Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Jhamai, Mila"'
Autor:
Luijk, René, Wu, Haoyu, Ward-Caviness, Cavin K., Hannon, Eilis, Carnero-Montoro, Elena, Min, Josine L., Mandaviya, Pooja, Müller-Nurasyid, Martina, Mei, Hailiang, van der Maarel, Silvere M., Beekman, Marian, der Breggen, Ruud van, Deelen, Joris, Lakenberg, Nico, Moed, Matthijs, Suchiman, H. Eka D., Arindrarto, Wibowo, van’t Hof, Peter, Jan Bonder, Marc, Deelen, Patrick, Tigchelaar, Ettje F., Zhernakova, Alexandra, Zhernakova, Dasha V., van Dongen, Jenny, Hottenga, Jouke J., Pool, René, Isaacs, Aaron, Hofman, Bert A., Jhamai, Mila, van der Kallen, Carla J.H., Schalkwijk, Casper G., Stehouwer, Coen D.A., van den Berg, Leonard H., van Galen, Michiel, Vermaat, Martijn, van Rooij, Jeroen, Uitterlinden, André G., Verbiest, Michael, Verkerk, Marijn, Kielbasa, P. Szymon M., Bot, Jan, Nooren, Irene, van Dijk, Freerk, Swertz, Morris A., van Heemst, Diana, Relton, Caroline, Mill, Jonathan, Waldenberger, Melanie, Bell, Jordana T., Jansen, Rick, Boomsma, D.I.
Publikováno v:
Nature Communications, 9(1):3738. Nature Publishing Group
Luijk, R, Wu, H, Ward-Caviness, C K, Hannon, E, Carnero-Montoro, E, Min, J L, Mandaviya, P, Müller-Nurasyid, M, Mei, H, van der Maarel, S M, Beekman, M, der Breggen, R V, Deelen, J, Lakenberg, N, Moed, M, Suchiman, H E D, Arindrarto, W, van’t Hof, P, Jan Bonder, M, Deelen, P, Tigchelaar, E F, Zhernakova, A, Zhernakova, D V, van Dongen, J, Hottenga, J J, Pool, R, Isaacs, A, Hofman, B A, Jhamai, M, van der Kallen, C J H, Schalkwijk, C G, Stehouwer, C D A, van den Berg, L H, van Galen, M, Vermaat, M, van Rooij, J, Uitterlinden, A G, Verbiest, M, Verkerk, M, Kielbasa, P S M, Bot, J, Nooren, I, van Dijk, F, Swertz, M A, van Heemst, D, Relton, C, Mill, J, Waldenberger, M, Bell, J T, Jansen, R, Boomsma, D I & BIOS Consortium 2018, ' Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation ', Nature Communications, vol. 9, no. 1, 3738, pp. 1-9 . https://doi.org/10.1038/s41467-018-05714-3
Nature Communications, Vol 9, Iss 1, Pp 1-9 (2018)
Nature Communications, 9:3738. Nature Publishing Group
BIOS Consortium, Luijk, R, Wu, H, Ward-Caviness, C K, Hannon, E, Carnero-Montoro, E, Min, J L, Mandaviya, P, Müller-Nurasyid, M, Mei, H, van der Maarel, S M, Beekman, M, der Breggen, R V, Deelen, J, Lakenberg, N, Moed, M, Suchiman, H E D, Arindrarto, W, van’t Hof, P, Jan Bonder, M, Deelen, P, Tigchelaar, E F, Zhernakova, A, Zhernakova, D V, van Dongen, J, Hottenga, J J, Pool, R, Isaacs, A, Hofman, B A, Jhamai, M, van der Kallen, C J H, Schalkwijk, C G, Stehouwer, C D A, van den Berg, L H, van Galen, M, Vermaat, M, van Rooij, J, Uitterlinden, A G, Verbiest, M, Verkerk, M, Kielbasa, P S M, Bot, J, Nooren, I, van Dijk, F, Swertz, M A, van Heemst, D, Relton, C, Mill, J, Waldenberger, M, Bell, J T & Jansen, R 2018, ' Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation ', Nature Communications, vol. 9, 3738 . https://doi.org/10.1038/s41467-018-05714-3
Nature Communications
