Marc S Williams
Overview
Explore the profile of Marc S Williams including associated specialties, affiliations and a list of published articles.
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Articles
252
Citations
7058
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Recent Articles
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Manolio T, Narula J, Rupert A, Bult C, Chisholm R, Ginsburg G, et al.
Am J Hum Genet
. 2024 Dec;
111(12):2585-2588.
PMID: 39642866
No abstract available.
3.
Justice A, Kelly M, Bellus G, Green J, Zaidi R, Kerrins T, et al.
HGG Adv
. 2024 Nov;
6(1):100388.
PMID: 39604264
Variation in the elastin gene (ELN) may contribute to connective tissue disease beyond the known disease associations of supravalvar aortic stenosis and cutis laxa. Exome data from MyCode Community Health...
4.
Baker A, Goehringer J, Woltz M, Romagnoli K, Campbell-Salome G, Sturm A, et al.
Public Health Genomics
. 2024 Nov;
27(1):197-209.
PMID: 39501610
Introduction: Previous research indicates that population genomic screening can benefit individuals who act on the genetic results. However, there remains a significant gap between individuals receiving genetic information and acting...
5.
Jiang S, Guzauskas G, Garbett S, Graves J, Williams M, Hao J, et al.
Genet Med
. 2024 Oct;
27(2):101285.
PMID: 39360752
Purpose: Genomic screening to identify individuals with Lynch Syndrome (LS) and those with a high polygenic risk score (PRS) promises to personalize colorectal cancer (CRC) screening. Understanding its clinical and...
6.
Justice A, Kelly M, Bellus G, Green J, Zaidi R, Kerrins T, et al.
medRxiv
. 2024 Sep;
PMID: 39314928
Etoc Blurb: Carriers of variants of interest in the elastin gene ( ) were evaluated for presence of findings that could be associated with the variation. Chart review and Phenome-wide...
7.
Cragun D, Salvati Z, Schneider J, Burnett-Hartman A, Epstein M, Hunter J, et al.
Genet Med
. 2024 Jul;
26(10):101201.
PMID: 38953292
Purpose: This study compared Lynch syndrome universal tumor screening (UTS) across multiple health systems (some of which had 2 or more distinct UTS programs) to understand multilevel factors that may...
8.
Pak C, Gilmore M, Bulkley J, Chakraborty P, Dagan-Rosenfeld O, Foreman A, et al.
Genet Med
. 2024 May;
26(8):101164.
PMID: 38757444
Purpose: The ClinGen Actionability Working Group (AWG) developed an evidence-based framework to generate actionability reports and scores of gene-condition pairs in the context of secondary findings from genome sequencing. Here...
9.
Johnson D, Del Fiol G, Kawamoto K, Romagnoli K, Sanders N, Isaacson G, et al.
J Am Med Inform Assoc
. 2024 Apr;
31(5):1183-1194.
PMID: 38558013
Objectives: Patient care using genetics presents complex challenges. Clinical decision support (CDS) tools are a potential solution because they provide patient-specific risk assessments and/or recommendations at the point of care....
10.
Baglaenko Y, Wagner C, Bhoj V, Brodin P, Gershwin M, Graham D, et al.
Camb Prism Precis Med
. 2024 Mar;
1:e25.
PMID: 38550937
Precision Medicine is an emerging approach for disease treatment and prevention that takes into account individual variability in genes, environment, and lifestyle. Autoimmune diseases are those in which the body's...