Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Yik Ying Teo"'
Autor:
Vijay Kumar Subbiah, Woei-Yuh Saw, Farhang Aghakhanian, Maude E. Phipps, Boon Peng Hoh, Lian Deng, Mohammad Zahirul Hoque, Chee Wei Yew, Shuhua Xu, Xiaoxi Zhang, Yik Ying Teo, Kai Yuan
Publikováno v:
Genome Biology and Evolution
North Borneo (NB) is home to more than 40 native populations. These natives are believed to have undergone local adaptation in response to environmental challenges such as the mosquito-abundant tropical rainforest. We attempted to trace the footprint
Autor:
Esteban J. Parra, E-Shyong Tai, Habiba Alsafar, Enrico Petretto, Jirong Long, Amelia Li Min Tan, Xueling Sim, Yik Ying Teo, Miguel Cruz, Huimei Chen, Qiuju Ding
Publikováno v:
Journal of Human Genetics. 65:411-420
Genome-wide association studies (GWASs) have identified many genetic variations associated with type 2 diabetes mellitus (T2DM) in Asians, but understanding the functional genetic variants that influence traits is often a complex process. In this stu
Autor:
Marju Orho-Melander, Humberto García-Ortiz, Xueling Sim, Amp-T D-Genes, Cheol Joo Park, Gina M. Peloso, Jason Flannick, Brian Tomlinson, Hyun Min Kang, Emilio J. Cordova, Stephen S. Rich, Richard A. Gibbs, Angélica Martínez-Hernández, Lorena Orozco, Harsha Doddapaneni, Lisa R. Yanek, Jiwon Lee, Namrata Gupta, Valeriya Lyssenko, Sohee Han, James B. Meigs, Bong-Jo Kim, Bruce M. Psaty, Leslie S. Emery, Kerrin S. Small, Pradeep Natarajan, May E. Montasser, Christian Gieger, Sharon L.R. Kardia, Sarah C. Nelson, Craig L. Hanis, Heikki A. Koistinen, María Elena González-Villalpando, Edmund Chan, Michael Y. Tsai, Benjamin Glaser, Thomas Meitinger, Matthew J. Bown, Mariaelisa Graff, John Danesh, Sekar Kathiresan, Tiinamaija Tuomi, Ramachandran S. Vasan, Gil Atzmon, Alyna T. Khan, Diego Ardissino, Yii-Der Ida Chen, David Zhang, Rob M. van Dam, Wendy S. Post, Barry I. Freedman, D. C. Rao, Michael Preuss, Donna M. Lehman, L. Adrienne Cupples, Colin N. A. Palmer, Claudia H. T. Tam, Hortensia Moreno-Macías, Markku Laakso, Peter Dornbos, Teresa Tusié-Luna, Stella Aslibekyan, Marguerite R. Irvin, Daniel J. Rader, Jee-Young Moon, Eimear E. Kenny, Lisa W. Martin, Jennifer A. Brody, Amit Khera, Erwin P. Bottinger, Sarah E. Graham, Myriam Fornage, Ruth McPherson, Nancy L. Heard-Costa, Michael Boehnke, Clicerio Gonzalez, Ryan W. Kim, Yi-Cheng Chang, Peter M. Nilsson, Yik Ying Teo, Robert Sladek, Cristen J. Willer, Fei Fei Wang, Donna K. Arnett, Mark Chaffin, Karine A. Viaud Martinez, Alanna C. Morrison, Leslie A. Lange, Ravindranath Duggirala, Donna M. Muzny, Kent D. Taylor, Niels Grarup, Soren Germer, Patricia A. Peyser, Brian E. Cade, Lewis C. Becker, Steven A. Lubitz, Nicholette D. Palmer, Susan K. Dutcher, Ronald C.W. Ma, Xuenan Mi, Xiuqing Guo, Hugh Watkins, Eric Boerwinkle, Qibin Qi, Johanna Kuusisto, Christie M. Ballantyne, Tanika N. Kelly, Rajiv Chowdhury, Elvia Mendoza-Caamal, Wing-Yee So, Tien Yin Wong, Torben Hansen, Cecilia Contreras-Cubas, Jeong-Sun Seo, Mi Yeong Hwang, Daekwan Seo, Dajiang