Variant Association Tools for Quality Control and Analysis of Large-Scale Sequence and Genotyping Array Data by Wang, Gao T., Peng, Bo, Leal, Suzanne M.

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The genetic contribution of the X chromosome in age-related hearing loss by Naderi, Elnaz, Cornejo-Sanchez, Diana M, Li, Guangyou, Schrauwen, Isabelle, Wang, Gao T, Dewan, Andrew T, Leal, Suzanne M

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Whole genome sequencing identifies candidate genes for familial essential tremor and reveals biological pathways implicated in essential tremor aetiology by Clark, Lorraine N., Gao, Yizhe, Wang, Gao T., Hernandez, Nora, Ashley-Koch, Allison, Jankovic, Joseph, Ottman, Ruth, Leal, Suzanne M., Rodriguez, Sandra M. Barral, Louis, Elan D.

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RNF213 Rare Variants in an Ethnically Diverse Population With Moyamoya Disease by 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

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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 by 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.

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Rare-variant association analysis reveals known and new age-related hearing loss genes by 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

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Regulatory variants in TCF7L2 are associated with thoracic aortic aneurysm by 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.

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Collapsed haplotype pattern method for linkage analysis of next-generation sequence data by Wang, Gao T, Zhang, Di, Li, Biao, Dai, Hang, Leal, Suzanne M

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Generation of sequence-based data for pedigree-segregating Mendelian or Complex traits by Li, Biao, Wang, Gao T, Leal, Suzanne M

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SEQSpark: A Complete Analysis Tool for Large-Scale Rare Variant Association Studies Using Whole-Genome and Exome Sequence Data by Zhang, Di, Zhao, Linhai, Li, Biao, He, Zongxiao, Wang, Gao T., Liu, Dajiang J., Leal, Suzanne M.

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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 by He, Zongxiao, Zhang, Di, Renton, Alan E., Li, Biao, Zhao, Linhai, Wang, Gao T., Goate, Alison M., Mayeux, Richard, Leal, Suzanne M.

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A quantitative trait rare variant nonparametric linkage method with application to age-at-onset of Alzheimer's disease by 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

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Power analysis and sample size estimation for sequence-based association studies by Wang, Gao T, Li, Biao, Santos-Cortez, Regie P Lyn, Peng, Bo, Leal, Suzanne M

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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 by 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

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SparsePro: An efficient fine-mapping method integrating summary statistics and functional annotations by Zhang, Wenmin, Najafabadi, Hamed, Li, Yue

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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 by He, Zongxiao, Zhang, Di, Renton, Alan E., Li, Biao, Zhao, Linhai, Wang, Gao T., Goate, Alison M., Mayeux, Richard, Leal, Suzanne M.

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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 by Zhao, Linhai, Zhang, Di, Broadbent, Carl A, Wang, Gao T, Goate, Alison M, Mayeux, Richard, Leal, Suzanne M

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Population-scale tissue transcriptomics maps long non-coding RNAs to complex disease by Gloudemans, Michael J., Smail, Craig, Eulalio, Tiffany Y., Aguet, François, Xu, Jishu, Kim-Hellmuth, Sarah, Park, YoSon, Scott, Alexandra J., Strober, Benjamin J., Gabriel, Stacey, Meier, Samuel R., Nguyen, Duyen T., Segrè, Ayellet V., Brown, Andrew, Cotter, Daniel J., Cox, Nancy, Dermitzakis, Emmanouil T., Einson, Jonah, Flynn, Elise D., Fresard, Laure, Gamazon, Eric R., Gay, Nicole R., Guigó, Roderic, Hamel, Andrew R., He, Yuan, Hoffman, Paul J., Hormozdiari, Farhad, Hou, Lei, Jo, Brian, Kashin, Seva, Mohammadi, Pejman, Oliva, Meritxell, Parsana, Princy, Sabatti, Chiara, Stranger, Barbara E., Teran, Nicole A., Viñuela, Ana, Wang, Gao, Wright, Fred, Ferreira, Pedro G., Li, Gen, Yeger-Lotem, Esti, Bradbury, Debra, Qi, Liqun, Robinson, Karna, Roche, Nancy V., Tabor, David E., Bridge, Jason, Gillard, Bryan M., Hasz, Richard, Hunter, Marcus, Kopen, Gene, Leinweber, William F., Moser, Michael T., Myer, Kevin, Washington, Michael, Wheeler, Joseph, Rohrer, Daniel C., Valley, Dana R., Branton, Philip A., Sobin, Leslie, Gardiner, Heather M., Mosavel, Maghboeba, Siminoff, Laura A., Flicek, Paul, Haeussler, Maximilian, Juettemann, Thomas, Ruffier, Magali, Sheppard, Dan, Taylor, Kieron, Abell, Nathan S., Akey, Joshua, Chen, Lin, Feinberg, Andrew P., Hansen, Kasper D., Jasmine, Farzana, Jiang, Lihua, Kaul, Rajinder, Kibriya, Muhammad G., Li, Jin Billy, Li, Qin, Lin, Shin, Pierce, Brandon L., Skol, Andrew D., Smith, Kevin S., Snyder, Michael, Stamatoyannopoulos, John, Tang, Hua, Guan, Ping, Little, A. Roger, Nierras, Concepcion R., Rao, Abhi K., Volpi, Simona, Brown, Christopher D., Wen, Xiaoquan, Hall, Ira M., Lappalainen, Tuuli, Im, Hae Kyung, Quertermous, Thomas, Kirkegaard, Karla

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A vast resource of allelic expression data spanning human tissues by Castel, Stephane E, Aguet, François, Mohammadi, Pejman, Ardlie, Kristin G, Lappalainen, Tuuli

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RNF213 Mutations in an Ethnically Diverse Population with Moyamoya Disease by 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.

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