Teresa M. Lee

Columbia University Irving Medical Center

Also affiliated with Columbia University

MedicineBiochemistry, 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 10 papers. Top paper: “The genetic architecture of pediatric cardiomyopathy”.

The genetic architecture of pediatric cardiomyopathy

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2021.12.006

N/A

0.624DataRank · unranked

63 citations

Surbhi Bhatnagar, Phillip J. Dexheimer, James D. Wilkinson, Arthi Sridhar, Xiao Fan +23 more

Cardiac imaging and biomarkers for assessing myocardial fibrosis in children with hypertrophic cardiomyopathy

American Heart Journal(2023)10.1016/j.ahj.2023.06.005

N/A

0.462DataRank · unranked

10 citations

Pamela K. Woodard, Ling Shi, Taye H. Hamza, Charles E. Canter, Steven D. Colan +23 more

Sigma non-opioid receptor 1 is a potential therapeutic target for long QT syndrome

Nature Cardiovascular Research(2022)10.1038/s44161-021-00016-2

N/A

0DataRank · unranked

14 citations

Ramsey Bekdash, Kumi Morikawa, Jose R. Quejada, Alison D. Klein, Danielle Aina-Badejo +14 more

Genetic, demographic and clinical variables act synergistically to impact neurodevelopmental outcomes in children with single ventricle heart disease

medRxiv(2022)10.1101/2022.10.01.22280594

N/A

0DataRank · unranked

1 citations

Edgar J. Hernández, J. William Gaynor, Mark W. Russell, Jane W. Newburger, Wendy K. Chung +18 more

Genetic and clinical variables act synergistically to impact neurodevelopmental outcomes in children with single ventricle heart disease

Communications Medicine(2023)10.1038/s43856-023-00361-2

N/A

0DataRank · unranked

8 citations

Edgar J. Hernández, J. William Gaynor, Mark W. Russell, Jane W. Newburger, Wendy K. Chung +18 more

Genetic Testing Resources and Practice Patterns Among Pediatric Cardiomyopathy Programs

Pediatric Cardiology(2024)10.1007/s00246-024-03498-6

N/A

0DataRank · unranked

1 citations

Emily H. Kim, Melanie D. Everitt, Wendy K. Chung, Irene D. Lytrivi, Sonya Kirmani +9 more

Biallelic potential disease-causing missense variants in TAF1A in two siblings with infantile restrictive cardiomyopathy

European Journal of Medical Genetics(2024)10.1016/j.ejmg.2024.104968

N/A

0DataRank · unranked

1 citations

Wenyuan Xu, Aliaa H. Abdelhakim, Anastasiya Matveyenko, Matthias Szabolcs, William C. Copeland +6 more

Variants in ADRB1 and CYP2C9: Association with Response to Atenolol and Losartan in Marfan Syndrome

The Journal of Pediatrics(2020)10.1016/j.jpeds.2020.03.064

N/A

0DataRank · unranked

17 citations

Lynn A. Sleeper, Bruce D. Gelb, Shaine A. Morris, Harry C. Dietz, Geoffrey A. Forbus +19 more

Genomics of pediatric cardiomyopathy

Pediatric Research(2025)10.1038/s41390-025-03819-2

N/A

0DataRank · unranked

11 citations

Stephanie M. Ware, Alicia M. Kamsheh, Surbhi Bhatnagar, Mohammed Absi, Elyse Miller +5 more

Bi-allelic missense disease-causing variants in RPL3L associate neonatal dilated cardiomyopathy with muscle-specific ribosome biogenesis

Human Genetics(2020)10.1007/s00439-020-02188-6

N/A

0DataRank · unranked

32 citations

Loukas Argyriou, Francisco Martínez‐Azorín, Susanne Morlot, Gökhan Yiğit, Teresa M. Lee +19 more