J. Liu, Cristina Revilla-Monsalve, Paul S. de Vries, Daniel R. Witte, Yi-Jen Hung, Olle Melander, Karen L. Mohlke, Lucinda Antonacci-Fulton, Francisco Barajas-Olmos, Soo Heon Kwak, Daniel E. Weeks, Claudia Schurmann, Ginger A. Metcalf, Young-Jin Kim, Adrienne M. Stilp, Lori L. Bonnycastle, John Blangero, Ralph A. DeFronzo, Donald W. Bowden, Rasika A. Mathias, Oluf Pedersen, Rozenn N. Lemaitre, Stephen T. McGarvey, Heribert Schunkert, Jaakko Tuomilehto, Farook Thameem, Valentin Fuster, Joshua C. Bis, George Hindy, Allan Linneberg, James G. Wilson, Kyong Soo Park, Sergio A. Islas-Andrade, Ching-Yu Cheng, Won Jung Choi, Minxian X. Wang, Xuzhi Wang, Adolfo Correa, Jai G. Broome, Gail P. Jarvik, Alexander P. Reiner, E. Shyong Tai, Juyoung Lee, Mark I. McCarthy, Nilesh J. Samani, Susan Redline, Carlos A. Aguilar-Salinas, Jerome I. Rotter, Ma. Eugenia Garay-Sevilla, Jiang He, Patrick T. Ellinor, Joseph Park, Joanne E. Curran, Nir Barzilai, Federico Centeno-Cruz, Seonwook Lee, Lawrence F. Bielak, Jianjun Liu, Charles Kooperberg, Juan M. Peralta, Jose C. Florez, Leif Groop, Noël P. Burtt, Margaret Sunitha Selvaraj, Jeffrey R. O'Connell, Ruth J. F. Loos
Large-scale gene sequencing studies for complex traits have the potential to identify causal genes with therapeutic implications. We performed gene-based association testing of blood lipid levels with rare (minor allele frequency170,000 individuals f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08cffcbe73ed87d1953f10593c831399
https://doi.org/10.1101/2020.12.22.423783
https://doi.org/10.1101/2020.12.22.423783
Autor:
Choong Leong Tang, Michelle Lo, Lai Fun Thean, Peh Yean Cheah, Min Hoe Chew, Woon-Puay Koh, Yik Ying Teo, Jian-Min Yuan, Yee Syuen Low
Publikováno v:
Journal of Medical Genetics. 55:181-188
BackgroundMultiple single nucleotide polymorphisms (SNPs) have been associated with colorectal cancer (CRC) risk. The role of structural or copy number variants (CNV) in CRC, however, remained unclear. We investigated the role of CNVs in patients wit
Autor:
Yechiel Friedlander, Jian-Min Yuan, Woon-Puay Koh, Tien Yin Wong, Chew-Kiat Heng, Ching-Yu Cheng, Rob M. van Dam, Chiea Chuen Khor, E. Shyong Tai, Tingjing Ke, Rajkumar Dorajoo, Daniel Y. T. Goh, Yik Ying Teo, Jianjun Liu, Yi Han
Publikováno v:
Annals of Human Genetics. 80:282-293
Summary Peroxisome proliferator activated receptors (PPARs) are transcription factors involved in the regulation of key metabolic pathways. Numerous in vivo and in vitro studies have established their important roles in lipid metabolism. A few SNPs i
Autor:
Su'Aidah Binte Mustaffa, Christian R. Marshall, Stephen W. Scherer, Rita Y.Y. Yong, Eric P.H. Yap, Pavandip S. Wasan, Yik Ying Teo, Liang Sheng
Publikováno v:
Human Mutation. 37:669-678
The human amylase gene locus at chromosome 1p21.1 is structurally complex. This region contains two pancreatic amylase genes, AMY2B, AMY2A, and a salivary gene AMY1. The AMY1 gene harbors extensive copy number variation (CNV), and recent studies have
Autor:
