Marc S. Williams

Also affiliated with Genomic Health (United States), Geisinger Health System

Biochemistry, Genetics and Molecular BiologyEconomics, Econometrics and FinanceMedicine

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

2in 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 2 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.

Penetrance of breast cancer genes from the eMERGE III Network

10.1101/2021.04.24.21255936

Top 100%

0DataRank

Top 100%0 citations

Julia Wynn, Ning Shang, Cong Liu, Alexander Fedotov, Miranda L.G. Hallquist +24 more

Papers

Driven by 41 papers — median percentile 0. Top paper: “Pediatric reporting of genomic results study (PROGRESS): a mixed-methods, longitudinal, observational cohort study protocol to explore disclosure of actionable adult- and pediatric-onset genomic variants to minors and their parents”.

Pediatric reporting of genomic results study (PROGRESS): a mixed-methods, longitudinal, observational cohort study protocol to explore disclosure of actionable adult- and pediatric-onset genomic variants to minors and their parents

BMC Pediatrics(2020)10.1186/s12887-020-02070-4

N/A

0.852DataRank · unranked

20 citations

Jennifer K. Wagner, Steven Joffe, Alanna Kulchak Rahm, Marc S. Williams, Angela R. Bradbury +13 more

A genome-wide association study of polycystic ovary syndrome identified from electronic health records

American Journal of Obstetrics and Gynecology(2020)10.1016/j.ajog.2020.04.004

N/A

0.698DataRank · unranked

104 citations

Kevin Ho, Jacob M. Keaton, Dustin N. Hartzel, Felix R. Day, Anne E. Justice +15 more

A picture is worth a thousand words: advancing the use of visualization tools in implementation science through process mapping and matrix heat mapping

Implementation Science Communications(2023)10.1186/s43058-023-00424-4

N/A

0.538DataRank · unranked

35 citations

Alanna Kulchak Rahm, Marc S. Williams, Ilene Ladd, Victoria Schlieder, Jamie Atondo +11 more

Administrative codes inaccurately identify recurrent venous thromboembolism: The CVRN VTE study

Thrombosis Research(2020)10.1016/j.thromres.2020.02.023

N/A

0.510DataRank · unranked

29 citations

Alan S. Go, Dongjie Fan, Sue Hee Sung, Daniel M. Witt, John R. Schmelzer +5 more

Reanalysis of eMERGE phase III sequence variants in 10,500 participants and infrastructure to support the automated return of knowledge updates

Genetics in Medicine(2021)10.1016/j.gim.2021.10.010

N/A

0.494DataRank · unranked

26 citations

Wanfeng Yu, Andrea M. Oza, Megan Hawley, Prathik K. Vijay Kumar, Christopher Koch +12 more

Evaluation of the portability of computable phenotypes with natural language processing in the eMERGE network

Scientific Reports(2023)10.1038/s41598-023-27481-y

N/A

0.489DataRank · unranked

25 citations

Luke V. Rasmussen, Ken Wiley, Thomas N. Person, David Cronkite, Sunghwan Sohn +34 more

Using implementation science to develop a familial hypercholesterolemia screening program in primary care: The CARE-FH study

Journal of clinical lipidology(2024)10.1016/j.jacl.2024.01.001

N/A

0.483DataRank · unranked

11 citations

Katrina M. Romagnoli, Tyler J. Schubert, Katarina Clegg, H. Lester Kirchner, Yirui Hu +6 more

The polygenic architecture of left ventricular mass mirrors the clinical epidemiology

Scientific Reports(2020)10.1038/s41598-020-64525-z

N/A

0.442DataRank · unranked

18 citations

Rebecca T. Levinson, Eric Farber‐Eger, Todd L. Edwards, Jacklyn N. Hellwege, Adriana M. Hung +20 more

Enabling the clinical application of artificial intelligence in genomics: a perspective of the AMIA Genomics and Translational Bioinformatics Workgroup

Journal of the American Medical Informatics Association(2023)10.1093/jamia/ocad211

N/A

0.434DataRank · unranked

17 citations

Radha Nagarajan, Chen Wang, Murat Sincan, Robert R. Freimuth, David B. Everman +14 more

A research agenda to support the development and implementation of genomics-based clinical informatics tools and resources

Journal of the American Medical Informatics Association(2022)10.1093/jamia/ocac057

N/A

0.345DataRank · unranked

9 citations

Laura Findley, Madison P. Goldrich, Tejinder Rakhra-Burris, Ana Stevens, Pamela A. Williams +34 more

Is the genomic translational pipeline being disrupted?

