Bibliotecas PUC-SP - Busca Integrada

HaploBuild: an algorithm to construct non-contiguous associated haplotypes in family based genetic studies

Tekijä Laramie, Jason M., Wilk, Jemma B., DeStefano, Anita L., Myers, Richard H.
Julkaistu 2007

Framingham Heart Study genome-wide association: results for pulmonary function measures

Tekijä Wilk, Jemma B, Walter, Robert E, Laramie, Jason M, Gottlieb, Daniel J, O'Connor, George T
Julkaistu 2007

Global gene expression in neuroendocrine tumors from patients with the MEN1 syndrome

Tekijä Dilley, William G, Kalyanaraman, Somasundaram, Verma, Sulekha, Cobb, J Perren, Laramie, Jason M, Lairmore, Terry C
Julkaistu 2005

Global gene expression in neuroendocrine tumors from patients with the MEN1 syndrome

Tekijä Laramie Jason M, Cobb J Perren, Verma Sulekha, Kalyanaraman Somasundaram, Dilley William G, Lairmore Terry C
Julkaisussa Molecular Cancer (2005-02-01)

Evidence for a gene influencing heart rate on chromosome 5p13-14 in a meta-analysis of genome-wide scans from the NHLBI Family Blood Pressure Program

Tekijä Laramie, Jason M, Wilk, Jemma B, Hunt, Steven C, Ellison, R Curtis, Chakravarti, Aravinda, Boerwinkle, Eric, Myers, Richard H
Julkaistu 2006

Evidence for a gene influencing heart rate on chromosome 5p13-14 in a meta-analysis of genome-wide scans from the NHLBI Family Blood Pressure Program

Tekijä Ellison R Curtis, Hunt Steven C, Wilk Jemma B, Laramie Jason M, Chakravarti Aravinda, Boerwinkle Eric, Myers Richard H
Julkaisussa BMC Medical Genetics (2006-03-01)

Leptin Is Associated With Blood Pressure and Hypertension in Women From the National Heart, Lung, and Blood Institute Family Heart Study

Tekijä Ma, Duanduan, Feitosa, Mary F., Wilk, Jemma B., Laramie, Jason M., Yu, Kai, Leiendecker-Foster, Catherine, Myers, Richard H., Province, Michael A., Borecki, Ingrid B.
Julkaistu 2009

Polymorphisms near EXOC4 and LRGUK on chromosome 7q32 are associated with Type 2 Diabetes and fasting glucose; The NHLBI Family Heart Study

Tekijä Laramie, 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
Julkaistu 2008

Polymorphisms near <it>EXOC4 </it>and <it>LRGUK </it>on chromosome 7q32 are associated with Type 2 Diabetes and fasting glucose; The NHLBI Family Heart Study

Tekijä Tobin Jennifer E, Latourelle Jeanne C, Nagle Michael W, Williamson Sally L, Wilk Jemma B, Laramie Jason M, Province Michael A, Borecki Ingrid B, Myers Richard H
Julkaisussa BMC Medical Genetics (2008-05-01)

Sepiapterin reductase expression is increased in Parkinson’s disease brain tissue.

Tekijä Tobin, Jennifer E., Cui, Jing, Wilk, Jemma B., Latourelle, Jeanne C., Laramie, Jason M., McKee, Ann C., Guttman, Mark, Karamohamed, Samer, DeStefano, Anita L., Myers, Richard H.
Julkaistu 2007

The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports

Tekijä Cupples, 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
Julkaistu 2007

The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study

Tekijä Latourelle, Jeanne C, Sun, Mei, Lew, Mark F, Suchowersky, Oksana, Klein, Christine, Golbe, Lawrence I, Mark, Margery H, Growdon, John 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, Sherman, Scott J, Roxburgh, Richard, Snow, Barry, Slevin, John T, Cambi, Franca, Gusella, James F, Myers, Richard H
Julkaistu 2008

The Gly2019Ser mutation in <it>LRRK2 </it>is not fully penetrant in familial Parkinson's disease: the GenePD study

Tekijä Corbett Alastair, Nicholson Garth, Litvan Irene, Itin Ilia, Baker Kenneth B, DeStefano Anita L, Laramie Jason M, Huskey Karen W, Massood Tiffany, Wilk Jemma B, Nagle Michael W, Williamson Sally, Hendricks Audrey E, Saint-Hilaire Marie H, Zini Michela, Pezzoli Gianni, Goldwurm Stefano, Singer Carlos, Shill Holly A, Ahmed Anwar, Perlmutter Joel S, Guttman Mark, Racette Brad A, Watts Ray L, Wooten G Frederick, Growdon John H, Mark Margery H, Golbe Lawrence I, Klein Christine, Suchowersky Oksana, Lew Mark F, Sun Mei, Latourelle Jeanne C, Nance Martha, Drasby Edward, Isaacson Stuart, Burn David J, Chinnery Patrick F, Pramstaller Peter P, Al-hinti Jomana, Moller Anette T, Ostergaard Karen, Sherman Scott J, Roxburgh Richard, Snow Barry, Slevin John T, Cambi Franca, Gusella James F, Myers Richard H
Julkaisussa BMC Medicine (2008-11-01)