Elizabeth Goldmuntz

Also affiliated with University of Pennsylvania

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

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome

Scientific Reports(2021)10.1038/s41598-021-94021-x

Top 100%

0DataRank

Top 100%0 citations

Aaron M. Holleman, Holly Corbitt, Cheryl L. Maslen, Tracie C. Rosser, David J. Cutler +21 more

Papers

Driven by 33 papers — median percentile 0. 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

Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome

Scientific Reports(2020)10.1038/s41598-020-74650-4

N/A

0.955DataRank · unranked

26 citations

Aaron M. Holleman, Holly Corbitt, Cheryl L. Maslen, Tracie C. Rosser, David J. Cutler +21 more

Genomic analyses implicate noncoding de novo variants in congenital heart disease

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

N/A

0.779DataRank · unranked

179 citations

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

Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations

Nature Communications(2020)10.1038/s41467-019-13624-1

N/A

0.672DataRank · unranked

87 citations

Joseph Glessner, Bradley P. Coe, Jin Li, Maedeh Mohebnasab, Xiao Chang +36 more

Association of genetic and sulcal traits with executive function in congenital heart disease

Annals of Clinical and Translational Neurology(2023)10.1002/acn3.51950

N/A

0.312DataRank · unranked

7 citations

Jane W. Newburger, David Wypij, Nina H. Thomas, Evdokia Anagnoustou, Martina Brueckner +17 more

Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States

Genes(2021)10.3390/genes12071030

N/A

0.250DataRank · unranked

4 citations

Fadi I. Musfee, Laura E. Mitchell, Elizabeth Goldmuntz, Hongbo M. Xie, Håkon Håkonarson +7 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

0.165DataRank · unranked

2 citations

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

Pulmonary Artery Shear Stress and Oscillatory Shear Index are Associated with Right Ventricular Remodeling in Repaired Tetralogy of Fallot

Annals of Biomedical Engineering(2025)10.1007/s10439-025-03793-0

N/A

0.165DataRank · unranked

2 citations

Anindro Bhattacharya, Fengling Hu, Russell T. Shinohara, Paris Perdikaris, Kevin K. Whitehead +4 more

Machine learning to infer neurocognitive testing scores among adolescents and young adults with congenital heart disease

Communications Medicine(2026)10.1038/s43856-026-01417-9

N/A

0.109DataRank · unranked

1 citations

Sheng He, Heather R. Adams, Evdokia Anagnoustou, David C. Bellinger, Martina Brueckner +25 more

Comparison of serum biomarkers of myocardial fibrosis with cardiac magnetic resonance in patients operated for tetralogy of Fallot

International Journal of Cardiology(2022)10.1016/j.ijcard.2022.04.064

N/A

0DataRank · unranked

9 citations

Grace DeCost, Anh Duc, Nkecha Hughes, Elizabeth Goldmuntz, Andrea L. Jones +3 more

Maternal effect genes as risk factors for congenital heart defects

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100098

N/A

0DataRank · unranked

5 citations

Omobola O. Oluwafemi, A. J. Agopian, Håkon Håkonarson, Elizabeth Goldmuntz, Laura E. Mitchell +1 more

Gene-Interaction-Sensitive enrichment analysis in congenital heart disease

BioData Mining(2022)10.1186/s13040-022-00287-w

N/A

0DataRank · unranked

4 citations

Deanne Taylor, Elizabeth Goldmuntz, Laura E. Mitchell, A. J. Agopian, Jason H. Moore +2 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

Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS and sporadic congenital heart disease

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.09.30.507111

N/A

0DataRank · unranked

0 citations

Yujue Wang, Lijie Shi, Donna M. McDonald‐McGinn, T. Blaine Crowley, Daniel E. McGinn +45 more

Prenatal vs postnatal diagnosis of 22q11.2 deletion syndrome: cardiac and noncardiac outcomes through 1 year of age

American Journal of Obstetrics and Gynecology(2023)10.1016/j.ajog.2023.09.005

N/A

0DataRank · unranked

15 citations

Stephanie Galloway, T. Blaine Crowley, Julie S. Moldenhauer, Ann Swillen, Jeroen Breckpot +57 more

Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS

npj Genomic Medicine(2023)10.1038/s41525-023-00363-y

N/A

0DataRank · unranked

12 citations

Yujue Wang, Lijie Shi, Donna M. McDonald‐McGinn, T. Blaine Crowley, Daniel E. McGinn +47 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

Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluation

Prenatal Diagnosis(2024)10.1002/pd.6566

N/A

0DataRank · unranked

7 citations

Anne S. Bassett, Erik Boot, Bruno Marino, Julie S. Moldenhauer, Sólveig Óskarsdóttir +6 more

Identifying novel data-driven subgroups in congenital heart disease using multi-modal measures of brain structure

