المؤلفون: Janina S. Ried, Janina Jeff M., Audrey Y. Chu, Jennifer L. Bragg-Gresham, Jenny van Dongen, Jennifer E. Huffman, Tarunveer S. Ahluwalia, Gemma Cadby, Niina Eklund, Joel Eriksson, Tõnu Esko, Mary F. Feitosa, Anuj Goel, Mathias Gorski, Caroline Hayward, Nancy L. Heard-Costa, Anne U. Jackson, Eero Jokinen, Stavroula Kanoni, Kati Kristiansson, Zoltán Kutalik, Jari Lahti, Jian'an Luan, Reedik Mägi, Anubha Mahajan, Massimo Mangino, Carolina Medina-Gomez, Keri L. Monda, Ilja M. Nolte, Louis Pérusse, Inga Prokopenko, Lu Qi, Lynda M. Rose, Erika Salvi, Megan T. Smith, Harold Snieder, Alena Stančáková, Yun Ju Sung, Ioanna Tachmazidou, Alexander Teumer, Gudmar Thorleifsson, Pim van der Harst, Ryan W. Walker, Sophie R. Wang, Sarah H. Wild, Sara M. Willems, Andrew Wong, Weihua Zhang, Eva Albrecht, Alexessander Couto Alves, Stephan J. L. Bakker, Cristina Barlassina, Traci M. Bartz, John Beilby, Claire Bellis, Richard N. Bergman, Sven Bergmann, John Blangero, Matthias Blüher, Eric Boerwinkle, Lori L. Bonnycastle, Stefan R. Bornstein, Marcel Bruinenberg, Harry Campbell, Yii-Der Ida Chen, Charleston W. K. Chiang, Peter S. Chines, Francis S Collins, Fracensco Cucca, L Adrienne Cupples, Francesca D’Avila, Eco J .C. de Geus, George Dedoussis, Maria Dimitriou, Angela Döring, Johan G. Eriksson, Aliki-Eleni Farmaki, Martin Farrall, Teresa Ferreira, Krista Fischer, Nita G. Forouhi, Nele Friedrich, Anette Prior Gjesing, Nicola Glorioso, Mariaelisa Graff, Harald Grallert, Niels Grarup, Jürgen Gräßler, Jagvir Grewal, Anders Hamsten, Marie Neergaard Harder, Catharina A. Hartman, Maija Hassinen, Nicholas Hastie, Andrew Tym Hattersley, Aki S. Havulinna, Markku Heliövaara, Hans Hillege, Albert Hofman, Oddgeir Holmen, Georg Homuth, Jouke-Jan Hottenga, Jennie Hui, Lise Lotte Husemoen, Pirro G. Hysi, Aaron Isaacs, Till Ittermann, Shapour Jalilzadeh, Alan L. James, Torben Jørgensen, Pekka Jousilahti, Antti Jula, Johanne Marie Justesen, Anne E. Justice, Mika Kähönen, Maria Karaleftheri, Kay Tee Khaw, Sirkka M. Keinanen-Kiukaanniemi, Leena Kinnunen, Paul B. Knekt, Heikki A. Koistinen, Ivana Kolcic, Ishminder K. Kooner, Seppo Koskinen, Peter Kovacs, Theodosios Kyriakou, Tomi Laitinen, Claudia Langenberg, Alexandra M. Lewin, Peter Lichtner, Cecilia M. Lindgren, Jaana Lindström, Allan Linneberg, Roberto Lorbeer, Mattias Lorentzon, Robert Luben, Valeriya Lyssenko, Satu Männistö, Paolo Manunta, Irene Mateo Leach, Wendy L. McArdle, Barbara Mcknight, Karen L. Mohlke, Evelin Mihailov, Lili Milani, Rebecca Mills, May E. Montasser, Andrew P. Morris, Gabriele Müller, Arthur W. Musk, Narisu Narisu, Ken K. Ong, Ben A. Oostra, Clive Osmond, Aarno Palotie, James S. Pankow, Lavinia Paternoster, Brenda W. Penninx, Irene Pichler, Maria G. Pilia, Ozren Polašek, Peter P. Pramstaller, Olli T Raitakari, Tuomo Rankinen, D. C. Rao, Nigel W. Rayner, Rasmus Ribel-Madsen, Treva K. Rice, Marcus Richards, Paul M. Ridker, Fernando Rivadeneira, Kathy A. Ryan, Serena Sanna, Mark A. Sarzynski, Salome Scholtens, Robert A. Scott, Sylvain Sebert, Lorraine Southam, Thomas Hempel Sparsø, Valgerdur Steinthorsdottir, Kathleen Stirrups, Ronald P. Stolk, Konstantin Strauch, Heather M. Stringham, Morris A. Swertz, Amy J. Swift, Anke Tönjes, Emmanouil Tsafantakis, Peter J. van der Most, Jana V. Van Vliet-Ostaptchouk, Liesbeth Vandenput, Erkki Vartiainen, Cristina Venturini, Niek Verweij, Jorma S. Viikari, Veronique Vitart, Marie-Claude Vohl, Judith M. Vonk, Gérard Waeber, Elisabeth Widén, Gonneke Willemsen, Tom Wilsgaard, Thomas W. Winkler, Alan F. Wright, Laura M. Yerges-Armstrong, Jing Hua Zhao, M. Carola Zillikens, Dorret I. Boomsma, Claude Bouchard, John C. Chambers, Daniel I. Chasman, Daniele Cusi, Ron T. Gansevoort, Christian Gieger, Torben Hansen, Andrew A. Hicks, Frank Hu, Kristian Hveem, Marjo-Riitta Jarvelin, Eero Kajantie, Jaspal S. Kooner, Diana Kuh, Johanna Kuusisto, Markku Laakso, Timo A. Lakka, Terho Lehtimäki, Andres Metspalu, Inger Njølstad, Claes Ohlsson, Albertine J. Oldehinkel, Lyle J. Palmer, Oluf Pedersen, Markus Perola, Annette Peters, Bruce M. Psaty, Hannu Puolijoki, Rainer Rauramaa, Igor Rudan, Veikko Salomaa, Peter E. H. Schwarz, Alan R. Shudiner, Jan H. Smit, Thorkild I. A. Sørensen, Timothy D. Spector, Kari Stefansson, Michael Stumvoll, Angelo Tremblay, Jaakko Tuomilehto, André G. Uitterlinden, Matti Uusitupa, Uwe Völker, Peter Vollenweider, Nicholas J. Wareham, Hugh Watkins, James F. Wilson, Eleftheria Zeggini, Goncalo R. Abecasis, Michael Boehnke, Ingrid B. Borecki, Panos Deloukas, Cornelia M. van Duijn, Caroline Fox, Leif C. Groop, Iris M. Heid, David J. Hunter, Robert C. Kaplan, Mark I. McCarthy, Kari E. North, Jeffrey R. O'Connell, David Schlessinger, Unnur Thorsteinsdottir, David P. Strachan, Timothy Frayling, Joel N. Hirschhorn, Martina Müller-Nurasyid, Ruth J. F. Loos

