Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 606 Records) |
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| Changes in antioxidant status and DNA repair capacity are corroborated with molecular alterations in malignant thyroid tissue of patients with papillary thyroid cancer. Frontiers in molecular biosciences 2023 9 10 1237548. Zing Hong Eng, Azlina Abdul Aziz, Khoon Leong Ng, Sarni Mat Jun |
| Multi-ancestry genome-wide association meta-analysis of Parkinson's disease. Nature genetics 2023 12 . Jonggeol Jeffrey Kim, Dan Vitale, Diego Véliz Otani, Michelle Mulan Lian, Karl Heilbron, , Hirotaka Iwaki, Julie Lake, Caroline Warly Solsberg, Hampton Leonard, Mary B Makarious, Eng-King Tan, Andrew B Singleton, Sara Bandres-Ciga, Alastair J Noyce, , Cornelis Blauwendraat, Mike A Nalls, Jia Nee Foo, Ignacio Ma |
| Risk-reducing mastectomy and breast cancer mortality in women with a BRCA1 or BRCA2 pathogenic variant: an international analysis. British journal of cancer 2023 11 . Kelly Metcalfe, Tomasz Huzarski, Jacek Gronwald, Joanne Kotsopoulos, Raymond Kim, Pal Moller, Tuya Pal, Amber Aeilts, Andrea Eisen, Beth Karlan, Louise Bordeleau, Nadine Tung, Olufunmilayo Olopade, Dana Zakalik, Christian F Singer, William Foulkes, Fergus Couch, Susan L Neuhausen, Charis Eng, Ping Sun, Jan Lubinski, Steven A Narod, |
| Is the MTHFR gene mutation associated with thrombosis? Cleveland Clinic journal of medicine 2023 11 90 (11): 661-663. Andrew Dhawan, Charis E |
| Genome-Wide Association Analysis of Protein-Coding Variants in IgA Nephropathy. Journal of the American Society of Nephrology : JASN 2023 10 . Ming Li, Yan-Na Wang, Ling Wang, Wee-Yang Meah, Dian-Chun Shi, Khai-Koon Heng, Li Wang, Chiea-Chuen Khor, Jin-Xin Bei, Ching-Yu Cheng, Tin Aung, Yun-Hua Liao, Qin-Kai Chen, Jie-Ruo Gu, Yao-Zhong Kong, Jimmy Lee, Siow-Ann Chong, Mythily Subramaniam, Jia-Nee Foo, Feng-Tao Cai, Geng-Ru Jiang, Gang Xu, Jian-Xin Wan, Meng-Hua Chen, Pei-Ran Yin, Xiu-Qing Dong, Shao-Zhen Feng, Xue-Qing Tang, Zhong Zhong, Eng-King Tan, Nan Chen, Hong Zhang, Zhi-Hong Liu, E Shyong Tai, Jian-Jun Liu, Xue-Qing |
| The Genomic Landscape of Benign and Malignant Thyroid Tumors from Individuals Carrying Germline PTEN Variants Is Distinct from Sporadic Thyroid Cancers. Cancer research 2024 9 OF1-OF12. Gilman Plitt, Takae Brewer, Lamis Yehia, Laura Rabinowitz, Christopher C Griffith, Charis E |
| Mutational Features and Tumor Microenvironment Alterations in High-Grade Appendiceal Cancers Treated With Iterative Hyperthermic Intraperitoneal Chemotherapy. JCO precision oncology 2024 9 8 e2400149. David G Su, Ankit Dhiman, Varun V Bansal, Yuanyuan Zha, Ardaman Shergill, Blasé Polite, Lindsay Alpert, Kiran K Turaga, Oliver S E |
| Single nucleotide polymorphisms (SNPs) that are associated with obesity and type 2 diabetes among Asians: a systematic review and meta-analysis. Scientific reports 2024 8 14 (1): 20062. Kevina Yanasegaran, Jeremy Yung Ern Ng, Eng Wee Chua, Azmawati Mohammed Nawi, Pei Yuen Ng, Mohd Rizal Abdul Man |
