Jason M. Laramie, Ph.D.
Affiliations: | Boston University, Boston, MA, United States |
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Parents
Sign in to add mentorRichard H. Myers | grad student | 2003-2008 | Boston University | |
(Genetic studies of obesity in the NHLBI Family Heart Study.) |
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Publications
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Jun G, Manning A, Almeida M, et al. (2017) Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees. Proceedings of the National Academy of Sciences of the United States of America |
Hunter Z, Xu L, Zhou Y, et al. (2011) Whole-Genome Sequencing Results From 30 Patients with Waldenstrom's Macroglobulinemia Blood. 118: 434-434 |
Laramie JM, Wilk JB, Williamson SL, et al. (2009) Multiple genes influence BMI on chromosome 7q31-34: the NHLBI Family Heart Study. Obesity (Silver Spring, Md.). 17: 2182-9 |
Ma D, Feitosa MF, Wilk JB, et al. (2009) Leptin is associated with blood pressure and hypertension in women from the National Heart, Lung, and Blood Institute Family Heart Study. Hypertension. 53: 473-9 |
Latourelle JC, Sun M, Lew MF, et al. (2008) The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study. Bmc Medicine. 6: 32 |
Tobin JE, Latourelle JC, Lew MF, et al. (2008) Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study. Neurology. 71: 28-34 |
Laramie JM, Wilk JB, Williamson SL, et al. (2008) Polymorphisms near EXOC4 and LRGUK on chromosome 7q32 are associated with Type 2 Diabetes and fasting glucose; the NHLBI Family Heart Study. Bmc Medical Genetics. 9: 46 |
Wilk JB, Laramie JM, Latourelle JC, et al. (2008) NYD-SP18 is associated with obesity in the NHLBI Family Heart Study. International Journal of Obesity (2005). 32: 930-5 |
Wilk JB, Walter RE, Laramie JM, et al. (2007) Framingham Heart Study genome-wide association: results for pulmonary function measures. Bmc Medical Genetics. 8: S8 |
Cupples LA, Arruda HT, Benjamin EJ, et al. (2007) The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports. Bmc Medical Genetics. 8: S1 |