المؤلفون: van den Berg, Stéphanie, de Moor, Marleen, Verweij, Karin, Krueger, Robert, Luciano, Michelle, Arias Vasquez, Alejandro, Matteson, Lindsay, Derringer, Jaime, Esko, Tõnu, Amin, Najaf, Gordon, Scott, Hansell, Narelle, Hart, Amy, Seppälä, Ilkka, Huffman, Jennifer, Konte, Bettina, Lahti, Jari, Lee, Minyoung, Miller, Mike, Nutile, Teresa, Tanaka, Toshiko, Teumer, Alexander, Viktorin, Alexander, Wedenoja, Juho, Abdellaoui, Abdel, Abecasis, Goncalo, Adkins, Daniel, Agrawal, Arpana, Allik, Jüri, Appel, Katja, Bigdeli, Timothy, Busonero, Fabio, Campbell, Harry, Costa, Paul, Smith, George, Davies, Gail, de Wit, Harriet, Ding, Jun, Engelhardt, Barbara, Eriksson, Johan, Fedko, Iryna, Ferrucci, Luigi, Franke, Barbara, Giegling, Ina, Grucza, Richard, Hartmann, Annette, Heath, Andrew, Heinonen, Kati, Henders, Anjali, Homuth, Georg, Hottenga, Jouke-Jan, Iacono, William, Janzing, Joost, Jokela, Markus, Karlsson, Robert, Kemp, John, Kirkpatrick, Matthew, Latvala, Antti, Lehtimäki, Terho, Liewald, David, Madden, Pamela, Magri, Chiara, Magnusson, Patrik, Marten, Jonathan, Maschio, Andrea, Mbarek, Hamdi, Medland, Sarah, Mihailov, Evelin, Milaneschi, Yuri, Montgomery, Grant, Nauck, Matthias, Nivard, Michel, Ouwens, Klaasjan, Palotie, Aarno, Pettersson, Erik, Polasek, Ozren, Qian, Yong, Pulkki-Råback, Laura, Raitakari, Olli, Realo, Anu, Rose, Richard, Ruggiero, Daniela, Schmidt, Carsten, Slutske, Wendy, Sorice, Rossella, Starr, John, St Pourcain, Beate, Sutin, Angelina, Timpson, Nicholas, Trochet, Holly, Vermeulen, Sita, Vuoksimaa, Eero, Widen, Elisabeth, Wouda, Jasper, Wright, Margaret, Zgaga, Lina, Porteous, David, Minelli, Alessandra, Rujescu, Dan, Ciullo, Marina

المصدر: Behavior Genetics: an international journal devoted to research in the inheritance of behavior in animals and man. 46(2)

مصطلحات موضوعية: Common genetic variants, Imputation, Personality, Phenotype harmonization, Polygenic risk, Cohort Studies, Extraversion, Psychological, Genome-Wide Association Study, Humans, Multifactorial Inheritance, Personality, Polymorphism, Single Nucleotide, Risk Factors

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/3v37p5wgTest

المؤلفون: P. Frid, H. Xu, B.D. Mitchell, M. Drake, J. Wasselius, B. Gaynor, K. Ryan, A.K. Giese, M. Schirmer, K.L. Donahue, R. Irie, M.J.R.J. Bouts, E.C. McIntosh, S.J.T. Mocking, A.V. Dalca, E. Giralt-Steinhauer, L. Holmegaard, K. Jood, J. Roquer, J.W. Cole, P.F. McArdle, J.P. Broderick, J. Jimenez-Conde, C. Jern, B.M. Kissela, D.O. Kleindorfer, R. Lemmens, J.F. Meschia, J. Rosand, T. Rundek, R.L. Sacco, R. Schmidt, P. Sharma, A. Slowik, V. Thijs, D. Woo, B.B. Worrall, S.J. Kittner, J. Petersson, P. Golland, O. Wu, N.S. Rost, A. Lindgren

مصطلحات موضوعية: Migraine without Aura, Rehabilitation, Migraine with Aura, education, Posterior circulation ischemic stroke, Diffusion Magnetic Resonance Imaging, Risk Factors, Common genetic variants, Humans, MRI phenotype, Surgery, Neurology (clinical), Cardiology and Cardiovascular Medicine, Migraine, Ischemic Stroke

وصف الملف: application/pdf; Print-Electronic

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ca438d84e784185271bdb5ecc3b5fecTest
http://hdl.handle.net/10230/54960Test

