Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 732 Records) |
Query Trace: Precision medicine[original query] |
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CETP and APOA2 polymorphisms are associated with weight loss and healthy eating behavior changes in response to digital lifestyle modifications. Scientific reports 2023 12 13 (1): 21615. Meelim Kim, Seolha Lee, Eun Cho, Kyung-Won Hong, So-Jin You, Hyung Jin Ch |
Associations Between Genetic Variation in the Targets of Low-Density Lipoprotein-Lowering Drugs and Rheumatoid Arthritis. Circulation. Genomic and precision medicine 2023 12 e004232. Chenxi Qin, Sara Hä |
Genetic Susceptibility of HLA Alleles to Non-Steroidal Anti-Inflammatory Drug Hypersensitivity in the Taiwanese Population. Biomedicines 2023 12 11 (12): . Szu-Ling Chang, Chih-Hung Lai, Guan-Cheng Lin, Yi-Ming Chen, Mei-Hsuan Lee, Han-Shui Hsu, I-Chieh Ch |
Risk adjustment model for tuberculosis compared to non-tuberculosis mycobacterium or latent tuberculosis infection: Center for Personalized Precision Medicine of Tuberculosis (cPMTb) cohort database. BMC pulmonary medicine 2023 11 23 (1): 471. Woo Jung Seo, Hyeon-Kyoung Koo, Ji Yeon Kang, Jieun Kang, So Hee Park, Hyung Koo Kang, Hye Kyeong Park, Sung-Soon Lee, Sangbong Choi, Tae Won Jang, Kyeong-Cheol Shin, Jee Youn Oh, Joon Young Choi, Jinsoo Min, Young-Kyung Choi, Jae-Gook Shin, Yong-Soon C |
Role of genetic polymorphisms in clopidogrel response variability: a systematic review. Open heart 2023 11 10 (2): . Jose Lopez, Justin Mark, Gustavo J Duarte, Mohammed Shaban, Franklin Sosa, Rishabh Mishra, Swati Jain, An Tran, Asma Khizar, Daniel Karpel, Giancarlo Acosta, Miguel Rodriguez-Guer |
Pathogenic alterations in PIK3CA and KMT2C are frequent and independent prognostic factors in anal squamous cell carcinoma treated with salvage abdominoperineal resection. International journal of cancer 2023 11 . Abderaouf Hamza, Julien Masliah-Planchon, Cindy Neuzillet, Jérémie H Lefèvre, Magali Svrcek, Sophie Vacher, Christine Bourneix, Matthieu Delaye, Diane Goéré, Peggy Dartigues, Emmanuelle Samalin, Marc Hilmi, Julien Lazartigues, Elodie Girard, Jean-François Emile, Eugénie Rigault, Virginie Dangles-Marie, Nathalie Rioux-Leclercq, Christelle de la Fouchardière, David Tougeron, Andrea Casadei-Gardini, Pascale Mariani, Frédérique Peschaud, Wulfran Cacheux, Astrid Lièvre, Ivan Bièc |
Comprehensive genomic profiling testing in Japanese castration-resistant prostate cancer patients: results of a single-center retrospective cohort study. Japanese journal of clinical oncology 2023 10 . Takafumi Fukushima, Keisuke Goto, Tetsutaro Hayashi, Kenichiro Ikeda, Tomoya Hatayama, Ryoken Yamanaka, Kyosuke Iwane, Ryo Tasaka, Yuki Kohada, Kenshiro Takemoto, Kohei Kobatake, Akihiro Goriki, Asuka Toshida, Hikaru Nakahara, Masanori Motonaga, Kentaro Tokumo, Yasutoshi Fujii, C Nelson Hayes, Wataru Okamoto, Toshio Kubo, Takashi Matsumoto, Masaki Shiota, Noboru Yamamoto, Yuji Urabe, Eiso Hiyama, Koji Arihiro, Takao Hinoi, Nobuyuki Hina |
[Expert consensus on the genetic counseling for Dystrophinopathies]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2024 5 41 (6): 651-660. Genetic Counseling Consensus Expert Group For Monogenic Disease Carrier Screening, Genetic Counseling Group Of Medical Genetics Branch Of Chinese Medical Association, Medical Genetics Branch Of Chinese Medical Doctor Association, Genetic Diagnosis And Precision Medicine Branch Of The Chinese Association Of Birth Health And Science, Xiaoliang Liu, Yanyan Zhao, Hua Wang, Jesse Li-Ling, Lingqian Wu, Yanping Lu, Qingxian Cha |