المصدر: Nature Communications, Vol 7, Iss 1, Pp 1-11 (2016)

مصطلحات موضوعية: Science

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2041-1723

URL الوصول: https://doaj.org/article/f36bd59969d44358bd7caf32e2240b93

المؤلفون: Cecilia M. Lindgren, Iris M. Heid, Joshua C. Randall, Claudia Lamina, Valgerdur Steinthorsdottir, Lu Qi, Elizabeth K. Speliotes, Gudmar Thorleifsson, Cristen J. Willer, Blanca M. Herrera, Anne U. Jackson, Noha Lim, Paul Scheet, Nicole Soranzo, Najaf Amin, Yurii S. Aulchenko, John C. Chambers, Alexander Drong, Jian'an Luan, Helen N. Lyon, Fernando Rivadeneira, Serena Sanna, Nicholas J. Timpson, M. Carola Zillikens, Jing Hua Zhao, Peter Almgren, Stefania Bandinelli, Amanda J. Bennett, Richard N. Bergman, Lori L. Bonnycastle, Suzannah J. Bumpstead, Stephen J. Chanock, Lynn Cherkas, Peter Chines, Lachlan Coin, Cyrus Cooper, Gabriel Crawford, Angela Doering, Anna Dominiczak, Alex S. F. Doney, Shah Ebrahim, Paul Elliott, Michael R. Erdos, Karol Estrada, Luigi Ferrucci, Guido Fischer, Nita G. Forouhi, Christian Gieger, Harald Grallert, Christopher J. Groves, Scott Grundy, Candace Guiducci, David Hadley, Anders Hamsten, Aki S. Havulinna, Albert Hofman, Rolf Holle, John W. Holloway, Thomas Illig, Bo Isomaa, Leonie C. Jacobs, Karen Jameson, Pekka Jousilahti, Fredrik Karpe, Johanna Kuusisto, Jaana Laitinen, G. Mark Lathrop, Debbie A. Lawlor, Massimo Mangino, Wendy L. McArdle, Thomas Meitinger, Mario A. Morken, Andrew P. Morris, Patricia Munroe, Narisu Narisu, Anna Nordström, Peter Nordström, Ben A. Oostra, Colin N. A. Palmer, Felicity Payne, John F. Peden, Inga Prokopenko, Frida Renström, Aimo Ruokonen, Veikko Salomaa, Manjinder S. Sandhu, Laura J. Scott, Angelo Scuteri, Kaisa Silander, Kijoung Song, Xin Yuan, Heather M. Stringham, Amy J. Swift, Tiinamaija Tuomi, Manuela Uda, Peter Vollenweider, Gerard Waeber, Chris Wallace, G. Bragi Walters, Michael N. Weedon, Jacqueline C. M. Witteman, Cuilin Zhang, Weihua Zhang, Mark J. Caulfield, Francis S. Collins, George Davey Smith, Ian N. M. Day, Paul W. Franks, Andrew T. Hattersley, Frank B. Hu, Marjo-Riitta Jarvelin, Augustine Kong, Jaspal S. Kooner, Markku Laakso, Edward Lakatta, Vincent Mooser, Andrew D. Morris, Leena Peltonen, Nilesh J. Samani, Timothy D. Spector, David P. Strachan, Toshiko Tanaka, Jaakko Tuomilehto, André G. Uitterlinden, Cornelia M. van Duijn, Nicholas J. Wareham, Hugh Watkins for the PROCARDIS consortia, Dawn M. Waterworth, Michael Boehnke, Panos Deloukas, Leif Groop, David J. Hunter, Unnur Thorsteinsdottir, David Schlessinger, H.-Erich Wichmann, Timothy M. Frayling, Gonçalo R. Abecasis, Joel N. Hirschhorn, Ruth J. F. Loos, Kari Stefansson, Karen L. Mohlke, Inês Barroso, Mark I. McCarthy for the GIANT consortium

المصدر: PLoS Genetics, Vol 5, Iss 7 (2009)

مصطلحات موضوعية: Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://europepmc.org/articles/PMC2722420; https://doaj.org/toc/1553-7390; https://doaj.org/toc/1553-7404

URL الوصول: https://doaj.org/article/e44f8db0afa249ddb81fb6414958ef65

المؤلفون: Inês Barroso, Gail Davies, H.-Erich Wichmann, Bjarke Feenstra, Peter Vollenweider, Nicholas J. Timpson, Alan F. Wright, Frank Geller, Gérard Waeber, John M. Starr, Benjamin M. Neale, George Davey Smith, Tõnu Esko, Ruth J. F. Loos, Andrew A. Hicks, Pedro Marques-Vidal, Dorret I. Boomsma, Harry Campbell, Zoltán Kutalik, David M. Evans, Scott D. Gordon, Eva Albrecht, Peter P. Pramstaller, Leena Peltonen, Jing Hua Zhao, Lavinia Paternoster, Thomas Hansen, Massimo Mangino, Fazil Aliev, Beate St Pourcain, Panos Deloukas, Heather A. Boyd, Guillaume Paré, Marco P. Boks, Monique M.B. Breteler, Jouke-Jan Hottenga, Xin Li, Kari Stefansson, Ian J. Deary, Jari Lahti, Inga Prokopenko, Nicholas Eriksson, Lili Milani, Nicholas J. Wareham, Jordan W. Smoller, Norman Klopp, Lynn Cherkas, Reedik Mägi, Margaret J. Wright, Peter Kraft, Jacques S. Beckmann, Brenda W.J.H. Penninx, Gabriel Cuellar-Partida, André G. Uitterlinden, Fernando Rivadeneira, Wendy L. McArdle, Johan G. Eriksson, Jiali Han, Jennifer E. Huffman, Andres Metspalu, J.M. Vink, Frank J. A. van Rooij, Christian Gieger, M. Arfan Ikram, Cecilia M. Lindgren, Aarno Palotie, Daniel I. Chasman, Joyce Y. Tung, Liang-Dar Hwang, David A. Hinds, Elisabeth Widen, Caroline Hayward, Michelle Luciano, Johannes H. Smit, Gonneke Willemsen, Dale R. Nyholt, Carolina Medina-Gomez, Nicole M. Warrington, Teemu Palviainen, Stacy Steinberg, Kay-Tee Khaw, Kevin S. O’Connell, Bettina Konte, Gudmar Thorleifsson, Eco J. C. de Geus, John P. Kemp, Mads Melbye, Mark I. McCarthy, Sarah E. Medland, Jaakko Kaprio, Cameron D. Palmer, Joel N. Hirschhorn, Ina Giegling, Scott Melville, Thomas Werge, Nicole Soranzo, Sigurdur H. Magnusson, Maris Teder-Laving, Hreinn Stefansson, Kauko Heikkilä, Cornelia M. van Duijn, David L. Duffy, Samuli Ripatti, Igor Rudan, Annette M. Hartmann, Ole A. Andreassen, Mari Nelis, Ozren Polasek, Vincent Mooser, Mousheng Xu, Eero Vuoksimaa, Katri Räikkönen, Nicholas G. Martin, Dan Rujescu, Tim D. Spector, Dawn M. Waterworth, Danielle M. Dick, Roel A. Ophoff