المؤلفون: van den Berg, Stéphanie M, de Moor, Marleen HM, Verweij, Karin JH, Krueger, Robert F, Luciano, Michelle, Arias Vasquez, Alejandro, Matteson, Lindsay K, Derringer, Jaime, Esko, Tõnu, Amin, Najaf, Gordon, Scott D, Hansell, Narelle K, Hart, Amy B, Seppälä, Ilkka, Huffman, Jennifer E, Konte, Bettina, Lahti, Jari, Lee, Minyoung, Miller, Mike, Nutile, Teresa, Tanaka, Toshiko, Teumer, Alexander, Viktorin, Alexander, Wedenoja, Juho, Abdellaoui, Abdel, Abecasis, Goncalo R, Adkins, Daniel E, Agrawal, Arpana, Allik, Jüri, Appel, Katja, Bigdeli, Timothy B, Busonero, Fabio, Campbell, Harry, Costa, Paul T, Smith, George Davey, Davies, Gail, de Wit, Harriet, Ding, Jun, Engelhardt, Barbara E, Eriksson, Johan G, Fedko, Iryna O, Ferrucci, Luigi, Franke, Barbara, Giegling, Ina, Grucza, Richard, Hartmann, Annette M, Heath, Andrew C, Heinonen, Kati, Henders, Anjali K, Homuth, Georg, Hottenga, Jouke-Jan, Iacono, William G, Janzing, Joost, Jokela, Markus, Karlsson, Robert, Kemp, John P, Kirkpatrick, Matthew G, Latvala, Antti, Lehtimäki, Terho, Liewald, David C, Madden, Pamela AF, Magri, Chiara, Magnusson, Patrik KE, Marten, Jonathan, Maschio, Andrea, Mbarek, Hamdi, Medland, Sarah E, Mihailov, Evelin, Milaneschi, Yuri, Montgomery, Grant W, Nauck, Matthias, Nivard, Michel G, Ouwens, Klaasjan G, Palotie, Aarno, Pettersson, Erik, Polasek, Ozren, Qian, Yong, Pulkki-Råback, Laura, Raitakari, Olli T, Realo, Anu, Rose, Richard J, Ruggiero, Daniela, Schmidt, Carsten O, Slutske, Wendy S, Sorice, Rossella, Starr, John M, St Pourcain, Beate, Sutin, Angelina R, Timpson, Nicholas J, Trochet, Holly, Vermeulen, Sita, Vuoksimaa, Eero, Widen, Elisabeth, Wouda, Jasper, Wright, Margaret J, Zgaga, Lina, Generation Scotland, Porteous, David, Minelli, Alessandra, Palmer, Abraham A

المصدر: Behavior Genetics, vol 46, iss 2

مصطلحات موضوعية: Biological Psychology, Epidemiology, Health Sciences, Psychology, Genetics, Prevention, Human Genome, Cohort Studies, Extraversion, Psychological, Genome-Wide Association Study, Humans, Multifactorial Inheritance, Personality, Polymorphism, Single Nucleotide, Risk Factors, Generation Scotland, Common genetic variants, Imputation, Phenotype harmonization, Polygenic risk, Zoology, Neurosciences, Genetics & Heredity, Biomedical and clinical sciences

جغرافية الموضوع: 170 - 182

العلاقة: qt526400ft; https://escholarship.org/uc/item/526400ftTest

الإتاحة: https://escholarship.org/uc/item/526400ftTest

المؤلفون: He, Yazhou, Theodoratou, Evropi, Li, Xue, Din, Farhat V.N., Vaughan‐Shaw, Peter, Svinti, Victoria, Farrington, Susan M., Campbell, Harry, Dunlop, Malcolm G., Timofeeva, Maria

المصدر: He, Y, Theodoratou, E, Li, X, Din, F V N, Vaughan-Shaw, P, Svinti, V, Farrington, S M, Campbell, H, Dunlop, M G & Timofeeva, M 2019, ' Effects of common genetic variants associated with colorectal cancer risk on survival outcomes after diagnosis: a large population-based cohort study. ', International Journal of Cancer . https://doi.org/10.1002/ijc.32550Test
International Journal of Cancer

مصطلحات موضوعية: Male, Genotype, Short Report, colorectal cancer, common genetic variants, Middle Aged, Prognosis, survival, Colorectal cancer, Cancer Genetics and Epigenetics, Cohort Studies, Scotland, Risk Factors, SURVIVAL, cohort study, Humans, Female, Genetic Predisposition to Disease, Colorectal Neoplasms, Aged, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::be1ce1a3001e2b7fd2b09eef7212b583Test
https://hdl.handle.net/20.500.11820/9ce6934b-3414-40da-83de-135dae834e1dTest

المؤلفون: Robert F. Krueger, Teresa Nutile, Georg Homuth, Ina Giegling, Aarno Palotie, Katja Appel, Grant W. Montgomery, Elisabeth Widen, Jouke-Jan Hottenga, Beate St Pourcain, Caroline Hayward, Andrea Maschio, Andrew C. Heath, Narelle K. Hansell, Terho Lehtimäki, Wendy S. Slutske, Sarah E. Medland, Johan G. Eriksson, John M. Starr, Antonio Terracciano, Jonathan Marten, Olli T. Raitakari, Liisa Keltikangas-Järvinen, Igor Rudan, Kati Heinonen, Brenda W.J.H. Penninx, David J. Porteous, Klaasjan G. Ouwens, Barbara Franke, Jaakko Kaprio, Erik Pettersson, Jueri Allik, Ian J. Deary, Alessandra Minelli, Nicholas G. Martin, William G. Iacono, Yuri Milaneschi, Ilkka Seppälä, David M. Evans, Lina Zgaga, John P. Kemp, Alexander Teumer, Dorret I. Boomsma, Harry Campbell, Margaret J. Wright, Abraham A. Palmer, Jun Ding, Patrik K. E. Magnusson, Marleen H. M. de Moor, James F. Wilson, Anu Realo, Paul T. Costa, Scott D. Gordon, Jaime Derringer, Michel G. Nivard, Cornelia M. van Duijn, David C. Liewald, David Schlessinger, Marina Ciullo, Juho Wedenoja, Amy B. Hart, Laura J. Bierut, Angelina R. Sutin, Hamdi Mbarek, Alexander Viktorin, Stéphanie Martine van den Berg, Ozren Polasek, Harriet de Wit, Jari Lahti, Dan Rujescu, Nicholas J. Timpson, Matthias Nauck, Fabio Busonero, Iryna O. Fedko, Evelin Mihailov, Gonçalo R. Abecasis, John M. Hettema, Daniel E. Adkins, Hans J. Grabe, Richard A. Grucza, Luigi Ferrucci, Alejandro Arias Vasquez, Barbara E. Engelhardt, Laura Pulkki-Råback, Antti Latvala, Bettina Konte, Michelle Luciano, Robert Karlsson, Chiara Magri, Sita H. Vermeulen, Tõnu Esko, Arpana Agrawal, Matt McGue, Holly Trochet, Joost G. E. Janzing, Gail Davies, Toshiko Tanaka, Rossella Sorice, Timothy B. Bigdeli, Abdel Abdellaoui, Karin J. H. Verweij, Andres Metspalu, Nancy L. Pedersen, Anjali K. Henders, Matthew G. Kirkpatrick, Yong Qian, Lindsay K. Matteson, Annette M. Hartmann, George Davey Smith, Michael B. Miller, Najaf Amin, Pamela A. F. Madden, Richard J. Rose, Minyoung Lee, Eero Vuoksimaa, Katri Räikkönen, Markus Jokela, Jennifer E. Huffman, Carsten Oliver Schmidt, Jasper Wouda, Daniela Ruggiero