BIOS Consortium 2018, ' Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation ', Nature Communications, vol. 9, no. 1, 3738 . https://doi.org/10.1038/s41467-018-05714-3
Nature Communications, 9
Nature Communications, 9(1):3738, 1-9. Nature Publishing Group
Luijk, R, Wu, H, Ward-Caviness, C K, Hannon, E, Carnero-Montoro, E, Min, J L, Mandaviya, P, Müller-Nurasyid, M, Mei, H, van der Maarel, S M, Beekman, M, der Breggen, R V, Deelen, J, Lakenberg, N, Moed, M, Suchiman, H E D, Arindrarto, W, van’t Hof, P, Jan Bonder, M, Deelen, P, Tigchelaar, E F, Zhernakova, A, Zhernakova, D V, van Dongen, J, Hottenga, J J, Pool, R, Isaacs, A, Hofman, B A, Jhamai, M, van der Kallen, C J H, Schalkwijk, C G, Stehouwer, C D A, van den Berg, L H, van Galen, M, Vermaat, M, van Rooij, J, Uitterlinden, A G, Verbiest, M, Verkerk, M, Kielbasa, P S M, Bot, J, Nooren, I, van Dijk, F, Swertz, M A, van Heemst, D, Relton, C, Mill, J, Waldenberger, M, Bell, J T, Jansen, R, Boomsma, D I & BIOS Consortium 2018, ' Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation ', Nature Communications, vol. 9, no. 1, 3738, pp. 1-9 . https://doi.org/10.1038/s41467-018-05714-3
Nature Communications, Vol 9, Iss 1, Pp 1-9 (2018)
Nature Communications, 9:3738. Nature Publishing Group
BIOS Consortium, Luijk, R, Wu, H, Ward-Caviness, C K, Hannon, E, Carnero-Montoro, E, Min, J L, Mandaviya, P, Müller-Nurasyid, M, Mei, H, van der Maarel, S M, Beekman, M, der Breggen, R V, Deelen, J, Lakenberg, N, Moed, M, Suchiman, H E D, Arindrarto, W, van’t Hof, P, Jan Bonder, M, Deelen, P, Tigchelaar, E F, Zhernakova, A, Zhernakova, D V, van Dongen, J, Hottenga, J J, Pool, R, Isaacs, A, Hofman, B A, Jhamai, M, van der Kallen, C J H, Schalkwijk, C G, Stehouwer, C D A, van den Berg, L H, van Galen, M, Vermaat, M, van Rooij, J, Uitterlinden, A G, Verbiest, M, Verkerk, M, Kielbasa, P S M, Bot, J, Nooren, I, van Dijk, F, Swertz, M A, van Heemst, D, Relton, C, Mill, J, Waldenberger, M, Bell, J T & Jansen, R 2018, ' Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation ', Nature Communications, vol. 9, 3738 . https://doi.org/10.1038/s41467-018-05714-3
Nature Communications
BIOS Consortium 2018, ' Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation ', Nature Communications, vol. 9, no. 1, 3738 . https://doi.org/10.1038/s41467-018-05714-3
Nature Communications, 9
Nature Communications, 9(1):3738, 1-9. Nature Publishing Group
X-chromosome inactivation (XCI), i.e., the inactivation of one of the female X chromosomes, restores equal expression of X-chromosomal genes between females and males. However, ~10% of genes show variable degrees of escape from XCI between females, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ab67788cb35f958f6a81d9ce7a4a391
https://research.vumc.nl/en/publications/18512c17-65c0-4011-9c66-5345ed8ffb26
https://research.vumc.nl/en/publications/18512c17-65c0-4011-9c66-5345ed8ffb26
Autor:
