-
1
-
-
0032910319
-
Environment and vulnerability to major psychiatric illness: a case control study of early parental loss in major depression, bipolar disorder and schizophrenia
-
Agid O., Shapira B., Zislin J., Ritsner M., Ritsner M., Hanin B., Murad H., Troudart T., Bloch M., Heresco-Levy U., Lerer B. Environment and vulnerability to major psychiatric illness: a case control study of early parental loss in major depression, bipolar disorder and schizophrenia. Molecular Psychiatry 1999, 4:163-172.
-
(1999)
Molecular Psychiatry
, vol.4
, pp. 163-172
-
-
Agid, O.1
Shapira, B.2
Zislin, J.3
Ritsner, M.4
Ritsner, M.5
Hanin, B.6
Murad, H.7
Troudart, T.8
Bloch, M.9
Heresco-Levy, U.10
Lerer, B.11
-
3
-
-
21744440098
-
Comorbidity and pathophysiology of obsessive-compulsive disorder in schizophrenia: is there evidence for a schizo-obsessive subtype of schizophrenia?
-
Bottas A., Cooke R.G., Richter M.A. Comorbidity and pathophysiology of obsessive-compulsive disorder in schizophrenia: is there evidence for a schizo-obsessive subtype of schizophrenia?. Journal of Psychiatry & Neuroscience 2005, 30:187-193.
-
(2005)
Journal of Psychiatry & Neuroscience
, vol.30
, pp. 187-193
-
-
Bottas, A.1
Cooke, R.G.2
Richter, M.A.3
-
4
-
-
78249256348
-
The environment and susceptibility to schizophrenia
-
Brown A.S. The environment and susceptibility to schizophrenia. Progress in Neurobiology 2011, 93:23-58.
-
(2011)
Progress in Neurobiology
, vol.93
, pp. 23-58
-
-
Brown, A.S.1
-
5
-
-
0036714750
-
Paternal age and risk of schizophrenia in adult offspring
-
Brown A.S., Schaefer C.A., Wyatt R.J., Begg M.D., Goetz R., Bresnahan M.A., Harkavy-Friedman J., Gorman J.M., Malaspina D., Susser E.S. Paternal age and risk of schizophrenia in adult offspring. The American Journal of Psychiatry 2002, 159:1528-1533.
-
(2002)
The American Journal of Psychiatry
, vol.159
, pp. 1528-1533
-
-
Brown, A.S.1
Schaefer, C.A.2
Wyatt, R.J.3
Begg, M.D.4
Goetz, R.5
Bresnahan, M.A.6
Harkavy-Friedman, J.7
Gorman, J.M.8
Malaspina, D.9
Susser, E.S.10
-
6
-
-
0037678577
-
Parental age and risk of schizophrenia: a case-control study
-
Byrne M., Agerbo E., Ewald H., Eaton W.W., Mortensen P.B. Parental age and risk of schizophrenia: a case-control study. Archives of General Psychiatry 2003, 60:673-678.
-
(2003)
Archives of General Psychiatry
, vol.60
, pp. 673-678
-
-
Byrne, M.1
Agerbo, E.2
Ewald, H.3
Eaton, W.W.4
Mortensen, P.B.5
-
7
-
-
77957124207
-
China's below-replacement fertility: government policy or socioeconomic development?
-
Cai Y. China's below-replacement fertility: government policy or socioeconomic development?. Population and Development Review 2010, 36:419-440.
-
(2010)
Population and Development Review
, vol.36
, pp. 419-440
-
-
Cai, Y.1
-
10
-
-
18644367074
-
Immigration and schizophrenia: the social causation hypothesis revisited
-
Cooper B. Immigration and schizophrenia: the social causation hypothesis revisited. The British Journal of Psychiatry 2005, 186:361-363.
-
(2005)
The British Journal of Psychiatry
, vol.186
, pp. 361-363
-
-
Cooper, B.1
-
11
-
-
63949088440
-
Effect of socioeconomic status and parents' education at birth on risk of schizophrenia in offspring
-
Corcoran C., Perrin M., Harlap S., Deutsch L., Fennig S., Manor O., Nahon D., Kimhy D., Malaspina D., Susser E. Effect of socioeconomic status and parents' education at birth on risk of schizophrenia in offspring. Social Psychiatry and Psychiatric Epidemiology 2009, 44:265-271.
-
(2009)
Social Psychiatry and Psychiatric Epidemiology
, vol.44
, pp. 265-271
-
-
Corcoran, C.1
Perrin, M.2
Harlap, S.3
Deutsch, L.4
Fennig, S.5
Manor, O.6
Nahon, D.7
Kimhy, D.8
Malaspina, D.9
Susser, E.10
-
13
-
-
0034303523
-
The origins, patterns and implications of human spontaneous mutation
-
Crow J.F. The origins, patterns and implications of human spontaneous mutation. Nature Reviews. Genetics 2000, 1:40-47.
-
(2000)
Nature Reviews. Genetics
, vol.1
, pp. 40-47
-
-
Crow, J.F.1
-
14
-
-
0036714734
-
Paternal age and schizophrenia: further support for an association
-
Dalman C., Allebeck P. Paternal age and schizophrenia: further support for an association. The American Journal of Psychiatry 2002, 159:1591-1592.
-
(2002)
The American Journal of Psychiatry
, vol.159
, pp. 1591-1592
-
-
Dalman, C.1
Allebeck, P.2
-
15
-
-
0029078029
-
Biological basis of germline mutation-comparisons of spontaneous germline mutation-rates among Drosophila, mouse, and human
-
Drost J.B., Lee W.R. Biological basis of germline mutation-comparisons of spontaneous germline mutation-rates among Drosophila, mouse, and human. Environmental and Molecular Mutagenesis 1995, 25:48-64.
-
(1995)
Environmental and Molecular Mutagenesis
, vol.25
, pp. 48-64
-
-
Drost, J.B.1
Lee, W.R.2
-
16
-
-
10744220971
-
Paternal and maternal age as risk factors for psychosis: findings from Denmark, Sweden and Australia
-
El-Saadi O., Pedersen C.B., McNeil T.F., Saha S., Welham J., O'Callaghan E., Cantor-Graae E., Chant D., Mortensen P.B., McGrath J. Paternal and maternal age as risk factors for psychosis: findings from Denmark, Sweden and Australia. Schizophrenia Research 2004, 67:227-236.
