日期 影响因子
日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:
–

CYP1B1 and MYOC Gene Analysis of Patients with Primary Congenital Glaucoma in the Cukurova Region of Türkiye

土耳其丘库罗瓦地区原发性先天性青光眼患者的CYP1B1和MYOC基因分析

期刊:Journal of Pediatric Genetics
影响因子:0.4
doi:10.1055/s-0043-1774294
Akbas, Ahsen Cavusoglu; Erdem, Elif; Bozdogan, Sevcan Tug; Harbiyeli, Ibrahim Inan; Yagmur, Meltem
青光眼
神经科学
发表日期：2024
文献求助 收藏

Germline landscape of BRCAs by 7-site collaborations as a BRCA consortium in Turkey

土耳其 BRCA 联盟通过 7 个研究中心合作开展的 BRCA 基因系图谱研究

期刊:Breast
影响因子:7.9
doi:10.1016/j.breast.2022.06.005
Bisgin, Atil; Sag, Sebnem Ozemri; Dogan, Muhammet E; Yildirim, Mahmut S; Gumus, Aydeniz Aydin; Akkus, Nejmiye; Balasar, Ozgur; Durmaz, Ceren D; Eroz, Recep; Altiner, Sule; Alemdar, Adem; Aliyeva, Lamia; Boga, Ibrahim; Cam, Fethi S; Dogan, Berkcan; Esbah, Onur; Hanta, Abdullah; Mujde, Cem; Ornek, Cemre; Ozer, Sinem; Rencuzogullari, Cagla; Sonmezler, Ozge; Bozdogan, Sevcan Tug; Dundar, Munis; Temel, Sehime G
发表日期：2022
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Analysis of ACE2 and TMPRSS2 coding variants as a risk factor for SARS-CoV-2 from 946 whole-exome sequencing data in the Turkish population

基于土耳其人群946例全外显子组测序数据的ACE2和TMPRSS2编码变异分析，探讨其作为SARS-CoV-2感染风险因素的作用

期刊:Journal of Medical Virology
影响因子:4.6
doi:10.1002/jmv.27976
Duman, Nilgun; Tuncel, Gulten; Bisgin, Atil; Bozdogan, Sevcan Tug; Sag, Sebnem Ozemri; Gul, Seref; Kiraz, Aslihan; Balta, Burhan; Erdogan, Murat; Uyanik, Bulent; Canbek, Sezin; Ata, Pinar; Geckinli, Bilgen Bilge; Arslan Ates, Esra; Alavanda, Ceren; Yesim Ozdemir, Sevda; Sezer, Ozlem; Ozgon, Gulay Oner; Gurkan, Hakan; Guler, Kubra; Boga, Ibrahim; Kaya, Niyazi; Alemdar, Adem; Sayan, Murat; Dundar, Munis; Ergoren, Mahmut Cerkez; Temel, Sehime Gulsun
炎症/感染
ACE2
SARS-CoV-2
发表日期：2022
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Current Status of Genetic Diagnosis Laboratories and Frequency of Genetic Variants Associated with Cystic Fibrosis through a Newborn-Screening Program in Turkey.

土耳其新生儿筛查计划中囊性纤维化相关基因变异频率及基因诊断实验室现状

期刊:Genes
影响因子:2.8
doi:10.3390/genes12020206
Bozdogan Sevcan Tug, Mujde Cem, Boga Ibrahim, Sonmezler Ozge, Hanta Abdullah, Rencuzogullari Cagla, Ozcan Dilek, Altintas Derya Ufuk, Bisgin Atil
其它
发表日期：2021
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Identification of a Novel Mutation in GRIN2A Gene with Global Developmental Delay and Refractory Epilepsy

GRIN2A基因新突变与全面发育迟缓和难治性癫痫的鉴定

期刊:Annals of Indian Academy of Neurology
影响因子:1.8
doi:10.4103/aian.AIAN_365_18
Sarigecili, Esra; Direk, Meltem Cobanogullari; Komur, Mustafa; Bozdogan, Sevcan Tug; Okuyaz, Cetin
发育与干细胞
癫痫
神经科学
发表日期：2020
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No Association between Polymorphisms of Vitamin D and Oxytocin Receptor Genes and Autistic Spectrum Disorder in a Sample of Turkish Children

土耳其儿童样本中维生素D和催产素受体基因多态性与自闭症谱系障碍之间无关联

期刊:Clinical Psychopharmacology and Neuroscience
影响因子:2.7
doi:10.9758/cpn.2018.16.4.415
Bozdogan, Sevcan Tug; Kutuk, Meryem Ozlem; Tufan, Evren; Altıntaş, Zuhal; Temel, Gülhan Orekici; Toros, Fevziye
自闭症
信号转导
神经科学
发表日期：2018
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Hereditary Spastic Paraplegia Type 35 with a Novel Mutation in Fatty Acid 2-Hydroxylase Gene and Literature Review of the Clinical Features

遗传性痉挛性截瘫35型伴脂肪酸2-羟化酶基因新突变及其临床特征的文献综述

期刊:Annals of Indian Academy of Neurology
影响因子:1.8
doi:10.4103/aian.AIAN_106_18
Incecik, Faruk; Besen, Seyda; Bozdogan, Sevcan Tug
代谢
发表日期：2018
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Global transcriptional disturbances underlie Cornelia de Lange syndrome and related phenotypes

整体转录紊乱是 Cornelia de Lange 综合征及其相关表型的基础

期刊:Journal of Clinical Investigation
影响因子:13.3
doi:10.1172/JCI77435
Bo Yuan, Davut Pehlivan, Ender Karaca, Nisha Patel, Wu-Lin Charng, Tomasz Gambin, Claudia Gonzaga-Jauregui, V Reid Sutton, Gozde Yesil, Sevcan Tug Bozdogan, Tulay Tos, Asuman Koparir, Erkan Koparir, Christine R Beck, Shen Gu, Huseyin Aslan, Ozge Ozalp Yuregir, Khalid Al Rubeaan, Dhekra Alnaqeb, Mune
信号转导
发表日期：2015
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β-Globin chain abnormalities with coexisting α-thalassemia mutations

β-珠蛋白链异常合并α-地中海贫血突变

期刊:Archives of Medical Science
影响因子:3.3
doi:10.5114/aoms.2012.28723
Guvenc, Birol; Canataroglu, Abdullah; Unsal, Cagatay; Yildiz, Sule Menziletoglu; Turhan, Ferda Tekin; Bozdogan, Sevcan Tug; Dincer, Suleyman; Erkman, Hakan
贫血
代谢
发表日期：2012
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β-Thalassemia mutations and hemoglobinopathies in Adana, Turkey: results from a single center study

土耳其阿达纳β-地中海贫血突变和血红蛋白病：单中心研究结果

期刊:Archives of Medical Science
影响因子:3.3
doi:10.5114/aoms.2012.28811
Guvenc, Birol; Canataroglu, Abdullah; Unsal, Cagatay; Yildiz, Sule Menziletoglu; Turhan, Ferda Tekin; Bozdogan, Sevcan Tug; Dincer, Suleyman; Erkman, Hakan
贫血
代谢
发表日期：2012
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