نتایج جستجو برای: asian continental ancestry group

تعداد نتایج: 1066264  

Journal: :American journal of human biology : the official journal of the Human Biology Council 2001
L Madrigal G Saenz M Chavez D Dykes

Variation in the frequency of twinning among human populations has been presumed to reflect genetic differences. It has been commonly reported that populations of African ancestry have the highest, those of Asian ancestry the lowest, and those of European and Middle-Eastern ancestry intermediate frequencies of twinning. Populations from the Americas have been reported to have intermediate twinn...

Journal: :Current opinion in genetics & development 2016
Pontus Skoglund David Reich

Whole-genome studies have documented that most Native American ancestry stems from a single population that diversified within the continent more than twelve thousand years ago. However, this shared ancestry hides a more complex history whereby at least four distinct streams of Eurasian migration have contributed to present-day and prehistoric Native American populations. Whole genome studies e...

Journal: :Movement Disorders 2021

Background A recently published East Asian genome-wide association study of Parkinson;s disease (PD) reported 2 novel risk loci, SV2C and WBSCR17. Objectives The objective this were to determine whether WBSCR17 loci contribute the developing PD in European ancestry populations. Methods We report an analysis variants with COURAGE-PD cohort (9673 patients; 8465 controls) comprising individuals an...

2017
Nelum Wickramasinghe V V Robin Uma Ramakrishnan Sushma Reddy Sampath S Seneviratne

Co-occurrence of closely related taxa on islands could be attributed to sympatric speciation or multiple colonization. Sympatric speciation is considered to be rare in small islands, however multiple colonizations are known to be common in both oceanic and continental islands. In this study we investigated the phylogenetic relatedness and means of origin of the two sympatrically co-occurring Zo...

2014
Henriët. Springelkamp René Höhn Aniket Mishra Pirro G. Hysi Chiea-Chuen Khor Stephanie J. Loomis Jessica N. Cooke Bailey Jane Gibson Gudmar Thorleifsson Sarah F. Janssen Xiaoyan Luo Wishal D. Ramdas Eranga Vithana Monisha E. Nongpiur Grant W. Montgomery Liang Xu Jenny E. Mountain Puya Gharahkhani Yi Lu Najaf Amin Lennart C. Karssen Kar-Seng Sim Elisabeth M. van Leeuwen Adriana I. Iglesias Virginie J. M. Verhoeven Michael A. Hauser Seng-Chee Loon Dominiek D. G. Despriet Abhishek Nag Cristina Venturini Paul G. Sanfilippo Arne Schillert Jae H. Kang John Landers Fridbert Jonasson Angela J. Cree Leonieke M. E. van Koolwijk Fernando Rivadeneira Emmanuelle Souzeau Vesteinn Jonsson Geeta Menon Paul Mitchell Jie Jin Wang Elena Rochtchina John Attia Rodney Scott Elizabeth G. Holliday Tien-Yin Wong Paul N. Baird Jing Xie Michael Inouye Ananth Viswanathan Xueling Sim Robert N. Weinreb Paulus T. V. M. de Jong Ben A. Oostra André G. Uitterlinden Albert Hofman Sarah Ennis Unnur Thorsteinsdottir Kathryn P. Burdon R. Rand Allingham Murray H. Brilliant Donald L. Budenz Jessica N. Cooke Bailey William G. Christen John Fingert David S. Friedman Douglas Gaasterland Terry Gaasterland Jonathan L. Haines Michael A. Hauser Jae Hee Kang Peter Kraft Richard K. Lee Paul R. Lichter Yutao Liu Stephanie J. Loomis Sayoko E. Moroi Louis R. Pasquale Margaret A. Pericak-Vance Anthony Realini Julia E. Richards Joel S. Schuman William K. Scott Kuldev Singh Arthur J. Sit Douglas Vollrath Robert N. Weinreb Janey L. Wiggs Gadi Wollstein Donald J. Zack Kang Zhang Peter Donnelly (Chair) Ines Barroso (Deputy Chair) Jenefer M. Blackwell Elvira Bramon Matthew A. Brown Juan P. Casas Aiden Corvin Panos Deloukas Audrey Duncanson Janusz Jankowski Hugh S. Markus Christopher G. Mathew Colin N. A. Palmer Robert Plomin Anna Rautanen Stephen J. Sawcer Richard C. Trembath Ananth C. Viswanathan Nicholas W. Wood Chris C. A. Spencer Gavin Band Céline Bellenguez Colin Freeman Garrett Hellenthal Eleni Giannoulatou Matti Pirinen Richard Pearson Amy Strange Zhan Su Damjan Vukcevic Peter Donnelly Cordelia Langford Sarah E. Hunt Sarah Edkins Rhian Gwilliam Hannah Blackburn Suzannah J. Bumpstead Serge Dronov Matthew Gillman Emma Gray Naomi Hammond Alagurevathi Jayakumar Owen T. McCann Jennifer Liddle Simon C. Potter Radhi Ravindrarajah Michelle Ricketts Matthew Waller Paul Weston Sara Widaa Pamela Whittaker Ines Barroso Christopher G. Mathew (Chair) Timothy D. Spector Alireza Mirshahi Seang-Mei Saw Johannes R. Vingerling Yik-Ying Teo Jonathan L. Haines Roger C. W. Wolfs Hans G. Lemij E-Shyong Tai Nomdo M. Jansonius Jost B. Jonas Ching-Yu Cheng Tin Aung Ananth C. Viswanathan Caroline C. W. Klaver Jamie E. Craig Stuart Macgregor David A. Mackey Andrew J. Lotery Kari Stefansson Arthur A. B. Bergen Terri L. Young Janey L. Wiggs Norbert Pfeiffer Tien-Yin Wong Louis R. Pasquale Alex W. Hewitt Cornelia M. van Duijn Christopher J. Hammond