-
(2004)
Schizophrenia Research
, vol.67
, pp. 227-236
-
-
El-Saadi, O.1
Pedersen, C.B.2
McNeil, T.F.3
Saha, S.4
Welham, J.5
O'Callaghan, E.6
Cantor-Graae, E.7
Chant, D.8
Mortensen, P.B.9
McGrath, J.10
-
17
-
-
0004085199
-
-
American Psychiatric Press, Washington, DC
-
First M.B., Spitzer R.L., Gibbon M., Williams J.B.W. Structured Clinical Interview for DSM-IV Axis I Disorders: Clinician Version (SCID-CV): Administration Booklet 1997, American Psychiatric Press, Washington, DC.
-
(1997)
Structured Clinical Interview for DSM-IV Axis I Disorders: Clinician Version (SCID-CV): Administration Booklet
-
-
First, M.B.1
Spitzer, R.L.2
Gibbon, M.3
Williams, J.B.W.4
-
18
-
-
77549086193
-
Fathers' behaviors and children's psychopathology
-
Flouri E. Fathers' behaviors and children's psychopathology. Clinical Psychology Review 2010, 30:363-369.
-
(2010)
Clinical Psychology Review
, vol.30
, pp. 363-369
-
-
Flouri, E.1
-
19
-
-
50949120272
-
Advancing paternal age and bipolar disorder
-
Frans E.M., Sandin S., Reichenberg A., Lichtenstein P., Langstrom N., Hultman C.M. Advancing paternal age and bipolar disorder. Archives of General Psychiatry 2008, 65:1034-1040.
-
(2008)
Archives of General Psychiatry
, vol.65
, pp. 1034-1040
-
-
Frans, E.M.1
Sandin, S.2
Reichenberg, A.3
Lichtenstein, P.4
Langstrom, N.5
Hultman, C.M.6
-
20
-
-
77952374703
-
De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia
-
S2d Team
-
Gauthier J., Champagne N., Lafreniere R.G., Xiong L., Spiegelman D., Brustein E., Lapointe M., Peng H.S., Cote M., Noreau A., Hamdan F.F., Addington A.M., Rapoport J.L., DeLisi L.E., Krebs M.O., Joober R., Fathalli F., Mouaffak F., Haghighi A.P., Neri C., Dube M.P., Samuels M.E., Marineau C., Stone E.A., Awadalla P., Barker P.A., Carbonetto S., Drapeau P., Rouleau G.A., S2d Team De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia. Proceedings of the National Academy of Sciences of the United States of America 2010, 107:7863-7868.
-
(2010)
Proceedings of the National Academy of Sciences of the United States of America
, vol.107
, pp. 7863-7868
-
-
Gauthier, J.1
Champagne, N.2
Lafreniere, R.G.3
Xiong, L.4
Spiegelman, D.5
Brustein, E.6
Lapointe, M.7
Peng, H.S.8
Cote, M.9
Noreau, A.10
Hamdan, F.F.11
Addington, A.M.12
Rapoport, J.L.13
DeLisi, L.E.14
Krebs, M.O.15
Joober, R.16
Fathalli, F.17
Mouaffak, F.18
Haghighi, A.P.19
Neri, C.20
Dube, M.P.21
Samuels, M.E.22
Marineau, C.23
Stone, E.A.24
Awadalla, P.25
Barker, P.A.26
Carbonetto, S.27
Drapeau, P.28
Rouleau, G.A.29
more..
-
21
-
-
0142059634
-
The paternal-age effect in Apert syndrome is due, in part, to the increased frequency of mutations in sperm
-
Glaser R.L., Broman K.W., Schulman R.L., Eskenazi B., Wyrobek A.J., Jabs E.W. The paternal-age effect in Apert syndrome is due, in part, to the increased frequency of mutations in sperm. American Journal of Human Genetics 2003, 73:939-947.
-
(2003)
American Journal of Human Genetics
, vol.73
, pp. 939-947
-
-
Glaser, R.L.1
Broman, K.W.2
Schulman, R.L.3
Eskenazi, B.4
Wyrobek, A.J.5
Jabs, E.W.6
-
23
-
-
77950587223
-
Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia
-
Wellcome Trust Case Control Consortium
-
Grozeva D., Kirov G., Ivanov D., Jones I.R., Jones L., Green E.K., St Clair D.M., Young A.H., Ferrier N., Farmer A.E., McGuffin P., Holmans P.A., Owen M.J., O'Donovan M.C., Craddock N. Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia. Archives of General Psychiatry 2010, 67:318-327. Wellcome Trust Case Control Consortium.
-
(2010)
Archives of General Psychiatry
, vol.67
, pp. 318-327
-
-
Grozeva, D.1
Kirov, G.2
Ivanov, D.3
Jones, I.R.4
Jones, L.5
Green, E.K.6
St Clair, D.M.7
Young, A.H.8
Ferrier, N.9
Farmer, A.E.10
McGuffin, P.11
Holmans, P.A.12
Owen, M.J.13
O'Donovan, M.C.14
Craddock, N.15
-
24
-
-
0037365627
-
Fertility of patients with schizophrenia, their siblings, and the general population: a cohort study from 1950 to 1959 in Finland
-
Haukka J., Suvisaari J., Lonnqvist J. Fertility of patients with schizophrenia, their siblings, and the general population: a cohort study from 1950 to 1959 in Finland. The American Journal of Psychiatry 2003, 160:460-463.
-
(2003)
The American Journal of Psychiatry
, vol.160
, pp. 460-463
-
-
Haukka, J.1
Suvisaari, J.2
Lonnqvist, J.3
-
25
-
-
0344199986
-
Parental age and risk of sporadic and familial cancer in offspring: implications for germ cell mutagenesis
-
Hemminki K., Kyyronen P. Parental age and risk of sporadic and familial cancer in offspring: implications for germ cell mutagenesis. Epidemiology 1999, 10:747-751.
-
(1999)
Epidemiology
, vol.10
, pp. 747-751
-
-
Hemminki, K.1
Kyyronen, P.2
-
26
-
-
51649107017
-
Rare chromosomal deletions and duplications increase risk of schizophrenia
-
International Schizophrenia Consortium
-
International Schizophrenia Consortium Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature 2008, 455:237-241.
-
(2008)
Nature
, vol.455
, pp. 237-241
-
-
-
27
-
-
68449086236
-
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
-
International Schizophrenia Consortium, Purcell S.M., Wray N.R., Stone J.L., Visscher P.M., O'Donovan M.C., Sullivan P.F.
-
International Schizophrenia Consortium, Purcell S.M., Wray N.R., Stone J.L., Visscher P.M., O'Donovan M.C., Sullivan P.F. Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature 2009, 460:748-752.
-
(2009)
Nature
, vol.460
, pp. 748-752
-
-
-
29
-
-
70449217362
-
A study of schizophrenia in the male: a psychiatric and social study based on 138 cases with follow up
-
Johanson E. A study of schizophrenia in the male: a psychiatric and social study based on 138 cases with follow up. Acta Psychiatrica et Neurologica Scandinavica supplementum 1958, 125:1-132.
