Rezultati - Lin, Chiao-Feng

Birth and death of gene overlaps in vertebrates od 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 od Lin, Chiao-Feng, Naj, Adam C, Wang, Li-San

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

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

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Spliceosomal small nuclear RNA genes in 11 insect genomes od 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 od 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 od 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 od 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 od 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 od 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 od 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 od 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 od 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 od 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 od 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 od 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 od 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 od 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 od 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 od 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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