Dan E. Arking

Johns Hopkins University

Biochemistry, Genetics and Molecular BiologyMedicine

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 1%percentile

11.0Author DataRank

Indexed papers

5in 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 5 indexed papers 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.

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Nature(2021)10.1038/s41586-021-03205-y

Top 3%

7.0DataRank

Top 3%2322 citations

Daniel Harris, Michael D. Kessler, Jedidiah Carlson, Zachary A. Szpiech, Raúl Torres +95 more

Papers

Driven by 83 papers — median percentile 79. Top paper: “Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data”.

Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data

Nature Genetics(2022)10.1038/s41588-021-00997-7

N/A

7.2DataRank · unranked

363 citations

Deepti Jain, Zhili Zheng, TOPMed Anthropometry Working Group, Stella Aslibekyan, Diane M. Becker +95 more

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Nature(2021)10.1038/s41586-021-03205-y

Top 3%

7.0DataRank

Top 3%2322 citations

Daniel Harris, Michael D. Kessler, Jedidiah Carlson, Zachary A. Szpiech, Raúl Torres +95 more

Clonal haematopoiesis and risk of chronic liver disease

Nature(2023)10.1038/s41586-023-05857-4

N/A

4.5DataRank · unranked

204 citations

Connor A. Emdin, Alexander G. Bick, Seyedeh M. Zekavat, Abhishek Niroula, James P. Pirruccello +95 more

A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

Nature Genetics(2021)10.1038/s41588-021-00935-7

N/A

4.0DataRank · unranked

191 citations

Masahiro Kanai, Wanson Choi, Xinyi Li, Saori Sakaue, Kenichi Yamamoto +95 more

Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

Nature Communications(2018)10.1038/s41467-018-04668-w

N/A

3.7DataRank · unranked

109 citations

Sanni Ruotsalainen, Robert E. Handsaker, Maris Alver, Jonathan M. Bloom, Timothy Poterba +442 more

Mitochondrial DNA copy number can influence mortality and cardiovascular disease via methylation of nuclear DNA CpGs

Genome Medicine(2020)10.1186/s13073-020-00778-7

N/A

3.0DataRank · unranked

123 citations

Ryan J. Longchamps, Jason A. Sumpter, Charles Newcomb, John Lane, Megan L. Grove +19 more

52 Genetic Loci Influencing Myocardial Mass

Journal of the American College of Cardiology(2016)10.1016/j.jacc.2016.07.729

N/A

2.4DataRank · unranked

135 citations

Jessica van Setten, Niek Verweij, Georg Vogler, Matthew T. Maurano, Xinchen Wang +172 more

Consistent RNA sequencing contamination in GTEx and other data sets

Nature Communications(2020)10.1038/s41467-020-15821-9

Top 10%

2.2DataRank

Top 10%93 citations

Stephanie Yang, Rohan Verma, Vamsee Pillalamarri, Dan E. Arking, Avi Z. Rosenberg +3 more

Clonal hematopoiesis of indeterminate potential is associated with acute kidney injury

Nature Medicine(2024)10.1038/s41591-024-02854-6

N/A

1.9DataRank · unranked

76 citations

Cassianne Robinson‐Cohen, Jianchun Chen, Elvis A. Akwo, Alyssa Parker, Samuel A. Silver +26 more

Whole genome sequence analysis of blood lipid levels in >66,000 individuals

Nature Communications(2022)10.1038/s41467-022-33510-7

N/A

1.6DataRank · unranked

75 citations

Xihao Li, Zilin Li, Akhil Pampana, David Zhang, Joseph Park +95 more

Genome sequencing unveils a regulatory landscape of platelet reactivity

Nature Communications(2021)10.1038/s41467-021-23470-9

N/A

1.5DataRank · unranked

54 citations

Ming‐Huei Chen, Benjamin A.T. Rodriguez, Lisa R. Yanek, Arunoday Bhan, Brady Gaynor +94 more

Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial Fibrillation

Circulation Genomic and Precision Medicine(2020)10.1161/circgen.119.002874

N/A

1.4DataRank · unranked

30 citations

Amelia Weber Hall, Seung Hoan Choi, Sean J. Jurgens, Jeffrey Haessler, Nathan A. Bihlmeyer +55 more

Association of mitochondrial DNA copy number with cardiometabolic diseases

Cell Genomics(2021)10.1016/j.xgen.2021.100006

N/A

1.4DataRank · unranked

62 citations

Ryan J. Longchamps, Kerri L. Wiggins, Laura M. Raffield, Lawrence F. Bielak, Wei Zhao +33 more

Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p

Nature Genetics(2022)10.1038/s41588-022-01203-y

N/A

1.3DataRank · unranked

55 citations

Emi Ling, Serkan Erdin, Derek J.C. Tai, Rachita Yadav, Jakob Grove +94 more

Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies

Nature Genetics(2022)10.1038/s41588-022-01225-6

N/A

1.2DataRank · unranked

63 citations

Corbin Quick, Hufeng Zhou, Sheila M. Gaynor, Yaowu Liu, Han Chen +95 more

Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals

Nature Communications(2022)10.1038/s41467-022-32275-3

N/A

1.1DataRank · unranked

63 citations

Daniel H. Katz, Julián Ávila-Pacheco, Alexander G. Bick, Akhil Pampana, Jeremy Robbins +95 more

Mitochondrial DNA copy number and diabetes: the Atherosclerosis Risk in Communities (ARIC) study

BMJ Open Diabetes Research & Care(2020)10.1136/bmjdrc-2020-001204

N/A

1.1DataRank · unranked

29 citations

Ryan J. Longchamps, Yiyi Zhang, Rita R. Kalyani, Eliseo Güallar, Dan E. Arking +3 more

Quantifying constraint in the human mitochondrial genome

Nature(2024)10.1038/s41586-024-08048-x

N/A

1.1DataRank · unranked

58 citations

Kaiyue Ma, Wei Liu, Stephanie L. Battle, Kristen M. Laricchia, Grace Tiao +12 more

Deleterious heteroplasmic mitochondrial mutations are associated with an increased risk of overall and cancer-specific mortality

Nature Communications(2023)10.1038/s41467-023-41785-7

N/A

1.1DataRank · unranked

44 citations

Stephanie L. Battle, Wen Shi, Daniela Puiu, Vamsee Pillalamarri, Jiaqi Xie +21 more

Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program

Genome Medicine(2021)10.1186/s13073-021-00917-8

Top 21%

0.976DataRank

Top 21%35 citations

Jiwon Lee, Tamar Sofer, Heming Wang, Man Zhang, Han Chen +94 more

Association Between Whole Blood–Derived Mitochondrial DNA Copy Number, Low‐Density Lipoprotein Cholesterol, and Cardiovascular Disease Risk

Journal of the American Heart Association(2023)10.1161/jaha.122.029090

N/A

0.920DataRank · unranked

30 citations

Xianbang Sun, Yuankai Zhang, Wenqing Jiang, M M Lai, Kerri L. Wiggins +40 more

Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases

Nature Genetics(2025)10.1038/s41588-024-02072-3

N/A

0.821DataRank · unranked

50 citations

Ida Surakka, Morten S. Olesen, Garðar Sveinbjörnsson, Nicholas Marston, Seung Hoan Choi +95 more

Evaluation of mitochondrial DNA copy number estimation techniques

PLoS ONE(2020)10.1371/journal.pone.0228166

N/A

0.760DataRank · unranked

158 citations

Christina A. Castellani, Stephanie Yang, Charles Newcomb, Jason A. Sumpter, John Lane +8 more

Blood-derived mitochondrial DNA copy number is associated with gene expression across multiple tissues and is predictive for incident neurodegenerative disease

Genome Research(2021)10.1101/gr.269381.120

N/A

0.704DataRank · unranked

108 citations

Christina A. Castellani, Ryan J. Longchamps, Vamsee Pillalamarri, Brian O’Rourke, Eliseo Güallar +2 more

Genome-wide analysis of mitochondrial DNA copy number reveals loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferation

Human Genetics(2021)10.1007/s00439-021-02394-w

N/A

0.648DataRank · unranked

74 citations

Stephanie Yang, Christina A. Castellani, Wen Shi, Jon D. Lane, Megan L. Grove +47 more

Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk

Nature Genetics(2025)10.1038/s41588-025-02074-9

N/A

0.628DataRank · unranked

28 citations

Sean J. Jurgens, Ling Xiao, Matthew C. Hill, Christopher M. Haggerty, Garðar Sveinbjörnsson +95 more

A bioinformatics pipeline for estimating mitochondrial DNA copy number and heteroplasmy levels from whole genome sequencing data

NAR Genomics and Bioinformatics(2022)10.1093/nargab/lqac034

N/A

0.584DataRank · unranked

48 citations

Daniela Puiu, TOPMed mtDNA Working Group, Joost Verlouw, Linda Broer, Eric Boerwinkle +9 more

