Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Kelly R. Ewen-White"'
Autor:
Grant W. Montgomery, Megan J. Campbell, Peter Dickson, Shane Herbert, Kirby Siemering, Kelly R. Ewen-White, Peter M. Visscher, Nicholas G. Martin
Publikováno v:
Twin Research and Human Genetics. 8:346-352
High density single nucleotide polymorphism (SNP) genotyping panels provide an alternative to microsatellite markers for genome scans. However, genotype errors have a major impact on power to detect linkage or association and are difficult to detect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de88d57ca8331ae3f35b52168bfa0fac
https://doi.org/10.1375/twin.8.4.346
https://doi.org/10.1375/twin.8.4.346
Autor:
Grant W, Montgomery, Megan J, Campbell, Peter, Dickson, Shane, Herbert, Kirby, Siemering, Kelly R, Ewen-White, Peter M, Visscher, Nicholas G, Martin
Publikováno v:
Twin research and human genetics : the official journal of the International Society for Twin Studies. 8(4)
High density single nucleotide polymorphism (SNP) genotyping panels provide an alternative to microsatellite markers for genome scans. However, genotype errors have a major impact on power to detect linkage or association and are difficult to detect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8f9de8bf2b437bb27d9aeeea95652604
https://pubmed.ncbi.nlm.nih.gov/16176719
https://pubmed.ncbi.nlm.nih.gov/16176719
Autor:
Gary Dawson, Nicholas G. Martin, David H. Barlow, Jacqueline Wicks, Stephen Kennedy, Kelly R. Ewen-White, Vicki Smith, Susan A. Treloar, Grant W. Montgomery, David L. Duffy, Daniel T. O'Connor, Melanie Bahlo, Simon T. Bennett, Dale R. Nyholt, Ian Mackay, Daniel E. Weeks, Alisoun H. Carey
Publikováno v:
ResearcherID
Endometriosis is a common gynecological disease that affects up to 10% of women in their reproductive years. It causes pelvic pain, severe dysmenorrhea, and subfertility. The disease is defined as the presence of tissue resembling endometrium in site
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a96f918a351cffd3d7bdebd77ba71887
https://europepmc.org/articles/PMC1226203/
https://europepmc.org/articles/PMC1226203/
Autor:
Douglas F. Levinson, Jeremy M. Silverman, Brien P. Riley, Dieter B. Wildenauer, Jean-Francois Deleuze, Jacques Mallet, Kenneth S. Kendler, Alan R. Sanders, George N. Papadimitriou, Brian J. Mowry, Sibylle G. Schwab, Claudine Laurent, Stéphane Soubigou, Kung Yee Liang, Gerald Nestadt, Margot Albus, Bernard Lerer, Anthony O'Neill, Peter Holmans, Nigel Williams, R. Ribble, Marilyn K. Walters, Kelly R. Ewen-White, Raymond R. Crowe, Deborah A. Nertney, Hywel Williams, M. Jay, Nicola DeMarchi, Laura Martinolich, Ann Weilbaecher, Eric B. Carpenter, Pablo V. Gejman, Nadine Norton, Wolfgang Maier, Dermot Walsh, Michael John Owen, Stephanie Bauche, Michael Conlon O'Donovan, Ann E. Pulver, Dimitris Dikeos, Brandon Wormley
Publikováno v:
Science
Science, 2002, 296 (5568), pp.739-741. ⟨10.1126/science.1069914⟩
Science, 2002, 296 (5568), pp.739-741. ⟨10.1126/science.1069914⟩
International audience; Reports of substantial evidence for genetic linkage of schizophrenia to chromosome 1q were evaluated by genotyping 16 DNA markers across 107 centimorgans of this chromosome in a multicenter sample of 779 informative schizophre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97370f423aec9fa231967ec1c5d42e35
https://hal.science/hal-03863693
https://hal.science/hal-03863693