المساهمون: Academic Medical Center, Helsinki Collegium for Advanced Studies, Behavioural Sciences, Clinicum, Department of Public Health, Johan Eriksson / Principal Investigator, Department of General Practice and Primary Health Care, Diabetes and Obesity Research Program, Research Programs Unit, Institute for Molecular Medicine Finland, Aarno Palotie / Principal Investigator, Elisabeth Ingrid Maria Widen / Principal Investigator, Jaakko Kaprio / Principal Investigator, Psychosocial factors and health, Developmental Psychology Research Group, Genomics of Neurological and Neuropsychiatric Disorders, Genetic Epidemiology, Genomic Discoveries and Clinical Translation, Faculty of Behavioural, Management and Social Sciences, Psychiatry, EMGO - Mental health, Amsterdam Neuroscience - Complex Trait Genetics, IOO, EMGO+ - Mental Health, Biological Psychology, Clinical Child and Family Studies, Erasmus MC other, Epidemiology

المصدر: Behavior Genetics
van den Berg, S M, de Moor, M H M, Verweij, C J H, Krueger, R F, Luciano, M, Vasquez, A A, Matteson, L K, Derringer, J, Esko, T, Amin, N, Gordon, S D, Hansell, N K, Hart, A B, Seppälä, I, Huffman, J E, Konte, B, Lahti, J, Miller, M, Nutile, T, Tanaka, T, Teumer, A, Viktorin, A, Wedenoja, J, Abdellaoui, A, Abecasis, G R, Adkins, D E, Agrawal, A, Allik, J, Appel, K, Bigdeli, T B, Busonero, F, Campbell, H, Costa, P T, Davey Smith, G, Davies, G, de Wit, H, Ding, J, Engelhardt, B E, Eriksson, J G, Fedko, I O, Ferrucci, L, Franke, B, Giegling, I, Grucza, R, Hartmann, A M, Heath, A C, Heinonen, K, Henders, A K, Homuth, G, Hottenga, J J, Iacono, W G, Janzing, J, Jokela, M, Karlsson, R, Kemp, J P, Kirkpatrick, M G, Latvala, A, Lehtimäki, T, Liewald, D C, Madden, P A F, Magri, C, Magnusson, P K E, Marten, J, Maschio, A, Mbarek, H, Medland, S E, Mihailov, E, Milaneschi, Y, Montgomery, G W, Nauck, M, Nivard, M G, Ouwens, K G, Palotie, A, Pettersson, E, Polasek, O, Qian, Y, Pulkki-Raback, L, Raitakari, O T, Realo, A, Rose, R J, Ruggiero, D, Schmidt, C O, Slutske, W S, Sorice, R, Starr, J M, St Pourcain, B, Sutin, A R, Timpson, N J, Trochet, H, Zgaga, L, Porteous, D, Minelli, A, Palmer, A A, Rujescu, D, Ciullo, M, Hayward, C, Rudan, I, Metspalu, A, Kaprio, J, Deary, I J, Räikkönen, K, Wilson, J F, Keltikangas-Järvinen, L, Bierut, L J, Hettema, J M, Grabe, H J, Penninx, B W J H, van Duijn, C M, Evans, D M, Schlessinger, D, Pedersen, N L, Terracciano, A, McGue, M, Martin, N G & Boomsma, D I 2016, ' Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium ', Behavior Genetics, vol. 46, no. 2, pp. 170-182 . https://doi.org/10.1007/s10519-015-9735-5Test
Behavior genetics, 46(2), 170-182. Springer New York
Behavior Genetics, 46, 2, pp. 170-82
Behavior genetics (2015). doi:10.1007/s10519-015-9735-5
info:cnr-pdr/source/autori:van Den Berg S.M.; de Moor M.H.M.; Verweij K.J.H.; Krueger R.F.; Luciano M.; Arias Vasquez A.; Matteson L.K.; Derringer J.; Esko T.; Amin N.; Gordon S.D.; Hansell N.K.; Hart A.B.; Seppala I.; Huffman J.E.; Konte B.; Lahti J.; Lee M.; Miller M.; Nutile T.; Tanaka T.; Teumer A.; Viktorin A.; Wedenoja J.; Abdellaoui A.; Abecasis G.R.; Adkins D.E.; Agrawal A.; Allik J.; Appel K.; Bigdeli T.B.; Busonero F.; Campbell H.; Costa P.T.; Smith G.D.; Davies G.; de Wit H.; Ding J.; Engelhardt B.E.; Eriksson J.G.; Fedko I.O.; Ferrucci L.; Franke B.; Giegling I.; Grucza R.; Hartmann A.M.; Heath A.C.; Heinonen K.; Henders A.K.; Homuth G.; Hottenga J.-J.; Iacono W.G.; Janzing J.; Jokela M.; Karlsson R.; Kemp J.P.; Kirkpatrick M.G.; Latvala A.; Lehtimaki T.; Liewald D.C.; Madden P.A.F.; Magri C.; Magnusson P.K.E.; Marten J.; Maschio A.; Mbarek H.; Medland S.E.; Mihailov E.; Milaneschi Y.; Montgomery G.W.; Nauck M.; Nivard M.G.; Ouwens K.G.; Palotie A.; Pettersson E.; Polasek O.; Qian Y.; Pulkki-Raback L.; Raitakari O.T.; Realo A.; Rose R.J.; Ruggiero D.; Schmidt C.O.; Slutske W.S.; Sorice R.; Starr J.M.; St Pourcain B.; Sutin A.R.; Timpson N.J.; Trochet H.; Vermeulen S.; Vuoksimaa E.; Widen E.; Wouda J.; Wright M.J.; Zgaga L.; Generation Scotland; Porteous D.; Minelli A.; Palmer A.A.; Rujescu D.; Ciullo M.; Hayward C.; Rudan I.; Metspalu A.; Kaprio J.; Deary I.J.; Raikkonen K.; Wilson J.F.; Keltikangas-Jarvinen L.; Bierut L.J.; Hettema J.M.; Grabe H.J.; Penninx B.W.J.H.; van Duijn C.M.; Evans D.M.; Schlessinger D.; Pedersen N.L.; Terracciano A.; McGue M.; Martin N.G.; Boomsma D.I./titolo:Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium/doi:10.1007%2Fs10519-015-9735-5/rivista:Behavior genetics/anno:2015/pagina_da:/pagina_a:/intervallo_pagine:/volume
van den Berg, S M, de Moor, M H M, Verweij, K J H, Krueger, R F, Luciano, M, Arias Vasquez, A, Matteson, L K, Derringer, J, Esko, T, Amin, N, Gordon, S D, Hansell, N K, Hart, A B, Seppälä, I, Huffman, J E, Konte, B, Lahti, J, Lee, M, Miller, M, Nutile, T, Tanaka, T, Teumer, A, Viktorin, A, Wedenoja, J, Abdellaoui, A, Abecasis, G R, Adkins, D E, Agrawal, A, Allik, J, Appel, K, Bigdeli, T B, Busonero, F, Campbell, H, Costa, P T, Smith, G D, Davies, G, de Wit, H, Ding, J, Engelhardt, B E, Eriksson, J G, Fedko, I O, Ferrucci, L, Franke, B, Giegling, I, Grucza, R, Kemp, J P, Medland, S E, St Pourcain, B, Timpson, N J, Evans, D M 2016, ' Meta-analysis of Genome-Wide Association Studies for Extraversion : Findings from the Genetics of Personality Consortium ', Behavior Genetics, vol. 46, no. 2, pp. 170-182 . https://doi.org/10.1007/s10519-015-9735-5Test