Comparison of diagnostic performance between Oncomine Dx target test and AmoyDx panel for detecting actionable mutations in lung cancer. Scientific reports 2024 5 14 (1): 12480. Yuki Nagakubo, Yosuke Hirotsu, Mona Yoshino, Kenji Amemiya, Ryota Saito, Yumiko Kakizaki, Toshiharu Tsutsui, Yoshihiro Miyashita, Taichiro Goto, Masao Oma |
Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood. medRxiv : the preprint server for health sciences 2024 5 . Yasminka A Jakubek, Xiaolong Ma, Adrienne M Stilp, Fulong Yu, Jason Bacon, Justin W Wong, Francois Aguet, Kristin Ardlie, Donna Arnett, Kathleen Barnes, Joshua C Bis, Tom Blackwell, Lewis C Becker, Eric Boerwinkle, Russell P Bowler, Matthew J Budoff, April P Carson, Jiawen Chen, Michael H Cho, Josef Coresh, Nancy Cox, Paul S de Vries, Dawn L DeMeo, David W Fardo, Myriam Fornage, Xiuqing Guo, Michael E Hall, Nancy Heard-Costa, Bertha Hidalgo, Marguerite Ryan Irvin, Andrew D Johnson, Eimear E Kenny, Dan Levy, Yun Li, Joao Ac Lima, Yongmei Liu, Ruth J F Loos, Mitchell J Machiela, Rasika A Mathias, Braxton D Mitchell, Joanne Murabito, Josyf C Mychaleckyj, Kari North, Peter Orchard, Stephen Cj Parker, Yash Pershad, Patricia A Peyser, Katherine A Pratte, Bruce M Psaty, Laura M Raffield, Susan Redline, Stephen S Rich, Jerome I Rotter, Sanjiv J Shah, Jennifer A Smith, Aaron P Smith, Albert Smith, Margaret Taub, Hemant K Tiwari, Russell Tracy, Bjoernar Tuftin, Alexander G Bick, Vijay G Sankaran, Alexander P Reiner, Paul Scheet, Paul L Au |
Precision medicine for pancreatic cancer: Characterizing the clinico-genomic landscape and outcomes of KRAS G12C-mutated disease. Journal of the National Cancer Institute 2024 5 . Fergus Keane, Joanne F Chou, Henry Walch, Joshua Schoenfeld, Anupriya Singhal, Darren Cowzer, Emily Harrold, Catherine O'Connor, Wungki Park, Anna Varghese, Imane El Dika, Fiyinfolu Balogun, Kenneth H Yu, Marinela Capanu, Nikolaus Schultz, Rona Yaeger, Eileen M O'Reil |
Meta-Analysis of Genome-Wide Association Studies Reveals Genetic Mechanisms of Supraventricular Arrhythmias. Circulation. Genomic and precision medicine 2024 5 e004320. Lu-Chen Weng, Shaan Khurshid, Amelia Weber Hall, Victor Nauffal, Valerie N Morrill, Yan V Sun, Joel T Rämö, Dominik Beer, Simon Lee, Girish Nadkarni, Renee Johnson, Laura Andreasen, Anne Clayton, Clive R Pullinger, Zachary T Yoneda, Daniel J Friedman, Matthew C Hyman, Renae L Judy, Allan C Skanes, Kate M Orland, Paloma Jordà, Timothy M Treu, Matthew T Oetjens, Rajesh Subbiah, Jacob P Hartmann, Heidi T May, John P Kane, Tariq Z Issa, Navid A Nafissi, Peter Leong-Sit, Marie-Pierre Dubé, Carolina Roselli, Seung Hoan Choi, , Jean-Claude Tardif, Habib R Khan, Stacey Knight, Jesper H Svendsen, Bruce Walker, Richard Karlsson Linnér, J Michael Gaziano, Rafik Tadros, Diane Fatkin, Daniel J Rader, Svati H Shah, Dan M Roden, Gregory M Marcus, Ruth J F Loos, Scott M Damrauer, Christopher M Haggerty, Kelly Cho, Aarno Palotie, Morten S Olesen, Lee L Eckhardt, Jason D Roberts, Michael J Cutler, M Benjamin Shoemaker, Peter W F Wilson, Patrick T Ellinor, Steven A Lubi |
Landscape of TPMT and NUDT15 Pharmacogenetic Variation in a Cohort of Canadian Pediatric Inflammatory Bowel Disease Patients. Inflammatory bowel diseases 2024 5 . April M Kennedy, Anne M Griffiths, Aleixo M Muise, Thomas D Walters, Amanda Ricciuto, Hien Q Huynh, Eytan Wine, Kevan Jacobson, Sally Lawrence, Nicholas Carman, David R Mack, Jennifer C deBruyn, Anthony R Otley, Colette Deslandres, Wael El-Matary, Mary Zachos, Eric I Benchimol, Jeffrey Critch, Rilla Schneider, Eileen Crowley, Michael Li, Neil Warner, Dermot P B McGovern, Dalin Li, Talin Haritunians, Sarah Rudin, Iris Co |
