نتایج جستجو برای: gwas

تعداد نتایج: 6259  

2016
Tiger Zhou Emmanuelle Souzeau Shiwani Sharma Owen M. Siggs Ivan Goldberg Paul R. Healey Stuart Graham Alex W. Hewitt David A. Mackey Robert J. Casson John Landers Richard Mills Jonathan Ellis Paul Leo Matthew A. Brown Stuart MacGregor Kathryn P. Burdon Jamie E. Craig

BACKGROUND Genome-wide association studies (GWAS) have identified association of common alleles with primary open-angle glaucoma (POAG) and its quantitative endophenotypes near numerous genes. This study aims to determine whether rare pathogenic variants in these disease-associated genes contribute to POAG. METHODS Participants fulfilled strict inclusion criteria of advanced POAG at a young a...

Journal: :American journal of human genetics 2012
Weihong Tang Christine Schwienbacher Lorna M Lopez Yoav Ben-Shlomo Tiphaine Oudot-Mellakh Andrew D Johnson Nilesh J Samani Saonli Basu Martin Gögele Gail Davies Gordon D O Lowe David-Alexandre Tregouet Adrian Tan James S Pankow Albert Tenesa Daniel Levy Claudia B Volpato Ann Rumley Alan J Gow Cosetta Minelli John W G Yarnell David J Porteous John M Starr John Gallacher Eric Boerwinkle Peter M Visscher Peter P Pramstaller Mary Cushman Valur Emilsson Andrew S Plump Nena Matijevic Pierre-Emmanuel Morange Ian J Deary Andrew A Hicks Aaron R Folsom

Activated partial thromboplastin time (aPTT) and prothrombin time (PT) are clinical tests commonly used to screen for coagulation-factor deficiencies. One genome-wide association study (GWAS) has been reported previously for aPTT, but no GWAS has been reported for PT. We conducted a GWAS and meta-analysis to identify genetic loci for aPTT and PT. The GWAS for aPTT was conducted in 9,240 individ...

2009
Zongli Xu Jack A. Taylor

We have developed a set of web-based SNP selection tools (freely available at http://www.niehs.nih.gov/snpinfo) where investigators can specify genes or linkage regions and select SNPs based on GWAS results, linkage disequilibrium (LD), and predicted functional characteristics of both coding and non-coding SNPs. The algorithm uses GWAS SNP P-value data and finds all SNPs in high LD with GWAS SN...

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2010
Melanie Bahlo Jim Stankovich Patrick Danoy Peter F Hickey Bruce V Taylor Sharon R Browning Matthew A Brown Justin P Rubio

As of June 2009, 361 genome-wide association studies (GWAS) had been referenced by the HuGE database. GWAS require DNA from many thousands of individuals, relying on suitable DNA collections. We recently performed a multiple sclerosis (MS) GWAS where a substantial component of the cases (24%) had DNA derived from saliva. Genotyping was done on the Illumina genotyping platform using the Infinium...

Journal: :Journal of medical genetics 2012
Peilin Jia Lily Wang Ayman H Fanous Xiangning Chen Kenneth S Kendler Zhongming Zhao

BACKGROUND After the recent successes of genome-wide association studies (GWAS), one key challenge is to identify genetic variants that might have a significant joint effect on complex diseases but have failed to be identified individually due to weak to moderate marginal effect. One popular and effective approach is gene set based analysis, which investigates the joint effect of multiple funct...

Journal: :Archives of neurology 2010
Alessandro Biffi Christopher D Anderson Rahul S Desikan Mert Sabuncu Lynelle Cortellini Nick Schmansky David Salat Jonathan Rosand

OBJECTIVE To investigate whether genome-wide association study (GWAS)-validated and GWAS-promising candidate loci influence magnetic resonance imaging measures and clinical Alzheimer's disease (AD) status. DESIGN Multicenter case-control study of genetic and neuroimaging data from the Alzheimer's Disease Neuroimaging Initiative. SETTING Multicenter GWAS. Patients A total of 168 individuals ...

Journal: :Human molecular genetics 2014
Xiaoling Zhang Andrew D Johnson Audrey E Hendricks Shih-Jen Hwang Kahraman Tanriverdi Santhi K Ganesh Nicholas L Smith Patricia A Peyser Jane E Freedman Christopher J O'Donnell

Genome-wide association studies (GWAS) have uncovered many genetic associations for cardiovascular disease (CVD). However, data are limited regarding causal genetic variants within implicated loci. We sought to identify regulatory variants (cis- and trans-eQTLs) affecting expression levels of 93 genes selected by their proximity to SNPs with significant associations in prior GWAS for CVD traits...

Journal: :Human molecular genetics 2012
Lara Bossini-Castillo Jose-Ezequiel Martin Jasper Broen Olga Gorlova Carmen P Simeón Lorenzo Beretta Madelon C Vonk Jose Luis Callejas Ivan Castellví Patricia Carreira Francisco José García-Hernández Mónica Fernández Castro Marieke J H Coenen Gabriela Riemekasten Torsten Witte Nicolas Hunzelmann Alexander Kreuter Jörg H W Distler Bobby P Koeleman Alexandre E Voskuyl Annemie J Schuerwegh Øyvind Palm Roger Hesselstrand Annika Nordin Paolo Airó Claudio Lunardi Raffaella Scorza Paul Shiels Jacob M van Laar Ariane Herrick Jane Worthington Christopher Denton Filemon K Tan Frank C Arnett Sandeep K Agarwal Shervin Assassi Carmen Fonseca Maureen D Mayes Timothy R D J Radstake Javier Martin

A single-nucleotide polymorphism (SNP) at the IL12RB2 locus showed a suggestive association signal in a previously published genome-wide association study (GWAS) in systemic sclerosis (SSc). Aiming to reveal the possible implication of the IL12RB2 gene in SSc, we conducted a follow-up study of this locus in different Caucasian cohorts. We analyzed 10 GWAS-genotyped SNPs in the IL12RB2 region (2...

2014
Luis M. Real Agustín Ruiz Javier Gayán Antonio González-Pérez María E. Sáez Reposo Ramírez-Lorca Francisco J. Morón Juan Velasco Ruth Marginet-Flinch Eva Musulén José M. Carrasco Concha Moreno-Rey Enrique Vázquez Manuel Chaves-Conde Jose A. Moreno-Nogueira Manuel Hidalgo-Pascual Eduardo Ferrero-Herrero Sergi Castellví-Bel Antoni Castells Ceres Fernandez-Rozadilla Clara Ruiz-Ponte Angel Carracedo Beatriz González Sergio Alonso Manuel Perucho

BACKGROUND Non-hereditary colorectal cancer (CRC) is a complex disorder resulting from the combination of genetic and non-genetic factors. Genome-wide association studies (GWAS) are useful for identifying such genetic susceptibility factors. However, the single loci so far associated with CRC only represent a fraction of the genetic risk for CRC development in the general population. Therefore,...

Journal: :Crop Science 2023

The National Plant Germplasm System (NPGS) is a vital resource for genetic diversity, yet utilization of this requires thorough understanding the germplasm and diversity. Intermediate wheatgrass (IWG, Thinopyrum intermedium) perennial grass species that has been improved forage production through breeding utilizing NPGS collection also targeted domestication as grain crop. To better characteriz...

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