Human Genome Epidemiology Literature Finder
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Urinary Analysis of FGFR3 and TERT Gene Mutations Enhances Performance of Cxbladder Tests and Improves Patient Risk Stratification. The Journal of urology 2022 12 209 (4): 762-772. Lotan Yair, Raman Jay D, Konety Badrinath, Daneshmand Siamak, Schroeck Florian, Shariat Shahrokh F, Black Peter, de Lange Michel, Asroff Scott, Goldfischer Evan, Efros Mitchell, Chong Kian Tai, Huang Eugene, Chua Hong Liang, Wu Qing Hui, Yeow Siying, Lau Weida, Yong Jin, Eng Mol |
Australian genome-wide association study confirms higher female risk for adult glioma associated with variants in the region of CCDC26. Neuro-oncology 2022 12 . Alpen Karen, Vajdic Claire M, MacInnis Robert J, Milne Roger L, Koh Eng-Siew, Hovey Elizabeth, Harrup Rosemary, Bruinsma Fiona, Nguyen Tuong L, Li Shuai, Joseph David, Benke Geza, Dugué Pierre-Antoine, Southey Melissa C, Giles Graham G, Rosenthal Mark, Drummond Katharine J, Nowak Anna K, Hopper John L, Kapuscinski Miroslaw, Makalic En |
Prevalence of Mutations in Mendelian Stroke Genes in Early Onset Stroke Patients. Annals of neurology 2022 12 . Park Hong-Kyun, Lee Keon-Joo, Park Jong-Moo, Kang Kyusik, Lee Soo Joo, Kim Jae Guk, Cha Jae-Kwan, Kim Dae-Hyun, Han Moon-Ku, Kang Jihoon, Kim Beom Joon, Park Tai Hwan, Park Moo-Seok, Lee Kyung Bok, Lee Jun, Hong Keun-Sik, Cho Yong-Jin, Lee Byung-Chul, Yu Kyung-Ho, Oh Mi Sun, Kim Joon-Tae, Choi Kang-Ho, Kim Dong-Eog, Ryu Wi-Sun, Choi Jay Chol, Kwon Jee-Hyun, Kim Wook-Joo, Shin Dong-Ick, Sohn Sung Il, Hong Jeong-Ho, Lee Juneyoung, Lee Kyunghoon, Song Junghan, Bae Joon Seol, Cheong Hyun Sub, Debette Stéphanie, Bae Hee-Jo |
Predicting atrial fibrillation after ischemic stroke: clinical, genetics and electrocardiogram modelling. Cerebrovascular diseases extra 2022 12 . Poh Mervyn Qi Wei, Tham Carol Huilian, Chee Jeremiah David Ming Siang, Saffari Seyed Ehsan, Tan Kenny Wee Kian, Tan Li Wei, Ng Ebonne Yulin, Yeo Celestia Pei Xuan, Seet Christopher Ying Hao, Xie Joanne Peiting, Lai Jonathan Yexian, Singh Rajinder, Tan Eng-King, Tu Tian Mi |
Interpretable deep learning translation of GWAS and multi-omics findings to identify pathobiology and drug repurposing in Alzheimer's disease. Cell reports 2022 11 41 (9): 111717. Xu Jielin, Mao Chengsheng, Hou Yuan, Luo Yuan, Binder Jessica L, Zhou Yadi, Bekris Lynn M, Shin Jiyoung, Hu Ming, Wang Fei, Eng Charis, Oprea Tudor I, Flanagan Margaret E, Pieper Andrew A, Cummings Jeffrey, Leverenz James B, Cheng Feixio |
PD-L1 score as a prognostic biomarker in asian early-stage epidermal growth factor receptor-mutated lung cancer. European journal of cancer (Oxford, England : 1990) 2022 11 178 139-149. Saw Stephanie P L, Ng Win Pin, Zhou Siqin, Lai Gillianne G Y, Tan Aaron C, Ang Mei-Kim, Lim Wan-Teck, Kanesvaran Ravindran, Ng Quan Sing, Jain Amit, Tan Wan Ling, Rajasekaran Tanujaa, Chan Johan W K, Teh Yi Lin, Pang Mengyuan, Yeo Jia-Chi, Takano Angela, Ong Boon-Hean, Tan Eng-Huat, Tan Sze Huey, Skanderup Anders J, Tan Daniel S |
A Randomized Phase 2 Trial of Nivolumab Versus Nivolumab-Ipilimumab Combination in EGFR-Mutant NSCLC. JTO clinical and research reports 2022 11 3 (12): 100416. Lai Gillianne G Y, Yeo Jia Chi, Jain Amit, Zhou Siqin, Pang Mengyuan, Alvarez Jacob J S, Sim Ngak Leng, Tan Aaron C, Suteja Lisda, Lim Tze Wei, Guo Yu Amanda, Shen Meixin, Saw Stephanie P L, Rohatgi Neha, Yeong Joe P S, Takano Angela, Lim Kiat Hon, Gogna Apoorva, Too Chow Wei, Da Zhuang Kun, Tan Wan Ling, Kanesvaran Ravindran, Ng Quan Sing, Ang Mei Kim, Rajasekaran Tanujaa, Wang Lanying, Toh Chee Keong, Lim Wan-Teck, Tam Wai Leong, Tan Sze Huey, Skanderup Anders M J, Tan Eng-Huat, Tan Daniel S |
