Search research articles
Contact Us
Filters
Showing results (41-50 of 103) with videos related to
Page
of 11
Sort By:
Inflammatory Bowel Diseases
|
April 3, 2004
A genome scan in 260 inflammatory bowel disease-affected relative pairs
M Michael Barmada, Steven R Brant, Dan L Nicolae, et al.
Inflammatory Bowel Diseases
|
October 9, 2004
A genome scan in 260 inflammatory bowel disease-affected relative pairs
M Michael Barmada, Steven R Brant, Dan L Nicolae, et al.
American Journal of Respiratory and Critical Care Medicine
|
October 17, 2015
Genome-Wide Methylation Study Identifies an IL-13-induced Epigenetic Signature in Asthmatic Airways
Jessie Nicodemus-Johnson, Katherine A Naughton, Jyotsna Sudi, et al.
American Journal of Human Genetics
|
April 5, 2016
Imputing Gene Expression in Uncollected Tissues Within and Beyond GTEx
Jiebiao Wang, Eric R Gamazon, Brandon L Pierce, et al.
Investigative Ophthalmology & Visual Science
|
March 20, 2012
Replication analysis for severe diabetic retinopathy
Michael A Grassi, Anna Tikhomirov, Sudha Ramalingam, et al.
Allergy
|
August 12, 2023
Epigenetic responses to rhinovirus exposure in airway epithelial cells are correlated with key transcriptional pathways in chronic rhinosinusitis
Marcus M Soliai, Atsushi Kato, Katherine A Naughton, et al.
The New England Journal of Medicine
|
March 29, 2013
Rhinovirus wheezing illness and genetic risk of childhood-onset asthma
Minal Calışkan, Yury A Bochkov, Eskil Kreiner-Møller, et al.
Gastroenterology
|
January 4, 2003
Crohn's disease-associated NOD2 variants share a signaling defect in response to lipopolysaccharide and peptidoglycan
Denise K Bonen, Yasunori Ogura, Dan L Nicolae, et al.
Nature Genetics
|
August 11, 2015
A gene-based association method for mapping traits using reference transcriptome data
Eric R Gamazon, Heather E Wheeler, Kaanan P Shah, et al.
Human Molecular Genetics
|
January 8, 2011
Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13
Minal Çalışkan, Jessica X Chong, Lawrence Uricchio, et al.
Page
of 11
Search research articles
Search
Showing results (41-50 of 103) with videos related to
Sort By:
Page
of 11
Inflammatory Bowel Diseases
|
April 3, 2004
A genome scan in 260 inflammatory bowel disease-affected relative pairs
M Michael Barmada, Steven R Brant, Dan L Nicolae, et al.
Inflammatory Bowel Diseases
|
October 9, 2004
A genome scan in 260 inflammatory bowel disease-affected relative pairs
M Michael Barmada, Steven R Brant, Dan L Nicolae, et al.
American Journal of Respiratory and Critical Care Medicine
|
October 17, 2015
Genome-Wide Methylation Study Identifies an IL-13-induced Epigenetic Signature in Asthmatic Airways
Jessie Nicodemus-Johnson, Katherine A Naughton, Jyotsna Sudi, et al.
American Journal of Human Genetics
|
April 5, 2016
Imputing Gene Expression in Uncollected Tissues Within and Beyond GTEx
Jiebiao Wang, Eric R Gamazon, Brandon L Pierce, et al.
Investigative Ophthalmology & Visual Science
|
March 20, 2012
Replication analysis for severe diabetic retinopathy
Michael A Grassi, Anna Tikhomirov, Sudha Ramalingam, et al.
Allergy
|
August 12, 2023
Epigenetic responses to rhinovirus exposure in airway epithelial cells are correlated with key transcriptional pathways in chronic rhinosinusitis
Marcus M Soliai, Atsushi Kato, Katherine A Naughton, et al.
The New England Journal of Medicine
|
March 29, 2013
Rhinovirus wheezing illness and genetic risk of childhood-onset asthma
Minal Calışkan, Yury A Bochkov, Eskil Kreiner-Møller, et al.
Gastroenterology
|
January 4, 2003
Crohn's disease-associated NOD2 variants share a signaling defect in response to lipopolysaccharide and peptidoglycan
Denise K Bonen, Yasunori Ogura, Dan L Nicolae, et al.
Nature Genetics
|
August 11, 2015
A gene-based association method for mapping traits using reference transcriptome data
Eric R Gamazon, Heather E Wheeler, Kaanan P Shah, et al.
Human Molecular Genetics
|
January 8, 2011
Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13
Minal Çalışkan, Jessica X Chong, Lawrence Uricchio, et al.
Page
of 11