-
(1958)
Acta Psychiatrica et Neurologica Scandinavica supplementum
, vol.125
, pp. 1-132
-
-
Johanson, E.1
-
30
-
-
21244503836
-
Obsessive-compulsive symptoms in schizophrenia: prevalence and clinical correlates
-
Kayahan B., Ozturk O., Veznedaroglu B., Eraslan D. Obsessive-compulsive symptoms in schizophrenia: prevalence and clinical correlates. Psychiatry and Clinical Neurosciences 2005, 59:291-295.
-
(2005)
Psychiatry and Clinical Neurosciences
, vol.59
, pp. 291-295
-
-
Kayahan, B.1
Ozturk, O.2
Veznedaroglu, B.3
Eraslan, D.4
-
32
-
-
84868665308
-
Resolving the evolutionary paradox of common, harmful, heritable mental disorders. American Journal of Medical Genetics. Part B
-
Keller M., Miller G. Resolving the evolutionary paradox of common, harmful, heritable mental disorders. American Journal of Medical Genetics. Part B. Neuropsychiatric Genetics 2006, 141B:385-452.
-
(2006)
Neuropsychiatric Genetics
, vol.141 B
, pp. 385-452
-
-
Keller, M.1
Miller, G.2
-
34
-
-
71449105010
-
A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression
-
Knight H.M., Pickard B.S., Maclean A., Malloy M.P., Soares D.C., McRae A.F., Condie A., White A., Hawkins W., McGhee K., van Beck M., MacIntyre D.J., Starr J.M., Deary I.J., Visscher P.M., Porteous D.J., Cannon R.E., St Clair D., Muir W.J., Blackwood D.H. A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression. American Journal of Human Genetics 2009, 85:833-846.
-
(2009)
American Journal of Human Genetics
, vol.85
, pp. 833-846
-
-
Knight, H.M.1
Pickard, B.S.2
Maclean, A.3
Malloy, M.P.4
Soares, D.C.5
McRae, A.F.6
Condie, A.7
White, A.8
Hawkins, W.9
McGhee, K.10
van Beck, M.11
MacIntyre, D.J.12
Starr, J.M.13
Deary, I.J.14
Visscher, P.M.15
Porteous, D.J.16
Cannon, R.E.17
St Clair, D.18
Muir, W.J.19
Blackwood, D.H.20
more..
-
35
-
-
0031788688
-
Lionel Sharples Penrose, 1898-1972: a personal memoir in celebration of the centenary of his birth
-
Laxova R. Lionel Sharples Penrose, 1898-1972: a personal memoir in celebration of the centenary of his birth. Genetics 1998, 150:1333-1340.
-
(1998)
Genetics
, vol.150
, pp. 1333-1340
-
-
Laxova, R.1
-
36
-
-
3343019031
-
Evidence for association between novel polymorphisms in the PRODH gene and schizophrenia in a Chinese population
-
Li T., Ma X.H., Sham P.C., Sun X.L., Hu X., Wang Q., Meng H.Q., Deng W., Liu X.H., Murray R.M., Collier D.A. Evidence for association between novel polymorphisms in the PRODH gene and schizophrenia in a Chinese population. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics 2004, 129B:13-15.
-
(2004)
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics
, vol.129 B
, pp. 13-15
-
-
Li, T.1
Ma, X.H.2
Sham, P.C.3
Sun, X.L.4
Hu, X.5
Wang, Q.6
Meng, H.Q.7
Deng, W.8
Liu, X.H.9
Murray, R.M.10
Collier, D.A.11
-
37
-
-
0033962482
-
Obsessive and compulsive symptoms in schizophrenia clinical and neurocognitive correlates
-
Lysaker P.H., Marks K.A., Picone J.B., Rollins A.L., Fastenau P.S., Bond G.R. Obsessive and compulsive symptoms in schizophrenia clinical and neurocognitive correlates. The Journal of Nervous and Mental Disease 2000, 188:78-83.
-
(2000)
The Journal of Nervous and Mental Disease
, vol.188
, pp. 78-83
-
-
Lysaker, P.H.1
Marks, K.A.2
Picone, J.B.3
Rollins, A.L.4
Fastenau, P.S.5
Bond, G.R.6
-
38
-
-
34250859540
-
Neurocognitive deficits in first-episode schizophrenic patients and their first-degree relatives
-
Ma X.H., Wang Q., Sham P.C., Liu X.H., Rabe-Hesketh S., Sun X.L., Hu J.M., Meng H.Q., Chen W., Chen E.Y.H., Deng W., Chan R.C.K., Murray R.M., Collier D.A., Li T. Neurocognitive deficits in first-episode schizophrenic patients and their first-degree relatives. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics 2007, 144B:407-416.
-
(2007)
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics
, vol.144 B
, pp. 407-416
-
-
Ma, X.H.1
Wang, Q.2
Sham, P.C.3
Liu, X.H.4
Rabe-Hesketh, S.5
Sun, X.L.6
Hu, J.M.7
Meng, H.Q.8
Chen, W.9
Chen, E.Y.H.10
Deng, W.11
Chan, R.C.K.12
Murray, R.M.13
Collier, D.A.14
Li, T.15
-
39
-
-
0035189109
-
Paternal factors and schizophrenia risk: de novo mutations and imprinting
-
Malaspina D. Paternal factors and schizophrenia risk: de novo mutations and imprinting. Schizophrenia Bulletin 2001, 27:379-393.
-
(2001)
Schizophrenia Bulletin
, vol.27
, pp. 379-393
-
-
Malaspina, D.1
-
40
-
-
18344371152
-
Paternal age and sporadic schizophrenia: evidence for de novo mutations
-
Malaspina D., Corcoran C., Fahim C., Berman A., Harkavy-Friedman J., Yale S., Goetz D., Goetz R., Harlap S., Gorman J. Paternal age and sporadic schizophrenia: evidence for de novo mutations. American Journal of Medical Genetics 2002, 114:299-303.
-
(2002)
American Journal of Medical Genetics
, vol.114
, pp. 299-303
-
-
Malaspina, D.1
Corcoran, C.2
Fahim, C.3
Berman, A.4
Harkavy-Friedman, J.5
Yale, S.6
Goetz, D.7
Goetz, R.8
Harlap, S.9
Gorman, J.10
-
41
-
-
20444503008
-
Paternal age and intelligence: implications for age-related genomic changes in male germ cells
-
Malaspina D., Reichenberg A., Weiser M., Fennig S., Davidson M., Harlap S., Wolitzky R., Rabinowitz J., Susser E., Knobler H.Y. Paternal age and intelligence: implications for age-related genomic changes in male germ cells. Psychiatric Genetics 2005, 15:117-125.
