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Journal Article 12

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Journal Article

Common variant at 16p11.2 conferring risk of psychosis

Steinberg, S.
2014

Molecular psychiatry, 19 (2014) 1, S. 108 - 114

“...Nöthen, M. M....”

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Replication Study and Meta-Analysis in European Samples Supports Association of the 3p21.1 Locus with Bipolar Disorder

Vassos, E.
2012

Biological psychiatry, 72 (2012) S. 645 - 650

“...Nöthen, M.M....”

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Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe

Rietschel, M.
2012

Molecular psychiatry, 17 (2012) S. 906 - 917

“...Nöthen, M.M....”

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Association Study of Nonsynonymous Single Nucleotide Polymorphisms in Schizophrenia

Carrera, N.
2012

Biological psychiatry, 71 (2012) S. 169 - 177

“...Nöthen, M.M....”

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Gene-Based Analysis of Regionally Enriched Cortical Genes in GWAS Data Sets of Cognitive Traits and Psychiatric Disorders

Ersland, K.M.
2012

PLoS one, 7 (2012) 2, S. e31687

“...Nöthen, M.M....”

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Dual association of a TRKA polymorphism with schizophrenia

Van Schijndel, J.E.
2011

Psychiatric genetics, 21 (2011) S. 125 - 131

“...Nöthen, M.M....”

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At-risk variant in TCF7L2 for type II diabetes increases risk of schizophrenia

Hansen, T.
2011

Biological psychiatry, 70 (2011) S. 59 - 63

“...Nöthen, M.M....”

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Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness

Ingason, A.
2011

The @American journal of psychiatry, 168 (2011) S. 408 - 417

“...Nöthen, M.M....”

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Expanding the range of ZNF804A variants conferring risk of psychosis

Steinberg, S.
2011

Molecular psychiatry, 16 (2011) S. 59 - 66

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Copy number variations of chromosome 16p13.1 region associated with schizophrenia.

Ingason, A.
2011

Molecular psychiatry, 16 (2011) S. 17 - 25

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Common variants on 8p12 and 1q24.2 confer risk of schizophrenia

Shi, Y.
2011

Nature genetics, 43 (2011) S. 1224 - 1227

“...Nöthen, M.M....”

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A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia

Ingason, A.
2010

Human molecular genetics, 19 (2010) S. 1379 - 1386

“...Nöthen, M.M....”

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Publications database 12 Open Access 1

Journal Article 12

Rietschel, M. 12 Werge, T. Cichon, S. 11 Nöthen, M.M. 11 Djurovic, S. 10 Rujescu, D. 10 more ... Tosato, S. 10 Andreassen, O.A. 9 Hansen, T. 9 Sigurdsson, E. 8 Stefansson, H. 8 Stefansson, K. 8 Collier, D.A. 7 Giegling, I. 7 Ingason, A. 7 Ophoff, R.A. 7 Steinberg, S. 7 Gustafsson, O. 6 Melle, I. 6 Peltonen, L. 6 Ruggeri, M. 6 Craddock, N. 5 Mors, O. 5 Murray, R. 5 Petursson, H. 5 Strengman, E. 5 Suvisaari, J. 5 Tuulio-Henriksson, A. 5 Vassos, E. 5 Bitter, I. 4 see all ... less ...

Connectivity and Activity 11 Funktion und Dysfunktion des Nervensystems 11 Copy Number Variation and Endophenotypes in Psychiatric Disorders 3 Copy number variations conferring risk of psychiatric disorders in children 1 Genomic variations underlying common behavior diseases and cognition trait in human populations 1 Pathophysiological Mechanisms of Neurological and Psychiatric Diseases 1

Strukturelle und funktionelle Organisation des Gehirns; INM-1 12

2011 6 2012 4 2010 1 2015 1

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