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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 4
2015 8
2016 10
2017 10
2018 11
2019 7
2020 3
2021 5
2022 4
2023 6
2024 4

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72 results

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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.
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 Free PMC article.
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.
CIAO1 and MMS19 deficiency: A lethal neurodegenerative phenotype caused by cytosolic Fe-S cluster protein assembly disorders.
van Karnebeek CDM, Tarailo-Graovac M, Leen R, Meinsma R, Correard S, Jansen-Meijer J, Prykhozhij SV, Pena IA, Ban K, Schock S, Saxena V, Pras-Raves ML, Drögemöller BI, Grootemaat AE, van der Wel NN, Dobritzsch D, Roseboom W, Schomakers BV, Jaspers YRJ, Zoetekouw L, Roelofsen J, Ferreira CR, van der Lee R, Ross CJ, Kochan J, McIntyre RL, van Klinken JB, van Weeghel M, Kramer G, Weschke B, Labrune P, Willemsen MA, Riva D, Garavaglia B, Moeschler JB, Filiano JJ, Ekker M, Berman JN, Dyment D, Vaz FM, Wassermann WW, Houtkooper RH, van Kuilenburg ABP. van Karnebeek CDM, et al. Among authors: tarailo graovac m. Genet Med. 2024 Feb 24;26(6):101104. doi: 10.1016/j.gim.2024.101104. Online ahead of print. Genet Med. 2024. PMID: 38411040 Free article.
72 results