-
(2005)
Psychiatric Genetics
, vol.15
, pp. 117-125
-
-
Malaspina, D.1
Reichenberg, A.2
Weiser, M.3
Fennig, S.4
Davidson, M.5
Harlap, S.6
Wolitzky, R.7
Rabinowitz, J.8
Susser, E.9
Knobler, H.Y.10
-
42
-
-
0032837374
-
Towards a molecular understanding of Prader-Willi and Angelman syndromes
-
Mann M.R.W., Bautolomei M.S. Towards a molecular understanding of Prader-Willi and Angelman syndromes. Human Molecular Genetics 1999, 8:1867-1873.
-
(1999)
Human Molecular Genetics
, vol.8
, pp. 1867-1873
-
-
Mann, M.R.W.1
Bautolomei, M.S.2
-
43
-
-
70349956433
-
Finding the missing heritability of complex diseases
-
Manolio T.A., Collins F.S., Cox N.J., Goldstein D.B., Hindorff L.A., Hunter D.J., McCarthy M.I., Ramos E.M., Cardon L.R., Chakravarti A., Cho J.H., Guttmacher A.E., Kong A., Kruglyak L., Mardis E., Rotimi C.N., Slatkin M., Valle D., Whittemore A.S., Boehnke M., Clark A.G., Eichler E.E., Gibson G., Haines J.L., Mackay T.F.C., McCarroll S.A., Visscher P.M. Finding the missing heritability of complex diseases. Nature 2009, 461:747-753.
-
(2009)
Nature
, vol.461
, pp. 747-753
-
-
Manolio, T.A.1
Collins, F.S.2
Cox, N.J.3
Goldstein, D.B.4
Hindorff, L.A.5
Hunter, D.J.6
McCarthy, M.I.7
Ramos, E.M.8
Cardon, L.R.9
Chakravarti, A.10
Cho, J.H.11
Guttmacher, A.E.12
Kong, A.13
Kruglyak, L.14
Mardis, E.15
Rotimi, C.N.16
Slatkin, M.17
Valle, D.18
Whittemore, A.S.19
Boehnke, M.20
Clark, A.G.21
Eichler, E.E.22
Gibson, G.23
Haines, J.L.24
Mackay, T.F.C.25
McCarroll, S.A.26
Visscher, P.M.27
more..
-
45
-
-
0033558028
-
Season of birth and schizophrenia: a systematic review and meta-analysis of data from the Southern Hemisphere
-
McGrath J.J., Welham J.L. Season of birth and schizophrenia: a systematic review and meta-analysis of data from the Southern Hemisphere. Schizophrenia Research 1999, 35:237-242.
-
(1999)
Schizophrenia Research
, vol.35
, pp. 237-242
-
-
McGrath, J.J.1
Welham, J.L.2
-
46
-
-
0032977944
-
The fertility and fecundity of patients with psychoses
-
McGrath J.J., Hearle J., Jenner L., Plant K., Drummond A., Barkla J.M. The fertility and fecundity of patients with psychoses. Acta Psychiatrica Scandinavica 1999, 99:441-446.
-
(1999)
Acta Psychiatrica Scandinavica
, vol.99
, pp. 441-446
-
-
McGrath, J.J.1
Hearle, J.2
Jenner, L.3
Plant, K.4
Drummond, A.5
Barkla, J.M.6
-
47
-
-
1642503730
-
Association analysis of the catechol-O-methyltransferase (COMT), serotonin transporter (5-HTT) and serotonin 2A receptor (5HT2A) gene polymorphisms with obsessive-compulsive disorder
-
Meira-Lima I., Shavitt R.G., Miguita K., Ikenaga E., Miguel E.C., Vallada H. Association analysis of the catechol-O-methyltransferase (COMT), serotonin transporter (5-HTT) and serotonin 2A receptor (5HT2A) gene polymorphisms with obsessive-compulsive disorder. Genes, Brain, and Behavior 2004, 3:75-79.
-
(2004)
Genes, Brain, and Behavior
, vol.3
, pp. 75-79
-
-
Meira-Lima, I.1
Shavitt, R.G.2
Miguita, K.3
Ikenaga, E.4
Miguel, E.C.5
Vallada, H.6
-
48
-
-
80052238644
-
Meta-analysis of paternal age and schizophrenia risk in male versus female offspring
-
Miller B., Messias E., Miettunen J., Alaraisanen A., Jarvelin M.R., Koponen H., Rasanen P., Isohanni M., Kirkpatrick B. Meta-analysis of paternal age and schizophrenia risk in male versus female offspring. Schizophrenia Bulletin 2011, 37:1039-1047.
-
(2011)
Schizophrenia Bulletin
, vol.37
, pp. 1039-1047
-
-
Miller, B.1
Messias, E.2
Miettunen, J.3
Alaraisanen, A.4
Jarvelin, M.R.5
Koponen, H.6
Rasanen, P.7
Isohanni, M.8
Kirkpatrick, B.9
-
49
-
-
33845904134
-
Environment and schizophrenia: environmental factors in schizophrenia: childhood trauma - a critical review
-
Morgan C., Fisher H. Environment and schizophrenia: environmental factors in schizophrenia: childhood trauma - a critical review. Schizophrenia Bulletin 2007, 33:3-10.
-
(2007)
Schizophrenia Bulletin
, vol.33
, pp. 3-10
-
-
Morgan, C.1
Fisher, H.2
-
50
-
-
0015314585
-
Parental age effects on the occurrence of new mutations for the Marfan syndrome
-
Murdoch J.L., Walker B.A., McKusick V.A. Parental age effects on the occurrence of new mutations for the Marfan syndrome. Annals of Human Genetics 1972, 35:331-336.
-
(1972)
Annals of Human Genetics
, vol.35
, pp. 331-336
-
-
Murdoch, J.L.1
Walker, B.A.2
McKusick, V.A.3
-
51
-
-
61449229353
-
A genome-wide investigation of SNPs and CNVs in schizophrenia
-
Need A.C., Ge D.L., Weale M.E., Maia J., Feng S., Heinzen E.L., Shianna K.V., Yoon W., Kasperaviciute D., Gennarelli M., Strittmatter W.J., Bonvicini C., Rossi G., Jayathilake K., Cola P.A., McEvoy J.P., Keefe R.S.E., Fisher E.M.C., St Jean P.L., Giegling I., Hartmann A.M., Moller H.J., Ruppert A., Fraser G., Crombie C., Middleton L.T., St Clair D., Roses A.D., Muglia P., Francks C., Rujescu D., Meltzer H.Y., Goldstein D.B. A genome-wide investigation of SNPs and CNVs in schizophrenia. PLoS Genetics 2009, 5:e1000373.
