المؤلفون: Cabrera-Mendoza B; Genomics of Psychiatric and Neurodegenerative Diseases Laboratory, National Institute of Genomic Medicine (INMEGEN), Mexico City, Mexico; PECEM, Faculty of Medicine, National Autonomous University of Mexico, Mexico City, Mexico., Martínez-Magaña JJ; Genomics of Psychiatric and Neurodegenerative Diseases Laboratory, National Institute of Genomic Medicine (INMEGEN), Mexico City, Mexico; Multidisciplinary Academic Division of Comalcalco, Juárez Autonomous University of Tabasco, Comalcalco, Tabasco, Mexico., Genis-Mendoza AD; Genomics of Psychiatric and Neurodegenerative Diseases Laboratory, National Institute of Genomic Medicine (INMEGEN), Mexico City, Mexico; Psychiatric Care Services, Child Psychiatric Hospital Dr. Juan N Navarro, Mexico City, Mexico., Sarmiento E; Child Psychiatric Hospital Dr. Juan N Navarro, Mexico City, Mexico., Ruíz-Ramos D; Multidisciplinary Academic Division of Health Sciences, Juárez Autonomous University of Tabasco, Villahermosa, Tabasco, Mexico., Tovilla-Zárate CA; Multidisciplinary Academic Division of Jalpa de Méndez, Juárez Autonomous University of Tabasco, Jalpa de Méndez, Tabasco, Mexico., González-Castro TB; Multidisciplinary Academic Division of Jalpa de Méndez, Juárez Autonomous University of Tabasco, Jalpa de Méndez, Tabasco, Mexico., Juárez-Rojop IE; Multidisciplinary Academic Division of Comalcalco, Juárez Autonomous University of Tabasco, Comalcalco, Tabasco, Mexico., García-de la Cruz DD; Multidisciplinary Academic Division of Health Sciences, Juárez Autonomous University of Tabasco, Villahermosa, Tabasco, Mexico., López-Armenta M; Institute of Forensic Sciences (INCIFO),CDMX, Mexico., Real F; Institute of Forensic Sciences (INCIFO),CDMX, Mexico., García-Dolores F; Institute of Forensic Sciences (INCIFO),CDMX, Mexico., Flores G; Neuropsychiatry Laboratory, Institute of Physiology, Meritorious Autonomous University of Puebla, Puebla, Mexico., Vázquez-Roque RA; Neuropsychiatry Laboratory, Institute of Physiology, Meritorious Autonomous University of Puebla, Puebla, Mexico., Lanzagorta N; Carracci Medical Group, Mexico City, Mexico., Escamilla M; Department of Psychiatry, School of Medicine, University of Texas Rio Grande Valley, Harlingen, TX, USA., Saucedo-Uribe E; Center of Advanced Neurosciences, Department of Psychiatry, Autonomous University of Nuevo Leon, University Hospital 'Dr. José Eleuterio González', Monterrey, Mexico., Rodríguez-Mayoral O; Palliative Care Unit, National Institute of Cancerology, Mexico city, Mexico., Jiménez-Genchi J; Psychiatric Care Services, Psychiatric Hospital Fray Bernardino Álvarez, Mexico City, Mexico., Castañeda-González C; Psychiatric Care Services, Psychiatric Hospital Fray Bernardino Álvarez, Mexico City, Mexico., Roche-Bergua A; Psychiatric Care Services, Psychiatric Hospital Fray Bernardino Álvarez, Mexico City, Mexico., Nicolini H; Genomics of Psychiatric and Neurodegenerative Diseases Laboratory, National Institute of Genomic Medicine (INMEGEN), Mexico City, Mexico. Electronic address: hnicolini@inmegen.gob.mx.

