Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 119 Records) |
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A Four-Gene-Based Risk Score With High Prognostic Value in Gastric Cancer. Frontiers in oncology 2021 11 584213. Zhang Bingdong, Li Yuerui, Yang Liu, Chen Yongbi |
The Alopecia Areata Phenotype Is Induced by the Water Avoidance Stress Test In cchcr1-Deficient Mice. Biomedicines 2021 8 9 (7): . Zhao Qiaofeng, Koyama Satoshi, Yoshihara Nagisa, Takagi Atsushi, Komiyama Etsuko, Wada Akino, Oka Akira, Ikeda Shiga |
Whole exome sequencing identifies deleterious rare variants in CCDC141 in familial self-limited delayed puberty. NPJ genomic medicine 2021 12 6 (1): 107. Saengkaew Tansit, Ruiz-Babot Gerard, David Alessia, Mancini Alessandra, Mariniello Katia, Cabrera Claudia P, Barnes Michael R, Dunkel Leo, Guasti Leonardo, Howard Sasha |
Genome-Wide Association Study of Peripheral Artery Disease.
Circulation. Genomic and precision medicine 2021 Oct CIRCGEN119002862. van Zuydam Natalie R, Stiby Alexander, Abdalla Moustafa, Austin Erin, Dahlström Emma H, McLachlan Stela, Vlachopoulou Efthymia, Ahlqvist Emma, Di Liao Chen, Sandholm Niina, Forsblom Carol, Mahajan Anubha, Robertson Neil R, Rayner N William, Lindholm Eero, Sinisalo Juha, Perola Markus, Kallio Milla, Weiss Emily, Price Jackie, Paterson Andrew, Klein Barbara, Salomaa Veikko, Palmer Colin N A, Groop Per-Henrik, Groop Leif, McCarthy Mark I, de Andrade Mariza, Morris Andrew P, Hopewell Jemma C, Colhoun Helen M, Kullo Iftikhar J, |
A genome-wide association study to investigate genetic loci associated with primary glaucoma in American Cocker Spaniels. American journal of veterinary research 2022 9 83 (11): 1-8. Gomes Filipe Espinheira, Casanova Maria Isabel, Mouttham Lara, Bannasch Danika L, Park Sangwan, Kim Soohyun, Young Laura J, Daley Nicole L, Thomasy Sara M, Castelhano Marta G, Ledbetter Eric C, Holmberg Bradford, Boyd Ryan, Van Der Woerdt Alexandra, McDonald Jessica, Hayward Jessica |
Genetic correlation of crizotinib efficacy and resistance in ALK- rearranged non-small-cell lung cancer. Lung cancer (Amsterdam, Netherlands) 2022 7 171 18-25. Liu Chang, Liu Cuicui, Liao Jiatao, Yin Jiani C, Wu Xianghua, Zhao Xinmin, Sun Si, Wang Huijie, Hu Zhihuang, Zhang Yao, Yu Hui, Shao Yang, Wang Jial |
Functional assessment of missense variants of uncertain significance in the cancer susceptibility gene PALB2. NPJ breast cancer 2022 7 8 (1): 86. Wu Shijie, Qi Lina, Chen Huihui, Zhang Kun, He Jiapan, Guo Xianan, Shen Lu, Zhou Yunxiang, Zhong Xi, Zheng Shu, Zhou Jiaojiao, Chen Yidi |
Association of a Novel DOCK2 Mutation-Related Gene Signature With Immune in Hepatocellular Carcinoma. Frontiers in genetics 2022 13 872224. Huang Yushen, Luo Wen, Chen Siyun, Su Hongmei, Zhu Wuchang, Wei Yuanyuan, Qiu Yue, Long Yan, Shi Yanxia, Wei Jinb |
Deciphering Genetic Susceptibility to Tuberculous Meningitis. Frontiers in neurology 2022 4 13 820168. Schurz Haiko, Glanzmann Brigitte, Bowker Nicholas, van Toorn Ronald, Solomons Regan, Schoeman Johan, van Helden Paul D, Kinnear Craig J, Hoal Eileen G, Möller Mar |
A recurrent homozygous missense mutation in CCDC103 causes asthenoteratozoospermia due to disorganized dynein arms. Asian journal of andrology 2022 3 24 (3): 255-259. Zubair Muhammad, Khan Ranjha, Ma Ao, Hameed Uzma, Khan Mazhar, Abbas Tanveer, Ahmad Riaz, Zhou Jian-Teng, Shah Wasim, Hussain Ansar, Ahmed Nisar, Khan Ihsan, Khan Khalid, Zhang Yuan-Wei, Zhang Huan, Wu Li-Min, Shi Qing-H |
Chromosomal Region 11p14.1 is Associated with Pharmacokinetics and Pharmacodynamics of Bisoprolol.