| Incidence of endometrial cancer in BRCA mutation carriers. Gynecologic oncology 2024 8 189 148-155. Joanne Kotsopoulos, Jan Lubinski, Tomasz Huzarski, Brittany L Bychkovsky, Pal Moller, Raymond H Kim, Nadine Tung, Andrea Eisen, William Foulkes, Christian F Singer, Amber Aeilts, Susan L Neuhausen, Louise Bordeleau, Beth Karlan, Robert Fruscio, Charis Eng, Olufunmilayo Olopade, Dana Zakalik, Fergus Couch, Teresa Ramon Y Cajal, Ping Sun, Jacek Gronwald, Steven A Nar |
| Identification of Genetic Variants in Progressive Supranuclear Palsy in Southeast Asia. Movement disorders : official journal of the Movement Disorder Society 2024 8 . Adeline Su Lyn Ng, Ai Huey Tan, Yi Jayne Tan, Jia Lun Lim, Michelle Mulan Lian, Alfand Marl Dy Closas, Azlina Ahmad-Annuar, Shanthi Viswanathan, Yuen Kang Chia, Jia Nee Foo, Weng Khong Lim, Eng-King Tan, Shen-Yang L |
| Investigation of the Genetic Determinants of Telangiectasia and Solid Organ Arteriovenous Malformation Formation in Hereditary Hemorrhagic Telangiectasia (HHT). International journal of molecular sciences 2024 7 25 (14): . Kevin J Whitehead, Doruk Toydemir, Whitney Wooderchak-Donahue, Gretchen M Oakley, Bryan McRae, Angelica Putnam, Jamie McDonald, Pinar Bayrak-Toydem |
| Impact of high-risk EBV strains on nasopharyngeal carcinoma gene expression. Oral oncology 2024 7 157 106941. Chee Yit Lim, Gwyneth W Y Ng, Chuan Keng Goh, Melvin Kiang Chua Lee, Ian Cheong, Eng Eong Ooi, Jianjun Liu, Robert B West, Kwok Seng Loh, Joshua K T |
| 5-HTP inhibits eosinophilia via intracellular endothelial 5-HTRs; SNPs in 5-HTRs associate with asthmatic lung function. Frontiers in allergy 2024 6 5 1385168. Matthew T Walker, Jeffrey C Bloodworth, Timothy S Kountz, Samantha L McCarty, Jeremy E Green, Ryan P Ferrie, Jackson A Campbell, Samantha H Averill, Kenneth B Beckman, Leslie C Grammer, Celeste Eng, Pedro C Avila, Harold J Farber, William Rodriguez-Cintron, Jose R Rodriguez-Santana, Denise Serebrisky, Shannon M Thyne, Max A Seibold, Esteban G Burchard, Rajesh Kumar, Joan M Cook-Mil |
| Interaction between Caffeine Consumption & Genetic susceptibility in Parkinson's disease: a systematic review. Ageing research reviews 2024 6 102381. Yujuan Yang, Zhi-Dong Zhou, Ling Xiao Yi, Brendan Jen-Wei Tan, Eng-King T |
| A common polymorphism in the Intelectin-1 gene influences mucus plugging in severe asthma. Nature communications 2024 5 15 (1): 3900. Jamie L Everman, Satria P Sajuthi, Maude A Liegeois, Nathan D Jackson, Erik H Collet, Michael C Peters, Maurizio Chioccioli, Camille M Moore, Bhavika B Patel, Nathan Dyjack, Roger Powell, Cydney Rios, Michael T Montgomery, Celeste Eng, Jennifer R Elhawary, Angel C Y Mak, Donglei Hu, Scott Huntsman, Sandra Salazar, Luigi Feriani, Ana Fairbanks-Mahnke, Gianna L Zinnen, Cole R Michel, Joe