R
Richard A. King
Researcher at University of Minnesota
Publications - 177
Citations - 10560
Richard A. King is an academic researcher from University of Minnesota. The author has contributed to research in topics: Oculocutaneous albinism & Albinism. The author has an hindex of 54, co-authored 172 publications receiving 10261 citations. Previous affiliations of Richard A. King include University of Utah.
Papers
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Journal ArticleDOI
A genome-wide search for asthma susceptibility loci in ethnically diverse populations
David G. Marsh,Nancy E. Maestri,Linda R. Freidhoff,Kathleen C. Barnes,Alkis Togias,Eva Ehrlich,Terri H. Beaty,David L. Duffy,Richard R. Rosenthal,Farhad Imani,Georgia M. Dunston,Paulette Furbert-Harris,Floyd J. Malveaux,Carole Ober,Nancy J. Cox,Lucille A. Lester,Rhonda Peterson,Heidi Gidley,Anna Pluzhnikov,Jennifer L. Anderson,Julian Solway,Alan R. Leff,Raoul L. Wolf,Mark Wylam,Bradley Kurtz,Anthony Richardson,Rodney Parry,Malcolm N. Blumenthal,Richard A. King,William S. Oetting,Delores Drury,Andreas Rosenberg,Lisa R. Daniels,Charlene McEvoy,Jay Lou,Mark Hamra,Marcia J. Brott,Stephen S. Rich,Beverly J. Spray,James L. Weber,Bo Yuan,Zhenyuan Wang,Eugene R. Bleecker,PJ Amelung,Betsy Rechstiner,Deborah A. Meyers,Jonathan M. Samet,Denise Wiesch,Jianfeng Xu,Shirley Murphy,Susan Banks-Schlegel +50 more
TL;DR: A genome-wide search in 140 families with ≥2 asthmatic sibs, from three racial groups and report evidence for linkage to six novel regions, including 5p15 (P= 0.0008) and 17p11.1–q11.2 (/> = 0.0015) in African Americans and 11p15 and 19q13 (P =0.0013) in Caucasians and Hispanics.
Journal ArticleDOI
Linkage analysis with multiplexed short tandem repeat polymorphisms using infrared fluorescence and M13 tailed primers.
TL;DR: A technique known as multiplexing STRPs with tailed primers (MSTP) using primers that have a 19-bp extension identical to the sequence of an M13 sequencing primer on the 5' end of the forward primer in conjunction with multiplexed several primer pairs in a single polymerase chain reaction (PCR) amplification.
Journal ArticleDOI
A genome-wide search for susceptibility genes in human systemic lupus erythematosus sib-pair families
Patrick M. Gaffney,Grainne M. Kearns,Grainne M. Kearns,Katherine B. Shark,Ward A. Ortmann,Scott A. Selby,Michelle L. Malmgren,Kristine E. Rohlf,Theresa C. Ockenden,Ronald P. Messner,Richard A. King,Stephen S. Rich,Timothy W. Behrens +12 more
TL;DR: The hypothesis that multiple genes, including one in the HLA region, influence susceptibility to human SLE is supported.
Book
The genetic basis of common diseases.
TL;DR: The Genetic Basis of Common Diseases is an excellent compilation of current knowledge that delineates the genetic aspects of common disorders and points out that the simply inherited mendelian disorders are uncommon or rare but that there are no chromosome abnormalities.
Journal ArticleDOI
Mutations in the Human Orthologue of the Mouse underwhite Gene (uw) Underlie a New Form of Oculocutaneous Albinism, OCA4
J. M. Newton,Orit Cohen-Barak,Nobuko Hagiwara,John M. Gardner,Muriel T. Davisson,Richard A. King,Murray H. Brilliant +6 more
TL;DR: The mouse underwhite gene and its human orthologue are identified, which underlies a new form of human OCA, termed "OCA4," and the encoded protein, MATP (for "membrane-associated transporter protein") is predicted to span the membrane 12 times and likely functions as a transporter.