Kết quả tìm kiếm - Lin, Chiao-Feng

Birth and death of gene overlaps in vertebrates Bằng Makałowska, Izabela, Lin, Chiao-Feng, Hernandez, Krisitina

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Analyzing Copy Number Variation using SNP Array Data: Protocols for Calling CNV and Association Tests Bằng Lin, Chiao-Feng, Naj, Adam C, Wang, Li-San

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Evolutionary dynamics of U12-type spliceosomal introns Bằng Lin, Chiao-Feng, Mount, Stephen M, Jarmołowski, Artur, Makałowski, Wojciech

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U12-type Spliceosomal Introns of Insecta Bằng Janice, Jessin, Pande, Amit, Weiner, January, Lin, Chiao-Feng, Makałowski, Wojciech

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Spliceosomal small nuclear RNA genes in 11 insect genomes Bằng Mount, Stephen M., Gotea, Valer, Lin, Chiao-Feng, Hernandez, Kristina, Makałowski, Wojciech

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Molecular Evolution in the Drosophila melanogaster Species Subgroup: Frequent Parameter Fluctuations on the Timescale of Molecular Divergence Bằng Akashi, Hiroshi, Ko, Wen-Ya, Piao, Shengfu, John, Anoop, Goel, Piyush, Lin, Chiao-Feng, Vitins, Alexa P.

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Bioinformatics Workflow for Clinical Whole Genome Sequencing at Partners HealthCare Personalized Medicine Bằng Tsai, Ellen A., Shakbatyan, Rimma, Evans, Jason, Rossetti, Peter, Graham, Chet, Sharma, Himanshu, Lin, Chiao-Feng, Lebo, Matthew S.

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HIPPIE: a high-throughput identification pipeline for promoter interacting enhancer elements Bằng Hwang, Yih-Chii, Lin, Chiao-Feng, Valladares, Otto, Malamon, John, Kuksa, Pavel P., Zheng, Qi, Gregory, Brian D., Wang, Li-San

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Determinants of Plant U12-Dependent Intron Splicing Efficiency Bằng Lewandowska, Dominika, Simpson, Craig G., Clark, Gillian P., Jennings, Nikki S., Barciszewska-Pacak, Maria, Lin, Chiao-Feng, Makalowski, Wojciech, Brown, John W.S., Jarmolowski, Artur

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DRAW+SneakPeek: Analysis workflow and quality metric management for DNA-seq experiments Bằng Lin, Chiao-Feng, Valladares, Otto, Childress, D. Micah, Klevak, Egor, Geller, Evan T., Hwang, Yih-Chii, Tsai, Ellen A., Schellenberg, Gerard D., Wang, Li-San

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A Rigorous Interlaboratory Examination of the Need to Confirm Next-Generation Sequencing–Detected Variants with an Orthogonal Method in Clinical Genetic Testing Bằng Lincoln, Stephen E., Truty, Rebecca, Lin, Chiao-Feng, Zook, Justin M., Paul, Joshua, Ramey, Vincent H., Salit, Marc, Rehm, Heidi L., Nussbaum, Robert L., Lebo, Matthew S.

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Assessing predictions of the impact of variants on splicing in CAGI5 Bằng Mount, Stephen M., Avsec, Žiga, Carmel, Liran, Casadio, Rita, Çelik, Muhammed Hasan, Chen, Ken, Cheng, Jun, Cohen, Noa E., Fairbrother, William G, Fenesh, Tzila, Gagneur, Julien, Gotea, Valer, Holzer, Tamar, Lin, Chiao-Feng, Martelli, Pier Luigi, Naito, Tatsuhiko, Nguyen, Thi Yen Duong, Savojardo, Castrense, Unger, Ron, Wang, Robert, Yang, Yuedong, Zhao, Huiying

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Corrigendum to: Detecting Genetic Ancestry and Adaptation in the Taiwanese Han People Bằng Lo, Yun-Hua, Cheng, Hsueh-Chien, Hsiung, Chia-Ni, Yang, Show-Ling, Wang, Han-Yu, Peng, Chia-Wei, Chen, Chun-Yu, Lin, Kung-Ping, Kang, Mei-Ling, Chen, Chien-Hsiun, Chu, Hou-Wei, Lin, Chiao-Feng, Lee, Mei-Hsuan, Liu, Quintin, Satta, Yoko, Lin, Cheng-Jui, Lin, Marie, Chaw, Shu-Miaw, Loo, Jun-Hun, Shen, Chen-Yang, Ko, Wen-Ya

