Miguel Verbitsky

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2004-2009 Department of Genetics Columbia University Medical Center, New York University School of Medicine 
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"Miguel Verbitsky"
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Zanoni F, Verbitsky M, Carlassara L, et al. (2020) P0355Family History Of Complex Traits In The Curegn Cohort: Associations With Renal Function, Comorbidity Burden And Disease Progression Nephrology Dialysis Transplantation. 35
Petukhova L, Patel AV, Rigo RK, et al. (2019) Integrative analysis of rare copy number variants and gene expression data in Alopecia Areata implicates an etiological role for autophagy. Experimental Dermatology
Lata S, Marasa M, Li Y, et al. (2017) Whole-Exome Sequencing in Adults With Chronic Kidney Disease: A Pilot Study. Annals of Internal Medicine
Sanna-Cherchi S, Khan K, Westland R, et al. (2017) Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations. American Journal of Human Genetics. 101: 789-802
Petukhova L, Patel A, Severin R, et al. (2017) 522 Integrative analysis of gene expression data and rare copy number variants in alopecia areata Journal of Investigative Dermatology. 137: S90
Westland R, Verbitsky M, Vukojevic K, et al. (2015) Copy number variation analysis identifies novel CAKUT candidate genes in children with a solitary functioning kidney. Kidney International
Vivante A, Kleppa MJ, Schulz J, et al. (2015) Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development. American Journal of Human Genetics
Verbitsky M, Sanna-Cherchi S, Fasel DA, et al. (2015) Genomic imbalances in pediatric patients with chronic kidney disease. The Journal of Clinical Investigation. 125: 2171-8
Kiryluk K, Li Y, Scolari F, et al. (2014) Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens. Nature Genetics. 46: 1187-96
Hoshino J, Suwabe T, Sumida K, et al. (2014) Cystic Disease And Ciliopathies Nephrology Dialysis Transplantation. 29
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