Per Hoffmann - Researcher Profile | RDL Research Database

Publications

6 shown

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

Naomi R. Wray , Stephan Ripke , Manuel Mattheisen +97 more

2018 Nature Genetics 3130 citations

Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease

Tom R. Webb , Jeanette Erdmann , Kathleen Stirrups +97 more

2017 Journal of the American College of Ca... 260 citations

Identification of loci associated with schizophrenia by genome-wide association and follow-up

Michael O’Donovan , Nicholas Craddock , Nadine Norton +53 more

2008 Nature Genetics 1074 citations

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

M. Rietschel , Manuel Mattheisen , F. Degenhardt +97 more

2011 Molecular Psychiatry 116 citations

Analysis of shared heritability in common disorders of the brain

Verneri Anttila , Brendan Bulik‐Sullivan , Hilary K. Finucane +97 more

Brainstorming diseases Consistent classification of neuropsychiatric diseases is problematic because it can lead to misunderstanding of etiology. The Brainstorm Consortium exami...

2018 Science 1928 citations

Genome-wide association study identifies 30 loci associated with bipolar disorder

Eli A. Stahl , Gerome Breen , Andreas J. Forstner +97 more

Bipolar disorder is a highly heritable psychiatric disorder. We performed a genome-wide association study (GWAS) including 20,352 cases and 31,358 controls of European descent, ...

2019 Nature Genetics 1565 citations

Frequent Co-Authors

Researcher Info

h-index: 6
Publications: 6
Citations: 8,073
Institution: University of Michigan

External Links

ORCID Profile Google Scholar

Identifiers

ORCID: 0000-0002-6573-983X

Impact Metrics

h-index 6

h-index: Number of publications with at least h citations each.