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DNA Methylation Signatures in Development and Aging of the Human Prefrontal Cortex
Numata, Shusuke, Ye, Tianzhang, Hyde, Thomas M., Guitart-Navarro, Xavier, Tao, Ran, Wininger, Michael, Colantuoni, Carlo, Weinberger, Daniel R., Kleinman, Joel E., Lipska, Barbara K.
Published in American journal of human genetics (10.02.2012)
Published in American journal of human genetics (10.02.2012)
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Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci
De Jager, Philip L, Jia, Xiaoming, Wang, Joanne, de Bakker, Paul I W, Ottoboni, Linda, Aggarwal, Neelum T, Piccio, Laura, Raychaudhuri, Soumya, Tran, Dong, Aubin, Cristin, Briskin, Rebeccah, Romano, Susan, Baranzini, Sergio E, McCauley, Jacob L, Pericak-Vance, Margaret A, Haines, Jonathan L, Gibson, Rachel A, Naeglin, Yvonne, Uitdehaag, Bernard, Matthews, Paul M, Kappos, Ludwig, Polman, Chris, McArdle, Wendy L, Strachan, David P, Evans, Denis, Cross, Anne H, Daly, Mark J, Compston, Alastair, Sawcer, Stephen J, Weiner, Howard L, Hauser, Stephen L, Hafler, David A, Oksenberg, Jorge R
Published in Nature genetics (01.07.2009)
Published in Nature genetics (01.07.2009)
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Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies
RIVADENEIRA, Fernando, STYRKARSDOTTIR, Unnur, CUPPLES, L. Adrienne, DELOUKAS, Panagiotis, DEMISSIE, Serkalem, GRUNDBERG, Elin, HOFMAN, Albert, KONG, Augustine, KARASIK, David, VAN MEURS, Joyce B, OOSTRA, Ben, PASTINEN, Tomi, ESTRADA, Karol, POLS, Huibert A. P, SIGURDSSON, Gunnar, SORANZO, Nicole, THORLEIFSSON, Gudmar, THORSTEINSDOTTIR, Unnur, WILLIAMS, Frances M. K, WILSON, Scott G, YANHUA ZHOU, RALSTON, Stuart H, VAN DUIJN, Cornelia M, HALLDORSSON, Bjarni V, SPECTOR, Timothy, KIEL, Douglas P, STEFANSSON, Kari, IOANNIDIS, John P. A, UITTERLINDEN, André G, HSU, Yi-Hsiang, RICHARDS, J. Brent, ZILLIKENS, M. Carola, KAWOURA, Fotini K, AMIN, Najaf, AULCHENKO, Yurii S
Published in Nature genetics (01.11.2009)
Published in Nature genetics (01.11.2009)
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In vivo expression of polyglutamine-expanded huntingtin by mouse striatal astrocytes impairs glutamate transport: a correlation with Huntington's disease subjects
Faideau, Mathilde, Kim, Jinho, Cormier, Kerry, Gilmore, Richard, Welch, Mackenzie, Auregan, Gwennaelle, Dufour, Noelle, Guillermier, Martine, Brouillet, Emmanuel, Hantraye, Philippe, Déglon, Nicole, Ferrante, Robert J., Bonvento, Gilles
Published in Human molecular genetics (01.08.2010)
Published in Human molecular genetics (01.08.2010)
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New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
