Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 211 Records) |
Query Trace: KIN[original query] |
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X-chromosome inactivation and PCDH19-associated epileptic encephalopathy: A novel PCDH19 variant in a Chinese family. Clinica chimica acta; international journal of clinical chemistry 2021 7 521 285-288. Hung Ling-Yin, Subramaniam Shreenidhi Ranganatha, Tong Tsz-Yan Tammy, Chan Wing-Ki, Yau Eric Kin-Cheong, Ching Chor-Kw |
Polymorphisms of ACE (I/D) and ACE2 receptor gene (Rs2106809, Rs2285666) are not related to the clinical course of COVID-19: A case study. Journal of medical virology 2021 Jun . Karaka? Çelik Sevim, Çakmak Genç Güne?, Pi?kin Nihal, Açikgöz Bilgehan, Altinsoy Bülent, Kurucu ??siz Ba?ak, Dursun Ahm |
Safety and feasibility of retrograde INOUE-BALLOON for balloon aortic valvuloplasty without rapid ventricular pacing during transcatheter aortic valve replacement. Cardiovascular intervention and therapeutics 2021 6 37 (2): 372-380. Ninomiya Ryo, Yoshizawa Michiko, Koeda Yorihiko, Ishikawa Yu, Kumagai Akiko, Ishida Masaru, Takahashi Fumiaki, Fusazaki Tetsuya, Tashiro Atsushi, Kin Hajime, Morino Yoshihi |
The IRM cell adhesion molecules Hibris, Kin of irre and Roughest control egg morphology by modulating ovarian muscle contraction in Drosophila. Journal of insect physiology 2021 12 136 104344. Valer Felipe Berti, Spegiorim Giulia Covolo, Espreafico Enilza Maria, Ramos Ricardo Guelerman Pinhei |
rs7903146 mutation of Type 2 diabetes mellitus-related gene TCF7L2 is not associated with polycystic ovary syndrome in a cohort of Turkey. Revista da Associacao Medica Brasileira (1992) 2021 Aug 67 (8): 1130-1136. Ta?kin Emre, Ero?lu Sem |
DNA Methylation Profiling Identifies Subgroups of Lung Adenocarcinoma with Distinct Immune Cell Composition, DNA Methylation Age, and Clinical Outcome. Clinical cancer research : an official journal of the American Association for Cancer Research 2022 7 28 (17): 3824-3835. Guidry Kayla, Vasudevaraja Varshini, Labbe Kristen, Mohamed Hussein, Serrano Jonathan, Guidry Brett W, DeLorenzo Michael, Zhang Hua, Deng Jiehui, Sahu Soumyadip, Almonte Christina, Moreira Andre L, Tsirigos Aristotelis, Papagiannakopoulos Thales, Pass Harvey, Snuderl Matija, Wong Kwok-K |
Limited Effect of Y Chromosome Variation on Coronary Artery Disease and Mortality in UK Biobank-Brief Report. Arteriosclerosis, thrombosis, and vascular biology 2022 7 42 (9): 1198-1206. Timmers Paul R H J, Wilson James |
Temozolomide and Radiotherapy versus Radiotherapy Alone in Patients with Glioblastoma, IDH-wildtype: Post Hoc Analysis of the EORTC Randomized Phase III CATNON Trial. Clinical cancer research : an official journal of the American Association for Cancer Research 2022 3 28 (12): 2527-2535. Tesileanu C Mircea S, Sanson Marc, Wick Wolfgang, Brandes Alba A, Clement Paul M, Erridge Sara C, Vogelbaum Michael A, Nowak Anna K, Baurain Jean-Francois, Mason Warren P, Wheeler Helen, Chinot Olivier L, Gill Sanjeev, Griffin Matthew, Rogers Leland, Taal Walter, Rudà Roberta, Weller Michael, McBain Catherine, van Linde Myra E, Aldape Kenneth, Jenkins Robert B, Kros Johan M, Wesseling Pieter, von Deimling Andreas, Hoogstrate Youri, de Heer Iris, Atmodimedjo Peggy N, Dubbink Hendrikus J, Brouwer Rutger W W, van IJcken Wilfred F J, Cheung Kin Jip, Golfinopoulos Vassilis, Baumert Brigitta G, Gorlia Thierry, French Pim J, van den Bent Martin |