Zheng, Hou-Feng, Forgetta, Vincenzo, Hsu, Yi-Hsiang, Estrada, Karol, Rosello-Diez, Alberto, Leo, Paul J, Dahia, Chitra L, Park-Min, Kyung Hyun, Tobias, Jonathan H, Kooperberg, Charles, Kleinman, Aaron, Styrkarsdottir, Unnur, Liu, Ching-Ti, Uggla, Charlotta, Evans, Daniel S, Nielson, Carrie M, Walter, Klaudia, Pettersson-Kymmer, Ulrika, McCarthy, Shane, Eriksson, Joel, Kwan, Tony, Jhamai, Mila, Trajanoska, Katerina, Memari, Yasin, Min, Josine, Huang, Jie, Danecek, Petr, Wilmot, Beth, Li, Rui, Chou, Wen-Chi, Mokry, Lauren E, Moayyeri, Alireza, Claussnitzer, Melina, Cheng, Chia-Ho, Cheung, Warren, Medina-Gómez, Carolina, Ge, Bing, Chen, Shu-Huang, Choi, Kwangbom, Oei, Ling, Fraser, James, Kraaij, Robert, Hibbs, Matthew A, Gregson, Celia L, Paquette, Denis, Hofman, Albert, Wibom, Carl, Tranah, Gregory J, Marshall, Mhairi, Gardiner, Brooke B, Cremin, Katie, Auer, Paul, Hsu, Li, Ring, Sue, Tung, Joyce Y, Thorleifsson, Gudmar, Enneman, Anke W, van Schoor, Natasja M, de Groot, Lisette CPGM, van der Velde, Nathalie, Melin, Beatrice, Kemp, John P, Christiansen, Claus, Sayers, Adrian, Zhou, Yanhua, Calderari, Sophie, van Rooij, Jeroen, Carlson, Chris, Peters, Ulrike, Berlivet, Soizik, Dostie, Josée, Uitterlinden, Andre G, Williams, Stephen R, Farber, Charles, Grinberg, Daniel, LaCroix, Andrea Z, Haessler, Jeff, Chasman, Daniel I, Giulianini, Franco, Rose, Lynda M, Ridker, Paul M, Eisman, John A, Nguyen, Tuan V, Center, Jacqueline R, Nogues, Xavier, Garcia-Giralt, Natalia, Launer, Lenore L, Gudnason, Vilmunder, Mellström, Dan, Vandenput, Liesbeth, Amin, Najaf, van Duijn, Cornelia M, Karlsson, Magnus K, Ljunggren, Östen, Svensson, Olle, Hallmans, Göran, Rousseau, François, Giroux, Sylvie, Bussière, Johanne, Arp, Pascal P, Koromani, Fjorda, Prince, Richard L, Lewis, Joshua R, Langdahl, Bente L, Hermann, A Pernille, Jensen, Jens-Erik B, Kaptoge, Stephen, Khaw, Kay-Tee, Reeve, Jonathan, Formosa, Melissa M, Xuereb-Anastasi, Angela, Åkesson, Kristina, McGuigan, Fiona E, Garg, Gaurav, Olmos, Jose M, Zarrabeitia, Maria T, Riancho, Jose A, Ralston, Stuart H, Alonso, Nerea, Jiang, Xi, Goltzman, David, Pastinen, Tomi, Grundberg, Elin, Gauguier, Dominique, Orwoll, Eric S, Karasik, David, Davey-Smith, George, AOGC Consortium, Smith, Albert V, Siggeirsdottir, Kristin, Harris, Tamara B, Zillikens, M Carola, van Meurs, Joyce BJ, Thorsteinsdottir, Unnur, Maurano, Matthew T, Timpson, Nicholas J, Soranzo, Nicole, Durbin, Richard, Wilson, Scott G, Ntzani, Evangelia E, Brown, Matthew A, Stefansson, Kari, Hinds, David A, Spector, Tim, Cupples, L Adrienne, Ohlsson, Claes, Greenwood, Celia MT, UK10K Consortium, Jackson, Rebecca D, Rowe, David W, Loomis, Cynthia A, Evans, David M, Ackert-Bicknell, Cheryl L, Joyner, Alexandra L, Duncan, Emma L, Kiel, Douglas P, Rivadeneira, Fernando, Richards, J Brent
Publikováno v:
Zheng, Hou-Feng; Forgetta, Vincenzo; Hsu, Yi-Hsiang; Estrada, Karol; Rosello-Diez, Alberto; Leo, Paul J; et al.(2015). Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.. Nature, 526(7571), 112-117. doi: 10.1038/nature14878. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/2t06828r
