المؤلفون: Geissler, Julia M, Romanos, Marcel, Sheerin, Una-Marie, Scheffer, Hans, Shaw, Karen, Shoulson, Ira, Sidransky, Ellen, Smith, Colin, Spencer, Chris C A, Stefánsson, Hreinn, Steinberg, Stacy, Stockton, Joanna D, Strange, Amy, Saad, Mohamad, Talbot, Kevin, Tanner, Carlie M, Tashakkori-Ghanbaria, Avazeh, Tison, François, Trabzuni, Daniah, Traynor, Bryan J, Uitterlinden, André G, Velseboer, Daan, Vidailhet, Marie, Walker, Robert, Simón-Sánchez, Javier, van de Warrenburg, Bart, Wickremaratchi, Mirdhu, Williams, Nigel, Williams-Gray, Caroline H, Winder-Rhodes, Sophie, Stefánsson, Kári, Martinez, Maria, Hardy, John, Heutink, Peter, Brice, Alexis, Schulte, Claudia, Gasser, Thomas, Singleton, Andrew B, Wood, Nicholas W, Lesage, Suzanne, Sveinbjörnsdóttir, Sigurlaug, Arepalli, Sampath, Barker, Roger, Ben-Shlomo, Yoav, Berendse, Henk W, Gerlach, Manfred, Berg, Daniela, Bhatia, Kailash, de Bie, Rob M A, Biffi, Alessandro, Bloem, Bas, Bochdanovits, Zoltan, Bonin, Michael, Bras, Jose M, Brockmann, Kathrin, Brooks, Janet, Burn, David J, Charlesworth, Gavin, Chen, Honglei, Chinnery, Patrick F, Chong, Sean, Clarke, Carl E, Cookson, Mark R, Cooper, J Mark, Corvol, Jean Christophe, Counsell, Carl, Damier, Philippe, Dartigues, Jean-François, Deloukas, Panos, Deuschl, Günther, Dexter, David T, van Dijk, Karin D, Dillman, Allissa, Durif, Frank, Dürr, Alexandra, Edkins, Sarah, members, International Parkinson Disease Genomics Consortium, Evans, Jonathan R, Foltynie, Thomas, Gao, Jianjun, Gardner, Michelle, Gibbs, J Raphael, Goate, Alison, Gray, Emma, Guerreiro, Rita, Gústafsson, Ómar, Harris, Clare, Nalls, Mike, van Hilten, Jacobus J, Hofman, Albert, Hollenbeck, Albert, Holton, Janice, Hu, Michele, Huang, Xuemei, Huber, Heiko, Hudson, Gavin, Hunt, Sarah E, Huttenlocher, Johanna, Plagnol, Vincent, Illig, Thomas, Jónsson, Pálmi V, Lambert, Jean-Charles, Langford, Cordelia, Lees, Andrew, Lichtner, Peter, Limousin, Patricia, Lopez, Grisel, Lorenz, Delia, McNeill, Alisdair, Hernandez, Dena G, Moorby, Catriona, Moore, Matthew, Morris, Huw R, Morrison, Karen E, Mudanohwo, Ese, O'Sullivan, Sean S, Pearson, Justin, Perlmutter, Joel S, Pétursson, Hjörvar, Pollak, Pierre, Sharma, Manu, Post, Bart, Potter, Simon, Ravina, Bernard, Revesz, Tamas, Riess, Olaf, Rivadeneira, Fernando, Rizzu, Patrizia, Ryten, Mina, Sawcer, Stephen, Schapira, Anthony

المساهمون: Human genetics, Neurology, Amsterdam Neuroscience - Neurodegeneration, Geissler, Julia M [0000-0003-1878-9647], Apollo - University of Cambridge Repository

