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

Year Number of Results
2002 4
2003 9
2004 5
2005 9
2006 4
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2008 9
2009 10
2010 9
2011 18
2012 17
2013 9
2014 13
2015 16
2016 12
2017 15
2018 14
2019 14
2020 16
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2022 12
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2024 2

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219 results

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Page 1
Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease.
Karaca E, Harel T, Pehlivan D, Jhangiani SN, Gambin T, Coban Akdemir Z, Gonzaga-Jauregui C, Erdin S, Bayram Y, Campbell IM, Hunter JV, Atik MM, Van Esch H, Yuan B, Wiszniewski W, Isikay S, Yesil G, Yuregir OO, Tug Bozdogan S, Aslan H, Aydin H, Tos T, Aksoy A, De Vivo DC, Jain P, Geckinli BB, Sezer O, Gul D, Durmaz B, Cogulu O, Ozkinay F, Topcu V, Candan S, Cebi AH, Ikbal M, Yilmaz Gulec E, Gezdirici A, Koparir E, Ekici F, Coskun S, Cicek S, Karaer K, Koparir A, Duz MB, Kirat E, Fenercioglu E, Ulucan H, Seven M, Guran T, Elcioglu N, Yildirim MS, Aktas D, Alikaşifoğlu M, Ture M, Yakut T, Overton JD, Yuksel A, Ozen M, Muzny DM, Adams DR, Boerwinkle E, Chung WK, Gibbs RA, Lupski JR. Karaca E, et al. Among authors: ozkinay f. Neuron. 2015 Nov 4;88(3):499-513. doi: 10.1016/j.neuron.2015.09.048. Neuron. 2015. PMID: 26539891 Free PMC article.
A Very Rare Pathogen of Osteomyelitis: Alcaligenes faecalis.
Avcu G, Erci E, Arslan SY, Arslan A, Bilen NM, Bal ZS, Ozkinay F, Kurugol Z, Gunay H, Aydemir S. Avcu G, et al. Among authors: ozkinay f. Pediatr Infect Dis J. 2023 Sep 1;42(9):e362-e363. doi: 10.1097/INF.0000000000003993. Epub 2023 Jun 7. Pediatr Infect Dis J. 2023. PMID: 37310887 No abstract available.
A Rare Cause of Orbital Cellulitis: Eikenella corrodens.
Erci E, Avcu G, Ozer EC, Bal ZS, Ozkinay F, Kurugol Z, Gode S, Aydemir SS. Erci E, et al. Among authors: ozkinay f. Pediatr Infect Dis J. 2023 Jul 1;42(7):e257. doi: 10.1097/INF.0000000000003909. Epub 2023 Mar 17. Pediatr Infect Dis J. 2023. PMID: 37000931 No abstract available.
Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium.
Dundar M, Fahrioglu U, Yildiz SH, Bakir-Gungor B, Temel SG, Akin H, Artan S, Cora T, Sahin FI, Dursun A, Sezer O, Gurkan H, Erdogan M, Gunduz CNS, Bisgin A, Ozdemir O, Ulgenalp A, Percin EF, Yildirim ME, Tekes S, Bagis H, Yuce H, Duman N, Bozkurt G, Yararbas K, Yildirim MS, Arman A, Mihci E, Eraslan S, Altintas ZM, Aymelek HS, Ruhi HI, Tatar A, Ergoren MC, Cetin GO, Altunoglu U, Caglayan AO, Yuksel B, Ozkul Y, Saatci C, Kenanoglu S, Karasu N, Dundar B, Ozcelik F, Demir M, Siniksaran BS, Kulak H, Kiranatlioglu K, Baysal K, Kazimli U, Akalin H, Dundar A, Boz M, Bayram A, Subasioglu A, Colak FK, Karaduman N, Gunes MC, Kandemir N, Aynekin B, Emekli R, Sahin IO, Ozdemir SY, Onal MG, Senel AS, Poyrazoglu MH, Kisaarslan ANP, Gursoy S, Baskol M, Calis M, Demir H, Zararsiz GE, Erdogan MO, Elmas M, Solak M, Ulu MS, Thahir A, Aydin Z, Atasever U, Sag SO, Aliyeva L, Alemdar A, Dogan B, Erguzeloglu CO, Kaya N, Ozkinay F, Cogulu O, Durmaz A, Onay H, Karaca E, Durmaz B, Aykut A, Cilingir O, Aras BD, Gokalp EE, Arslan S, Temena A, Haziyeva K, Kocagil S, Bas H, Susam E, Keklikci AR, Sarac E, Kocak N, Nergiz S, Terzi YK, Dincer SA, Baskin ES, Genc GC, Bahadir O, Sanri A, Yigit S, Tozkir H, Y… See abstract for full author list ➔ Dundar M, et al. Among authors: ozkinay f. Funct Integr Genomics. 2022 Jun;22(3):291-315. doi: 10.1007/s10142-021-00819-3. Epub 2022 Jan 31. Funct Integr Genomics. 2022. PMID: 35098403
Immunodeficiency in a Child with Alström Syndrome.
Ozdemir TR, Karaca NE, Marshall JD, Kutukculer N, Aksu G, Ozgul RK, Ozanturk A, Isik E, Akgun B, Ozdemir HH, Darcan S, Ozkinay F, Cogulu O. Ozdemir TR, et al. Among authors: ozkinay f. Indian J Pediatr. 2018 Oct;85(10):924-926. doi: 10.1007/s12098-018-2740-y. Epub 2018 Aug 28. Indian J Pediatr. 2018. PMID: 30155784 No abstract available.
LSM1 is the new candidate gene for neurodevelopmental disorder.
Kok Kilic G, Isik E, Alpay O, Atik T, Aykut A, Durmaz A, Cogulu O, Ozkinay F. Kok Kilic G, et al. Among authors: ozkinay f. Eur J Med Genet. 2022 Nov;65(11):104610. doi: 10.1016/j.ejmg.2022.104610. Epub 2022 Sep 12. Eur J Med Genet. 2022. PMID: 36100156
219 results