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Schizophrenia Susceptibility Associated with Interstitial Deletions of Chromosome 22q11

Proceedings of the National Academy of Sciences - PNAS, 1995-08, Vol.92 (17), p.7612-7616

1995

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Genetic heterogeneity in schizophrenia : stratification of genome scan data using co-segregating related phenotypes

Molecular psychiatry, 2000-11, Vol.5 (6), p.650-653

2000

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Dense SNP association study for bipolar I disorder on chromosome 18p11 suggests two loci with excess paternal transmission

Molecular psychiatry, 2007-04, Vol.12 (4), p.367-375

2007

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Psychotic Illness in Patients Diagnosed with Velo-Cardio-Facial Syndrome and Their Relatives

The journal of nervous and mental disease, 1994-08, Vol.182 (8), p.476-477

1994

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Genetic heterogeneity in schizophrenia II: conditional analyses of affected schizophrenia sibling pairs provide evidence for an interaction between markers on chromosome 8p and 14q

Molecular psychiatry, 2002-01, Vol.7 (6), p.658-664

2002

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Identification of Sequence Variants and Analysis of the Role of the Catechol- O-Methyl-Transferase Gene in Schizophrenia Susceptibility

Biological psychiatry (1969), 1998-03, Vol.43 (6), p.425-431

1998

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Multiple variants aggregate in the neuregulin signaling pathway in a subset of schizophrenia patients

Translational psychiatry, 2013-05, Vol.3 (5), p.e264-e264

2013

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Genomewide Linkage Scan for Bipolar-Disorder Susceptibility Loci among Ashkenazi Jewish Families

American journal of human genetics, 2004-08, Vol.75 (2), p.204-219

2004

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Schizophrenia and chromosomal deletions within 22q11.2

American journal of human genetics, 1995-06, Vol.56 (6), p.1502-1503

1995

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Five Latent Factors Underlying Schizophrenia: Analysis and Relationship to Illnesses in Relatives

Schizophrenia bulletin, 2004-01, Vol.30 (4), p.855-873

2004

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An epidemiologic investigation of alcohol-dependent schizophrenics

Acta psychiatrica Scandinavica, 1989-06, Vol.79 (6), p.603-612

1989

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Schizophrenia: Gender and familial risk

Journal of psychiatric research, 1992, Vol.26 (1), p.17-27

1992

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Bipolar I Disorder and Schizophrenia: A 440–Single-Nucleotide Polymorphism Screen of 64 Candidate Genes among Ashkenazi Jewish Case-Parent Trios

American journal of human genetics, 2005-12, Vol.77 (6), p.918-936

2005

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Season of Birth of Siblings of Schizophrenic Patients

British journal of psychiatry, 1992-01, Vol.160 (1), p.71-75

1992

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Genotype and phenotype analysis at the 22q11 schizophrenia susceptibility locus

Cold Spring Harbor Symposia on Quantitative Biology, 1996, Vol.61, p.835

1996

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The Johns Hopkins University Collaborative Schizophrenia Study: an epidemiologic-genetic approach to test the heterogeneity hypothesis and identify schizophrenia susceptibility genes

Cold Spring Harbor Symposia on Quantitative Biology, 1996, Vol.61, p.797

1996

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Age-incidence artifacts do not account for the season-of-birth effect in schizophrenia

Schizophrenia bulletin, 1990, Vol.16 (1), p.13-15

1990

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Stage II follow-up on a linkage scan for bipolar disorder in the Ashkenazim provides suggestive evidence for chromosome 12p and the GRIN2B gene

Genetics in medicine, 2007-11, Vol.9 (11), p.745-751

2007

Volltextzugriff (PDF)

Genomewide Linkage Scan for Schizophrenia Susceptibility Loci among Ashkenazi Jewish Families Shows Evidence of Linkage on Chromosome 10q22

American journal of human genetics, 2003-09, Vol.73 (3), p.601-611

2003

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Report from the Maryland epidemiology schizophrenia linkage study: No evidence for linkage between schizophrenia and a number of candidate and other genomic regions using a complex dominant model

American journal of medical genetics, 1994-12, Vol.54 (4), p.345-353

1994

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Psychiatric morbidity in the relatives of patients with DSM-III schizophreniform disorder: Comparisons with the relatives of schizophrenic and bipolar disorder patients

Journal of psychiatric research, 1991, Vol.25 (1), p.19-29

1991

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An indirect test of the new mutation hypothesis associating advanced paternal age with the etiology of schizophrenia

American journal of medical genetics, 2004-01, Vol.124B (1), p.6-9

2004

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Follow-up report of potential linkage for schizophrenia on chromosome 22q: Part 3

American journal of medical genetics, 1995-04, Vol.60 (2), p.172-173

1995

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Season of birth of siblings of schizophrenic patients

British journal of psychiatry, 1992, Vol.160 (JAN), p.71-75

1992

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Schizophrenia Susceptibility Associated with Interstitial Deletions of Chromosome 22q11

Genetic heterogeneity in schizophrenia : stratification of genome scan data using co-segregating related phenotypes

Dense SNP association study for bipolar I disorder on chromosome 18p11 suggests two loci with excess paternal transmission

Psychotic Illness in Patients Diagnosed with Velo-Cardio-Facial Syndrome and Their Relatives

Genetic heterogeneity in schizophrenia II: conditional analyses of affected schizophrenia sibling pairs provide evidence for an interaction between markers on chromosome 8p and 14q

Identification of Sequence Variants and Analysis of the Role of the Catechol- O-Methyl-Transferase Gene in Schizophrenia Susceptibility

Multiple variants aggregate in the neuregulin signaling pathway in a subset of schizophrenia patients

Genomewide Linkage Scan for Bipolar-Disorder Susceptibility Loci among Ashkenazi Jewish Families

Schizophrenia and chromosomal deletions within 22q11.2

Five Latent Factors Underlying Schizophrenia: Analysis and Relationship to Illnesses in Relatives

An epidemiologic investigation of alcohol-dependent schizophrenics

Schizophrenia: Gender and familial risk

Bipolar I Disorder and Schizophrenia: A 440–Single-Nucleotide Polymorphism Screen of 64 Candidate Genes among Ashkenazi Jewish Case-Parent Trios

Season of Birth of Siblings of Schizophrenic Patients

Genotype and phenotype analysis at the 22q11 schizophrenia susceptibility locus

The Johns Hopkins University Collaborative Schizophrenia Study: an epidemiologic-genetic approach to test the heterogeneity hypothesis and identify schizophrenia susceptibility genes

Age-incidence artifacts do not account for the season-of-birth effect in schizophrenia

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

Stage II follow-up on a linkage scan for bipolar disorder in the Ashkenazim provides suggestive evidence for chromosome 12p and the GRIN2B gene

Genomewide Linkage Scan for Schizophrenia Susceptibility Loci among Ashkenazi Jewish Families Shows Evidence of Linkage on Chromosome 10q22

Report from the Maryland epidemiology schizophrenia linkage study: No evidence for linkage between schizophrenia and a number of candidate and other genomic regions using a complex dominant model

Psychiatric morbidity in the relatives of patients with DSM-III schizophreniform disorder: Comparisons with the relatives of schizophrenic and bipolar disorder patients

An indirect test of the new mutation hypothesis associating advanced paternal age with the etiology of schizophrenia

Follow-up report of potential linkage for schizophrenia on chromosome 22q: Part 3

Season of birth of siblings of schizophrenic patients

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