المؤلفون: Eising, Else, Mirza-Schreiber, Nazinin, de Zeeuw, Eveline L., Wang, Carol A., Truong, Dongnhu T., Allegrini, Andrea G., Shapland, Chin Yang, Zhu, Gu, Wigg, Karen G., Gerritse, Margot, Molz, Barbara, Alagöz, Gökberk, Gialluisi, Alessandro, Abbondanza, Filippo, Rimfeld, Kaili, van Donkelaar, Marjolein, Liao, Zhijie, Jansen, Philip R., Andlauer, Till F. M., Bates, Timothy C., Bernard, Manon, Blokland, Kirsten, Bonte, Milene, Børglum, Anders D., Bourgeron, Thomas, Brandeis, Daniel, Ceroni, Fabiola, Csépe, Valéria, Dale, Philip S., de Jong, Peter F., DeFries, John C., Démonet, Jean-François, Demontis, Ditte, Feng, Yu, Gordon, Scott D., Guger, Sharon L., Hayiou-Thomas, Marianna E., Hernández-Cabrera, Juan A., Hottenga, Jouke-Jan, Hulme, Charles, Kere, Juha, Kerr, Elizabeth N., Koomar, Tanner, Landerl, Karin, Leonard, Gabriel, Lovett, Maureen W., Lyytinen, Heikki, Martin, Nicholas G., Martinelli, Angela, Maurer, Urs, Michaelson, Jacob, Moll, Kristina, Monaco, Anthony P., Morgan, Angela T., Nőthen, Markus M., Pausova, Zdenka, Pennell, Craig E., Pennington, Bruce F., Price, Kaitlyn M., Rajagopal, Veera M., Ramus, Franck, Richer, Louis, Simpson, Nuala H., Smith, Shelley, Snowling, Margaret J., Stein, John, Strug, Lisa J., Talcott, Joel B., Tiemeier, Henning, van der Schroeff, Marc M.P., Verhoef, Ellen, Watkins, Kate E., Wilkinson, Margaret, Wright, Margaret J., Barr, Cathy L., Boomsma, Dorret I., Carreiras, Manuel, Franken, Marie-Christine J., Gruen, Jeffrey R., Luciano, Michelle, Müller-Myhsok, Bertram, Newbury, Dianne F., Olson, Richard ., Paracchini, Silvia, Paus, Tomáš, Plomin, Robert, Reilly, Sheena, Schulte-Körne, Gerd, Tomblin, Bruce, van Bergen, Elsje, Whitehouse, Andrew J.O., Willcutt, Erik G., St Pourcain, Beate, Francks, Clyde, Fisher, Simon E.

المساهمون: The Royal Society, University of St Andrews. Cellular Medicine Division, University of St Andrews. School of Medicine, University of St Andrews. Centre for Biophotonics, University of St Andrews. Biomedical Sciences Research Complex, University of St Andrews. Institute of Behavioural and Neural Sciences, University of St Andrews. St Andrews Bioinformatics Unit

مصطلحات موضوعية: Reading, Language, Genome-wide association study, Meta-analysis, QH426 Genetics, RA0421 Public health. Hygiene. Preventive Medicine, DAS, SDG 3 - Good Health and Well-being, MCC, QH426, RA0421

وصف الملف: application/pdf

العلاقة: Proceedings of the National Academy of Sciences of the United States of America; Eising , E , Mirza-Schreiber , N , de Zeeuw , E L , Wang , C A , Truong , D T , Allegrini , A G , Shapland , C Y , Zhu , G , Wigg , K G , Gerritse , M , Molz , B , Alagöz , G , Gialluisi , A , Abbondanza , F , Rimfeld , K , van Donkelaar , M , Liao , Z , Jansen , P R , Andlauer , T F M , Bates , T C , Bernard , M , Blokland , K , Bonte , M , Børglum , A D , Bourgeron , T , Brandeis , D , Ceroni , F , Csépe , V , Dale , P S , de Jong , P F , DeFries , J C , Démonet , J-F , Demontis , D , Feng , Y , Gordon , S D , Guger , S L , Hayiou-Thomas , M E , Hernández-Cabrera , J A , Hottenga , J-J , Hulme , C , Kere , J , Kerr , E N , Koomar , T , Landerl , K , Leonard , G , Lovett , M W , Lyytinen , H , Martin , N G , Martinelli , A , Maurer , U , Michaelson , J , Moll , K , Monaco , A P , Morgan , A T , Nőthen , M M , Pausova , Z , Pennell , C E , Pennington , B F , Price , K M , Rajagopal , V M , Ramus , F , Richer , L , Simpson , N H , Smith , S , Snowling , M J , Stein , J , Strug , L J , Talcott , J B , Tiemeier , H , van der Schroeff , M M P , Verhoef , E , Watkins , K E , Wilkinson , M , Wright , M J , Barr , C L , Boomsma , D I , Carreiras , M , Franken , M-C J , Gruen , J R , Luciano , M , Müller-Myhsok , B , Newbury , D F , Olson , R , Paracchini , S , Paus , T , Plomin , R , Reilly , S , Schulte-Körne , G , Tomblin , B , van Bergen , E , Whitehouse , A J O , Willcutt , E G , St Pourcain , B , Francks , C & Fisher , S E 2022 , ' Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people ' , Proceedings of the National Academy of Sciences of the United States of America , vol. 119 , no. 35 , e2202764119 . https://doi.org/10.1073/pnas.2202764119Test; PURE: 280149201; PURE UUID: 9d568cd6-3246-4956-a351-c451e6febd63; ORCID: /0000-0001-9934-8602/work/114641547; Scopus: 85136345356; WOS: 000911585800009; http://hdl.handle.net/10023/25885Test; https://doi.org/10.1073/pnas.2202764119Test; RGF\EA\180141