Jackson, Anne U, Wheeler, Eleanor, Bouatia-Naji, Nabila, Morris, Andrew P, Rybin, Denis, Thorleifsson, Gudmar, Steinthorsdottir, Valgerdur, Grallert, Harald, Dehghan, Abbas, Franklin, Christopher S, Song, Kijoung, Egan, Josephine M, Lajunen, Taina, Doney, Alex, Kanoni, Stavroula, Qi, Lu, Gieger, Christian, Payne, Felicity, Roccasecca, Rosa Maria, Sethupathy, Praveen, Balkau, Beverley, Barter, Philip, Beilby, John P, Benediktsson, Rafn, Bergmann, Sven, Bumpstead, Suzannah J, Chines, Peter, Cornelis, Marilyn, Day, Ian N M, de Geus, Eco J C, Dina, Christian, Erdos, Michael R, Fedson, Annette C, Fischer-Rosinsky, Antje, Graessler, Jürgen, Grundy, Scott, Hartikainen, Anna-Liisa, Hassanali, Neelam, Hayward, Caroline, Heath, Simon C, Herder, Christian, Hicks, Andrew A, Hillman, David R, Hingorani, Aroon D, Hui, Jennie, Isomaa, Bo, Johnson, Paul R V, Jula, Antti, Kaakinen, Marika, Kesaniemi, Y Antero, Kivimaki, Mika, Knight, Beatrice, Mahley, Robert, Mangino, Massimo, McAteer, Jarred B, McPherson, Ruth, Morken, Mario A, Mukherjee, Sutapa, Naitza, Silvia, Narisu, Narisu, Pattaro, Cristian, Pedersen, Nancy L, Pichler, Irene, Polasek, Ozren, Posthuma, Danielle, Province, Michael A, Psaty, Bruce M, Roden, Michael, Sanna, Serena, Sayer, Avan Aihie, Scheet, Paul, Scott, Laura J, Seedorf, Udo, Shields, Beverley, Simpson, Laila, Swift, Amy, Syvänen, Ann-Christine, Tanaka, Toshiko, Thorand, Barbara, Tichet, Jean, Varma, Dhiraj, Vitart, Veronique, Waeber, Gérard, Walley, Andrew, Walters, G Bragi, Wild, Sarah H, Zelenika, Diana, Zhai, Guangju, Zillikens, M Carola, Meneton, Pierre, Magnusson, Patrik K E, Salomaa, Veikko, Schwarz, Peter, Karpe, Fredrik, Dedoussis, George V, Kuusisto, Johanna, Pedersen, Oluf, Pramstaller, Peter Paul, Wichmann, H Erich, Stumvoll, Michael
Published in Nature genetics (01.02.2010)
Published in Nature genetics (01.02.2010)
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The splicing regulator Rbfox1 (A2BP1) controls neuronal excitation in the mammalian brain
Gehman, Lauren T, Stoilov, Peter, Maguire, Jamie, Damianov, Andrey, Lin, Chia-Ho, Shiue, Lily, Ares, Manuel, Mody, Istvan, Black, Douglas L
Published in Nature genetics (01.07.2011)
Published in Nature genetics (01.07.2011)
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Identification of loci associated with schizophrenia by genome-wide association and follow-up
O'Donovan, Michael C, Craddock, Nicholas, Norton, Nadine, Williams, Hywel, Peirce, Timothy, Moskvina, Valentina, Nikolov, Ivan, Hamshere, Marian, Carroll, Liam, Georgieva, Lyudmila, Dwyer, Sarah, Holmans, Peter, Marchini, Jonathan L, Spencer, Chris C A, Howie, Bryan, Leung, Hin-Tak, Hartmann, Annette M, Möller, Hans-Jürgen, Morris, Derek W, Shi, YongYong, Feng, GuoYin, Hoffmann, Per, Propping, Peter, Vasilescu, Catalina, Maier, Wolfgang, Rietschel, Marcella, Zammit, Stanley, Schumacher, Johannes, Quinn, Emma M, Schulze, Thomas G, Williams, Nigel M, Giegling, Ina, Iwata, Nakao, Ikeda, Masashi, Darvasi, Ariel, Shifman, Sagiv, He, Lin, Duan, Jubao, Sanders, Alan R, Levinson, Douglas F, Gejman, Pablo V, Cichon, Sven, Nöthen, Markus M, Gill, Michael, Corvin, Aiden, Rujescu, Dan, Kirov, George, Owen, Michael J
Published in Nature genetics (01.09.2008)
Published in Nature genetics (01.09.2008)
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Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases
