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Miguel Verbitsky

Showing results (11-20 of 49) with videos related to

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Experimental Dermatology|June 7, 2019
Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagyLynn Petukhova, Aakash V Patel, Rachel K Rigo, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 18, 2005
Gene expression differences in mice divergently selected for methamphetamine sensitivityAbraham A Palmer, Miguel Verbitsky, Rathi Suresh, et al.
Journal of the American Society of Nephrology : JASN|March 11, 2025
Family History in the Context of CKDFrancesca Zanoni, Maddalena Marasa, Lucrezia Carlassara, et al.
The Journal of Clinical Investigation|April 21, 2015
Genomic imbalances in pediatric patients with chronic kidney diseaseMiguel Verbitsky, Simone Sanna-Cherchi, David A Fasel, et al.
Medrxiv : the Preprint Server for Health Sciences|March 4, 2025
Interstitial Cystitis: a phenotype and rare variant exome sequencing study: Interstitial Cystitis: a phenotype and exome sequencing studyJoshua E Motelow, Ayan Malakar, Sarath Babu Krishna Murthy, et al.
BMC Medical Genetics|August 5, 2011
Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish populationXinmin Liu, Rong Cheng, Miguel Verbitsky, et al.
Archives of Neurology|May 13, 2009
Association of glucocerebrosidase mutations with dementia with lewy bodiesLorraine N Clark, Lykourgos A Kartsaklis, Rebecca Wolf Gilbert, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 15, 2010
Polyamine pathway contributes to the pathogenesis of Parkinson diseaseNicole M Lewandowski, Shulin Ju, Miguel Verbitsky, et al.
Kidney International|September 10, 2015
Copy number variation analysis identifies novel CAKUT candidate genes in children with a solitary functioning kidneyRik Westland, Miguel Verbitsky, Katarina Vukojevic, et al.
Ebiomedicine|February 19, 2026
Interstitial cystitis: a phenotype and rare variant exome sequencing studyJoshua E Motelow, Ayan Malakar, Sarath Babu Krishna Murthy, et al.
Pageof 5

Showing results (11-20 of 49) with videos related to

Sort By:
Pageof 5
Experimental Dermatology|June 7, 2019
Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagyLynn Petukhova, Aakash V Patel, Rachel K Rigo, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 18, 2005
Gene expression differences in mice divergently selected for methamphetamine sensitivityAbraham A Palmer, Miguel Verbitsky, Rathi Suresh, et al.
Journal of the American Society of Nephrology : JASN|March 11, 2025
Family History in the Context of CKDFrancesca Zanoni, Maddalena Marasa, Lucrezia Carlassara, et al.
The Journal of Clinical Investigation|April 21, 2015
Genomic imbalances in pediatric patients with chronic kidney diseaseMiguel Verbitsky, Simone Sanna-Cherchi, David A Fasel, et al.
Medrxiv : the Preprint Server for Health Sciences|March 4, 2025
Interstitial Cystitis: a phenotype and rare variant exome sequencing study: Interstitial Cystitis: a phenotype and exome sequencing studyJoshua E Motelow, Ayan Malakar, Sarath Babu Krishna Murthy, et al.
BMC Medical Genetics|August 5, 2011
Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish populationXinmin Liu, Rong Cheng, Miguel Verbitsky, et al.
Archives of Neurology|May 13, 2009
Association of glucocerebrosidase mutations with dementia with lewy bodiesLorraine N Clark, Lykourgos A Kartsaklis, Rebecca Wolf Gilbert, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 15, 2010
Polyamine pathway contributes to the pathogenesis of Parkinson diseaseNicole M Lewandowski, Shulin Ju, Miguel Verbitsky, et al.
Kidney International|September 10, 2015
Copy number variation analysis identifies novel CAKUT candidate genes in children with a solitary functioning kidneyRik Westland, Miguel Verbitsky, Katarina Vukojevic, et al.
Ebiomedicine|February 19, 2026
Interstitial cystitis: a phenotype and rare variant exome sequencing studyJoshua E Motelow, Ayan Malakar, Sarath Babu Krishna Murthy, et al.
Pageof 5