Association of smoking, lung function and COPD in COVID-19 risk: a two-step Mendelian randomization study. Addiction (Abingdon, England) 2022 Feb . Au Yeung Shiu Lun, Li Albert Martin, He Baoting, Kwok Kin On, Schooling C Ma |
Genetic association of ANGPT2 with primary open-angle glaucoma. Eye and vision (London, England) 2022 Oct 9 (1): 37. He Jing Na, Ng Tsz Kin, Lu Shi Yao, Tam Pancy Oi Sin, Chan Poemen P, Tham Clement C, Pang Chi Pui, Chen Li Jia, Chu Wai K |
The relationship between PD-L1 expression and tumor driver gene mutations and survival in non small cell lung carcinoma. Polish journal of pathology : official journal of the Polish Society of Pathologists 2021 72 (3): 222-228. Chan Kin, Vong Hong, Chu Wai, Cheng Kun, Zhong Xue, Wen Ji |
Investigation of the genetic etiology in male infertility with apparently balanced chromosomal structural rearrangements by genome sequencing. Asian journal of andrology 2022 1 24 (3): 248-254. Chau Matthew Hoi Kin, Li Ying, Dai Peng, Shi Mengmeng, Zhu Xiaofan, Wah Chung Jacqueline Pui, Kwok Yvonne K, Choy Kwong Wai, Kong Xiangdong, Dong Zir |
Does ACE2 mediate the detrimental effect of exposures related to COVID-19 risk: A Mendelian randomization investigation. Journal of medical virology 2022 Oct . Au Yeung Shiu Lun, Wong Tommy Hon Ting, He Baoting, Luo Shan, Kwok Kin |
Disparities in ethnicity and metabolic disease burden in referrals to nephrology. Singapore medical journal 2023 9 . Yan Ting Chua, Cheang Han Leo, Horng Ruey Chua, Weng Kin Wong, Gek Cher Chan, Anantharaman Vathsala, Ye Lu Mavis Gan, Boon Wee T |
Interactive effects between CDHR3 genotype and rhinovirus species for diagnosis and severity of respiratory tract infections in hospitalized children. Microbiology spectrum 2023 9 e0118123. Yu P Song, Man F Tang, Agnes S Y Leung, Kin P Tao, Oi M Chan, Gary W K Wong, Paul K S Chan, Renee W Y Chan, Ting F Leu |
Influence of the Bile Acid Transporter Genes ABCB4, ABCB8, and ABCB11 and the Farnesoid X Receptor on the Response to Ursodeoxycholic Acid in Patients with Nonalcoholic Steatohepatitis. Journal of personalized medicine 2023 7 13 (7): . Henriette Kreimeyer, Katharina Vogt, Tobias Götze, Jan Best, Oliver Götze, Jochen Weigt, Alisan Kahraman, Mustafa Özçürümez, Julia Kälsch, Wing-Kin Syn, Svenja Sydor, Ali Canbay, Paul Man |
Primary open-angle glaucoma risk prediction with ABCA1 and LOC102723944 variants and their genotype-phenotype correlations in southern Chinese population. Molecular genetics and genomics : MGG 2023 7 . Zhenggen Wu, Chukai Huang, Yuqian Zheng, Xiang-Ling Yuan, Shaowan Chen, Yanxuan Xu, Li Jia Chen, Chi Pui Pang, Mingzhi Zhang, Tsz Kin |
