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

Year Number of Results
1977 1
1985 1
1988 1
1989 4
1990 1
1992 1
1994 2
1995 2
1996 3
1997 1
1998 3
1999 3
2002 1
2003 4
2004 2
2005 4
2006 6
2007 1
2008 10
2009 11
2010 11
2011 14
2012 11
2013 19
2014 21
2015 20
2016 11
2017 19
2018 27
2019 40
2020 44
2021 6
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277 results
Results by year
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Page 1
De Novo Variants in TAOK1 Cause Neurodevelopmental Disorders.
Dulovic-Mahlow M, Trinh J, Kandaswamy KK, Braathen GJ, Di Donato N, Rahikkala E, Beblo S, Werber M, Krajka V, Busk ØL, Baumann H, Al-Sannaa NA, Hinrichs F, Affan R, Navot N, Al Balwi MA, Oprea G, Holla ØL, Weiss MER, Jamra RA, Kahlert AK, Kishore S, Tveten K, Vos M, Rolfs A, Lohmann K. Dulovic-Mahlow M, et al. Among authors: kishore s. Am J Hum Genet. 2019 Jul 3;105(1):213-220. doi: 10.1016/j.ajhg.2019.05.005. Epub 2019 Jun 20. Am J Hum Genet. 2019. PMID: 31230721 Free PMC article.
Malignant Venous Obstruction: Superior Vena Cava Syndrome and Beyond.
Friedman T, Quencer KB, Kishore SA, Winokur RS, Madoff DC. Friedman T, et al. Among authors: kishore sa. Semin Intervent Radiol. 2017 Dec;34(4):398-408. doi: 10.1055/s-0037-1608863. Epub 2017 Dec 14. Semin Intervent Radiol. 2017. PMID: 29249864 Free PMC article. Review.
Clinical exome sequencing: results from 2819 samples reflecting 1000 families.
Trujillano D, Bertoli-Avella AM, Kumar Kandaswamy K, Weiss ME, Köster J, Marais A, Paknia O, Schröder R, Garcia-Aznar JM, Werber M, Brandau O, Calvo Del Castillo M, Baldi C, Wessel K, Kishore S, Nahavandi N, Eyaid W, Al Rifai MT, Al-Rumayyan A, Al-Twaijri W, Alothaim A, Alhashem A, Al-Sannaa N, Al-Balwi M, Alfadhel M, Rolfs A, Abou Jamra R. Trujillano D, et al. Among authors: kishore s. Eur J Hum Genet. 2017 Feb;25(2):176-182. doi: 10.1038/ejhg.2016.146. Epub 2016 Nov 16. Eur J Hum Genet. 2017. PMID: 27848944 Free PMC article.
Medicare For All: An Analysis Of Key Policy Issues.
Johnson M, Kishore S, Berwick DM. Johnson M, et al. Among authors: kishore s. Health Aff (Millwood). 2020 Jan;39(1):133-141. doi: 10.1377/hlthaff.2019.01040. Health Aff (Millwood). 2020. PMID: 31905054
Modeling Monogenic Diabetes using Human ESCs Reveals Developmental and Metabolic Deficiencies Caused by Mutations in HNF1A.
Cardenas-Diaz FL, Osorio-Quintero C, Diaz-Miranda MA, Kishore S, Leavens K, Jobaliya C, Stanescu D, Ortiz-Gonzalez X, Yoon C, Chen CS, Haliyur R, Brissova M, Powers AC, French DL, Gadue P. Cardenas-Diaz FL, et al. Among authors: kishore s. Cell Stem Cell. 2019 Aug 1;25(2):273-289.e5. doi: 10.1016/j.stem.2019.07.007. Cell Stem Cell. 2019. PMID: 31374199 Free PMC article.
277 results
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