Stephanie M. Fullerton

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 1%percentile

60.5Author DataRank

Indexed papers

11in 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 11 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.

A global reference for human genetic variation

Nature(2015)10.1038/nature15393

Top 1%

10.6DataRank

Top 1%20166 citations

Gonçalo R. Abecasis, Richard M. Durbin, Panagiotis Deloukas, Aravinda Chakravarti, Peter Donnelly +516 more

Papers

Driven by 51 papers — median percentile 97. Top paper: “A global reference for human genetic variation”.

A global reference for human genetic variation

Nature(2015)10.1038/nature15393

Top 1%

10.6DataRank

Top 1%20166 citations

Gonçalo R. Abecasis, Richard M. Durbin, Panagiotis Deloukas, Aravinda Chakravarti, Peter Donnelly +516 more

A framework for human microbiome research

Nature(2012)10.1038/nature11209

Top 2%

8.4DataRank

Top 2%2766 citations

Barbara A. Methé, William Nelson, Mihai Pop, Heather H. Creasy, Michelle Giglio +236 more

Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel

Nature Communications(2014)10.1038/ncomms4934

Top 2%

8.3DataRank

Top 2%460 citations

Jonathan Marchini, Peter Donnelly, Gerton Lunter, Jonathan L. Marchini, Simon Myers +364 more

An Integrated TCGA Pan-Cancer Clinical Data Resource to Drive High-Quality Survival Outcome Analytics

Cell(2018)10.1016/j.cell.2018.02.052

Top 2%

8.1DataRank

Top 2%3980 citations

Katherine A. Hoadley, Laila M. Poisson, Alexander J. Lazar, Andrew D. Cherniack, Albert J. Kovatich +866 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

Perspective on Oncogenic Processes at the End of the Beginning of Cancer Genomics

Cell(2018)10.1016/j.cell.2018.03.033

Top 3%

6.4DataRank

Top 3%447 citations

Matthew H. Bailey, Hoifung Poon, Vesteinn Thorsson, Antonio Colaprico, Andreas Bender +883 more

Pan-cancer analysis of whole genomes

Nature(2020)10.1038/s41586-020-1969-6

Top 3%

5.9DataRank

Top 3%3307 citations

Lauri A. Aaltonen, Federico Abascal, Adam Abeshouse, Hiroyuki Aburatani, David J. Adams +1244 more

Machine Learning Detects Pan-cancer Ras Pathway Activation in The Cancer Genome Atlas

Cell Reports(2018)10.1016/j.celrep.2018.03.046

N/A

5.5DataRank · unranked

186 citations

Francisco Sanchez-Vega, Konnor C. La, Joshua Armenia, Walid K. Chatila, Augustin Luna +869 more

Analyses of non-coding somatic drivers in 2,658 cancer whole genomes

Nature(2020)10.1038/s41586-020-1965-x

Top 5%

4.6DataRank

Top 5%668 citations

Federico Abascal, Jeremiah A. Wala, Ofer Shapira, Grace Tiao, Henrik Hornshøj +1240 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

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

Structure, function and diversity of the healthy human microbiome

Nature(2012)10.1038/nature11234

N/A

1.4DataRank · unranked

10088 citations

Curtis Huttenhower, Dirk Gevers, Rob Knight, Sahar Abubucker, Jonathan H. Badger +235 more

Integrated genomic analyses of ovarian carcinoma

Nature(2011)10.1038/nature10166

N/A

1.3DataRank · unranked

8094 citations

Debra Bell, Andrew Berchuck, Michael J. Birrer, Jeremy Chien, D. W. Cramer +268 more

Oncogenic Signaling Pathways in The Cancer Genome Atlas

Cell(2018)10.1016/j.cell.2018.03.035

N/A

1.2DataRank · unranked

3322 citations

Marco Mina, Joshua Armenia, Walid K. Chatila, Augustin Luna, Konnor C. La +891 more

