Matthew T. Oetjens

Also affiliated with Autism & Developmental Medicine Institute, Geisinger Neuroscience Institute, Geisinger Health System

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 2%percentile

2.4Author 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.

Electronic health record analysis identifies kidney disease as the leading risk factor for hospitalization in confirmed COVID-19 patients

PLoS ONE(2020)10.1371/journal.pone.0242182

Top 9%

2.4DataRank

Top 9%43 citations

Jonathan Z. Luo, Alex R. Chang, Joseph B. Leader, Dustin N. Hartzel, Bryn S. Moore +7 more

Papers

Driven by 15 papers — median percentile 91. Top paper: “Whole-genome sequencing reveals host factors underlying critical COVID-19”.

Whole-genome sequencing reveals host factors underlying critical COVID-19

Nature(2022)10.1038/s41586-022-04576-6

N/A

7.3DataRank · unranked

350 citations

Erola Pairo-Castineira, Konrad Rawlik, A. Stuckey, Christopher A. Odhams, Susan Walker +84 more

Electronic health record analysis identifies kidney disease as the leading risk factor for hospitalization in confirmed COVID-19 patients

PLoS ONE(2020)10.1371/journal.pone.0242182

Top 9%

2.4DataRank

Top 9%43 citations

Jonathan Z. Luo, Alex R. Chang, Joseph B. Leader, Dustin N. Hartzel, Bryn S. Moore +7 more

Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank

Nature Genetics(2022)10.1038/s41588-021-01011-w

N/A

0.775DataRank · unranked

174 citations

Seung Hoan Choi, Valerie N. Morrill, Mark Chaffin, James P. Pirruccello, Jennifer L. Halford +65 more

Family-GWAS reveals effects of environment and mating on genetic associations

medRxiv(2024)10.1101/2024.10.01.24314703

N/A

0.553DataRank · unranked

39 citations

Hariharan Jayashankar, Junming Guan, Seyed Moeen Nehzati, Mahdi Mir, Michael Bennett +60 more

Frequency of truncating FLCN variants and Birt-Hogg-Dubé–associated phenotypes in a health care system population

Genetics in Medicine(2022)10.1016/j.gim.2022.05.006

N/A

0.529DataRank · unranked

33 citations

Hermela Shimelis, Andrés Moreno-De-Luca, Natasha T. Strande, Matthew T. Oetjens, David H. Ledbetter +4 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

A genome-first study of sex chromosome aneuploidies provides evidence of Y chromosome dosage effects on autism risk

Nature Communications(2024)10.1038/s41467-024-53211-7

N/A

0.416DataRank · unranked

15 citations

Brenda Finucane, Scott M. Myers, Lauren K. Walsh, John M. Seibert, Christa Lese Martin +3 more

Meta-Analysis of Genome-Wide Association Studies Reveals Genetic Mechanisms of Supraventricular Arrhythmias

Circulation Genomic and Precision Medicine(2024)10.1161/circgen.123.004320

N/A

0.413DataRank · unranked

10 citations

Shaan Khurshid, Amelia Weber Hall, Victor Nauffal, Valerie N. Morrill, Yan V. Sun +54 more

Genetic modifiers and ascertainment drive variable expressivity of complex disorders

medRxiv(2024)10.1101/2024.08.27.24312158

N/A

0.269DataRank · unranked

5 citations

Corrine Smolen, Anastasia Tyryshkina, Lucilla Pizzo, Deepro Banerjee, Matthew T. Oetjens +65 more

X and Y gene dosage effects are primary contributors to human sexual dimorphism: The case of height

Proceedings of the National Academy of Sciences(2025)10.1073/pnas.2503039122

N/A

0DataRank · unranked

4 citations

Brenda Finucane, Scott M. Myers, Christa L. Martin, David H. Ledbetter, Huntington F. Willard +2 more

Association of the FTO Obesity Risk Variant rs8050136 With Percentage of Energy Intake From Fat in Multiple Racial/Ethnic Populations

UNC Libraries(2020)10.17615/p1nk-s136

N/A

0DataRank · unranked

0 citations

Sarah A. Pendergrass, Fredrick R. Schumacher, Laurence N. Kolonel, Matthew T. Oetjens, Unhee Lim +18 more

Frequency of FLCN Loss of Function Variants and Birt-Hogg-Dubé-Associated Phenotypes in a Healthcare System Population

medRxiv(2022)10.1101/2022.01.31.22269926

N/A

0DataRank · unranked

0 citations

Hermela Shimelis, Andrés Moreno-De-Luca, Natasha T. Strande, Matthew T. Oetjens, David H. Ledbetter +4 more

Response to van Riel et al

Genetics in Medicine(2022)10.1016/j.gim.2022.10.008

N/A

0DataRank · unranked

0 citations

Matthew T. Oetjens, Scott M. Myers, Brenda Finucane, Juliann M. Savatt

Systematic analysis of variants escaping nonsense-mediated decay uncovers candidate Mendelian diseases

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.11.007

N/A

0DataRank · unranked

37 citations

María J. Guillen Sacoto, Francisca Millan, Zhancheng Zhang, Stephen McGee, Matthew T. Oetjens +11 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

Matthew T. Oetjens

Indexed papers

Top data-sharing exemplar

Papers