المصدر: Journal of psychiatric research [J Psychiatr Res] 2020 Apr; Vol. 123, pp. 62-71. Date of Electronic Publication: 2020 Jan 29.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Pergamon Press Country of Publication: England NLM ID: 0376331 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-1379 (Electronic) Linking ISSN: 00223956 NLM ISO Abbreviation: J Psychiatr Res Subsets: MEDLINE

مواضيع طبية MeSH: DNA Methylation* , Multifactorial Inheritance* , Suicidal Ideation* , Suicide, Attempted*, Epigenesis, Genetic ; Humans

المؤلفون: Marees AT; Department of Psychiatry, Amsterdam Medical Center, Amsterdam, The Netherlands.; Inserm, UMR-S 1144, Paris, France.; Université Paris Descartes, UMR-S 1144, Paris, France.; Université Paris Diderot, Sorbonne Paris Cité, UMR-S 1144, Paris, France.; QIMR Berghofer, Translational Neurogenomics Group, Brisbane, Australia., de Kluiver H; GGZ inGeest and Department of Psychiatry, Amsterdam Public Health research institute, VU University Medical Center, Amsterdam, The Netherlands., Stringer S; Department of Complex Trait Genetics, VU University, Amsterdam, The Netherlands., Vorspan F; Department of Psychiatry, Amsterdam Medical Center, Amsterdam, The Netherlands.; Inserm, UMR-S 1144, Paris, France.; Université Paris Descartes, UMR-S 1144, Paris, France.; Université Paris Diderot, Sorbonne Paris Cité, UMR-S 1144, Paris, France.; Service de Médecine Addictologique, APHP, Hôpital Fernand Widal, Paris, France.; Faculté de Médecine, Université Paris Diderot, Paris, France., Curis E; Université Paris Descartes, UMR-S 1144, Paris, France.; Laboratoire de biomathématiques, faculté de pharmacie de Paris, Université Paris Descartes, Paris, France.; Service de biostatistiques et informatique médicales, Hôpital Saint-Louis, APHP, Paris, France., Marie-Claire C; Inserm, UMR-S 1144, Paris, France.; Université Paris Descartes, UMR-S 1144, Paris, France.; Université Paris Diderot, Sorbonne Paris Cité, UMR-S 1144, Paris, France., Derks EM; Department of Psychiatry, Amsterdam Medical Center, Amsterdam, The Netherlands.; QIMR Berghofer, Translational Neurogenomics Group, Brisbane, Australia.

المصدر: International journal of methods in psychiatric research [Int J Methods Psychiatr Res] 2018 Jun; Vol. 27 (2), pp. e1608. Date of Electronic Publication: 2018 Feb 27.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 9111433 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1557-0657 (Electronic) Linking ISSN: 10498931 NLM ISO Abbreviation: Int J Methods Psychiatr Res Subsets: MEDLINE

مواضيع طبية MeSH: Data Interpretation, Statistical* , Guidelines as Topic* , Multifactorial Inheritance* , Quality Control*, Genome-Wide Association Study/*methods , Polymorphism, Single Nucleotide/*genetics , Risk Assessment/*methods, Humans

المؤلفون: Chaudhury S; Human Genetics Group, University of Nottingham, Nottingham, UK., Patel T; Human Genetics Group, University of Nottingham, Nottingham, UK., Barber IS; Human Genetics Group, University of Nottingham, Nottingham, UK., Guetta-Baranes T; Human Genetics Group, University of Nottingham, Nottingham, UK., Brookes KJ; Human Genetics Group, University of Nottingham, Nottingham, UK., Chappell S; Human Genetics Group, University of Nottingham, Nottingham, UK., Turton J; Human Genetics Group, University of Nottingham, Nottingham, UK., Guerreiro R; Department of Molecular Neuroscience, Institute of Neurology, University College London, London, UK; Department of Medical Sciences, Institute of Biomedicine-iBiMED, University of Aveiro, Aveiro, Portugal; UK Dementia Research Institute at UCL (UK DRI), London, UK., Bras J; Department of Molecular Neuroscience, Institute of Neurology, University College London, London, UK; Department of Medical Sciences, Institute of Biomedicine-iBiMED, University of Aveiro, Aveiro, Portugal; UK Dementia Research Institute at UCL (UK DRI), London, UK., Hernandez D; Laboratory of Neurogenetics, National Institute of Aging, National Institute of Health, Bethesda, MD, USA., Singleton A; Laboratory of Neurogenetics, National Institute of Aging, National Institute of Health, Bethesda, MD, USA., Hardy J; Department of Molecular Neuroscience, Institute of Neurology, University College London, London, UK; UK Dementia Research Institute at UCL (UK DRI), London, UK., Mann D; Faculty of Medical and Human Sciences, Institute of Brain, Behaviour and Mental Health, University of Manchester, Manchester, UK., Morgan K; Human Genetics Group, University of Nottingham, Nottingham, UK. Electronic address: kevin.morgan@nottingham.ac.uk.

