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

Marc S. Williams

Geisinger

65H指数

562论文数

1.9W被引数

收录论文 147

发表时间

Prevalence and significance of family history of kidney disease in the electronic health record in three United States health systems 电子健康记录中三个美国医疗体系中肾脏病家族史的发生率及意义

Kidney International

IF12.6

2026-09-28

PREAI

Andrei Bucaloiu; Aditya Surapaneni; Sneha Mehta; Richard Bradshaw; Yirui Hu; Morgan E. Grams; Marc S. Williams; Guilherme Del Fiol; Kensaku Kawamoto; Alexander R. Chang

Assessing the views and opinions of psychiatric patients receiving genome-guided treatment within the scope of the PREPARE preemptive pharmacogenomics clinical study 评估PREPARE抢先药理基因组学临床研究中接受基因组指导治疗的精神性疾病患者（psychiatric patients）的观点和意见

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

Advancing the science of genomic learning healthcare systems 推进基因组学习型医疗系统的科学

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

Genomic Screening at a Single Health System 单一医疗系统的基因组筛查

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.

Performance of recommended management among pediatric patients identified through genomic screening 通过基因组筛查识别的儿科患者中推荐管理措施的执行情况

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.

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.

An Implementation Strategy Package to Improve Familial Hypercholesterolemia Recognition in Primary Care: The CAREFH Study 一项旨在提高初级保健中家族性高胆固醇血症识别率的实施策略方案：CAREFH研究

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

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

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

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.

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.

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.

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

Population Genomic Screening for Three Common Hereditary Conditions Response 三种常见遗传条件反应的群体基因组筛选

ANNALS OF INTERNAL MEDICINE

IF15.2

2023-11-01

PREAI

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

Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing 临床测序可采取的单基因结果后医疗保健利用的前瞻性，多站点研究

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.

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.

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.

Population Genomic Screening for Three Common Hereditary Conditions A Cost-Effectiveness Analysis 三种常见遗传条件的群体基因组筛查成本效益分析

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.

Familial Hypercholesterolemia in the Electronic Medical Records and Genomics Network: Prevalence, Penetrance, Cardiovascular Risk, and Outcomes After Return of Results 电子病历和基因组学网络中的家族性高胆固醇血症: 患病率，外显率，心血管风险和结果返回后的结果

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.

Evaluation of the portability of computable phenotypes with natural language processing in the eMERGE network 在eMERGE网络中使用自然语言处理评估可计算表型的可移植性

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

研究方向