Behavior Genetics, 46, 170-182
Behavior genetics, 46(2), 170-182. Springer
Behavior Genetics, 46(2), 170-182. Springer US
Behavior Genetics, 46(2), 170-182. Springer
Behavior Genetics, 46, 170-82
van den Berg, S M, de Moor, M H M, Verweij, K J H, Krueger, R F, Luciano, M, Vasquez, A A, Matteson, L K, Derringer, J, Esko, T, Amin, N, Gordon, S D, Hansell, N K, Hart, A B, Seppala, I, Huffman, J E, Konte, B, Lahti, J, Lee, M, Miller, M, Nutile, T, Tanaka, T, Teumer, A, Viktorin, A, Wedenoja, J, Abdellaoui, A, Abecasis, G R, Adkins, D E, Agrawal, A, Allik, J, Appel, K, Bigdeli, T B, Busonero, F, Campbell, H, Costa, P T, Smith, G D, Davies, G, de Wit, H, Ding, J, Engelhardt, B E, Eriksson, J G, Fedko, I O, Ferrucci, L, Franke, B, Giegling, I, Grucza, R, Hartmann, A M, Heath, A C, Heinonen, K, Henders, A K, Homuth, G, Hottenga, J-J, Iacono, W G, Janzing, J, Jokela, M, Karlsson, R, Kemp, J P, Kirkpatrick, M G, Latvala, A, Lehtimaki, T, Liewald, D C, Madden, P A F, Magri, C, Magnusson, P K E, Marten, J, Maschio, A, Mbarek, H, Medland, S E, Mihailov, E, Milaneschi, Y, Montgomery, G W, Nauck, M, Nivard, M G, Ouwens, K G, Palotie, A, Pettersson, E, Polasek, O, Qian, Y, Pulkki-Raback, L, Raitakari, O T, Realo, A, Rose, R J, Ruggiero, D, Schmidt, C O, Slutske, W S, Sorice, R, Starr, J M, St Pourcain, B, Sutin, A R, Timpson, N J, Trochet, H, Vermeulen, S, Vuoksimaa, E, Widen, E, Wouda, J, Wright, M J, Zgaga, L, Porteous, D, Minelli, A, Palmer, A A, Rujescu, D, Ciullo, M, Hayward, C, Rudan, I, Metspalu, A, Kaprio, J, Deary, I J, Raikkonen, K, Wilson, J F, Keltikangas-Jarvinen, L, Bierut, L J, Hettema, J M, Grabe, H J, Penninx, B W J H, van Duijn, C M, Evans, D M, Schlessinger, D, Pedersen, N L, Terracciano, A, McGue, M, Martin, N G & Boomsma, D I 2016, ' Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium ', Behavior Genetics, vol. 46, no. 2, pp. 170-182 . https://doi.org/10.1007/s10519-015-9735-5Test
Behavior Genetics, 46(2), 170-182. Springer New York
van den Berg, S M, de Moor, M H M, Verweij, K J H, Krueger, R F, Luciano, M, Arias Vasquez, A, Matteson, L K, Derringer, J, Esko, T, Amin, N, Gordon, S D, Hansell, N K, Hart, A B, Seppälä, I, Huffman, J E, Konte, B, Lahti, J, Lee, M, Miller, M, Nutile, T, Tanaka, T, Teumer, A, Viktorin, A, Wedenoja, J, Abdellaoui, A, Abecasis, G R, Adkins, D E, Agrawal, A, Allik, J, Appel, K, Bigdeli, T B, Busonero, F, Campbell, H, Costa, P T, Smith, G D, Davies, G, de Wit, H, Ding, J, Engelhardt, B E, Eriksson, J G, Fedko, I O, Liewald, D C, Polasek, O, Starr, J M, Zgaga, L, Porteous, D, Hayward, C, Rudan, I & Deary, I J & Wilson, J F 2015, ' Meta-analysis of genome-wide association studies for extraversion : Findings from the Genetics of Personality Consortium ', Behavior Genetics . https://doi.org/10.1007/s10519-015-9735-5Test
van den Berg, S M, de Moor, M H M, Verweij, K J H, Krueger, R F, Luciano, M, Arias Vasquez, A, Matteson, L K, Derringer, J, Esko, T, Amin, D N, Gordon, S D, Hansell, N K, Hart, A B, Seppälä, I, Huffman, J E, Konte, B, Lahti, J, Lee, J M, Miller, M, Nutile, T, Tanaka, T, Teumer, A, Viktorin, A, Wedenoja, J, Abdellaoui, A, Abecasis, G R, Adkins, D E, Agrawal, A, Allik, J, Appel, K, Bigdeli, T B, Busonero, F, Campbell, H, Costa, P T, Smith, G D, Davies, G, De Wit, H, Ding, J Z, Engelhardt, B E, Eriksson, J G, Fedko, I O, Ferrucci, L, Franke, B, Giegling, I, Grucza, R, Hartmann, A M, Heath, A C, Heinonen, K, Henders, A K, Homuth, G, Hottenga, J J, Iacono, W G, Janzing, J, Jokela, M, Karlsson, R, Kemp, J P, Kirkpatrick, M G, Latvala, A, Lehtimäki, T, Liewald, D C, Madden, P A F, Magri, C, Magnusson, P K E, Marten, J, Maschio, A, Mbarek, H, Medland, S E, Mihailov, E, Milaneschi, Y, Montgomery, G W, Nauck, M, Nivard, M G, Ouwens, K G, Palotie, A, Pettersson, E, Polasek, O, Qian, Y-P, Pulkki-Råback, L, Raitakari, O T, Realo, A, Rose, R J, Ruggiero, D, Schmidt, C O, Slutske, W S, Sorice, R, Starr, J M, St Pourcain, B, Sutin, A R, Timpson, N J, Trochet, H, Vermeulen, S H, Vuoksimaa, E, Widen, E, Wouda, J, Wright, M J, Zgaga, L, Generation, S, Porteous, D J, Minelli, A, Palmer, L A, Rujescu, D, Ciullo, M, Hayward, C, Rudan, I, Metspalu, A, Kaprio, J, Deary, I J, Räikkönen, K, Wilson, J F, Keltikangas-Järvinen, L, Bierut, L J, Hettema, J M, Grabe, H-J, Penninx, B W J H, van Duijn, C M, Evans, D M, Schlessinger, D, Pedersen, N L, Terracciano, A, McGue, M, Martin, N G & Boomsma, D I 2016, ' Meta-analysis of Genome-Wide Association Studies for Extraversion : Findings from the Genetics of Personality Consortium ', Behavior Genetics, vol. 46, no. 2, pp. 170-182 . https://doi.org/10.1007/s10519-015-9735-5Test
Behavior Genetics, 46, 2, pp. 170-182

