P. Hoffmann

发表

First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children

B Müller-Myhsok, H Remschmidt, B. Müller-Myhsok, 2011, Molecular Psychiatry.

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

Thomas W. Mühleisen, A. Hofman, A. Uitterlinden, 2012, Molecular Psychiatry.

GWAS for executive function and processing speed suggests involvement of the CADM2 gene

Blair H. Smith, J. Bressler, M. Fornage, 2016, Molecular Psychiatry.

Genetically elevated high-density lipoprotein cholesterol through the cholesteryl ester transfer protein gene does not associate with risk of Alzheimer ' s disease

D. G. Clark, M. Fornage, A. Hofman, 2022 .

Strong Association of Variants around FOXE1 and Orofacial Clefting

M. Nöthen, M. Rubini, B. Peterlin, 2014, Journal of dental research.

Orofacial Clefting FOXE 1 Strong Association of Variants around

M. Nöthen, M. Rubini, B. Peterlin, 2014 .

Edinburgh Research Explorer Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia

I. Giegling, S. Djurovic, R. Ophoff, 2017 .

Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deﬁcit/hyperactivity disorder

S. Cichon, H. Wichmann, K. Jöckel, 2013 .

Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder

S Cichon, S. Cichon, C. Freitag, 2012, Molecular Psychiatry.

Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia

Thomas W. Mühleisen, N. Wray, D. Rujescu, 2017, Translational Psychiatry.

Genome-wide analysis of rare copy number variations reveals PARK 2 as a candidate gene for attention-deficit / hyperactivity disorder

S. Cichon, C. Freitag, K. Lesch, 2013 .

Genetic effects influencing risk for major depressive disorder in China and Europe

John P. Rice, N. Wray, S. Cichon, 2017, Translational Psychiatry.

Genetic effects influencing risk for major depressive disorder in China and Europe

John P. Rice, Till F. M. Andlauer, N. Wray, 2017, Translational Psychiatry.

Supporting evidence for LRRTM1 imprinting effects in schizophrenia

S. Cichon, M. Rietschel, R. Breuer, 2009, Molecular Psychiatry.

A common variant in Myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults

M. Nöthen, M. Czisch, R. Plomin, 2013, Translational Psychiatry.

Association analyses identify 31 new risk loci for colorectal cancer susceptibility

Aung Ko Win, I. Deary, V. Salomaa, 2019 .

Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2

M C O'Donovan, M J Owen, T G Schulze, 2009, Molecular Psychiatry.

Genome-wide association study of immunoglobulin light chain amyloidosis in three patient cohorts: comparison with myeloma

M. Nöthen, H. Goldschmidt, A. Jauch, 2017, Leukemia.

Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder

Janice M. Fullerton, Thomas W. Mühleisen, S. Cichon, 2015, Translational Psychiatry.

Evidence for the involvement of ZNF804A in cognitive processes of relevance to reading and spelling

M. Nöthen, D. Brandeis, B. Müller-Myhsok, 2012, Translational Psychiatry.