المساهمون: Epidemiology, Internal Medicine, Psychiatry, Biological Psychology, APH - Mental Health, APH - Methodology, APH - Health Behaviors & Chronic Diseases, APH - Personalized Medicine, Epidemiology and Data Science, Amsterdam Neuroscience - Complex Trait Genetics, Amsterdam Neuroscience - Mood, Anxiety, Psychosis, Stress & Sleep, Pediatric surgery, APH - Digital Health

المصدر: Cuellar-Partida, G, Tung, J Y, Eriksson, N, Albrecht, E, Aliev, F, Andreassen, O A, Barroso, I, Beckmann, J S, Boks, M P, Boomsma, D I, Boyd, H A, Breteler, M M B, Campbell, H, Chasman, D I, Cherkas, L F, Davies, G, de Geus, E J C, Deary, I J, Deloukas, P, Dick, D M, Duffy, D L, Eriksson, J G, Esko, T, Feenstra, B, Geller, F, Gieger, C, Giegling, I, Gordon, S D, Han, J, Hansen, T F, Hartmann, A M, Hayward, C, Heikkila, K, Hicks, A A, Hirschhorn, J N, Hottenga, J-J, Huffman, J E, Hwang, L-D, Ikram, M A, Kaprio, J, Kemp, J P, Khaw, K-T, Klopp, N, Konte, B, Kutalik, Z, Lahti, J, Li, X, Loos, R J F, Luciano, M, Magnusson, S H, Mangino, M, Marques-Vidal, P, Martin, N G, McArdle, W L, McCarthy, M I, Medina-Gomez, C, Melbye, M, Melville, S A, Metspalu, A, Milani, L, Mooser, V, Nelis, M, Nyholt, D R, O'Connell, K S, Ophoff, R A, Palmer, C, Palotie, A, Palviainen, T, Pare, G, Paternoster, L, Peltonen, L, Penninx, B W J H, Polasek, O, Pramstaller, P P, Prokopenko, I, Raikkonen, K, Ripatti, S, Rivadeneira, F, Rudan, I, Rujescu, D, Smit, J H, Smith, G D, Smoller, J W, Soranzo, N, Spector, T D, Pourcain, B S, Starr, J M, Stefansson, H, Steinberg, S, Teder-Laving, M, Thorleifsson, G, Stefansson, K, Timpson, N J, Uitterlinden, A G, van Duijn, C M, van Rooij, F J A, Vink, J M, Vollenweider, P, Vuoksimaa, E, Waeber, G, Wareham, N J, Warrington, N, Waterworth, D, Werge, T, Wichmann, H-E, Widen, E, Willemsen, G, Wright, A F, Wright, M J, Xu, M, Zhao, J H, Kraft, P, Hinds, D A, Lindgren, C M, Magi, R, Neale, B M, Evans, D M & Medland, S E 2021, ' Genome-wide association study identifies 48 common genetic variants associated with handedness ', Nature Human Behaviour, vol. 5, pp. 59-70 . https://doi.org/10.1038/s41562-020-00956-y
Partida, G C, Tung, J Y, Eriksson, N, Albrecht, E, Aliev, F, Andreassen, O A, Barroso, I, Beckmann, J S, Boks, M P, Boomsma, D I, Boyd, H A, Breteler, M MB, Campbell, H, Chasman, D I, Cherkas, L F, Davies, G, de Geus, E JC, Deary, I J, Deloukas, P, Dick, D M, Duffy, D L, Eriksson, J G, Esko, T, Feenstra, B, Geller, F, Gieger, C, Giegling, I, Gordon, S D, Han, J, Hansen, T F, Hartmann, A M, Hayward, C, Heikkilä, K, Hicks, A A, Hirschhorn, J N, Hottenga, J-J, Huffman, J E, Hwang, L-D, Ikram, M A, Kaprio, J, Kemp, J P, Khaw, K-T, Klopp, N, Konte, B, Kutalik, Z, Lahti, J, Li, X, Loos, R JF, Luciano, M, Magnusson, S H, Mangino, M, Marques-Vidal, P, Martin, N G, McArdle, W L, McCarthy, M I, Medina-Gomez, C, Melbye, M, Melville, S A, Metspalu, A, Milani, L, Mooser, V, Nelis, M, Nyholt, D R, O’Connell, K S, Ophoff, R A, Palmer, C, Palotie, A, Palviainen, T, Pare, G, Paternoster, L, Peltonen, L, Penninx, B WJH, Polasek, O, Pramstaller, P P, Prokopenko, I, Raikkonen, K, Ripatti, S, Rivadeneira, F, Rudan, I, Rujescu, D, Smit, J H, Smith, G D, Smoller, J W, Soranzo, N, Spector, T D, St Pourcain, B, Starr, J M, Stefánsson, H, Steinberg, S, Teder-Laving, M, Thorleifsson, G, Stefansson, K, Timpson, N J, Uitterlinden, A G, van Duijn, C M, van Rooij, F JA, Vink, J M, Vollenweider, P, Vuoksimaa, E, Waeber, G, Wareham, N J, Warrington, N, Waterworth, D, Werge, T, Wichmann, H-E, Widen, E, Willemsen, G, Wright, A F, Wright, M J, Xu, M, Zhao, J H, Kraft, P, Hinds, D A, Lindgren, C M, Magi, R, Neale, B M, Evans, D M & Medland, S E 2020, ' Genome-wide association study identifies 48 common genetic variants associated with handedness ', Nature Human Behaviour . https://doi.org/10.1038/s41562-020-00956-y
Cuellar-Partida, G, Tung, J Y, Eriksson, N, Albrecht, E, Aliev, F, Andreassen, O A, Barroso, I, Beckmann, J S, Boks, M P, Boomsma, D I, Boyd, H A, Breteler, M M B, Campbell, H, Chasman, D I, Cherkas, L F, Davies, G, de Geus, E J C, Deary, I J, Deloukas, P, Dick, D M, Duffy, D L, Eriksson, J G, Esko, T, Feenstra, B, Geller, F, Gieger, C, Giegling, I, Gordon, S D, Han, J, Hansen, T F, Hartmann, A M, Hayward, C, Heikkilä, K, Hicks, A A, Hirschhorn, J N, Hottenga, J J, Huffman, J E, Hwang, L D, Ikram, M A, Kaprio, J, Kemp, J P, Khaw, K T, Klopp, N, Konte, B, Kutalik, Z, Lahti, J, Li, X, Loos, R J F, Luciano, M, Magnusson, S H, Mangino, M, Marques-Vidal, P, Martin, N G, McArdle, W L, McCarthy, M I, Medina-Gomez, C, Melbye, M, Melville, S A, Metspalu, A, Milani, L, Mooser, V, Nelis, M, Nyholt, D R, O’Connell, K S, Ophoff, R A, Palmer, C, Palotie, A, Palviainen, T, Pare, G, Paternoster, L, Peltonen, L, Penninx, B W J H, Polasek, O, Pramstaller, P P, Prokopenko, I, Raikkonen, K, Ripatti, S, Rivadeneira, F, Rudan, I, Rujescu, D, Smit, J H, Smith, G D, Smoller, J W, Soranzo, N, Spector, T D, Pourcain, B S, Starr, J M, Stefánsson, H, Steinberg, S, Teder-Laving, M, Thorleifsson, G, Stefánsson, K, Timpson, N J, Uitterlinden, A G, van Duijn, C M, van Rooij, F J A, Vink, J M, Vollenweider, P, Vuoksimaa, E, Waeber, G, Wareham, N J, Warrington, N, Waterworth, D, Werge, T, Wichmann, H E, Widen, E, Willemsen, G, Wright, A F, Wright, M J, Xu, M, Zhao, J H, Kraft, P, Hinds, D A, Lindgren, C M, Mägi, R, Neale, B M, Evans, D M & Medland, S E 2021, ' Genome-wide association study identifies 48 common genetic variants associated with handedness ', Nature Human Behaviour, vol. 5, no. 1, pp. 59-70 . https://doi.org/10.1038/s41562-020-00956-y
Nature Human Behaviour, 5, 1, pp. 59-70
Nature Human Behaviour, 5(1), 59-70. Nature Publishing Group
Nat Hum Behav
Nature Human Behaviour, 5(1), 59-70. Springer Nature
Nature Human Behaviour
Nat. Hum. Behav. 5, 59–70 (2021)
Nature Human Behaviour, 5, 59-70
Nature human behaviour 5(1), 59-70 (2021). doi:10.1038/s41562-020-00956-y
Cuellar-Partida, G, Deloukas, P, Kemp, J P, McArdle, W L, Paternoster, L, Davey Smith, G, Timpson, N J, Medland, S E & al., E 2020, ' Genome-wide association study identifies 48 common genetic variants associated with handedness ', Nature Human Behaviour, vol. 5, pp. 59–70 . https://doi.org/10.1038/s41562-020-00956-y

