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Maternal BMI at the start of pregnancy and offspring epigenome-wide DNA methylation: findings from the pregnancy and childhood epigenetics (PACE) consortium

by Sharp, Gemma C, Salas, Lucas A, Monnereau, Claire, Allard, Catherine, Yousefi, Paul, Everson, Todd M, Bohlin, Jon, Xu, Zongli, Huang, Rae-Chi, Reese, Sarah E, Xu, Cheng-Jian, Baïz, Nour, Hoyo, Cathrine, Agha, Golareh, Roy, Ritu, Holloway, John W, Ghantous, Akram, Merid, Simon K, Bakulski, Kelly M, Küpers, Leanne K, Zhang, Hongmei, Richmond, Rebecca C, Page, Christian M, Duijts, Liesbeth, Lie, Rolv T, Melton, Phillip E, Vonk, Judith M, Nohr, Ellen A, Williams-DeVane, ClarLynda, Huen, Karen, Rifas-Shiman, Sheryl L, Ruiz-Arenas, Carlos, Gonseth, Semira, Rezwan, Faisal I, Herceg, Zdenko, Ekström, Sandra, Croen, Lisa, Falahi, Fahimeh, Perron, Patrice, Karagas, Margaret R, Quraishi, Bilal M, Suderman, Matthew, Magnus, Maria C, Jaddoe, Vincent W V, Taylor, Jack A, Anderson, Denise, Zhao, Shanshan, Smit, Henriette A, Josey, Michele J, Bradman, Asa, Baccarelli, Andrea A, Bustamante, Mariona, Håberg, Siri E, Pershagen, Göran, Hertz-Picciotto, Irva, Newschaffer, Craig, Corpeleijn, Eva, Bouchard, Luigi, Lawlor, Debbie A, Maguire, Rachel L, Barcellos, Lisa F, Davey Smith, George, Eskenazi, Brenda, Karmaus, Wilfried, Marsit, Carmen J, Hivert, Marie-France, Snieder, Harold, Fallin, M Daniele, Melén, Erik, Munthe-Kaas, Monica C, Arshad, Hasan, Wiemels, Joseph L, Annesi-Maesano, Isabella, Vrijheid, Martine, Oken, Emily, Holland, Nina, Murphy, Susan K, Sørensen, Thorkild I A, Koppelman, Gerard H, Newnham, John P, Wilcox, Allen J, Nystad, Wenche, London, Stephanie J, Felix, Janine F, Relton, Caroline L
Published in Human molecular genetics (15.10.2017)

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Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