مؤلفون مشاركون: ARUK Consortium

المصدر: Neurobiology of aging [Neurobiol Aging] 2018 Feb; Vol. 62, pp. 244.e1-244.e8. Date of Electronic Publication: 2017 Oct 10.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Elsevier Country of Publication: United States NLM ID: 8100437 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1558-1497 (Electronic) Linking ISSN: 01974580 NLM ISO Abbreviation: Neurobiol Aging Subsets: MEDLINE

مواضيع طبية MeSH: Genome-Wide Association Study* , Multifactorial Inheritance*, Alzheimer Disease/*diagnosis , Alzheimer Disease/*genetics , Apolipoproteins E/*genetics, Aged ; Alleles ; Cohort Studies ; Female ; Gene-Environment Interaction ; Genome, Human/genetics ; Genotyping Techniques/methods ; Humans ; Logistic Models ; Male ; Middle Aged ; Phenotype ; Polymorphism, Single Nucleotide ; Risk

المؤلفون: Gunter Kenis, Edwin van Dellen, Martijn Arns, Tom K. Birkenhäger, Esmée Verwijk, Bochao Lin, Iris E. C. Sommer, Metten Somers, Linda van Diermen, Bart P. F. Rutten, Dore Loef, Karen M. Ryan, Suzanne C. van Bronswijk, Bernhard T. Baune, Declan M. McLoughlin, Jasper O. Nuninga, Eric van Exel, Mardien L. Oudega, Marco P. Boks, Jurjen J. Luykx, D Rhebergen, Baer Arts, Philip van Eijndhoven, Geert Schurgers, Annemiek Dols, Didier Schrijvers, Sinan Guloksuz, Sigfried Schouws

المساهمون: Amsterdam Neuroscience - Mood, Anxiety, Psychosis, Stress & Sleep, Psychiatry, APH - Aging & Later Life, APH - Mental Health, Amsterdam Neuroscience - Neurodegeneration, Neurology, Psychiatrie & Neuropsychologie, MUMC+: MA Med Staf Spec Psychiatrie (9), RS: FPN CPS III, Section Clinical Psychology, RS: MHeNs - R3 - Neuroscience, MUMC+: MA Niet Med Staf Psychiatrie (9), Basic Neuroscience 1, MUMC+: MA AIOS Psychiatrie (9), RS: MHeNs - R2 - Mental Health, Psychiatry 1, MUMC+: MA Psychiatrie (3), Cognition, RS: FPN CN 4, Medical Psychology, Adult Psychiatry, Movement Disorder (MD), Clinical Cognitive Neuropsychiatry Research Program (CCNP), Brein en Cognitie (Psychologie, FMG)

