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

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The genetic contribution of the X chromosome in age-related hearing loss von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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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Rare A2ML1 variants confer susceptibility to otitis media von 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

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Power analysis and sample size estimation for sequence-based association studies von 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 von 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 von 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 von 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 von 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 von 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 von Castel, Stephane E., Aguet, Francois, Mohammadi, Pejman, Ardlie, Kristin G., Lappalainen, Tuuli

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