Jiin Ying Lim, Zenia Tiang, Wilson Lek Wen Tan, Angeline Lai, Maggie Brett, Byrappa Venkatesh, Bruno Reversade, Yik Ying Teo, Wendy K.M. Liew, Hai-Yang Law, Jyn Ling Kuan, Ee Shien Tan, Ivy Ng, Roger Foo, Asif Javed, Saumya Shekhar Jamuar, Woei Kang Liew, Ene-Choo Tan
Publikováno v:
EBioMedicine
EBioMedicine, Vol 5, Iss C, Pp 211-216 (2016)
EBioMedicine, 5, 211-216. Elsevier BV
EBioMedicine, Vol 5, Iss C, Pp 211-216 (2016)
EBioMedicine, 5, 211-216. Elsevier BV
Background In Western cohorts, the prevalence of incidental findings (IFs) or incidentalome, referring to variants in genes that are unrelated to the patient's primary condition, is between 0.86% and 8.8%. However, data on prevalence and type of IFs
Autor:
Humberto García-Ortiz, Loos R, Frederick E. Dewey, Farook Thameem, John C. Chambers, Mi Yeong Hwang, Nancy L. Heard-Costa, Danish Saleheen, Shuai Wang, Morris Ad, Josep M. Mercader, Noël P. Burtt, Laura J. Scott, Torben Hansen, Mark I. McCarthy, Clicerio Gonzalez, Matsuo K, Mark Seielstad, Marijana Vujkovic, Teresa Tusié-Luna, Alanna C. Morrison, Christian Gieger, Dana Dabelea, Colm O'Dushlaine, Niels Grarup, Elvia Mendoza-Caamal, Amanda F. Elliott, Ryan P. Welch, Craig L. Hanis, Kirchner Hl, Song Chen, Jennifer A. Brody, Maria L. Cortes, Asif Rasheed, Russel Tracy, Nancy J. Cox, Miriam S. Udler, Myron D. Gross, Donald W. Bowden, Oluf Pedersen, Marit E. Jørgensen, J. Tuomilehto, Yik Ying Teo, Andrew P. Morris, Zeitler P, T. M. Strom, Aris Baras, Colin N. A. Palmer, Shin Yc, Johanna Kuusisto, Lin Chen, Donna M. Lehman, Edmund Chan, Heikki A. Koistinen, Anthony Marcketta, Boehnke M, Francis S. Collins, Rayner Nw, Leslie A. Lange, Nir Barzilai, Brian E. Henderson, Jennifer Wessel, David J. Carey, Jaspal S. Kooner, Ralph A. DeFronzo, Anthony Payne, Carlos A. Aguilar-Salinas, Tien Yin Wong, Thomas Meitinger, Lyssenko, Claudia Ht Tam, Cristina Revilla-Monsalve, Daniel R. Witte, Jerome I. Rotter, Michael Preuss, Allan Linneberg, Jose C. Florez, Alisa K. Manning, Gonçalo R. Abecasis, Hyun Min Kang, van Dam Rm, Jason M. Torres, Anubha Mahajan, Claudia Schurmann, Markku Laakso, Leif Groop, Lori L. Bonnycastle, Sohee Han, Jason Flannick, Bong-Jo Kim, Lawrence M. Dolan, Brian Burke, Ma Elena Gonzalez, Kerrin S. Small, Ching-Ti Liu, Ronald C.W. Ma, Peter M. Nilsson, Eric Boerwinkle, Garay-Sevilla Me, Ravindranath Duggirala, Anne Ndungu, Cecilia Contreras-Cubas, Wendy S. Post, Tanya M. Teslovich, Brian Tomlinson, Kimberly L. Drews, Lizz Caulkins, Lee J, Philippe M. Frossard, Jianjun Liu, Hanks S, Ki-Sun Park, Tai Es, Kelsey M, S. Gabriel, Erwin P. Bottinger, Alexander P. Reiner, Tim D. Spector, Lorena Orozco, James S. Pankow, Juliana C.N. Chan, Wing-Yee So, Tiinamaija Tuomi, Malacara-Hernandez Jm, Karen L. Mohlke, S. S. Rich, de Vries Ps, Konstantin Strauch, Graeme I. Bell, Angélica Martínez-Hernández, Elizabeth J. Mayer-Davis, Thomas W. Blackwell, Heather M. Stringham, Bruce M. Psaty, Soo Heon Kwak, Catherine Pihoker, James S. Floyd, Christian Fuchsberger, Ching-Yu Cheng, Neil R. Robertson, Adolfo Correa, James G. Wilson, Ramachandran S. Vasan, Robert Sladek, James B. Meigs, Benjamin Glaser, Gil Atzmon, David Altshuler, Josée Dupuis, Xueling Sim, John Blangero, Emilio J. Cordova, C.J. O'Donnell, Maggie C.Y. Ng, Heckbert, Young-Jin Kim, Joseph B. Leader, Anne U. Jackson, Ryan Koesterer, Nicola Santoro, Christopher A. Haiman
