المؤلفون: Scerri, Thomas S., Schulte-Körne, Gerd

الوصول الحر: https://www.europeana.eu/item/2048425/item_IVANKBI3PCKGLT32Q36ERPGDJRKZ6UZD?utm_source=api&utm_medium=api&utm_campaign=YuvuWBeCaTest

المؤلفون: Gialluisi, Alessandro, Andlauer, Till F. M., Mirza-Schreiber, Nazanin, Moll, Kristina, Becker, Jessica, Hoffmann, Per, Ludwig, Kerstin U., Czamara, Darina, St Pourcain, Beate, Honbolygo, Ferenc, Toth, Denes, Csepe, Valeria, Huguet, Guillaume, Chaix, Yves, Iannuzzi, Stephanie, Demonet, Jean-Francois, Morris, Andrew P., Hulslander, Jacqueline, Willcutt, Erik G., DeFries, John C., Olson, Richard K., Smith, Shelley D., Pennington, Bruce F., Vaessen, Anniek, Maurer, Urs, Lyytinen, Heikki, Peyrard-Janvid, Myriam, Leppanen, Paavo H. T., Brandeis, Daniel, Bonte, Milene, Stein, John F., Talcott, Joel B., Fauchereau, Fabien, Wilcke, Arndt, Kirsten, Holger, Mueller, Bent, Francks, Clyde, Bourgeron, Thomas, Monaco, Anthony P., Ramus, Franck, Landerl, Karin, Kere, Juha, Scerri, Thomas S., Paracchini, Silvia, Fisher, Simon E., Schumacher, Johannes, Noethen, Markus M., Mueller-Myhsok, Bertram, Schulte-Koerne, Gerd

المساهمون: STEMM - Stem Cells and Metabolism Research Program, Juha Kere / Principal Investigator, Research Programs Unit, University of Helsinki

مصطلحات موضوعية: READING-DISABILITY, INDIVIDUAL-DIFFERENCES, SUSCEPTIBILITY GENE, MOLECULAR-GENETICS, LANGUAGE, COMORBIDITY, LOCUS, AGE, SCHIZOPHRENIA, INTELLIGENCE, Neurology and psychiatry

وصف الملف: application/pdf

العلاقة: AG and TFMA were supported by the Munich Cluster for Systems Neurology (SyNergy). AG was supported by Fondazione Umberto Veronesi. SP is a Royal Society University Research fellow. BMM, CF, BSP and SEF are supported by the Max Planck Society. AW, BM and HK were funded by the Fraunhofer Society and the Max Planck Society within the "Pakt fur Forschung und Innovation". HK was also supported by LIFE-Leipzig Research Center for Civilization Diseases funded by means of the European Union; the European Regional Development Fund (ERDF); and the Free State of Saxony within the excellence initiative. FR is supported by Agence Nationale de la Recherche (ANR-06-NEURO-019-01, ANR-17-EURE-0017 IEC, ANR-10-IDEX-0001-02 PSL, ANR-11-BSV4-014-01), European Commission (LSHM-CT-2005-018696). TFMA was supported by the B.M.B.F. through the DIFUTURE consortium of the Medical Informatics Initiative Germany (grant 01ZZ1804A) and by the European Union's Horizon 2020 Research and Innovation Programme (grant MultipleMS, EU RIA 733161). We would also like to acknowledge our project partners Catherine Billard, Caroline Bogliotti, Vanessa Bongiovanni, Laure Bricout, Camille Chabernaud, Isabelle Comte-Gervais, Florence Delteil-Pinton, Florence George, Christophe-Loic Gerard, Marie Lageat, Marie-France Leheuzey, Marie-Therese Lenormand, Marion Liebert, Emilie Longeras, Emilie Racaud, Isabelle Soares-Boucaud, Sylviane Valdois, Nadege Villiermet, and Johannes Ziegler. This study makes use of data generated by the WTCCC. A full list of the investigators who contributed to the generation of the data is available at www.wtccc.org.uk. Funding for the WTCCC project was provided by the Wellcome Trust under awards 076113 and 085475. Open Access funding enabled and organized by Projekt DEAL.; Gialluisi , A , Andlauer , T F M , Mirza-Schreiber , N , Moll , K , Becker , J , Hoffmann , P , Ludwig , K U , Czamara , D , St Pourcain , B , Honbolygo , F , Toth , D , Csepe , V , Huguet , G , Chaix , Y , Iannuzzi , S , Demonet , J-F , Morris , A P , Hulslander , J , Willcutt , E G , DeFries , J C , Olson , R K , Smith , S D , Pennington , B F , Vaessen , A , Maurer , U , Lyytinen , H , Peyrard-Janvid , M , Leppanen , P H T , Brandeis , D , Bonte , M , Stein , J F , Talcott , J B , Fauchereau , F , Wilcke , A , Kirsten , H , Mueller , B , Francks , C , Bourgeron , T , Monaco , A P , Ramus , F , Landerl , K , Kere , J , Scerri , T S , Paracchini , S , Fisher , S E , Schumacher , J , Noethen , M M , Mueller-Myhsok , B & Schulte-Koerne , G 2021 , ' Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia ' , Molecular Psychiatry , vol. 26 , pp. 3004–3017 . https://doi.org/10.1038/s41380-020-00898-xTest; http://hdl.handle.net/10138/353203Test; 2d9ac1fa-de81-4870-98b2-8d57a71adad0; 000577244500002

