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Page 1
Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification.
Schottlaender LV, Abeti R, Jaunmuktane Z, Macmillan C, Chelban V, O'Callaghan B, McKinley J, Maroofian R, Efthymiou S, Athanasiou-Fragkouli A, Forbes R, Soutar MPM, Livingston JH, Kalmar B, Swayne O, Hotton G; SYNAPS Study Group; Pittman A, Mendes de Oliveira JR, de Grandis M, Richard-Loendt A, Launchbury F, Althonayan J, McDonnell G, Carr A, Khan S, Beetz C, Bisgin A, Tug Bozdogan S, Begtrup A, Torti E, Greensmith L, Giunti P, Morrison PJ, Brandner S, Aurrand-Lions M, Houlden H. Schottlaender LV, et al. Among authors: tug bozdogan s. Am J Hum Genet. 2020 Mar 5;106(3):412-421. doi: 10.1016/j.ajhg.2020.02.007. Am J Hum Genet. 2020. PMID: 32142645 Free PMC article.
A Multicenter Study of Genotype Variation/Demographic Patterns in 2475 Individuals Including 1444 Cases With Breast Cancer in Turkey.
Boga I, Ozemri Sag S, Duman N, Ozdemir SY, Ergoren MC, Dalci K, Mujde C, Parsak CK, Rencuzogullari C, Sonmezler O, Yalav O, Alemdar A, Aliyeva L, Bozkurt O, Cetintas S, Cubukcu E, Deligonul A, Dogan B, Ornek Erguzeloglu C, Evrensel T, Gokgoz S, Senol K, Tolunay S, Akyurek E, Basgoz N, Gökçe N, Dundar B, Ozturk F, Taskin D, Demirtas M, Cag M, Diker O, Olgun P, Tug Bozdogan S, Dundar M, Bisgin A, Temel SG. Boga I, et al. Among authors: tug bozdogan s. Eur J Breast Health. 2023 Jul 3;19(3):235-252. doi: 10.4274/ejbh.galenos.2023.2023-2-5. eCollection 2023 Jul. Eur J Breast Health. 2023. PMID: 37415649 Free PMC article.
Vandetanib in a Child Affected by Neurofibromatosis Type 1 and Medullary Thyroid Carcinoma with Both NF1 and Homozygous RET Proto-oncogen Germ-line Mutations.
Demir Gündoğan B, Sağcan F, Tuğ Bozdoğan S, Balcı Y, Tuncel Daloğlu F, Çağlar Çıtak E. Demir Gündoğan B, et al. Among authors: tug bozdogan s. J Clin Res Pediatr Endocrinol. 2021 Aug 23;13(3):342-346. doi: 10.4274/jcrpe.galenos.2020.2020.0051. Epub 2020 Jul 23. J Clin Res Pediatr Endocrinol. 2021. PMID: 32702947 Free PMC article.
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: tug bozdogan s. Neuron. 2015 Nov 4;88(3):499-513. doi: 10.1016/j.neuron.2015.09.048. Neuron. 2015. PMID: 26539891 Free PMC article.
13 results