Marc S. Williams - Publications, H-index & Citations

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Marc S. Williams

Geisinger

65H-index

561Paper Count

1.9WCitation Count

Published Papers 146

Publication Date

Assessing the views and opinions of psychiatric patients receiving genome-guided treatment within the scope of the PREPARE preemptive pharmacogenomics clinical study

Frontiers in Pharmacology

IF4.8

2025-11-21

OAAI

Margarita-Ioanna Koufaki; Maria-Theodora Pandi; Maria Skokou; Kariofyllis Karamperis; Konstantinos Vasileiou; Christina Mitropoulou; Marc S. Williams; George P. Patrinos

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Advancing the science of genomic learning healthcare systems

Learning Health Systems

IF2.6

2025-07-23

OAAI

Teri A. Manolio; Renee Rider; Carol J. Bult; Rex L. Chisholm; Patricia A. Deverka; Geoffrey S. Ginsburg; Eric D. Green; Gail P. Jarvik; George A. Mensah; Jahnavi Narula; Erin M. Ramos; Mary V. Relling; Dan M. Roden; Robb Rowley; Noura S. Abul-Husn; Adam H. Buchanan; Christopher G. Chute; Guilherme Del Fiol; Gai Elhanan; Susanne B. Haga; Rizwan Hamid; Carol R. Horowitz; Peter J. Hulick; Cynthia A. James; Janina M. Jeff; Bruce Korf; Latrice Landry; Deven McGraw; Howard L. McLeod; Nancy J. Mendelsohn; Travis Osterman; Casey Overby Taylor; Daryl Pritchard; Heidi L. Rehm; Krystal S. Tsosie; Jason L. Vassy; Karriem Watson; Ken Wiley Jr; Marc S. Williams

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Genomic Screening at a Single Health System

JAMA NETWORK OPEN

IF9.7

2025-03-17

OAAI

Savatt, Juliann M.; Kelly, Melissa A.; Sturm, Amy C.; Mccormick, Cara Z.; Williams, Marc S.; Nixon, Michelle Pistner; Rolston, David D.; Strande, Natasha T.; Wain, Karen E.; Willard, Huntington F.; Faucett, W. Andrew; Ledbetter, David H.; Buchanan, Adam H.; Martin, Christa L.

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Performance of recommended management among pediatric patients identified through genomic screening

TRANSLATIONAL BEHAVIORAL MEDICINE

IF3

2025-01-01

PREAI

Savatt, Juliann M.; Urban, Gretchen M.; Floyd, Alyson E.; Leitzel, Tracey; Murray, John A. C.; Hu, Yirui; Williams, Marc S.; Buchanan, Adam H.

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Phenotypic findings associated with variation in elastin

HUMAN GENETICS AND GENOMICS ADVANCES

IF3.6

2025-01-01

OAAI

Justice, Anne; Kelly, Melissa A.; Bellus, Gary; Green, Joshua D.; Zaidi, Raza; Kerrins, Taylor; Josyula, Navya; Luperchio, Teresa R.; Kozel, Beth A.; Williams, Marc S.

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An Implementation Strategy Package to Improve Familial Hypercholesterolemia Recognition in Primary Care: The CAREFH Study

CIRCULATION

IF38.6

2024-11-12

PREAI

Gidding, Samuel; Jones, Laney; Cawley, Dylan; Carr, Lauren; Colonie, Ryan; Romagnoli, Katrina; Kirchner, H. Lester; Hu, Yirui; Williams, Marc

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

GENETICS IN MEDICINE

IF6.2

2024-10-01

PREAI

Cragun, Deborah; Salvati, Zachary M.; Schneider, Jennifer L.; Burnett-Hartman, Andrea N.; Epstein, Mara M.; Hunter, Jessica Ezzell; Liang, Su-Ying; Lowery, Jan; Lu, Christine Y.; Pawloski, Pamala A.; Schlieder, Victoria; Sharaf, Ravi N.; Williams, Marc S.; Rahm, Alanna Kulchak

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

GENETICS IN MEDICINE

IF6.2

2024-08-01

PREAI

Pak, Christine M.; Gilmore, Marian J.; Bulkley, Joanna E.; Chakraborty, Pranesh; Dagan-Rosenfeld, Orit; Foreman, Ann Katherine M.; Gollob, Michael H.; Jenkins, Charisma L.; Katz, Alexander E.; Lee, Kristy; Meeks, Naomi; O'Daniel, Julianne M.; Posey, Jennifer E.; Rego, Shannon M.; Shah, Neethu; Steiner, Robert D.; Stergachis, Andrew B.; Subramanian, Sai Lakshmi; Trotter, Tracy; Wallace, Kathleen; Williams, Marc S.; Goddard, Katrina A. B.; Buchanan, Adam H.; Manickam, Kandamurugu; Powell, Bradford; Hunter, Jessica Ezzell