NAT8 Variants, N-Acetylated Amino Acids, and Progression of CKD

Clinical Journal of the American Society of Nephrology(2020)10.2215/cjn.08600520

N/A

0.581DataRank · unranked

47 citations

Aditya Surapaneni, Zihe Zheng, Eugene P. Rhee, Josef Coresh, Adriana M. Hung +10 more

Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension

Kidney International(2022)10.1016/j.kint.2022.07.005

N/A

0.574DataRank · unranked

45 citations

Pascal Schlosser, Linda Zhou, Celina Liu, Nilanjan Chatterjee, Dan E. Arking +5 more

The functional impact of rare variation across the regulatory cascade

Cell Genomics(2023)10.1016/j.xgen.2023.100401

N/A

0.526DataRank · unranked

15 citations

Nicole M. Ferraro, Benjamin J. Strober, François Aguet, Silva Kasela, Marios Arvanitis +33 more

Association of Mitochondrial DNA Copy Number with Risk of Progression of Kidney Disease

Clinical Journal of the American Society of Nephrology(2022)10.2215/cjn.15551121

N/A

0.524DataRank · unranked

32 citations

Changwei Li, Zhijie Huang, Siyi Geng, Varun S. Rao, Tanika N. Kelly +6 more

Transcriptome- and proteome-wide association studies nominate determinants of kidney function and damage

Genome biology(2023)10.1186/s13059-023-02993-y

N/A

0.524DataRank · unranked

32 citations

Jingning Zhang, Hongbo Liu, Aditya Surapaneni, Eugene P. Rhee, Dan E. Arking +8 more

Multi-ancestry genome-wide gene–sleep interactions identify novel loci for blood pressure

Molecular Psychiatry(2021)10.1038/s41380-021-01087-0

N/A

0.483DataRank · unranked

24 citations

Raymond Noordam, Brian E. Cade, Karen Schwander, Thomas W. Winkler, Jiwon Lee +95 more

Multi-Ethnic Genome-Wide Association Study of Decomposed Cardioelectric Phenotypes Illustrates Strategies to Identify and Characterize Evidence of Shared Genetic Effects for Complex Traits

Circulation Genomic and Precision Medicine(2020)10.1161/circgen.119.002680

Top 41%

0.466DataRank

Top 41%13 citations

Colleen M. Sitlani, Heather M. Highland, Dan E. Arking, Steven Buyske, Dawood Darbar +27 more

Trans-ethnic genome-wide association study of blood metabolites in the Chronic Renal Insufficiency Cohort (CRIC) study

Kidney International(2022)10.1016/j.kint.2022.01.014

N/A

0.464DataRank · unranked

21 citations

Aditya Surapaneni, Zihe Zheng, Linda Zhou, Diptavo Dutta, Dan E. Arking +21 more

The impact of common and rare genetic variants on bradyarrhythmia development

Nature Genetics(2025)10.1038/s41588-024-01978-2

N/A

0.464DataRank · unranked

21 citations

Joel Rämö, Sean J. Jurgens, Shaan Khurshid, Mark Chaffin, Amelia Weber Hall +95 more

Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease

Nature Communications(2023)10.1038/s41467-023-36997-w

N/A

0.434DataRank · unranked

17 citations

Jeffrey Haessler, Jan Walter Benjamins, L. Repetto, Jie Yao, Aaron Isaacs +89 more

Multi-ancestry genome-wide association study accounting for gene-psychosocial factor interactions identifies novel loci for blood pressure traits

Human Genetics and Genomics Advances(2020)10.1016/j.xhgg.2020.100013

N/A

0.406DataRank · unranked

14 citations

Melissa A. Richard, Solomon K. Musani, Yun Ju Sung, Thomas W. Winkler, Karen Schwander +95 more

A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies

Nature Computational Science(2025)10.1038/s43588-024-00764-8

N/A

0.393DataRank · unranked

10 citations

Han Chen, Margaret Sunitha Selvaraj, Eric Van Buren, Hufeng Zhou, Yuxuan Wang +95 more

Plasma proteins associated with plant-based diets: Results from the Atherosclerosis Risk in Communities (ARIC) study and Framingham Heart Study (FHS)

Clinical Nutrition(2024)10.1016/j.clnu.2024.07.005

N/A

0.385DataRank · unranked

12 citations

Jingsha Chen, Brenton Prescott, Maura E. Walker, Morgan E. Grams, Bing Yu +8 more

