-
2
-
-
0028198920
-
Imprinting and anticipation: Are they relevant to genetic studies of schizophrenia?
-
(1994)
British Journal of Psychiatry
, vol.164
, pp. 619-624
-
-
Asherson, P.1
Walsh, C.2
Williams, J.3
Sargeant, M.4
Taylor, C.5
Clements, A.6
Gill, M.7
Owen, M.8
McGuffin, P.9
-
3
-
-
0020580436
-
Decrease of learning capacity in offspring with increasing paternal age in the rat
-
(1983)
Teratology
, vol.27
, pp. 141-148
-
-
Auroux, M.1
-
13
-
-
0034082294
-
Repeat sizes at CAG/CTG loci CTG18.1, ERDA1 and TGC13-7a in schizophrenia
-
(2000)
Psychiatric Genetics
, vol.10
, pp. 33-37
-
-
Bowen, T.1
Guy, C.A.2
Cardno, A.G.3
Vincent, J.B.4
Kennedy, J.L.5
Jones, L.A.6
Gray, M.7
Sanders, R.D.8
McCarthy, G.9
Murphy, K.C.10
Owen, M.J.11
O'Donovan, M.C.12
-
18
-
-
0032458026
-
Prader-Willi syndromepsychotic symptoms: II. A preliminary study of prevalence using the Psychopathology Assessment Schedule for Adults with Developmental Disability checklist
-
(1998)
Journal of Intellectual and Disability Research
, vol.42
, Issue.PART 6
, pp. 451-454
-
-
Clarke, D.1
-
20
-
-
16944364326
-
Autism or atypical autism in maternally but not paternally derived proximal 15q duplication
-
(1997)
American Journal of Human Genetics
, vol.60
, pp. 928-934
-
-
Cook E.H., Jr.1
Lindgren, V.2
Leventhal, B.L.3
Courchesne, R.4
Lincoln, A.5
Shulman, C.6
Lord, C.7
Courchesne, E.8
-
32
-
-
0027080030
-
A genetic study of type 2 neurofibromatosis in the United Kingdom: H. Guidelines for genetic counselling
-
(1992)
Journal of Medical Genetics
, vol.29
, pp. 847-852
-
-
Evans, D.G.1
Huson, S.M.2
Donnai, D.3
Neary, W.4
Blair, V.5
Newton, V.6
Strachan, T.7
Harris, R.8
-
33
-
-
11944267671
-
A genetic study of type 2 neurofibromatosis in the United Kingdom: I. Prevalence, mutation rate, fitness, and confirmation of maternal transmission effect on severity
-
(1992)
Journal of Medical Genetics
, vol.29
, pp. 841-846
-
-
Evans, D.G.1
Huson, S.M.2
Donnai, D.3
Neary, W.4
Blair, V.5
Teare, D.6
Newton, V.7
Strachan, T.8
Ramsden, R.9
Harris, R.10
-
39
-
-
12644303225
-
Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus
-
(1997)
Proceedings of the National Academy of Sciences of the United States of America
, vol.94
, pp. 587-592
-
-
Freedman, R.1
Coon, H.2
Myles-Worsley, M.3
Orr-Urtreger, A.4
Olincy, A.5
Davis, A.6
Polymeropoulos, M.7
Holik, J.8
Hopkins, J.9
Hoff, M.10
Rosenthal, J.11
Waldo, M.C.12
Reimherr, F.13
Wender, P.14
Yaw, J.15
Young, D.A.16
Breese, C.R.17
Adams, C.18
Patterson, D.19
Adler, L.E.20
Kruglyak, L.21
Leonard, S.22
Byerley, W.23
more..