The PRIMED Consortium: Reducing disparities in polygenic risk assessment

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.10.010

N/A

0.893DataRank · unranked

37 citations

Matthew P. Conomos, Sarah C. Nelson, Sally N. Adebamowo, Ananyo Choudhury, David V. Conti +90 more

Effect of predicted protein-truncating genetic variants on the human transcriptome

Science(2015)10.1126/science.1261877

N/A

0.877DataRank · unranked

345 citations

Matti Pirinen, Donald F. Conrad, Monkol Lek, Emily K. Tsang, Konrad J. Karczewski +206 more

Automated assembly of high-quality diploid human reference genomes

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.03.06.483034

Top 28%

0.719DataRank

Top 28%22 citations

Giulio Formenti, Arang Rhie, Andrea Guarracino, Chentao Yang, Jonathan M. D. Wood +77 more

Toward better governance of human genomic data

Nature Genetics(2021)10.1038/s41588-020-00742-6

N/A

0.631DataRank · unranked

66 citations

Mahsa Shabani, Edward S. Dove, Heidi Beate Bentzen, Pascal Borry, Michael Burgess +19 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

Using the linear references from the pangenome to discover missing autism variants

Nature Communications(2026)10.1038/s41467-026-68378-4

Top 65%

0.208DataRank

Top 65%3 citations

Jiadong Lin, Michelle D. Noyes, Young-Jun Kwon, Isaac Wong, Nidhi Koundinya +252 more

Author Correction: Cancer LncRNA Census reveals evidence for deep functional conservation of long noncoding RNAs in tumorigenesis

Communications Biology(2022)10.1038/s42003-022-03769-z

N/A

0.165DataRank · unranked

2 citations

Lars Feuerbach, Chen Hong, David Mas-Ponte, Randi Istrup Pedersen, PCAWG Drivers and Functional Interpretation Group +1255 more

IGG in the trenches: Results of an in-depth interview study on the practice, politics, and future of investigative genetic genealogy

Forensic Science International(2024)10.1016/j.forsciint.2024.111946

N/A

0DataRank · unranked

12 citations

Whitney Bash Brooks, Jill O. Robinson, Stephanie M. Fullerton, Emily Zoorob, Amy L. McGuire +1 more

Applying health equity implementation science frameworks to population genetic screening

Frontiers in Health Services(2024)10.3389/frhs.2024.1455365

N/A

0DataRank · unranked

5 citations

Stephanie M. Fullerton, Brian H. Shirts, Annie Chen, Nora B. Henrikson, Nandana D. Rao

Public Perspectives on Investigative Genetic Genealogy: Findings from a National Focus Group Study

AJOB Empirical Bioethics(2024)10.1080/23294515.2024.2336904

N/A

0DataRank · unranked

4 citations

Jill O. Robinson, Amira Daoud, Whitney Bash‐Brooks, Amy L. McGuire, Christi J. Guerrini +2 more

The PRIMED Consortium: Reducing disparities in polygenic risk assessment

UNC Libraries(2024)10.17615/67cq-h633

N/A

0DataRank · unranked

0 citations

John S. Witte, Iman K. Martin, Sally N. Adebamowo, Maggie C. Y. Ng, Eimear E. Kenny +22 more

FIGG at 5: An update on U.S. public perspectives on forensic investigative genetic genealogy five years after its introduction to criminal investigations

Forensic Science International(2025)10.1016/j.forsciint.2025.112372

N/A

0DataRank · unranked

8 citations

Jill O. Robinson, Mohamed I. Elsaid, Whitney Bash Brooks, Ariel Levchenko, Stephanie M. Fullerton +9 more

When families bridge the research-clinical divide: An exploration of values regarding cascade screening in genomic research

Genetics in Medicine Open(2025)10.1016/j.gimo.2025.103440

N/A

0DataRank · unranked

1 citations

Lauren Desrosiers, Ann Katherine M. Foreman, Nuriye Sahin‐Hodoglugil, Mary A. Majumder, Candice R. Finnila +9 more

