نتایج جستجو برای: wide association study

تعداد نتایج: 4492963  

Journal: :Science progress 2016
Andreas Scherer G Bryce Christensen

Genome-wide association study (GWAS) technology has been a primary method for identifying the genes responsible for diseases and other traits for the past 10 years. Over 2,000 human GWAS reports now appear in the scientific journals. The technology is continuing to improve, and has recently become accessible to researchers studying a wide variety of animals, plants and model organisms. Here, we...

2011
Yungang He Cong Li Christopher I. Amos Momiao Xiong Hua Ling Li Jin

The genome-wide association study (GWAS) has become a routine approach for mapping disease risk loci with the advent of large-scale genotyping technologies. Multi-allelic haplotype markers can provide superior power compared with single-SNP markers in mapping disease loci. However, the application of haplotype-based analysis to GWAS is usually bottlenecked by prohibitive time cost for haplotype...

Journal: :Twin research and human genetics : the official journal of the International Society for Twin Studies 2016
Bochao D Lin Gonneke Willemsen Abdel Abdellaoui Meike Bartels Erik A Ehli Gareth E Davies Dorret I Boomsma Jouke J Hottenga

We identified the genetic variants for eye color by Genome-Wide Association Study (GWAS) in a Dutch Caucasian family-based population sample and examined the genetic correlation between hair and eye color using data from unrelated participants from the Netherlands Twin Register. With the Genome-wide Complex Trait Analysis software package, we found strong genetic correlations between various co...

Journal: :Plant, cell & environment 2016
Yan Lv Zilong Guo Xiaokai Li Haiyan Ye Xianghua Li Lizhong Xiong

In order to understand cold adaptability and explore additional genetic resources for the cold tolerance improvement of rice, we investigated the genetic variation of 529 rice accessions under natural chilling and cold shock stress conditions at the seedling stage using genome-wide association studies; a total of 132 loci were identified. Among them, 12 loci were common for both chilling and co...

2015
Yohei Takahashi Ikuyo Inaba Katsuki Kono Noriaki Kawakami Koki Uno Manabu Ito Shohei Minami Haruhisa Yanagida Hiroshi Taneichi Ikuho Yonezawa Yoji Ogura Taichi Tsuji Teppei Suzuki Hideki Sudo Toshiaki Kotani Kota Watanabe Yoshiaki Toyama Morio Matsumoto Shiro Ikegawa

Objective We previously conducted a genome-wide association study for AIS susceptibility in Japanese and identified a SNP, rs11190870 near the LBX1 gene on chromosome 10q24.1 that showed significant association. The association is replicated in other populations of different ethnicities. However, it is controversial whether rs11190870 is also associated with severity of the scoliosis curve in A...

Journal: :JAMA neurology 2016
Frederick W Vonberg Tim B Bigdeli

Genetic Correlation Between Schizophrenia and Epilepsy Neuropathological, clinical, and epidemiological data suggest that schizophrenia and epilepsy are associated.1 Reported estimates of the prevalence of schizophrenia among people with epilepsy vary, depending on phenotypic definition, but may be around 7%.2 One hypothesis to account for the relationship is that the 2 diseases share a common ...

Journal: :American journal of human genetics 2015
Marc A Coram Sophie I Candille Qing Duan Kei Hang K Chan Yun Li Charles Kooperberg Alex P Reiner Hua Tang

Elucidating the genetic basis of complex traits and diseases in non-European populations is particularly challenging because US minority populations have been under-represented in genetic association studies. We developed an empirical Bayes approach named XPEB (cross-population empirical Bayes), designed to improve the power for mapping complex-trait-associated loci in a minority population by ...

2016
Orhun H. Kantarci

Before the genomics technology revolution allowed us to do genome-wide science, genetics research relied on our limited knowledge about a subject to generate hypothesis and candidate genes to study. Despite the level of naiveté, several associations with susceptibility to a complex disease such as multiple sclerosis (MS) were discovered. Of these, HLA-DRB1 and IL7R (1) stand out as being confir...

2016
Ailbhe Jane Brazel Douglas Vernimmen

Over the past 30 years, a plethora of pathogenic mutations affecting enhancer regions and epigenetic regulators have been identified. Coupled with more recent genome-wide association studies (GWAS) and epigenome-wide association studies (EWAS) implicating major roles for regulatory mutations in disease, it is clear that epigenetic mechanisms represent important biomarkers for disease developmen...

Journal: :Genetics 2016
Jianfei Huang Kai Wang Peng Wei Xiangtao Liu Xiaoming Liu Kai Tan Eric Boerwinkle James B Potash Shizhong Han

Genome-wide association studies (GWAS) have been widely used for identifying common variants associated with complex diseases. Despite remarkable success in uncovering many risk variants and providing novel insights into disease biology, genetic variants identified to date fail to explain the vast majority of the heritability for most complex diseases. One explanation is that there are still a ...

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