مصطلحات موضوعية: Male, Netherlands Twin Register (NTR), Linkage disequilibrium, Genome-wide association study, LANGUAGE DOMINANCE, Functional Laterality, Linkage Disequilibrium, Behavioral Neuroscience, 0302 clinical medicine, ddc:150, Gene Frequency, SCHIZOPHRENIA, Genetics, 0303 health sciences, Middle Aged, genetics [Genetic Variation], genetics [Functional Laterality], Schizophrenia, ASYMMETRY, genetics [Polymorphism, Single Nucleotide], Female, Adult, Social Psychology, LATERALIZATION, Experimental and Cognitive Psychology, genetics [Genetic Loci], Biology, Quantitative trait locus, Genetic correlation, Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, LINKAGE ANALYSIS, METAANALYSIS, MICROTUBULE, AUTISM, ORIGINS, SCREEN, Quantitative Trait, Heritable, Sex Factors, Genetic linkage, medicine, Humans, Bipolar disorder, 030304 developmental biology, Genetic association study, Aged, Genetic Variation, medicine.disease, Genetic Loci, Autism, genetics [Gene Frequency], Developmental Psychopathology, 030217 neurology & neurosurgery, Neuroscience, Genome-Wide Association Study

وصف الملف: application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document; application/vnd.openxmlformats-officedocument.spreadsheetml.sheet

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::986a1504a38fc87e9588fa425872923b
https://curis.ku.dk/portal/da/publications/genomewide-association-study-identifies-48-common-genetic-variants-associated-with-handedness(3aa476e7-e13d-48f1-af0d-544a2ee787fd).html