Gomez, Xing Zhang, Vivian Medina, Hong Wei Chu, Pietro Cicuta, Erin D Gordon, Pamela Zeitlin, Victor E Ortega, Nichole Reisdorph, Eleanor M Dunican, Monica Tang, Brett M Elicker, Travis S Henry, Eugene R Bleecker, Mario Castro, Serpil C Erzurum, Elliot Israel, Bruce D Levy, David T Mauger, Deborah A Meyers, Kaharu Sumino, David S Gierada, Annette T Hastie, Wendy C Moore, Loren C Denlinger, Nizar N Jarjour, Mark L Schiebler, Sally E Wenzel, Prescott G Woodruff, Jose Rodriguez-Santana, Chad G Pearson, Esteban G Burchard, John V Fahy, Max A Seibo |
| Integrative multi-omics analyses to identify the genetic and functional mechanisms underlying ovarian cancer risk regions. American journal of human genetics 2024 5 . Eileen O Dareng, Simon G Coetzee, Jonathan P Tyrer, Pei-Chen Peng, Will Rosenow, Stephanie Chen, Brian D Davis, Felipe Segato Dezem, Ji-Heui Seo, Robbin Nameki, Alberto L Reyes, Katja K H Aben, Hoda Anton-Culver, Natalia N Antonenkova, Gerasimos Aravantinos, Elisa V Bandera, Laura E Beane Freeman, Matthias W Beckmann, Alicia Beeghly-Fadiel, Javier Benitez, Marcus Q Bernardini, Line Bjorge, Amanda Black, Natalia V Bogdanova, Kelly L Bolton, James D Brenton, Agnieszka Budzilowska, Ralf Butzow, Hui Cai, Ian Campbell, Rikki Cannioto, Jenny Chang-Claude, Stephen J Chanock, Kexin Chen, Georgia Chenevix-Trench, , Yoke-Eng Chiew, Linda S Cook, Anna DeFazio, Joe Dennis, Jennifer A Doherty, Thilo Dörk, Andreas du Bois, Matthias Dürst, Diana M Eccles, Gabrielle Ene, Peter A Fasching, James M Flanagan, Renée T Fortner, Florentia Fostira, Aleksandra Gentry-Maharaj, Graham G Giles, Marc T Goodman, Jacek Gronwald, Christopher A Haiman, Niclas Håkansson, Florian Heitz, Michelle A T Hildebrandt, Estrid Høgdall, Claus K Høgdall, Ruea-Yea Huang, Allan Jensen, Michael E Jones, Daehee Kang, Beth Y Karlan, Anthony N Karnezis, Linda E Kelemen, Catherine J Kennedy, Elza K Khusnutdinova, Lambertus A Kiemeney, Susanne K Kjaer, Jolanta Kupryjanczyk, Marilyne Labrie, Diether Lambrechts, Melissa C Larson, Nhu D Le, Jenny Lester, Lian Li, Jan Lubi?ski, Michael Lush, Jeffrey R Marks, Keitaro Matsuo, Taymaa May, John R McLaughlin, Iain A McNeish, Usha Menon, Stacey Missmer, Francesmary Modugno, Melissa Moffitt, Alvaro N Monteiro, Kirsten B Moysich, Steven A Narod, Tu Nguyen-Dumont, Kunle Odunsi, Håkan Olsson, N Charlotte Onland-Moret, Sue K Park, Tanja Pejovic, Jennifer B Permuth, Anna Piskorz, Darya Prokofyeva, Marjorie J Riggan, Harvey A Risch, Cristina Rodríguez-Antona, Mary Anne Rossing, Dale P Sandler, V Wendy Setiawan, Kang Shan, Honglin Song, Melissa C Southey, Helen Steed, Rebecca Sutphen, Anthony J Swerdlow, Soo Hwang Teo, Kathryn L Terry, Pamela J Thompson, Liv Cecilie Vestrheim Thomsen, Linda Titus, Britton Trabert, Ruth Travis, Shelley S Tworoger, Ellen Valen, Els Van Nieuwenhuysen, Digna Velez Edwards, Robert A Vierkant, Penelope M Webb, , Clarice R Weinberg, Rayna Matsuno Weise, Nicolas Wentzensen, Emily White, Stacey J Winham, Alicja Wolk, Yin-Ling Woo, Anna H Wu, Li Yan, Drakoulis Yannoukakos, Nur Zeinomar, Wei Zheng, Argyrios Ziogas, Andrew Berchuck, Ellen L Goode, David G Huntsman, Celeste L Pearce, Susan J Ramus, Thomas A Sellers, , Matthew L Freedman, Kate Lawrenson, Joellen M Schildkraut, Dennis Hazelett, Jasmine T Plummer, Siddhartha Kar, Michelle R Jones, Paul D P Pharoah, Simon A Gayth |