الإتاحة: https://doi.org/10.1073/pnas.2202764119Test
http://hdl.handle.net/10023/25885Test

المؤلفون: Pettigrew, Kerry A., Reeves, Emily, Leavett, Ruth, Hayiou-Thomas, Marianna E., Sharma, Anahita, Simpson, Nuala H., Martinelli, Angela, Thompson, Paul, Hulme, Charles, Snowling, Margaret J., Newbury, Dianne F., Paracchini, Silvia

المساهمون: The Wellcome Trust, University of St Andrews. School of Medicine, University of St Andrews. Biomedical Sciences Research Complex

مصطلحات موضوعية: R Medicine, QH426 Genetics, Biochemistry, Genetics and Molecular Biology(all), Agricultural and Biological Sciences(all), NDAS, QH426

وصف الملف: application/pdf

العلاقة: PLoS ONE; Pettigrew , K A , Reeves , E , Leavett , R , Hayiou-Thomas , M E , Sharma , A , Simpson , N H , Martinelli , A , Thompson , P , Hulme , C , Snowling , M J , Newbury , D F & Paracchini , S 2015 , ' Copy number variation screen identifies a rare de novo deletion at chromosome 15q13.1-13.3 in a child with language impairment ' , PLoS ONE , vol. 10 , no. 8 , e0134997 . https://doi.org/10.1371/journal.pone.0134997Test; PURE: 209628100; PURE UUID: 03497e3f-4dc7-4e36-b183-844ae161889f; RIS: urn:84643DEF495D04A64FFFCE9E5914145D; Scopus: 84942891872; PubMed: 26262844; ORCID: /0000-0001-9934-8602/work/60428067; WOS: 000359353300049; http://hdl.handle.net/10023/7231Test; https://doi.org/10.1371/journal.pone.0134997Test; http://www.scopus.com/inward/record.url?scp=84942891872&partnerID=8YFLogxKTest; 097831/z/11/z

الإتاحة: https://doi.org/10.1371/journal.pone.0134997Test
http://hdl.handle.net/10023/7231Test
http://www.scopus.com/inward/record.url?scp=84942891872&partnerID=8YFLogxKTest

المؤلفون: Martinelli, Angela, Rice, Mabel, Talcott, Joel B., Diaz, Rebeca, Smith, Shelley, Hashim Raza, Muhammad, Snowling, Margaret J., Hulme, Charles, Stein, John, Hayiou-Thomas, Marianna E., Hawi, Ziarih, Kent, Lindsey, Pitt, Samantha J., Newbury, Dianne F., Paracchini, Silvia

المساهمون: The Royal Society, Cunningham Trust, The Wellcome Trust, University of St Andrews. Cellular Medicine Division, University of St Andrews. School of Medicine, University of St Andrews. Institute of Behavioural and Neural Sciences, University of St Andrews. Centre for Biophotonics, University of St Andrews. Biomedical Sciences Research Complex, University of St Andrews. St Andrews Bioinformatics Unit

مصطلحات موضوعية: QH426 Genetics, RC0321 Neuroscience. Biological psychiatry. Neuropsychiatry, 3rd-DAS, QH426, RC0321

وصف الملف: application/pdf

العلاقة: Human Molecular Genetics; 273792703; 599de033-ae48-40aa-a6be-6dfd6e72c2a5; 000670925600008; 85108023007; Martinelli , A , Rice , M , Talcott , J B , Diaz , R , Smith , S , Hashim Raza , M , Snowling , M J , Hulme , C , Stein , J , Hayiou-Thomas , M E , Hawi , Z , Kent , L , Pitt , S J , Newbury , D F & Paracchini , S 2021 , ' A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures ' , Human Molecular Genetics , vol. 30 , no. 12 , ddab111 , pp. 1160–1171 . https://doi.org/10.1093/hmg/ddab111Test; ORCID: /0000-0002-5315-3399/work/92774987; ORCID: /0000-0003-2257-1595/work/92775310; ORCID: /0000-0003-0937-5928/work/92775382; ORCID: /0000-0001-9934-8602/work/92775867; https://hdl.handle.net/10023/23634Test; RGF\EA\180141; N/A; 105621/Z/14/Z

الإتاحة: https://doi.org/10.1093/hmg/ddab111Test
https://hdl.handle.net/10023/23634Test

المؤلفون: Scerri, Thomas S., Macpherson, Ellen, Martinelli, Angela, Wa, Wong Cheuk, Monaco, Anthony P., Stein, John, Zheng, Mo, Ho, Connie Suk-Han, McBride, Catherine, Snowling, Margaret, Hulme, Charles, Hayiou-Thomas, Marianna E., Waye, Mary M. Y., Talcott, Joel B., Paracchini, Silvia

المساهمون: The Wellcome Trust, University of St Andrews. School of Medicine, University of St Andrews. Cellular Medicine Division, University of St Andrews. Biomedical Sciences Research Complex

مصطلحات موضوعية: QH426 Genetics, RC0321 Neuroscience. Biological psychiatry. Neuropsychiatry, NDAS, BDC, QH426, RC0321, demo, psy

العلاقة: http://hdl.handle.net/10023/11295Test

الإتاحة: http://hdl.handle.net/10023/11295Test