المؤلفون: Giuseppe Matullo, John R. B. Perry, Meena Kumari, Gemma C Sharp, Tomáš Paus, E. Giralt-Steinhauer, Marta E. Alarcón-Riquelme, Koen F. Dekkers, F. Gagnon, Simonetta Guarrera, Cilla Söderhäll, Rosie M. Walker, Therese Tillin, M. Smarts, Juan E. Castillo-Fernandez, John M. Starr, Jean Shin, Dan Mason, T Esko, Christopher Shaw, Hannah R Elliott, Manon Bernard, David L. Corcoran, Yvonne Awaloff, Ahmad Al Khleifat, Bert Brunekreef, Clara Viberti, John Wright, Gibran Hemani, Kathryn L. Evans, Camilla Schmidt Morgen, Jouke J. Hottenga, Susan M. Ring, Terrie E. Moffitt, Silva Kasela, C. Hale, Idil Yet, Katri Räikkönen, René Luijk, Vanessa Schmoll, Kimberley Burrows, Annelot M. Dekker, D. VanHeemst, Jordana T. Bell, Jordi Jimenez-Conde, Carlotta Sacerdote, Salvatore Panico, Lili Milani, Nabila Kazmi, Torben Hansen, Aleksey Shatunov, J L Min, Richa Gupta, Henning Tiemeier, Grant W. Montgomery, Vincent W. V. Jaddoe, E.J.C. de Geus, Fernando Rivadeneira, Debbie A Lawlor, Carol A. Wang, Toni-Kim Clarke, Susanne Lucae, Nicholas J. Wareham, Jordi Sunyer, Felix R. Day, C. Soriano-Tarraga, Christoph Bock, Juan R. González, D. Aissi, J.B. van Meurs, Ian J. Deary, Ken K. Ong, Louise Arseneault, Eilis Hannon, Bastiaan T. Heijmans, Philip E. Melton, Ashok Kumar, Pierre-Emmanuel Morange, Zdenka Pausova, T.D. Spector, Nicholas G. Martin, J. Mill, Francesc Català-Moll, Alun D. Hughes, Leonard C. Schalkwyk, Giovanni Cugliari, Carlos Ruiz-Arenas, Elena Carnero-Montoro, Marine Germain, Yanni Zeng, Andrew M. McIntosh, Riccardo E. Marioni, Wilfried Karmaus, Ikram, Gonneke Willemsen, Miina Ollikainen, Karen M Ho, Craig E. Pennell, F.I. Rezwan, Darina Czamara, Ramona A. J. Zwamborn, Dorret I. Boomsma, Wendy L. McArdle, J. M. van Dongen, Guillermo Barturen, Matthew Suderman, Richie Poulton, Daniel Lawson, A. Metspalu, David-Alexandre Trégouët, Marian Beekman, Andrew D. Bretherick, Johanna Klughammer, Hongmei Zhang, M.H. van IJzendoorn, Nish Chaturvedi, Jari Lahti, Karen Sugden, Jan H. Veldink, Mariona Bustamante, Avshalom Caspi, Pooja R. Mandaviya, Judith M. Vonk, Tom R. Gaunt, Cheng-Jian Xu, John W. Holloway, Tian Lin, Tom G. Richardson, Caroline L Relton, Naomi R. Wray, Allan F. McRae, George Davey Smith, Erik Melén, Valentina Iotchkova, Ellen A. Nohr, Jaakko Kaprio, Göran Pershagen, Elisabeth B. Binder, A. al Chalabi, T.J. Gorrie-Stone, K. van Eijk, Gerard H. Koppelman, M. Lerro, Alexia Cardona, Sailalitha Bollepalli, P.E. Slagboom, Thorkild I. A. Sørensen, André G. Uitterlinden, Jaume Roquer, Peter M. Visscher, Janine F. Felix, Martin Kerick, Gail Davies, Rae-Chi Huang, Alfredo Iacoangeli, Alison D. Murray

المساهمون: Helsinki Institute of Life Science HiLIFE, Institute for Molecular Medicine Finland, Epigenetics of Complex Diseases and Traits, Department of Public Health, Department of Psychology and Logopedics, Biological Psychology, APH - Mental Health, APH - Personalized Medicine, APH - Health Behaviors & Chronic Diseases, APH - Methodology, Groningen Research Institute for Asthma and COPD (GRIAC), Bordeaux population health (BPH), Université de Bordeaux (UB)-Institut de Santé Publique, d'Épidémiologie et de Développement (ISPED)-Institut National de la Santé et de la Recherche Médicale (INSERM), Centre recherche en CardioVasculaire et Nutrition = Center for CardioVascular and Nutrition research (C2VN), Aix Marseille Université (AMU)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), Epidemiology, Internal Medicine, Pediatrics, Child and Adolescent Psychiatry / Psychology, Clinical Child and Family Studies

المصدر: Nature Genetics
Digital.CSIC. Repositorio Institucional del CSIC
instname
Nature genetics, 53(9), 1311-1321. Nature Publishing Group
Nature Genetics, 53, 1311-1321. Nature Publishing Group
Nature Genetics, Nature Publishing Group, 2021, 53 (9), pp.1311-1321. ⟨10.1038/s41588-021-00923-x⟩
et al., Min, J L, Hemani, G, Hannon, E, dekkers, K, Castillo-Fernandez, J, Luijk, R, Carnero-Montoro, E, Lawson, D J, Burrows, K, Suderman, M J, Bretherick, A D, Richardson, T G, Klughammer, J, Lochkova, V, Sharp, G C, Al Khleifat, A, Shatunov, A, Lacoangeli, A, Mcardle, W L, Ho, K M, Kumar, A, Soderhall, C, Soriano-Tárraga, C, Giralt-Steinhauer, E, Kazmi, N, Mason, D, McRae, A F, Corcoran, D L, Elliott, H R, Ring, S M, Lawlor, D A, Sørensen, T I A, Davey Smith, G, Gaunt, T R & Relton, C L 2021, ' Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation ', Nature Genetics, vol. 53, no. 9, pp. 1311-1321 . https://doi.org/10.1038/s41588-021-00923-x
Min, J L, Hemani, G, Hannon, E, Dekkers, K F, Castillo-Fernandez, J, Luijk, R, Carnero-Montoro, E, Lawson, D J, Burrows, K, Suderman, M, Bretherick, A D, Richardson, T G, Klughammer, J, Iotchkova, V, Sharp, G, Al Khleifat, A, Shatunov, A, Iacoangeli, A, McArdle, W L, Ho, K M, Kumar, A, Söderhäll, C, Soriano-Tárraga, C, Giralt-Steinhauer, E, Kazmi, N, Mason, D, McRae, A F, Corcoran, D L, Sugden, K, Kasela, S, Cardona, A, Day, F R, Cugliari, G, Viberti, C, Guarrera, S, Lerro, M, Gupta, R, Bollepalli, S, Mandaviya, P, Zeng, Y, Clarke, T K, Walker, R M, Schmoll, V, Czamara, D, Ruiz-Arenas, C, Elliott, H R, Nohr, E A, Sørensen, T I A, Hansen, T, Morgen, C S & BIOS Consortium 2021, ' Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation ', Nature Genetics, vol. 53, no. 9, pp. 1311-1321 . https://doi.org/10.1038/s41588-021-00923-x
Min, J L, van Dongen, J, Hottenga, J J, Willemsen, G, de Geus, E J C, Boomsma, D I, Relton, C L & BIOS Consortium 2021, ' Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation ', Nature genetics, vol. 53, no. 9, pp. 1311-1321 . https://doi.org/10.1038/s41588-021-00923-x
Min, J L, Hemani, G, Hannon, E, Dekkers, K F, Castillo-Fernandez, J, Luijk, R, Carnero-Montoro, E, Lawson, D J, Burrows, K, Suderman, M, Bretherick, A D, Richardson, T G, Klughammer, J, Iotchkova, V, Sharp, G, Al Khleifat, A, Shatunov, A, Iacoangeli, A, McArdle, W L, Ho, K M, Kumar, A, Söderhäll, C, Soriano-Tárraga, C, Giralt-Steinhauer, E, Kazmi, N, Mason, D, McRae, A F, Corcoran, D L, Sugden, K, Kasela, S, Cardona, A, Day, F R, Cugliari, G, Viberti, C, Guarrera, S, Lerro, M, Gupta, R, Bollepalli, S, Mandaviya, P, Zeng, Y, Clarke, T K, Walker, R M, Schmoll, V, Czamara, D, Ruiz-Arenas, C, Rezwan, F I, Marioni, R E, Nohr, E A, Sørensen, T I A, Morgen, C S & BIOS Consortium 2021, ' Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation ', Nature Genetics, vol. 53, no. 9, pp. 1311-1321 . https://doi.org/10.1038/s41588-021-00923-x
Nature Genetics, 53(9), 1311-1321. NATURE PORTFOLIO
Nature Genetics, 2021, 53 (9), pp.1311-1321. ⟨10.1038/s41588-021-00923-x⟩
Nature Genetics, 53(9), 1311-1321. Nature Publishing Group