-
(2009)
PLoS Genetics
, vol.5
-
-
Need, A.C.1
Ge, D.L.2
Weale, M.E.3
Maia, J.4
Feng, S.5
Heinzen, E.L.6
Shianna, K.V.7
Yoon, W.8
Kasperaviciute, D.9
Gennarelli, M.10
Strittmatter, W.J.11
Bonvicini, C.12
Rossi, G.13
Jayathilake, K.14
Cola, P.A.15
McEvoy, J.P.16
Keefe, R.S.E.17
Fisher, E.M.C.18
St Jean, P.L.19
Giegling, I.20
Hartmann, A.M.21
Moller, H.J.22
Ruppert, A.23
Fraser, G.24
Crombie, C.25
Middleton, L.T.26
St Clair, D.27
Roses, A.D.28
Muglia, P.29
Francks, C.30
Rujescu, D.31
Meltzer, H.Y.32
Goldstein, D.B.33
more..
-
52
-
-
0035158090
-
Evidence of a dose-response relationship between urbanicity during upbringing and schizophrenia risk
-
Pedersen C.B., Mortensen P.B. Evidence of a dose-response relationship between urbanicity during upbringing and schizophrenia risk. Archives of General Psychiatry 2001, 58:1039-1046.
-
(2001)
Archives of General Psychiatry
, vol.58
, pp. 1039-1046
-
-
Pedersen, C.B.1
Mortensen, P.B.2
-
53
-
-
0034940960
-
Family history, place and season of birth as risk factors for schizophrenia in Denmark: a replication and reanalysis
-
Pedersen C.B., Mortensen P.B. Family history, place and season of birth as risk factors for schizophrenia in Denmark: a replication and reanalysis. The British Journal of Psychiatry 2001, 179:46-52.
-
(2001)
The British Journal of Psychiatry
, vol.179
, pp. 46-52
-
-
Pedersen, C.B.1
Mortensen, P.B.2
-
54
-
-
50449119163
-
Parental age and mutation
-
Penrose L. Parental age and mutation. Lancet 1955, 269:312.
-
(1955)
Lancet
, vol.269
, pp. 312
-
-
Penrose, L.1
-
55
-
-
35648963256
-
Aberrant epigenetic regulation could explain the relationship of paternal age to schizophrenia
-
Perrin M.C., Brown A.S., Malaspina D. Aberrant epigenetic regulation could explain the relationship of paternal age to schizophrenia. Schizophrenia Bulletin 2007, 33:1270-1273.
-
(2007)
Schizophrenia Bulletin
, vol.33
, pp. 1270-1273
-
-
Perrin, M.C.1
Brown, A.S.2
Malaspina, D.3
-
57
-
-
78049450213
-
Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function
-
International Schizophrenia Consortium
-
Raychaudhuri S., Korn J.M., McCarroll S.A., Altshuler D., Sklar P., Purcell S., Daly M.J., International Schizophrenia Consortium Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function. PLoS Genetics 2010, 6:e1001097.
-
(2010)
PLoS Genetics
, vol.6
-
-
Raychaudhuri, S.1
Korn, J.M.2
McCarroll, S.A.3
Altshuler, D.4
Sklar, P.5
Purcell, S.6
Daly, M.J.7
-
58
-
-
33748297511
-
Advancing paternal age and autism
-
Reichenberg A., Gross R., Weiser M., Bresnahan M., Silverman J., Harlap S., Rabinowitz J., Shulman C., Malaspina D., Lubin G., Knobler H.Y., Davidson M., Susser E. Advancing paternal age and autism. Archives of General Psychiatry 2006, 63:1026-1032.
-
(2006)
Archives of General Psychiatry
, vol.63
, pp. 1026-1032
-
-
Reichenberg, A.1
Gross, R.2
Weiser, M.3
Bresnahan, M.4
Silverman, J.5
Harlap, S.6
Rabinowitz, J.7
Shulman, C.8
Malaspina, D.9
Lubin, G.10
Knobler, H.Y.11
Davidson, M.12
Susser, E.13
-
59
-
-
20544462411
-
Obsessive and compulsive symptoms in schizophrenia patients - from neuropsychology to clinical typology and classification
-
Reznik I., Kotler M., Weizman A. Obsessive and compulsive symptoms in schizophrenia patients - from neuropsychology to clinical typology and classification. The Journal of Neuropsychiatry and Clinical Neurosciences 2005, 17:254-255.
-
(2005)
The Journal of Neuropsychiatry and Clinical Neurosciences
, vol.17
, pp. 254-255
-
-
Reznik, I.1
Kotler, M.2
Weizman, A.3
-
60
-
-
0023201611
-
Spontaneous mutation and parental age in humans
-
Risch N., Reich E.W., Wishnick M.M., McCarthy J.G. Spontaneous mutation and parental age in humans. American Journal of Human Genetics 1987, 41:218-248.
-
(1987)
American Journal of Human Genetics
, vol.41
, pp. 218-248
-
-
Risch, N.1
Reich, E.W.2
Wishnick, M.M.3
McCarthy, J.G.4
-
61
-
-
63549147533
-
Advanced paternal age is associated with impaired neurocognitive outcomes during infancy and childhood
-
Saha S., Barnett A.G., Foldi C., Burne T.H., Eyles D.W., Buka S.L., McGrath J.J. Advanced paternal age is associated with impaired neurocognitive outcomes during infancy and childhood. PLoS medicine 2009, 6:e1000040.
-
(2009)
PLoS medicine
, vol.6
-
-
Saha, S.1
Barnett, A.G.2
Foldi, C.3
Burne, T.H.4
Eyles, D.W.5
Buka, S.L.6
McGrath, J.J.7
-
62
-
-
18344413881
-
Autism and maternally derived aberrations of chromosome 15q
-
Schroer R.J., Phelan M.C., Michaelis R.C., Crawford E.C., Skinner S.A., Cuccaro M., Simensen R.J., Bishop J., Skinner C., Fender D., Stevenson R.E. Autism and maternally derived aberrations of chromosome 15q. American Journal of Medical Genetics 1998, 76:327-336.
-
(1998)
American Journal of Medical Genetics
, vol.76
, pp. 327-336
-
-
Schroer, R.J.1
Phelan, M.C.2
Michaelis, R.C.3
Crawford, E.C.4
Skinner, S.A.5
Cuccaro, M.6
Simensen, R.J.7
Bishop, J.8
Skinner, C.9
Fender, D.10
Stevenson, R.E.11
-
63
-
-
70449732249
-
Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders
-
Sebat J., Levy D.L., McCarthy S.E. Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders. Trends in Genetics 2009, 25:528-535.