-
41
-
-
0033941757
-
Paternal origin of FGFR2 mutations in sporadic cases of Crouzon syndrome and Pfeiffer syndrome
-
(2000)
American Journal of Human Genetics
, vol.66
, pp. 768-777
-
-
Glaser, R.L.1
Jiang, W.2
Boyadjiev, S.A.3
Tran, A.K.4
Zachary, A.A.5
Van Maldergem, L.6
Johnson, D.7
Walsh, S.8
Oldridge, M.9
Wall, S.A.10
Wilkie, A.O.11
Jabs, E.W.12
-
47
-
-
0026036288
-
Genomic imprinting and the strange case of the insulin-like growth factor II receptor
-
(1991)
Cell
, vol.64
, pp. 1045-1046
-
-
Haig, D.1
Graham, C.2
-
50
-
-
0029974119
-
The schizophrenogenic mother concept in American psychiatry
-
(1996)
Psychiatry
, vol.59
, pp. 274-297
-
-
Hartwell, C.E.1
-
58
-
-
13044276244
-
A decrease of reelin expression as a putative vulnerability factor in schizophrenia
-
(1998)
Proceedings of the National Academy of Sciences U S A
, vol.95
, pp. 15718-15723
-
-
Impagnatiello, F.1
Guidotti, A.R.2
Pesold, C.3
Dwivedi, Y.4
Caruncho, H.5
Pisu, M.G.6
Uzunov, D.P.7
Smalheiser, N.R.8
Davis, J.M.9
Pandey, G.N.10
Pappas, G.D.11
Tueting, P.12
Sharma, R.P.13
Costa, E.14
-
63
-
-
0030951904
-
Anticipation in schizophrenia: Biology or bias?
-
(1997)
American Journal of Medical Genetics
, vol.74
, pp. 275-280
-
-
Johnson, J.E.1
Cleary, J.2
Ahsan, H.3
Harkavy, F.J.4
Malaspina, D.5
Cloninger, C.R.6
Faraone, S.V.7
Tsuang, M.T.8
Kaufmann, C.A.9
-
65
-
-
0032516032
-
A third member of the synapsin gene family
-
(1998)
Proceedings of the National Academy of Sciences of the United States of America
, vol.95
, pp. 4667-4672
-
-
Kao, H.T.1
Porton, B.2
Czernik, A.J.3
Feng, J.4
Yiu, G.5
Haring, M.6
Benfenati, F.7
Greengard, P.8
-
68
-
-
0032503891
-
NIMH Genetics Initiative Millenium Schizophrenia Consortium: Linkage analysis of African-American pedigrees
-
(1998)
American Journal of Medical Genetics
, vol.81
, pp. 282-289
-
-
Kaufmann, C.A.1
Suarez, B.2
Malaspina, D.3
Pepple, J.4
Svrakic, D.5
Markel, P.D.6
Meyer, J.7
Zambuto, C.T.8
Schmitt, K.9
Matise, T.C.10
Harkavy Friedman, J.M.11
Hampe, C.12
Lee, H.13
Shore, D.14
Wynne, D.15
Faraone, S.V.16
Tsuang, M.T.17
Cloninger, C.R.18
-
72
-
-
0032897901
-
Analysis of germline mutation spectra at the Huntington's disease locus supports a mitotic mutation mechanism
-
(1999)
Human Molecular Genetics
, vol.8
, pp. 173-183
-
-
Leeflang, E.P.1
Tavare, S.2
Marjoram, P.3
Neal, C.O.4
Srinidhi, J.5
MacFarlane, H.6
MacDonald, M.E.7
Gusella, J.F.8
De Young, M.9
Wexler, N.S.10
Arnheim, N.11
-
78
-
-
0027363951
-
Gametic but not somatic instability of CAG repeat length in Huntington's disease
-
(1993)
Journal of Medical Genetics
, vol.30
, pp. 982-986
-
-
MacDonald, M.E.1
Barnes, G.2
Srinidhi, J.3
Duyao, M.P.4
Ambrose, C.M.5
Myers, R.H.6
Gray, J.7
Conneally, P.M.8
Young, A.9
Penney, J.10
-
79
-
-
12944257359
-
Relation of familial schizophrenia to negative symptoms but not to the deficit syndrome
-
(2000)
American Journal of Psychiatry
, vol.157
, pp. 994-1003
-
-
Malaspina, D.1
Goetz, R.R.2
Yale, S.3
Berman, A.4
Friedman, J.H.5
Tremeau, F.6
Printz, D.7
Amador, X.8
Johnson, J.9
Brown, A.10
Gorman, J.M.11
-
87
-
-
0034035450