NeuroImage(2024)10.1016/j.neuroimage.2024.120721

N/A

0DataRank · unranked

4 citations

Ami Norris‐Brilliant, Anum Rahman, Stephania Assimopoulos, Sarah U. Morton, Azadeh Kushki +26 more

Genome sequencing is critical for forecasting outcomes following congenital cardiac surgery

Nature Communications(2025)10.1038/s41467-025-61625-0

N/A

0DataRank · unranked

4 citations

Edgar J. Hernández, Thomas A. Miller, Nathan R. Blue, Raquel M. Zimmerman, Eric R. Griffiths +21 more

Cardiovascular magnetic resonance imaging traits associated with adverse right ventricular remodeling in repaired tetralogy of Fallot: A Single Center Outcomes Using cardiovascular magnetic resonance in Tetralogy of Fallot study

Journal of Cardiovascular Magnetic Resonance(2025)10.1016/j.jocmr.2025.101855

N/A

0DataRank · unranked

2 citations

Ningiun J. Dong, Jin-seo Kim, Abhijit Bhattaru, Phuong Vu, Fengling Hu +15 more

Graph-based prototype inverse-projection for identifying cortical sulcal pattern abnormalities in congenital heart disease

Medical Image Analysis(2025)10.1016/j.media.2025.103538

N/A

0DataRank · unranked

0 citations

Seungyeon Son, Sarah U. Morton, David Wypij, John D. Cleveland, Caitlin K. Rollins +18 more

Machine Learning to Infer Neurocognitive Testing Scores Among Adolescents and Young Adults with Congenital Heart Disease

Research Square(2025)10.21203/rs.3.rs-6787532/v1

N/A

0DataRank · unranked

0 citations

Sheng He, Heather Adams, Evdokia Anagnostou, David C. Bellinger, Martina Brueckner +19 more

Prevalence and spectrum of congenital heart disease in individuals with distal chromosome 22q11.22-23 deletions

medRxiv(2025)10.1101/2025.10.15.25337915

N/A

0DataRank · unranked

0 citations

Daniel E. McGinn, T. Blaine Crowley, Lydia Rockart, Audrey Green, Victoria Giunta +18 more

Prevalence and Spectrum of Congenital Heart Disease in Individuals With Distal Chromosome 22q11.22–23 Deletions

Clinical Genetics(2025)10.1111/cge.70118

N/A

0DataRank · unranked

0 citations

Daniel E. McGinn, T. Blaine Crowley, Lydia Rockart, Audrey Green, Victoria Giunta +18 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

NKX2‐6 related congenital heart disease: Biallelic homeodomain‐disrupting variants and truncus arteriosus

American Journal of Medical Genetics Part A(2020)10.1002/ajmg.a.61550

N/A

0DataRank · unranked

8 citations

Petra Werner, Brande Latney, Bryon L. Krock, Avni Santani, Emma Bedoukian +4 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

Systems Analysis Implicates WAVE2 Complex in the Pathogenesis of Developmental Left-Sided Obstructive Heart Defects

JACC Basic to Translational Science(2020)10.1016/j.jacbts.2020.01.012

N/A

0DataRank · unranked

28 citations

Andrew D. Rouillard, Nicolas Fernandez, Zichen Wang, Alexander Lachmann, Sunita S. Shankaran +21 more

Identifying Risk Factors for Complicated Post-operative Course in Tetralogy of Fallot Using a Machine Learning Approach

Frontiers in Cardiovascular Medicine(2021)10.3389/fcvm.2021.685855

N/A

0DataRank · unranked

17 citations

Jing Huang, Xuemei Zhang, Lihai Song, Grace DeCost, Christopher E. Mascio +7 more

Common Variation in Cytoskeletal Genes Is Associated with Conotruncal Heart Defects

Genes(2021)10.3390/genes12050655

N/A

0DataRank · unranked

3 citations

A. J. Agopian, Elizabeth Goldmuntz, Håkon Håkonarson, Bernice E. Morrow, Deanne Taylor +5 more

Natural history of the aortic root in Tetralogy of Fallot after repair

International Journal of Cardiology Congenital Heart Disease(2021)10.1016/j.ijcchd.2021.100092

N/A

0DataRank · unranked

4 citations

Max T. Geisinger, Tanmay Bhamare, Melissa Wasserman, Jungwon Min, Elizabeth Goldmuntz +1 more

Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome

Scientific Reports(2021)10.1038/s41598-021-94021-x

Top 100%

0DataRank

Top 100%0 citations

Aaron M. Holleman, Holly Corbitt, Cheryl L. Maslen, Tracie C. Rosser, David J. Cutler +21 more

Elizabeth Goldmuntz

Indexed papers

Top data-sharing exemplar

Papers