| Transcriptomic imputation of genetic risk variants uncovers novel whole-blood biomarkers of Parkinson's disease. NPJ Parkinson's disease 2024 5 10 (1): 99. Gabriel Chew, Aaron Shengting Mai, John F Ouyang, Yueyue Qi, Yinxia Chao, Qing Wang, Enrico Petretto, Eng-King T |
| Molecular profiling of metastatic breast cancer and target-based therapeutic matching in an Asian tertiary phase I oncology unit. Frontiers in oncology 2024 5 14 1342346. Robert John Walsh, Rebecca Ong, Seng Wee Cheo, Peter Q J Low, Aishwarya Jayagopal, Matilda Lee, Natalie Ngoi, Samuel G Ow, Andrea L A Wong, Siew Eng Lim, Yi Wan Lim, Valerie Heong, Raghav Sundar, Ross A Soo, Cheng Ean Chee, Wei Peng Yong, Boon Cher Goh, Soo Chin Lee, David S P Tan, Joline S J L |
| The risk of skin cancer in women who carry BRCA1 or BRCA2 mutations. Hereditary cancer in clinical practice 2024 5 22 (1): 7. Steven A Narod, Kelly Metcalfe, Amy Finch, An-Wen Chan, Susan Randall Armel, Amber Aeilts, Andrea Eisen, Beth Karlan, Louise Bordeleau, Nadine Tung, William D Foulkes, Susan L Neuhausen, Charis Eng, Olufunmilayo Olopade, Dana Zakalik, Fergus Couch, Carey Cullinane, Tuya Pal, Ping Sun, Joanne Kotsopoulos, |
| Newborn Screening for ?-Thalassemia Identifies a Complex Genotype Involving a Novel ?-Globin Gene Mutation (HBB:c.336dup). Hemoglobin 2024 4 1-3. John S Waye, Meredith Hanna, Betty-Ann Hohenadel, Lisa Nakamura, Lynda Walker, Barry Eng, Landry E Nfons |
| Parkinson's Disease Risk Variant rs9638616 is Non-Specifically Associated with Altered Brain Structure and Function. Journal of Parkinson's disease 2024 4 . Thomas Welton, Thomas Wei Jun Teo, Ling Ling Chan, Eng-King Tan, Louis Chew Seng T |
| Novel genomic variants influencing methotrexate delayed clearance in pediatric patients with acute lymphoblastic leukemia. Frontiers in pharmacology 2024 11 15 1480657. Jung Yoon Choi, Hoshik Kwon, Hyery Kim, Kyung Taek Hong, Youngeun Ma, Kyung-Nam Koh, Sunmin Yun, Keon Hee Yoo, Sang Hoon Song, Ho Joon Im, Ju Han Kim, Hyoung Jin Ka |
| The incidence of pancreatic cancer in women with a BRCA1 or BRCA2 mutation. Cancer 2024 11 . Bryson W Katona, Jan Lubinski, Tuya Pal, Tomasz Huzarski, William D Foulkes, Pal Moller, Andrea Eisen, Susan Randall Armel, Susan L Neuhausen, Rebecca Raj, Amber Aeilts, Christian F Singer, Louise Bordeleau, Beth Karlan, Olufunmilayo Olopade, Nadine Tung, Dana Zakalik, Joanne Kotsopoulos, Robert Fruscio, Charis Eng, Ping Sun, Steven A Narod, |
