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Monika Mozere

Showing results (1-10 of 12) with videos related to

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Bioinformatics (Oxford, England)|September 30, 2017
HaploForge: a comprehensive pedigree drawing and haplotype visualization web applicationMehmet Tekman, Alan Medlar, Monika Mozere, et al.
BMC Bioinformatics|February 10, 2018
OVAS: an open-source variant analysis suite with inheritance modellingMonika 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) syndromeFahad 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 nephropathyCătălin 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 BiobankKittiya 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 elementsPeter 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 GlomerulopathyAdam 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 SyndromeStephanie 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 2Oscar 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 DeafnessNaomi Issler, Sara Afonso, Irith Weissman, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Bioinformatics (Oxford, England)|September 30, 2017
HaploForge: a comprehensive pedigree drawing and haplotype visualization web applicationMehmet Tekman, Alan Medlar, Monika Mozere, et al.
BMC Bioinformatics|February 10, 2018
OVAS: an open-source variant analysis suite with inheritance modellingMonika 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) syndromeFahad 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 nephropathyCătălin 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 BiobankKittiya 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 elementsPeter 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 GlomerulopathyAdam 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 SyndromeStephanie 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 2Oscar 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 DeafnessNaomi Issler, Sara Afonso, Irith Weissman, et al.
Pageof 2