Browsing by Contributors Laramie, Jason M

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PreviewIssue DateTitleContributor(s)
2017 AJC Volume 119 Issue 12 May (33).pdf.jpg2017Coronary Artery DiseaseReuwer, Anne Q; Arsenault, Benoit J; Lemieux, Isabelle; Ha, Sang Jin; Kim, Seok Yeon; Bae, Jong-hoa; Kim, Kwon Sam; Winkle, Roger a; Mead, R Hardwin; Engel, Gregory; Patrawala, Rob a; Prasad, Sandhir B; See, Valerie; Brown, Paula; Jones, W Schuyler; Clare, Robert; Ellis, Stephen J; Mills, James S; Fischman, David L; Kraus, William E; Whellan, David J; Connor, Christopher M O; Capranzano, Piera; Chisari, Alberto; Ministeri, Margherita; Mangiameli, Andrea; Ronsivalle, Giuseppe; Ricca, Giovanni; Barrano, Giombattista; Guey, Lin T; Pullinger, Clive R; Ishida, Brian Y; Francone, Omar L; Laramie, Jason M
2006Evidence for a Gene Influencing Heart Rate on Chromosome 5P13-14 in a Meta-Analysis of Genome-Wide Scans from the NHLBI Family Blood Pressure ProgramLaramie, Jason M; Wilk, Jemma B; Hunt, Steven C; Ellison, R Curtis; Chakravarti, Aravinda; Boerwinkle, Eric; Myers, Richard H
2007Framingham Heart Study Genome-Wide Association: Results for Pulmonary Function MeasuresWilk, Jemma B; Walter, Robert E; Laramie, Jason M; Gottlieb, Daniel J; O'Connor, George T
2008Polymorphisms Near EXOC4 and LRGUK on Chromosome 7q32 Are Associated With Type 2 Diabetes and Fasting Glucose; The NHLBI Family Heart StudyLaramie, Jason M; Wilk, Jemma B; Williamson, Sally L; Nagle, Michael W; Latourelle, Jeanne C; Tobin, Jennifer E; Province, Michael A; Borecki, Ingrid B; Myers, Richard H
2007The Framingham Heart Study 100K SNP Genome-Wide Association Study Resource: Overview of 17 Phenotype Working Group ReportsCupples, L Adrienne; Arruda, Heather T; Benjamin, Emelia J; D'Agostino, Ralph B; Demissie, Serkalem; DeStefano, Anita L; Dupuis, Josée; Falls, Kathleen M; Fox, Caroline S; Gottlieb, Daniel J; Govindaraju, Diddahally R; Guo, Chao-Yu; Heard-Costa, Nancy L; Hwang, Shih-Jen; Kathiresan, Sekar; Kiel, Douglas P; Laramie, Jason M; Larson, Martin G; Levy, Daniel; Liu, Chun-Yu; Lunetta, Kathryn L; Mailman, Matthew D; Manning, Alisa K; Meigs, James B; Murabito, Joanne M; Newton-Cheh, Christopher; O'Connor, George T; O'Donnell, Christopher J; Pandey, Mona; Seshadri, Sudha; Vasan, Ramachandran S; Wang, Zhen Y; Wilk, Jemma B; Wolf, Philip A; Yang, Qiong; Atwood, Larry D
2008The Gly2019Ser Mutation in LRRK2 is not Fully Penetrant in Familial Parkinson's Disease: The GenePD StudyLatourelle, Jeanne C; Lew, Mark F; Suchowersky, Oksana; Klein, Christine; Golbe, Lawrence I; Mark, Margery H; Wooten, G Frederick; Watts, Ray L; Guttman, Mark; Racette, Brad A; Perlmutter, Joel S; Ahmed, Anwar; Shill, Holly A; Singer, Carlos; Goldwurm, Stefano; Pezzoli, Gianni; Zini, Michela; Saint-Hilaire, Marie H; Hendricks, Audrey E; Williamson, Sally; Nagle, Michael W; Wilk, Jemma B; Massood, Tiffany; Huskey, Karen W; Laramie, Jason M; DeStefano, Anita L; Baker, Kenneth B; Itin, Ilia; Litvan, Irene; Nicholson, Garth; Corbett, Alastair; Nance, Martha; Drasby, Edward; Isaacson, Stuart; Burn, David J; Chinnery, Patrick F; Pramstaller, Peter P; Al-hinti, Jomana; Moller, Anette T; Ostergaard, Karen; Roxburgh, Richard; Snow, Barry; Slevin, John T; Cambi, Franca; Growdon, John Herbert; Gusella, James Francis; Sun, Mei; Sherman, Scott J; Myers, Richard Hepworth