الإتاحة: http://hdl.handle.net/10138/353203Test

المؤلفون: Morgan, Angela T, Scerri, Thomas S, Vogel, Adam P, Reid, Christopher A, Quach, Mara, Jackson, Victoria E, McKenzie, Chaseley, Burrows, Emma L, Bennett, Mark F, Turner, Samantha J, Reilly, Sheena, Horton, Sarah E, Block, Susan, Kefalianos, Elaina, Frigerio-Domingues, Carlos

مصطلحات موضوعية: Proteomics and metabolomics, Biomedical and clinical sciences, Health sciences, Psychology, PPID gene, brain MRI, chaperone, cyclophilin-40, stuttering

العلاقة: Brain; Morgan, AT; Scerri, TS; Vogel, AP; Reid, CA; Quach, M; Jackson, VE; McKenzie, C; Burrows, EL; Bennett, MF; Turner, SJ; Reilly, S; Horton, SE; Block, S; Kefalianos, E; Frigerio-Domingues, C; Sainz, E; Rigbye, KA; Featherby, TJ; Richards, KL; Kueh, A; Herold, MJ; Corbett, MA; Gecz, J; Helbig, I; Thompson-Lake, DGY; Liégeois, FJ; Morell, RJ; Hung, A; Drayna, D; Scheffer, IE; Wright, DK; Bahlo, M; Hildebrand, MS, Stuttering associated with a pathogenic variant in the chaperone protein cyclophilin 40., Brain, 2023, 146 (12), pp. 5086-5097; http://hdl.handle.net/10072/427505Test

الإتاحة: https://doi.org/10.1093/brain/awad314Test
http://hdl.handle.net/10072/427505Test

المؤلفون: Gialluisi, Alessandro, Andlauer, Till F. M., Mirza-Schreiber, Nazanin, Moll, Kristina, Becker, Jessica, Hoffmann, Per, Ludwig, Kerstin U., Czamara, Darina, St Pourcain, Beate, Honbolygo, Ferenc, Toth, Denes, Csepe, Valeria, Huguet, Guillaume, Chaix, Yves, Iannuzzi, Stephanie, Demonet, Jean-Francois, Morris, Andrew P., Hulslander, Jacqueline, Willcutt, Erik G., DeFries, John C., Olson, Richard K., Smith, Shelley D., Pennington, Bruce F., Vaessen, Anniek, Maurer, Urs, Lyytinen, Heikki, Peyrard-Janvid, Myriam, Leppanen, Paavo H. T., Brandeis, Daniel, Bonte, Milene, Stein, John F., Talcott, Joel B., Fauchereau, Fabien, Wilcke, Arndt, Kirsten, Holger, Mueller, Bent, Francks, Clyde, Bourgeron, Thomas, Monaco, Anthony P., Ramus, Franck, Landerl, Karin, Kere, Juha, Scerri, Thomas S., Paracchini, Silvia, Fisher, Simon E., Schumacher, Johannes, Noethen, Markus M., Mueller-Myhsok, Bertram, Schulte-Koerne, Gerd

المصدر: Gialluisi , A , Andlauer , T F M , Mirza-Schreiber , N , Moll , K , Becker , J , Hoffmann , P , Ludwig , K U , Czamara , D , St Pourcain , B , Honbolygo , F , Toth , D , Csepe , V , Huguet , G , Chaix , Y , Iannuzzi , S , Demonet , J-F , Morris , A P , Hulslander , J , Willcutt , E G , DeFries , J C , Olson , R K , Smith , S D , Pennington , ....