Pharmacogenomics and personalized medicine 2022 4 15 249-260. Fontana Vanessa, Turner Richard Myles, Francis Ben, Yin Peng, Pütz Benno, Hiltunen Timo P, Ruotsalainen Sanni, Kontula Kimmo K, Müller-Myhsok Bertam, Pirmohamed Mun |
Outflow angle: a risk factor for thromboembolic complications in coil embolisation for treating unruptured middle cerebral artery bifurcation aneurysms. Acta neurochirurgica 2022 2 164 (3): 795-803. Suzuki Ryotaro, Takigawa Tomoji, Nariai Yasuhiko, Nagaishi Masaya, Hyodo Akio, Suzuki Kensu |
A Comparative Evaluation of Standard and Balloon-Assisted Coiling of Intracranial Aneurysms Based on Neurophysiological Monitoring. Journal of clinical medicine 2022 2 11 (3): . Waldeck Stephan, Chapot René, von Falck Christian, Froelich Matthias F, Brockmann Marc, Overhoff Dani |
Association between a single nucleotide polymorphism in the R3HCC1 gene and irinotecan toxicity. Cancer medicine 2022 10 . Kanesada Kou, Tsunedomi Ryouichi, Hazama Shoichi, Ogihara Hiroyuki, Hamamoto Yoshihiko, Shindo Yoshitaro, Matsui Hiroto, Tokumitsu Yukio, Yoshida Shin, Iida Michihisa, Suzuki Nobuaki, Takeda Shigeru, Ioka Tatsuya, Nagano Hiroa |
Two New Variants in FYCO1 Are Responsible for Autosomal Recessive Congenital Cataract in Iranian Population. Cell journal 2022 10 24 (9): 546-551. Shirzadeh Ebrahim, Piryaei Fahimeh, Naddaf Hanieh, Barabadi Zah |
Genome-Wide Association Study for eGFR in a Taiwanese Population.
Clinical journal of the American Society of Nephrology : CJASN 2022 Oct . Chen Ying-Chun, Wong Henry Sung-Ching, Wu Mei-Yi, Chou Wan-Hsuan, Kao Chih-Chin, Chao Ching-Hsuan, Chang Wei-Chiao, Wu Mai-S |
A Nonsense Variant in CCDC65 Gene Causes Respiratory Failure Associated with Increased Lamb Mortality in French Lacaune Dairy Sheep. Genes 2022 1 13 (1): . Ben Braiek Maxime, Moreno-Romieux Carole, Allain Charlotte, Bardou Philippe, Bordes Arnaud, Debat Frédéric, Drögemüller Cord, Plisson-Petit Florence, Portes David, Sarry Julien, Tadi Némuel, Woloszyn Florent, Fabre Stépha |
Genomic landscape of TCR?? and TCR?? T-large granular lymphocyte leukemia. Blood 2022 1 139 (20): 3058-3072. Cheon HeeJin, Xing Jeffrey C, Moosic Katharine B, Ung Johnson, Chan Vivian W, Chung David S, Toro Mariella F, Elghawy Omar, Wang John S, Hamele Cait E, Hardison Ross C, Olson Thomas L, Tan Su-Fern, Feith David J, Ratan Aakrosh, Loughran Thomas |
Identification of risk genes in Chinese nonobstructive azoospermia patients based on whole-exome sequencing. Asian journal of andrology 2022 Oct . Liu Yu-Jun, Zhuang Xin-Jie, An Jian-Ting, Jiang Hui, Li Rong, Qiao Jie, Yan Li-Ying, Zhi |
Bladder cancer course, four genetic high-risk variants, and histopathological findings. EXCLI journal 2023 9 22 867-879. Thura Kadhum, Silvia Selinski, Meinolf Blaszkewicz, Jörg Reinders, Emanuel Roth, Frank Volkert, Daniel Ovsiannikov, Oliver Moormann, Holger Gerullis, Dimitri Barski, Thomas Otto, Svetlana Höhne, Jan G Hengstler, Klaus Gol |
