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

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1961 1
1962 1
1964 1
1965 1
1966 1
1967 1
1980 1
1996 1
2006 2
2007 1
2008 1
2011 1
2012 1
2013 3
2014 1
2015 3
2016 4
2017 2
2018 2
2019 5
2020 5
2021 4
2022 6
2023 5
2024 4
2025 5

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

57 results

Results by year

Filters applied: . Clear all
Page 1
Whole-exome sequencing reveals a monogenic cause in 56% of individuals with laterality disorders and associated congenital heart defects.
Bolkier Y, Barel O, Marek-Yagel D, Atias-Varon D, Kagan M, Vardi A, Mishali D, Katz U, Salem Y, Tirosh-Wagner T, Jacobson JM, Raas-Rothschild A, Chorin O, Eliyahu A, Sarouf Y, Shlomovitz O, Veber A, Shalva N, Javasky E, Ben Moshe Y, Staretz-Chacham O, Rechavi G, Mane S, Anikster Y, Vivante A, Pode-Shakked B. Bolkier Y, et al. Among authors: veber a. J Med Genet. 2022 Jul;59(7):691-696. doi: 10.1136/jmedgenet-2021-107775. Epub 2021 Jul 2. J Med Genet. 2022. PMID: 34215651
The infinitesimal model with dominance.
Barton NH, Etheridge AM, Véber A. Barton NH, et al. Among authors: veber a. Genetics. 2023 Oct 4;225(2):iyad133. doi: 10.1093/genetics/iyad133. Genetics. 2023. PMID: 37450606 Free PMC article.
Mono and Biallelic Variants in TRIM63 Are Frequently Associated With a Unique Form of Hypertrophic Cardiomyopathy.
Ruhrman Shahar N, Marek-Yagel D, Greenberg R, Isakov O, Naftali M, Friedman E, Bazak L, Monakier D, Veber A, Shalva N, Segev A, Haim M, Sagi-Dain L, Benyamini L, Shalata A, Josefsberg Ben Yehoshua S, Basel Salmon L, Hoss S, Ben-Shachar S. Ruhrman Shahar N, et al. Among authors: veber a. Circ Genom Precis Med. 2025 Feb;18(1):e004864. doi: 10.1161/CIRCGEN.124.004864. Epub 2025 Jan 27. Circ Genom Precis Med. 2025. PMID: 39866098 No abstract available.
Decision-making tools for healthcare structures in times of pandemic.
Garaix T, Gaubert S, Josse J, Vayatis N, Véber A. Garaix T, et al. Among authors: veber a. Anaesth Crit Care Pain Med. 2022 Apr;41(2):101052. doi: 10.1016/j.accpm.2022.101052. Epub 2022 Mar 2. Anaesth Crit Care Pain Med. 2022. PMID: 35247640 Free PMC article. No abstract available.
Why do sex chromosomes progressively lose recombination?
Jay P, Jeffries D, Hartmann FE, Véber A, Giraud T. Jay P, et al. Among authors: veber a. Trends Genet. 2024 Jul;40(7):564-579. doi: 10.1016/j.tig.2024.03.005. Epub 2024 Apr 27. Trends Genet. 2024. PMID: 38677904 Review.
Ancestries of a recombining diploid population.
Sainudiin R, Thatte B, Véber A. Sainudiin R, et al. Among authors: veber a. J Math Biol. 2016 Jan;72(1-2):363-408. doi: 10.1007/s00285-015-0886-z. Epub 2015 Apr 30. J Math Biol. 2016. PMID: 25925241
57 results