Coppola, Giovanni, Chinnathambi, Subashchandrabose, Lee, Jason JiYong, Dombroski, Beth A., Baker, Matt C., Soto-Ortolaza, Alexandra I., Lee, Suzee E., Klein, Eric, Huang, Alden Y., Sears, Renee, Lane, Jessica R., Karydas, Anna M., Kenet, Robert O., Biernat, Jacek, Wang, Li-San, Cotman, Carl W., DeCarli, Charles S., Levey, Allan I., Ringman, John M., Mendez, Mario F., Chui, Helena C., Le Ber, Isabelle, Brice, Alexis, Lupton, Michelle K., Preza, Elisavet, Lovestone, Simon, Powell, John, Graff-Radford, Neill, Petersen, Ronald C., Boeve, Bradley F., Lippa, Carol F., Bigio, Eileen H., Mackenzie, Ian, Finger, Elizabeth, Kertesz, Andrew, Caselli, Richard J., Gearing, Marla, Juncos, Jorge L., Ghetti, Bernardino, Spina, Salvatore, Bordelon, Yvette M., Tourtellotte, Wallace W., Frosch, Matthew P., Vonsattel, Jean Paul G., Zarow, Chris, Beach, Thomas G., Albin, Roger L., Lieberman, Andrew P., Lee, Virginia M., Trojanowski, John Q., Van Deerlin, Vivianna M., Bird, Thomas D., Galasko, Douglas R., Masliah, Eliezer, White, Charles L., Troncoso, Juan C., Hannequin, Didier, Boxer, Adam L., Geschwind, Michael D., Kumar, Satish, Mandelkow, Eva-Maria, Wszolek, Zbigniew K., Uitti, Ryan J., Dickson, Dennis W., Haines, Jonathan L., Mayeux, Richard, Pericak-Vance, Margaret A., Farrer, Lindsay A., Ross, Owen A., Rademakers, Rosa, Schellenberg, Gerard D., Miller, Bruce L., Mandelkow, Eckhard, Geschwind, Daniel H.
Published in Human molecular genetics (01.08.2012)
Published in Human molecular genetics (01.08.2012)
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Divergent Whole-Genome Methylation Maps of Human and Chimpanzee Brains Reveal Epigenetic Basis of Human Regulatory Evolution
Zeng, Jia, Konopka, Genevieve, Hunt, Brendan G., Preuss, Todd M., Geschwind, Dan, Yi, Soojin V.
Published in American journal of human genetics (07.09.2012)
Published in American journal of human genetics (07.09.2012)
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CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs
Merveille, Anne-Christine, Davis, Erica E, Becker-Heck, Anita, Legendre, Marie, Amirav, Israel, Bataille, Géraldine, Belmont, John, Beydon, Nicole, Billen, Frédéric, Clément, Annick, Clercx, Cécile, Coste, André, Crosbie, Rachelle, de Blic, Jacques, Deleuze, Stephane, Duquesnoy, Philippe, Escalier, Denise, Escudier, Estelle, Fliegauf, Manfred, Horvath, Judith, Hill, Kent, Jorissen, Mark, Just, Jocelyne, Kispert, Andreas, Lathrop, Mark, Loges, Niki Tomas, Marthin, June K, Momozawa, Yukihide, Montantin, Guy, Nielsen, Kim G, Olbrich, Heike, Papon, Jean-François, Rayet, Isabelle, Roger, Gilles, Schmidts, Miriam, Tenreiro, Henrique, Towbin, Jeffrey A, Zelenika, Diana, Zentgraf, Hanswalter, Georges, Michel, Lequarré, Anne-Sophie, Katsanis, Nicholas, Omran, Heymut, Amselem, Serge
Published in Nature genetics (01.01.2011)
Published in Nature genetics (01.01.2011)
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The continuing value of twin studies in the omics era
van Dongen, Jenny, Slagboom, P. Eline, Draisma, Harmen H. M., Martin, Nicholas G., Boomsma, Dorret I.