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Detecting Genetic Ancestry and Adaptation in the Taiwanese Han People Bằng Lo, Yun-Hua, Cheng, Hsueh-Chien, Hsiung, Chia-Ni, Yang, Show-Ling, Wang, Han-Yu, Peng, Chia-Wei, Chen, Chun-Yu, Lin, Kung-Ping, Kang, Mei-Ling, Chen, Chien-Hsiun, Chu, Hou-Wei, Lin, Chiao-Feng, Lee, Mei-Hsuan, Liu, Quintin, Satta, Yoko, Lin, Cheng-Jui, Lin, Marie, Chaw, Shu-Miaw, Loo, Jun-Hun, Shen, Chen-Yang, Ko, Wen-Ya

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Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders Bằng Lim, Elaine T., Raychaudhuri, Soumya, Sanders, Stephan J., Stevens, Christine, Sabo, Aniko, MacArthur, Daniel G., Neale, Benjamin M., Kirby, Andrew, Ruderfer, Douglas M., Fromer, Menachem, Lek, Monkol, Liu, Li, Flannick, Jason, Ripke, Stephan, Nagaswamy, Uma, Muzny, Donna, Reid, Jeffrey G., Hawes, Alicia, Newsham, Irene, Wu, Yuanqing, Lewis, Lora, Dinh, Huyen, Gross, Shannon, Wang, Li-San, Lin, Chiao-Feng, Valladares, Otto, Gabriel, Stacey B., dePristo, Mark, Altshuler, David M., Purcell, Shaun M., State, Matthew W., Boerwinkle, Eric, Buxbaum, Joseph D., Cook, Edwin H., Gibbs, Richard A., Schellenberg, Gerard D., Sutcliffe, James S., Devlin, Bernie, Roeder, Kathryn, Daly, Mark J.

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Rarity of the Alzheimer Disease–Protective APP A673T Variant in the United States Bằng Wang, Li-San, Naj, Adam C., Graham, Robert R., Crane, Paul K., Kunkle, Brian W., Cruchaga, Carlos, Gonzalez Murcia, Josue D., Cannon-Albright, Lisa, Baldwin, Clinton T., Zetterberg, Henrik, Blennow, Kaj, Kukull, Walter A., Faber, Kelley M., Schupf, Nicole, Norton, Maria C., Tschanz, JoAnn T., Munger, Ronald G., Corcoran, Christopher D., Rogaeva, Ekaterina, Lin, Chiao-Feng, Dombroski, Beth A., Cantwell, Laura B., Partch, Amanda, Valladares, Otto, Hakonarson, Hakon, St George-Hyslop, Peter, Green, Robert C., Goate, Alison M., Foroud, Tatiana M., Carney, Regina M., Larson, Eric B., Behrens, Timothy W., Kauwe, John S. K., Haines, Jonathan L., Farrer, Lindsay A., Pericak-Vance, Margaret A., Mayeux, Richard, Schellenberg, Gerard D.

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Variants in the ATP-Binding Cassette Transporter (ABCA7), Apolipoprotein E ε4, and the Risk of Late-Onset Alzheimer Disease in African Americans Bằng Reitz, Christiane, Jun, Gyungah, Naj, Adam, Rajbhandary, Ruchita, Vardarajan, Badri Narayan, Wang, Li-San, Valladares, Otto, Lin, Chiao-Feng, Larson, Eric B., Graff-Radford, Neill R., Evans, Denis, De Jager, Philip L., Crane, Paul K., Buxbaum, Joseph D., Murrell, Jill R., Raj, Towfique, Ertekin-Taner, Nilufer, Logue, Mark, Baldwin, Clinton T., Green, Robert C., Barnes, Lisa L., Cantwell, Laura B., Fallin, M. Daniele, Go, Rodney C. P., Griffith, Patrick, Obisesan, Thomas O., Manly, Jennifer J., Lunetta, Kathryn L., Kamboh, M. Ilyas, Lopez, Oscar L., Bennett, David A., Hendrie, Hugh, Hall, Kathleen S., Goate, Alison M., Byrd, Goldie S., Kukull, Walter A., Foroud, Tatiana M., Haines, Jonathan L., Farrer, Lindsay A., Pericak-Vance, Margaret A., Schellenberg, Gerard D., Mayeux, Richard

