Human Genome Epidemiology Literature Finder
|
Records 1 - 19 (of 19 Records) |
| Query Trace: KARS[original query] |
|---|
| Dihydropyrimidine dehydrogenase enzyme deficiency: clinical and genetic assessment of prevalence in Turkish cancer patients. Cancer investigation 2002 20 (3): 333-9. Celik Ismail, Kars Ay?e, Guc Dicle, Tekuzman Gülten, Ruacan Sevk |
| Potentially functional polymorphisms in aminoacyl-tRNA synthetases genes are associated with breast cancer risk in a Chinese population. Molecular carcinogenesis 2015 Jul 54 (7): 577-83. He Yisha, Gong Jianhang, Wang Yanru, Qin Zhenzhen, Jiang Yue, Ma Hongxia, Jin Guangfu, Chen Jiaping, Hu Zhibin, Guan Xiaoxiang, Shen Hongbi |
| Genomic analysis of the interleukin-1ß-511 and interleukin-6-174 gene polymorphisms in Turkish patients with epilepsy. Genetics and molecular research : GMR 2014 13 (4): 8552-60. Gök I, Esen V, Kose Ozlece |
| Genetic variants in multisynthetase complex genes are associated with DNA damage levels in Chinese populations. Mutation research 2016 Jan 786 8-13. Liu Jia, Zhu Meng, Chen Weihong, Xie Kaipeng, Shen Wei, Yuan Jing, Cheng Yang, Geng Liguo, Wang Yuzhuo, Jin Guangfu, Dai Juncheng, Ma Hongxia, Du Jiangbo, Wang Meilin, Zhang Zhengdong, Hu Zhibin, Wu Tangchun, Shen Hongbi |
| Association of DARS gene polymorphisms with the risk of isolated ventricular septal defects in the Chinese Han population. Italian journal of pediatrics 2016 Nov 42 (1): 102. Feng Yu, Chen Runsen, Mo Xumi |
| Mutations in KARS cause early-onset hearing loss and leukoencephalopathy: Potential pathogenic mechanism. Human mutation 2017 9 38 (12): 1740-1750. Zhou Xiao-Long, He Long-Xia, Yu Li-Jia, Wang Yong, Wang Xi-Jin, Wang En-Duo, Yang T |
| [Gene Expression and Clinical Characteristics of Molecular Targeted Therapy ?in Non-small Cell Lung Cancer Patients in Shandong]. Zhongguo fei ai za zhi = Chinese journal of lung cancer 2017 Jan 20 (1): 14-20. Qiao Xiuli, Ai Dan, Liang Honglu, Mu Dianbin, Guo Qis |
| The role of ABO blood groups in glial neoplasms. British journal of neurosurgery 2019 Feb 33 (1): 43-46. Alkan Ali, Yaz?c? Gözde, Cengiz Mustafa, Karaka? Yusuf, Çelik ?smail, Kars Ay?e, Zorlu Far |
| Liquid biopsies using pleural effusion-derived exosomal DNA in advanced lung adenocarcinoma. Translational lung cancer research 2019 Aug 8 (4): 392-400. Song Zhengbo, Cai Zhijian, Yan Junrong, Shao Yang W, Zhang Yipi |
| Whole genome sequencing and rare variant analysis in essential tremor families. PloS one 2019 8 14 (8): e0220512. Odgerel Zagaa, Sonti Shilpa, Hernandez Nora, Park Jemin, Ottman Ruth, Louis Elan D, Clark Lorraine |
| Damaging coding variants within kainate receptor channel genes are enriched in individuals with schizophrenia, autism and intellectual disabilities. Scientific reports 2019 Dec 9 (1): 19215. Koromina Maria, Flitton Miles, Blockley Alix, Mellor Ian R, Knight Helen |
| Cardiomyopathy in children with mitochondrial disease: Prognosis and genetic background. International journal of cardiology 2019 1 279 115-121. Imai-Okazaki Atsuko, Kishita Yoshihito, Kohda Masakazu, Mizuno Yosuke, Fushimi Takuya, Matsunaga Ayako, Yatsuka Yukiko, Hirata Tomoko, Harashima Hiroko, Takeda Atsuhito, Nakaya Akihiro, Sakata Yasushi, Kogaki Shigetoyo, Ohtake Akira, Murayama Kei, Okazaki Yasus |
| Human CRY1 variants associate with attention deficit/hyperactivity disorder. The Journal of clinical investigation 2020 6 130 (7): 3885-3900. Onat O Emre, Kars M Ece, Gül ?eref, Bilguvar Kaya, Wu Yiming, Özhan Ay?e, Ayd?n Cihan, Ba?ak A Nazl?, Trusso M Allegra, Goracci Arianna, Fallerini Chiara, Renieri Alessandra, Casanova Jean-Laurent, Itan Yuval, Atba?o?lu Cem E, Saka Meram C, Kavakl? ? Halil, Özçelik Tayf |
| The genetic structure of the Turkish population reveals high levels of variation and admixture. Proceedings of the National Academy of Sciences of the United States of America 2021 8 118 (36): . Kars M Ece, Ba?ak A Nazl?, Onat O Emre, Bilguvar Kaya, Choi Jungmin, Itan Yuval, Ça?lar Caner, Palvadeau Robin, Casanova Jean-Laurent, Cooper David N, Stenson Peter D, Yavuz Alper, Bulu? Hakan, Günel Murat, Friedman Jeffrey M, Özçelik Tayf |
| Integration of clinicopathological and mutational data offers insight into lung cancer with tumor spread through air spaces. Annals of translational medicine 2021 Jun 9 (12): 985. Tian Yu, Feng Jing, Jiang Long, Ning Junwei, Gu Zenan, Huang Jia, Luo Qingqu |
| Report of rare and novel mutations in candidate genes in a cohort of hearing-impaired patients. Molecular genetics & genomic medicine 2022 2 10 (4): e1887. Liu Min, Liang Yue, Huang Bixue, Sun Jincangjian, Chen Kaiti |
| Identifying high-impact variants and genes in exomes of Ashkenazi Jewish inflammatory bowel disease patients. Nature communications 2023 4 14 (1): 2256. Yiming Wu, Kyle Gettler, Meltem Ece Kars, Mamta Giri, Dalin Li, Cigdem Sevim Bayrak, Peng Zhang, Aayushee Jain, Patrick Maffucci, Ksenija Sabic, Tielman Van Vleck, Girish Nadkarni, Lee A Denson, Harry Ostrer, Adam P Levine, Elena R Schiff, Anthony W Segal, Subra Kugathasan, Peter D Stenson, David N Cooper, L Philip Schumm, Scott Snapper, Mark J Daly, Talin Haritunians, Richard H Duerr, Mark S Silverberg, John D Rioux, Steven R Brant, Dermot P B McGovern, Judy H Cho, Yuval It |
| Prion Mutations in Republic of Republic of Korea, China, and Japan. International journal of molecular sciences 2023 1 24 (1): . Kim Dan Yeong, Shim Kyu Hwan, Bagyinszky Eva, An Seong Soo |
| The landscape of rare genetic variation associated with inflammatory bowel disease and Parkinson's disease comorbidity. Genome medicine 2024 5 16 (1): 66. Meltem Ece Kars, Yiming Wu, Peter D Stenson, David N Cooper, Johan Burisch, Inga Peter, Yuval It |
- Page last reviewed:Feb 1, 2024
- Content source: