Megan J. Puckelwartz

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 3%percentile

1.7Author 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.

Pathogenic and Uncertain Genetic Variants Have Clinical Cardiac Correlates in Diverse Biobank Participants

Journal of the American Heart Association(2020)10.1161/jaha.119.013808

Top 12%

1.7DataRank

Top 12%41 citations

Megan J. Puckelwartz, Lorenzo L. Pesce, Avery Robinson, Samuel Kearns, Jennifer A. Pacheco +5 more

Papers

Driven by 22 papers — median percentile 88. Top paper: “Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations”.

Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations

Nature Medicine(2024)10.1038/s41591-024-02796-z

N/A

4.8DataRank · unranked

196 citations

Leah C. Kottyan, Christopher Kachulis, Noura S. Abul‐Husn, Joshua Arias, Gillian M. Belbin +73 more

Returning integrated genomic risk and clinical recommendations: The eMERGE study

Genetics in Medicine(2023)10.1016/j.gim.2023.100006

N/A

2.6DataRank · unranked

121 citations

Aimee Allworth, Harris T. Bland, Pedro J. Caraballo, Rex L. Chisholm, Ellen Wright Clayton +95 more

Pathogenic and Uncertain Genetic Variants Have Clinical Cardiac Correlates in Diverse Biobank Participants

Journal of the American Heart Association(2020)10.1161/jaha.119.013808

Top 12%

1.7DataRank

Top 12%41 citations

Megan J. Puckelwartz, Lorenzo L. Pesce, Avery Robinson, Samuel Kearns, Jennifer A. Pacheco +5 more

Risk factors affecting polygenic score performance across diverse cohorts

eLife(2023)10.7554/elife.88149

N/A

0.312DataRank · unranked

7 citations

Scott Dudek, Krzysztof Kiryluk, Theresa L. Walunas, Iftikhar J. Kullo, Wei‐Qi Wei +16 more

Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure

Nature Communications(2022)10.1038/s41467-022-34216-6

N/A

0DataRank · unranked

150 citations

Noah L. Tsao, Pankhuri Singhal, Chang Liu, Ha My T. Vy, Ishan Paranjpe +38 more

Opposing effects of genetic variation in MTCH2 for obesity versus heart failure

Human Molecular Genetics(2022)10.1093/hmg/ddac176

N/A

0DataRank · unranked

9 citations

Tanner O. Monroe, Lorenzo L. Pesce, Konrad Teodor Sawicki, Mattia Quattrocelli, Rosemary Bauer +5 more

Quantifying factors that affect polygenic risk score performance across diverse ancestries and age groups for body mass index

medRxiv(2022)10.1101/2022.05.27.22275647

N/A

0DataRank · unranked

5 citations

Brenda Xiao, Ozan Dikilitas, Robert R. Freimuth, Marguerite R. Irvin, Gail P. Jarvik +14 more

Identification of Clinical Drivers of Left Atrial Enlargement Through Genomics of Left Atrial Size

Circulation Heart Failure(2023)10.1161/circheartfailure.123.010557

N/A

0DataRank · unranked

7 citations

Ali Manouchehri, Nataraja Sarma Vaitinadin, Mingjian Shi, Minoo Bagheri, Deepak K. Gupta +8 more

Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations

medRxiv(2023)10.1101/2023.05.25.23290535

N/A

0DataRank · unranked

7 citations

Leah C. Kottyan, Christopher Kachulis, Noura S. Abul‐Husn, Josh Arias, Gillian M. Belbin +71 more

Common- and rare-variant genetic architecture of heart failure across the allele frequency spectrum

medRxiv(2023)10.1101/2023.07.16.23292724

N/A

0DataRank · unranked

6 citations

Kathleen M. Cardone, David Y. Zhang, Noah L. Tsao, Sarah Abramowitz, Pranav Sharma +30 more

The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young

medRxiv(2023)10.1101/2023.03.27.23287711

N/A

0DataRank · unranked

1 citations

Lorenzo L. Pesce, Edgar J. Hernández, Gregory Webster, Lisa Dellefave‐Castillo, Mark W. Russell +17 more

Susceptibility to innate immune activation in genetically mediated myocarditis

Journal of Clinical Investigation(2024)10.1172/jci180254

N/A

0DataRank · unranked

29 citations

Dominic E. Fullenkamp, Ivana A. Chychula, Binjie Li, Lisa Dellefave‐Castillo, Adi D. Dubash +14 more

The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young

Genome Medicine(2024)10.1186/s13073-024-01284-w

N/A

0DataRank · unranked

13 citations

Lorenzo L. Pesce, Edgar J. Hernández, Gregory Webster, Lisa Dellefave‐Castillo, Mark W. Russell +18 more

Reduction of Filamin C Results in Altered Proteostasis, Cardiomyopathy, and Arrhythmias

Journal of the American Heart Association(2024)10.1161/jaha.123.030467

N/A

0DataRank · unranked

12 citations

Lisa Dellefave‐Castillo, Garima Tomar, Lisa D. Wilsbacher, Lubna Choudhury, David Y. Barefield +11 more

Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrum

Nature Genetics(2025)10.1038/s41588-025-02140-2

N/A

0DataRank · unranked

33 citations

Kathleen M. Cardone, David Zhang, Noah L. Tsao, Sarah Abramowitz, Pranav Sharma +35 more

Identification of candidate cardiomyopathy modifier genes through genome sequencing and RNA profiling

Frontiers in Cardiovascular Medicine(2025)10.3389/fcvm.2025.1546493

N/A

0DataRank · unranked

2 citations

Sarah Abramowitz, Daryl Waggott, Megan E. Grove, Frederick E. Dewey, Cuiping Pan +17 more

A novel, rapidly progressive ataxia due to a spontaneous Myo5a mutation in mice impairs transport proteins and alters mitochondria

The FASEB Journal(2025)10.1096/fj.202402274r

N/A

0DataRank · unranked

0 citations

Ryan R. Hsieh, Gabrielle Cowen, Eoin P. Sode, Jason M. Kwon, Andy H. Vo +9 more

Engineered heart tissues facilitate functional characterization of noncoding variants implicated in Hypertrophic and Dilated Cardiomyopathy

Research Square(2025)10.21203/rs.3.rs-7696371/v1

N/A

0DataRank · unranked

0 citations

Tanner O. Monroe, Cory Holgren, Robert M. Mitchell, Li Zhang, Alexis G. Thornburg +6 more

A combined genomic arrhythmia propensity score delineates cumulative risk

Cell Reports Medicine(2025)10.1016/j.xcrm.2025.102455

N/A

0DataRank · unranked

0 citations

Megan J. Puckelwartz, Lorenzo L. Pesce, Samuel Kearns, Patrick Page, Nora Ibrahim +10 more

Trajectory analysis of cardiovascular phenotypes from biobank data uncovers novel genetic associations

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.10.087130

N/A

0DataRank · unranked

1 citations

Lorenzo L. Pesce, Anthony Gacita, Lindsey E. Montefiori, Nathan Hodge, Samuel Kearns +9 more

Identification of Cardiac Fibrosis in Young Adults With a Homozygous Frameshift Variant in SERPINE1

JAMA Cardiology(2021)10.1001/jamacardio.2020.6909

N/A

0DataRank · unranked

24 citations

Sanjiv J. Shah, Jennifer L. Strande, Abigail S. Baldridge, Panagiotis Flevaris, Megan J. Puckelwartz +11 more

South Asian-Specific MYBPC3Δ25bp Deletion Carriers Display Hypercontraction and Impaired Diastolic Function Under Exercise Stress

Frontiers in Cardiovascular Medicine(2021)10.3389/fcvm.2021.766339

N/A

0DataRank · unranked

6 citations

Robert Sibilia, Saavia Girgla, Shiv Kumar Viswanathan, Megan J. Puckelwartz, Kiranpal S. Sangha +9 more

Megan J. Puckelwartz

Indexed papers

Top data-sharing exemplar

Papers