مصطلحات موضوعية: Multifactorial Inheritance, ADN, Quantitative Trait Loci, Genome-wide association study, VARIANTS, Biology, Quantitative trait locus, Polymorphism, Single Nucleotide, LINKS, Epigenesis, Genetic, 03 medical and health sciences, 0302 clinical medicine, Quantitative Trait, Heritable, Genetic variation, Genetics, WIDE ASSOCIATION, GWAS, Humans, Genetic Predisposition to Disease, Genotip, METAANALYSIS, EQTL, 030304 developmental biology, Epigenesis, SNP ANALYSIS, 0303 health sciences, COMPLEX, dNaM, Chromosome Mapping, DNA, DNA Methylation, Phenotype, Genetic architecture, MODEL, Fenotip, Gene Expression Regulation, DNA methylation, MENDELIAN RANDOMIZATION, [SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie, 3111 Biomedicine, Metilació, Transcriptome, Genètica, 030217 neurology & neurosurgery, Genome-Wide Association Study

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URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9f18b02f6a59803fa5fa39c1daf1e4d
https://pubmed.ncbi.nlm.nih.gov/34493871

المؤلفون: Carol A. Wang, Simonetta Guarrera, Avshalom Caspi, Eilis Hannon, Marta E. Alarcón-Riquelme, P. Eline Slagboom, Pooja R. Mandaviya, Koen F. Dekkers, Cheng-Jian Xu, Jari Lahti, Juan E. Castillo-Fernandez, Dan Mason, Dylan Aïssi, Jan H. Veldink, Mariona Bustamante, Melissa C. Smart, Guillermo Barturen, Zdenka Pausova, Jenny van Dongen, Jordi Jimenez-Conde, Craig E. Pennell, Gibran Hemani, Tom R. Gaunt, Camilla Schmidt Morgen, Ken K. Ong, Toni-Kim Clarke, Alexia Cardona, Susanne Lucae, René Luijk, T.J. Gorrie-Stone, Phillip E. Melton, Thorkild I. A. Sørensen, André G. Uitterlinden, Jordana T. Bell, Jouke-Jan Hottenga, Meena Kumari, Francesc Català-Moll, Jonathan Mill, Tõnu Esko, Sailalitha Bollepalli, Dorret I. Boomsma, Torben Hansen, Hongmei Zhang, Yanni Zeng, John Wright, Wilfried Karmaus, Martin Kerick, Carolina Soriano-Tárraga, Jaakko Kaprio, Miina Ollikainen, Eco J. C. de Geus, Jordi Sunyer, Therese Tillin, Juan R. González, Yvonne Awaloff, Faisal I. Rezwan, Karen Sugden, Nicholas G. Martin, Karen M Ho, Andres Metspalu, Marine Germain, Kristel R. van Eijk, Ramona A. J. Zwamborn, George Davey Smith, Judith M. Vonk, Tian Lin, Henning Tiemeier, Grant W. Montgomery, Naomi R. Wray, Rae-Chi Huang, Alfredo Iacoangeli, Wendy L. McArdle, Jean Shin, Michael Lerro, Darina Czamara, Valentina Iotchkova, David-Alexandre Trégouët, Johanna Klughammer, Elena Carnero-Montoro, Pierre-Emmanuel Morange, Andrew M. McIntosh, Gemma C Sharp, Alun D. Hughes, Carlos Ruiz-Arenas, John M. Starr, Riccardo E. Marioni, Peter M. Visscher, Nabila Kazmi, Ian J. Deary, Kathryn L. Evans, Terrie E. Moffitt, Janine F. Felix, Tomáš Paus, Ashok Kumar, Jaume Roquer, Christopher Shaw, Hannah R Elliott, Susan M. Ring, Nish Chaturvedi, Giovanni Cugliari, Ahmad Al Khleifat, Joyce B. J. van Meurs, Kimberley Burrows, Bert Brunekreef, Debbie A Lawlor, Clara Viberti, Louise Arseneault, Silva Kasela, Cilla Söderhäll, Idil Yet, Manon Bernard, Christoph Bock, Vincent W. V. Jaddoe, Felix R. Day, Diana van Heemst, Alison D. Murray, Nicholas J. Wareham, Giuseppe Matullo, John R. B. Perry, Gerard H. Koppelman, M. Arfan Ikram, Ammar Al Chalabi, Gonneke Willemsen, Richie Poulton, Daniel Lawson, Andrew D. Bretherick, Vanessa Schmoll, Carlotta Sacerdote, Annelot M. Dekker, Lili Milani, Fernando Rivadeneira, Erik Melén, John W. Holloway, Gareth E. Davies, Tom G. Richardson, Caroline L Relton, Josine L. Min, Göran Pershagen, Elisabeth B. Binder, Marian Beekman, Chris Haley, Richa Gupta, Bastiaan T. Heijmans, Ellen A. Nohr, Allan F. McRae, Matthew Suderman, Rosie M. Walker, David L. Corcoran, Katri Räikkönen, Marinus H. van IJzendoorn, Eva Giralt-Steinhauer, Leonard C. Schalkwyk, Aleksey Shatunov, Tim D. Spector

