Thomas Hays

Columbia University Irving Medical Center

Environmental ScienceSocial SciencesBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 9 papers. Top paper: “Genetic testing for kidney disease of unknown etiology”.

Genetic testing for kidney disease of unknown etiology

Kidney International(2020)10.1016/j.kint.2020.03.031

N/A

0DataRank · unranked

74 citations

Emily Groopman, Ali G. Gharavi, Thomas Hays

Genetic testing for unexplained perinatal disorders

Current Opinion in Pediatrics(2021)10.1097/mop.0000000000000999

N/A

0DataRank · unranked

26 citations

Ronald J. Wapner, Thomas Hays

Learning the Language of Medical Device Innovation: A Longitudinal Interdisciplinary Elective for Medical Students

Academic Medicine(2022)10.1097/acm.0000000000004723

N/A

0DataRank · unranked

13 citations

Mathew Hakimi, Thomas Hays, Joseph Adachi, Annie Chau, Brecken Esper +10 more

Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis

Journal of the American Society of Nephrology(2023)10.1681/asn.0000000000000132

N/A

0DataRank · unranked

15 citations

Tze Yin Lim, Juntao Ke, Gina Jin, Miguel Verbitsky, Monica Bodria +77 more

The utility of gene sequencing in identifying an underlying genetic disorder in prenatally suspected lower urinary tract obstruction

Prenatal Diagnosis(2023)10.1002/pd.6425

N/A

0DataRank · unranked

8 citations

Karin J. Blakemore, Christine Hertenstein, Jena L. Miller, Kristen A. Miller, Hanan E. Shamseldin +11 more

The Contribution of Commonly Diagnosed Genetic Disorders to Small for Gestational Age Birth and Subsequent Morbidity and Mortality in Preterm Infants

medRxiv(2023)10.1101/2023.07.14.23292682

N/A

0DataRank · unranked

0 citations

Selin Everett, Alex Lyford, Rakesh Sahni, Faith Kim, Caitlin Baptiste +5 more

A Deep Intronic PKHD1 Variant Identified by SpliceAI in a Deceased Neonate With Autosomal Recessive Polycystic Kidney Disease

American Journal of Kidney Diseases(2024)10.1053/j.ajkd.2023.12.011

N/A

0DataRank · unranked

12 citations

Kayleigh D. Rutherford, Anisha J. Cooke, Malorie Meshkati, Vanessa Eddy-Abrams, Daniel Greene +20 more

The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart disease

Prenatal Diagnosis(2024)10.1002/pd.6527

N/A

0DataRank · unranked

10 citations

Miles Bomback, Atlas Khan, Sarath Krishna Murthy, David E. Solowiejczyk, Neeta L. Vora +9 more

Exome analysis links kidney malformations to developmental disorders and reveals causal genes

Nature Communications(2025)10.1038/s41467-025-62319-3

N/A

0DataRank · unranked

9 citations

Sarath Babu Krishna Murthy, Natalie Vena, Gundula Povysil, Andrew Beenken, Miguel Verbitsky +95 more