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 NCBI Filters

Results by year

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

Year Number of Results
2008 1
2009 2
2010 2
2011 1
2012 3
2014 5
2015 8
2016 11
2017 13
2018 11
2019 7
2020 3
2021 5
2022 4
2023 6
2024 3

Text availability

Article attribute

Article type

Publication date

Search Results

75 results

Results by year

Filters applied: . Clear all
Page 1
Genome-wide sequencing and the clinical diagnosis of genetic disease: The CAUSES study.
Elliott AM, Adam S, du Souich C, Lehman A, Nelson TN, van Karnebeek C, Alderman E, Armstrong L, Aubertin G, Blood K, Boelman C, Boerkoel C, Bretherick K, Brown L, Chijiwa C, Clarke L, Couse M, Creighton S, Watts-Dickens A, Gibson WT, Gill H, Tarailo-Graovac M, Hamilton S, Heran H, Horvath G, Huang L, Hulait GK, Koehn D, Lee HK, Lewis S, Lopez E, Louie K, Niederhoffer K, Matthews A, Meagher K, Peng JJ, Patel MS, Race S, Richmond P, Rupps R, Salvarinova R, Seath K, Selby K, Steinraths M, Stockler S, Tang K, Tyson C, van Allen M, Wasserman W, Mwenifumbo J, Friedman JM. Elliott AM, et al. Among authors: tarailo graovac m. HGG Adv. 2022 Apr 18;3(3):100108. doi: 10.1016/j.xhgg.2022.100108. eCollection 2022 Jul 14. HGG Adv. 2022. PMID: 35599849 Free PMC article.
Genetic Modifiers and Rare Mendelian Disease.
Rahit KMTH, Tarailo-Graovac M. Rahit KMTH, et al. Among authors: tarailo graovac m. Genes (Basel). 2020 Feb 25;11(3):239. doi: 10.3390/genes11030239. Genes (Basel). 2020. PMID: 32106447 Free PMC article. Review.
Uncovering Missing Heritability in Rare Diseases.
Maroilley T, Tarailo-Graovac M. Maroilley T, et al. Among authors: tarailo graovac m. Genes (Basel). 2019 Apr 4;10(4):275. doi: 10.3390/genes10040275. Genes (Basel). 2019. PMID: 30987386 Free PMC article. Review.
Integration of genomics and metabolomics for prioritization of rare disease variants: a 2018 literature review.
Graham E, Lee J, Price M, Tarailo-Graovac M, Matthews A, Engelke U, Tang J, Kluijtmans LAJ, Wevers RA, Wasserman WW, van Karnebeek CDM, Mostafavi S. Graham E, et al. Among authors: tarailo graovac m. J Inherit Metab Dis. 2018 May;41(3):435-445. doi: 10.1007/s10545-018-0139-6. Epub 2018 May 2. J Inherit Metab Dis. 2018. PMID: 29721916 Free PMC article. Review.
Mitogen-induced defective mitosis transforms neural progenitor cells.
Omairi HK, Grisdale CJ, Meode M, Bohm AK, Black S, Adam NJ, Chapman CP, Maroilley T, Kelly JJ, Tarailo-Graovac M, Jones SJM, Blough MD, Cairncross JG. Omairi HK, et al. Among authors: tarailo graovac m. Neuro Oncol. 2023 Oct 3;25(10):1763-1774. doi: 10.1093/neuonc/noad082. Neuro Oncol. 2023. PMID: 37186014
75 results