مصطلحات موضوعية: Genetics, Regulation of gene expression, 0303 health sciences, Natural selection, dNaM, Biology, Genetic architecture, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, chemistry, Genetic variation, DNA methylation, Trait, 030217 neurology & neurosurgery, DNA, 030304 developmental biology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::b75e7cd42d80892eb39c80d045871ad8
https://doi.org/10.1101/2020.09.01.20180406

المؤلفون: Christian Gieger, Teemu Palviainen, Bettina Konte, Peter P. Pramstaller, Aarno Palotie, Elisabeth Widen, Monique M.B. Breteler, Caroline Hayward, Xin Li, Tim D. Spector, Jing Hua Zhao, John M. Starr, David M. Evans, Nicholas G. Martin, Wendy L. McArdle, Nicole Soranzo, Mads Melbye, Peter Kraft, André G. Uitterlinden, Beate St Pourcain, Massimo Mangino, Daniel I. Chasman, Jacques S. Beckmann, Gabriel Cuellar Partida, George Davey Smith, Cecilia M. Lindgren, Johan G. Eriksson, Alan F. Wright, Kauko Heikkilä, Eva Albrecht, Gudmar Thorleifsson, Mari Nelis, Nicholas Eriksson, Dawn M. Waterworth, Leena Peltonen, Frank J. A. van Rooij, Jari Lahti, Maris Teder-Laving, Igor Rudan, Annette M. Hartmann, Guillaume Paré, Ole A. Andreassen, Mohammad Arfan Ikram, Stacy Steinberg, Bjarke Feenstra, Peter Vollenweider, Sarah E. Medland, Brenda W.J.H. Penninx, Mark I. McCarthy, Jordan W. Smoller, Fazil Aliev, Joel N. Hirschhorn, Dan Rujescu, J.M. Vink, Dorret I. Boomsma, Harry Campbell, Pedro Marques-Vidal, David A. Hinds, Tõnu Esko, Ruth J. F. Loos, Zoltán Kutalik, Jouke-Jan Hottenga, Reedik Mägi, Dale R. Nyholt, Kari Stefansson, Kevin S. O’Connell, Hreinn Stefansson, Scott Melville, Andres Metspalu, Inês Barroso, Marco P. Boks, Gail Davies, Lavinia Paternoster, Thomas Hansen, Norman Klopp, H.-Erich Wichmann, David L. Duffy, Lili Milani, Heather A. Boyd, Michelle Luciano, Benjamin M. Neale, Margaret J. Wright, Fernando Rivadeneira, Liang-Dar Hwang, Scott D. Gordon, Jiali Han, Jennifer E. Huffman, Danielle M. Dick, Roel A. Ophoff, Ozren Polasek, Nicholas J. Wareham, Vincent Mooser, Mousheng Xu, Johannes H. Smit, Gonneke Willemsen, Ian J. Deary, Panos Deloukas, John P. Kemp, Cornelia M. van Duijn, Samuli Ripatti, Joyce Y. Tung, Eco J. C. de Geus, Cameron D. Palmer, Ina Giegling, Katri Räikkönen, Thomas Werge, Eero Vuoksimaa, Andrew A. Hicks, Inga Prokopenko, Lynn Cherkas, Sigurdur H. Magnusson, Gérard Waeber, Nicholas J. Timpson, Frank Geller, Carolina Medina-Gomez, Nicole M. Warrington, Kay-Tee Khaw, Jaakko Kaprio

مصطلحات موضوعية: Genetics, 0303 health sciences, 03 medical and health sciences, 0302 clinical medicine, Genetic variants, Biology, Association (psychology), Biobank, 030217 neurology & neurosurgery, 030304 developmental biology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c40c6c48a726fe619cb07c4402e42b6
https://doi.org/10.1101/831321

المؤلفون: Sarah J Lewis, Amy Davies, Caroline L Relton, George Davey Smith, Karen M Ho, Gemma C Sharp, Evie Stergiakouli, Jonathan R Sandy, Wendy L. McArdle, Kerry Humphries

المصدر: Clinical Epigenetics, Vol 9, Iss 1, Pp 1-17 (2017)
Sharp, G, Ho, K, Davies, A, Stergiakouli, E, Humphries, K, McArdle, W, Sandy, J, Davey Smith, G, Lewis, S & Relton, C 2017, ' Distinct DNA methylation profiles in subtypes of orofacial cleft ', Clinical Epigenetics, vol. 9, 63 (2017) . https://doi.org/10.1186/s13148-017-0362-2
Clinical Epigenetics

مصطلحات موضوعية: Epigenomics, Male, 0301 basic medicine, TBX1, lcsh:QH426-470, lcsh:Medicine, Orofacial clefts, PDGFRA, 030105 genetics & heredity, Biology, Cleft Collective, Cohort Studies, 03 medical and health sciences, Epigenome-wide association study, Genetics, Humans, Gene Regulatory Networks, Genetic Predisposition to Disease, Epigenetics, Molecular Biology, Gene, Genetics (clinical), Genetic association, EWAS, DNA methylation, Research, Cleft lip, lcsh:R, Infant, Methylation, Human genetics, stomatognathic diseases, lcsh:Genetics, 030104 developmental biology, Cleft palate, Female, Genome-Wide Association Study, Developmental Biology

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::846a40014944e4186256813fc4aa7fbf
http://link.springer.com/article/10.1186/s13148-017-0362-2

المؤلفون: Jordana T. Bell, Nicholas J. Timpson, Eilis Hannon, Gibran Hemani, Oliver Lyttleton, Jonathan Mill, Hashem A. Shihab, Elena Carnero-Montoro, Colin Campbell, Tom R. Gaunt, Jie Zheng, Susan M. Ring, Wendy L. McArdle, Santiago Rodriguez, Tom G. Richardson, Caroline L Relton, George Davey Smith