Polygenic risk score predicting susceptibility and outcome of benign prostatic hyperplasia in the Han Chinese. Human genomics 2024 5 18 (1): 49. Sheng-Chun Hung, Li-Wen Chang, Tzu-Hung Hsiao, Guan-Cheng Lin, Shian-Shiang Wang, Jian-Ri Li, I-Chieh Ch |
Polygenic Risk Scores Validated in Patient-Derived Cells Stratify for Mitochondrial Subtypes of Parkinson's Disease. Annals of neurology 2024 5 . Giuseppe Arena, Zied Landoulsi, Dajana Grossmann, Thomas Payne, Armelle Vitali, Sylvie Delcambre, Alexandre Baron, Paul Antony, Ibrahim Boussaad, Dheeraj Reddy Bobbili, Ashwin Ashok Kumar Sreelatha, Lukas Pavelka, Nico J Diederich, Christine Klein, Philip Seibler, Enrico Glaab, Thomas Foltynie, Oliver Bandmann, Manu Sharma, Rejko Krüger, Patrick May, Anne Grünewald, |
A deep catalogue of protein-coding variation in 983,578 individuals. Nature 2024 5 . Kathie Y Sun, Xiaodong Bai, Siying Chen, Suying Bao, Chuanyi Zhang, Manav Kapoor, Joshua Backman, Tyler Joseph, Evan Maxwell, George Mitra, Alexander Gorovits, Adam Mansfield, Boris Boutkov, Sujit Gokhale, Lukas Habegger, Anthony Marcketta, Adam E Locke, Liron Ganel, Alicia Hawes, Michael D Kessler, Deepika Sharma, Jeffrey Staples, Jonas Bovijn, Sahar Gelfman, Alessandro Di Gioia, Veera M Rajagopal, Alexander Lopez, Jennifer Rico Varela, Jesus Alegre, Jaime Berumen, Roberto Tapia-Conyer, Pablo Kuri-Morales, Jason Torres, Jonathan Emberson, Rory Collins, , , Michael Cantor, Timothy Thornton, Hyun Min Kang, John D Overton, Alan R Shuldiner, M Laura Cremona, Mona Nafde, Aris Baras, Goncalo Abecasis, Jonathan Marchini, Jeffrey G Reid, William Salerno, Suganthi Balasubramani |
Polymorphisms of HLA genes and hypersensitivity to penicillin among patients in a Taiwanese population. International journal of immunogenetics 2024 5 . Chih-Chun Wang, I-Chieh Chen, Guan-Cheng Lin, Yi-Ming Chen, Ching-Hui Sh |
Somatic mutational profiling and clinical impact of driver genes in Latin-Iberian medulloblastomas: Towards precision medicine. Neuropathology : official journal of the Japanese Society of Neuropathology 2024 5 . Letícia Ganem Rillo Paz Barateiro, Rodrigo de Oliveira Cavagna, Mariana Bisarro Dos Reis, Flávia Escremim de Paula, Gustavo Ramos Teixeira, Daniel Antunes Moreno, Murilo Bonatelli, Iara Santana, Fabiano Pinto Saggioro, Luciano Neder, João Norberto Stavale, Suzana Maria Fleury Malheiros, Hernan Garcia-Rivello, Silvia Christiansen, Susana Nunes, Maria João Gil da Costa, Jorge Pinheiro, Carlos Almeida Júnior, Bruna Minniti Mançano, Rui Manuel Re |
Distinct Driver Pathway Enrichments and a High Prevalence of TSC2 Mutations in Right Colon Cancer in Chile: A Preliminary Comparative Analysis. International journal of molecular sciences 2024 5 25 (9): . Camilo Tapia-Valladares, Guillermo Valenzuela, Evelin González, Ignacio Maureira, Jessica Toro, Matías Freire, Gonzalo Sepúlveda-Hermosilla, Diego Ampuero, Alejandro Blanco, Iván Gallegos, Fernanda Morales, José I Erices, Olga Barajas, Mónica Ahumada, Héctor R Contreras, Jaime González, Ricardo Armisén, Katherine Marcela |
Consumption of dietary fiber and APOA5 genetic variants in metabolic syndrome: baseline data from the Korean Medicine Daejeon Citizen Cohort Study. Nutrition & metabolism 2024 4 21 (1): 19. Jimi Kim, Younghwa Baek, Siwoo L |
Assessing the Occurrence and Influence of Cancer Chemotherapy-Related Pharmacogenetic Alleles in the Chilean Population. Pharmaceutics 2024 4 16 (4): . Gareth I Owen, Miguel Cordova-Delgado, Bernabé I Bustos, Leslie C Cerpa, Pamela Gonzalez, Sebastián Morales-Pison, Benjamín Garcia-Bloj, Marcelo Garrido, Juan Francisco Miquel, Luis A Quiñon |