مصطلحات موضوعية: 0301 basic medicine, Netherlands Twin Register (NTR), Multifactorial Inheritance, Genome-wide association study, Cohort Studies, Extraversion, Psychological, 0302 clinical medicine, Risk Factors, NEUROTICISM, Genetics(clinical), IR-99241, Big Five personality traits, Genetics (clinical), Original Research, media_common, Genetics, Ecology, HERITABILITY, METIS-315471, Polymorphism, Single Nucleotide/genetics, Neuroticism, 3142 Public health care science, environmental and occupational health, Common genetic variants, Urological cancers Radboud Institute for Health Sciences [Radboudumc 15], Trait, Psychology, Personality, DIMENSIONS, NEUROTROPHIC FACTOR BDNF, Evolution, 515 Psychology, media_common.quotation_subject, Single-nucleotide polymorphism, Phenotype harmonization, Polymorphism, Single Nucleotide, Imputation, Polygenic risk, Ecology, Evolution, Behavior and Systematics, 03 medical and health sciences, Behavior and Systematics, Personality/genetics, CLONINGERS TEMPERAMENT SCALES, 5-FACTOR MODEL, Humans, Multifactorial Inheritance/genetics, PSYCHOBIOLOGICAL MODEL, Extraversion and introversion, Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7], Other Research Radboud Institute for Health Sciences [Radboudumc 0], Extraversion (Psychology), COMMON SNPS EXPLAIN, 030104 developmental biology, LARGE PROPORTION, 3111 Biomedicine, Developmental Psychopathology, HUMAN HEIGHT, 030217 neurology & neurosurgery, Genome-Wide Association Study

