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

المصدر: Journal of Stroke and Cerebrovascular Diseases EpiHealth: Epidemiology for Health. 31(8)

مصطلحات موضوعية: Common genetic variants, Migraine, MRI phenotype, Posterior circulation ischemic stroke, Medicin och hälsovetenskap, Klinisk medicin, Neurologi, Medical and Health Sciences, Clinical Medicine, Neurology

الوصول الحر: https://lup.lub.lu.se/record/28f9978f-e3e8-4318-b18f-664aa2bb2065Test
http://dx.doi.org/10.1016/j.jstrokecerebrovasdis.2022.106546Test

المؤلفون: Ellul, Pierre, Delorme, Richard, Pignon, Baptiste, Chaumette, Boris, Peyre, Hugo, Baghdadli, Amaria, Iftimovici, Anton, Krebs, Marie Odile

المساهمون: Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Institut National de la Santé et de la Recherche Médicale (INSERM), Université Paris Cité (UPCité), Centre de recherche en épidémiologie et santé des populations (CESP), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Paul Brousse-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris-Saclay, Institut National de la Santé et de la Recherche Médicale, Fondation Bettencourt Schueller, GHU, ANR-18-RHUS-0014, Fondation pour la Recherche Médicale

المصدر: ISSN: 1018-8827.

مصطلحات موضوعية: Attention deficit hyperactivity disorder, Bipolar disorder, Colocalization, Common genetic variants, GWAS, Schizophrenia, SNP, [SDV]Life Sciences [q-bio]

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/38836921; hal-04623757; https://hal.science/hal-04623757Test; PUBMED: 38836921

الإتاحة: https://doi.org/10.1007/s00787-024-02479-7Test
https://hal.science/hal-04623757Test

المؤلفون: Priyanka Upadhyai, Pooja U. Shenoy, Bhavya Banjan, Mohammed F. Albeshr, Shahid Mahboob, Irfan Manzoor, Ranajit Das

المصدر: Life; Volume 12; Issue 9; Pages: 1300

مصطلحات موضوعية: COVID-19 host genetics, genetic variation in COVID-19 patients, exome-wide association study for COVID-19 patients, common genetic variants

جغرافية الموضوع: agris

وصف الملف: application/pdf

العلاقة: Epidemiology; https://dx.doi.org/10.3390/life12091300Test

الإتاحة: https://doi.org/10.3390/life12091300Test

المؤلفون: Peyre, H, Schoeler, T, Liu, C, Williams, CM, Hoertel, N, Havdahl, A, Pingault, J-B

المصدر: Journal of Child Psychology and Psychiatry , 62 (11) pp. 1285-1296. (2021)

مصطلحات موضوعية: Autism spectrum disorder, attention deficit hyperactivity disorder, comorbidity, common genetic variants, SNP, colocalization, genomic structural equation modelling, GWAS

وصف الملف: text

العلاقة: https://discovery.ucl.ac.uk/id/eprint/10135518/10/Pingault_Hugo.C_MAP_JCPP.R3.v1.pdfTest; https://discovery.ucl.ac.uk/id/eprint/10135518/16/Pingault_Hugo.C_MAP_JCPP_Figures.R3.v1.pdfTest; https://discovery.ucl.ac.uk/id/eprint/10135518/22/Pingault_Hugo.C_MAP_JCPP_Table.R1_vf7.pdfTest; https://discovery.ucl.ac.uk/id/eprint/10135518/4/Hugo.Supp_ASD%20and%20ADHD.R3.v1.pdfTest; https://discovery.ucl.ac.uk/id/eprint/10135518Test/

الإتاحة: https://discovery.ucl.ac.uk/id/eprint/10135518/10/Pingault_Hugo.C_MAP_JCPP.R3.v1.pdfTest
https://discovery.ucl.ac.uk/id/eprint/10135518/16/Pingault_Hugo.C_MAP_JCPP_Figures.R3.v1.pdfTest
https://discovery.ucl.ac.uk/id/eprint/10135518/22/Pingault_Hugo.C_MAP_JCPP_Table.R1_vf7.pdfTest
https://discovery.ucl.ac.uk/id/eprint/10135518/4/Hugo.Supp_ASD%20and%20ADHD.R3.v1.pdfTest
https://discovery.ucl.ac.uk/id/eprint/10135518Test/

المؤلفون: Martin, C, Lambiase, P

المساهمون: Kumar, D, Elliott, P

المصدر: In: Kumar, D and Elliott, P, (eds.) Cardiovascular Genetics and Genomics: Principles and Clinical Practice. (pp. 481-522). Springer: Cham, Switzerland. (2018)

مصطلحات موضوعية: Inherited conduction disease, Atrial fibrillation, Genomics, Mutations, Common genetic variants

وصف الملف: text

العلاقة: https://discovery.ucl.ac.uk/id/eprint/10061674/3/Martin_Inherited%20Conduction%20Disease_Atrial%20Fibrillation270716.pdfTest; https://discovery.ucl.ac.uk/id/eprint/10061674Test/

الإتاحة: https://discovery.ucl.ac.uk/id/eprint/10061674/3/Martin_Inherited%20Conduction%20Disease_Atrial%20Fibrillation270716.pdfTest
https://discovery.ucl.ac.uk/id/eprint/10061674Test/

