Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

137 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Digital Health Tools in Genomics: Advancing Diversity, Equity, and Inclusion.
Assamad D, Majeed S, Aguda V, Grewal S, Butkowsky C, Clausen M, D'Amours G, Bombard Y. Assamad D, et al. Among authors: bombard y. Public Health Genomics. 2023;26(1):194-200. doi: 10.1159/000534804. Epub 2023 Oct 26. Public Health Genomics. 2023. PMID: 37883926 Free article. No abstract available.
"Game Changer": Health Professionals' Views on the Clinical Utility of Circulating Tumor DNA Testing in Hereditary Cancer Syndrome Management.
Shickh S, Oldfield LE, Clausen M, Mighton C, Sebastian A, Calvo A, Baxter NN, Dawson L, Penney LS, Foulkes W, Basik M, Sun S, Schrader KA, Regier DA, Karsan A, Pollett A, Pugh TJ, Kim RH, Bombard Y; CHARM Consortium. Shickh S, et al. Among authors: bombard y. Oncologist. 2022 May 6;27(5):e393-e401. doi: 10.1093/oncolo/oyac039. Oncologist. 2022. PMID: 35385106 Free PMC article.
Genetics Adviser: The development and usability testing of a new patient digital health application to support clinical genomic testing.
Clausen M, Krishnapillai S, Hirjikaka D, Kodida R, Shickh S, Reble E, Mighton C, Sam J, Adi-Wauran E, Baxter NN, Feldman G, Glogowski E, Lerner-Ellis J, Scheer A, Shastri-Estrada S, Shuman C, Armel SR, Aronson M, Graham T, Panchal S, Thorpe KE, Carroll JC, Eisen A, Elser C, Kim RH, Faghfoury H, Schrader KA, Seto E, Bombard Y. Clausen M, et al. Among authors: bombard y. Genet Med Open. 2024 Jan 23;2:101814. doi: 10.1016/j.gimo.2024.101814. eCollection 2024. Genet Med Open. 2024. PMID: 39669596 Free PMC article.
Clinical Utility of Genomic Sequencing for Hereditary Cancer Syndromes: An Observational Cohort Study.
Shickh S, Mighton C, Clausen M, Sam J, Hirjikaka D, Reble E, Graham T, Panchal S, Eisen A, Elser C, Schrader KA, Baxter NN, Laupacis A, Lerner-Ellis J, Kim RH, Bombard Y; Incidental Genomics Study Team. Shickh S, et al. Among authors: bombard y. JCO Precis Oncol. 2024 Dec;8:e2400407. doi: 10.1200/PO-24-00407. Epub 2024 Dec 12. JCO Precis Oncol. 2024. PMID: 39666930
Offering complex genomic screening in acute pediatric settings: Family decision-making and outcomes.
Martyn M, Lee L, Jan A, Tytherleigh R, Lynch F, Mighton C, Bouffler SE, Lynch E, Macciocca I, Curnow L, McCorkell G, Lunke S, Chong B, Delatycki MB, Downie L, Vears D, Best S, Clausen M, Bombard Y, Stark Z, Gaff C. Martyn M, et al. Among authors: bombard y. Genet Med. 2024 Nov 14;27(2):101327. doi: 10.1016/j.gim.2024.101327. Online ahead of print. Genet Med. 2024. PMID: 39548854 Free article.
Opportunistic genomic screening has clinical utility: An interventional cohort study.
Mighton C, Kodida R, Shickh S, Clausen M, Reble E, Sam J, Grewal S, Hirjikaka D, Panchal S, Piccinin C, Aronson M, Ward T, Armel SR, Hofstedter R, Graham T, Mancuso T, Forster N, Capo-Chichi JM, Greenfeld E, Noor A, Cohn I, Morel CF, Elser C, Eisen A, Carroll JC, Glogowksi E, Schrader KA, Chan KKW, Thorpe KE, Lerner-Ellis J, Kim RH, Bombard Y; Incidental Genomics Study Team. Mighton C, et al. Among authors: bombard y. Genet Med. 2024 Nov 8:101323. doi: 10.1016/j.gim.2024.101323. Online ahead of print. Genet Med. 2024. PMID: 39530317
"Should I Let Them Know I Have This?": Multifaceted Genetic Discrimination and Limited Awareness of Legal Protections among Individuals with Hereditary Cancer Syndromes.
Gopalakrishnan R, Sam J, Butkowsky C, Reble E, Clausen M, Rajeziesfahani S, Sparkes B, Aguda V, Aronson M, Bishop D, Dawson L, Eisen A, Graham T, Green J, Mighton C, Pauling J, Pavao C, Pechlivanoglou P, Remocker C, Savas S, Sun S, Tiano T, Tilley A, Schrader K, Etchegary H, Bombard Y. Gopalakrishnan R, et al. Among authors: bombard y. Public Health Genomics. 2024;27(1):240-254. doi: 10.1159/000542210. Epub 2024 Oct 24. Public Health Genomics. 2024. PMID: 39447549 Free article.
The Key Features of a Genetic Nondiscrimination Policy: A Delphi Consensus Statement.
Uberoi D, Dalpé G, Cheung K, Kondrup E, Palmour N, Arawi T, Arych M, Ramiro Aviles MA, Ayuso C, Bentzen HB, Blizinsky K, Bombard Y, Chandrasekharan S, Chung BHY, de Paor A, Doerr M, Dove ES, Dupras C, Granados-Moreno P, Greenbaum D, Gunnarsdóttir HD, Haidar H, Ho CH, Jamuar SS, Kim H, Lebret A, Macdonald A, Minssen T, Nasir J, Nicol D, Nicolás P, Otlowski M, Nair APS, Prince AER, Rothstein M, Ryan R, Sillon G, Singh KK, Stedman I, Tiller J, Van Hoyweghen I, Zawati MH, Joly Y. Uberoi D, et al. Among authors: bombard y. JAMA Netw Open. 2024 Sep 3;7(9):e2435355. doi: 10.1001/jamanetworkopen.2024.35355. JAMA Netw Open. 2024. PMID: 39325459 Free article.
A Genomic Counseling Model for Population-Based Sequencing: A Pre-Post Intervention Study.
Casalino S, Mighton C, Clausen M, Frangione E, Aujla N, MacDonald G, Young J, Fung CYJ, Morgan G, Arnoldo S, Bearss E, Binnie A, Borgundvaag B, Chowdhary S, Dagher M, Devine L, Friedman SM, Hao L, Khan Z, Lane W, Lapadula E, Lebo M, Richardson D, Stern S, Strug L, Taher A, Greenfeld E, Noor A, Faghfoury H, Taher J, Bombard Y, Lerner-Ellis J; GENCOV Study Workgroup. Casalino S, et al. Among authors: bombard y. Genet Med. 2024 Dec;26(12):101272. doi: 10.1016/j.gim.2024.101272. Epub 2024 Sep 17. Genet Med. 2024. PMID: 39301805
137 results