Variant Association Tools for Quality Control and Analysis of Large-Scale Sequence and Genotyping Array Data
Wang, Gao T., Peng, Bo, Leal, Suzanne M.
Published in American journal of human genetics (01.05.2014)
Published in American journal of human genetics (01.05.2014)
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The genetic contribution of the X chromosome in age-related hearing loss
Naderi, Elnaz, Cornejo-Sanchez, Diana M, Li, Guangyou, Schrauwen, Isabelle, Wang, Gao T, Dewan, Andrew T, Leal, Suzanne M
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Published in Frontiers in genetics (21.02.2023)
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Whole genome sequencing identifies candidate genes for familial essential tremor and reveals biological pathways implicated in essential tremor aetiology
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Published in EBioMedicine (01.11.2022)
Published in EBioMedicine (01.11.2022)
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RNF213 Rare Variants in an Ethnically Diverse Population With Moyamoya Disease
CECCHI, Alana C, DONGCHUAN GUO, BAMSHAD, Michael J, GROTTA, James C, NICKERSON, Deborah A, PANNU, Hariyadarshi, MILEWICZ, Dianna M, ZHAO REN, FLYNN, Kelly, SANTOS-CORTEZ, Regie Lyn P, LEAL, Suzanne M, WANG, Gao T, REGALADO, Ellen S, STEINBERG, Gary K, SHENDURE, Jay
Published in Stroke (1970) (01.11.2014)
Published in Stroke (1970) (01.11.2014)
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A Rare Variant Nonparametric Linkage Method for Nuclear and Extended Pedigrees with Application to Late-Onset Alzheimer Disease via WGS Data
Zhao, Linhai, He, Zongxiao, Zhang, Di, Wang, Gao T., Renton, Alan E., Vardarajan, Badri N., Nothnagel, Michael, Goate, Alison M., Mayeux, Richard, Leal, Suzanne M.
Published in American journal of human genetics (03.10.2019)
Published in American journal of human genetics (03.10.2019)
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Rare-variant association analysis reveals known and new age-related hearing loss genes
Cornejo-Sanchez, Diana M, Li, Guangyou, Fabiha, Tabassum, Wang, Ran, Acharya, Anushree, Everard, Jenna L, Kadlubowska, Magda K, Huang, Yin, Schrauwen, Isabelle, Wang, Gao T, DeWan, Andrew T, Leal, Suzanne M
Published in European journal of human genetics : EJHG (01.06.2023)
Published in European journal of human genetics : EJHG (01.06.2023)
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Collapsed haplotype pattern method for linkage analysis of next-generation sequence data
Wang, Gao T, Zhang, Di, Li, Biao, Dai, Hang, Leal, Suzanne M
Published in European journal of human genetics : EJHG (01.12.2015)
Published in European journal of human genetics : EJHG (01.12.2015)
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Regulatory variants in TCF7L2 are associated with thoracic aortic aneurysm
Roychowdhury, Tanmoy, Lu, Haocheng, Hornsby, Whitney E., Crone, Bradley, Wang, Gao T., Guo, Dong-chuan, Sendamarai, Anoop K., Devineni, Poornima, Lin, Maoxuan, Zhou, Wei, Graham, Sarah E., Wolford, Brooke N., Surakka, Ida, Wang, Zhenguo, Chang, Lin, Zhang, Jifeng, Mathis, Michael, Brummett, Chad M., Melendez, Tori L., Shea, Michael J., Kim, Karen Meekyong, Deeb, G. Michael, Patel, Himanshu J., Eliason, Jonathan, Eagle, Kim A., Yang, Bo, Ganesh, Santhi K., Brumpton, Ben, Åsvold, Bjørn Olav, Skogholt, Anne Heidi, Hveem, Kristian, Pyarajan, Saiju, Klarin, Derek, Tsao, Philip S., Damrauer, Scott M., Leal, Suzanne M., Milewicz, Dianna M., Chen, Y. Eugene, Garcia-Barrio, Minerva T., Willer, Cristen J.
Published in American journal of human genetics (02.09.2021)
Published in American journal of human genetics (02.09.2021)
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SEQSpark: A Complete Analysis Tool for Large-Scale Rare Variant Association Studies Using Whole-Genome and Exome Sequence Data
Zhang, Di, Zhao, Linhai, Li, Biao, He, Zongxiao, Wang, Gao T., Liu, Dajiang J., Leal, Suzanne M.
Published in American journal of human genetics (06.07.2017)
Published in American journal of human genetics (06.07.2017)
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The Rare-Variant Generalized Disequilibrium Test for Association Analysis of Nuclear and Extended Pedigrees with Application to Alzheimer Disease WGS Data
He, Zongxiao, Zhang, Di, Renton, Alan E., Li, Biao, Zhao, Linhai, Wang, Gao T., Goate, Alison M., Mayeux, Richard, Leal, Suzanne M.