Mitochondrial heteroplasmy improves risk prediction for myeloid neoplasms

Nature Communications(2024)10.1038/s41467-024-54443-3

N/A

0.360DataRank · unranked

10 citations

Sergiu Paşca, Wen Shi, Daniela Puiu, Nicole J. Lake, Monkol Lek +9 more

Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization

Wellcome Open Research(2023)10.12688/wellcomeopenres.18754.1

N/A

0.357DataRank · unranked

7 citations

Natasha Hui Jin Ng, Juan Fernandez, Rebecca S. Fine, Eleanor Wheeler, Jennifer Wessel +95 more

Monogenic and Polygenic Contributions to QTc Prolongation in the Population

medRxiv(2021)10.1101/2021.06.18.21258578

N/A

0.320DataRank · unranked

5 citations

Valerie N. Morrill, Sean J. Jurgens, Seung Hoan Choi, Amelia Weber Hall, Lu‐Chen Weng +33 more

Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

Nature Communications(2020)10.1038/s41467-020-15236-6

Top 57%

0.275DataRank

Top 57%2 citations

Sanni Ruotsalainen, Robert E. Handsaker, Maris Alver, Jonathan M. Bloom, Timothy Poterba +442 more

Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels

Digital Commons@Becker (Washington University School of Medicine)(2020)10.17615/5y99-4w88

N/A

0.269DataRank · unranked

5 citations

Terho Lehtimäki, P. Eline Slagboom, Albert V. Smith, Dennis O. Mook‐Kanamori, Paul Elliott +93 more

Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.29.123505

N/A

0.208DataRank · unranked

3 citations

Raymond Noordam, Brian E. Cade, Karen Schwander, Thomas W. Winkler, Jiwon Lee +95 more

Association analysis of mitochondrial DNA heteroplasmic variants: Methods and application

Mitochondrion(2024)10.1016/j.mito.2024.101954

N/A

0.165DataRank · unranked

2 citations

Katia Bulekova, Jian Yang, M M Lai, Achilleas Pitsillides, Xue Liu +19 more

Epigenome-wide association study of nuclear DNA methylation in relation to mitochondrial heteroplasmy

Nature Communications(2025)10.1038/s41467-025-65845-2

N/A

0.104DataRank · unranked

1 citations

Kyeezu Kim, Yinan Zheng, Christina A. Castellani, Scott M. Ratliff, Mengyao Wang +41 more

The association between mitochondrial DNA copy number, low-density lipoprotein cholesterol, and cardiovascular disease risk

medRxiv(2022)10.1101/2022.10.23.22281418

N/A

0.104DataRank · unranked

1 citations

Xianbang Sun, Yuankai Zhang, Wenqing Jiang, Lai Meng, Kerri L. Wiggins +40 more

Associations of Blood Mitochondrial DNA Quality and Quantity with Risk of Kidney Function Decline

Clinical Journal of the American Society of Nephrology(2025)10.2215/cjn.0000000893

N/A

0DataRank · unranked

0 citations

Ronit Katz, Dan E. Arking, Wen Shi, Charles Newcomb, Gregory J. Tranah +9 more

Author Index Vol. 64, 2007

Human Heredity(2007)10.1159/000105464

N/A

0DataRank · unranked

0 citations

John P. A. Ioannidis, Wendy S. Post, Haiqing Shen, Coleen Damcott, Dan E. Arking +20 more

Contents Vol. 64, 2007

Human Heredity(2007)10.1159/000105467

N/A

0DataRank · unranked

0 citations

John P. A. Ioannidis, Wendy S. Post, Haiqing Shen, Coleen Damcott, Dan E. Arking +20 more

Thinking outside the nucleus: Mitochondrial DNA copy number in health and disease

Mitochondrion(2020)10.1016/j.mito.2020.06.004

N/A

0DataRank · unranked

367 citations

Ryan J. Longchamps, Jing Sun, Eliseo Güallar, Dan E. Arking, Christina A. Castellani

Analysis of putative cis-regulatory elements regulating blood pressure variation

Human Molecular Genetics(2020)10.1093/hmg/ddaa098

N/A

0DataRank · unranked

13 citations

Dongwon Lee, Thomas J. Hoffmann, Georg Ehret, Dan E. Arking, Dilrini K. Ranatunga +9 more