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Patterns and rates of exonic de novo mutations in autism spectrum disorders Bằng Neale, Benjamin M., Kou, Yan, Liu, Li, Ma'ayan, Avi, Samocha, Kaitlin E., Sabo, Aniko, Lin, Chiao-Feng, Stevens, Christine, Wang, Li-San, Makarov, Vladimir, Polak, Paz, Yoon, Seungtai, Maguire, Jared, Crawford, Emily L., Campbell, Nicholas G., Geller, Evan T., Valladares, Otto, Shafer, Chad, Liu, Han, Zhao, Tuo, Cai, Guiqing, Lihm, Jayon, Dannenfelser, Ruth, Jabado, Omar, Peralta, Zuleyma, Nagaswamy, Uma, Muzny, Donna, Reid, Jeffrey G., Newsham, Irene, Wu, Yuanqing, Lewis, Lora, Han, Yi, Voight, Benjamin F., Lim, Elaine, Rossin, Elizabeth, Kirby, Andrew, Flannick, Jason, Fromer, Menachem, Shakir, Khalid, Fennell, Tim, Garimella, Kiran, Banks, Eric, Poplin, Ryan, Gabriel, Stacey, DePristo, Mark, Wimbish, Jack R., Boone, Braden E., Levy, Shawn E., Betancur, Catalina, Sunyaev, Shamil, Boerwinkle, Eric, Buxbaum, Joseph D., Cook, Edwin H., Devlin, Bernie, Gibbs, Richard A., Roeder, Kathryn, Schellenberg, Gerard D., Sutcliffe, James S., Daly, Mark J.

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Synaptic, transcriptional, and chromatin genes disrupted in autism Bằng De Rubeis, Silvia, He, Xin, Goldberg, Arthur P., Poultney, Christopher S., Samocha, Kaitlin, Cicek, A Ercument, Kou, Yan, Liu, Li, Fromer, Menachem, Walker, Susan, Singh, Tarjinder, Klei, Lambertus, Kosmicki, Jack, Fu, Shih-Chen, Aleksic, Branko, Biscaldi, Monica, Bolton, Patrick F., Brownfeld, Jessica M., Cai, Jinlu, Campbell, Nicholas J., Carracedo, Angel, Chahrour, Maria H., Chiocchetti, Andreas G., Coon, Hilary, Crawford, Emily L., Crooks, Lucy, Curran, Sarah R., Dawson, Geraldine, Duketis, Eftichia, Fernandez, Bridget A., Gallagher, Louise, Geller, Evan, Guter, Stephen J., Hill, R. Sean, Ionita-Laza, Iuliana, Gonzalez, Patricia Jimenez, Kilpinen, Helena, Klauck, Sabine M., Kolevzon, Alexander, Lee, Irene, Lei, Jing, Lehtimäki, Terho, Lin, Chiao-Feng, Ma'ayan, Avi, Marshall, Christian R., McInnes, Alison L., Neale, Benjamin, Owen, Michael J., Ozaki, Norio, Parellada, Mara, Parr, Jeremy R., Purcell, Shaun, Puura, Kaija, Rajagopalan, Deepthi, Rehnström, Karola, Reichenberg, Abraham, Sabo, Aniko, Sachse, Michael, Sanders, Stephan J., Schafer, Chad, Schulte-Rüther, Martin, Skuse, David, Stevens, Christine, Szatmari, Peter, Tammimies, Kristiina, Valladares, Otto, Voran, Annette, Wang, Li-San, Weiss, Lauren A., Willsey, A. Jeremy, Yu, Timothy W., Yuen, Ryan K.C., Cook, Edwin H., Freitag, Christine M., Gill, Michael, Hultman, Christina M., Lehner, Thomas, Palotie, Aarno, Schellenberg, Gerard D., Sklar, Pamela, State, Matthew W., Sutcliffe, James S., Walsh, Christopher A., Scherer, Stephen W., Zwick, Michael E., Barrett, Jeffrey C., Cutler, David J., Roeder, Kathryn, Devlin, Bernie, Daly, Mark J., Buxbaum, Joseph D.

