J
Julie A. Douglas
Researcher at University of Michigan
Publications - 52
Citations - 8859
Julie A. Douglas is an academic researcher from University of Michigan. The author has contributed to research in topics: Cancer & Prostate cancer. The author has an hindex of 24, co-authored 47 publications receiving 8493 citations. Previous affiliations of Julie A. Douglas include Skidmore College & Johns Hopkins University.
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The International HapMap Project
John W. Belmont,Paul Hardenbol,Thomas D. Willis,Fuli Yu,Huanming Yang,Lan Yang Ch'Ang,Wei Huang,Bin Liu,Yan Shen,Paul K.H. Tam,Lap-Chee Tsui,Mary M.Y. Waye,Jeffrey Tze Fei Wong,Changqing Zeng,Qingrun Zhang,Mark S. Chee,Luana Galver,Semyon Kruglyak,Sarah S. Murray,Arnold Oliphant,Alexandre Montpetit,Fanny Chagnon,Vincent Ferretti,Martin Leboeuf,Michael S. Phillips,Andrei Verner,Shenghui Duan,Denise L. Lind,Raymond D. Miller,John P. Rice,Nancy L. Saccone,Patricia Taillon-Miller,Ming Xiao,Akihiro Sekine,Koki Sorimachi,Yoichi Tanaka,Tatsuhiko Tsunoda,Eiji Yoshino,David R. Bentley,Sarah E. Hunt,Don Powell,Houcan Zhang,Ichiro Matsuda,Yoshimitsu Fukushima,Darryl Macer,Eiko Suda,Charles N. Rotimi,Clement Adebamowo,Toyin Aniagwu,Patricia A. Marshall,Olayemi Matthew,Chibuzor Nkwodimmah,Charmaine D.M. Royal,Mark Leppert,Missy Dixon,Fiona Cunningham,Ardavan Kanani,Gudmundur A. Thorisson,Peter E. Chen,David J. Cutler,Carl S. Kashuk,Peter Donnelly,Jonathan Marchini,Gilean McVean,Simon Myers,Lon R. Cardon,Andrew P. Morris,Bruce S. Weir,James C. Mullikin,Michael Feolo,Mark J. Daly,Renzong Qiu,Alastair Kent,Georgia M. Dunston,Kazuto Kato,Norio Niikawa,Jessica Watkin,Richard A. Gibbs,Erica Sodergren,George M. Weinstock,Richard K. Wilson,Lucinda Fulton,Jane Rogers,Bruce W. Birren,Hua Han,Hongguang Wang,Martin Godbout,John C. Wallenburg,Paul L'Archevêque,Guy Bellemare,Kazuo Todani,Takashi Fujita,Satoshi Tanaka,Arthur L. Holden,Francis S. Collins,Lisa D. Brooks,Jean E. McEwen,Mark S. Guyer,Elke Jordan,Jane Peterson,Jack Spiegel,Lawrence M. Sung,Lynn F. Zacharia,Karen Kennedy,Michael Dunn,Richard Seabrook,Mark Shillito,Barbara Skene,John Stewart,David Valle,Ellen Wright Clayton,Lynn B. Jorde,Aravinda Chakravarti,Mildred K. Cho,Troy Duster,Troy Duster,Morris W. Foster,Maria Jasperse,Bartha Maria Knoppers,Pui-Yan Kwok,Julio Licinio,Jeffrey C. Long,Pilar N. Ossorio,Vivian Ota Wang,Charles N. Rotimi,Patricia Spallone,Patricia Spallone,Sharon F. Terry,Eric S. Lander,Eric H. Lai,Deborah A. Nickerson,Gonçalo R. Abecasis,David Altshuler,Michael Boehnke,Panos Deloukas,Julie A. Douglas,Stacey Gabriel,Richard R. Hudson,Thomas J. Hudson,Leonid Kruglyak,Yusuke Nakamura,Robert L. Nussbaum,Stephen F. Schaffner,Stephen T. Sherry,Lincoln Stein,Toshihiro Tanaka +145 more
TL;DR: The HapMap will allow the discovery of sequence variants that affect common disease, will facilitate development of diagnostic tools, and will enhance the ability to choose targets for therapeutic intervention.
