نتایج جستجو برای: to assess heritability

تعداد نتایج: 10618307  

Journal: :بینا 0
محمد پاکرولن m pakravan ophthalmic research center, shahid beheshti university of medical sciences, tehran, iranتهران- پاسداران- بوستان نهم- بیمارستان لبافی نژاد- مرکز تحقیقات چشم فریده شریفی پور f sharifipoor jondi shapoor university of medical sciences, ahvaz, iranدانشگاه علوم پزشکی اهواز شاهین یزدانی sh yazdani ophthalmic research center, shahid beheshti university of medical sciences, tehran, iranتهران- پاسداران- بوستان نهم- بیمارستان لبافی نژاد- مرکز تحقیقات چشم نسیم کوهستانی n kohestani ophthalmic research center, shahid beheshti university of medical sciences, tehran, iranتهران- پاسداران- بوستان نهم- بیمارستان لبافی نژاد- مرکز تحقیقات چشم نسیم عموهاشمی n amohashemi ophthalmic research center, shahid beheshti university of medical sciences, tehran, iranتهران- پاسداران- بوستان نهم- بیمارستان لبافی نژاد- مرکز تحقیقات چشم مهدی یاسری m yaseri دانشکده بهداشت- دانشگاه علوم پزشکی تهران

purpose: to compare anterior segment and ocular biometric parameters of unaffected fellow eyes of patients with a previous attack of acute angle closure (aac), primary angle closure suspect (pacs) eyes, and normal eyes; and to assess the risk of developing aac in pacs. methods: in this prospective comparative observational case series, 16 unaffected fellow eyes of patients with a previous attac...

Journal: :Schizophrenia bulletin 2014
Gregory Light Tiffany A Greenwood Neal R Swerdlow Monica E Calkins Robert Freedman Michael F Green Raquel E Gur Ruben C Gur Laura C Lazzeroni Keith H Nuechterlein Ann Olincy Allen D Radant Larry J Seidman Larry J Siever Jeremy M Silverman Joyce Sprock William S Stone Catherine A Sugar Debby W Tsuang Ming T Tsuang Bruce I Turetsky David L Braff

BACKGROUND Twin and multiplex family studies have established significant heritability for schizophrenia (SZ), often summarized as 81%. The Consortium on the Genetics of Schizophrenia (COGS-1) family study was designed to deconstruct the genetic architecture of SZ using neurocognitive and neurophysiological endophenotypes, for which heritability estimates ranged from 18% to 50% (mean = 30%). Th...

Journal: :Investigative ophthalmology & visual science 2008
Yingfeng Zheng Jian Ge Guofu Huang Jian Zhang Bin Liu Yoon-Mi Hur Mingguang He

PURPOSE To assess the heritability of central corneal thickness (CCT) in Chinese children in a classic twin study. METHODS Twins aged 8 to 16 years were recruited from the Guangzhou Twin Registry. Pachymetry data were obtained by one operator using the same imaging system. Zygosity was confirmed by genotyping with 16 polymorphic markers in all same-sex twin pairs. The CCT of the right eyes wa...

Journal: :Environmental health perspectives 2015
Jianjun Gao Lin Tong Maria Argos Molly Scannell Bryan Alauddin Ahmed Muhammad Rakibuz-Zaman Muhammad G Kibriya Farzana Jasmine Vesna Slavkovich Joseph H Graziano Habibul Ahsan Brandon L Pierce

BACKGROUND Consumption of arsenic-contaminated drinking water adversely affects health. There is interindividual variation in arsenic metabolism efficiency, partially due to genetic variation in the arsenic methyltransferase (AS3MT) gene region. OBJECTIVES The goal of this study was to assess the overall contribution of genetic factors to variation in arsenic metabolism efficiency, as measure...

Journal: :Journal of the American Academy of Child and Adolescent Psychiatry 2016
Christel M Middeldorp Anke R Hammerschlag Klaasjan G Ouwens Maria M Groen-Blokhuis Beate St Pourcain Corina U Greven Irene Pappa Carla M T Tiesler Wei Ang Ilja M Nolte Natalia Vilor-Tejedor Jonas Bacelis Jane L Ebejer Huiying Zhao Gareth E Davies Erik A Ehli David M Evans Iryna O Fedko Mònica Guxens Jouke-Jan Hottenga James J Hudziak Astanand Jugessur John P Kemp Eva Krapohl Nicholas G Martin Mario Murcia Ronny Myhre Johan Ormel Susan M Ring Marie Standl Evie Stergiakouli Camilla Stoltenberg Elisabeth Thiering Nicholas J Timpson Maciej Trzaskowski Peter J van der Most Carol Wang Dale R Nyholt Sarah E Medland Benjamin Neale Bo Jacobsson Jordi Sunyer Catharina A Hartman Andrew J O Whitehouse Craig E Pennell Joachim Heinrich Robert Plomin George Davey Smith Henning Tiemeier Danielle Posthuma Dorret I Boomsma

OBJECTIVE The aims of this study were to elucidate the influence of common genetic variants on childhood attention-deficit/hyperactivity disorder (ADHD) symptoms, to identify genetic variants that explain its high heritability, and to investigate the genetic overlap of ADHD symptom scores with ADHD diagnosis. METHOD Within the EArly Genetics and Lifecourse Epidemiology (EAGLE) consortium, gen...

Journal: :BMC public health 2015
Ronja Foraita Mirko Brandes Frauke Günther Karin Bammann Iris Pigeot Wolfgang Ahrens

BACKGROUND Overweight/obesity is an important public health burden worldwide, increasing the risk for the development of cardiovascular diseases or the metabolic syndrome. This risk may be reduced by a good aerobic fitness (AF) that can be improved by physical activity but is also influenced by genetic factors. The aim of this study was to test for familial aggregation of AF measured by maximal...

2013
Sven Stringer Eske M. Derks René S. Kahn William G. Hill Naomi R. Wray

For most complex traits, results from genome-wide association studies show that the proportion of the phenotypic variance attributable to the additive effects of individual SNPs, that is, the heritability explained by the SNPs, is substantially less than the estimate of heritability obtained by standard methods using correlations between relatives. This difference has been called the "missing h...

Journal: :Twin research : the official journal of the International Society for Twin Studies 2004
Maurice P A Zeegers Fruhling Rijsdijk Pak Sham Robert Fagard Marij Gielen Peter W De Leeuw Robert Vlietinck

The heritability of blood pressure estimated in previous studies may be confounded by the influence of potential blood pressure risk factors. We applied the classical twin design to estimate the contribution of these covariates to blood pressure heritability. The study consisted of 173 dizygotic and 251 monozygotic twin pairs aged 18-34 years, randomly selected from the East Flanders Prospectiv...

Journal: :Arthritis Research & Therapy 2006
Guangju Zhai James Stankovich Flavia Cicuttini Changhai Ding Graeme Jones

The aim of this study was to estimate the heritability and describe the correlates of bone marrow lesions in knee subchondral bone. A sibpair design was used. T2- and T1-weighted MRI scans were performed on the right knee to assess bone marrow lesions at lateral tibia and femora and medial tibia and femora, as well as chondral defects. A radiograph was taken on the same knee and scored for indi...

C. Robert Granie F. Alanoshahr, R. Imany-Nabiyyi S. Alijani S.A. Rafat

The success of genomic selection mainly depends on the extent of linkage disequilibrium (LD) between markers and quantitative trait loci (QTL), number of QTL and heritability (h2) of the traits. The extent of LD depends on the genetic structure of the population and marker density. This study was conducted to determine the effects of marker density, level of heritability, number of QTL, and to ...

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