Search research articles
Contact Us
Filters
Showing results (31-40 of 48) with videos related to
Page
of 5
Sort By:
Digestive Diseases and Sciences
|
September 5, 2018
A New Look at Familial Risk of Inflammatory Bowel Disease in the Ashkenazi Jewish Population
Elena R Schiff, Matthew Frampton, Francesca Semplici, et al.
Inflammatory Bowel Diseases
|
August 30, 2014
Mucosal transcriptomics implicates under expression of BRINP3 in the pathogenesis of ulcerative colitis
Philip J Smith, Adam P Levine, Jenny Dunne, et al.
Kidney International Reports
|
August 7, 2023
Common Risk Variants in <i>AHI1</i> Are Associated With Childhood Steroid Sensitive Nephrotic Syndrome
Mallory L Downie, Sanjana Gupta, Catalin Voinescu, et al.
Pediatric Nephrology (Berlin, Germany)
|
November 10, 2022
Shared genetic risk across different presentations of gene test-negative idiopathic nephrotic syndrome
Mallory L Downie, Sanjana Gupta, Melanie M Y Chan, et al.
NPJ Digital Medicine
|
December 21, 2022
A survey on clinical natural language processing in the United Kingdom from 2007 to 2022
Honghan Wu, Minhong Wang, Jinge Wu, et al.
Nature Communications
|
August 17, 2022
GWAS meta-analysis of intrahepatic cholestasis of pregnancy implicates multiple hepatic genes and regulatory elements
Peter H Dixon, Adam P Levine, Inês Cebola, et al.
Elife
|
September 20, 2022
Diverse ancestry whole-genome sequencing association study identifies <i>TBX5</i> and <i>PTK7</i> as susceptibility genes for posterior urethral valves
Melanie M Y Chan, Omid Sadeghi-Alavijeh, Filipa M Lopes, et al.
Journal of the American Society of Nephrology : JASN
|
January 11, 2020
Large-Scale Whole-Genome Sequencing Reveals the Genetic Architecture of Primary Membranoproliferative GN and C3 Glomerulopathy
Adam P Levine, Melanie M Y Chan, Omid Sadeghi-Alavijeh, et al.
Human Molecular Genetics
|
November 1, 2016
Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance
Steven J Lubbe, Valentina Escott-Price, J Raphael Gibbs, et al.
Journal of the American Society of Nephrology : JASN
|
July 3, 2019
Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome
Stephanie Dufek, Chris Cheshire, Adam P Levine, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 48) with videos related to
Sort By:
Page
of 5
Digestive Diseases and Sciences
|
September 5, 2018
A New Look at Familial Risk of Inflammatory Bowel Disease in the Ashkenazi Jewish Population
Elena R Schiff, Matthew Frampton, Francesca Semplici, et al.
Inflammatory Bowel Diseases
|
August 30, 2014
Mucosal transcriptomics implicates under expression of BRINP3 in the pathogenesis of ulcerative colitis
Philip J Smith, Adam P Levine, Jenny Dunne, et al.
Kidney International Reports
|
August 7, 2023
Common Risk Variants in <i>AHI1</i> Are Associated With Childhood Steroid Sensitive Nephrotic Syndrome
Mallory L Downie, Sanjana Gupta, Catalin Voinescu, et al.
Pediatric Nephrology (Berlin, Germany)
|
November 10, 2022
Shared genetic risk across different presentations of gene test-negative idiopathic nephrotic syndrome
Mallory L Downie, Sanjana Gupta, Melanie M Y Chan, et al.
NPJ Digital Medicine
|
December 21, 2022
A survey on clinical natural language processing in the United Kingdom from 2007 to 2022
Honghan Wu, Minhong Wang, Jinge Wu, et al.
Nature Communications
|
August 17, 2022
GWAS meta-analysis of intrahepatic cholestasis of pregnancy implicates multiple hepatic genes and regulatory elements
Peter H Dixon, Adam P Levine, Inês Cebola, et al.
Elife
|
September 20, 2022
Diverse ancestry whole-genome sequencing association study identifies <i>TBX5</i> and <i>PTK7</i> as susceptibility genes for posterior urethral valves
Melanie M Y Chan, Omid Sadeghi-Alavijeh, Filipa M Lopes, et al.
Journal of the American Society of Nephrology : JASN
|
January 11, 2020
Large-Scale Whole-Genome Sequencing Reveals the Genetic Architecture of Primary Membranoproliferative GN and C3 Glomerulopathy
Adam P Levine, Melanie M Y Chan, Omid Sadeghi-Alavijeh, et al.
Human Molecular Genetics
|
November 1, 2016
Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance
Steven J Lubbe, Valentina Escott-Price, J Raphael Gibbs, et al.
Journal of the American Society of Nephrology : JASN
|
July 3, 2019
Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome
Stephanie Dufek, Chris Cheshire, Adam P Levine, et al.
Page
of 5