Marc S. Williams

19.4k total citations · 3 hit papers
227 papers, 7.1k citations indexed

About

Marc S. Williams is a scholar working on Genetics, Public Health, Environmental and Occupational Health and Molecular Biology. According to data from OpenAlex, Marc S. Williams has authored 227 papers receiving a total of 7.1k indexed citations (citations by other indexed papers that have themselves been cited), including 114 papers in Genetics, 41 papers in Public Health, Environmental and Occupational Health and 38 papers in Molecular Biology. Recurrent topics in Marc S. Williams's work include Genomics and Rare Diseases (82 papers), BRCA gene mutations in cancer (60 papers) and Health Systems, Economic Evaluations, Quality of Life (33 papers). Marc S. Williams is often cited by papers focused on Genomics and Rare Diseases (82 papers), BRCA gene mutations in cancer (60 papers) and Health Systems, Economic Evaluations, Quality of Life (33 papers). Marc S. Williams collaborates with scholars based in United States, United Kingdom and Canada. Marc S. Williams's co-authors include Heidi L. Rehm, Robert L. Nussbaum, Michael S. Watson, Christa Lese Martin, Leslie G. Biesecker, Jonathan S. Berg, Robert C. Green, Bruce R. Korf, Kelly E. Ormond and Wayne W. Grody and has published in prestigious journals such as The Lancet, JAMA and Journal of Clinical Oncology.

In The Last Decade

Marc S. Williams

219 papers receiving 6.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

2013 1.6k citations Marc S. Williams et al. Genetics in Medicine profile →
Standardizing terms for clinical pharmacogenetic test results: consensus terms from the Clinical Pharmacogenetics Implementation Consortium (CPIC)

2016 354 citations Robert R. Freimuth, Josh F. Peterson et al. Genetics in Medicine profile →
Pharmacogenomics

2019 238 citations Marc S. Williams, Josh F. Peterson et al. profile →

Peers

Countries citing papers authored by Marc S. Williams

Since Specialization

Citations

This map shows the geographic impact of Marc S. Williams's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Marc S. Williams with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marc S. Williams more than expected).

Fields of papers citing papers by Marc S. Williams

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marc S. Williams. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Marc S. Williams. The network helps show where Marc S. Williams may publish in the future.

