نتایج جستجو برای: genotyped individuals

تعداد نتایج: 340120  

Journal: :Human molecular genetics 2005
Xiayi Ke Marcos M Miretti John Broxholme Sarah Hunt Stephan Beck David R Bentley Panos Deloukas Lon R Cardon

Single-nucleotide polymorphism (SNP) tagging is widely used as a way of saving genotyping costs in association studies. A number of different tagging methods have been developed to reduce the number of markers to be genotyped while maintaining power for detecting effects on non-assayed SNPs. How the different methods perform in different settings, the degree to which they overlap and share comm...

Journal: :Genetic epidemiology 2000
R J Carroll M H Gail J Benichou D Pee

In the genotyped-proband design, a proband is selected based on an observed phenotype, the genotype of the proband is observed, and then the phenotypes of all first-degree relatives are obtained. The genotypes of these first-degree relatives are not observed. Gail et al. [(1999) Genet Epidemiol] discuss likelihood analysis of this design under the assumption that the phenotypes are conditionall...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه شهید چمران اهواز - دانشکده ادبیات و علوم انسانی 1386

the purpose of the present study is to find out whether bilinguals of khuzestan-arab origin or monolinguals of iranian origin code-switch during learning or speaking english and which group is more susceptible to code-switch. to this end, the students of 24 classes from high schools and pre- university centers were screened out, and interviewed and their voices and code-switchings were recorded...

Journal: :Genome research 2011
Yun Li Carlo Sidore Hyun Min Kang Michael Boehnke Gonçalo R Abecasis

New sequencing technologies allow genomic variation to be surveyed in much greater detail than previously possible. While detailed analysis of a single individual typically requires deep sequencing, when many individuals are sequenced it is possible to combine shallow sequence data across individuals to generate accurate calls in shared stretches of chromosome. Here, we show that, as progressiv...

2017
Giovanna C Cavalcante Marcos AT Amador André M Ribeiro dos Santos Darlen C Carvalho Roberta B Andrade Esdras EB Pereira Marianne R Fernandes Danielle F Costa Ney PC Santos Paulo P Assumpção Ândrea Ribeiro dos Santos Sidney Santos

AIM To evaluate the relation between 12 polymorphisms and the development of gastric cancer (GC) and colorectal cancer (CRC). METHODS In this study, we included 125 individuals with GC diagnosis, 66 individuals with CRC diagnosis and 475 cancer-free individuals. All participants resided in the North region of Brazil and authorized the use of their samples. The 12 polymorphisms (in CASP8, CYP2...

2017
Xuecai Zhang Paulino Pérez-Rodríguez Juan Burgueño Michael Olsen Edward Buckler Gary Atlin Boddupalli M Prasanna Mateo Vargas Félix San Vicente José Crossa

Genomic selection (GS) increases genetic gain by reducing the length of the selection cycle, as has been exemplified in maize using rapid cycling recombination of biparental populations. However, no results of GS applied to maize multi-parental populations have been reported so far. This study is the first to show realized genetic gains of rapid cycling genomic selection (RCGS) for four recombi...

Journal: :American journal of human genetics 2007
Michele Cargill Steven J Schrodi Monica Chang Veronica E Garcia Rhonda Brandon Kristina P Callis Nori Matsunami Kristin G Ardlie Daniel Civello Joseph J Catanese Diane U Leong Jackie M Panko Linda B McAllister Christopher B Hansen Jason Papenfuss Stephen M Prescott Thomas J White Mark F Leppert Gerald G Krueger Ann B Begovich

We performed a multitiered, case-control association study of psoriasis in three independent sample sets of white North American individuals (1,446 cases and 1,432 controls) with 25,215 genecentric single-nucleotide polymorphisms (SNPs) and found a highly significant association with an IL12B 3'-untranslated-region SNP (rs3212227), confirming the results of a small Japanese study. This SNP was ...

Journal: :BMC Nephrology 2008
Stephen J Tonna Alexander Needham Krishna Polu Andrea Uscinski Gerald B Appel Ronald J Falk Avi Katz Salah Al-Waheeb Bernard S Kaplan George Jerums Judy Savige Jennifer Harmon Kang Zhang Gary C Curhan Martin R Pollak

BACKGROUND Focal and segmental glomerulosclerosis (FSGS) is the most common histologic pattern of renal injury seen in adults with idiopathic proteinuria. Homozygous or compound heterozygous mutations in the podocin gene NPHS2 are found in 10-30% of pediatric cases of steroid resistant nephrosis and/or FSGS. METHODS We studied the spectrum of genetic variation in 371 individuals with predomin...

Journal: :Hypertension 2010
Yasuharu Tabara Katsuhiko Kohara Yoshikuni Kita Nobuhito Hirawa Tomohiro Katsuya Takayoshi Ohkubo Yumiko Hiura Atsushi Tajima Takayuki Morisaki Toshiyuki Miyata Tomohiro Nakayama Naoyuki Takashima Jun Nakura Ryuichi Kawamoto Norio Takahashi Akira Hata Masayoshi Soma Yutaka Imai Yoshihiro Kokubo Tomonori Okamura Hitonobu Tomoike Naoharu Iwai Toshio Ogihara Itsuro Inoue Katsushi Tokunaga Toby Johnson Mark Caulfield Patricia Munroe Satoshi Umemura Hirotsugu Ueshima Tetsuro Miki

Hypertension is one of the most common complex genetic disorders. We have described previously 38 single nucleotide polymorphisms (SNPs) with suggestive association with hypertension in Japanese individuals. In this study we extend our previous findings by analyzing a large sample of Japanese individuals (n=14 105) for the most associated SNPs. We also conducted replication analyses in Japanese...

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