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

Year Number of Results
2006 2
2007 7
2008 6
2010 3
2011 1
2012 3
2013 2
2014 4
2015 6
2016 7
2017 3
2018 4
2019 3
2020 4
2021 2
2022 4
2024 2

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56 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: karaer k. Neuron. 2015 Nov 4;88(3):499-513. doi: 10.1016/j.neuron.2015.09.048. Neuron. 2015. PMID: 26539891 Free PMC article.
A case with bilateral radio-ulnar synostosis.
Koç A, Kaymak AO, Karaer K, Ergün MA, Aksu T, Perçin EF. Koç A, et al. Among authors: karaer k. Genet Couns. 2008;19(2):193-8. Genet Couns. 2008. PMID: 18618994 Review.
Kept in Mind Infantile Neuroaxonal Dystrophy.
Karalok ZS, Taskin BD, Aydogmus U, Ceylaner S, Karaer K, Yilmaz C. Karalok ZS, et al. Among authors: karaer k. Genet Couns. 2016;27(2):279-82. Genet Couns. 2016. PMID: 29485838 No abstract available.
Ring chromosome 9 in a newborn.
Aldemir O, Celik IH, Karaer K, Ceylaner G. Aldemir O, et al. Among authors: karaer k. Genet Couns. 2013;24(4):357-60. Genet Couns. 2013. PMID: 24551976
Novel mutations in the LRP5 gene in patients with Osteoporosis-pseudoglioma syndrome.
Pekkinen M, Grigelioniene G, Akin L, Shah K, Karaer K, Kurtoğlu S, Ekbote A, Aycan Z, Sağsak E, Danda S, Åström E, Mäkitie O. Pekkinen M, et al. Among authors: karaer k. Am J Med Genet A. 2017 Dec;173(12):3132-3135. doi: 10.1002/ajmg.a.38491. Epub 2017 Oct 21. Am J Med Genet A. 2017. PMID: 29055141 No abstract available.
56 results