Roel A Ophoff

发表

Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights

Alexander Gusev, Bogdan Pasaniuc, Nicholas Mancuso, 2016, Nature Genetics.

Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4

Dennis E Bulman, Ronald van Eijk, Peter J Oefner, 1996, Cell.

Genetic architecture of subcortical brain structures in 38,851 individuals

Benjamin S Aribisala, Tien Yin Wong, Wiro J Niessen, 2019, Nature Genetics.

European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene.

Paolo Vineis, Abbas Ghaderi, Simonetta Guarrera, 2011, Human molecular genetics.

Genomewide linkage disequilibrium mapping of severe bipolar disorder in a population isolate.

Nelson B Freimer, Susan K Service, Lodewijk A Sandkuijl, 2002, American journal of human genetics.

A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer

Paolo Vineis, Simonetta Guarrera, Giuseppe Matullo, 2010, Nature Genetics.

Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47

Tariq Ahmad, Katherine I. Morley, Vibeke Andersen, 2011, Nature Genetics.

Wnt signaling and Dupuytren's disease.

Peter Nürnberg, Andre Franke, Cisca Wijmenga, 2011, The New England journal of medicine.

Genetic contributions to social impulsivity and aggressiveness in vervet monkeys

Jeffrey Rogers, Lisa J. Martin, Lisa J Martin, 2004, Biological Psychiatry.

Is human blood a good surrogate for brain tissue in transcriptional studies?

Peter Langfelder, Steve Horvath, Chaochao Cai, 2010, BMC Genomics.

A genome-wide association study identifies a functional ERAP2 haplotype associated with birdshot chorioretinopathy.

Stephan Ripke, Carel B Hoyng, Flip Mulder, 2014, Human molecular genetics.

Cortical Brain Abnormalities in 4474 Individuals With Schizophrenia and 5098 Control Subjects via the Enhancing Neuro Imaging Genetics Through Meta Analysis (ENIGMA) Consortium

Adrian Preda, Peter Kochunov, Elliot Hong, 2018, Biological Psychiatry.

Novel genetic loci associated with hippocampal volume

Benjamin S Aribisala, Wiro J Niessen, Peter Kochunov, 2017, Nature Communications.

Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis

Frank Baas, Cisca Wijmenga, Lude Franke, 2008, Nature Genetics.

Identification of schizophrenia-associated loci by combining DNA methylation and gene expression data from whole blood

Steve Horvath, Eric Strengman, Simone de Jong, 2014, European Journal of Human Genetics.

Novel genetic loci underlying human intracranial volume identified through genome-wide association

Benjamin S Aribisala, Wiro J Niessen, Peter Kochunov, 2016, Nature Neuroscience.

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

Qi Xu, Peng Wang, Dengtang Liu, 2011, Nature Genetics.

A quantitative trait locus for variation in dopamine metabolism mapped in a primate model using reference sequences from related species

Ken Dewar, Nelson B Freimer, Rita M Cantor, 2007, Proceedings of the National Academy of Sciences.

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Jianxin Shi, Susmita Datta, Aribert Rothenberger, 2013, Nature Genetics.

Genetic analysis of DNA methylation and gene expression levels in whole blood of healthy human subjects

Peter Langfelder, Steve Horvath, Fabrice Colas, 2012, BMC Genomics.

Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder

Jakob Grove, Esben Agerbo, Andres Metspalu, 2017, bioRxiv.

Weighted gene co-expression network analysis of the peripheral blood from Amyotrophic Lateral Sclerosis patients

Peter Langfelder, Steve Horvath, Joseph DeYoung, 2009, BMC Genomics.

No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder

Irene Lee, Kari Stefansson, Wouter Staal, 2011, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Disruption of the neurexin 1 gene is associated with schizophrenia.

Elvira Bramon, Chiara Sabatti, Kari Stefansson, 2009, Human molecular genetics.

Expression QTL analysis of top loci from GWAS meta-analysis highlights additional schizophrenia candidate genes

Wiepke Cahn, Eric Strengman, Simone de Jong, 2012, European Journal of Human Genetics.

Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen

Lude Franke, J Peter H Burbach, R. Ophoff, 2008, The Lancet Neurology.

Accurate and fast multiple-testing correction in eQTL studies.

Eleazar Eskin, Buhm Han, Jae Hoon Sul, 2015, American journal of human genetics.

Whole genome sequencing in psychiatric disorders: the WGSPD consortium

Hailiang Huang, Chiara Sabatti, Kevin Eggan, 2017, bioRxiv.

Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis

Ewout J N Groen, Machiel J Zwarts, Fernando Rivadeneira, 2009, Nature Genetics.

Seasonal changes in gene expression represent cell-type composition in whole blood.

Steve Horvath, Eric Strengman, Jacobine E Buizer-Voskamp, 2014, Human molecular genetics.

Transcriptome analysis in whole blood reveals increased microbial diversity in schizophrenia

Eleazar Eskin, Serghei Mangul, David Koslicki, 2018 .