-
A gene for ataxic cerebral palsy maps to chromosome 9p12-q12
-
(2000)
European Journal of Human Genetics
, vol.8
, pp. 267-272
-
-
McHale, D.P.1
Jackson, A.P.2
Campbell, D.A.3
Levene, M.I.4
Corry, P.5
Woods, C.G.6
Lench, N.J.7
Mueller, R.F.8
Markham, A.F.9
-
93
-
-
0030687684
-
Evidence for uniparental, paternal expression of the human GABAA receptor subunit genes, using microcell-mediated chromosome transfer
-
(1997)
Human Molecular Genetics
, vol.6
, pp. 2127-2133
-
-
Meguro, M.1
Mitsuya, K.2
Sui, H.3
Shigenami, K.4
Kugoh, H.5
Nakao, M.6
Oshimura, M.7
-
94
-
-
0033365230
-
Proteolipoprotein gene analysis in 82 patients with sporadic Pelizaeus-Merzbacher Disease: Duplications, the major cause of the disease, originate more frequently in male germ cells, but point mutations do not. The Clinical European Network on Brain Dysmyelinating Disease
-
(1999)
American Journal of Human Genetics
, vol.65
, pp. 360-369
-
-
Mimault, C.1
Giraud, G.2
Courtois, V.3
Cailloux, F.4
Boire, J.Y.5
Dastugue, B.6
Boespflug-Tanguy, O.7
-
101
-
-
10544244172
-
Confirmation of association between expanded CAG/CTG repeats and both schizophrenia and bipolar disorder
-
(1996)
Psychological Medicine
, vol.26
, pp. 1145-1153
-
-
O'Donovan, M.C.1
Guy, C.2
Craddock, N.3
Bowen, T.4
McKeon, P.5
Macedo, A.6
Maier, W.7
Wildenauer, D.8
Aschauer, H.N.9
Sorbi, S.10
Feldman, E.11
Mynett-Johnson, L.12
Claffey, E.13
Nacmias, B.14
Valente, J.15
Dourado, A.16
Grassi, E.17
Lenzinger, E.18
Heiden, A.M.19
Moorhead, S.20
Harrison, D.21
Williams, J.22
McGuffin, P.23
Owen, M.J.24
more..
-
103
-
-
0025335637
-
Wilms' tumor and paternal occupation
-
(1990)
Cancer Research
, vol.50
, pp. 3212-3217
-
-
Olshan, A.F.1
Breslow, N.E.2
Daling, J.R.3
Falletta, J.M.4
Grufferman, S.5
Robison, L.L.6
Waskerwitz, M.7
Hammond, G.D.8
-
106
-
-
0028365603
-
Unstable trinucleotide repeats and the diagnosis of neurodegenerative disease
-
(1994)
Human Pathology
, vol.25
, pp. 598-601
-
-
Orr, H.T.1
-
112
-
-
0032559241
-
Pfeiffer syndrome type 2: Further delineation and review of the literature
-
(1998)
American Journal of Medical Genetics
, vol.75
, pp. 245-251
-
-
Plomp, A.S.1
Hamel, B.C.2
Cobben, J.M.3
Verloes, A.4
Offermans, J.P.5
Lajeunie, E.6
Fryns, J.P.7
Die-Smulders, C.E.8
-
117
-
-
0025355888
-
Genetic linkage and complex diseases, with special reference to psychiatric disorders
-
(1990)
Genetic Epidemiology
, vol.7
, pp. 3-16
-
-
Risch, N.1
-
120
-
-
0028093135
-
Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia
-
(1994)
Nature
, vol.371
, pp. 252-254
-
-
Rousseau, F.1
Bonaventure, J.2
Legeai-Mallet, L.3
Pelet, A.4
Rozet, J.M.5
Maroteaux, P.6
Le Merrer, M.7
Munnich, A.8
-
122
-
-
0031671781
-
Ionizing radiationgenetic risks IX. Estimates of the frequencies of mendelian diseases and spontaneous mutation rates in human populations: A 1998 perspective
-
(1998)
Mutation Research
, vol.411
, pp. 129-178
-
-
Sankaranarayanan, K.1
-
125
-
-
0028930046
-
Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndrome
-
(1995)
Human Molecular Genetics
, vol.4
, pp. 323-328
-
-
Schell, U.1
