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David Fasel

5PUBLICATIONS

34CO-AUTHORS

Disease surveillanceNeurogeneticsGene expression (incl. microarray and other genome-wide approaches)Cardiovascular medicine and haematology not elsewhere classifiedCancer genetics

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Publications (5)

Sort by Publication Date:

|Apr 14, 2021

Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studies.

Ning Shang, Atlas Khan, Fernanda Polubriaginof

|Feb 18, 2021

Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux.

Miguel Verbitsky, Priya Krithivasan, Ekaterina Batourina

|Dec 28, 2020

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

|Mar 01, 2019

Author Correction: The copy number variation landscape of congenital anomalies of the kidney and urinary tract.

Miguel Verbitsky, Rik Westland, Alejandra Perez

|Dec 23, 2018

The copy number variation landscape of congenital anomalies of the kidney and urinary tract.

Miguel Verbitsky, Rik Westland, Alejandra Perez

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Frequent Collaborators

4 joint publications

Maddalena Marasà

2 joint publications

Miguel Verbitsky

2 joint publications

Matthew G Sampson

2 joint publications

Erin L Heinzen

2 joint publications

Maddalena Gigante

2 joint publications

David E Barton

2 joint publications

Nan Wu

2 joint publications

Friedhelm Hildebrandt

2 joint publications

Virginia E Papaioannou

2 joint publications

Cathy L Mendelsohn

Frequent Collaborators

4 joint publications

Maddalena Marasà

2 joint publications

Miguel Verbitsky

2 joint publications

Matthew G Sampson

2 joint publications

Erin L Heinzen

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