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

Year Number of Results
1962 2
1964 2
1965 1
1967 1
1968 1
1969 4
1970 1
1971 1
1972 1
1974 1
1977 1
1979 1
1985 1
1986 1
1994 1
2002 1
2007 2
2008 1
2009 2
2010 1
2011 2
2012 3
2013 3
2014 2
2015 6
2016 4
2017 9
2018 14
2019 7
2020 7
2021 17
2022 0
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Article attribute
Article type
Publication date

Search Results

94 results
Results by year
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Page 1
Improving diagnostics of rare genetic diseases with NGS approaches.
Vinkšel M, Writzl K, Maver A, Peterlin B. Vinkšel M, et al. Among authors: maver a. J Community Genet. 2021 Apr;12(2):247-256. doi: 10.1007/s12687-020-00500-5. Epub 2021 Jan 15. J Community Genet. 2021. PMID: 33452619 Free PMC article.
De novo mutations in idiopathic male infertility-A pilot study.
Hodžić A, Maver A, Plaseska-Karanfilska D, Ristanović M, Noveski P, Zorn B, Terzic M, Kunej T, Peterlin B. Hodžić A, et al. Among authors: maver a. Andrology. 2021 Jan;9(1):212-220. doi: 10.1111/andr.12897. Epub 2020 Sep 17. Andrology. 2021. PMID: 32860660 Free article.
Analysis of blood-based gene expression in idiopathic Parkinson disease.
Shamir R, Klein C, Amar D, Vollstedt EJ, Bonin M, Usenovic M, Wong YC, Maver A, Poths S, Safer H, Corvol JC, Lesage S, Lavi O, Deuschl G, Kuhlenbaeumer G, Pawlack H, Ulitsky I, Kasten M, Riess O, Brice A, Peterlin B, Krainc D. Shamir R, et al. Among authors: maver a. Neurology. 2017 Oct 17;89(16):1676-1683. doi: 10.1212/WNL.0000000000004516. Epub 2017 Sep 15. Neurology. 2017. PMID: 28916538 Free PMC article.
De Novo SOX6 Variants Cause a Neurodevelopmental Syndrome Associated with ADHD, Craniosynostosis, and Osteochondromas.
Tolchin D, Yeager JP, Prasad P, Dorrani N, Russi AS, Martinez-Agosto JA, Haseeb A, Angelozzi M, Santen GWE, Ruivenkamp C, Mercimek-Andrews S, Depienne C, Kuechler A, Mikat B, Ludecke HJ, Bilan F, Le Guyader G, Gilbert-Dussardier B, Keren B, Heide S, Haye D, Van Esch H, Keldermans L, Ortiz D, Lancaster E, Krantz ID, Krock BL, Pechter KB, Arkader A, Medne L, DeChene ET, Calpena E, Melistaccio G, Wilkie AOM, Suri M, Foulds N; Genomics England Research Consortium, Begtrup A, Henderson LB, Forster C, Reed P, McDonald MT, McConkie-Rosell A, Thevenon J, Le Tanno P, Coutton C, Tsai ACH, Stewart S, Maver A, Gorazd R, Pichon O, Nizon M, Cogné B, Isidor B, Martin-Coignard D, Stoeva R, Lefebvre V, Le Caignec C. Tolchin D, et al. Among authors: maver a. Am J Hum Genet. 2020 Jun 4;106(6):830-845. doi: 10.1016/j.ajhg.2020.04.015. Epub 2020 May 21. Am J Hum Genet. 2020. PMID: 32442410 Free PMC article.
94 results