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Horia Stanescu

Showing results (1-10 of 30) with videos related to

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Pediatric Nephrology (Berlin, Germany)|September 5, 2024
Distal renal tubular acidosis and WDR72: some answers, more questionsDetlef Bockenhauer, Horia Stanescu
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 20, 2011
Filtering the genes and sorting the glomerular filter: a new piece in the puzzle?Robert Kleta, Enriko Klootwijk, Horia Stanescu, et al.
Rare Diseases (Austin, Tex.)|August 9, 2016
EAST syndrome: Clinical, pathophysiological, and genetic aspects of mutations in KCNJ10Ola Abdelhadi, Daniela Iancu, Horia Stanescu, et al.
Bioinformatics (Oxford, England)|December 15, 2012
SwiftLink: parallel MCMC linkage analysis using multicore CPU and GPUAlan Medlar, Dorota Głowacka, Horia Stanescu, et al.
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.
Molecular Genetics & Genomic Medicine|September 22, 2016
Founder mutation in KCNJ10 in Pakistani patients with EAST syndromeOla Abdelhadi, Daniela Iancu, Mehmet Tekman, et al.
Journal of the American Society of Nephrology : JASN|September 11, 2025
Fifty Shades of Risk: Population Studies and the Genetic Architecture of Kidney DiseasesOmid Sadeghi-Alavijeh, Melanie M Y Chan, Horia Stanescu, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|November 19, 2013
Consanguinity in Saudi Arabia: a unique opportunity for pediatric kidney researchJameela A Kari, Detlef Bockenhauer, Horia Stanescu, et al.
BMC Dermatology|July 30, 2009
Description of familial keloids in five pedigrees: evidence for autosomal dominant inheritance and phenotypic heterogeneityJason A Clark, Maria L Turner, Lillian Howard, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Pediatric Nephrology (Berlin, Germany)|September 5, 2024
Distal renal tubular acidosis and WDR72: some answers, more questionsDetlef Bockenhauer, Horia Stanescu
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 20, 2011
Filtering the genes and sorting the glomerular filter: a new piece in the puzzle?Robert Kleta, Enriko Klootwijk, Horia Stanescu, et al.
Rare Diseases (Austin, Tex.)|August 9, 2016
EAST syndrome: Clinical, pathophysiological, and genetic aspects of mutations in KCNJ10Ola Abdelhadi, Daniela Iancu, Horia Stanescu, et al.
Bioinformatics (Oxford, England)|December 15, 2012
SwiftLink: parallel MCMC linkage analysis using multicore CPU and GPUAlan Medlar, Dorota Głowacka, Horia Stanescu, et al.
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.
Molecular Genetics & Genomic Medicine|September 22, 2016
Founder mutation in KCNJ10 in Pakistani patients with EAST syndromeOla Abdelhadi, Daniela Iancu, Mehmet Tekman, et al.
Journal of the American Society of Nephrology : JASN|September 11, 2025
Fifty Shades of Risk: Population Studies and the Genetic Architecture of Kidney DiseasesOmid Sadeghi-Alavijeh, Melanie M Y Chan, Horia Stanescu, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|November 19, 2013
Consanguinity in Saudi Arabia: a unique opportunity for pediatric kidney researchJameela A Kari, Detlef Bockenhauer, Horia Stanescu, et al.
BMC Dermatology|July 30, 2009
Description of familial keloids in five pedigrees: evidence for autosomal dominant inheritance and phenotypic heterogeneityJason A Clark, Maria L Turner, Lillian Howard, et al.
Pageof 3