المصدر: Richardson, T G, Shihab, H A, Hemani, G, Zheng, J, Hannon, E, Mill, J, Carnero-Montoro, E, Bell, J T, Lyttleton, O, McArdle, W L, Ring, S M, Rodriguez, S, Campbell, C, Smith, G D, Relton, C L, Timpson, N J & Gaunt, T R 2016, ' Collapsed methylation quantitative trait loci analysis for low frequency and rare variants ', Human Molecular Genetics, vol. 25, no. 19, pp. 4339-4349 . https://doi.org/10.1093/hmg/ddw283
Richardson, T, Shihab, H, Hemani, G, Zheng, J, Hannon, E, Mill, J, Carnero-Montoro, E, Bell, J T, Lyttleton, O, McArdle, W, Ring, S, Rodriguez, S, Campbell, C, Davey Smith, G, Relton, C, Timpson, N & Gaunt, T 2016, ' Collapsed Methylation Quantitative Trait Loci analysis for Low Frequency and Rare variants ', Human Molecular Genetics, vol. 25, no. 19, pp. 4339-4349 . https://doi.org/10.1093/hmg/ddw283
Human Molecular Genetics

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Adolescent, Genotype, Quantitative Trait Loci, Genome-wide association study, Quantitative trait locus, Biology, Polymorphism, Single Nucleotide, 03 medical and health sciences, Gene Frequency, Genetics, Humans, Child, Molecular Biology, Allele frequency, Genetics (clinical), Association Studies Articles, Infant, Newborn, Genetic Variation, Infant, General Medicine, Methylation, DNA Methylation, Middle Aged, 030104 developmental biology, Gene Expression Regulation, CpG site, Child, Preschool, DNA methylation, Expression quantitative trait loci, CpG Islands, Female, Genome-Wide Association Study

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea9d5d9d80804f2248a70df4c5caf6cd
https://doi.org/10.1093/hmg/ddw283

المؤلفون: Nabila Kazmi, Tom R. Gaunt, Michael Pawlita, Miranda Pring, Andy R Ness, Wendy L. McArdle, Steve J Thomas, Christopher Penfold, Ryan Langdon, Tim Waterboer, Devin C. Koestler, Susan M. Ring, Karen M Ho, Caroline L Relton, George Davey Smith, Karl T. Kelsey, Matthew Suderman, Srikant Ambatipudi, Rebecca C Richmond

المصدر: Ambatipudi, S, Langdon, R, Richmond, R C, Suderman, M, Koestler, D C, Kelsey, K T, Kazmi, N, Penfold, C, Ho, K M, McArdle, W, Ring, S M, Pring, M, Waterboer, T, Pawlita, M, Gaunt, T R, Davey Smith, G, Thomas, S, Ness, A R & Relton, C L 2018, ' DNA methylation derived systemic inflammation indices are associated with head and neck cancer development and survival ', Oral Oncology, vol. 85, pp. 87-94 . https://doi.org/10.1016/j.oraloncology.2018.08.021

مصطلحات موضوعية: Male, 0301 basic medicine, Oncology, Cancer Research, Multivariate statistics, Lymphocyte-to-monocyte ratio, Datasets as Topic, Comorbidity, Kaplan-Meier Estimate, Antibodies, Viral, Logistic regression, Leukocyte Count, 0302 clinical medicine, Odds Ratio, Medicine, Overall survival, Prospective cohort study, Head and neck cancer, Neutrophil-to-lymphocyte ratio, Aged, 80 and over, Human papillomavirus 16, DNA methylation, Smoking, Middle Aged, C-Reactive Protein, Head and Neck Neoplasms, 030220 oncology & carcinogenesis, Female, ICEP, Oral Surgery, Adult, medicine.medical_specialty, Alcohol Drinking, Article, 03 medical and health sciences, Internal medicine, Biomarkers, Tumor, Humans, Neutrophil to lymphocyte ratio, Aged, Proportional Hazards Models, Inflammation, Systemic inflammation, Squamous Cell Carcinoma of Head and Neck, business.industry, Proportional hazards model, Papillomavirus Infections, mdNLR, Oncogene Proteins, Viral, DNA Methylation, medicine.disease, Head and neck squamous-cell carcinoma, Repressor Proteins, stomatognathic diseases, 030104 developmental biology, Case-Control Studies, CpG Islands, business

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c14376f8a0c4e2ae5f4c33d500b07bd2
https://hdl.handle.net/1983/af8f772c-112f-4ac3-8c31-3b15ce147cc9

المؤلفون: Andrea Danese, Wendy L. McArdle, Sarah K. G. Jensen, Sara R. Jaffee, Tom R. Gaunt, Esther Walton, Carmine M. Pariante, Lotte C Houtepen, Caroline L Relton, Edward D. Barker, Susanna Roberts, Charlotte A.M. Cecil, Thomas G. O'Connor

المصدر: Dev Psychopathol
Barker, E D, Cecil, C A M, Walton, E, Houtepen, L C, O'Connor, T G, Danese, A, Jaffee, S R, Jensen, S K G, Pariante, C, McArdle, W, Gaunt, T R, Relton, C L & Roberts, S 2018, ' Inflammation-related epigenetic risk and child and adolescent mental health : A prospective study from pregnancy to middle adolescence ', Development and Psychopathology, vol. 30, no. 3, pp. 1145-1156 . https://doi.org/10.1017/S0954579418000330

مصطلحات موضوعية: 0301 basic medicine, Male, medicine.medical_specialty, Adolescent, education, postnatal adversity, Child Behavior Disorders, Article, 03 medical and health sciences, 0302 clinical medicine, Pregnancy, Risk Factors, Epidemiology, Developmental and Educational Psychology, medicine, Humans, Prospective Studies, Prospective cohort study, Child, Depression (differential diagnoses), Inflammation, DNA methylation, conduct disorder, attention deficit hyperactivity, Cognition, ALSPAC, medicine.disease, anxiety, prenatal adversity, Mental health, Psychiatry and Mental health, polyepigenetic score, 030104 developmental biology, oppositional defiant disorder, Mental Health, Conduct disorder, inflammation, depression, Anxiety, Female, medicine.symptom, Psychology, 030217 neurology & neurosurgery, Clinical psychology

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c840f21d532d1b36d4d612a0b29a65bb
https://europepmc.org/articles/PMC7612578/