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

JOURNAL OF CLINICAL LIPIDOLOGY

IF4.6

2024-03-01

OAAI

Jones, Laney K.; Romagnoli, Katrina M.; Schubert, Tyler J.; Clegg, Katarina; Kirchner, H. Lester; Hu, Yirui; Cawley, Dylan; Norelli, Victoria; Williams, Marc S.; Gidding, Samuel S.; Rahm, Alanna K.

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Should secondary pharmacogenomic variants be actively screened and reported when diagnostic genome-wide sequencing is performed in a child?

GENETICS IN MEDICINE

IF6.2

2024-02-01

OAAI

Friedman, Jan M.; Bombard, Yvonne; Carleton, Bruce; Issa, Amalia M.; Knoppers, Bartha; Plon, Sharon E.; Rahimzadeh, Vasiliki; V. Relling, Mary; Williams, Marc S.; van Karnebeek, Clara; Vears, Danya; Cornel, Martina C.

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Low adenoma burden in unselected patients with a pathogenic APC variant

GENETICS IN MEDICINE

IF6.2

2023-12-01

PREAI

Schwiter, Rachel; Rocha, Heather; Johns, Alicia; Savatt, Juliann M.; Diehl, David L.; Kelly, Melissa A.; Williams, Marc S.; Buchanan, Adam H.

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Using Implementation Science to Develop a Familial Hypercholesterolemia Screening Program in Primary Care: The CAREFH Study

CIRCULATION

IF38.6

2023-11-07

PREAI

Jones, Laney K.; Romagnoli, Katrina M.; Schubert, Tyler J.; Clegg, Katarina; Kirchner, H. Lester; Hu, Yirui; Cawley, Dylan; Norelli, Victoria; Williams, Marc S.; Gidding, Sam S.; Rahm, Alanna Kulchak

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Population Genomic Screening for Three Common Hereditary Conditions Response

ANNALS OF INTERNAL MEDICINE

IF15.2

2023-11-01

PREAI

Peterson, Josh F.; Veenstra, David L.; Williams, Marc S.; Hao, Jing; Guzauskas, Gregory F.

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Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2023-11-01

OAAI

Linder, Jodell E.; Tao, Ran; Chung, Wendy K.; Kiryluk, Krzysztof; Liu, Cong; Weng, Chunhua; Connolly, John J.; Hakonarson, Hakon; Harr, Margaret; Leppig, Kathleen A.; Jarvik, Gail P.; Veenstra, David L.; Aufox, Sharon; Chisholm, Rex L.; Gordon, Adam S.; Hoell, Christin; Rasmussen-Torvik, Laura J.; Smith, Maureen E.; Holm, Ingrid A.; Miller, Erin M.; Prows, Cynthia A.; Elskeally, Omar; Kullo, Iftikhar J.; Lee, Christopher; Jose, Sheethal; Manolio, Teri A.; Rowley, Robb; Padi-Adjirackor, Nana Addo; Wilmayani, Ni Ketut; City, Brittany; Wei, Wei-Qi; Wiesner, Georgia L.; Rahm, Alanna Kulchak; Williams, Janet L.; Williams, Marc S.; Peterson, Josh F.

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Evaluation of Malignant Hyperthermia Features in Patients with Pathogenic or Likely Pathogenic RYR1 Variants Disclosed through a Population Genomic Screening Program

ANESTHESIOLOGY

IF9.1

2023-10-03

PREAI

Yu, Kristen D.; Betts, Megan N.; Urban, Gretchen M.; Schwartz, Marci L. B.; Robinson, Tanisha O.; Moyer, Robert J.; Taddonio, Scott W.; Vasudevan, Anasuya; Johns, Alicia; Sturm, Amy C.; Kelly, Melissa A.; Williams, Marc S.; Poler, S. Mark; Buchanan, Adam H.

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Yield of Familial Hypercholesterolemia Genetic and Phenotypic Diagnoses After Electronic Health Record and Genomic Data Screening

JOURNAL OF THE AMERICAN HEART ASSOCIATION

IF5.3

2023-07-04

OAAI

Gidding, Samuel S.; Kirchner, H. Lester; Brangan, Andrew; Howard, William; Kelly, Melissa A.; Myers, Kelly D.; Morgan, Kelly M.; Oetjens, Matthew T.; Shuey, Timothy C.; Staszak, David; Strande, Natasha T.; Walters, Nicole L.; Yu, Kristen D. D.; Wilemon, Katherine A.; Williams, Marc S.; Sturm, Amy C.; Jones, Laney K.