Herr, A.2
Feldman, G.J.3
Robin, N.H.4
Zackai, E.H.5
Die-Smulders, C.6
Viskochil, D.H.7
Stewart, J.M.8
Wolff, G.9
Ohashi, H.10
-
131
-
-
0020457589
-
Family history and schizophrenia: Characteristics of groups with and without positive family histories
-
(1982)
Psychological Medicine
, vol.12
, pp. 591-594
-
-
Shur, E.1
-
134
-
-
16944366964
-
Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function
-
(1997)
Nature
, vol.387
, pp. 705-708
-
-
Skuse, D.H.1
James, R.S.2
Bishop, D.V.3
Coppin, B.4
Dalton, P.5
Aamodt-Leeper, G.6
Bacarese-Hamilton, M.7
Creswell, C.8
McGurk, R.9
Jacobs, P.A.10
-
140
-
-
0029988921
-
Somatic mosaicism of expanded CAG repeats in brains of patients with dentatorubral-pallidoluysian atrophy: Cellular population-dependent dynamics of mitotic instability
-
(1996)
American Journal of Human Genetics
, vol.58
, pp. 1212-1222
-
-
Takano, H.1
Onodera, O.2
Takahashi, H.3
Igarashi, S.4
Yamada, M.5
Oyake, M.6
Ikeuchi, T.7
Koide, R.8
Tanaka, H.9
Iwabuchi, K.10
Tsuji, S.11
-
143
-
-
0027381482
-
Molecular analysis of juvenile Huntington disease: The major influence on (CAG)n repeat length is the sex of the affected parent
-
(1993)
Human Molecular Genetics
, vol.2
, pp. 1535-1540
-
-
Telenius, H.1
Kremer, H.P.2
Theilmann, J.3
Andrew, S.E.4
Almqvist, E.5
Anvret, M.6
Greenberg, C.7
Greenberg, J.8
Lucotte, G.9
Squitieri, F.10
-
144
-
-
0032513590
-
CHARGE syndrome: Report of 47 cases and review
-
(1998)
American Journal of Medical Genetics
, vol.76
, pp. 402-409
-
-
Tellier, A.L.1
Cormier-Daire, V.2
Abadie, V.3
Amiel, J.4
Sigaudy, S.5
Bonnet, D.6
Lonlay-Debeney, P.7
Morrisseau-Durand, M.P.8
Hubert, P.9
Michel, J.L.10
Jan, D.11
Dollfus, H.12
Baumann, C.13
Labrune, P.14
Lacombe, D.15
Philip, N.16
LeMerrer, M.17
Briard, M.L.18
Munnich, A.19
Lyonnet, S.20
more..
-
146
-
-
0030867052
-
Birth prevalence, mutation rate, sex ratio, parents' age, and ethnicity in Apert syndrome
-
(1997)
American Journal of Medical Genetics
, vol.72
, pp. 394-398
-
-
Tolarova, M.M.1
Harris, J.A.2
Ordway, D.E.3
Vargervik, K.4
-
149
-
-
0034464005
-
The molecular and genetic basis of fibroblast growth factor receptor 3 disorders: The achondroplasia family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricans
-
(2000)
Endocrine Reviews
, vol.21
, pp. 23-39
-
-
Vajo, Z.1
Francomano, C.A.2
Wilkin, D.J.3
-
156
-
-
0032231407
-
Mutations in fibroblast growth-factor receptor 3 in sporadic cases of achondroplasia occur exclusively on the paternally derived chromosome
-
(1998)
American Journal of Human Genetics
, vol.63
, pp. 711-716
-
-
Wilkin, D.J.1
Szabo, J.K.2
Cameron, R.3
Henderson, S.4
Bellus, G.A.5
Mack, M.L.6
Kaitila, I.7
Loughlin, J.8
Munnich, A.9
Sykes, B.10
Bonaventure, J.11
Francomano, C.A.12
-
160
-
-
0033485719
-
Parental age at child's birth and son's risk of prostate cancer: The Framingham Study
-
(1999)
American Journal of Epidemiology
, vol.150
, pp. 1208-1212
-
-
Zhang, Y.1
Kreger, B.E.2
Dorgan, J.F.3
Cupples, L.A.4
Myers, R.H.5
Splansky, G.L.6
Schatzkin, A.7
Ellison, R.C.8
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