-
(2009)
Trends in Genetics
, vol.25
, pp. 528-535
-
-
Sebat, J.1
Levy, D.L.2
McCarthy, S.E.3
-
64
-
-
8544276579
-
Paternal age and schizophrenia: a population based cohort study
-
Sipos A., Rasmussen F., Harrison G., Tynelius P., Lewis G., Leon D.A., Gunnell D. Paternal age and schizophrenia: a population based cohort study. British Medical Journal 2004, 329:1070-1073.
-
(2004)
British Medical Journal
, vol.329
, pp. 1070-1073
-
-
Sipos, A.1
Rasmussen, F.2
Harrison, G.3
Tynelius, P.4
Lewis, G.5
Leon, D.A.6
Gunnell, D.7
-
65
-
-
16944366964
-
Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function
-
Skuse D.H., James R.S., Bishop D.V.M., Coppin B., Dalton P., Aamodt-Leeper G., Bacarese-Hamilton M., Creswell C., McGurk R., Jacobs P.A. Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function. Nature 1997, 387:705-708.
-
(1997)
Nature
, vol.387
, pp. 705-708
-
-
Skuse, D.H.1
James, R.S.2
Bishop, D.V.M.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
-
66
-
-
49949085933
-
Large recurrent microdeletions associated with schizophrenia
-
Group
-
Stefansson H., Rujescu D., Cichon S., Pietilainen O.P.H., Ingason A., Steinberg S., Fossdal R., Sigurdsson E., Sigmundsson T., Buizer-Voskamp J.E., Hansen T., Jakobsen K.D., Muglia P., Francks C., Matthews P.M., Gylfason A., Halldorsson B.V., Gudbjartsson D., Thorgeirsson T.E., Sigurdsson A., Jonasdottir A., Jonasdottir A., Bjornsson A., Mattiasdottir S., Blondal T., Haraldsson M., Magnusdottir B.B., Giegling I., Moller H.J., Hartmann A., Shianna K.V., Ge D.L., Need A.C., Crombie C., Fraser G., Walker N., Lonnqvist J., Suvisaari J., Tuulio-Henriksson A., Paunio Tm, Toulopoulou T., Bramon E., Di Forti M., Murray R., Ruggeri M., Vassos E., Tosato S., Walshe M., Li T., Vasilescu C., Muhleisen T.W., Wang A.G., Ullum H., Djurovic S., Melle I., Olesen J., Kiemeney L.A., Franke B., Sabatti C., Freimer N.B., Gulcher J.R., Thorsteinsdottir U., Kong A., Andreassen O.A., Ophoff R.A., Georgi A., Rietschel M., Werge T., Petursson H., Goldstein D.B., Nothen M.M., Peltonen L., Collier D.A., St Clair D., Stefansson K., Group Large recurrent microdeletions associated with schizophrenia. Nature 2008, 455:232-261.
-
(2008)
Nature
, vol.455
, pp. 232-261
-
-
Stefansson, H.1
Rujescu, D.2
Cichon, S.3
Pietilainen, O.P.H.4
Ingason, A.5
Steinberg, S.6
Fossdal, R.7
Sigurdsson, E.8
Sigmundsson, T.9
Buizer-Voskamp, J.E.10
Hansen, T.11
Jakobsen, K.D.12
Muglia, P.13
Francks, C.14
Matthews, P.M.15
Gylfason, A.16
Halldorsson, B.V.17
Gudbjartsson, D.18
Thorgeirsson, T.E.19
Sigurdsson, A.20
Jonasdottir, A.21
Jonasdottir, A.22
Bjornsson, A.23
Mattiasdottir, S.24
Blondal, T.25
Haraldsson, M.26
Magnusdottir, B.B.27
Giegling, I.28
Moller, H.J.29
Hartmann, A.30
Shianna, K.V.31
Ge, D.L.32
Need, A.C.33
Crombie, C.34
Fraser, G.35
Walker, N.36
Lonnqvist, J.37
Suvisaari, J.38
Tuulio-Henriksson, A.39
Paunio, T.40
Toulopoulou, T.41
Bramon, E.42
Di Forti, M.43
Murray, R.44
Ruggeri, M.45
Vassos, E.46
Tosato, S.47
Walshe, M.48
Li, T.49
Vasilescu, C.50
Muhleisen, T.W.51
Wang, A.G.52
Ullum, H.53
Djurovic, S.54
Melle, I.55
Olesen, J.56
Kiemeney, L.A.57
Franke, B.58
Sabatti, C.59
Freimer, N.B.60
Gulcher, J.R.61
Thorsteinsdottir, U.62
Kong, A.63
Andreassen, O.A.64
Ophoff, R.A.65
Georgi, A.66
Rietschel, M.67
Werge, T.68
Petursson, H.69
Goldstein, D.B.70
Nothen, M.M.71
Peltonen, L.72
Collier, D.A.73
St Clair, D.74
Stefansson, K.75
more..
-
67
-
-
68449090594
-
Common variants conferring risk of schizophrenia
-
Group
-
Stefansson H., Ophoff R.A., Steinberg S., Andreassen O.A., Cichon S., Rujescu D., Werge T., Pietilainen O.P.H., Mors O., Mortensen P.B., Sigurdsson E., Gustafsson O., Nyegaard M., Tuulio-Henriksson A., Ingason A., Hansen T., Suvisaari J., Lonnqvist J., Paunio T., Borglum A.D., Hartmann A., Fink-Jensen A., Nordentoft M., Hougaard D., Norgaard-Pedersen B., Bottcher Y., Olesen J., Breuer R., Moller H.J., Giegling I., Rasmussen H.B., Timm S., Mattheisen M., Bitter I., Rethelyi J.M., Magnusdottir B.B., Sigmundsson T., Olason P., Mason G., Gulcher J.R., Haraldsson M., Fossdal R., Thorgeirsson T.E., Thorsteinsdottir U., Ruggeri M., Tosato S., Franke B., Strengman E., Kiemeney L.A., Melle I., Djurovic S., Abramova L., Kaleda V., Sanjuan J., de Frutos R., Bramon E., Vassos E., Fraser G., Ettinger U., Picchioni M., Walker N., Toulopoulou T., Need A.C., Ge D., Yoon J.L., Shianna K.V., Freimer N.B., Cantor R.M., Murray R., Kong A., Golimbet V., Carracedo A., Arango C., Costas J., Jonsson E.G., Terenius L., Agartz I., Petursson H., Nothen M.M., Rietschel M., Matthews P.M., Muglia P., Peltonen L., St Clair D., Goldstein D.B., Stefansson K., Collier D.A., Group Common variants conferring risk of schizophrenia. Nature 2009, 460(7256):744-U799.