Inherited Cancer Susceptibility Gene Sequence Variations Among Patients With Appendix Cancer. JAMA oncology 2022 11 9 (1): 95-101. Holowatyj Andreana N, Washington Mary K, Tavtigian Sean V, Eng Cathy, Horton Carol |
WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE. medRxiv : the preprint server for health sciences 2023 9 . Xinruo Zhang, Jennifer A Brody, Mariaelisa Graff, Heather M Highland, Nathalie Chami, Hanfei Xu, Zhe Wang, Kendra Ferrier, Geetha Chittoor, Navya S Josyula, Xihao Li, Zilin Li, Matthew A Allison, Diane M Becker, Lawrence F Bielak, Joshua C Bis, Meher Preethi Boorgula, Donald W Bowden, Jai G Broome, Erin J Buth, Christopher S Carlson, Kyong-Mi Chang, Sameer Chavan, Yen-Feng Chiu, Lee-Ming Chuang, Matthew P Conomos, Dawn L DeMeo, Margaret Du, Ravindranath Duggirala, Celeste Eng, Alison E Fohner, Barry I Freedman, Melanie E Garrett, Xiuqing Guo, Chris Haiman, Benjamin D Heavner, Bertha Hidalgo, James E Hixson, Yuk-Lam Ho, Brian D Hobbs, Donglei Hu, Qin Hui, Chii-Min Hwu, Rebecca D Jackson, Deepti Jain, Rita R Kalyani, Sharon L R Kardia, Tanika N Kelly, Ethan M Lange, Michael LeNoir, Changwei Li, Loic Le Marchand, Merry-Lynn N McDonald, Caitlin P McHugh, Alanna C Morrison, Take Naseri, , Jeffrey O'Connell, Christopher J O'Donnell, Nicholette D Palmer, James S Pankow, James A Perry, Ulrike Peters, Michael H Preuss, D C Rao, Elizabeth A Regan, Sefuiva M Reupena, Dan M Roden, Jose Rodriguez-Santana, Colleen M Sitlani, Jennifer A Smith, Hemant K Tiwari, Ramachandran S Vasan, Zeyuan Wang, Daniel E Weeks, Jennifer Wessel, Kerri L Wiggins, Lynne R Wilkens, Peter W F Wilson, Lisa R Yanek, Zachary T Yoneda, Wei Zhao, Sebastian Zöllner, Donna K Arnett, Allison E Ashley-Koch, Kathleen C Barnes, John Blangero, Eric Boerwinkle, Esteban G Burchard, April P Carson, Daniel I Chasman, Yii-Der Ida Chen, Joanne E Curran, Myriam Fornage, Victor R Gordeuk, Jiang He, Susan R Heckbert, Lifang Hou, Marguerite R Irvin, Charles Kooperberg, Ryan L Minster, Braxton D Mitchell, Mehdi Nouraie, Bruce M Psaty, Laura M Raffield, Alexander P Reiner, Stephen S Rich, Jerome I Rotter, M Benjamin Shoemaker, Nicholas L Smith, Kent D Taylor, Marilyn J Telen, Scott T Weiss, Yingze Zhang, Nancy Heard- Costa, Yan V Sun, Xihong Lin, L Adrienne Cupples, Leslie A Lange, Ching-Ti Liu, Ruth J F Loos, Kari E North, Anne E Justi |
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 |
Caffeine intake interacts with Asian gene variants in Parkinson's disease: a study in 4488 subjects. The Lancet regional health. Western Pacific 2023 9 40 100877. Yi-Lin Ong, Xiao Deng, Hui-Hua Li, K Narasimhalu, Ling-Ling Chan, Kumar M Prakash, Wing-Lok Au, Pavanni Ratnagopal, Louis C S Tan, Eng-King T |
Unsupervised machine learning algorithms identify expected haemorrhage relationships but define unexplained coagulation profiles mapping to thrombotic phenotypes in hereditary haemorrhagic telangiectasia. EJHaem 2023 8 4 (3): 602-611. Ghazel Mukhtar, Claire L Shovl |
Integrating somatic CNV and gene expression in breast cancers from women with PTEN hamartoma tumor syndrome. NPJ genomic medicine 2023 7 8 (1): 14. Takae Brewer, Lamis Yehia, Peter Bazeley, Charis E |
Bioinformatics Analysis of the Genetic and Epigenetic Alterations of Bone Morphogenetic Protein Receptors in Metastatic Breast Cancer. Biochemical genetics 2023 7 . Adam Hermawan, Herwandhani Put |