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

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b75ed1f400f905ec72792b1d1c9d3e0Test
https://doi.org/10.1007/s10519-015-9735-5Test

المؤلفون: George Dedoussis, Lorraine Southam, Eleftheria Zeggini, Ioanna Ntalla, Panagiota Vlachou, Nigel W. Rayner, Kalliope Panoutsopoulou

المصدر: Annals of Human Genetics

مصطلحات موضوعية: Male, Adolescent, Short Communication, Alpha-Ketoglutarate-Dependent Dioxygenase FTO, common genetic variants, Genome-wide association study, Biology, Overweight, Polymorphism, Single Nucleotide, Childhood obesity, Body Mass Index, Cohort Studies, BMI, 03 medical and health sciences, 0302 clinical medicine, Risk Factors, Genetics, medicine, Humans, Genetic Predisposition to Disease, Obesity, adolescents, Allele, Child, Alleles, Genetics (clinical), 030304 developmental biology, 2. Zero hunger, 0303 health sciences, Greece, Membrane Proteins, Proteins, medicine.disease, Genetic Loci, Cohort, Female, medicine.symptom, Apoptosis Regulatory Proteins, Body mass index, 030217 neurology & neurosurgery, Genome-Wide Association Study, Demography, Cohort study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c152be5716585bb938328415a8c99919Test
https://doi.org/10.1111/ahg.12012Test

المؤلفون: Andrea Fuhs, Juliane Winkelmann, H.-Erich Wichmann, Werner Poewe, Emmanuel Mignot, Christopher J. Earley, Claire Fontenille, Matthew J. Farrer, Wolfgang H. Oertel, David Kemlink, Olli Polo, Darina Czamara, William G. Ondo, Viola Gschliesser, Marcella Francavilla, Barbara Schormair, Walter Paulus, Franziska Knauf, Birgit Högl, Karel Sonka, Klaus Berger, Bertram Müller-Myhsok, Maria Kaffe, Siong Chi Lin, Ingo Fietze, Wei Dong Le, Nadine Gross, Kaisa Silander, Juliette Faraco, Zbigniew K. Wszolek, Thomas Meitinger, Birgit Frauscher, Pavel Vodicka, Paul E. Peppard, Claudia Trenkwalder, Lan Xiong, Jana Vavrova, Markus Perola, Cornelius G. Bachmann, Thomas Illig, Guy A. Rouleau, Christian Gieger, Sona Nevsimalova, Richard P. Allen, Holger Prokisch, Carles Vilariño-Güell, Karin Stiasny-Kolster, Yves Dauvilliers, Derek Spieler, Johannes Kettunen, Tina Falkenstetter, Isabelle Cournu-Rebeix, Eva C. Schulte, Peter Lichtner, Jacques Montplaisir, Bertrand Fontaine, Alexander Zimprich

