Bibliotecas PUC-SP - Busca Integrada

On the launch of Genetics in Medicine Open: Disseminating knowledge and wisdom in genomic medicine

per Robert G. Best, Marc S. Williams
Publicat a Genetics in Medicine Open (2023-01-01)

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

per Kee Chan, Amy Brower, Marc S. Williams
Publicat a Frontiers in Genetics (2022-09-01)

Beyond the hype of big data and artificial intelligence: building foundations for knowledge and wisdom

per Josip Car, Aziz Sheikh, Paul Wicks, Marc S. Williams
Publicat a BMC Medicine (2019-07-01)

Geisinger's effort to realize its potential as a learning health system: A progress report

per F. Daniel Davis, Marc S. Williams, Rebecca A. Stametz
Publicat a Learning Health Systems (2021-04-01)

Polycystic Ovary Syndrome Susceptibility Loci Inform Disease Etiological Heterogeneity

per Yanfei Zhang, Vani C. Movva, Marc S. Williams, Ming Ta Michael Lee
Publicat a Journal of Clinical Medicine (2021-06-01)

Are providers prepared for genomic medicine: interpretation of Direct-to-Consumer genetic testing (DTC-GT) results and genetic self-efficacy by medical professionals

per Scott P. McGrath, Nephi Walton, Marc S. Williams, Katherine K. Kim, Kiran Bastola
Publicat a BMC Health Services Research (2019-11-01)

Exome-Wide Analysis of the DiscovEHR Cohort Reveals Novel Candidate Pharmacogenomic Variants for Clinical Pharmacogenomics

per Maria-Theodora Pandi, Marc S. Williams, Peter van der Spek, Maria Koromina, George P. Patrinos
Publicat a Genes (2020-05-01)

Implementation of a patient-facing genomic test report in the electronic health record using a web-application interface

per Marc S. Williams, Melissa S. Kern, Virginia R. Lerch, Jonathan Billet, Janet L. Williams, Gregory J. Moore
Publicat a BMC Medical Informatics and Decision Making (2018-05-01)

GSTM1 Copy Number Is Not Associated With Risk of Kidney Failure in a Large Cohort

per Yanfei Zhang, Waleed Zafar, Dustin N. Hartzel, Marc S. Williams, Adrienne Tin, Alex R. Chang, Ming Ta Michael Lee
Publicat a Frontiers in Genetics (2019-08-01)

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

per Whitney S. McDonald, Jennifer K. Wagner, Patricia A. Deverka, Laura A. Woods, Josh F. Peterson, Marc S. Williams
Publicat a Molecular Genetics & Genomic Medicine (2020-10-01)

Dissecting genetic factors affecting phenylephrine infusion rates during anesthesia: a genome-wide association study employing EHR data

per Yanfei Zhang, S. Mark Poler, Jiang Li, Vida Abedi, Sarah A. Pendergrass, Marc S. Williams, Ming Ta Michael Lee
Publicat a BMC Medicine (2019-08-01)

Predicting phenotypic severity of uncertain gene variants in the RET proto-oncogene.

per David K Crockett, Stephen R Piccolo, Perry G Ridge, Rebecca L Margraf, Elaine Lyon, Marc S Williams, Joyce A Mitchell
Publicat a PLoS ONE (2011-03-01)

Barriers, facilitators, and solutions to familial hypercholesterolemia treatment.

per Laney K Jones, Amy C Sturm, Terry L Seaton, Christina Gregor, Samuel S Gidding, Marc S Williams, Alanna Kulchak Rahm
Publicat a PLoS ONE (2020-01-01)

Phenotypic findings associated with variation in elastin

per Anne Justice, Melissa A. Kelly, Gary Bellus, Joshua D. Green, Raza Zaidi, Taylor Kerrins, Navya Josyula, Teresa R. Luperchio, Beth A. Kozel, Marc S. Williams
Publicat a HGG Advances (2025-01-01)

Anxiety, Depression, and Adverse Clinical Outcomes in Patients With Atrial Fibrillation Starting Warfarin: Cardiovascular Research Network WAVE Study

per Christine Baumgartner, Dongjie Fan, Margaret C. Fang, Daniel E. Singer, Daniel M. Witt, John R. Schmelzer, Marc S. Williams, Jerry H. Gurwitz, Sue Hee Sung, Alan S. Go
Publicat a Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease (2018-04-01)

Economic Evaluation of Universal Lynch Syndrome Screening Protocols among Newly Diagnosed Patients with Colorectal Cancer

per Jing Hao, Dina Hassen, James M. Gudgeon, Susan R. Snyder, Heather Hampel, Marc S. Williams, Ravi N. Sharaf, Christine Y. Lu, Janet L. Williams, Victoria Schlieder, Alanna Kulchak Rahm
Publicat a Journal of Personalized Medicine (2021-12-01)

Healthcare Utilization and Costs after Receiving a Positive <i>BRCA1/2</i> Result from a Genomic Screening Program

per Jing Hao, Dina Hassen, Kandamurugu Manickam, Michael F. Murray, Dustin N. Hartzel, Yirui Hu, Kunpeng Liu, Alanna Kulchak Rahm, Marc S. Williams, Amanda Lazzeri, Adam Buchanan, Amy Sturm, Susan R. Snyder
Publicat a Journal of Personalized Medicine (2020-02-01)

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

per Laney K. Jones, Megan McMinn, David Kann, Michael Lesko, Amy C. Sturm, Nicole Walters, Nan Chen, Kerrianne Fry, Ross C. Brownson, Samuel S. Gidding, Marc S. Williams, Alanna Kulchak Rahm
Publicat a Implementation Science Communications (2021-03-01)

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

per Anna Baker, Kasia Tolwinski, Jamie Atondo, F. Daniel Davis, Jessica Goehringer, Laney K. Jones, Cassandra J. Pisieczko, Amy C. Sturm, Janet L. Williams, Marc S. Williams, Alanna Kulchak Rahm, Adam H. Buchanan
Publicat a Journal of Personalized Medicine (2022-09-01)

Variants at the MHC Region Associate With Susceptibility to Clostridioides difficile Infection: A Genome-Wide Association Study Using Comprehensive Electronic Health Records

per Jiang Li, Yanfei Zhang, Alexandria L. Jilg, Donna M. Wolk, Harshit S. Khara, Amy Kolinovsky, David D. K. Rolston, Raquel Hontecillas, Josep Bassaganya-Riera, Marc S. Williams, Vida Abedi, Ming Ta Michael Lee
Publicat a Frontiers in Immunology (2021-03-01)