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

المصدر: Behavior Genetics vol. 46 no. 2, pp. 170-182

مصطلحات موضوعية: Common genetic variants, Imputation, Personality, Phenotype harmonization, Polygenic risk

وصف الملف: application/pdf

العلاقة: info:eu-repo/grantAgreement/EC/FP7/201413; info:eu-repo/grantAgreement/EC/FP7/212111; info:eu-repo/grantAgreement/EC/FP7/205419; http://repub.eur.nl/pub/90500Test; urn:hdl:1765/90500

الإتاحة: https://doi.org/10.1007/s10519-015-9735-5Test
http://repub.eur.nl/pub/90500Test

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

المساهمون: Institute for Molecular Medicine Finland

مصطلحات موضوعية: COMMON GENETIC-VARIANTS, RISK, TRANSCRIPTION, TOX3, 3111 Biomedicine

وصف الملف: application/pdf

العلاقة: Winkelmann , J , Czamara , D , Schormair , B , Knauf , F , Schulte , E C , Trenkwalder , C , Dauvilliers , Y , Polo , O , Hoegl , B , Berger , K , Fuhs , A , Gross , N , Stiasny-Kolster , K , Oertel , W , Bachmann , C G , Paulus , W , Xiong , L , Montplaisir , J , Rouleau , G A , Fietze , I , Vavrova , J , Kemlink , D , Sonka , K , Nevsimalova , S , Lin , S-C , Wszolek , Z , Vilarino-Gueell , C , Farrer , M J , Gschliesser , V , Frauscher , B , Falkenstetter , T , Poewe , W , Allen , R P , Earley , C J , Ondo , W G , Le , W-D , Spieler , D , Kaffe , M , Zimprich , A , Kettunen , J , Perola , M , Silander , K , Cournu-Rebeix , I , Francavilla , M , Fontenille , C , Fontaine , B , Vodicka , P , Prokisch , H , Lichtner , P , Peppard , P , Faraco , J , Mignot , E , Gieger , C , Illig , T , Wichmann , H -E , Mueller-Myhsok , B & Meitinger , T 2011 , ' Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1 ' , PLoS Genetics , vol. 7 , no. 7 , pp. e1002171 . https://doi.org/10.1371/journal.pgen.1002171Test; 79960819049; 40eb74ee-0edf-4fe6-a3a3-4d59a6339892; http://hdl.handle.net/10138/162555Test; 000293338600020

الإتاحة: http://hdl.handle.net/10138/162555Test

المؤلفون: Oerlemans, Anoek M., Hartman, Catharina A., Franke, Barbara, Buitelaar, Jan K., Rommelse, Nanda N. J.

المصدر: Oerlemans , A M , Hartman , C A , Franke , B , Buitelaar , J K & Rommelse , N N J 2016 , ' Does the cognitive architecture of simplex and multiplex ASD families differ? ' , Journal of Autism and Developmental Disorders , vol. 46 , no. 2 , pp. 489-501 . https://doi.org/10.1007/s10803-015-2572-9Test

مصطلحات موضوعية: Autism Spectrum Disorder (ASD), Simplex-multiplex stratification, Family, Unaffected siblings, Cognition, AUTISM SPECTRUM DISORDERS, COMMON GENETIC-VARIANTS, DE-NOVO MUTATIONS, COMPREHENSIVE METAANALYSIS, EXECUTIVE FUNCTION, RISK-FACTORS, QUOTIENT AQ, CHILDREN, PARENTS, PROFILES

وصف الملف: application/pdf

العلاقة: https://research.rug.nl/en/publications/4e65e688-6e9c-4de2-a85b-41891db6ee5aTest

الإتاحة: https://doi.org/10.1007/s10803-015-2572-9Test
https://hdl.handle.net/11370/4e65e688-6e9c-4de2-a85b-41891db6ee5aTest
https://research.rug.nl/en/publications/4e65e688-6e9c-4de2-a85b-41891db6ee5aTest
https://pure.rug.nl/ws/files/62782097/Does_the_cognitive_architecture_of_simplex_and_multiplex_ASD_families_differ.pdfTest

المؤلفون: van den Berg, Stéphanie M, de Moor, Marleen H M, Verweij, Karin J H, 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, Kemp, John P, Medland, Sarah E, St Pourcain, Beate, Timpson, Nicholas J, Evans, David M

المصدر: 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 , ....

مصطلحات موضوعية: Personality, Phenotype harmonization, Common genetic variants, Imputation, Polygenic risk

وصف الملف: application/pdf

العلاقة: https://research-information.bris.ac.uk/en/publications/f76312dd-0b81-4fa8-8ca9-f5933491ee51Test

الإتاحة: https://doi.org/10.1007/s10519-015-9735-5Test
https://hdl.handle.net/1983/f76312dd-0b81-4fa8-8ca9-f5933491ee51Test
https://research-information.bris.ac.uk/en/publications/f76312dd-0b81-4fa8-8ca9-f5933491ee51Test
https://research-information.bris.ac.uk/ws/files/101612998/art_3A10.1007_2Fs10519_015_9735_5.pdfTest