Glaucoma is characterized by irreversible optic nerve degeneration and is the most frequent cause of irreversible blindness worldwide. Here, the International Glaucoma Genetics Consortium conducts a meta-analysis of genome-wide association studies of vertical cup-disc ratio (VCDR), an important disease-related optic nerve parameter. In 21,094 individuals of European ancestry and 6,784 individua...

2014
Noraidatulakma Abdullah John Attia Christopher Oldmeadow Rodney J Scott Elizabeth G Holliday

The prevalence of Type 2 diabetes is rising rapidly in both developed and developing countries. Asia is developing as the epicentre of the escalating pandemic, reflecting rapid transitions in demography, migration, diet, and lifestyle patterns. The effective management of Type 2 diabetes in Asia may be complicated by differences in prevalence, risk factor profiles, genetic risk allele frequenci...

Journal: :Immunohematology 2013
Lilian Castilho Marion E Reid

The JR blood group system (ISBT 032) consists of one antigen,Jra, which is of high prevalence in all populations. The rare Jr(a-) phenotype has been found mostly in Japanese and other Asian populations, but also in people of northern European ancestry, in Bedouin Arabs, and in one Mexican. Anti-Jra has caused transfusion reactions and is involved in hemolytic disease of the fetus and newborn. T...

2010
Mary N. Haan Elizabeth R. Mayeda

The apolipoprotein E (APOE) genotype is a genetic risk factor for dementia, Alzheimer's disease, and cardiovascular disease (CVD). It includes three alleles (e2, e3, e4) that are located on chromosome 19q3.2. The e3 allele is the most common and is more common in people of Northern European ancestry and less common in those of Asian ancestry. Those with at least one e4 allele are at increased r...

Journal: :Social science & medicine 1989
J P Rushton A F Bogaert

Previously we have reported population differences in sexual restraint such that, higher socio-economic status greater than lower socio-economic status, and Mongoloids greater than Caucasoids greater than Negroids. This ordering was predicted from a gene-based evolutionary theory of r/K reproductive strategies in which a trade-off occurs between gamete production and social behaviors such as in...

Journal: :Genomics 2008
Marilyn Menotti-Raymond Victor A David Solveig M Pflueger Kerstin Lindblad-Toh Claire M Wade Stephen J O'Brien Warren E Johnson

Genetic variation in cat breeds was assessed utilizing a panel of short tandem repeat (STR) loci genotyped in 38 cat breeds and 284 single-nucleotide polymorphisms (SNPs) genotyped in 24 breeds. Population structure in cat breeds generally reflects their recent ancestry and absence of strong breed barriers between some breeds. There is a wide range in the robustness of population definition, fr...

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