Mitochondrial DNA copy number and incident atrial fibrillation

BMC Medicine(2020)10.1186/s12916-020-01715-6

N/A

0DataRank · unranked

40 citations

Traci M. Bartz, Nona Sotoodehnia, Wendy S. Post, Susan R. Heckbert, Álvaro Alonso +12 more

Blood-derived mitochondrial DNA copy number is associated with gene expression across multiple tissues and is predictive for incident neurodegenerative disease

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.17.209023

N/A

0DataRank · unranked

13 citations

Christina A. Castellani, Ryan J. Longchamps, Vamsee Pillalamarri, Brian O’Rourke, Eliseo Güallar +2 more

Stratifying Type 2 Diabetes Cases by BMI Identifies Genetic Risk Variants in LAMA1 and Enrichment for Risk Variants in Lean Compared to Obese Cases

UNC Libraries(2020)10.17615/9k4n-rx53

N/A

0DataRank · unranked

0 citations

Francis S. Collins, Christian Gieger, Martha Ganser, Valgerður Steinthórsdóttir, Eric Boerwinkle +27 more

Genetic diversity is a predictor of mortality in humans

UNC Libraries(2020)10.17615/kwh0-eh07

N/A

0DataRank · unranked

0 citations

John M. Starr, David A. Bennett, Kathryn L. Lunetta, Hans J. Grabe, Lei Yu +47 more

Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans

UNC Libraries(2020)10.17615/gng9-yn62

N/A

0DataRank · unranked

0 citations

Jonathan D. H. Smith, Steven Buyske, Erin N. Smith, Kathleen F. Kerr, Toshiko Tanaka +56 more

Fine-Mapping and Initial Characterization of QT Interval Loci in African Americans

UNC Libraries(2020)10.17615/arb6-r827

N/A

0DataRank · unranked

0 citations

Qianchuan He, Nona Sotoodehnia, Megan D. Fesinmeyer, Christopher A. Haiman, D. Y. Lin +17 more

The QT interval and risk of incident atrial fibrillation

UNC Libraries(2020)10.17615/cpmn-as06

N/A

0DataRank · unranked

0 citations

Karen Stocke, Mala C. Mandyam, Álvaro Alonso, Javed Butler, Dan E. Arking +14 more

Epigenetic Age and the Risk of Incident Atrial Fibrillation

Circulation(2021)10.1161/circulationaha.121.056456

N/A

0DataRank · unranked

118 citations

Eric Vittinghoff, Ake T. Lu, Álvaro Alonso, Biqi Wang, Colleen M. Sitlani +23 more

Proteins Associated with Risk of Kidney Function Decline in the General Population

Journal of the American Society of Nephrology(2021)10.1681/asn.2020111607

N/A

0DataRank · unranked

57 citations

Aditya Surapaneni, Jingsha Chen, Linda Zhou, Zhi Yu, Diptavo Dutta +20 more

Development and optimization of an in vivo electrocardiogram recording method and analysis program for adult zebrafish

Disease Models & Mechanisms(2021)10.1242/dmm.048827

N/A

0DataRank · unranked

7 citations

Rebecca Rose, Adriana Blazeski, Noah Fine, Courtney E. Woods, Joseph F. Thole +6 more

A Bioinformatics Pipeline for Estimating Mitochondria DNA Copy Number and Heteroplasmy Levels from Whole Genome Sequencing Data

medRxiv(2021)10.1101/2021.12.28.21268452

N/A

0DataRank · unranked

3 citations

Daniela Puiu, TOPMed mtDNA Working Group, Eric Boerwinkle, Kent D. Taylor, Jerome I. Rotter +7 more

A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies

Nature Methods(2022)10.1038/s41592-022-01640-x

N/A

0DataRank · unranked

109 citations

Xihao Li, Hufeng Zhou, Sheila M. Gaynor, Margaret Sunitha Selvaraj, Theodore Arapoglou +95 more

Monogenic and Polygenic Contributions to QTc Prolongation in the Population

Circulation(2022)10.1161/circulationaha.121.057261

N/A

0DataRank · unranked

50 citations

Valerie N. Morrill, Sean J. Jurgens, Seung Hoan Choi, Amelia W. Hall, Lu-Chen Weng +34 more

Resting heart rate and incident atrial fibrillation: A stratified Mendelian randomization in the AFGen consortium

PLoS ONE(2022)10.1371/journal.pone.0268768

N/A

0DataRank · unranked

15 citations

Bastiaan Geelhoed, Carolina Roselli, Boyi Wang, Henry J. Lin, Stefan Weiß +28 more