مصطلحات موضوعية: READING-DISABILITY, INDIVIDUAL-DIFFERENCES, SUSCEPTIBILITY GENE, MOLECULAR-GENETICS, LANGUAGE, COMORBIDITY, LOCUS, AGE, SCHIZOPHRENIA, INTELLIGENCE

العلاقة: https://cris.maastrichtuniversity.nl/en/publications/8b76c901-ca76-4687-8b5d-daa0dad811ecTest

الإتاحة: https://doi.org/10.1038/s41380-020-00898-xTest
https://cris.maastrichtuniversity.nl/en/publications/8b76c901-ca76-4687-8b5d-daa0dad811ecTest

المؤلفون: Gialluisi, Alessandro, Andlauer, Till F M, Mirza-Schreiber, Nazanin, Moll, Kristina, Becker, Jessica, Hoffman, Per, Ludwig, Krestin U, Czamara, Darina, St Pourcain, Beate, Honbolygó, Ferenc, Tóth, Dénes, Csépe, Valéria, Huguet, Guillaume, Chaix, Yves, Iannuzzi, Stephanie, Demonet, Jean-Francois, Morris, Andrew P, Hulslander, Jacqueline, Willcutt, Erik G, DeFries, John C, Olson, Richard K, Smith, Shelley D, Pennington, Bruce F, Vaessen, Anniek, Maurer, Urs, Lyytinen, Heikki, Peyrard-Janvid, Myriam, Leppänen, Paavo H T, Brandeis, Daniel, Bonte, Milene, Stein, John F, Talcott, Joel B, Fauchereau, Fabien, Wilcke, Arndt, Kirsten, Holger, Müller, Bent, Francks, Clyde, Bourgeron, Thomas, Monaco, Anthony P, Ramus, Franck, Landerl, Karin, Kere, Juha, Scerri, Thomas S, Paracchini, Silvia, Fisher, Simon E, Schumacher, Johannes, Nöthen, Markus M, Müller-Myhsok, Bertram, Schulte-Körne, Gerd

المصدر: Gialluisi , A , Andlauer , T F M , Mirza-Schreiber , N , Moll , K , Becker , J , Hoffman , P , Ludwig , K U , Czamara , D , St Pourcain , B , Honbolygó , F , Tóth , D , Csépe , V , Huguet , G , Chaix , Y , Iannuzzi , S , Demonet , J-F , Morris , A P , Hulslander , J , Willcutt , E G , DeFries , J C , Olson , R K , Smith , S D , Pennington , ....

مصطلحات موضوعية: Developmental dyslexia, GWAS, Reading, Genetics, Heritability, Polygenic risk, Schizophrenia, ADHD, Bipolar disorder, Educational attaintment, Intelligence, Brain cortical thickness, Transverse temporal gyrus

وصف الملف: application/pdf

العلاقة: https://research-portal.st-andrews.ac.uk/en/researchoutput/genome-wide-association-study-reveals-new-insights-into-the-heritability-and-genetic-correlates-of-developmental-dyslexiaTest(be047dd1-4235-448f-ba0f-9041d4ebdf5e).html

الإتاحة: https://doi.org/10.1038/s41380-020-00898-xTest
https://research-portal.st-andrews.ac.uk/en/researchoutput/genome-wide-association-study-reveals-new-insights-into-the-heritability-and-genetic-correlates-of-developmental-dyslexiaTest(be047dd1-4235-448f-ba0f-9041d4ebdf5e).html
https://research-repository.st-andrews.ac.uk/bitstream/10023/20788/1/Gialluisi_2020_Genome_wide_association_MolPsych_CCBY.pdfTest