المصدر: Biological Psychiatry, 91(6), 531-539. Elsevier USA
Biological Psychiatry, 91(9), S55-S55. Elsevier Science
Luykx, J J, Loef, D, Lin, B, van Diermen, L, Nuninga, J O, van Exel, E, Oudega, M L, Rhebergen, D, Schouws, S N T M, van Eijndhoven, P, Verwijk, E, Schrijvers, D, Birkenhager, T K, Ryan, K M, Arts, B, van Bronswijk, S C, Kenis, G, Schurgers, G, Baune, B T, Arns, M, van Dellen, E E, Somers, M, Sommer, I E C, Boks, M P, Gülöksüz, S, McLoughlin, D M, Dols, A & Rutten, B P F 2022, ' Interrogating Associations Between Polygenic Liabilities and Electroconvulsive Therapy Effectiveness ', Biological Psychiatry, vol. 91, no. 6, pp. 531-539 . https://doi.org/10.1016/j.biopsych.2021.10.013
Biological Psychiatry, 91, 6, pp. 531-539
Biological Psychiatry, 91(6), 531-539. Elsevier Inc.
Biological psychiatry
Biological Psychiatry, 91(6), 531-539. Elsevier Science
Biological psychiatry. Elsevier USA
Maastricht University
Biological Psychiatry, 91, 531-539
Biological Psychiatry, 91(6), 531-539. ELSEVIER SCIENCE INC
Biological Psychiatry, 91(6), 531-539. Elsevier

مصطلحات موضوعية: Multifactorial Inheritance, medicine.medical_treatment, Stress-related disorders Donders Center for Medical Neuroscience [Radboudumc 13], Polygenic liabilities, behavioral disciplines and activities, Electroconvulsive therapy, All institutes and research themes of the Radboud University Medical Center, Rating scale, Linear regression, mental disorders, Medicine, Humans, RATING-SCALE, Electroconvulsive Therapy, Depression (differential diagnoses), Biological Psychiatry, POPULATION, Depressive Disorder, Major, Electroconvulsive Therapy - ECT, business.industry, Depression, Polygenic Risk Score (PRS), MAJOR DEPRESSION, Explained variation, medicine.disease, Antidepressive Agents, Treatment Outcome, Schizophrenia, Major depressive disorder, Antidepressant, Human medicine, business, Clinical psychology, Electroconvulsive therapy (ECT)

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12dad662e4aff1b3a838fc55b82fb838
https://pubmed.ncbi.nlm.nih.gov/34955169

المؤلفون: Sebastian Lundström, Marjo-Riitta Järvelin, Henning Tiemeier, Cathryn M. Lewis, Ville Karhunen, Andrea G. Allegrini, Ralf Kuja-Halkola, Jouke-Jan Hottenga, Anita Thapar, Bart M. L. Baselmans, Alexandra Havdahl, Helga Ask, Eshim S. Jami, Martin Steen Tesli, Fernando Rivadeneira, Elizabeth W Diemer, Christel M. Middeldorp, Per Magnus, Wonuola A. Akingbuwa, Ragna Bugge Askeland, Ted Reichborn-Kjennerud, Hamdi Mbarek, Kaili Rimfeld, Fiona A. Hagenbeek, Michel G. Nivard, Eivind Ystrom, Paul Lichtenstein, Marcus R. Munafò, Gerome Breen, Robert Plomin, Anke R. Hammerschlag, Hannah M Sallis, Catharina E. M. van Beijsterveldt, Meike Bartels, Dorret I. Boomsma

المساهمون: Biological Psychology, APH - Health Behaviors & Chronic Diseases, APH - Mental Health, APH - Personalized Medicine, APH - Methodology, Commission of the European Communities, Child and Adolescent Psychiatry / Psychology, Epidemiology, Internal Medicine