Common driver mutations and programmed death-ligand 1 expression in advanced non-small cell lung cancer in smokers and never smokers. BMC cancer 2023 7 23 (1): 659. Chong Kin Liam, Chian Yih Yew, Yong Kek Pang, Chee Kuan Wong, Mau Ern Poh, Jiunn Liang Tan, Chun Ian Soo, Thian Chee Loh, Ka Kiat Chin, Vijayan Munusamy, Yong Sheng Liam, Nur Husna Ibrah |
Creating the Pick's disease International Consortium: Association study of MAPT H2 haplotype with risk of Pick's disease. medRxiv : the preprint server for health sciences 2023 5 . Rebecca R Valentino, William J Scotton, Shanu F Roemer, Tammaryn Lashley, Michael G Heckman, Maryam Shoai, Alejandro Martinez-Carrasco, Nicole Tamvaka, Ronald L Walton, Matthew C Baker, Hannah L Macpherson, Raquel Real, Alexandra I Soto-Beasley, Kin Mok, Tamas Revesz, Thomas T Warner, Zane Jaunmuktane, Bradley F Boeve, Elizabeth A Christopher, Michael DeTure, Ranjan Duara, Neill R Graff-Radford, Keith A Josephs, David S Knopman, Shunsuke Koga, Melissa E Murray, Kelly E Lyons, Rajesh Pahwa, Joseph E Parisi, Ronald C Petersen, Jennifer Whitwell, Lea T Grinberg, Bruce Miller, Athena Schlereth, William W Seeley, Salvatore Spina, Murray Grossman, David J Irwin, Edward B Lee, EunRan Suh, John Q Trojanowski, Vivianna M Van Deerlin, David A Wolk, Theresa R Connors, Patrick M Dooley, Matthew P Frosch, Derek H Oakley, Iban Aldecoa, Mircea Balasa, Ellen Gelpi, Sergi Borrego-Écija, Rosa Maria de Eugenio Huélamo, Jordi Gascon-Bayarri, Raquel Sánchez-Valle, Pilar Sanz-Cartagena, Gerard Piñol-Ripoll, Laura Molina-Porcel, Eileen H Bigio, Margaret E Flanagan, Tamar Gefen, Emily J Rogalski, Sandra Weintraub, Javier Redding-Ochoa, Koping Chang, Juan C Troncoso, Stefan Prokop, Kathy L Newell, Bernardino Ghetti, Matthew Jones, Anna Richardson, Andrew C Robinson, Federico Roncaroli, Julie Snowden, Kieren Allinson, Oliver Green, James B Rowe, Poonam Singh, Thomas G Beach, Geidy E Serrano, Xena E Flowers, James E Goldman, Allison C Heaps, Sandra P Leskinen, Andrew F Teich, Sandra E Black, Julia L Keith, Mario Masellis, Istvan Bodi, Andrew King, Safa-Al Sarraj, Claire Troakes, Glenda M Halliday, John R Hodges, Jillian J Kril, John B Kwok, Olivier Piguet, Marla Gearing, Thomas Arzberger, Sigrun Roeber, Johannes Attems, Christopher M Morris, Alan J Thomas, Bret M Evers, Charles L White, Naguib Mechawar, Anne A Sieben, Patrick P Cras, Bart B De Vil, Peter Paul P P De Deyn, Charles Duyckaerts, Isabelle Le Ber, Danielle Seihean, Sabrina Turbant-Leclere, Ian R MacKenzie, Catriona McLean, Matthew D Cykowski, John F Ervin, Shih-Hsiu J Wang, Caroline Graff, Inger Nennesmo, Rashed M Nagra, James Riehl, Gabor G Kovacs, Giorgio Giaccone, Benedetta Nacmias, Manuela Neumann, Lee-Cyn Ang, Elizabeth C Finger, Cornelis Blauwendraat, Mike A Nalls, Andrew B Singleton, Dan Vitale, Cristina Cunha, Agostinho Carvalho, Zbigniew K Wszolek, Huw R Morris, Rosa Rademakers, John A Hardy, Dennis W Dickson, Jonathan D Rohrer, Owen A Ro |