المصدر: ADHD Attention Deficit and Hyperactivity Disorders, 9(2), 121-127
ADHD Attention Deficit and Hyperactivity Disorders 9(2), 121-127 (2017). doi:10.1007/s12402-017-0219-8
ADHD Attention Deficit and Hyperactivity Disorders, 9(2), 121-127. Springer Wien
Attention Deficit and Hyperactivity Disorders, 9, 121-127
Geissler, J M, Schulte, C, Berg, D & International Parkinson Disease Genomics Consortium members 2017, ' No genetic association between attention-deficit/hyperactivity disorder (ADHD) and Parkinson’s disease in nine ADHD candidate SNPs ', ADHD Attention Deficit and Hyperactivity Disorders, vol. 9, no. 2, pp. 121-127 . https://doi.org/10.1007/s12402-017-0219-8Test
Attention Deficit and Hyperactivity Disorders, 9, 2, pp. 121-127

مصطلحات موضوعية: 0301 basic medicine, Parkinson's disease, Single-nucleotide polymorphism, Genome-wide association study, genetics [Attention Deficit Disorder with Hyperactivity], Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, 0302 clinical medicine, SDG 3 - Good Health and Well-being, genetics [Parkinson Disease], medicine, Attention deficit hyperactivity disorder, ADHD, GWAS, Humans, Genetic Predisposition to Disease, ddc:610, genetics [Genetic Predisposition to Disease], Genetic Association Studies, Genetic association, Dopamine transporter, Genetics, TPH2, biology, Parkinson Disease, General Medicine, Disorders of movement Donders Center for Medical Neuroscience [Radboudumc 3], medicine.disease, Psychiatry and Mental health, Clinical Psychology, 030104 developmental biology, Norepinephrine transporter, Attention Deficit Disorder with Hyperactivity, biology.protein, genetics [Polymorphism, Single Nucleotide], Parkinson’s disease, Psychology, 030217 neurology & neurosurgery, CDH13, SNPs

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c64dc92688c2a4ae8420a2ef6ebe5479Test

المؤلفون: Tobias J. Renner, Andrea Boreatti-Hümmer, Sebastian Heinzel, Andreas Reif, Christian Jacob, Monika Heine, Thomas Dresler, Christina G. Baehne, Klaus-Peter Lesch, Ann-Christine Ehlis, Andreas J. Fallgatter

المساهمون: Psychiatrie & Neuropsychologie, Farmacologie en Toxicologie, RS: MHeNs School for Mental Health and Neuroscience

المصدر: Cerebral Cortex, 23(6), 1453-1462. Oxford University Press
Cerebral cortex 23(6), 1453-1462 (2012). doi:10.1093/cercor/bhs132

مصطلحات موضوعية: Male, genetics [Catechol O-Methyltransferase], Minisatellite Repeats, Neuropsychological Tests, Electroencephalography, genetics [Attention Deficit Disorder with Hyperactivity], Vocabulary, Gene Frequency, NoGo-anteriorization, Prefrontal cortex, Evoked Potentials, Brain Mapping, genetics [Receptors, Dopamine D4], medicine.diagnostic_test, attention-deficit, Cognition, Middle Aged, physiology [Decision Making], DRD4 protein, human, genetics [Reaction Time], Female, hyperactivity disorder (ADHD), dopamine, Psychology, electroencephalography, medicine.drug, Cognitive psychology, Adult, Genotype, Cognitive Neuroscience, Decision Making, Prefrontal Cortex, genetics [Polymorphism, Genetic], Catechol O-Methyltransferase, Inhibitory postsynaptic potential, Young Adult, Cellular and Molecular Neuroscience, Dopamine, mental disorders, Reaction Time, medicine, Humans, Attention deficit hyperactivity disorder, ddc:610, genetics [Evoked Potentials], genetic epistasis, Analysis of Variance, Neural correlates of consciousness, Polymorphism, Genetic, Catechol-O-methyl transferase, genetics [Minisatellite Repeats], Receptors, Dopamine D4, Epistasis, Genetic, pathology [Attention Deficit Disorder with Hyperactivity], medicine.disease, pathology [Prefrontal Cortex], Attention Deficit Disorder with Hyperactivity, genetics [Epistasis, Genetic], Neuroscience

