Showing 1 - 20 results of 42 for search '"PITTELOUD, N"', query time: 2.27s Refine Results  

SOX11 variants cause a neurodevelopmental disorder with infrequent ocular malformations and hypogonadotropic hypogonadism and with distinct DNA methylation profile

by Al-Jawahiri, Reem, Foroutan, Aidin, McConkey, Haley, Levy, Michael, Haghshenas, Sadegheh, Rooney, Kathleen, Turner, Jasmin, Shears, Debbie, Holder, Muriel, Lefroy, Henrietta, Castle, Bruce, Reis, Linda M., Semina, Elena V., Nickerson, Deborah, Bamshad, Michael, Leal, Suzanne, Lachlan, Katherine, Chandler, Kate, Clayton-Smith, Jill, Hug, Franziska Phan, Pitteloud, Nelly, Bartoloni, Lucia, Hoffjan, Sabine, Park, Soo-Mi, Thankamony, Ajay, Lees, Melissa, Wakeling, Emma, Naik, Swati, Hanker, Britta, Girisha, Katta M., Agolini, Emanuele, Giuseppe, Zampino, Alban, Ziegler, Tessarech, Marine, Keren, Boris, Afenjar, Alexandra, Zweier, Christiane, Smol, Thomas, Nobuhiko, Okamoto, Sekiguchi, Futoshi, Tsuchida, Naomi, Matsumoto, Naomichi, Kou, Ikuyo, Yonezawa, Yoshiro, Ikegawa, Shiro, Callewaert, Bert, Ambrose, John C., Arumugam, Prabhu, Bleda, Marta, Boardman-Pretty, Freya, Boustred, Christopher R., Brittain, Helen, Caulfield, Mark J., Chan, Georgia C., Fowler, Tom, Giess, Adam, Hamblin, Angela, Henderson, Shirley, Hubbard, Tim J.P., Jones, Louise J., Kasperaviciute, Dalia, Kayikci, Melis, Kousathanas, Athanasios, Lahnstein, Lea, Leigh, Sarah E.A., Leong, Ivonne U.S., Lopez, Javier F., FionaMaleady-Crowe, McEntagart, Meriel, Minneci, Federico, Moutsianas, Loukas, Mueller, Michael, Murugaesu, Nirupa, Need, Anna C., Odhams, Chris A., Patch, Christine, Perez-Gil, Daniel, Pullinger, John, Rendon, Augusto, TimRogers, Savage, Kevin, Sawant, Kushmita, Scott, Richard H., Siddiq, Afshan, Sieghart, Alexander, Smith, Samuel C., Sosinsky, Alona, Stuckey, Alexander, Tanguy, Mélanie, Taylor Tavares, Ana Lisa, Thomas, Ellen R.A., Thompson, Simon R., Tucci, Arianna, Williams, Eleanor, Kleinendorst, Lotte, Donaldson, Alan, Alders, Marielle, De Paepe, Anne, Sadikovic, Bekim, McNeill, Alisdair
Published in Genetics in medicine (01.06.2022)

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Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum

by Kaisinger, Lena R, Stankovic, Stasa, Messina, Andrea, Busch, Alexander S, Santoni, Federico, Petricek, Konstantin M, Huang-Doran, Isabel, Gudbjartsson, Daniel F, Gardner, Eugene J, Bolla, Manjeet K, Campbell, Archie, Joshi, Peter K, Karlsson, Robert, Medland, Sarah E, Meisinger, Christa, Polašek, Ozren, Porcu, Eleonora, Smith, Albert V, Tanaka, Toshiko, van der Most, Peter J, Vitart, Veronique, Wang, Carol A, Willemsen, Gonneke, Ahearn, Thomas U, Andrulis, Irene L, Bogdanova, Natalia V, Buring, Julie E, Canzian, Federico, Couch, Fergus J, Cox, Angela, Crisponi, Laura, Daly, Mary B, Devilee, Peter, Dörk, Thilo, Dunning, Alison M, Fasching, Peter A, Fernandez-Rhodes, Lindsay, Ferreli, Liana, Fletcher, Olivia, García-Closas, Montserrat, Guénel, Pascal, Haiman, Christopher A, Hall, Per, Hakonarson, Hakon, Hart, Roger J, Hooning, Maartje J, Hoppe, Reiner, Hu, Frank B, Huebner, Hanna, Jernström, Helena, Khusnutdinova, Elza K, Lacey, James V, Launer, Lenore J, Magnusson, Patrik K E, Mannermaa, Arto, McCarthy, Mark I, Meitinger, Thomas, Millwood, Iona Y, Milne, Roger L, Montgomery, Grant W, Nolte, Ilja M, Obi, Nadia, Offit, Kenneth, Ostrowski, Sisse R, Palotie, Aarno, Pedersen, Ole B, Saloustros, Emmanouil, Sandler, Dale P, Schmidt, Carsten O, Stampfer, Meir, Tamimi, Rulla M, Turman, Constance, Wolk, Alicja, Zheng, Wei, Alizadeh, Behrooz Z, Bandinelli, Stefania, Boerwinkle, Eric, Gieger, Christian, Hayward, Caroline, Nøhr, Ellen A, Snieder, Harold, Sovio, Ulla, Stöckl, Doris, Sudlow, Cathie, Timpson, Nic J, Toniolo, Daniela, Ulivi, Sheila, Völzke, Henry, Wareham, Nicholas J, Widen, Elisabeth, Pharoah, Paul D P, Easton, Douglas F, Njølstad, Pål R, Manousaki, Despoina, Juul, Anders, Stefansson, Kari, Horikoshi, Momoko, Farooqi, I Sadaf, Pitteloud, Nelly, Johansson, Stefan
Published in Nature genetics (01.08.2024)

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Understanding the genetic complexity of puberty timing across the allele frequency spectrum

by Kaisinger, Lena R, Stankovic, Stasa, Messina, Andrea, Busch, Alexander S, Santoni, Federico, Petricek, Konstantin M, Huang-Doran, Isabel, Gudbjartsson, Daniel F, Gardner, Eugene J, Bolla, Manjeet K, Campbell, Archie, Joshi, Peter K, Karlsson, Robert, Medland, Sarah E, Meisinger, Christa, Polašek, Ozren, Porcu, Eleonora, Smith, Albert V, Tanaka, Toshiko, van der Most, Peter J, Vitart, Veronique, Wang, Carol A, Willemsen, Gonneke, Ahearn, Thomas U, Andrulis, Irene L, Bogdanova, Natalia V, Buring, Julie E, Canzian, Federico, Couch, Fergus J, Cox, Angela, Crisponi, Laura, Daly, Mary B, Devilee, Peter, Dörk, Thilo, Dunning, Alison M, Fasching, Peter A, Fernandez-Rhodes, Lindsay, Ferreli, Liana, Fletcher, Olivia, García-Closas, Montserrat, Guénel, Pascal, Haiman, Christopher A, Hall, Per, Hakonarson, Hakon, Hart, Roger J, Hooning, Maartje J, Hoppe, Reiner, Hu, Frank B, Huebner, Hanna, Jernström, Helena, Khusnutdinova, Elza K, Lacey, James V, Launer, Lenore J, Magnusson, Patrik K E, Mannermaa, Arto, McCarthy, Mark I, Meitinger, Thomas, Millwood, Iona Y, Milne, Roger L, Montgomery, Grant W, Nolte, Ilja M, Obi, Nadia, Offit, Kenneth, Ostrowski, Sisse R, Palotie, Aarno, Pedersen, Ole B, Saloustros, Emmanouil, Sandler, Dale P, Schmidt, Carsten O, Stampfer, Meir, Tamimi, Rulla M, Turman, Constance, Wolk, Alicja, Zheng, Wei, Alizadeh, Behrooz Z, Bandinelli, Stefania, Boerwinkle, Eric, Gieger, Christian, Hayward, Caroline, Nøhr, Ellen A, Snieder, Harold, Sovio, Ulla, Stöckl, Doris, Sudlow, Cathie, Timpson, Nic J, Toniolo, Daniela, Ulivi, Sheila, Völzke, Henry, Wareham, Nicholas J, Widen, Elisabeth, Pharoah, Paul D P, Easton, Douglas F, Njølstad, Pål R, Manousaki, Despoina, Juul, Anders, Stefansson, Kari, Horikoshi, Momoko, Farooqi, I Sadaf, Pitteloud, Nelly, Johansson, Stefan
Published in Nature genetics (01.07.2024)

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