| Exome sequencing in Asian populations identifies low-frequency and rare coding variation influencing Parkinson's disease risk. Nature aging 2024 11 . Elaine Gy Chew, Zhehao Liu, Zheng Li, Sun Ju Chung, Michelle M Lian, Moses Tandiono, Yue Jing Heng, Ebonne Y Ng, Louis Cs Tan, Wee Ling Chng, Tiak Ju Tan, Esther Kl Peh, Ying Swan Ho, Xiao Yin Chen, Erin Yt Lim, Chu Hua Chang, Jonavan J Leong, Ting Xuan Peh, Ling Ling Chan, Yinxia Chao, Wing-Lok Au, Kumar M Prakash, Jia Lun Lim, Yi Wen Tay, Vincent Mok, Anne Yy Chan, Juei-Jueng Lin, Beom S Jeon, Kyuyoung Song, Clement C Tham, Chi Pui Pang, Jeeyun Ahn, Kyu Hyung Park, Janey L Wiggs, Tin Aung, Ai Huey Tan, Azlina Ahmad Annuar, Mary B Makarious, Cornelis Blauwendraat, Mike A Nalls, Laurie A Robak, Roy N Alcalay, Ziv Gan-Or, Richard Reynolds, Shen-Yang Lim, Yun Xia, Chiea Chuen Khor, Eng-King Tan, Zhenxun Wang, Jia Nee F |
| Germline Genetic Susceptibility Testing Among Emirati Nationals at Risk for Hereditary Breast and Ovarian Cancer Syndrome. JCO global oncology 2024 11 10 e2400352. Rifaat R Rawashdeh, Holly Pederson, Rafal Iskanderian, Fawad Khan, Basel Altrabulsi, Stephanie Ricci, Charis Eng, Bassel Jallad, Asma Ibrahim Al Mannaei, Mohamed Salem Alameri, Azza Attia, Stephen R Grobmy |
| Genetic susceptibility to caffeine intake and metabolism: a systematic review. Journal of translational medicine 2024 10 22 (1): 961. Jazreel Ju-Li Low, Brendan Jen-Wei Tan, Ling-Xiao Yi, Zhi-Dong Zhou, Eng-King T |
| Region-based analyses of existing genome-wide association studies identifies novel potential genetic susceptibility regions for glioma. Cancer research communications 2024 10 . Karen Alpen, Robert J Maclnnis, Claire M Vajdic, John Lai, James G Dowty, Eng-Siew Koh, Elizabeth Hovey, Rosemary Harrup, Tuong L Nguyen, Shuai Li, David Joseph, Geza Benke, Pierre-Antoine Dugué, Melissa C Southey, Graham G Giles, Anna K Nowak, Katharine J Drummond, Daniel F Schmidt, John L Hopper, Miroslaw K Kapuscinski, Enes Makal |
| Loss-of-function SMPD1 gene variant in Progressive Supranuclear Palsy-Richardson Syndrome patients of Chinese ancestry. Journal of movement disorders 2024 1 . Shen-Yang Lim, Ai Huey Tan, Jia Nee Foo, Yi Jayne Tan, Elaine Gy Chew, Azlina Ahmad Annuar, Alfand Marl Dy Closas, Azalea Pajo, Jia Lun Lim, Yi Wen Tay, Anis Nadhirah, Jia Wei Hor, Tzi Shin Toh, Lei Cheng Lit, Jannah Zulkefli, Su Juen Ngim, Weng Khong Lim, Huw R Morris, Eng-King Tan, Adeline Sl |
| Genetic Association Studies in Restless Legs Syndrome: Risk variants & Ethnic differences. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2024 1 1-31. Brendan Jen-Wei Tan, Xin-Ler Pang, Sarah Png, Zhi Dong Zhou, Eng-King T |
| Generation of a human induced pluripotent stem cell line NTUHi006-A from a polycystic ovarian syndrome patient. Stem cell research 2025 1 82 103647. Chia-Eng Wu, Hsiang-Po Huang, Hong-Nerng Ho, Mei-Jou Ch |
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