-
(2009)
Nature
, vol.460
, Issue.7256
-
-
Stefansson, H.1
Ophoff, R.A.2
Steinberg, S.3
Andreassen, O.A.4
Cichon, S.5
Rujescu, D.6
Werge, T.7
Pietilainen, O.P.H.8
Mors, O.9
Mortensen, P.B.10
Sigurdsson, E.11
Gustafsson, O.12
Nyegaard, M.13
Tuulio-Henriksson, A.14
Ingason, A.15
Hansen, T.16
Suvisaari, J.17
Lonnqvist, J.18
Paunio, T.19
Borglum, A.D.20
Hartmann, A.21
Fink-Jensen, A.22
Nordentoft, M.23
Hougaard, D.24
Norgaard-Pedersen, B.25
Bottcher, Y.26
Olesen, J.27
Breuer, R.28
Moller, H.J.29
Giegling, I.30
Rasmussen, H.B.31
Timm, S.32
Mattheisen, M.33
Bitter, I.34
Rethelyi, J.M.35
Magnusdottir, B.B.36
Sigmundsson, T.37
Olason, P.38
Mason, G.39
Gulcher, J.R.40
Haraldsson, M.41
Fossdal, R.42
Thorgeirsson, T.E.43
Thorsteinsdottir, U.44
Ruggeri, M.45
Tosato, S.46
Franke, B.47
Strengman, E.48
Kiemeney, L.A.49
Melle, I.50
Djurovic, S.51
Abramova, L.52
Kaleda, V.53
Sanjuan, J.54
de Frutos, R.55
Bramon, E.56
Vassos, E.57
Fraser, G.58
Ettinger, U.59
Picchioni, M.60
Walker, N.61
Toulopoulou, T.62
Need, A.C.63
Ge, D.64
Yoon, J.L.65
Shianna, K.V.66
Freimer, N.B.67
Cantor, R.M.68
Murray, R.69
Kong, A.70
Golimbet, V.71
Carracedo, A.72
Arango, C.73
Costas, J.74
Jonsson, E.G.75
Terenius, L.76
Agartz, I.77
Petursson, H.78
Nothen, M.M.79
Rietschel, M.80
Matthews, P.M.81
Muglia, P.82
Peltonen, L.83
St Clair, D.84
Goldstein, D.B.85
Stefansson, K.86
Collier, D.A.87
more..
-
69
-
-
79961114905
-
Early versus late onset obsessive-compulsive disorder: evidence for distinct subtypes
-
Taylor S. Early versus late onset obsessive-compulsive disorder: evidence for distinct subtypes. Clinical Psychology Review 2011, 31:1083-1100.
-
(2011)
Clinical Psychology Review
, vol.31
, pp. 1083-1100
-
-
Taylor, S.1
-
70
-
-
0032972847
-
Obsessive-compulsive disorder in schizophrenia: epidemiologic and biologic overlap
-
Tibbo P., Warneke L. Obsessive-compulsive disorder in schizophrenia: epidemiologic and biologic overlap. Journal of Psychiatry & Neuroscience 1999, 24:15-24.
-
(1999)
Journal of Psychiatry & Neuroscience
, vol.24
, pp. 15-24
-
-
Tibbo, P.1
Warneke, L.2
-
71
-
-
20444367662
-
Advanced paternal age associated with an elevated risk for schizophrenia in offspring in a Japanese population
-
Tsuchiya K.J., Takagai S., Kawai M., Matsumoto H., Nakamura K., Minabe Y., Mori N., Takei N. Advanced paternal age associated with an elevated risk for schizophrenia in offspring in a Japanese population. Schizophrenia Research 2005, 76:337-342.
-
(2005)
Schizophrenia Research
, vol.76
, pp. 337-342
-
-
Tsuchiya, K.J.1
Takagai, S.2
Kawai, M.3
Matsumoto, H.4
Nakamura, K.5
Minabe, Y.6
Mori, N.7
Takei, N.8
-
72
-
-
53949105679
-
Paternal age at birth and high-functioning autistic-spectrum disorder in offspring
-
Tsuchiya K.J., Matsumoto K., Miyachi T., Tsujii M., Nakamura K., Takagai S., Kawai M., Yagi A., Iwaki K., Suda S., Sugihara G., Iwata Y., Matsuzaki H., Sekine Y., Suzuki K., Sugiyama T., Mori N., Takei N. Paternal age at birth and high-functioning autistic-spectrum disorder in offspring. The British Journal of Psychiatry 2008, 193:316-321.
-
(2008)
The British Journal of Psychiatry
, vol.193
, pp. 316-321
-
-
Tsuchiya, K.J.1
Matsumoto, K.2
Miyachi, T.3
Tsujii, M.4
Nakamura, K.5
Takagai, S.6
Kawai, M.7
Yagi, A.8
Iwaki, K.9
Suda, S.10
Sugihara, G.11
Iwata, Y.12
Matsuzaki, H.13
Sekine, Y.14
Suzuki, K.15
Sugiyama, T.16
Mori, N.17
Takei, N.18
-
73
-
-
84858860265
-
Neurological soft signs in schizophrenia and obsessive compulsive disorder spectrum
-
Tumkaya S., Karadag F., Oguzhanoglu N.K. Neurological soft signs in schizophrenia and obsessive compulsive disorder spectrum. European Psychiatry 2010, 10.1016/j.eurpsy.2010.03.005.
-
(2010)
European Psychiatry
-
-
Tumkaya, S.1
Karadag, F.2
Oguzhanoglu, N.K.3
-
74
-
-
70450224887
-
The role of genetic variation in the causation of mental illness: an evolution-informed framework
-
Uher R. The role of genetic variation in the causation of mental illness: an evolution-informed framework. Molecular Psychiatry 2009, 14:1072-1082.
-
(2009)
Molecular Psychiatry
, vol.14
, pp. 1072-1082
-
-
Uher, R.1
-
75
-
-
33845319214
-
Reaction time of the Continuous Performance Test is an endophenotypic marker for schizophrenia: a study of first-episode neuroleptic-naive schizophrenia, their non-psychotic first-degree relatives and healthy population controls
-
Wang Q., Chan R., Sun J.H., Yao J., Deng W., Sun X.L., Liu X.H., Sham P.C., Ma X.H., Meng H.Q., Murray R.M., Collier D.A., Li T. Reaction time of the Continuous Performance Test is an endophenotypic marker for schizophrenia: a study of first-episode neuroleptic-naive schizophrenia, their non-psychotic first-degree relatives and healthy population controls. Schizophrenia Research 2007, 89:293-298.
