J. Körner

发表

An association study of a neurotrophic3 (NT‐3) gene polymorphism with schizophrenia

R. Murray, M. Rietschel, M. Nöthen, 1995, Acta psychiatrica Scandinavica.

Lack of association between schizophrenia and alleles of the dopamine D1, D2, D3 and D4 receptor loci1

S. Cichon, H. Möller, M. Rietschel, 1993 .

Dopamine D2 receptor molecular variant and schizophrenia

S. Cichon, M. Rietschel, M. Nöthen, 1994, The Lancet.

No evidence of association between dopamine D4 receptor variants and bipolar affective disorder.

R. Murray, M. Rietschel, M. Nöthen, 1994, American journal of medical genetics.

Mutation in the β amyloid precursor protein gene and schizophrenia

M. Rietschel, M. Nöthen, W. Maier, 1993, Biological Psychiatry.

Tyrosine hydroxylase polymorphisms and manic-depressive illness

M. Nöthen, P. Propping, J. Fritze, 1990, The Lancet.

RFLP alleles at the tyrosine hydroxylase locus: No association found to affective disorders

P. Propping, J. Fritze, J. Körner, 1990, Psychiatry Research.

No evidence of association between dopamine D3 receptor gene and bipolar affective disorder.

R. Murray, M. Rietschel, M. Nöthen, 1997 .

Association and haplotype analysis at the tyrosine hydroxylase locus in a combined German‐British sample of manic depressive patients and controls

H. Möller, M. Rietschel, M. Nöthen, 1994, Psychiatric genetics.

Pseudoautosomal marker DXYS20 and manic depression.

S. Cichon, M. Rietschel, M. Nöthen, 1993, American Journal of Human Genetics.

Lack of association between dopamine D1 and D2 receptor genes and bipolar affective disorder.

M. Nöthen, R. Fimmers, D. Grandy, 1992, The American journal of psychiatry.

[Pemphigus chronicus benignus familiaris (Hailey-Hailey disease) and bipolar affective disease in 3 members of a family].

H. Möller, M. Rietschel, M. Nöthen, 1994, Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete.

Familial Cosegregation of Affective Disorder and Hailey-Hailey Disease

H. Möller, M. Rietschel, M. Nöthen, 1993, British Journal of Psychiatry.

Association analysis of the monoamine oxidase A gene in bipolar affective disorder by using family-based internal controls.

M. Rietschel, M. Nöthen, W. Maier, 1995, American journal of human genetics.

A serine to glycine substitution at position 9 in the extracellular N-terminal part of the dopamine D3 receptor protein: No role in the genetic predisposition to bipolar affective disorder

S. Cichon, M. Rietschel, M. Nöthen, 1993, Psychiatry Research.

[Spontaneous liver rupture in eclampsia].

J. Körner, F. Mörl, R. Behrend, 1987, Geburtshilfe und Frauenheilkunde.

The human serotonin 7 (5-HT7) receptor gene: genomic organization and systematic mutation screening in schizophrenia and bipolar affective disorder.

M. Rietschel, M. Nöthen, R. Fimmers, 1996, Molecular psychiatry.

Partial trisomy 16p in an adolescent with autistic disorder and Tourette's syndrome.

J. Hebebrand, H. Remschmidt, J. Körner, 1994, American journal of medical genetics.

HLA-DR2–frequencies in affective disorders

P. Propping, J. Fritze, J. Körner, 1990, British Journal of Psychiatry.

Further RFLPs at the human tyrosine hydroxylase locus.

J. Mallet, P. Propping, A. Gal, 1988, Nucleic acids research.

Systematic screening for mutations in the human serotonin-2A (5-HT2A) receptor gene: Identification of two naturally occurring receptor variants and association analysis in schizophrenia

M. Rietschel, M. Nöthen, W. Maier, 1996, Human Genetics.

Systematic screening for mutations in the human serotonin 1F receptor gene in patients with bipolar affective disorder and schizophrenia.

M. Rietschel, M. Nöthen, W. Maier, 1996, American journal of medical genetics.

Systematic screening for mutations in the 5'-regulatory region of the human dopamine D1 receptor (DRD1) gene in patients with schizophrenia and bipolar affective disorder.

S. Cichon, M. Rietschel, M. Nöthen, 1996, American journal of medical genetics.

Single-strand conformation analysis (SSCA) of the dopamine D1 receptor gene (DRD1) reveals no significant mutation in patients with schizophrenia and manic depression

S. Cichon, M. Rietschel, M. Nöthen, 1994, Biological Psychiatry.

Identification of two novel polymorphisms and a rare deletion variant in the human dopamine D4 receptor gene

S. Cichon, M. Rietschel, M. Nöthen, 1995, Psychiatric genetics.

Dopamine D3 receptor Gly9/Ser9 polymorphism and schizophrenia: no increased frequency of homozygosity in German familial cases

H. Möller, M. Rietschel, M. Nöthen, 1996, Schizophrenia Research.

Assessing the statistical power to detect linkage in a sample of 51 bipolar affective disorder pedigrees

M. Rietschel, N. Craddock, P. McGuffin, 1996, Behavior genetics.

Apolipoprotein E genotype distribution in schizophrenia

M. Rietschel, M. Nöthen, R. Fimmers, 1996, Psychiatric genetics.

What can twin studies contribute to the understanding of adult psychopathology

M. Rietschel, P. McGuffin, J. Kaprio, 1993 .

An association study of debrisoquine hydroxylase (CYP2D6) polymorphisms in schizophrenia

M. Rietschel, M. Nöthen, M. Gill, 1994, Psychiatric genetics.

Systematic screening for mutations in the promoter and the coding region of the 5-HT1A gene.

S. Cichon, W. Maier, J. Erdmann, 1995, American journal of medical genetics.