Human Genomics(2015)10.1186/s40246-015-0032-4

N/A

0.292DataRank · unranked

6 citations

Marc S. Williams

Trends in Incidence of Hospitalized Acute Myocardial Infarction in the Cardiovascular Research Network (CVRN)

UNC Libraries(2020)10.17615/zqh1-bv71

N/A

0DataRank · unranked

0 citations

Wayne D. Rosamond, R. Novotny, Denise M. Boudreau, Jerry H. Gurwitz, Marc S. Williams +16 more

A dyadic approach to the delineation of diagnostic entities in clinical genomics

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2020.11.013

N/A

0DataRank · unranked

116 citations

Margaret P Adam, Fowzan S. Alkuraya, Anne Amemiya, Michael J. Bamshad, Anita E. Beck +42 more

Implementation strategies to improve statin utilization in individuals with hypercholesterolemia: a systematic review and meta-analysis

Implementation Science(2021)10.1186/s13012-021-01108-0

N/A

0DataRank · unranked

41 citations

Stephanie Tilberry, Christina Gregor, Lauren Yaeger, Yirui Hu, Amy C. Sturm +9 more

Evaluation of a multidisciplinary lipid clinic to improve the care of individuals with severe lipid conditions: a RE-AIM framework analysis

Implementation Science Communications(2021)10.1186/s43058-021-00135-8

N/A

0DataRank · unranked

40 citations

Megan McMinn, David Kann, Michael Lesko, Amy C. Sturm, Nicole Walters +7 more

User testing of a diagnostic decision support system with machine-assisted chart review to facilitate clinical genomic diagnosis

BMJ Health & Care Informatics(2021)10.1136/bmjhci-2021-100331

N/A

0DataRank · unranked

15 citations

Nephi Walton, Lynn Feldman, Conner Jenkins, Troy Jenkins, Thomas N. Person +7 more

Evaluation of a multidisciplinary lipid clinic to improve the care of individuals with severe lipid conditions: a RE-AIM Framework Analysis

Research Square(2021)10.21203/rs.3.rs-51142/v2

N/A

0DataRank · unranked

0 citations

Megan McMinn, David Kann, Michael Lesko, Amy C. Sturm, Nicole Walters +7 more

The clinical utility of polygenic risk scores in genomic medicine practices: a systematic review

Human Genetics(2022)10.1007/s00439-022-02452-x

N/A

0DataRank · unranked

85 citations

Brittany Zick, Angeliki Balasopoulou, Constantina Chalikiopoulou, Collet Dandara, Ghada El‐Kamah +15 more

Population-Based Screening of Newborns: Findings From the NBS Expansion Study (Part One)

Frontiers in Genetics(2022)10.3389/fgene.2022.867337

N/A

0DataRank · unranked

21 citations

Kee Chan, Marc S. Williams, Susan A. Berry, Robert J. Currier, Piero Rinaldo +22 more

ClinGen’s Pediatric Actionability Working Group: Clinical actionability of secondary findings from genome-scale sequencing in children and adolescents

Genetics in Medicine(2022)10.1016/j.gim.2022.02.019

N/A

0DataRank · unranked

13 citations

Charisma L. Jenkins, Joanna E. Bulkley, Marian J. Gilmore, Kristy Lee, Christine M. Pak +17 more

Understanding the Patient Experience of Receiving Clinically Actionable Genetic Results from the MyCode Community Health Initiative, a Population-Based Genomic Screening Initiative

Journal of Personalized Medicine(2022)10.3390/jpm12091511

N/A

0DataRank · unranked

12 citations

Kasia Tolwinski, Jamie Atondo, F. Daniel Davis, Jessica Goehringer, Laney K. Jones +7 more

Population-based screening of newborns: Findings from the newborn screening expansion study (part two)

Frontiers in Genetics(2022)10.3389/fgene.2022.867354

N/A

0DataRank · unranked

6 citations

Amy Brower, Marc S. Williams, Kee Chan

Designing implementation strategies to improve identification, cascade testing, and management of families with familial hypercholesterolemia: An intervention mapping approach

Frontiers in Health Services(2023)10.3389/frhs.2023.1104311

N/A

0DataRank · unranked

7 citations

Evan M. Calvo, Gemme Campbell‐Salome, Nicole Walters, Andrew Brangan, Gabriela Rodriguez +11 more

Genomics in nephrology: identifying informatics opportunities to improve diagnosis of genetic kidney disorders using a human-centered design approach

medRxiv(2023)10.1101/2023.10.06.23296660

N/A

0DataRank · unranked

0 citations

Zachary Salvati, Darren K. Johnson, Heather M. Ramey, Alex R. Chang, Marc S. Williams +1 more

Implementing evidence-based assertions of clinical actionability in the context of secondary findings: Updates from the ClinGen Actionability Working Group

Genetics in Medicine(2024)10.1016/j.gim.2024.101164

N/A

0DataRank · unranked

4 citations

Marian J. Gilmore, Joanna E. Bulkley, Pranesh Chakraborty, Orit Dagan‐Rosenfeld, Ann Katherine M. Foreman +21 more

Identifying factors and causal chains associated with optimal implementation of Lynch syndrome tumor screening: An application of coincidence analysis

