THE FRAGILE-X | 14 | 16 |
| 1983 | 35 | 63 | 1510 1996 PRENATAL DIAGNOSIS 16(13):1199-1211 Sutherland GR; Mulley JC Fragile X syndrome and Fragile XE mental retardation | 3 | 9 |
| 1984 | 17 | 34 | 1129 1993 MEDICAL JOURNAL OF AUSTRALIA 158(7):482-485 SUTHERLAND GR; MULLEY JC; RICHARDS RI FRAGILE-X SYNDROME - THE MOST COMMON CAUSE OF FAMILIAL INTELLECTUAL HANDICAP | 1 | 5 |
| 1985 | 17 | 33 | 1516 1996 VARIATION IN THE HUMAN GENOME 197:119-126 Sutherland GR; Richards RI Unusual inheritance patterns due to dynamic mutation in fragile X syndrome | 0 | 0 |
| 1986 | 4 | 22 | 664 1989 SCIENCE 246(4935):1298-1300 SUTHERS GK; CALLEN DF; HYLAND VJ; KOZMAN HM; BAKER E; EYRE H; HARPER PS; ROBERTS SH; HORSCAYLA MC; DAVIES KE; BELL MV; SUTHERLAND GR A NEW DNA MARKER TIGHTLY LINKED TO THE FRAGILE-X LOCUS (FRAXA) | 31 | 66 |
| 1987 | 6 | 38 | 674 1990 AMERICAN JOURNAL OF HUMAN GENETICS 47(2):187-195 SUTHERS GK; HYLAND VJ; CALLEN DF; OBERLE I; ROCCHI M; THOMAS NS; MORRIS CP; SCHWARTZ CE; SCHMIDT M; ROPERS HH; BAKER E; OOSTRA BA; DAHL N; WILSON PJ; HOPWOOD JJ; SUTHERLAND GR PHYSICAL MAPPING OF NEW DNA PROBES NEAR THE FRAGILE-X MUTATION (FRAXA) BY USING A PANEL OF CELL-LINES | 26 | 64 |
| 1988 | 16 | 33 | 735 1991 AMERICAN JOURNAL OF HUMAN GENETICS 48(3):460-467 SUTHERS GK; MULLEY JC; VOELCKEL MA; DAHL N; VAISANEN ML; STEINBACH P; GLASS IA; SCHWARTZ CE; VANOOST BA; THIBODEAU SN; HAITES NE; OOSTRA BA; GINE R; CARBALLO M; MORRIS CP; HOPWOOD JJ; SUTHERLAND GR GENETIC-MAPPING OF NEW DNA PROBES AT XQ27 DEFINES A STRATEGY FOR DNA STUDIES IN THE FRAGILE-X SYNDROME | 30 | 47 |
| 1989 | 18 | 35 | 858 1991 GENOMICS 10(3):576-582 SUTHERS GK; MULLEY JC; VOELCKEL MA; DAHL N; VAISANEN ML; STEINBACH P; GLASS IA; SCHWARTZ CE; VANOOST BA; THIBODEAU SN; HAITES NE; OOSTRA BA; SCHINZEL A; CARBALLO M; MORRIS CP; HOPWOOD JJ; SUTHERLAND GR LINKAGE HOMOGENEITY NEAR THE FRAGILE-X LOCUS IN NORMAL AND FRAGILE-X FAMILIES | 9 | 13 |
| 1990 | 5 | 7 | 703 1990 HUMAN GENETICS 85(1):141-142 SUTHERS GK; SUTHERLAND GR RECOMBINATION AND THE FRAGILE-X | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1991 | 0 | 2 | 565 1988 AUSTRALIAN PAEDIATRIC JOURNAL 24(1):97-97 SUTHERS GK; THODE A; TURNER GL CASE-REPORT - FRAGILE-X SYNDROME AND NEPHROGENIC DIABETES-INSIPIDUS | 0 | 0 |
| 1992 | 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 |
| 1993 | 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 |
| 1994 | 7 | 9 | 1120 1993 JOURNAL OF MEDICAL GENETICS 30(9):785-787 SUZUMORI K; YAMAUCHI M; SEKI N; KONDO I; HORI T PRENATAL-DIAGNOSIS OF A HYPERMETHYLATED FULL FRAGILE-X MUTATION IN CHORIONIC VILLI OF A MALE FETUS | 1 | 4 |
| 1995 | 5 | 14 | 668 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 |
| 1996 | 17 | 43 | 2226 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 118A(2):115-121 Symons FJ; Clark RD; Hatton DD; Skinner M; Bailey DB Self-injurious behavior in young boys with fragile X syndrome | 0 | 0 |
| 1997 | 15 | 47 | 2041 2001 JOURNAL OF SPECIAL EDUCATION 34(4):194-202 Symons FJ; Clark RD; Roberts JP; Bailey DB Classroom behavior of elementary school-age boys with fragile X syndrome | 2 | 3 |
| 1998 | 4 | 11 | 1758 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):306-308 Syrrou M; Georgiou I; Patsalis PC; Bouba I; Adonakis G; Papoulatos GN Fragile X premutations and (TA)n estrogen receptor polymorphism in women with ovarian dysfunction | 1 | 9 |
| 1999 | 13 | 20 | 1417 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):234-238 Syrrou M; Patsalis PC; Georgiou I; Hadjimarcou MI; ConstantinouDeltas CD; Pagoulatos G Evidence for high-risk haplotypes and (CGG)n expansion in fragile X syndrome in the Hellenic population of Greece and Cyprus | 5 | 15 |
| 2000 | 1 | 1 | 1447 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(3):527-527 Syrrou M; Patsalis PC; Georgiou I; Hadjimarcou MI; ConstantinouDeltas CD; Pagoulatos G Evidence for high-risk haplotypes and (CGG)n expansion in fragile X syndrome in the Hellenic population of Greece and Cyprus (vol 64, pg 234, 1996) | 0 | 0 |
Page 20: 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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