GWAS reveals genetic basis of a predisposition to severe COVID-19 through in silico modeling of the FYCO1 protein. Frontiers in medicine 2023 8 10 1178939. Mariya S Gusakova, Mikhail V Ivanov, Daria A Kashtanova, Anastasiia N Taraskina, Veronika V Erema, Valeriya M Mikova, Robert I Loshkarev, Olga A Ignatyeva, Aleksandra I Akinshina, Sergey I Mitrofanov, Ekaterina A Snigir, Vladimir S Yudin, Valentin V Makarov, Anton A Keskinov, Sergey M Yud |
TBK1 variants in Chinese patients with amyotrophic lateral sclerosis: genetic analysis and clinical features. European journal of neurology 2023 7 . Bi Zhao, Qirui Jiang, Junyu Lin, Qianqian Wei, Chunyu Li, Yanbing Hou, Bei Cao, Lingyu Zhang, Ruwei Ou, Kuncheng Liu, Tianmi Yang, Yi Xiao, Huifang Sha |
The association between the CCDC88A gene polymorphism at rs1437396 and alcohol use disorder, with or without major depression disorder. Arhiv za higijenu rada i toksikologiju 2023 6 74 (2): 127-133. Maria Bonea, Constantin-Ionut Coroama, Radu Anghel Popp, Ioana Valentina Miclut |
Loss of Primary Cilia Potentiates BRAF/MAPK Pathway Activation in Rhabdoid Colorectal Carcinoma: A Series of 21 Cases Showing Ciliary Rootlet CoiledCoil (CROCC) Alterations. Genes 2023 5 14 (5): . Andrea Remo, Federica Grillo, Luca Mastracci, Michele Simbolo, Matteo Fassan, Maria Paola Cecchini, Giuseppe Miscio, Antonio Sassano, Paola Parente, Alessandro Vanoli, Giovanna Sabella, Guido Giordano, Emanuele Damiano Urso, Luigi Cerulo, Aldo Scarpa, Francesco Fiorica, Massimo Pancio |
Single-Voxel MR Spectroscopy of Gliomas with s-LASER at 7T. Diagnostics (Basel, Switzerland) 2023 5 13 (10): . Martin Prener, Giske Opheim, Zahra Shams, Christian Baastrup Søndergaard, Ulrich Lindberg, Henrik B W Larsson, Morten Ziebell, Vibeke Andrée Larsen, Mark Bitsch Vestergaard, Olaf B Pauls |
The genetic architecture of fornix white matter microstructure and their involvement in neuropsychiatric disorders. Translational psychiatry 2023 5 13 (1): 180. Ya-Nan Ou, Yi-Jun Ge, Bang-Sheng Wu, Yi Zhang, Yu-Chao Jiang, Kevin Kuo, Liu Yang, Lan Tan, Jian-Feng Feng, Wei Cheng, Jin-Tai |
A de novo low-frequency mosaic variant of KIF1A causes hereditary spastic paraplegia: A literature review. Annals of human genetics 2023 3 . Liu Mengyuan, Li Bing, Wang Xiaona, Li Dongxiao, Xie Zhenhua, Li Yuke, Gao Yang, Chen Baiyun, Zhang Huichun, Wang Yanli, Gao Ch |
Polymorphism of rs599839 in the PSRC1 gene is associated with coronary artery disease in an Iranian population. Journal of cardiovascular and thoracic research 2023 11 15 (3): 168-173. Golnaz Houshmand, Mohammad Javad Alemzadeh-Ansari, Saeideh Mazloumzadeh, Niloofar Naderi, Maryam Pourirahim, Katayoun Heshmatzad, Majid Maleki, Samira Kalayin |
CCDC103 as a Prognostic Biomarker Correlated with Tumor Progression and Immune Infiltration in Glioma. OncoTargets and therapy 2023 10 16 819-837. Zhixing Xu, Haitao Xu, Xi Chen, Xiaobing Huang, Jintao Tian, Jinxi Zhao, Bohu Liu, Fengcai Shi, Jin Wu, Jun |
CCDC88C variants are associated with focal epilepsy and genotype-phenotype correlation. Clinical genetics 2024 1 . Yu-Jie Chen, Wen-Jie Wang, Dong-Fang Zou, Jun-Xia Luo, Pei-Yan Jin, Liang Jin, Xiao-Rong Liu, Wei-Ping Liao, Bin Li, Yong-Jun Chen, |
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- Page last updated:Apr 16, 2024
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