Protein-coding genetic variants that strongly affect disease risk can provide important clues into disease pathogenesis. Here we report an exome sequence analysis of 20,791 type 2 diabetes (T2D) cases and 24,440 controls from five ancestries. We iden
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7772bf67b60c38438ff7f4b6fdf05c9
Autor:
Takanori Mizoguchi, Donald T.H. Tan, Renyi Wu, Hon-Tym Wong, Simon W. M. John, Shamira A. Perera, Michael A. Hauser, Tien Yin Wong, Azhany Yaakub, Yasuo Kurimoto, Jin-Xin Bei, Zheng Li, Eranga N. Vithana, Tina T. Wong, Mineo Ozaki, Serena M. L. Ting, Ningli Wang, Lingam Vijaya, Sancy Low, Chiea Chuen Khor, Ileana Soto, E-Shyong Tai, Hua Wang, Saleh A. Al-Obeidan, Hailin Meng, R. Rand Allingham, Govindasamy Kumaramanickavel, K. Saidas Nair, Ya Xing Wang, Kee Seng Chia, Daniel H. Su, Tran Nguyen Bich Chau, Seang-Mei Saw, Chunyan Qiao, Clement C Y Tham, Seng-Chee Loon, Victor H. K. Yong, Do Nhu Hon, Chi Pui Pang, Essam A. Osman, Shomi S. Bhattacharya, Paul T K Chew, Do Tan, Vedam L. Ramprasad, Ching-Lin Ho, Yik Ying Teo, Naushin Waseem, Liza-Sharmini Ahmad Tajudin, Cameron P. Simmons, Li Jia Chen, Hongyan Jia, Belinda K. Cornes, Alicia C. How, Monisha E. Nongpiur, Liang Xu, Khaled K. Abu-Amero, Bo Feng, Ronnie George, Yingfeng Zheng, Guangxian Tang, Jost B. Jonas, Ching-Yu Cheng, Yang Li, Nagaswamy Soumittra, Sujie Fan, Yi Xin Zeng, Mingzhi Zhang, Masako Kuroda, Balekudaru Shantha, Paul J. Foster, Tin Aung, Raghavan Lavanya
Publikováno v:
PLoS Genetics, Vol 10, Iss 3, p e1004089 (2014)
PLoS Genetics
PLoS Genetics
Anterior chamber depth (ACD) is a key anatomical risk factor for primary angle closure glaucoma (PACG). We conducted a genome-wide association study (GWAS) on ACD to discover novel genes for PACG on a total of 5,308 population-based individuals of As
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f10cb594c045fad4ca65ad405f94d718
https://ora.ox.ac.uk/objects/uuid:6facdebc-4c5e-4a75-ad14-fdb2f0f66aa5
https://ora.ox.ac.uk/objects/uuid:6facdebc-4c5e-4a75-ad14-fdb2f0f66aa5
Autor:
Angkana Chaiprasert, Arirat Thanormchat, Nongnard Thamnongdee, Arisa Phurattanakornkul, Somcharn Rattanarangsee, Rick Twee-Hee Ong, Eryu Xia, Nampueng Makhao, Jun Hao Tan, Chate Ratanajaraya, Ditthawat Nonghanphithak, Therdsak Prammananan, Yik Ying Teo, Prapat Suriyaphol, Kiatichai Faksri
Publikováno v:
Scientific Reports
Scientific Reports, Vol 8, Iss 1, Pp 1-10 (2018)
Scientific Reports, Vol 8, Iss 1, Pp 1-10 (2018)
Tuberculous meningitis (TBM) is a severe form of tuberculosis with a high mortality rate. The factors associated with TBM pathogenesis are still unclear. Using comparative whole-genome sequence analysis we compared Mycobacterium tuberculosis (Mtb) is