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a169148b49281d9fc39682a5bfec69cTest
https://doi.org/10.1093/cercor/bhs132Test

المؤلفون: T. T. Nguyen, André Scherag, Klaus-Peter Lesch, Joachim Heinrich, Ivonne Jarick, Markus M. Nöthen, Benno G. Schimmelmann, Johannes Hebebrand, Gerd Lehmkuhl, Karl-Heinz Jöckel, Christine M. Freitag, Sebastian Beck, Carolin Pütter, Franziska Degenhardt, Sonali Pechlivanis, Andreas Reif, Susanne Gilsbach, H-Erich Wichmann, Anna-Lena Volckmar, Beate Herpertz-Dahlmann, Stefan Schreiber, Per Hoffmann, Andreas Warnke, Marcel Romanos, Tobias J. Renner, Carla M. T. Tiesler, Sven Cichon, Judith Sinzig, Stephen V. Faraone, Anke Hinney, Susann Scherag, Susanne Walitza, Jobst Meyer, Özgür Albayrak, Maria R. Dauvermann

المساهمون: Psychiatrie & Neuropsychologie, RS: MHeNs - R3 - Neuroscience, University of Zurich, Hinney, Anke

المصدر: Molecular Psychiatry, 19(1), 115-121. Nature Publishing Group
Molecular Psychiatry
Jarick, I; Volckmar, A-L; Pütter, C; Pechlivanis, S; Nguyen, T T; Dauvermann, M R; Beck, S; Albayrak, O; Scherag, S; Gilsbach, S; Cichon, S; Hoffmann, P; Degenhardt, F; Nöthen, M M; Schreiber, S; Wichmann, H-E; Jöckel, K-H; Heinrich, J; Tiesler, C M T; Faraone, S V; ... (2014). Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder. Molecular psychiatry, 19(1), pp. 115-121. Basingstoke: Nature Publishing Group 10.1038/mp.2012.161 <http://dx.doi.org/10.1038/mp.2012.161Test>
Molecular psychiatry 19(1), 115-121 (2012). doi:10.1038/mp.2012.161
Mol. Psychiatry 19, 115–121 (2014)

مصطلحات موضوعية: Male, Candidate gene, Medizin, 2804 Cellular and Molecular Neuroscience, parkin protein, Genome-wide association study, genetics [Attention Deficit Disorder with Hyperactivity], 2738 Psychiatry and Mental Health, 0302 clinical medicine, Neurodevelopmental disorder, GWAS, Copy-number variation, Child, Genetics, genetics [Ubiquitin-Protein Ligases], 0303 health sciences, ADHD, children, CNVs, PARK2, Middle Aged, 10058 Department of Child and Adolescent Psychiatry, 3. Good health, Psychiatry and Mental health, Female, Original Article, Adult, Adolescent, DNA Copy Number Variations, genetics [DNA Copy Number Variations], Ubiquitin-Protein Ligases, Locus (genetics), 610 Medicine & health, Biology, Polymorphism, Single Nucleotide, Community Health Planning, 03 medical and health sciences, Cellular and Molecular Neuroscience, mental disorders, medicine, Genetic predisposition, 1312 Molecular Biology, Attention deficit hyperactivity disorder, Humans, Genetic Predisposition to Disease, ddc:610, Molecular Biology, 030304 developmental biology, Genetic association, Aged, medicine.disease, Attention Deficit Disorder with Hyperactivity, 030217 neurology & neurosurgery, Genome-Wide Association Study

وصف الملف: application/pdf; Jarick_2012,_Genome-wide_analysis_of_rare_copy_number_variations.pdf - application/pdf; application/octet-stream