المؤلفون: Hildebrand, Joanne M, Kauppi, Maria, Majewski, Ian J, Liu, Zikou, Cox, Allison J, Miyake, Sanae, Petrie, Emma J, Silk, Michael A, Li, Zhixiu, Tanzer, Maria C, Brumatti, Gabriela, Young, Samuel N, Hall, Cathrine, Garnish, Sarah E, Corbin, Jason, Stutz, Michael D, Di Rago, Ladina, Gangatirkar, Pradnya, Josefsson, Emma C, Rigbye, Kristin, Anderton, Holly, Rickard, James A, Tripaydonis, Anne, Sheridan, Julie, Scerri, Thomas S, Jackson, Victoria E, Czabotar, Peter E, Zhang, Jian-Guo, Varghese, Leila, Allison, Cody C, Pellegrini, Marc, Tannahill, Gillian M, Hatchell, Esme C, Willson, Tracy A, Stockwell, Dina, de Graaf, Carolyn A, Collinge, Janelle, Hilton, Adrienne, Silke, Natasha, Spall, Sukhdeep K, Chau, Diep, Athanasopoulos, Vicki, Metcalf, Donald, Laxer, Ronald M, Bassuk, Alexander G, Darbro, Benjamin W, Fiatarone Singh, Maria A, Vlahovich, Nicole, Hughes, David, Kozlovskaia, Maria, Ascher, David B, Warnatz, Klaus, Venhoff, Nils, Thiel, Jens, Biben, Christine, Blum, Stefan, Reveille, John, Hildebrand, Michael S, Vinuesa, Carola G, McCombe, Pamela, Brown, Matthew A, Kile, Benjamin T, McLean, Catriona, Bahlo, Melanie, Masters, Seth L, Nakano, Hiroyasu, Ferguson, Polly J, Murphy, James M, Alexander, Warren S, Silke, John

المساهمون: UCL - SSS/DDUV - Institut de Duve, UCL - SSS/DDUV/SIGN - Cell signalling

المصدر: Nature communications, Vol. 11, no.1, p. 3150 [1-16] (2020)

مصطلحات موضوعية: Animals, Newborn, Hematopoietic Stem Cells, Hematopoietic System, Hereditary Autoinflammatory Diseases, Humans, Inflammation, Mice, Mutation, Missense, Necroptosis, Osteomyelitis, Protein Kinases

العلاقة: boreal:253587; http://hdl.handle.net/2078.1/253587Test; info:pmid/32561755; urn:EISSN:2041-1723

الإتاحة: https://doi.org/10.1038/s41467-020-16819-zTest
http://hdl.handle.net/2078.1/253587Test

المؤلفون: Hildebrand, Michael S., Jackson, Victoria E., Scerri, Thomas S., Van Reyk, Olivia, Coleman, Matthew, Braden, Ruth O., Turner, Samantha, Rigbye, Kristin A., Boys, Amber, Barton, Sarah, Webster, Richard, Fahey, Michael, Saunders, Kerryn, Parry-Fielder, Bronwyn, Paxton, Georgia, Hayman, Michael, Coman, David, Goel, Himanshu, Baxter, Anne, Ma, Alan, Davis, Noni, Reilly, Sheena, Delatycki, Martin, Liégeois, Frederique J., Connelly, Alan, Gecz, Jozef, Fisher, Simon E., Amor, David J., Scheffer, Ingrid E., Bahlo, Melanie, Morgan, Angela T.

المصدر: Hildebrand , M S , Jackson , V E , Scerri , T S , Van Reyk , O , Coleman , M , Braden , R O , Turner , S , Rigbye , K A , Boys , A , Barton , S , Webster , R , Fahey , M , Saunders , K , Parry-Fielder , B , Paxton , G , Hayman , M , Coman , D , Goel , H , Baxter , A , Ma , A , Davis , N , Reilly , S , Delatycki , M , Liégeois ....

وصف الملف: application/pdf

الإتاحة: https://doi.org/10.1212/WNL.0000000000009441Test
https://research.monash.edu/en/publications/4b80fea8-005f-4dfb-8d5e-12e0aaf3054fTest
https://researchmgt.monash.edu/ws/files/313842797/310620470_oa.pdfTest
http://www.scopus.com/inward/record.url?scp=85084786942&partnerID=8YFLogxKTest