المساهمون: Institute for Molecular Medicine Finland, Institute of Human Genetics, Technische Universität Munchen - Université Technique de Munich [Munich, Allemagne] (TUM), Department of Neurology, Technische Universität Munchen - Université Technique de Munich [Munich, Allemagne] (TUM)-Helmholtz-Zentrum München (HZM)-German Research Center for Environmental Health, Max-Planck-Institut für Psychiatrie, Max-Planck-Gesellschaft, Center of Parkinsonism and Movement Disorders, Paracelsus-Elena-Hospital, Neuropsychiatrie : recherche épidémiologique et clinique (PSNREC), Université Montpellier 1 (UM1)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM), Sleep Research Unit, University of Turku, Department of Pulmonary Medicine, Tampere University Hospital, Innsbruck Medical University [Austria] (IMU), Institute of Epidemiology and Social Medicine, Westfälische Wilhelms-Universität Münster (WWU), Somnomar, Sleep Research Institute, Philipps University-Center of Nervous Diseases, Department of Clinical Neurophysiology, Georg-August-University [Göttingen], Center of Excellence in Neuroscience, CHU de Montréal, Laboratoire d'étude des maladies du cerveau, Université de Montréal (UdeM)-Hopital Notre-Dame-Centre de Recherche du Centre Hospitalier de l’Université de Montréal (CR CHUM), Centre Hospitalier de l'Université de Montréal (CHUM), Université de Montréal (UdeM)-Université de Montréal (UdeM)-Centre Hospitalier de l'Université de Montréal (CHUM), Université de Montréal (UdeM), Centre d'étude du sommeil, Hôpital du Sacré-Coeur de Montréal, Interdisciplinary Center of Sleep Medicine, Universitätsmedizin Berlin-Internetseiten der Charité, Charles University [Prague] (CU)-1st Faculty of Medicine, Centre for Molecular Medicine and Therapeutics, University of British Columbia (UBC), Johns Hopkins University (JHU), Baylor College of Medecine, Medizinische Universität Wien = Medical University of Vienna, Institute for Molecular Medicine Finland [Helsinki] (FIMM), Helsinki Institute of Life Science (HiLIFE), University of Helsinki-University of Helsinki, Department of Chronic Disease Prevention, National Institute for Health and Welfare [Helsinki], Centre de Recherche de l'Institut du Cerveau et de la Moelle épinière (CRICM), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Institute of Experimental Medicine, Czech Academy of Sciences [Prague] (CAS), Department of Population Health Sciences, University of Wisconsin-Madison, Center For Narcolepsy, Stanford University, Institute of Genetic Epidemiology, German Research Center for Environmental Health-Helmholtz-Zentrum München (HZM), Unit for Molecular Epidemiology, Institute of Medical Informatics, Biometry, and Epidemiology, Ludwig-Maximilians-Universität München (LMU)-Chair of Epidemiology, Institute of Epidemiology I, Klinikum Großhadern, Technische Universität Munchen - Université Technique de Munich [Munich, Allemagne] (TUM)-Campus Großhadern, The replication phase was supported by a grant from the US RLS Foundation. Part of this work was financed by the National Genome Research Network (NGFN). The KORA study group consists of H-E Wichmann (speaker), R Holle, J John, T Illig, C Meisinger, A Peters, and their coworkers, who are responsible for the design and conduction of the KORA studies. The KORA research platform (KORA, Cooperative Research in the Region of Augsburg) was initiated and financed by the Helmholtz Zentrum München, which is funded by the German Federal Ministry of Education and Research and by the State of Bavaria. The collection of sociodemographic and clinical data in the Dortmund Health Study was supported by the German Migraine & Headache Society (DMKG) and by unrestricted grants of equal share from Astra Zeneca, Berlin Chemie, Boots Healthcare, Glaxo-Smith-Kline, McNeil Pharma (former Woelm Pharma), MSD Sharp & Dohme, and Pfizer to the University of Muenster. Blood collection in the Dortmund Health Study was done through funds from the Institute of Epidemiology and Social Medicine, University of Muenster. Data collection in the COR-Study was supported by unrestricted grants of the German RLS Society (Deutsche Restless Legs Vereinigung e.V.) and Axxonis Pharma, Boehringer Ingelheim Pharma, Mundipharma Research, Roche Pharma, and UCB to the University of Muenster. CG Bachmann was supported by grants of the German RLS Society, Deutsche Restless Legs Vereinigung, e.V. H Prokisch and T Meitinger were supported by the German Federal Ministry of Education and Research (BMBF) project Systems Biology of Metabotypes (SysMBo #0315494A). RP Allen and CJ Earley were supported by the grant PO1-AG21190 National Institute of Health, USA, the Canadian part of the study was supported by a Canadian Institutes of Health Research (CIHR) grant to GA Rouleau and J Montplaisir. D Kemlink and S Nevsimalova were supported by an ESRS grant MSM0021620849, Jávrová and K Sonka were supported by grant MSM0021620816. Recruitment of Czech controls was funded by grant IGA NR 8563-5, Ministry of Health of the Czech Republic. B Frauscher, I Cournu-Rebeix, M Francavilla, and C Fontenille are co-authors on behalf of BRC-REFGENSEP, which is supported by INSERM, AFM (Généthon), ARSEP, and GIS-IBISA., Technische Universität Munchen - Université Technique de Munich [Munich, Allemagne] (TUM)-Helmholtz Zentrum München = German Research Center for Environmental Health, Innsbruck Medical University = Medizinische Universität Innsbruck (IMU), Westfälische Wilhelms-Universität Münster = University of Münster (WWU), Georg-August-University = Georg-August-Universität Göttingen, Helsingin yliopisto = Helsingfors universitet = University of Helsinki-Helsingin yliopisto = Helsingfors universitet = University of Helsinki, Helmholtz Zentrum München = German Research Center for Environmental Health, Autard, Delphine

المصدر: PLoS Genetics
PLoS Genetics, Vol 7, Iss 7, p e1002171 (2011)
PLoS Genetics, Public Library of Science, 2011, 7 (7), pp.e1002171. ⟨10.1371/journal.pgen.1002171⟩
PLoS Genetics, 2011, 7 (7), pp.e1002171. ⟨10.1371/journal.pgen.1002171⟩
PLoS Genet. 7:e1002171 (2011)