Journal ArticleDOI
A common variant associated with prostate cancer in European and African populations
Laufey T. Amundadottir,Patrick Sulem,Julius Gudmundsson,Agnar Helgason,Adam Baker,Bjarni A. Agnarsson,Asgeir Sigurdsson,Kristrun R. Benediktsdottir,Jean-Baptiste Cazier,Jesus Sainz,Margret Jakobsdottir,Jelena Kostic,Droplaug N Magnusdottir,Shyamali Ghosh,Kari Agnarsson,Birgitta Birgisdottir,Louise le Roux,Adalheidur Olafsdottir,Thorarinn Blondal,Margret B. Andresdottir,Olafia S Gretarsdottir,Jon Thor Bergthorsson,Daniel F. Gudbjartsson,Arnaldur Gylfason,Gudmar Thorleifsson,Andrei Manolescu,Kristleifur Kristjansson,Gudmundur Geirsson,Helgi J Isaksson,Julie A. Douglas,Jan-Erik Johansson,Katarina Bälter,Fredrik Wiklund,James E. Montie,Xiaoying Yu,Brian K. Suarez,Carole Ober,Kathleen A. Cooney,Henrik Grönberg,William J. Catalona,Gudmundur V. Einarsson,Rosa B. Barkardottir,Jeffrey R. Gulcher,Augustine Kong,Unnur Thorsteinsdottir,Kari Stefansson +45 more
TL;DR: Allele −8 of the microsatellite DG8S737 was associated with prostate cancer in three case-control series of European ancestry from Iceland, Sweden and the US, and the association was replicated in an African American case- control group with a similar OR, leading to a greater estimated PAR.
Journal ArticleDOI
The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2 diabetes.
Soumitra Ghosh,Richard M. Watanabe,Timo T. Valle,Elizabeth R. Hauser,Victoria L. Magnuson,Carl D. Langefeld,Delphine S. Ally,Karen L. Mohlke,Kaisa Silander,Kimmo Kohtamäki,Peter S. Chines,James E. Balow,Gunther Birznieks,Jennie Chang,William Eldridge,Michael R. Erdos,Zarir E. Karanjawala,Julie I. Knapp,Kristina Kudelko,Colin Martin,Anabelle Morales-Mena,Anjene Musick,Tiffany Musick,Carrie Pfahl,Rachel Porter,Joseph B. Rayman,David Rha,Leonid Segal,Shane A. Shapiro,Ravi Sharaf,Ben Shurtleff,Alistair So,Joyce Tannenbaum,Catherine Te,Jason Tovar,Arun M. Unni,Christian Welch,Ray Whiten,Alyson Witt,Jillian Blaschak-Harvan,Julie A. Douglas,William L. Duren,Michael P. Epstein,Tasha E. Fingerlin,Hong Shi Kaleta,Ethan M. Lange,Chun Li,Richard C. McEachin,Heather M. Stringham,Edward H. Trager,Peggy P. White,Johan G. Eriksson,Liisa Toivanen,Gabriele Vidgren,Stella J. Nylund,Eva Tuomilehto-Wolf,Edna H. Ross,Elza Demirchyan,William Hagopian,Thomas A. Buchanan,Jaakko Tuomilehto,Richard N. Bergman,Francis S. Collins,Michael Boehnke +63 more
TL;DR: An ordered-subsets analysis based on families with high or low diabetes-related quantitative traits yielded results that support the possible existence of disease-predisposing genes on chromosomes 6 and 10, and Genomewide linkage-disequilibrium analysis using microsatellite marker data revealed strong evidence of association for D22S423.
Journal ArticleDOI
Experimentally-derived haplotypes substantially increase the efficiency of linkage disequilibrium studies.
TL;DR: It is shown that, particularly when phenotyping is expensive, conversion-based haplotyping can be more efficient and cost-effective than standard genotyping.
Journal ArticleDOI
A Multipoint Method for Detecting Genotyping Errors and Mutations in Sibling-Pair Linkage Data
TL;DR: A hidden Markov method for detecting genotyping errors and mutations in multilocus linkage data designed for use with sibling-pair data when parental genotypes are unavailable, which generally flags those errors that have the largest impact on linkage results.