Investigating the Potential Influence of TAS2R16 Genetic Variants and Protein Levels on Multiple Sclerosis Development. Journal of personalized medicine 2024 4 14 (4): . Greta Gedvilaite, Enrika Pileckaite, Ignas Ramanauskas, Loresa Kriauciuniene, Renata Balnyte, Rasa Liutkevicie |
Meta-analysis of the global distribution of clinically relevant CYP2C8 alleles and their inferred functional consequences. Human genomics 2024 4 18 (1): 40. Mahamadou D Camara, Yitian Zhou, Taís Nóbrega De Sousa, José P Gil, Abdoulaye A Djimde, Volker M Lausch |
Vascular Ehlers-Danlos Syndrome: A Comprehensive Natural History Study in a Dutch National Cohort of 142 Patients. Circulation. Genomic and precision medicine 2024 4 e003978. Serwet Demirdas, Lisa M van den Bersselaar, Rosan Lechner, Jessica Bos, Suzanne I M Alsters, Marieke J H Baars, Annette F Baas, Özlem Baysal, Saskia N van der Crabben, Eelco Dulfer, Noor A A Giesbertz, Apollonia T J M Helderman-van den Enden, Yvonne Hilhorst-Hofstee, Marlies J E Kempers, Fenne L Komdeur, Bart Loeys, Daniëlle Majoor-Krakauer, Charlotte W Ockeloen, Eline Overwater, Peter J van Tintelen, Marsha Voorendt, Vivian de Waard, Alessandra Maugeri, Hennie T Brüggenwirth, Ingrid M B H van de Laar, Arjan C Houweli |
Genetic variants, haplotype determination, and function of novel alleles of CYP2B6 in a Han Chinese population. Heliyon 2024 4 10 (7): e28952. Li-Qun Zhang, Xin-Yue Li, Lian-Guo Chen, Zhe Chen, Ren-Ai Xu, Jian-Chang Qian, Xiao-Yang Zhou, Da-Peng Dai, Guo-Xin Hu, Jian-Ping C |
Genetic contribution of breast cancer genes in women of black African origin. Frontiers in genetics 2024 1 14 1302645. Rokhaya Ndiaye, Jean Pascal Demba Diop, Ahmadou Dem, Alioune Die |
Polygenic liability for antipsychotic dosage and polypharmacy - a real-world registry and biobank study. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2024 1 . Elise Koch, Anders Kämpe, Maris Alver, Sindri Sigurðarson, Guðmundur Einarsson, Juulia Partanen, Robert L Smith, Piotr Jaholkowski, Heidi Taipale, Markku Lähteenvuo, Nils Eiel Steen, Olav B Smeland, Srdjan Djurovic, Espen Molden, , , Engilbert Sigurdsson, Hreinn Stefánsson, Kári Stefánsson, Aarno Palotie, Lili Milani, Kevin S O'Connell, Ole A Andreass |
Association study between genetic polymorphisms in MTHFR and stroke susceptibility in Egyptian population: a case-control study. Scientific reports 2024 1 14 (1): 114. Omali Y El-Khawaga, Mohammed F Al-Azzawy, Aliaa N El-Dawa, Afaf M ElSaid, Wessam Mustafa, Mariam Sa |
A novel AllGlo probe-quantitative PCR method for detecting single nucleotide polymorphism in CYP2C19 to evaluate the antiplatelet activity of clopidogrel. Scientific reports 2024 1 14 (1): 2358. Hongwei Li, Yizhen Fang, Yongquan Chen, Yuning Lin, Zanxi Fang, Zhiyuan Lin, Huabin Xie, Zhongying Zha |
Prevalence and Significance of Rare Genetic Variants in AKAP9 in Inherited Cardiac Diseases. Circulation. Genomic and precision medicine 2024 1 e004260. Alexis Hermida, Flavie Ader, Guillaume Jedraszak, Guillaume Viboud, Véronique Fressart, Anne Claire Bréhin, Marion Gérard, Diala Khraiche, Asurélien Palmyre, Olivier Paziaud, Elena Popescu, Julie Proukhnitzky, Mikael Laredo, Pascale Richard, Geraldine Vedrenne, Agathe Vernier, Philippe Charron, Estelle Gandjbakh |
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- Page last updated:Jun 03, 2024
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