مصطلحات موضوعية: Cancer Research, Linkage disequilibrium, Genome-wide association study, [SDV.GEN] Life Sciences [q-bio]/Genetics, 0302 clinical medicine, MESH: Risk Factors, Risk Factors, Restless legs syndrome, TRANSCRIPTION, Genetics (clinical), Genetics, RISK, 0303 health sciences, education.field_of_study, Movement Disorders, MESH: Polymorphism, Single Nucleotide, MESH: Genetic Predisposition to Disease, 3. Good health, MESH: Reproducibility of Results, COMMON GENETIC-VARIANTS, Neurology, Chromosomes, Human, Pair 2, Medicine, Research Article, lcsh:QH426-470, Population, education, MESH: Chromosomes, Human, Pair 2, Locus (genetics), Single-nucleotide polymorphism, Biology, MESH: Genetic Loci, Polymorphism, Single Nucleotide, 03 medical and health sciences, Restless Legs Syndrome, MESH: Restless Legs Syndrome, medicine, Humans, Genetic Predisposition to Disease, Molecular Biology, Ecology, Evolution, Behavior and Systematics, 030304 developmental biology, [SDV.GEN]Life Sciences [q-bio]/Genetics, MESH: Humans, TOX3, Reproducibility of Results, medicine.disease, Common genetic-variants, Risk, Transcription, Tox3, lcsh:Genetics, BTBD9, Genetic Loci, MESH: Genome-Wide Association Study, 3111 Biomedicine, Sleep Disorders, MESH: Chromosomes, Human, Pair 16, 030217 neurology & neurosurgery, Chromosomes, Human, Pair 16, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d40590c29234b719bd96ebc654f44cebTest
http://hdl.handle.net/10138/162555Test

المؤلفون: Christine Helsen, Hendrik Van Poppel, Frank Claessens, Thomas Van den Broeck, Liesbeth Clinckemalie, Lien Spans, Lorenzo Tosco, Stefan Prekovic, Steven Joniau

المصدر: BioMed Research International, Vol 2014 (2014)
BioMed Research International

مصطلحات موضوعية: Male, medicine.medical_specialty, CLINICAL-OUTCOMES, SUSCEPTIBILITY LOCI, Decision Making, MEDLINE, lcsh:Medicine, Single-nucleotide polymorphism, Review Article, Biology, Research & Experimental Medicine, urologic and male genital diseases, Bioinformatics, Polymorphism, Single Nucleotide, BIOMARKER LEVELS, General Biochemistry, Genetics and Molecular Biology, Prostate cancer, Risk Factors, DNA-REPAIR GENES, Epidemiology, Health care, medicine, SEQUENCE VARIANTS, Humans, SNP, GENOME-WIDE ASSOCIATION, Prostate cancer risk, Science & Technology, ANTIGEN RECURRENCE, General Immunology and Microbiology, business.industry, lcsh:R, RADICAL PROSTATECTOMY, Prostatic Neoplasms, General Medicine, Therapeutic decision making, medicine.disease, COMMON GENETIC-VARIANTS, Biotechnology & Applied Microbiology, Medicine, Research & Experimental, ANDROGEN-DEPRIVATION THERAPY, business, Life Sciences & Biomedicine

وصف الملف: Print-Electronic

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ecf958ad184ab28b3fac6da1495e9daaTest
https://lirias.kuleuven.be/handle/123456789/682244Test

المؤلفون: Vorstman, Jacob A. S., Anney, Richard J. L., Derks, Eske M., Gallagher, Louise, Gill, Michael, De Jonge, Maretha V., Engeland, Herman, Kahn, René S., Ophoff, Roel A., Betancur, Catalina, Autism Genome Project, The, International Schizophrenia Consortium, The

المساهمون: University Medical Center [Utrecht], Trinity College Dublin, Academic Medical Center - Academisch Medisch Centrum [Amsterdam] (AMC), University of Amsterdam [Amsterdam] (UvA), University of California [Los Angeles] (UCLA), University of California, Génétique de l'autisme = Genetics of Autism (NPS-01), Neuroscience Paris Seine (NPS), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de Biologie Paris Seine (IBPS), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de Biologie Paris Seine (IBPS), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Department of Psychiatry, Human Genetics Branch, National Institutes of Health [Bethesda] (NIH)-National Institute of Mental Health (NIMH), Mazalérat, Charlotte, University of California (UC), ANS - Amsterdam Neuroscience, APH - Amsterdam Public Health, Adult Psychiatry

المصدر: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, Wiley, 2013, 162 (1), pp.55-60. ⟨10.1002/ajmg.b.32121⟩
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 2013, 162 (1), pp.55-60. ⟨10.1002/ajmg.b.32121⟩
American journal of medical genetics. Part B, Neuropsychiatric genetics, 162(1), 55-60. Wiley-Liss Inc.

مصطلحات موضوعية: Genetic Markers, Multifactorial Inheritance, Schizophrenia (object-oriented programming), Autism, Biology, behavioral disciplines and activities, 03 medical and health sciences, Cellular and Molecular Neuroscience, 0302 clinical medicine, Risk Factors, Common Genetic Variants, mental disorders, medicine, Humans, Genetic Predisposition to Disease, [SDV.NEU] Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC], Autistic Disorder, Genetic risk, Genetics (clinical), 030304 developmental biology, Genetics, 0303 health sciences, Polygenic Risk Score, Genetic variants, Genetic Variation, medicine.disease, Genetic architecture, 3. Good health, schizophrenia, Psychiatry and Mental health, Variation (linguistics), Case-Control Studies, Risk allele, Etiology, [SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC], 030217 neurology & neurosurgery

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc92b0ee58aff36d6a5069102673f731Test
https://hal.archives-ouvertes.fr/hal-01541310Test