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Translational Behavioral Medicine
|
June 25, 2020
Relationship between genetic knowledge and familial communication of CRC risk and intent to communicate CRCP genetic information: insights from FamilyTalk eMERGE III
Sukh Makhnoon, Deborah J Bowen, Brian H Shirts, et al.
Human Molecular Genetics
|
April 28, 2010
Aging-related atherosclerosis is exacerbated by arterial expression of tumor necrosis factor receptor-1: evidence from mouse models and human association studies
Lisheng Zhang, Jessica J Connelly, Karsten Peppel, et al.
American Journal of Human Genetics
|
June 25, 2011
Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate
Iftikhar J Kullo, Keyue Ding, Khader Shameer, et al.
Circulation. Cardiovascular Genetics
|
February 23, 2010
Association of a peripheral blood metabolic profile with coronary artery disease and risk of subsequent cardiovascular events
Svati H Shah, James R Bain, Michael J Muehlbauer, et al.
Scandinavian Journal of Infectious Diseases
|
July 11, 2008
Clinical outcomes and costs among patients with Staphylococcus aureus bacteremia and orthopedic device infections
Tahaniyat Lalani, Vivian H Chu, Chelsea A Grussemeyer, et al.
American Heart Journal
|
December 22, 2005
The cost of acute myocardial infarction in the new millennium: evidence from a multinational registry
Teresa L Kauf, Eric J Velazquez, David R Crosslin, et al.
Pain
|
March 17, 2021
Genome-wide association studies of low back pain and lumbar spinal disorders using electronic health record data identify a locus associated with lumbar spinal stenosis
Pradeep Suri, Ian B Stanaway, Yanfei Zhang, et al.
Human Molecular Genetics
|
January 22, 2008
Comprehensive genetic analysis of the platelet activating factor acetylhydrolase (PLA2G7) gene and cardiovascular disease in case-control and family datasets
Beth S Sutton, David R Crosslin, Svati H Shah, et al.
Frontiers in Genetics
|
July 3, 2014
eMERGEing progress in genomics-the first seven years
Dana C Crawford, David R Crosslin, Gerard Tromp, et al.
Genes and Immunity
|
November 22, 2018
Unfolding of hidden white blood cell count phenotypes for gene discovery using latent class mixed modeling
Taryn O Hall, Ian B Stanaway, David S Carrell, et al.
Page
of 12
Search research articles
Search
Showing results (21-30 of 116) with videos related to
Sort By:
Page
of 12
Translational Behavioral Medicine
|
June 25, 2020
Relationship between genetic knowledge and familial communication of CRC risk and intent to communicate CRCP genetic information: insights from FamilyTalk eMERGE III
Sukh Makhnoon, Deborah J Bowen, Brian H Shirts, et al.
Human Molecular Genetics
|
April 28, 2010
Aging-related atherosclerosis is exacerbated by arterial expression of tumor necrosis factor receptor-1: evidence from mouse models and human association studies
Lisheng Zhang, Jessica J Connelly, Karsten Peppel, et al.
American Journal of Human Genetics
|
June 25, 2011
Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate
Iftikhar J Kullo, Keyue Ding, Khader Shameer, et al.
Circulation. Cardiovascular Genetics
|
February 23, 2010
Association of a peripheral blood metabolic profile with coronary artery disease and risk of subsequent cardiovascular events
Svati H Shah, James R Bain, Michael J Muehlbauer, et al.
Scandinavian Journal of Infectious Diseases
|
July 11, 2008
Clinical outcomes and costs among patients with Staphylococcus aureus bacteremia and orthopedic device infections
Tahaniyat Lalani, Vivian H Chu, Chelsea A Grussemeyer, et al.
American Heart Journal
|
December 22, 2005
The cost of acute myocardial infarction in the new millennium: evidence from a multinational registry
Teresa L Kauf, Eric J Velazquez, David R Crosslin, et al.
Pain
|
March 17, 2021
Genome-wide association studies of low back pain and lumbar spinal disorders using electronic health record data identify a locus associated with lumbar spinal stenosis
Pradeep Suri, Ian B Stanaway, Yanfei Zhang, et al.
Human Molecular Genetics
|
January 22, 2008
Comprehensive genetic analysis of the platelet activating factor acetylhydrolase (PLA2G7) gene and cardiovascular disease in case-control and family datasets
Beth S Sutton, David R Crosslin, Svati H Shah, et al.
Frontiers in Genetics
|
July 3, 2014
eMERGEing progress in genomics-the first seven years
Dana C Crawford, David R Crosslin, Gerard Tromp, et al.
Genes and Immunity
|
November 22, 2018
Unfolding of hidden white blood cell count phenotypes for gene discovery using latent class mixed modeling
Taryn O Hall, Ian B Stanaway, David S Carrell, et al.
Page
of 12