Published in American journal of human genetics (02.02.2017)
Published in American journal of human genetics (02.02.2017)
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A quantitative trait rare variant nonparametric linkage method with application to age-at-onset of Alzheimer's disease
Zhao, Linhai, Zhang, Zhihui, Rodriguez, Sandra M Barral, Vardarajan, Badri N, Renton, Alan E, Goate, Alison M, Mayeux, Richard, Wang, Gao T, Leal, Suzanne M
Published in European journal of human genetics : EJHG (01.12.2020)
Published in European journal of human genetics : EJHG (01.12.2020)
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Power analysis and sample size estimation for sequence-based association studies
Wang, Gao T, Li, Biao, Santos-Cortez, Regie P Lyn, Peng, Bo, Leal, Suzanne M
Published in Bioinformatics (Oxford, England) (15.08.2014)
Published in Bioinformatics (Oxford, England) (15.08.2014)
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Rare A2ML1 variants confer susceptibility to otitis media
Santos-Cortez, Regie Lyn P, Chiong, Charlotte M, Reyes-Quintos, Ma Rina T, Tantoco, Ma Leah C, Wang, Xin, Acharya, Anushree, Abbe, Izoduwa, Giese, Arnaud P, Smith, Joshua D, Allen, E Kaitlynn, Li, Biao, Cutiongco-de la Paz, Eva Maria, Garcia, Marieflor Cristy, Llanes, Erasmo Gonzalo D V, Labra, Patrick John, Gloria-Cruz, Teresa Luisa I, Chan, Abner L, Wang, Gao T, Daly, Kathleen A, Shendure, Jay, Bamshad, Michael J, Nickerson, Deborah A, Patel, Janak A, Riazuddin, Saima, Sale, Michele M, Chonmaitree, Tasnee, Ahmed, Zubair M, Abes, Generoso T, Leal, Suzanne M
Published in Nature genetics (01.08.2015)
Published in Nature genetics (01.08.2015)
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Rare variant associations with waist-to-hip ratio in European-American and African-American women from the NHLBI-Exome Sequencing Project
Kan, Mengyuan, Auer, Paul L, Wang, Gao T, Bucasas, Kristine L, Hooker, Stanley, Rodriguez, Alejandra, Li, Biao, Ellis, Jaclyn, Adrienne Cupples, L, Ida Chen, Yii-Der, Dupuis, Josée, Fox, Caroline S, Gross, Myron D, Smith, Joshua D, Heard-Costa, Nancy, Meigs, James B, Pankow, James S, Rotter, Jerome I, Siscovick, David, Wilson, James G, Shendure, Jay, Jackson, Rebecca, Peters, Ulrike, Zhong, Hua, Lin, Danyu, Hsu, Li, Franceschini, Nora, Carlson, Chris, Abecasis, Goncalo, Gabriel, Stacey, Bamshad, Michael J, Altshuler, David, Nickerson, Deborah A, North, Kari E, Lange, Leslie A, Reiner, Alexander P, Leal, Suzanne M
Published in European journal of human genetics : EJHG (01.08.2016)
Published in European journal of human genetics : EJHG (01.08.2016)
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The Rare-Variant Generalized Disequilibrium Test for Association Analysis of Nuclear and Extended Pedigrees with Application to Alzheimer Disease WGS Data
He, Zongxiao, Zhang, Di, Renton, Alan E., Li, Biao, Zhao, Linhai, Wang, Gao T., Goate, Alison M., Mayeux, Richard, Leal, Suzanne M.
Published in American journal of human genetics (02.02.2017)
Published in American journal of human genetics (02.02.2017)
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A Rare Variant Nonparametric Linkage Method for Nuclear and Extended Pedigrees with Application to Late Onset Alzheimer’s Disease Whole Genome Sequence
Zhao, Linhai, Zhang, Di, Broadbent, Carl A, Wang, Gao T, Goate, Alison M, Mayeux, Richard, Leal, Suzanne M
Published in Human heredity (01.06.2018)
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Published in Human heredity (01.06.2018)
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RNF213 Mutations in an Ethnically Diverse Population with Moyamoya Disease
Cecchi, Alana C., Guo, Dongchuan, Ren, Zhao, Flynn, Kelly, Santos-Cortez, Regie Lyn P., Leal, Suzanne M., Wang, Gao T., Regalado, Ellen S., Steinberg, Gary K., Shendure, Jay, Bamshad, Michael J., Grotta, James C., Nickerson, Deborah A., Pannu, Hariyadarshi, Milewicz, Dianna M.
Published in Stroke (1970) (02.10.2014)
Published in Stroke (1970) (02.10.2014)
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Erratum: The Rare-Variant Generalized Disequilibrium Test for Association Analysis of Nuclear and Extended Pedigrees with Application to Alzheimer Disease WGS Data
He, Zongxiao, Zhang, Di, Renton, Alan E, Li, Biao, Zhao, Linhai, Wang, Gao T, Goate, Alison M, Mayeux, Richard, Leal, Suzanne M
Published in American journal of human genetics (02.02.2017)
Published in American journal of human genetics (02.02.2017)
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Even-odd harmonics generated from above-threshold ionization
Guo, Dong-Sheng, Zhang, Jing-Tao, Sun, Zhen-Rong, Wang, Jin T., Gao, Ju, Sun, Zhi-Wei, Freeman, R. R.
Published in Frontiers of physics (01.02.2014)
Published in Frontiers of physics (01.02.2014)
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