Next generation sequencing aids diagnosis and management in a case of encephalocraniocutaneous lipomatosis. Pediatric dermatology 2023 7 . Kelly K Barry, Marilyn G Liang, Daniel M Balkin, Siddharth Srivastava, Alanna J Church, Whitney E |
Landscape of germline pathogenic variants in patients with dual primary breast and lung cancer. Human genomics 2023 7 17 (1): 66. Ning-Yuan Lee, Melissa Hum, Sabna Zihara, Lanying Wang, Matthew K Myint, Darren Wan-Teck Lim, Chee-Keong Toh, Anders Skanderup, Jens Samol, Min-Han Tan, Peter Ang, Soo-Chin Lee, Eng-Huat Tan, Gillianne G Y Lai, Daniel S W Tan, Yoon-Sim Yap, Ann S G L |
Tamoxifen and the risk of breast cancer in women with a BRCA1 or BRCA2 mutation. Breast cancer research and treatment 2023 7 . Joanne Kotsopoulos, Jacek Gronwald, Tomasz Huzarski, Amber Aeilts, Susan Randall Armel, Beth Karlan, Christian F Singer, Andrea Eisen, Nadine Tung, Olufunmilayo Olopade, Louise Bordeleau, Charis Eng, William D Foulkes, Susan L Neuhausen, Carey A Cullinane, Tuya Pal, Robert Fruscio, Jan Lubinski, Kelly Metcalfe, Ping Sun, Steven A Narod, |
Human Genetics Influences Microbiome Composition Involved in Asthma Exacerbations despite Inhaled Corticosteroid Treatment. The Journal of allergy and clinical immunology 2023 6 . Javier Perez-Garcia, Antonio Espuela-Ortiz, José M Hernández-Pérez, Ruperto González-Pérez, Paloma Poza-Guedes, Elena Martin-Gonzalez, Celeste Eng, Olaia Sardón-Prado, Elena Mederos-Luis, Paula Corcuera-Elosegui, Inmaculada Sánchez-Machín, Javier Korta-Murua, Jesús Villar, Esteban G Burchard, Fabian Lorenzo-Diaz, Maria Pino-Yan |
Parkinson's disease GWAS-linked Park16 variant is associated with a lower risk of cognitive impairment: a 4-year observational study. European journal of neurology 2023 5 . Bin Xiao, Xiao Deng, Ebonne Yu-Lin Ng, Yew-Long Lo, Zheyu Xu, Kay-Yaw Tay, Wing-Lok Au, Adeline Ng, Louis C S Tan, Eng-King T |
The Immunogenomic Landscape of Neuroendocrine Prostate Cancer. Clinical cancer research : an official journal of the American Association for Cancer Research 2023 5 . Bhavneet Bhinder, Alison Ferguson, Michael Sigouros, Manik Uppal, Ahmed G Elsaeed, Rohan Bareja, Hussein Alnajar, Kenneth Wha Eng, Vincenza Conteduca, Andrea Sboner, Juan Miguel Mosquera, Olivier Elemento, Himisha Beltr |
The mitochondrial genome as a modifier of autism versus cancer phenotypes in PTEN hamartoma tumor syndrome. HGG advances 2023 5 4 (3): 100199. Ruipeng Wei, Lamis Yehia, Ying Ni, Charis E |
Rare germline variants in pancreatic cancer and multiple primary cancers: an autopsy study. European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP) 2023 3 . Fujitani Hiroo, Eguchi Hidetaka, Kochi Yuta, Arai Tomio, Muramatsu Masaaki, Okazaki Yasus |
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 |
Whole-exome sequencing and bioinformatic analyses revealed differences in gene mutation profiles in papillary thyroid cancer patients with and without benign thyroid goitre background. Frontiers in endocrinology 2023 1 13 1039494. Eng Zing Hong, Abdullah Mardiaty Iryani, Ng Khoon Leong, Abdul Aziz Azlina, Arba'ie Nurul Hannis, Mat Rashid Nurullainy, Mat Junit Sar |
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 |
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 |
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- Page last updated:Apr 16, 2024
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