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Bioinformatics (Oxford, England)
|
September 30, 2017
HaploForge: a comprehensive pedigree drawing and haplotype visualization web application
Mehmet Tekman, Alan Medlar, Monika Mozere, et al.
BMC Bioinformatics
|
February 10, 2018
OVAS: an open-source variant analysis suite with inheritance modelling
Monika Mozere, Mehmet Tekman, Jameela Kari, et al.
Disease Models & Mechanisms
|
March 9, 2013
Generation and validation of a zebrafish model of EAST (epilepsy, ataxia, sensorineural deafness and tubulopathy) syndrome
Fahad Mahmood, Monika Mozere, Anselm A Zdebik, et al.
Kidney International
|
February 17, 2024
A Neanderthal haplotype introgressed into the human genome confers protection against membranous nephropathy
Cătălin D Voinescu, Monika Mozere, Giulio Genovese, et al.
Kidney International Reports
|
October 26, 2020
IgA Nephropathy Genetic Risk Score to Estimate the Prevalence of IgA Nephropathy in UK Biobank
Kittiya Sukcharoen, Seth A Sharp, Nicholas J Thomas, 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.
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.
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.
Journal of the American Society of Nephrology : JASN
|
April 5, 2017
Polycystic Kidney Disease with Hyperinsulinemic Hypoglycemia Caused by a Promoter Mutation in Phosphomannomutase 2
Oscar Rubio Cabezas, Sarah E Flanagan, Horia Stanescu, et al.
Journal of the American Society of Nephrology : JASN
|
February 12, 2022
A Founder Mutation in <i>EHD1</i> Presents with Tubular Proteinuria and Deafness
Naomi Issler, Sara Afonso, Irith Weissman, et al.
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Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Bioinformatics (Oxford, England)
|
September 30, 2017
HaploForge: a comprehensive pedigree drawing and haplotype visualization web application
Mehmet Tekman, Alan Medlar, Monika Mozere, et al.
BMC Bioinformatics
|
February 10, 2018
OVAS: an open-source variant analysis suite with inheritance modelling
Monika Mozere, Mehmet Tekman, Jameela Kari, et al.
Disease Models & Mechanisms
|
March 9, 2013
Generation and validation of a zebrafish model of EAST (epilepsy, ataxia, sensorineural deafness and tubulopathy) syndrome
Fahad Mahmood, Monika Mozere, Anselm A Zdebik, et al.
Kidney International
|
February 17, 2024
A Neanderthal haplotype introgressed into the human genome confers protection against membranous nephropathy
Cătălin D Voinescu, Monika Mozere, Giulio Genovese, et al.
Kidney International Reports
|
October 26, 2020
IgA Nephropathy Genetic Risk Score to Estimate the Prevalence of IgA Nephropathy in UK Biobank
Kittiya Sukcharoen, Seth A Sharp, Nicholas J Thomas, 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.
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.
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.
Journal of the American Society of Nephrology : JASN
|
April 5, 2017
Polycystic Kidney Disease with Hyperinsulinemic Hypoglycemia Caused by a Promoter Mutation in Phosphomannomutase 2
Oscar Rubio Cabezas, Sarah E Flanagan, Horia Stanescu, et al.
Journal of the American Society of Nephrology : JASN
|
February 12, 2022
A Founder Mutation in <i>EHD1</i> Presents with Tubular Proteinuria and Deafness
Naomi Issler, Sara Afonso, Irith Weissman, et al.
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of 2