المؤلفون: Gialluisi, Alessandro, Andlauer, Till F. M., Mirza-schreiber, Nazanin, Moll, Kristina, Becker, Jessica, Hoffmann, Per, Ludwig, Kerstin U., Czamara, Darina, St Pourcain, Beate, Brandler, William, Honbolygó, Ferenc, Tóth, Dénes, Csépe, Valéria, Huguet, Guillaume, Morris, Andrew P., Hulslander, Jacqueline, Willcutt, Erik G., Defries, John C., Olson, Richard K., Smith, Shelley D., Pennington, Bruce F., Vaessen, Anniek, Maurer, Urs, Lyytinen, Heikki, Peyrard-janvid, Myriam, Leppänen, Paavo H. T., Brandeis, Daniel, Bonte, Milene, Stein, John F., Talcott, Joel B., Fauchereau, Fabien, Wilcke, Arndt, Francks, Clyde, Bourgeron, Thomas, Monaco, Anthony P., Ramus, Franck, Landerl, Karin, Kere, Juha, Scerri, Thomas S., Paracchini, Silvia, Fisher, Simon E., Schumacher, Johannes, Nöthen, Markus M., Müller-myhsok, Bertram, Schulte-körne, Gerd

المصدر: Gialluisi , A , Andlauer , T F M , Mirza-schreiber , N , Moll , K , Becker , J , Hoffmann , P , Ludwig , K U , Czamara , D , St Pourcain , B , Brandler , W , Honbolygó , F , Tóth , D , Csépe , V , Huguet , G , Morris , A P , Hulslander , J , Willcutt , E G , Defries , J C , Olson , R K , Smith , S D , Pennington , B F , Vaessen , A , Maurer ....

وصف الملف: application/pdf

العلاقة: https://research-portal.st-andrews.ac.uk/en/researchoutput/genomewide-association-scan-identifies-new-variants-associated-with-a-cognitive-predictor-of-dyslexiaTest(d487cab7-bcaf-430d-97a1-0c917e53eb13).html

الإتاحة: https://doi.org/10.1038/s41398-019-0402-0Test
https://research-portal.st-andrews.ac.uk/en/researchoutput/genomewide-association-scan-identifies-new-variants-associated-with-a-cognitive-predictor-of-dyslexiaTest(d487cab7-bcaf-430d-97a1-0c917e53eb13).html
https://research-repository.st-andrews.ac.uk/bitstream/10023/17043/1/Gialluisi_2019_TP_Genome_wideassociation_CC.pdfTest
https://www.biorxiv.org/content/early/2018/05/02/309336Test

المؤلفون: Khan, Kamal, Zech, Michael, Morgan, Angela T., Amor, David J., Skorvanek, Matej, Khan, Tahir N., Hildebrand, Michael S., Jackson, Victoria E., Scerri, Thomas S., Coleman, Matthew, Rigbye, Kristin A., Scheffer, Ingrid E., Bahlo, Melanie, Wagner, Matias, Lam, Daniel D., Berutti, Riccardo, Havránková, Petra, Fečíková, Anna, Strom, Tim M., Han, Vladimir, Dosekova, Petra, Gdovinova, Zuzana, Laccone, Franco, Jameel, Muhammad, Mooney, Marie R., Baig, Shahid M., Jech, Robert, Davis, Erica E., Katsanis, Nicholas, Winkelmann, Juliane

المساهمون: National Institutes of Health, Grantová Agentura České Republiky, Deutsche Forschungsgemeinschaft, National Health and Medical Research Council

المصدر: Genetics in Medicine ; volume 21, issue 11, page 2532-2542 ; ISSN 1098-3600

مصطلحات موضوعية: Genetics (clinical)

الإتاحة: https://doi.org/10.1038/s41436-019-0523-0Test
http://www.nature.com/articles/s41436-019-0523-0.pdfTest
http://www.nature.com/articles/s41436-019-0523-0Test
https://api.elsevier.com/content/article/PII:S109836002101056X?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S109836002101056X?httpAccept=text/plainTest

المؤلفون: Eising, Else, Carrion-Castillo, Amaia, Vino, Arianna, Strand, Edythe A., Jakielski, Kathy J., Scerri, Thomas S., Hildebrand, Michael S., Webster, Richard, Ma, Alan, Mazoyer, Bernard, Francks, Clyde, Bahlo, Melanie, Scheffer, Ingrid E., Morgan, Angela T., Shriberg, Lawrence D., Fisher, Simon E.

المصدر: Molecular Psychiatry ; volume 24, issue 7, page 1065-1078 ; ISSN 1359-4184 1476-5578

مصطلحات موضوعية: Cellular and Molecular Neuroscience, Psychiatry and Mental health, Molecular Biology

الإتاحة: https://doi.org/10.1038/s41380-018-0020-xTest
http://www.nature.com/articles/s41380-018-0020-xTest
http://www.nature.com/articles/s41380-018-0020-x.pdfTest