Steven R. DePalma

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 11 papers. Top paper: “GATA6 mutations in hiPSCs inform mechanisms for maldevelopment of the heart, pancreas, and diaphragm”.

GATA6 mutations in hiPSCs inform mechanisms for maldevelopment of the heart, pancreas, and diaphragm

eLife(2020)10.7554/elife.53278

N/A

1.4DataRank · unranked

63 citations

Lauren K. Wasson, Jon A. L. Willcox, Sarah U. Morton, Joshua M. Gorham, Daniel M. DeLaughter +22 more

Rare genetic variation at transcription factor binding sites modulates local DNA methylation profiles

PLoS Genetics(2020)10.1371/journal.pgen.1009189

N/A

0DataRank · unranked

43 citations

Nihir Patel, Felix Richter, Bharati Jadhav, Paras Garg, Sarah U. Morton +16 more

BET bromodomain proteins regulate transcriptional reprogramming in genetic dilated cardiomyopathy

JCI Insight(2020)10.1172/jci.insight.138687

N/A

0DataRank · unranked

37 citations

Hiroko Wakimoto, Zhe Jiao, Joshua M. Gorham, Steven R. DePalma, Madeleine E. Lemieux +10 more

Cardiomyocyte Proliferative Capacity Is Restricted in Mice With Lmna Mutation

Frontiers in Cardiovascular Medicine(2021)10.3389/fcvm.2021.639148

N/A

0DataRank · unranked

15 citations

Hiroko Wakimoto, Jiangming Jiang, Michael Parfenov, Steven R. DePalma, David A. Conner +6 more

Pathogenesis of Cardiomyopathy Caused by Variants in ALPK3 , an Essential Pseudokinase in the Cardiomyocyte Nucleus and Sarcomere

Circulation(2022)10.1161/circulationaha.122.059688

N/A

0DataRank · unranked

50 citations

Hiroko Wakimoto, Joao A. Paulo, Qi Zhang, Daniel Reichart, Christopher N. Toepfer +9 more

Damaging variants in FOXI3 cause microtia and craniofacial microsomia

Genetics in Medicine(2022)10.1016/j.gim.2022.09.005

N/A

0DataRank · unranked

21 citations

Andrew T. Timberlake, Justin J. Curran, Michael L. Cunningham, Barbara McDonough, Maria A. Artunduaga +21 more

Genetic Contribution to End-Stage Cardiomyopathy Requiring Heart Transplantation

Circulation Genomic and Precision Medicine(2023)10.1161/circgen.123.004062

N/A

0DataRank · unranked

13 citations

Oddný Brattberg Gunnarsdóttir, Anissa Viveiros, Daniel Reichart, Daniel Quiat, Jon A. L. Willcox +12 more

Increased endothelial sclerostin caused by elevated DSCAM mediates multiple trisomy 21 phenotypes

Journal of Clinical Investigation(2024)10.1172/jci167811

N/A

0DataRank · unranked

6 citations

Qi Zhang, Priyanka Narayan, Sarah U. Morton, Viktoria Strohmenger, Vi T. Tang +18 more

Noncoding variants and sulcal patterns in congenital heart disease: Machine learning to predict functional impact

iScience(2024)10.1016/j.isci.2024.111707

N/A

0DataRank · unranked

2 citations

Jane W. Newburger, Steven R. DePalma, Martina Brueckner, John D. Cleveland, Wendy K. Chung +16 more

Genomic analyses implicate noncoding de novo variants in congenital heart disease

Nature Genetics(2020)10.1038/s41588-020-0652-z

N/A

0DataRank · unranked

179 citations

Sarah U. Morton, Seong Won Kim, Alexander Kitaygorodsky, Lauren K. Wasson, Kathleen Chen +30 more

Enrichment of tandem repeat element variants near CHD genes identified by short- and long-read genome sequencing

BMC Medical Genomics(2025)10.1186/s12920-025-02191-8

N/A

0DataRank · unranked

2 citations

Sarah U. Morton, Daniel Quiat, Steven R. DePalma, Joshua M. Gorham, Martina Brueckner +5 more