An IL1RL1 genetic variant lowers soluble ST2 levels and the risk effects of APOE-?4 in female patients with Alzheimer's disease. Nature aging 2023 4 2 (7): 616-634. Yuanbing Jiang, Xiaopu Zhou, Hiu Yi Wong, Li Ouyang, Fanny C F Ip, Vicky M N Chau, Shun-Fat Lau, Wei Wu, Daniel Y K Wong, Heukjin Seo, Wing-Yu Fu, Nicole C H Lai, Yuewen Chen, Yu Chen, Estella P S Tong, , Vincent C T Mok, Timothy C Y Kwok, Kin Y Mok, Maryam Shoai, Benoit Lehallier, Patricia Morán Losada, Eleanor O'Brien, Tenielle Porter, Simon M Laws, John Hardy, Tony Wyss-Coray, Colin L Masters, Amy K Y Fu, Nancy Y |
The 3'UTR region of the DNA repair gene PARP-1 May increase the severity of COVID-19 by altering the binding of antiviral miRNAs. Virology 2023 4 583 29-35. Bü?ra Y?lmaz, Güne? Çakmak Genç, Sevim Karaka? Çelik, Nihal Pi?kin, Emre Horuz, Ahmet Durs |
Multi-Polymorphism Analysis Reveals Joint Effects in Males With Chronic Central Serous Chorioretinopathy. Investigative ophthalmology & visual science 2023 4 64 (4): 19. Chen Zhen Ji, Ng Danny S C, Cen Ling-Ping, Ng Tsz Kin, Ho Mary, Brelen Marten E, Li Tai-Ping, Lu Shi Yao, Tam Pancy O S, Young Alvin L, Chen Weiqi, Yam Jason C, Chen Haoyu, Tham Clement C, Pang Chi Pui, Chen Li J |
The evolution of lung cancer and impact of subclonal selection in TRACERx. Nature 2023 4 616 (7957): 525-533. Frankell Alexander M, Dietzen Michelle, Al Bakir Maise, Lim Emilia L, Karasaki Takahiro, Ward Sophia, Veeriah Selvaraju, Colliver Emma, Huebner Ariana, Bunkum Abigail, Hill Mark S, Grigoriadis Kristiana, Moore David A, Black James R M, Liu Wing Kin, Thol Kerstin, Pich Oriol, Watkins Thomas B K, Naceur-Lombardelli Cristina, Cook Daniel E, Salgado Roberto, Wilson Gareth A, Bailey Chris, Angelova Mihaela, Bentham Robert, Martínez-Ruiz Carlos, Abbosh Christopher, Nicholson Andrew G, Le Quesne John, Biswas Dhruva, Rosenthal Rachel, Puttick Clare, Hessey Sonya, Lee Claudia, Prymas Paulina, Toncheva Antonia, Smith Jon, Xing Wei, Nicod Jerome, Price Gillian, Kerr Keith M, Naidu Babu, Middleton Gary, Blyth Kevin G, Fennell Dean A, Forster Martin D, Lee Siow Ming, Falzon Mary, Hewish Madeleine, Shackcloth Michael J, Lim Eric, Benafif Sarah, Russell Peter, Boleti Ekaterini, Krebs Matthew G, Lester Jason F, Papadatos-Pastos Dionysis, Ahmad Tanya, Thakrar Ricky M, Lawrence David, Navani Neal, Janes Sam M, Dive Caroline, Blackhall Fiona H, Summers Yvonne, Cave Judith, Marafioti Teresa, Herrero Javier, Quezada Sergio A, Peggs Karl S, Schwarz Roland F, Van Loo Peter, Miedema Daniël M, Birkbak Nicolai J, Hiley Crispin T, Hackshaw Allan, Zaccaria Simone, , Jamal-Hanjani Mariam, McGranahan Nicholas, Swanton Charl |
The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young. medRxiv : the preprint server for health sciences 2023 4 . Puckelwartz Megan J, Pesce Lorenzo L, Hernandez Edgar J, Webster Gregory, Dellefave-Castillo Lisa M, Russell Mark W, Geisler Sarah S, Kearns Samuel D, Etheridge Felix K, Etheridge Susan P, Monroe Tanner O, Pottinger Tess D, Kannankeril Prince J, Shoemaker M Benjamin, Fountain Darlene, Roden Dan M, MacLeod Heather, Burns Kristin M, Yandell Mark, Tristani-Firouzi Martin, George Alfred L, McNally Elizabeth |