Whole-exome sequencing in 415,422 individuals identifies rare variants associated with mitochondrial DNA copy number

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100147

N/A

0DataRank · unranked

12 citations

Wen Shi, Conrad Say, Stephanie Yang, John Lane, Eliseo Güallar +3 more

Frequency of the PNPLA3 rs738409 polymorphism and other genetic loci for liver disease in a Guatemalan adult population

Liver International(2022)10.1111/liv.15268

N/A

0DataRank · unranked

8 citations

Jiaqi Xie, Christian S. Álvarez, Dominick Parisi, Stephanie Yang, Alvaro Rivera‐Andrade +7 more

Quantifying constraint in the human mitochondrial genome

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.12.16.520778

N/A

0DataRank · unranked

10 citations

Wei Liu, Stephanie L. Battle, Kristen M. Laricchia, Grace Tiao, Daniela Puiu +9 more

Deleterious heteroplasmic mitochondrial mutations increase risk of overall and cancer-specific mortality

medRxiv(2022)10.1101/2022.09.20.22280151

N/A

0DataRank · unranked

2 citations

Yun Soo Hong, Wen Shi, Daniela Puiu, Vamsee Pillalamarri, Nathan Pankratz +5 more

Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma

EBioMedicine(2023)10.1016/j.ebiom.2023.104758

N/A

0DataRank · unranked

19 citations

Priyadarshini Kachroo, Tianxiao Huan, David Van Den Berg, Gha Young Lee, Helena Bui +95 more

Long-Term Air Pollution Exposure and Mitochondrial DNA Copy Number: An Analysis of UK Biobank Data

Environmental Health Perspectives(2023)10.1289/ehp11946

N/A

0DataRank · unranked

12 citations

Stephanie L. Battle, Daniela Puiu, Wen Shi, Nathan Pankratz, Di Zhao +3 more

Common and Rare Variant Contributions to Bradyarrhythmias from Multi-Ancestry Meta-Analyses

medRxiv(2023)10.1101/2023.09.24.23295485

N/A

0DataRank · unranked

0 citations

Joel Rämö, Sean J. Jurgens, Shaan Khurshid, Mark Chaffin, Amelia Weber Hall +56 more

Association of Blood Mitochondrial DNA Copy Number With Risk of Acute Kidney Injury After Cardiac Surgery

American Journal of Kidney Diseases(2024)10.1053/j.ajkd.2024.03.013

N/A

0DataRank · unranked

6 citations

Heather Thiessen‐Philbrook, Dan E. Arking, Stephanie Yang, Eric McArthur, Amit X. Garg +10 more

Rare and common genetic determinants of mitochondrial function determine severity but not risk of amyotrophic lateral sclerosis

Heliyon(2024)10.1016/j.heliyon.2024.e24975

N/A

0DataRank · unranked

11 citations

Marcel Weinreich, James Lee, Allan C. Shaw, Laura Ferraiuolo, Heather Mortiboys +20 more

Mitochondrial DNA copy number reduction via in vitro TFAM knockout remodels the nuclear epigenome and transcriptome

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.01.29.577835

N/A

0DataRank · unranked

2 citations

Phyo W. Win, Tyler Shin Nagano, Elly H. Shin, Charles Newcomb, Dan E. Arking +2 more

Association analysis of mitochondrial DNA heteroplasmic variants: methods and application

medRxiv(2024)10.1101/2024.01.12.24301233

N/A

0DataRank · unranked

0 citations

Katia Bulekova, Jian Yang, M M Lai, Achilleas Pitsillides, Xue Liu +20 more

Mitochondrial heteroplasmy improves risk prediction for myeloid neoplasms

medRxiv(2024)10.1101/2024.04.07.24305454

N/A

0DataRank · unranked

0 citations

Sergiu Paşca, Wen Shi, Daniela Puiu, Nicole J. Lake, Monkol Lek +9 more

Plant-Based Diets and Cardiovascular Events: A Proteomics Approach to Examine the Underlying Pathways

Journal of Nutrition(2025)10.1016/j.tjnut.2025.04.011

N/A

0DataRank · unranked

2 citations

Jingsha Chen, Brenton Prescott, Maura E. Walker, Morgan E. Grams, Bing Yu +8 more

Multi-ancestry genome-wide association analyses incorporating SNP-by-psychosocial interactions identify novel loci for serum lipids

Translational Psychiatry(2025)10.1038/s41398-025-03418-z

N/A

0DataRank · unranked

0 citations

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bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.11.10.687605

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