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Cell Genomics
|
April 5, 2025
Integration of biobank-scale genetics and plasma proteomics reveals evidence for causal processes in asthma risk and heterogeneity
Lauren J Donoghue, Christian Benner, Diana Chang, et al.
Plos One
|
April 20, 2023
Rare CIDEC coding variants enriched in age-related macular degeneration patients with small low-luminance deficit cause lipid droplet and fat storage defects
Sehyun Kim, Amy Stockwell, Han Qin, et al.
Bioinformatics (Oxford, England)
|
May 7, 2016
Pathway analysis by randomization incorporating structure-PARIS: an update
Mariusz Butkiewicz, Jessica N Cooke Bailey, Alex Frase, et al.
Human Genetics
|
February 1, 2011
Genetic analysis of biological pathway data through genomic randomization
Brian L Yaspan, William S Bush, Eric S Torstenson, et al.
Scientific Reports
|
February 14, 2024
Apolipoprotein L1 (APOL1) renal risk variant-mediated podocyte cytotoxicity depends on African haplotype and surface expression
Nidhi Gupta, Bridget Waas, Daniel Austin, et al.
Molecular Autism
|
August 20, 2013
Rare coding variants of the adenosine A3 receptor are increased in autism: on the trail of the serotonin transporter regulome
Nicholas G Campbell, Chong-Bin Zhu, Kathryn M Lindler, et al.
Thorax
|
June 10, 2022
Genome-wide association study across five cohorts identifies five novel loci associated with idiopathic pulmonary fibrosis
Richard J Allen, Amy Stockwell, Justin M Oldham, et al.
American Journal of Respiratory and Critical Care Medicine
|
January 5, 2023
Identification of a Genetic Susceptibility Locus for Idiopathic Pulmonary Fibrosis in the 16p Subtelomere Using Whole-Genome Sequencing
Lauren J Donoghue, Amy D Stockwell, Margaret Neighbors, et al.
European Journal of Human Genetics : EJHG
|
April 28, 2011
Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders
Richard J L Anney, Elaine M Kenny, Colm O'Dushlaine, et al.
Cancer Research
|
June 19, 2007
Haplotype analysis of CYP11A1 identifies promoter variants associated with breast cancer risk
Brian L Yaspan, Joan P Breyer, Qiuyin Cai, et al.
Page
of 7
Search research articles
Search
Showing results (11-20 of 68) with videos related to
Sort By:
Page
of 7
Cell Genomics
|
April 5, 2025
Integration of biobank-scale genetics and plasma proteomics reveals evidence for causal processes in asthma risk and heterogeneity
Lauren J Donoghue, Christian Benner, Diana Chang, et al.
Plos One
|
April 20, 2023
Rare CIDEC coding variants enriched in age-related macular degeneration patients with small low-luminance deficit cause lipid droplet and fat storage defects
Sehyun Kim, Amy Stockwell, Han Qin, et al.
Bioinformatics (Oxford, England)
|
May 7, 2016
Pathway analysis by randomization incorporating structure-PARIS: an update
Mariusz Butkiewicz, Jessica N Cooke Bailey, Alex Frase, et al.
Human Genetics
|
February 1, 2011
Genetic analysis of biological pathway data through genomic randomization
Brian L Yaspan, William S Bush, Eric S Torstenson, et al.
Scientific Reports
|
February 14, 2024
Apolipoprotein L1 (APOL1) renal risk variant-mediated podocyte cytotoxicity depends on African haplotype and surface expression
Nidhi Gupta, Bridget Waas, Daniel Austin, et al.
Molecular Autism
|
August 20, 2013
Rare coding variants of the adenosine A3 receptor are increased in autism: on the trail of the serotonin transporter regulome
Nicholas G Campbell, Chong-Bin Zhu, Kathryn M Lindler, et al.
Thorax
|
June 10, 2022
Genome-wide association study across five cohorts identifies five novel loci associated with idiopathic pulmonary fibrosis
Richard J Allen, Amy Stockwell, Justin M Oldham, et al.
American Journal of Respiratory and Critical Care Medicine
|
January 5, 2023
Identification of a Genetic Susceptibility Locus for Idiopathic Pulmonary Fibrosis in the 16p Subtelomere Using Whole-Genome Sequencing
Lauren J Donoghue, Amy D Stockwell, Margaret Neighbors, et al.
European Journal of Human Genetics : EJHG
|
April 28, 2011
Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders
Richard J L Anney, Elaine M Kenny, Colm O'Dushlaine, et al.
Cancer Research
|
June 19, 2007
Haplotype analysis of CYP11A1 identifies promoter variants associated with breast cancer risk
Brian L Yaspan, Joan P Breyer, Qiuyin Cai, et al.
Page
of 7