المصدر: JAMA Psychiatry, 77(7), 715-728. American Medical Association
Akingbuwa, W A, Hammerschlag, A R, Jami, E S, Allegrini, A G, Karhunen, V, Sallis, H, Ask, H, Askeland, R B, Baselmans, B, Diemer, E, Hagenbeek, F A, Havdahl, A, Hottenga, J-J, Mbarek, H, Rivadeneira, F, Tesli, M, van Beijsterveldt, C, Breen, G, Lewis, C M, Thapar, A, Boomsma, D I, Kuja-Halkola, R, Reichborn-Kjennerud, T, Magnus, P, Rimfeld, K, Ystrom, E, Jarvelin, M-R, Lichtenstein, P, Lundstrom, S, Munafò, M R, Plomin, R, Tiemeier, H, Nivard, M G, Bartels, M, Middeldorp, C M & and the Bipolar Disorder and Major Depressive Disorder Working Groups of the Psychiatric Genomics Consortium 2020, ' Genetic Associations Between Childhood Psychopathology and Adult Depression and Associated Traits in 42 998 Individuals : A Meta-analysis ', JAMA Psychiatry, vol. 77, no. 7, pp. 715-728 . https://doi.org/10.1001/jamapsychiatry.2020.0527
Akingbuwa, W, Hammerschlag, A, Jami, E, Allegrini, A, Karhunen, V, Sallis, H M, Ask, H, Askeland, R B, Baselmans, B M L, Diemer, E, Hagenbeek, F, Havdahl, K A, Hottenga, J-J, Mbarek, H, Rivadeneira, F, Tesli, M, van Beijsterveldt, C, Breen, G, Lewis, C, Thapar, A, Boomsma, D, Kuja-Halkola, R, Reichborn-Kjennerud, T, Magnus, P, Rimfeld, K, Ystrom, E, Järvelin, M-R, Lichtenstein, P, Lundström, S, Munafo, M R, Plomin, R, Tiemeier, HW, Nivard, M, Bartels, M & Middeldorp, C M 2020, ' Genetic Associations Between Childhood Psychopathology and Adult Depression and Associated Traits in 42 998 Individuals : A Meta-Analysis ', JAMA Psychiatry . https://doi.org/10.1001/jamapsychiatry.2020.0527
Print: 2168-622X
Akingbuwa, W A, Hammerschlag, A R, Jami, E S, Baselmans, B, Hagenbeek, F A, Hottenga, J-J, Mbarek, H, Boomsma, D I, Nivard, M G, Bartels, M, Middeldorp, C M & Bipolar Disorder and Major Depressive Disorder Working Groups of the Psychiatric Genomics Consortium 2020, ' Genetic Associations Between Childhood Psychopathology and Adult Depression and Associated Traits in 42 998 Individuals : A Meta-Analysis ', JAMA Psychiatry, vol. 77, no. 7, pp. 715-728 . https://doi.org/10.1001/jamapsychiatry.2020.0527
JAMA psychiatry

مصطلحات موضوعية: Netherlands Twin Register (NTR), Multifactorial Inheritance, Bipolar Disorder, 1702 Cognitive Sciences, Behavioral Symptoms, Personal Satisfaction, POLYGENIC SCORES, Body Mass Index, 0302 clinical medicine, Sleep Initiation and Maintenance Disorders, Medicine, Longitudinal Studies, RATING-SCALE, Child, MoBa, Psychiatry, RISK, Generation R, ATTENTION-DEFICIT/HYPERACTIVITY DISORDER, and the Bipolar Disorder and Major Depressive Disorder Working Groups of the Psychiatric Genomics Consortium, PSYCHIATRIC-DISORDERS, ALSPAC, Neuroticism, 3. Good health, Europe, TEDS, Psychiatry and Mental health, Major depressive disorder, Educational Status, Life Sciences & Biomedicine, Developmental psychopathology, Psychopathology, Clinical psychology, Adult, Adolescent, Child psychopathology, polygenic risk score (PRS), Childhood psychopathology, NTR, BF, CATSS, 03 medical and health sciences, Young Adult, Genetics, Attention deficit hyperactivity disorder, Humans, Bipolar disorder, GENOME-WIDE ASSOCIATION, Social Behavior, MODEL SELECTION, EDUCATIONAL-ATTAINMENT, Depressive Disorder, Major, Science & Technology, business.industry, MAJOR DEPRESSION, NFBC86, medicine.disease, 030227 psychiatry, Mood disorders, 1701 Psychology, Attention Deficit Disorder with Hyperactivity, RC0321, business, 030217 neurology & neurosurgery, Meta analysis, 1199 Other Medical and Health Sciences

