Zobrazeno 1 - 10
of 114
pro vyhledávání: '"Howard M. Cann"'
Autor:
Dimitrios Trichopoulos, Anne Tjonneland, Michael J. Thun, Gilles Thomas, Daniel O. Stram, V. Wendy Setiawan, Elio Riboli, Malcolm C. Pike, Petra H. Peeters, Carmen Navarro, William Modi, Jakob Linseisen, Loic LeMarchand, Peter Kraft, Laurence N. Kolonel, David Hunter, Joel N. Hirschhorn, Richard B. Hayes, Susan E. Hankinson, Christopher A. Haiman, Matthew L. Freedman, W. Ryan Diver, Graham Colditz, Francoise Clavel-Chapelon, Stephen J. Chanock, Eugenia E. Calle, Noel P. Burtt, Julie E. Buring, Sheila Bingham, Franco Berrino, Goran Berglund, David Altshuler, Demetrius Albanes, Brian E. Henderson, Rudolf Kaaks, Sholom Wacholder, Howard M. Cann, David G. Cox, Heather Spencer Feigelson
Supplementary Tables 1S-7S, Figure 1S from Haplotype Analysis of the HSD17B1 Gene and Risk of Breast Cancer: A Comprehensive Approach to Multicenter Analyses of Prospective Cohort Studies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0330a9ce56583cf9b4cf404e67dd84af
https://doi.org/10.1158/0008-5472.22366805.v1
https://doi.org/10.1158/0008-5472.22366805.v1
Autor:
Alicia R Martin, Helio A Costa, Tuuli Lappalainen, Brenna M Henn, Jeffrey M Kidd, Muh-Ching Yee, Fabian Grubert, Howard M Cann, Michael Snyder, Stephen B Montgomery, Carlos D Bustamante
Publikováno v:
PLoS Genetics, Vol 10, Iss 8, p e1004549 (2014)
Large-scale sequencing efforts have documented extensive genetic variation within the human genome. However, our understanding of the origins, global distribution, and functional consequences of this variation is far from complete. While regulatory v
Externí odkaz:
https://doaj.org/article/034634dd18804c91bad00abc6cb5c6c2
Autor:
Howard M. Cann, Shane A. McCarthy, Chris Tyler-Smith, David Reich, Aylwyn Scally, Qasim Ayub, Pontus Skoglund, Petr Danecek, Jean-François Deleuze, Manjinder S. Sandhu, Pille Hallast, Ruoyun Hui, Yuan Chen, Swapan Mallick, Yali Xue, Sabine Felkel, Anders Bergström, Hélène Blanché, Mohamed A. Almarri, Jack Kamm, Richard Durbin
Publikováno v:
Science
INTRODUCTION: Large-scale human genome sequencing studies to date have been limited to large, metropolitan populations or to small numbers of genomes from each group. Much remains to be understood about the extent and structure of genetic variation i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30f59d64f25c414f16049ef25f89093f
https://www.repository.cam.ac.uk/handle/1810/302417
https://www.repository.cam.ac.uk/handle/1810/302417
Autor:
Blandine Patillon, Pierre Luisi, Hélène Blanché, Etienne Patin, Howard M Cann, Emmanuelle Génin, Audrey Sabbagh
Publikováno v:
PLoS ONE, Vol 7, Iss 12, p e53049 (2012)
VKORC1 (vitamin K epoxide reductase complex subunit 1, 16p11.2) is the main genetic determinant of human response to oral anticoagulants of antivitamin K type (AVK). This gene was recently suggested to be a putative target of positive selection in Ea
Externí odkaz:
https://doaj.org/article/9e6d86977cab4257bbcca362cc407418
Autor:
Laurent Excoffier, Laura R. Botigué, Howard M. Cann, Jeffrey M. Kidd, Shaila Musharoff, Brian K. Maples, Brenna M. Henn, Carlos Bustamante, Michael Snyder, Mikhail Lipatov, Alicia R. Martin, Isabelle Dupanloup, Stephan Peischl
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, vol 113, iss 4
Proc Natl Acad Sci U S A
Proc Natl Acad Sci U S A
The Out-of-Africa (OOA) dispersal ~50,000 years ago is characterized by a series of founder events as modern humans expanded into multiple continents. Population genetics theory predicts an increase of mutational load in populations undergoing serial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65c436e2b0db0e8b594aa78dab334835
https://escholarship.org/uc/item/15f7c94w
https://escholarship.org/uc/item/15f7c94w
Publikováno v:
European Journal of Human Genetics. 19:583-587
Inbreeding coefficients and consanguineous mating types are usually inferred from population surveys or pedigree studies. Here, we present a method to estimate them from dense genome-wide single-nucleotide polymorphism genotypes and apply it to 940 u
Autor:
Hongzhi Cao, Hélène Blanche, Jing Wang, Hongmei Zhu, Junjie Qin, Jinxiang Li, Xiuqing Zhang, Xin Jin, Honglong Wu, Huanming Yang, Lars Bolund, Guangyu Zhou, Xueda Hu, Ruiqiang Li, Xuan Zhu, Hancheng Zheng, Ruibang Luo, Qibin Li, Yingrui Li, Geng Tian, Wubin Qian, Howard M. Cann, Yuanyuan Ren, Dongfang Li, Songgang Li, Jun Wang, Karsten Kristiansen
Publikováno v:
Li, R, Li, Y, Zheng, H, Luo, R, Zhu, H, Li, Q, Qian, W, Ren, Y, Tian, G, Li, J, Zhou, G, Zhu, X, Wu, H, Qin, J, Jin, X, Li, D, Cao, H, Hu, X, Blanche, H, Cann, H, Zhang, X, Li, S, Bolund, L, Kristiansen, K, Yang, H, Wang, J & Wang, J 2009, ' Building the sequence map of the human pan-genome ', Nature Biotechnology, vol. 28, no. 1, pp. 57-63 . https://doi.org/10.1038/nbt.1596
Udgivelsesdato: 2010-Jan Here we integrate the de novo assembly of an Asian and an African genome with the NCBI reference human genome, as a step toward constructing the human pan-genome. We identified approximately 5 Mb of novel sequences not presen
Autor:
J.F. Shaw, H. Perkins, Rose Payne, Howard M. Cann, F.E. Ward, A. Biegel, Rene J. Duquesnoy, J. G. Bodmer, Marcus W. Feldman, Glenn E. Rodey, P. Stastny
Publikováno v:
Tissue Antigens. 9:135-147
For purposes of genetic comparison, the available HLA data on United States and African Black, together with United States Caucasoid populations, are summarized. Antigen frequencies and pairwise linkage disequilibria are presented for the HLA-A, -B a
Publikováno v:
Scopus-Elsevier
HL–A phenotype and gene frequencies are presented for a population sample of Nahua Indians from Mexico. These Indians showed restricted variability in the first and second segregant HL–A series as compared to Caucasian, Black and Mongoloid popula
Autor:
Richard M. Myers, Howard M. Cann, Marcus W. Feldman, Gregory S. Barsh, Hua Tang, Luigi Luca Cavalli-Sforza, Audrey Southwick, Devin Absher, Jun Li, Sohini Ramachandran, Amanda M. Casto
Publikováno v:
Science. 319:1100-1104
Human genetic diversity is shaped by both demographic and biological factors and has fundamental implications for understanding the genetic basis of diseases. We studied 938 unrelated individuals from 51 populations of the Human Genome Diversity Pane