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

Year Number of Results
2007 2
2009 1
2011 2
2012 2
2013 3
2014 2
2015 5
2016 2
2017 6
2018 11
2019 5
2020 7
2021 17
2022 12
2023 12
2024 2

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86 results

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Page 1
GiOPARK Project: The Genetic Study of Parkinson's Disease in the Croatian Population.
Rački V, Bergant G, Papić E, Kovanda A, Hero M, Rožmarić G, Starčević Čizmarević N, Ristić S, Ostojić S, Kapović M, Maver A, Peterlin B, Vuletić V. Rački V, et al. Among authors: maver a. Genes (Basel). 2024 Feb 19;15(2):255. doi: 10.3390/genes15020255. Genes (Basel). 2024. PMID: 38397244 Free PMC article.
Variant-specific pathophysiological mechanisms of AFF3 differently influence transcriptome profiles.
Bassani S, Chrast J, Ambrosini G, Voisin N, Schütz F, Brusco A, Sirchia F, Turban L, Schubert S, Jamra RA, Schlump JU, DeMille D, Bayrak-Toydemir P, Nelson GR, Wong KN, Duncan L, Mosera M, Gilissen C, Vissers LELM, Pfundt R, Kersseboom R, Yttervik H, Hansen GÅM, Falkenberg Smeland M, Butler KM, Lyons MJ, Carvalho CMB, Zhang C, Lupski JR, Potocki L, Flores-Gallegos L, Morales-Toquero R, Petit F, Yalcin B, Tuttle A, Elloumi HZ, Mccormick L, Kukolich M, Klaas O, Horvath J, Scala M, Iacomino M, Operto F, Zara F, Writzl K, Maver A, Haanpää MK, Pohjola P, Arikka H, Iseli C, Guex N, Reymond A. Bassani S, et al. Among authors: maver a. medRxiv [Preprint]. 2024 Jan 17:2024.01.14.24301100. doi: 10.1101/2024.01.14.24301100. medRxiv. 2024. PMID: 38293053 Free PMC article. Preprint.
A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans-A cohort study.
Vodnjov N, Toplišek J, Maver A, Čuturilo G, Jaklič H, Teran N, Višnjar T, Škrjanec Pušenjak M, Hodžić A, Miljanović O, Peterlin B, Writzl K. Vodnjov N, et al. Among authors: maver a. PLoS One. 2023 Dec 5;18(12):e0294969. doi: 10.1371/journal.pone.0294969. eCollection 2023. PLoS One. 2023. PMID: 38051749 Free PMC article.
Transcriptomic signatures for human male infertility.
Hodžić A, Maver A, Zorn B, Petrovič D, Kunej T, Peterlin B. Hodžić A, et al. Among authors: maver a. Front Mol Biosci. 2023 Aug 21;10:1226829. doi: 10.3389/fmolb.2023.1226829. eCollection 2023. Front Mol Biosci. 2023. PMID: 37670815 Free PMC article.
Oral microbiome and preterm birth.
Vidmar Šimic M, Maver A, Zimani AN, Hočevar K, Peterlin B, Kovanda A, Premru-Sršen T. Vidmar Šimic M, et al. Among authors: maver a. Front Med (Lausanne). 2023 Aug 7;10:1177990. doi: 10.3389/fmed.2023.1177990. eCollection 2023. Front Med (Lausanne). 2023. PMID: 37608830 Free PMC article.
The Expanding Phenotypical Spectrum of WARS2-Related Disorder: Four Novel Cases with a Common Recurrent Variant.
Pauly MG, Korenke GC, Diaw SH, Grözinger A, Cazurro-Gutiérrez A, Pérez-Dueñas B, González V, Macaya A, Serrano Antón AT, Peterlin B, Božović IB, Maver A, Münchau A, Lohmann K. Pauly MG, et al. Among authors: maver a. Genes (Basel). 2023 Mar 29;14(4):822. doi: 10.3390/genes14040822. Genes (Basel). 2023. PMID: 37107582 Free PMC article. Review.
Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14.
Jackson A, Lin SJ, Jones EA, Chandler KE, Orr D, Moss C, Haider Z, Ryan G, Holden S, Harrison M, Burrows N, Jones WD, Loveless M, Petree C, Stewart H, Low K, Donnelly D, Lovell S, Drosou K; Genomics England Research Consortium; Solve-RD consortium; Varshney GK, Banka S. Jackson A, et al. HGG Adv. 2023 Mar 3;4(2):100186. doi: 10.1016/j.xhgg.2023.100186. eCollection 2023 Apr 13. HGG Adv. 2023. PMID: 37009414 Free PMC article.
86 results