Genetics in Medicine(2024)10.1016/j.gim.2024.101201

N/A

0DataRank · unranked

4 citations

Zachary M Salvati, Jennifer L Schneider, Andrea N. Burnett‐Hartman, Mara M. Epstein, Jessica Ezzell Hunter +9 more

Phenotypic findings associated with variation in elastin

Human Genetics and Genomics Advances(2024)10.1016/j.xhgg.2024.100388

N/A

0DataRank · unranked

1 citations

Melissa Kelly, Gary A. Bellus, Joshua D Green, Raza Zaidi, Taylor Kerrins +5 more

Genomics in nephrology: identifying informatics opportunities to improve diagnosis of genetic kidney disorders using a human-centered design approach

Journal of the American Medical Informatics Association(2024)10.1093/jamia/ocae053

N/A

0DataRank · unranked

0 citations

Zachary Salvati, Darren K. Johnson, Heather M. Ramey, Alex R. Chang, Marc S. Williams +1 more

Using Coincidence Analysis to Identify Causal Chains of Factors Associated with Implementation and Optimization of Lynch Syndrome Tumor Screening Across Multiple Health care Systems

medRxiv(2024)10.1101/2024.02.22.24301533

N/A

0DataRank · unranked

0 citations

Zachary M Salvati, Jennifer L. Schneider, Andrea N. Burnett‐Hartman, Mara M. Epstein, Jessica Ezzell Hunter +9 more

Contributors

Genomic and Personalized Medicine(2013)10.1016/b978-0-12-382227-7.00124-5

N/A

0DataRank · unranked

0 citations

Minhaz Uddin Ahmed, Sun Hee Ahn, R. Rand Allingham, Jude Alsarraj, Matthew L. Anderson +228 more

Penetrance of breast cancer genes from the eMERGE III Network

10.1101/2021.04.24.21255936

Top 100%

0DataRank

Top 100%0 citations

Julia Wynn, Ning Shang, Cong Liu, Alexander Fedotov, Miranda L.G. Hallquist +24 more

Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic Groups

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.04.002

N/A

0DataRank · unranked

175 citations

Daniel J. Schaid, Matthew Kosel, Robert J. Carroll, Christopher G. Chute, Joshua C. Denny +17 more

Clinical outcomes of a genomic screening program for actionable genetic conditions

Genetics in Medicine(2020)10.1038/s41436-020-0876-4

N/A

0DataRank · unranked

154 citations

H. Lester Kirchner, M. Schwartz, Melissa Kelly, Tara Schmidlen, Laney K. Jones +15 more

Management of Secondary Genomic Findings

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.05.002

N/A

0DataRank · unranked

60 citations

Robert L. Nussbaum, Benjamin D. Solomon, Heidi L. Rehm, Marc S. Williams, Leslie G. Biesecker +1 more

Barriers, facilitators, and solutions to familial hypercholesterolemia treatment

PLoS ONE(2020)10.1371/journal.pone.0244193

N/A

0DataRank · unranked

50 citations

Amy C. Sturm, Terry Seaton, Christina Gregor, Samuel S. Gidding, Marc S. Williams +2 more

Functional biology of the Steel syndrome founder allele and evidence for clan genomics derivation of COL27A1 pathogenic alleles worldwide

European Journal of Human Genetics(2020)10.1038/s41431-020-0632-x

N/A

0DataRank · unranked

40 citations

Gözde Yeşil, Harikiran Nistala, Alper Gezdirici, Yavuz Bayram, Kalyan C. Nannuru +32 more

Genetic testing and employer‐sponsored wellness programs: An overview of current vendors, products, and practices

Molecular Genetics & Genomic Medicine(2020)10.1002/mgg3.1414

N/A

0DataRank · unranked

23 citations

Jennifer K. Wagner, Patricia A. Deverka, Laura Woods, Josh F. Peterson, Marc S. Williams +1 more

Loci identified by a genome‐wide association study of carotid artery stenosis in the eMERGE network

Genetic Epidemiology(2020)10.1002/gepi.22360

N/A

0DataRank · unranked

10 citations

Daniel Seung Kim, David R. Crosslin, Ian B. Stanaway, Elisabeth A. Rosenthal, David Carrell +19 more

A standardized, evidence-based protocol to assess clinical actionability of genetic disorders associated with genomic variation

UNC Libraries(2020)10.17615/0tee-nv95

N/A

0DataRank · unranked

1 citations

Christa Lese Martin, Evans, James P., Meredith Weaver, Katrina A.B. Goddard, Margaret Piper +19 more

Evaluation of a Multidisciplinary Lipid Clinic to Improve the Care of Individuals With Severe Lipid Conditions: a RE-AIM Framework Analysis

Research Square(2020)10.21203/rs.3.rs-51142/v1

N/A

0DataRank · unranked

0 citations

Megan McMinn, David Kann, Michael Lesko, Amy C. Sturm, Nicole Walters +7 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

Marc S. Williams

Indexed papers

Top data-sharing exemplar

Papers