-
(2007)
Schizophrenia Research
, vol.89
, pp. 293-298
-
-
Wang, Q.1
Chan, R.2
Sun, J.H.3
Yao, J.4
Deng, W.5
Sun, X.L.6
Liu, X.H.7
Sham, P.C.8
Ma, X.H.9
Meng, H.Q.10
Murray, R.M.11
Collier, D.A.12
Li, T.13
-
76
-
-
33846643157
-
Paternal ages below or above 35 years old are associated with a different risk of schizophrenia in the offspring
-
Wohl M., Gorwood P. Paternal ages below or above 35 years old are associated with a different risk of schizophrenia in the offspring. European Psychiatry 2007, 22:22-26.
-
(2007)
European Psychiatry
, vol.22
, pp. 22-26
-
-
Wohl, M.1
Gorwood, P.2
-
77
-
-
77649209124
-
The genetic interpretation of area under the ROC curve in genomic profiling
-
Wray N.R., Yang J., Goddard M.E., Visscher P.M. The genetic interpretation of area under the ROC curve in genomic profiling. PLoS Genetics 2010, 6:e1000864.
-
(2010)
PLoS Genetics
, vol.6
-
-
Wray, N.R.1
Yang, J.2
Goddard, M.E.3
Visscher, P.M.4
-
78
-
-
79959536362
-
The association between paternal age and schizophrenia in a Chinese Han population. [Article in Chinese, abstract in English]
-
Wu Y.J., Liu X., Zhao G.F., Ma X.H., Li T. The association between paternal age and schizophrenia in a Chinese Han population. [Article in Chinese, abstract in English]. Chinese Journal of Medical Genetics 2011, 28:266-269.
-
(2011)
Chinese Journal of Medical Genetics
, vol.28
, pp. 266-269
-
-
Wu, Y.J.1
Liu, X.2
Zhao, G.F.3
Ma, X.H.4
Li, T.5
-
79
-
-
84868650170
-
Parenting and fatherhood in urban China - a sociological perspective
-
Xu Q. Parenting and fatherhood in urban China - a sociological perspective. China Postgraduate Network Conference 2009, 2:24-36.
-
(2009)
China Postgraduate Network Conference
, vol.2
, pp. 24-36
-
-
Xu, Q.1
-
80
-
-
46249093584
-
Strong association of de novo copy number mutations with sporadic schizophrenia
-
Xu B., Roos J.L., Levy S., Van Rensburg E.J., Gogos J.A., Karayiorgou M. Strong association of de novo copy number mutations with sporadic schizophrenia. Nature Genetics 2008, 40:880-885.
-
(2008)
Nature Genetics
, vol.40
, pp. 880-885
-
-
Xu, B.1
Roos, J.L.2
Levy, S.3
Van Rensburg, E.J.4
Gogos, J.A.5
Karayiorgou, M.6
-
81
-
-
68249084502
-
The ups and downs of mutation frequencies during aging can account for the Apert syndrome paternal age effect
-
Yoon S.R., Qin J., Glaser R.L., Wang Jabs E., Wexler N.S., Sokol R., Arnheim N., Calabrese P. The ups and downs of mutation frequencies during aging can account for the Apert syndrome paternal age effect. PLoS Genetics 2009, 5:e1000558.
-
(2009)
PLoS Genetics
, vol.5
-
-
Yoon, S.R.1
Qin, J.2
Glaser, R.L.3
Wang Jabs, E.4
Wexler, N.S.5
Sokol, R.6
Arnheim, N.7
Calabrese, P.8
-
82
-
-
0242320340
-
Paternal age and risk for schizophrenia
-
Zammit S., Allebeck P., Dalman C., Lundberg I., Hemmingson T., Owen M.J., Lewis G. Paternal age and risk for schizophrenia. The British Journal of Psychiatry 2003, 183:405-408.
-
(2003)
The British Journal of Psychiatry
, vol.183
, pp. 405-408
-
-
Zammit, S.1
Allebeck, P.2
Dalman, C.3
Lundberg, I.4
Hemmingson, T.5
Owen, M.J.6
Lewis, G.7
-
83
-
-
50249177587
-
Investigating if psychosis-like symptoms (PLIKS) are associated with family history of schizophrenia or paternal age in the ALSPAC birth cohort
-
Zammit S., Horwood J., Thompson A., Thomas K., Menezes P., Gunnell D., Hollis C., Wolke D., Lewis G., Harrison G. Investigating if psychosis-like symptoms (PLIKS) are associated with family history of schizophrenia or paternal age in the ALSPAC birth cohort. Schizophrenia Research 2008, 104:279-286.
-
(2008)
Schizophrenia Research
, vol.104
, pp. 279-286
-
-
Zammit, S.1
Horwood, J.2
Thompson, A.3
Thomas, K.4
Menezes, P.5
Gunnell, D.6
Hollis, C.7
Wolke, D.8
Lewis, G.9
Harrison, G.10
-
85
-
-
5644258510
-
Molecular pharmacogenetic studies of drug responses to obsessive-compulsive disorder and six functional genes [article in Chinese, abstract in English]
-
Zhang L., Liu X., Li T., Yang Y., Hu X., Collier D. Molecular pharmacogenetic studies of drug responses to obsessive-compulsive disorder and six functional genes [article in Chinese, abstract in English]. Chinese Journal of Medical Genetics 2004, 21:479-481.
-
(2004)
Chinese Journal of Medical Genetics
, vol.21
, pp. 479-481
-
-
Zhang, L.1
Liu, X.2
Li, T.3
Yang, Y.4
Hu, X.5
Collier, D.6
-
86
-
-
77957121696
-
Below-replacement fertility and childbearing intention in Jiangsu Province, China
-
Zhenzhen Z., Cai Y., Feng W., Baochang G. Below-replacement fertility and childbearing intention in Jiangsu Province, China. Asian Population Studies 2009, 5:329-347.
-
(2009)
Asian Population Studies
, vol.5
, pp. 329-347
-
-
Zhenzhen, Z.1
Cai, Y.2
Feng, W.3
Baochang, G.4
-
87
-
-
36448948280
-
Catechol-O-methyltransferase gene and obsessive-compulsive symptoms in patients with recent-onset schizophrenia: preliminary results
-
Zinkstok J., van Nimwegen L., Van Amelsvoort T., De Haan L., Yusuf M.A., Baas F., Linszen D. Catechol-O-methyltransferase gene and obsessive-compulsive symptoms in patients with recent-onset schizophrenia: preliminary results. Psychiatry Research 2008, 157:1-8.
-
(2008)
Psychiatry Research
, vol.157
, pp. 1-8
-
-
Zinkstok, J.1
van Nimwegen, L.2
Van Amelsvoort, T.3
De Haan, L.4
Yusuf, M.A.5
Baas, F.6
Linszen, D.7
|