A genome-wide survey of segmental duplications that mediate common human genetic variation of chromosomal architecture

por Mehan, Michael R, Freimer, Nelson B, Ophoff, Roel A
Publicado 2004

A summary-statistics-based approach to examine the role of serotonin transporter promoter tandem repeat polymorphism in psychiatric phenotypes

por Majumdar, Arunabha, Patel, Preksha, Pasaniuc, Bogdan, Ophoff, Roel A.
Publicado 2021

Significant variation in the performance of DNA methylation predictors across data preprocessing and normalization strategies

por Ori, Anil P. S., Lu, Ake T., Horvath, Steve, Ophoff, Roel A.
Publicado 2022

Large-Scale Whole Genome Sequence Analysis of >22,000 Subjects Provides no Evidence of FMR1 Premutation Allele Involvement in Autism Spectrum Disorder

por Chubick, Alex, Wang, Evan, Au, Cora, Grody, Wayne W., Ophoff, Roel A.
Publicado 2023

Investigation of the Genetic Association between Quantitative Measures of Psychosis and Schizophrenia: A Polygenic Risk Score Analysis

por Derks, Eske M., Vorstman, Jacob A. S., Ripke, Stephan, Kahn, Rene S., Ophoff, Roel A.
Publicado 2012

Correction: Investigation of the Genetic Association between Quantitative Measures of Psychosis and Schizophrenia: A Polygenic Risk Score Analysis

por Derks, Eske M., Vorstman, Jacob A. S., Ripke, Stephan, Kahn, Rene S., Ophoff, Roel A.
Publicado 2013

Sex-Dependent Novelty Response in Neurexin-1α Mutant Mice

por Laarakker, Marijke C., Reinders, Niels R., Bruining, Hilgo, Ophoff, Roel A., Kas, Martien J. H.
Publicado 2012

An Integrative Multi-scale Analysis of the Dynamic DNA Methylation Landscape in Aging

por Yuan, Tian, Jiao, Yinming, de Jong, Simone, Ophoff, Roel A., Beck, Stephan, Teschendorff, Andrew E.
Publicado 2015

Gene expression profiling in C57BL/6J and A/J mouse inbred strains reveals gene networks specific for brain regions independent of genetic background

por de Jong S, Simone, Fuller, Tova F, Janson, Esther, Strengman, Eric, Horvath, Steve, Kas, Martien JH, Ophoff, Roel A
Publicado 2010

Integrative analysis of Dupuytren's disease identifies novel risk locus and reveals a shared genetic etiology with BMI

por Major, Megan, Freund, Malika K., Burch, Kathryn S., Mancuso, Nicholas, Ng, Michael, Furniss, Dominic, Pasaniuc, Bogdan, Ophoff, Roel A.
Publicado 2019

Epigenetic age analysis of children who seem to evade aging

por Walker, Richard F., Liu, Jia Sophie, Peters, Brock A., Ritz, Beate R., Wu, Timothy, Ophoff, Roel A., Horvath, Steve
Publicado 2015

Methylation age acceleration does not predict mortality in schizophrenia

por Kowalec, Kaarina, Hannon, Eilis, Mansell, Georgina, Burrage, Joe, Ori, Anil P. S., Ophoff, Roel A., Mill, Jonathan, Sullivan, Patrick F.
Publicado 2019

Common inversion polymorphism at 17q21.31 affects expression of multiple genes in tissue-specific manner

por de Jong, Simone, Chepelev, Iouri, Janson, Esther, Strengman, Eric, van den Berg, Leonard H, Veldink, Jan H, Ophoff, Roel A
Publicado 2012

The Relationship of DNA Methylation with Age, Gender and Genotype in Twins and Healthy Controls

por Boks, Marco P., Derks, Eske M., Weisenberger, Daniel J., Strengman, Erik, Janson, Esther, Sommer, Iris E., Kahn, René S., Ophoff, Roel A.
Publicado 2009

Evaluating Historical Candidate Genes for Schizophrenia

por Farrell, Martilias, Werge, Thomas, Sklar, Pamela, Owen, Michael J., Ophoff, Roel, O’Donovan, Michael, Corvin, Aiden, Cichon, Sven, Sullivan, Patrick F
Publicado 2015

Lithium Use during Pregnancy and the Risk of Miscarriage

por Poels, Eline M. P., Kamperman, Astrid M., Vreeker, Annabel, Gilden, Janneke, Boks, Marco P., Kahn, René S., Ophoff, Roel A., Bergink, Veerle
Publicado 2020

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

por Cai, Chaochao, Langfelder, Peter, Fuller, Tova F, Oldham, Michael C, Luo, Rui, van den Berg, Leonard H, Ophoff, Roel A, Horvath, Steve
Publicado 2010

Aging effects on DNA methylation modules in human brain and blood tissue

por Horvath, Steve, Zhang, Yafeng, Langfelder, Peter, Kahn, René S, Boks, Marco PM, van Eijk, Kristel, van den Berg, Leonard H, Ophoff, Roel A
Publicado 2012

Powerful eQTL mapping through low-coverage RNA sequencing

por Schwarz, Tommer, Boltz, Toni, Hou, Kangcheng, Bot, Merel, Duan, Chenda, Loohuis, Loes Olde, Boks, Marco P., Kahn, René S., Ophoff, Roel A., Pasaniuc, Bogdan
Publicado 2022

A Genetic Population Isolate in The Netherlands Showing Extensive Haplotype Sharing and Long Regions of Homozygosity

por Somers, Metten, Olde Loohuis, Loes M., Aukes, Maartje F., Pasaniuc, Bogdan, de Visser, Kees C. L., Kahn, René S., Sommer, Iris E., Ophoff, Roel A.
Publicado 2017