by Beaumont, Robin N., Day, Felix R., Peng, Shouneng, Hao, Ke, Feenstra, Bjarke, Qiao, Zhen, Moen, Gunn-Helen, Marsit, Carmen J., Nodzenski, Michael, Bradfield, Jonathan P., Grarup, Niels, Kooijman, Marjolein N., Li-Gao, Ruifang, Ahluwalia, Tarunveer S., Paternoster, Lavinia, Rueedi, Rico, Huikari, Ville, Metrustry, Sarah, Thiering, Elisabeth, Wang, Carol A., Joshi, Peter K., Myhre, Ronny, Pitkänen, Niina, van Leeuwen, Elisabeth M., Lagou, Vasiliki, Richmond, Rebecca C., Espinosa, Ana, Inskip, Hazel M., Holloway, John W., Santa-Marina, Loreto, Estivill, Xavier, Hocher, Berthold, Hivert, Marie-France, Muglia, Louis J., Heikkinen, Jani, van Kampen, Antoine H. C., van Schaik, Barbera D. C., Luan, Jian’an, Scott, Robert A., Zhao, Jing Hua, Ring, Susan M., Fernandez-Tajes, Juan, van Zuydam, Natalie R., Medina-Gomez, Carolina, de Haan, Hugoline G., Müller-Nurasyid, Martina, Fonvig, Cilius E., van Beijsterveldt, Catharina E. M., Bustamante, Mariona, Bonas-Guarch, Sílvia, Hougaard, David M., Mercader, Josep M., Linneberg, Allan, Knight, Bridget A., Bartels, Meike, Willems, Sara M., Chawes, Bo L., Kovacs, Peter, Prokopenko, Inga, Tuke, Marcus A., Yaghootkar, Hanieh, Loh, Po-Ru, Murray, Anna, Tönjes, Anke, Michaelsen, Kim F., Körner, Antje, Niinikoski, Harri, Pahkala, Katja, Jacobsson, Bo, Dedoussis, George V., Vrijkotte, Tanja G. M., Vrijheid, Martine, de Geus, Eco J. C. N., Kadarmideen, Haja N., Beilin, Lawrence J., Heinrich, Joachim, Borja, Judith B., Widén, Elisabeth E., Hattersley, Andrew T., Lehtimäki, Terho, Vollenweider, Peter, Sørensen, Thorkild I. A., Melbye, Mads, Rivadeneira, Fernando, Jaddoe, Vincent W. V., Hansen, Torben, Pisinger, Charlotta, Vaag, Allan A., Pedersen, Oluf, Uitterlinden, André G., Hyppönen, Elina, Scholtens, Denise M., Lowe, William L., Timpson, Nicholas J., Wareham, Nicholas J., Hakonarson, Hakon, Lawlor, Debbie A., Johansson, Stefan, Ong, Ken K., Evans, David M.
Published in Nature genetics (01.05.2019)

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Rare pathogenic variants in WNK3 cause X-linked intellectual disability

by Küry, Sébastien, Zhang, Jinwei, Besnard, Thomas, Caro-Llopis, Alfonso, Zeng, Xue, Robert, Stephanie M., Josiah, Sunday S., Kiziltug, Emre, Denommé-Pichon, Anne-Sophie, Cogné, Benjamin, Kundishora, Adam J., Hao, Le T., Li, Hong, Stevenson, Roger E., Louie, Raymond J., Deb, Wallid, Torti, Erin, Vignard, Virginie, McWalter, Kirsty, Raymond, F. Lucy, Rajabi, Farrah, Ranza, Emmanuelle, Grozeva, Detelina, Coury, Stephanie A., Blanc, Xavier, Brischoux-Boucher, Elise, Keren, Boris, Õunap, Katrin, Reinson, Karit, Ilves, Pilvi, Wentzensen, Ingrid M., Barr, Eileen E., Guihard, Solveig Heide, Charles, Perrine, Seaby, Eleanor G., Monaghan, Kristin G., Rio, Marlène, van Bever, Yolande, van Slegtenhorst, Marjon, Chung, Wendy K., Wilson, Ashley, Quinquis, Delphine, Bréhéret, Flora, Retterer, Kyle, Lindenbaum, Pierre, Scalais, Emmanuel, Rhodes, Lindsay, Stouffs, Katrien, Pereira, Elaine M., Berger, Sara M., Milla, Sarah S., Jaykumar, Ankita B., Cobb, Melanie H., Panchagnula, Shreyas, Duy, Phan Q., Vincent, Marie, Mercier, Sandra, Gilbert-Dussardier, Brigitte, Le Guillou, Xavier, Audebert-Bellanger, Séverine, Odent, Sylvie, Schmitt, Sébastien, Boisseau, Pierre, Bonneau, Dominique, Toutain, Annick, Colin, Estelle, Pasquier, Laurent, Redon, Richard, Bouman, Arjan, Rosenfeld, Jill. A., Friez, Michael J., Pérez-Peña, Helena, Akhtar Rizvi, Syed Raza, Haider, Shozeb, Antonarakis, Stylianos E., Schwartz, Charles E., Martínez, Francisco, Bézieau, Stéphane, Kahle, Kristopher T., Isidor, Bertrand
Published in Genetics in medicine (01.09.2022)

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