The extent to which low-frequency (minor allele frequency (MAF) between 1-5%) and rare (MAF ≤ 1%) variants contribute to complex traits and disease in the general population is mainly unknown. Bone mineral density (BMD) is highly heritable, a major
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::3bec1f5300fe91cd5fede9a2d49c5019
http://www.escholarship.org/uc/item/2t06828r
http://www.escholarship.org/uc/item/2t06828r
Autor:
Peters, Marjolein J, Joehanes, Roby, Pilling, Luke C, Schurmann, Claudia, Conneely, Karen N, Powell, Joseph, Reinmaa, Eva, Sutphin, George L, Zhernakova, Alexandra, Schramm, Katharina, Wilson, Yana A, Kobes, Sayuko, Tukiainen, Taru, NABEC/UKBEC Consortium, Ramos, Yolande F, Göring, Harald HH, Fornage, Myriam, Liu, Yongmei, Gharib, Sina A, Stranger, Barbara E, De Jager, Philip L, Aviv, Abraham, Levy, Daniel, Murabito, Joanne M, Munson, Peter J, Huan, Tianxiao, Hofman, Albert, Uitterlinden, André G, Rivadeneira, Fernando, van Rooij, Jeroen, Stolk, Lisette, Broer, Linda, Verbiest, Michael MPJ, Jhamai, Mila, Arp, Pascal, Metspalu, Andres, Tserel, Liina, Milani, Lili, Samani, Nilesh J, Peterson, Pärt, Kasela, Silva, Codd, Veryan, Peters, Annette, Ward-Caviness, Cavin K, Herder, Christian, Waldenberger, Melanie, Roden, Michael, Singmann, Paula, Zeilinger, Sonja, Illig, Thomas, Homuth, Georg, Grabe, Hans-Jörgen, Völzke, Henry, Steil, Leif, Kocher, Thomas, Murray, Anna, Melzer, David, Yaghootkar, Hanieh, Bandinelli, Stefania, Moses, Eric K, Kent, Jack W, Curran, Joanne E, Johnson, Matthew P, Williams-Blangero, Sarah, Westra, Harm-Jan, McRae, Allan F, Smith, Jennifer A, Kardia, Sharon LR, Hovatta, Iiris, Perola, Markus, Ripatti, Samuli, Salomaa, Veikko, Henders, Anjali K, Martin, Nicholas G, Smith, Alicia K, Mehta, Divya, Binder, Elisabeth B, Nylocks, K Maria, Kennedy, Elizabeth M, Klengel, Torsten, Ding, Jingzhong, Suchy-Dicey, Astrid M, Enquobahrie, Daniel A, Brody, Jennifer, Rotter, Jerome I, Chen, Yii-Der I, Houwing-Duistermaat, Jeanine, Kloppenburg, Margreet, Slagboom, P Eline, Helmer, Quinta, den Hollander, Wouter, Bean, Shannon, Raj, Towfique, Bakhshi, Noman, Wang, Qiao Ping, Oyston, Lisa J, Psaty, Bruce M, Tracy, Russell P, Montgomery, Grant W, Turner, Stephen T
Publikováno v:
Nature communications, vol 6, iss 1
Disease incidences increase with age, but the molecular characteristics of ageing that lead to increased disease susceptibility remain inadequately understood. Here we perform a whole-blood gene expression meta-analysis in 14,983 individuals of Europ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::311608e871b7e760f7e8677386195d9f
https://escholarship.org/uc/item/7935g8z3
https://escholarship.org/uc/item/7935g8z3
Akademický článek
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Publikováno v:
Apoptosis, 7, 13-21. Springer Netherlands
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::3b3279f113083717834bd73e04562191
https://pure.eur.nl/en/publications/3c96d8fc-66d4-46da-96d2-fb2ac4f9b6cb
https://pure.eur.nl/en/publications/3c96d8fc-66d4-46da-96d2-fb2ac4f9b6cb
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