Investigation of associations between apolipoprotein A5 and C3 gene polymorphisms with plasma triglyceride and lipid levels. Revista da Associacao Medica Brasileira (1992) 2023 3 69 (3): 415-420. Ta?kin Emre, Ba?ci Hasan, Turan Muhammed Kam |
Evaluating High-Confidence Genes in Conotruncal Cardiac Defects by Gene Burden Analyses. Journal of the American Heart Association 2023 2 12 (4): e028226. Chui Martin M C, Mak Christopher C Y, Yu Mullin H C, Wong Sandra Y Y, Lun Kin-Shing, Yung Tak-Cheung, Kwong Anna K Y, Chow Pak-Cheong, Chung Brian H |
Association of body mass index and PXDNL gene variants with acute primary angle closure in southern Chinese population. Heliyon 2023 11 9 (11): e22240. Jiawei Chen, Shaowan Chen, Yuqian Zheng, Yanxuan Xu, Xin Zhong, Yuqiang Huang, Tsz Kin Ng, Chukai Hua |
Smoking-informed methylation and expression QTLs in human brain and colocalization with smoking-associated genetic loci. medRxiv : the preprint server for health sciences 2023 10 . Megan Ulmer Carnes, Bryan C Quach, Linran Zhou, Shizhong Han, Ran Tao, Meisha Mandal, Amy Deep-Soboslay, Jesse A Marks, Grier P Page, Brion S Maher, Andrew E Jaffe, Hyejung Won, Laura J Bierut, Thomas M Hyde, Joel E Kleinman, Eric O Johnson, Dana B Hanco |
MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study. The Lancet. Neurology 2024 4 23 (5): 487-499. Rebecca R Valentino, William J Scotton, Shanu F Roemer, Tammaryn Lashley, Michael G Heckman, Maryam Shoai, Alejandro Martinez-Carrasco, Nicole Tamvaka, Ronald L Walton, Matthew C Baker, Hannah L Macpherson, Raquel Real, Alexandra I Soto-Beasley, Kin Mok, Tamas Revesz, Elizabeth A Christopher, Michael DeTure, William W Seeley, Edward B Lee, Matthew P Frosch, Laura Molina-Porcel, Tamar Gefen, Javier Redding-Ochoa, Bernardino Ghetti, Andrew C Robinson, Christopher Kobylecki, James B Rowe, Thomas G Beach, Andrew F Teich, Julia L Keith, Istvan Bodi, Glenda M Halliday, Marla Gearing, Thomas Arzberger, Christopher M Morris, Charles L White, Naguib Mechawar, Susana Boluda, Ian R MacKenzie, Catriona McLean, Matthew D Cykowski, Shih-Hsiu J Wang, Caroline Graff, Rashed M Nagra, Gabor G Kovacs, Giorgio Giaccone, Manuela Neumann, Lee-Cyn Ang, Agostinho Carvalho, Huw R Morris, Rosa Rademakers, John A Hardy, Dennis W Dickson, Jonathan D Rohrer, Owen A Ross, |
The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young. Genome medicine 2024 1 16 (1): 13. Megan J Puckelwartz, Lorenzo L Pesce, Edgar J Hernandez, Gregory Webster, Lisa M Dellefave-Castillo, Mark W Russell, Sarah S Geisler, Samuel D Kearns, Felix Karthik, Susan P Etheridge, Tanner O Monroe, Tess D Pottinger, Prince J Kannankeril, M Benjamin Shoemaker, Darlene Fountain, Dan M Roden, Meghan Faulkner, Heather M MacLeod, Kristin M Burns, Mark Yandell, Martin Tristani-Firouzi, Alfred L George, Elizabeth M McNal |
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- Page last updated:May 06, 2024
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