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4c7700e4c5d4a3b6b2d4ffacd22714aTest
https://cris.maastrichtuniversity.nl/en/publications/d8e7b4df-ec04-41e4-bd62-b0381415a8aaTest

المؤلفون: Stephanie Le Hellard, Vidar M. Steen, Benno G. Schimmelmann, Ole A. Andreassen, Michael Conlon O'Donovan, Markus M. Nöthen, Clive R. Bramham, Özgür Albayrak, Anke Hinney, Sven Cichon, Judith Sinzig, Andreas Warnke, Andrea Christoforou, Michael John Owen, Thomas W. Mühleisen, Jan Haavik, André Scherag, Franziska Degenhardt, Sudheer Giddaluru, Marcella Rietschel, Stefan Johansson, Johannes Hebebrand, Kari Merete Ersland, Bjarte Håvik, Nicholas John Craddock, Srdjan Djurovic, Thomas Werge, Helle Lybæk, Carla P. D. Fernandes, Beate Herpertz-Dahlmann, Manuel Mattheisen, Tobias J. Renner

المصدر: PLoS one 7(4), e35424 (2012). doi:10.1371/journal.pone.0035424
PLoS ONE, Vol 7, Iss 4, p e35424 (2012)
PLOS ONE 7(4), e35424 (2012). doi:10.1371/journal.pone.0035424
Håvik, Bjarte; Degenhardt, Franziska A; Johansson, Stefan; Fernandes, Carla P D; Hinney, Anke; Scherag, André; Lybæk, Helle; Djurovic, Srdjan; Christoforou, Andrea; Ersland, Kari M; Giddaluru, Sudheer; O'Donovan, Michael C; Owen, Michael J; Craddock, Nick; Mühleisen, Thomas W; Mattheisen, Manuel; Schimmelmann, Benno G; Renner, Tobias; Warnke, Andreas; Herpertz-Dahlmann, Beate; ... (2012). DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder. PLoS ONE, 7(4), e35424. Lawrence, Kans.: Public Library of Science 10.1371/journal.pone.0035424 <http://dx.doi.org/10.1371/journal.pone.0035424Test>
PLoS ONE

مصطلحات موضوعية: Bipolar Disorder, Medizin, Genome-wide association study, genetics [Attention Deficit Disorder with Hyperactivity], Doublecortin-Like Kinases, Cognition, 0302 clinical medicine, Polymorphism (computer science), Neurobiology of Disease and Regeneration, Odds Ratio, genetics [Schizophrenia], Psychiatry, Genetics, 0303 health sciences, Multidisciplinary, ddc:618, DCLK1 protein, human, metabolism [Protein-Serine-Threonine Kinases], Intracellular Signaling Peptides and Proteins, Genomics, Protein-Serine-Threonine Kinases, Mental Health, Phenotype, Schizophrenia, Medicine, ddc:500, metabolism [Intracellular Signaling Peptides and Proteins], Research Article, Genotype, Cognitive Neuroscience, Science, Neuropsychiatric Disorders, Single-nucleotide polymorphism, Protein Serine-Threonine Kinases, Biology, Polymorphism, Single Nucleotide, genetics [Protein-Serine-Threonine Kinases], 03 medical and health sciences, Developmental Neuroscience, Genome Analysis Tools, mental disorders, Genome-Wide Association Studies, Genetic predisposition, medicine, Attention deficit hyperactivity disorder, Humans, Genetic Predisposition to Disease, Bipolar disorder, ddc:610, QH426, 030304 developmental biology, Mood Disorders, Computational Biology, medicine.disease, R1, Introns, Attention Deficit Disorder with Hyperactivity, RC0321, genetics [Intracellular Signaling Peptides and Proteins], Verbal memory, 030217 neurology & neurosurgery, genetics [Bipolar Disorder], Neuroscience, Synaptic Plasticity, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5346bc3a71a18cb2f80a8c01637ae42Test
https://hdl.handle.net/1956/6478Test