Publications by authors named "David A Fasel"

Claim this Profile
G
GeneLiFT: A novel test to facilitate rapid screening of genetic literacy in a diverse population undergoing genetic testing.
Hila Milo Rasouly, Nicole Cuneo, Maddalena Marasa, Natalia DeMaria, Debanjana Chatterjee, David A Fasel

J Genet Couns· June 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux.
Miguel Verbitsky, Priya Krithivasan, Ekaterina Batourina, Atlas Khan, Sarah E Graham, David A Fasel

J Am Soc Nephrol· April 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Author Correction: The copy number variation landscape of congenital anomalies of the kidney and urinary tract.
Miguel Verbitsky, Rik Westland, Alejandra Perez, Krzysztof Kiryluk, Qingxue Liu, David A Fasel

Nat Genet· April 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The Burden of Candidate Pathogenic Variants for Kidney and Genitourinary Disorders Emerging From Exome Sequencing.
Hila Milo Rasouly, Emily E Groopman, Reuben Heyman-Kantor, David A Fasel, Adele Mitrotti

Ann Intern Med· January 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The copy number variation landscape of congenital anomalies of the kidney and urinary tract.
Miguel Verbitsky, Rik Westland, Alejandra Perez, Krzysztof Kiryluk, Qingxue Liu, David A Fasel

Nat Genet· January 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Diagnostic Utility of Exome Sequencing for Kidney Disease.
Emily E Groopman, Maddalena Marasa, Sophia Cameron-Christie, Slavé Petrovski, Vimla S Aggarwal, David A Fasel

N Engl J Med· January 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
W
Whole-Exome Sequencing in Adults With Chronic Kidney Disease: A Pilot Study.
Sneh Lata, Maddalena Marasa, Yifu Li, David A Fasel, Emily Groopman

Ann Intern Med· January 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.
Simone Sanna-Cherchi, Kamal Khan, Rik Westland, Priya Krithivasan, Lorraine Fievet, David A Fasel

Am J Hum Genet· December 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.
Simone Sanna-Cherchi, Kamal Khan, Rik Westland, Priya Krithivasan, Lorraine Fievet, David A Fasel

Am J Hum Genet· November 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genetic Drivers of Kidney Defects in the DiGeorge Syndrome.
Esther Lopez-Rivera, Yangfan P Liu, Miguel Verbitsky, Blair R Anderson, Valentina P Capone, David A Fasel

N Engl J Med· February 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Copy number variation analysis identifies novel CAKUT candidate genes in children with a solitary functioning kidney.
Rik Westland, Miguel Verbitsky, Katarina Vukojevic, Brittany J Perry, David A Fasel

Kidney Int· December 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genomic imbalances in pediatric patients with chronic kidney disease.
Miguel Verbitsky, Simone Sanna-Cherchi, David A Fasel, Brynn Levy, Krzysztof Kiryluk

J Clin Invest· May 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis