David Goldstein

16PUBLICATIONS
137CO-AUTHORS
NeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Respiratory diseasesEpidemiological methods
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Publications (16)

|Aug 07, 2025
Exome analysis links kidney malformations to developmental disorders and reveals causal genes.

Hila Milo Rasouly, Sarath Babu Krishna Murthy, Natalie Vena

|Feb 19, 2025
Assessing the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases.

Jonathan Mitchell, Niedzica Camacho, Patrick Shea

|Nov 30, 2023
Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease.

Yask Gupta, David J Friedman, Michelle T McNulty

|Aug 02, 2023
Africa-specific human genetic variation near CHD1L associates with HIV-1 load.

Paul J McLaren, Immacolata Porreca, Gennaro Iaconis

|Aug 26, 2022
Utility of whole genome sequencing in assessing risk and clinically relevant outcomes for pulmonary fibrosis.

David Zhang, Chad A Newton, Binhan Wang

|Jun 29, 2021
Exome sequencing in obsessive-compulsive disorder reveals a burden of rare damaging coding variants.

Mathew Halvorsen, Jack Samuels, Ying Wang

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Frequent Collaborators

4 joint publications

Ali G Gharavi

3 joint publications

Slavé Petrovski

3 joint publications

Antonio Amoroso

3 joint publications

Pietro Canetta