Investigative genetic genealogy practices warranting policy attention: Results of a modified policy Delphi

PLoS Genetics(2025)10.1371/journal.pgen.1011520

N/A

0DataRank · unranked

3 citations

Louiza Kalokairinou, Jill O. Robinson, Whitney Bash Brooks, Stephanie M. Fullerton, Sara Huston +7 more

Transparency and ongoing communication with participants in brain organoid research: Consensus of an interdisciplinary working group

Stem Cell Reports(2025)10.1016/j.stemcr.2025.102546

N/A

0DataRank · unranked

3 citations

Megan Doerr, Pamela Feliciano, Stephanie M. Fullerton, Saskia Hendriks, Søren Holm +8 more

Polygenic risk scores in the clinic: Health-system leaders and primary care providers weigh in

Genetics in Medicine(2025)10.1016/j.gim.2025.101575

N/A

0DataRank · unranked

2 citations

Stephanie M. Fullerton, Betty Cohn, David R. Crosslin, Gail P. Jarvik, Susan Brown Trinidad

A data model for population descriptors in genomic research

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.05.011

N/A

0DataRank · unranked

1 citations

Clement Adebamowo, Stephanie M. Fullerton, Jibril Hirbo, Iain R. Konigsberg, Peter Kraft +20 more

cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regions

Nature Methods(2025)10.1038/s41592-025-02919-5

N/A

0DataRank · unranked

0 citations

Yi Zhang, Xihao Li, Margaret Sunitha Selvaraj, Zilin Li, Hufeng Zhou +544 more

Author Correction: Combined burden and functional impact tests for cancer driver discovery using DriverPower

Nature Communications(2022)10.1038/s41467-022-32343-8

N/A

0DataRank · unranked

0 citations

PCAWG Drivers and Functional Interpretation Working Group, Federico Abascal, Samirkumar B. Amin, Pratiti Bandopadhayay, Rameen Beroukhim +1242 more

At the Research-Clinical Interface

Clinical Journal of the American Society of Nephrology(2020)10.2215/cjn.09670819

N/A

0DataRank · unranked

18 citations

Erika Blacksher, Kerri L. Cavanaugh, Stephanie M. Fullerton, Ebele M. Umeukeje, Bessie A. Young +2 more

Generalizability of Polygenic Risk Scores for Breast Cancer in the Multiethnic eMERGE Study

medRxiv(2020)10.1101/2020.08.17.20176685

N/A

0DataRank · unranked

0 citations

Nur Zeinomar, Wendy K. Chung, Krzysztof Kiryluk, Ali G. Ghravi, George Hripcsak +17 more

Return of Genomic Results to Research Participants: The Floor, the Ceiling, and the Choices In Between

UNC Libraries(2020)10.17615/rpzn-a165

N/A

0DataRank · unranked

0 citations

Gail P. Jarvik, Nanibaa’ A. Garrison, Wylie Burke, Jonathan S. Berg, John F. Connolly +27 more

Recommendations for ethical approaches to genotype-driven research recruitment

UNC Libraries(2020)10.17615/4ftw-cg79

N/A

0DataRank · unranked

0 citations

Laura M. Beskow, Benjamin S. Wilfond, Arlene M. Davis, Stephanie M. Fullerton, Emily Namey +1 more

Patient and Family Preferences on Health System-Led Direct Contact for Cascade Screening

Journal of Personalized Medicine(2021)10.3390/jpm11060538

N/A

0DataRank · unranked

46 citations

Paula R. Blasi, Marlaine Figueroa Gray, Brooks Tiffany, Aaron Scrol, James D. Ralston +5 more

Four misconceptions about investigative genetic genealogy

Journal of Law and the Biosciences(2021)10.1093/jlb/lsab001

N/A

0DataRank · unranked

54 citations

Ray Wickenheiser, Blaine T. Bettinger, Amy L. McGuire, Stephanie M. Fullerton, Christi J. Guerrini

What improves the likelihood of people receiving genetic test results communicating to their families about genetic risk?

