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Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
October 27, 2009
[Genetics in chronic obstructive pulmonary disease]
Inga-Cecilie Sørheim, Amund Gulsvik, Per Sigvald Bakke, et al.
BMC Medical Genetics
|
January 1, 2009
Folliculin mutations are not associated with severe COPD
Michael H Cho, Barbara J Klanderman, Augusto A Litonjua, et al.
The Journal of Allergy and Clinical Immunology
|
February 8, 2006
Eotaxin polymorphisms and serum total IgE levels in children with asthma
Benjamin A Raby, Kristel Van Steen, Ross Lazarus, et al.
Genetic Epidemiology
|
June 18, 2016
Family-Based Rare Variant Association Analysis: A Fast and Efficient Method of Multivariate Phenotype Association Analysis
Longfei Wang, Sungyoung Lee, Jungsoo Gim, et al.
American Journal of Respiratory and Critical Care Medicine
|
November 30, 2023
Reply to Neder, to Ogata <i>et al.</i>, and to Graham
Surya P Bhatt, Arie Nakhmani, Spyridon Fortis, et al.
Respiratory Research
|
November 8, 2011
COPD association and repeatability of blood biomarkers in the ECLIPSE cohort
Jennifer A Dickens, Bruce E Miller, Lisa D Edwards, et al.
BMC Systems Biology
|
November 29, 2014
Sexually-dimorphic targeting of functionally-related genes in COPD
Kimberly Glass, John Quackenbush, Edwin K Silverman, et al.
Respiratory Research
|
October 31, 2018
Childhood asthma is associated with COPD and known asthma variants in COPDGene: a genome-wide association study
Lystra P Hayden, Michael H Cho, Benjamin A Raby, et al.
Plos Medicine
|
August 13, 2024
Identification of factors directly linked to incident chronic obstructive pulmonary disease: A causal graph modeling study
Robert W Gregg, Chad M Karoleski, Edwin K Silverman, et al.
American Journal of Respiratory and Critical Care Medicine
|
June 20, 2023
FEV<sub>1</sub>/FVC Severity Stages for Chronic Obstructive Pulmonary Disease
Surya P Bhatt, Arie Nakhmani, Spyridon Fortis, et al.
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of 64
Search research articles
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Showing results (61-70 of 636) with videos related to
Sort By:
Page
of 64
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
October 27, 2009
[Genetics in chronic obstructive pulmonary disease]
Inga-Cecilie Sørheim, Amund Gulsvik, Per Sigvald Bakke, et al.
BMC Medical Genetics
|
January 1, 2009
Folliculin mutations are not associated with severe COPD
Michael H Cho, Barbara J Klanderman, Augusto A Litonjua, et al.
The Journal of Allergy and Clinical Immunology
|
February 8, 2006
Eotaxin polymorphisms and serum total IgE levels in children with asthma
Benjamin A Raby, Kristel Van Steen, Ross Lazarus, et al.
Genetic Epidemiology
|
June 18, 2016
Family-Based Rare Variant Association Analysis: A Fast and Efficient Method of Multivariate Phenotype Association Analysis
Longfei Wang, Sungyoung Lee, Jungsoo Gim, et al.
American Journal of Respiratory and Critical Care Medicine
|
November 30, 2023
Reply to Neder, to Ogata <i>et al.</i>, and to Graham
Surya P Bhatt, Arie Nakhmani, Spyridon Fortis, et al.
Respiratory Research
|
November 8, 2011
COPD association and repeatability of blood biomarkers in the ECLIPSE cohort
Jennifer A Dickens, Bruce E Miller, Lisa D Edwards, et al.
BMC Systems Biology
|
November 29, 2014
Sexually-dimorphic targeting of functionally-related genes in COPD
Kimberly Glass, John Quackenbush, Edwin K Silverman, et al.
Respiratory Research
|
October 31, 2018
Childhood asthma is associated with COPD and known asthma variants in COPDGene: a genome-wide association study
Lystra P Hayden, Michael H Cho, Benjamin A Raby, et al.
Plos Medicine
|
August 13, 2024
Identification of factors directly linked to incident chronic obstructive pulmonary disease: A causal graph modeling study
Robert W Gregg, Chad M Karoleski, Edwin K Silverman, et al.
American Journal of Respiratory and Critical Care Medicine
|
June 20, 2023
FEV<sub>1</sub>/FVC Severity Stages for Chronic Obstructive Pulmonary Disease
Surya P Bhatt, Arie Nakhmani, Spyridon Fortis, et al.
Page
of 64