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Population Genomic Screening for Three Common Hereditary Conditions A Cost-Effectiveness Analysis

ANNALS OF INTERNAL MEDICINE

IF15.2

2023-05-01

PREAI

Guzauskas, Gregory F.; Garbett, Shawn; Zhou, Zilu; Schildcrout, Jonathan S.; Graves, John A.; Williams, Marc S.; Hao, Jing; Jones, Laney K.; Spencer, Scott J.; Jiang, Shangqing; Veenstra, David L.; Peterson, Josh F.

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Familial Hypercholesterolemia in the Electronic Medical Records and Genomics Network: Prevalence, Penetrance, Cardiovascular Risk, and Outcomes After Return of Results

CIRCULATION-GENOMIC AND PRECISION MEDICINE

IF5.5

2023-04-01

OAAI

Dikilitas, Ozan; Sherafati, Alborz; Saadatagah, Seyedmohammad; Satterfield, Benjamin A.; Kochan, David C.; Anderson, Katherine C.; Chung, Wendy K.; Hebbring, Scott J.; Salvati, Zachary M.; Sharp, Richard R.; Sturm, Amy C.; Gibbs, Richard A.; Rowley, Robb; Venner, Eric; Linder, Jodell E.; Jones, Laney K.; Perez, Emma F.; Peterson, Josh F.; Jarvik, Gail P.; Rehm, Heidi L.; Zouk, Hana; Roden, Dan M.; Williams, Marc S.; Manolio, Teri A.; Kullo, Iftikhar J.

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

SCIENTIFIC REPORTS

IF3.9

2023-02-03

OAAI

Pacheco, Jennifer A.; Rasmussen, Luke V.; Wiley Jr, Ken; Person, Thomas Nate; Cronkite, David J.; Sohn, Sunghwan; Murphy, Shawn; Gundelach, Justin H.; Gainer, Vivian; Castro, Victor M.; Liu, Cong; Mentch, Frank; Lingren, Todd; Sundaresan, Agnes S.; Eickelberg, Garrett; Willis, Valerie; Furmanchuk, Al'ona; Patel, Roshan; Carrell, David S.; Deng, Yu; Walton, Nephi; Satterfield, Benjamin A.; Kullo, Iftikhar J.; Dikilitas, Ozan; Smith, Joshua C.; Peterson, Josh F.; Shang, Ning; Kiryluk, Krzysztof; Ni, Yizhao; Li, Yikuan; Nadkarni, Girish N.; Rosenthal, Elisabeth A.; Walunas, Theresa L.; Williams, Marc S.; Karlson, Elizabeth W.; Linder, Jodell E.; Luo, Yuan; Weng, Chunhua; Wei, WeiQi

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The Reckoning: The Return of Genomic Results to 1444 Participants Across the eMERGE3 Network

OBSTETRICAL & GYNECOLOGICAL SURVEY

IF3.6

2022-11-01

PREAI

Leppig, Kathleen A.; Rahm, Alanna Kulchak; Appelbaum, Paul; Aufox, Sharon; Bland, Sarah T.; Buchanan, Adam; Christensen, Kurt D.; Chung, Wendy K.; Clayton, Ellen Wright; Crosslin, David; Denny, Josh; DeVange, Shannon; Gordon, Adam; Green, Robert C.; Hakonarson, Hakon; Harr, Margaret H.; Henrikson, Nora; Hoell, Christin; Holm, Ingrid A.; Kullo, Iftikhar J.; Jarvik, Gail P.; Lammers, Philip E.; Larson, Eric B.; Lindor, Noralane M.; Marasa, Maddalena; Myers, Melanie F.; Perez, Emma; Peterson, Josh F.; Pratap, Siddharth; Prows, Cynthia A.; Ralston, James D.; Rasouly, Hila Milo; Roden, Dan M.; Sharp, Richard R.; Singh, Rajbir; Shaibi, Gabriel; Smith, Maureen E.; Sturm, Amy; Thiese, Heidi A.; Van Driest, Sara L.; Williams, Janet; Williams, Marc S.; Wynn, Julia; Blout Zawatsky, Carrie L.; Wiesner, Georgia L.

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Research Directions