Patient Education and Counseling(2021)10.1016/j.pec.2021.01.001

N/A

0DataRank · unranked

15 citations

Sukh Makhnoon, Brian H. Shirts, Stephanie M. Fullerton, Eric B. Larson, James D. Ralston +5 more

Neptune: an environment for the delivery of genomic medicine

Genetics in Medicine(2021)10.1038/s41436-021-01230-w

N/A

0DataRank · unranked

8 citations

Victoria Yi, David R. Murdock, Sara E. Kalla, Tsung-Jung Wu, Aniko Sabo +93 more

Strategies of inclusion: The tradeoffs of pursuing “baked in” diversity through place-based recruitment

Social Science & Medicine(2022)10.1016/j.socscimed.2022.115132

N/A

0DataRank · unranked

25 citations

Michael L. Bentz, Emily E. Vasquez, Melanie Jeske, Aliya Saperstein, Stephanie M. Fullerton +4 more

Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100120

N/A

0DataRank · unranked

12 citations

Laura M. Amendola, Tia L. Kauffman, Kathleen F. Mittendorf, Jeannette T. Bensen, Flavia Chen +15 more

Social and scientific motivations to move beyond groups in allele frequencies: The TOPMed experience

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.07.008

N/A

0DataRank · unranked

6 citations

Stephanie M. Gogarten, Stephanie M. Fullerton, Carmen R. Isasi, Braxton D. Mitchell, Kari E. North +5 more

Environmental scan of family chart linking for genetic cascade screening in a U.S. integrated health system

Frontiers in Genetics(2022)10.3389/fgene.2022.886650

N/A

0DataRank · unranked

3 citations

James D. Ralston, Stephanie M. Fullerton, Aaron Scrol, Nora B. Henrikson, Cameron B. Haas

Trustworthiness matters: Building equitable and ethical science

Cell(2023)10.1016/j.cell.2023.01.008

N/A

0DataRank · unranked

27 citations

Sandra Soo‐Jin Lee, Sara Goering, Stephanie M. Fullerton, Mildred K. Cho, Aaron Panofsky +2 more

Cloud-based biomedical data storage and analysis for genomic research: Landscape analysis of data governance in emerging NIH-supported platforms

Human Genetics and Genomics Advances(2023)10.1016/j.xhgg.2023.100196

N/A

0DataRank · unranked

14 citations

Sarah C. Nelson, Stephanie M. Fullerton, Jacklyn M. Dahlquist

Community Engagement in Precision Medicine Research: Organizational Practices and Their Impacts for Equity

AJOB Empirical Bioethics(2023)10.1080/23294515.2023.2201478

N/A

0DataRank · unranked

13 citations

Nicole Foti, Emily E. Vasquez, Stephanie M. Fullerton, Michael L. Bentz, Melanie Jeske +2 more

Interrogating the Value of Return of Results for Diverse Populations: Perspectives from Precision Medicine Researchers

AJOB Empirical Bioethics(2023)10.1080/23294515.2023.2279965

N/A

0DataRank · unranked

8 citations

Nicole Foti, Melanie Jeske, William Britton, Stephanie M. Fullerton, Janet K. Shim +2 more

Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience

UNC Libraries(2023)10.17615/wbfb-8h23

N/A

0DataRank · unranked

2 citations

P. Murali, Fangjing Chen, R. Green, Mark Kvale, David R. Crosslin +15 more

Advancing genomics to improve health equity

Nature Genetics(2024)10.1038/s41588-024-01711-z

N/A

0DataRank · unranked

53 citations

Lucia A. Hindorff, Vence L. Bonham, Tabia Henry Akintobi, Esteban G. Burchard, Kellan Baker +32 more

Stephanie M. Fullerton

Indexed papers

Top data-sharing exemplar

Papers