Co-authorship network of co-authors of Marc S. Williams

This figure shows the co-authorship network connecting the top 25 collaborators of Marc S. Williams. A scholar is included among the top collaborators of Marc S. Williams based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Marc S. Williams. Marc S. Williams is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Genomic Screening at a Single Health System 2025 ·JAMA Network Open ·Juliann M. Savatt, Melissa Kelly, Amy C. Sturm, Cara Z. McCormick, Marc S. Williams, (unknown), David D.K. Rolston, Natasha T. Strande, Karen E. Wain, Huntington F. Willard, W. Andrew Faucett, (unknown), Adam H. Buchanan, Alastair J. Martin	5
2	Using implementation science to develop a familial hypercholesterolemia screening program in primary care: The CARE-FH study 2024 ·Journal of clinical lipidology ·Laney K. Jones, (unknown), (unknown), (unknown), H. Lester Kirchner, Yirui Hu, (unknown), (unknown), Marc S. Williams, Samuel S. Gidding, Alanna Kulchak Rahm	3
3	Yield of Familial Hypercholesterolemia Genetic and Phenotypic Diagnoses After Electronic Health Record and Genomic Data Screening 2023 ·Journal of the American Heart Association ·Samuel S. Gidding, H. Lester Kirchner, (unknown), William H. Howard, Melissa Kelly, Kelly D. Myers, (unknown), Matthew T. Oetjens, (unknown), (unknown), Natasha T. Strande, (unknown), (unknown), Katherine Wilemon, Marc S. Williams, Amy C. Sturm, Laney K. Jones	7
4	Evaluation of Malignant Hyperthermia Features in Patients with Pathogenic or Likely Pathogenic RYR1 Variants Disclosed through a Population Genomic Screening Program 2023 ·Anesthesiology ·(unknown), (unknown), (unknown), M. Schwartz, (unknown), (unknown), (unknown), (unknown), (unknown), Amy C. Sturm, Melissa Kelly, Marc S. Williams, S. Mark Poler, Adam H. Buchanan	6
5	Low adenoma burden in unselected patients with a pathogenic APC variant 2023 ·Genetics in Medicine ·(unknown), Heather Rocha, (unknown), Juliann M. Savatt, David L. Diehl, Melissa Kelly, Marc S. Williams, Adam H. Buchanan	1
6	Collaborative Approach to Reach Everyone with Familial Hypercholesterolemia: CARE-FH Protocol 2022 ·Journal of Personalized Medicine ·Laney K. Jones, Marc S. Williams, Ilene Ladd, (unknown), (unknown), Jing Hao, (unknown), Yirui Hu, H. Lester Kirchner, (unknown), (unknown), (unknown), Alanna Kulchak Rahm, David D.K. Rolston, (unknown), (unknown), (unknown), Amy C. Sturm, Samuel S. Gidding	9
7	Impact of a Population Genomic Screening Program on Health Behaviors Related to Familial Hypercholesterolemia Risk Reduction 2022 ·Circulation Genomic and Precision Medicine ·Laney K. Jones, Nan Chen, (unknown), (unknown), (unknown), Dustin N. Hartzel, David L. Veenstra, Scott Spencer, Susan Snyder, Josh F. Peterson, (unknown), Amy C. Sturm, Samuel S. Gidding, Marc S. Williams, Jing Hao	3
8	User testing of a diagnostic decision support system with machine-assisted chart review to facilitate clinical genomic diagnosis 2021 ·BMJ Health & Care Informatics ·Alanna Kulchak Rahm, Nephi Walton, (unknown), (unknown), (unknown), Thomas N. Person, (unknown), (unknown), Peter N. Robinson, (unknown), Marc S. Williams, Michael M. Segal	7
9	Cost-effectiveness analysis of genotyping for HLA-B15:02 in Indonesian patients with epilepsy using a generic model 2021 ·The Pharmacogenomics Journal* ·Rika Yuliwulandari, Jae Gook Shin, Erna Kristin, (unknown), (unknown), (unknown), Surakameth Mahasirimongkol, Larisa H. Cavallari, Christina Mitropoulou, George P. Patrinos, Jing Hao, Marc S. Williams, Susan Snyder	11
10	Atypical presentation of a vertical penile fracture 2021 ·BMJ Case Reports ·(unknown), (unknown), (unknown), Marc S. Williams	1
11	Exome-Wide Analysis of the DiscovEHR Cohort Reveals Novel Candidate Pharmacogenomic Variants for Clinical Pharmacogenomics 2020 ·Genes ·(unknown), Marc S. Williams, Peter J. van der Spek, Maria Koromina, George P. Patrinos	4
12	Robot-assisted orthotopic “W” ileal neobladder in male patients: step-by-step video-illustrated technique and preliminary outcomes 2020 ·Journal of Robotic Surgery ·François‐Xavier Nouhaud, Marc S. Williams, William Yaxley, (unknown), Marlon Perera, Isaac Thangasamy, Rachel Esler, Geoffrey D. Coughlin	2
13	Prototype Development: Context-Driven Dynamic XML Ophthalmologic Data Capture Application 2017 ·JMIR Medical Informatics ·Peggy Peissig, (unknown), (unknown), (unknown), (unknown), Catherine A. McCarty, (unknown), (unknown), Jennifer A. Pacheco, Jyotishman Pathak, Stephen B. Ellis, Joshua C. Denny, Luke V. Rasmussen, Gerard Tromp, Marc S. Williams, Tamara R. Vrabec, Murray H. Brilliant	2
14	Practical considerations for implementing genomic information resources 2016 ·Applied Clinical Informatics ·Casey Lynnette Overby, John J. Connolly, Christopher G. Chute, Joshua C. Denny, Robert R. Freimuth, Andrea L. Hartzler, Ingrid A. Holm, Shannon Manzi, Jyotishman Pathak, Peggy Peissig, Maureen E. Smith, Marc S. Williams, Brian H. Shirts, Elena M. Stoffel, Peter Tarczy‐Hornoch, Carolyn R. Rohrer Vitek, Wendy A. Wolf, Justin Starren, Luke V. Rasmussen	22
15	User-centered design of multi-gene sequencing panel reports for clinicians 2016 ·Journal of Biomedical Informatics ·(unknown), (unknown), Amber L. Beitelshees, James J. Cimino, Guilherme Del Fiol, Ayşe P. Gürses, Mark A. Hoffman, Linda Jo Bone Jeng, Kensaku Kawamoto, Mark D. Kelemen, Harold Alan Pincus, Alan R. Shuldiner, Marc S. Williams, Toni I. Pollin, Casey Lynnette Overby	15
16	Implementation of genomic medicine in a health care delivery system: A value proposition? 2014 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·(unknown), David H. Ledbetter, Marc S. Williams	12
17	Building Global Democracy? 2011 ·Cambridge University Press eBooks ·Jan Aart Scholte, Kerstin Martens, Alnoor Ebrahim, Marc S. Williams, Timothy M. Shaw, Saied Reza Ameli, Morten Ougaard, Peter I. Hajnal, Julie Gilson, Peter Newell, (unknown), (unknown), (unknown)	116
18	Community-Centered Family Health History: A Customized Approach to Increased Health Communication and Awareness 2011 ·Progress in community health partnerships ·James O’Leary, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Marc S. Williams, Sharon F. Terry, Deborah J. Bowen	18
19	Comparison of compliance for colorectal cancer screening and surveillance by colonoscopy based on risk 2011 ·Genetics in Medicine ·David P. Taylor, Lisa Cannon‐Albright, Carol Sweeney, Marc S. Williams, Peter J. Haug, Joyce A. Mitchell, Randall W. Burt	56
20	Clinician Perspectives about Molecular Genetic Testing for Heritable Conditions and Development of a Clinician-Friendly Laboratory Report 2009 ·Journal of Molecular Diagnostics ·Ira M. Lubin, Margaret M. McGovern, (unknown), Susan J. Gross, Elaine Lyon, Roberta A Pagon, Victoria M. Pratt, (unknown), Colleen Shaw, (unknown), Tracy L. Trotter, Marc S. Williams, Jean Amos Wilson, Kenneth A. Pass	41

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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