Published in Nature reviews. Genetics (01.09.2012)
Published in Nature reviews. Genetics (01.09.2012)
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The Shaping of Modern Human Immune Systems by Multiregional Admixture with Archaic Humans
Abi-Rached, Laurent, Jobin, Matthew J., Kulkarni, Subhash, McWhinnie, Alasdair, Dalva, Klara, Gragert, Loren, Babrzadeh, Farbod, Gharizadeh, Baback, Luo, Ma, Plummer, Francis A., Kimani, Joshua, Carrington, Mary, Middleton, Derek, Rajalingam, Raja, Beksac, Meral, Marsh, Steven G. E., Maiers, Martin, Guethlein, Lisbeth A., Tavoularis, Sofia, Little, Ann-Margaret, Green, Richard E., Norman, Paul J., Parham, Peter
Published in Science (American Association for the Advancement of Science) (07.10.2011)
Published in Science (American Association for the Advancement of Science) (07.10.2011)
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Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease
Hamza, Taye H, Zabetian, Cyrus P, Tenesa, Albert, Laederach, Alain, Montimurro, Jennifer, Yearout, Dora, Kay, Denise M, Doheny, Kimberly F, Paschall, Justin, Pugh, Elizabeth, Kusel, Victoria I, Collura, Randall, Roberts, John, Griffith, Alida, Samii, Ali, Scott, William K, Nutt, John, Factor, Stewart A, Payami, Haydeh
Published in Nature genetics (01.09.2010)
Published in Nature genetics (01.09.2010)
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Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia
Chen, Wan-Jin, Lin, Yu, Xiong, Zhi-Qi, Wei, Wei, Ni, Wang, Tan, Guo-He, Guo, Shun-Ling, He, Jin, Chen, Ya-Fang, Zhang, Qi-Jie, Li, Hong-Fu, Lin, Yi, Murong, Shen-Xing, Xu, Jianfeng, Wang, Ning, Wu, Zhi-Ying
Published in Nature genetics (01.12.2011)
Published in Nature genetics (01.12.2011)
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De Novo Mutations in MLL Cause Wiedemann-Steiner Syndrome
Jones, Wendy D., Dafou, Dimitra, McEntagart, Meriel, Woollard, Wesley J., Elmslie, Frances V., Holder-Espinasse, Muriel, Irving, Melita, Saggar, Anand K., Smithson, Sarah, Trembath, Richard C., Deshpande, Charu, Simpson, Michael A.
Published in American journal of human genetics (10.08.2012)
Published in American journal of human genetics (10.08.2012)
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A genome-wide association study identifies two new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese
Hu, Zhibin, Wu, Chen, Shi, Yongyong, Guo, Huan, Zhao, Xueying, Yin, Zhihua, Yang, Lei, Dai, Juncheng, Hu, Lingmin, Tan, Wen, Li, Zhiqiang, Deng, Qifei, Wang, Jiucun, Wu, Wei, Jin, Guangfu, Jiang, Yue, Yu, Dianke, Zhou, Guoquan, Chen, Hongyan, Guan, Peng, Chen, Yijiang, Shu, Yongqian, Xu, Lin, Liu, Xiangyang, Liu, Li, Xu, Ping, Han, Baohui, Bai, Chunxue, Zhao, Yuxia, Zhang, Haibo, Yan, Ying, Ma, Hongxia, Chen, Jiaping, Chu, Mingjie, Lu, Feng, Zhang, Zhengdong, Chen, Feng, Wang, Xinru, Jin, Li, Lu, Jiachun, Zhou, Baosen, Lu, Daru, Wu, Tangchun, Lin, Dongxin, Shen, Hongbing
Published in Nature genetics (01.08.2011)
Published in Nature genetics (01.08.2011)
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