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Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer’s disease Bằng Lambert, Jean-Charles, Ibrahim-Verbaas, Carla A, Harold, Denise, Naj, Adam C, Sims, Rebecca, Bellenguez, Céline, Jun, Gyungah, DeStefano, Anita L, Bis, Joshua C, Beecham, Gary W, Grenier-Boley, Benjamin, Russo, Giancarlo, Thornton-Wells, Tricia A, Jones, Nicola, Smith, Albert V, Chouraki, Vincent, Thomas, Charlene, Ikram, M Arfan, Zelenika, Diana, Vardarajan, Badri N, Kamatani, Yoichiro, Lin, Chiao-Feng, Gerrish, Amy, Schmidt, Helena, Kunkle, Brian, Dunstan, Melanie L, Ruiz, Agustin, Bihoreau, Marie-Thérèse, Choi, Seung-Hoan, Reitz, Christiane, Pasquier, Florence, Hollingworth, Paul, Ramirez, Alfredo, Hanon, Olivier, Fitzpatrick, Annette L, Buxbaum, Joseph D, Campion, Dominique, Crane, Paul K, Baldwin, Clinton, Becker, Tim, Gudnason, Vilmundur, Cruchaga, Carlos, Craig, David, Amin, Najaf, Berr, Claudine, Lopez, Oscar L, De Jager, Philip L, Deramecourt, Vincent, Johnston, Janet A, Evans, Denis, Lovestone, Simon, Letenneur, Luc, Morón, Francisco J, Rubinsztein, David C, Eiriksdottir, Gudny, Sleegers, Kristel, Goate, Alison M, Fiévet, Nathalie, Huentelman, Matthew J, Gill, Michael, Brown, Kristelle, Kamboh, M Ilyas, Keller, Lina, Barberger-Gateau, Pascale, McGuinness, Bernadette, Larson, Eric B, Green, Robert, Myers, Amanda J, Dufouil, Carole, Todd, Stephen, Wallon, David, Love, Seth, Rogaeva, Ekaterina, Gallacher, John, St George-Hyslop, Peter, Clarimon, Jordi, Lleo, Alberto, Bayer, Anthony, Tsuang, Debby W, Yu, Lei, Tsolaki, Magda, Bossù, Paola, Spalletta, Gianfranco, Proitsi, Petroula, Collinge, John, Sorbi, Sandro, Sanchez-Garcia, Florentino, Fox, Nick C, Hardy, John, Deniz Naranjo, Maria Candida, Bosco, Paolo, Clarke, Robert, Brayne, Carol, Galimberti, Daniela, Mancuso, Michelangelo, Matthews, Fiona, Moebus, Susanne, Mecocci, Patrizia, Zompo, Maria Del, Maier, Wolfgang, Hampel, Harald, Pilotto, Alberto, Bullido, Maria, Panza, Francesco, Caffarra, Paolo, Nacmias, Benedetta, Gilbert, John R, Mayhaus, Manuel, Lannfelt, Lars, Hakonarson, Hakon, Pichler, Sabrina, Carrasquillo, Minerva M, Ingelsson, Martin, Beekly, Duane, Alvarez, Victoria, Zou, Fanggeng, Valladares, Otto, Younkin, Steven G, Coto, Eliecer, Hamilton-Nelson, Kara L, Gu, Wei, Razquin, Cristina, Pastor, Pau, Mateo, Ignacio, Owen, Michael J, Faber, Kelley M, Jonsson, Palmi V, Combarros, Onofre, O’Donovan, Michael C, Cantwell, Laura B, Soininen, Hilkka, Blacker, Deborah, Mead, Simon, Mosley, Thomas H, Bennett, David A, Harris, Tamara B, Fratiglioni, Laura, Holmes, Clive, de Bruijn, Renee F A G, Passmore, Peter, Montine, Thomas J, Bettens, Karolien, Rotter, Jerome I, Brice, Alexis, Morgan, Kevin, Foroud, Tatiana M, Kukull, Walter A, Hannequin, Didier, Powell, John F, Nalls, Michael A, Ritchie, Karen, Lunetta, Kathryn L, Kauwe, John S K, Boerwinkle, Eric, Riemenschneider, Matthias, Boada, Mercè, Hiltunen, Mikko, Martin, Eden R, Schmidt, Reinhold, Rujescu, Dan, Wang, Li-san, Dartigues, Jean-François, Mayeux, Richard, Tzourio, Christophe, Hofman, Albert, Nöthen, Markus M, Graff, Caroline, Psaty, Bruce M, Jones, Lesley, Haines, Jonathan L, Holmans, Peter A, Lathrop, Mark, Pericak-Vance, Margaret A, Launer, Lenore J, Farrer, Lindsay A, van Duijn, Cornelia M, Van Broeckhoven, Christine, Moskvina, Valentina, Seshadri, Sudha, Williams, Julie, Schellenberg, Gerard D, Amouyel, Philippe

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