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf84a09fd8fc811e6599be688015514f
https://research.vu.nl/en/publications/1ecd9566-2da2-4e34-bc4d-c8b35fef6a63

المؤلفون: Evie Stergiakouli, Hannah M Sallis, Debbie A Lawlor, George Davey Smith, Jack Euesden, Kate Tilling, Marcus R. Munafò, Amy E Taylor, Stanley Zammit, Neil M Davies, Hannah J. Jones

المصدر: Taylor, A, Jones, H, Sallis, H, Davey Smith, G, Lawlor, D, Davies, N, Stergiakouli, E, Munafo, M, Euesden, J, Tilling, K & Zammit, S 2018, ' Exploring the association of genetic factors with participation in the Avon Longitudinal Study of Parents and Children ', International Journal of Epidemiology, vol. 47, no. 4, dyy060, pp. 1207-1216 . https://doi.org/10.1093/ije/dyy060
International Journal of Epidemiology

مصطلحات موضوعية: Male, 0301 basic medicine, Multifactorial Inheritance, Longitudinal study, Adolescent, Epidemiology, Genome-wide association study, Brain and Behaviour, Polymorphism, Single Nucleotide, Body Mass Index, Young Adult, missing data, 03 medical and health sciences, MISSING DATA, Risk Factors, Mendelian randomization, Humans, Medicine, participation, GWAS, Genetic Predisposition to Disease, selection bias, genetics, Longitudinal Studies, Child, Genetic association, 2. Zero hunger, business.industry, Infant, Newborn, Genetic Variation, Infant, General Medicine, Odds ratio, Heritability, ALSPAC, Neuroticism, United Kingdom, Polygenic risk score (PRS), 030104 developmental biology, Child, Preschool, Genetic Epidemiology, Female, business, Body mass index, Genome-Wide Association Study, Demography

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00ef3a54432a72e88325382cb5c8f4b4
https://orca.cardiff.ac.uk/id/eprint/111862/1/dyy060.pdf

المؤلفون: Jari Lipsanen, Timo E. Strandberg, Katri Räikkönen, Johan G. Eriksson, Sture Andersson, Eero Kajantie, Jari Lahti, Siddheshwar Utge, Rebecca M. Reynolds

المساهمون: Medicum, Department of Psychology and Logopedics, Lastentautien yksikkö, Children's Hospital, Clinicum, HUS Children and Adolescents, Timo Strandberg / Principal Investigator, Department of Medicine, Geriatrian yksikkö, HUS Internal Medicine and Rehabilitation, Johan Eriksson / Principal Investigator, Department of General Practice and Primary Health Care, Helsinki University Hospital Area, Helsinki Collegium for Advanced Studies, Developmental Psychology Research Group, Teachers' Academy

المصدر: Utge, S, Räikkönen, K, Kajantie, E, Lipsanen, J, Andersson, S, Strandberg, T, Reynolds, R, Eriksson, J G & Lahti, J 2018, ' Polygenic risk score of SERPINA6/SERPINA1 associates with diurnal and stress-induced HPA axis activity in children ', Psychoneuroendocrinology . https://doi.org/10.1016/j.psyneuen.2018.04.009

مصطلحات موضوعية: Male, SALIVARY CORTISOL, Multifactorial Inheritance, Hydrocortisone, Endocrinology, Diabetes and Metabolism, Pituitary-Adrenal System, FATIGUE, 0302 clinical medicine, Endocrinology, Transcortin, Gene Frequency, Risk Factors, Trier social stress test, Child, LICORICE CONSUMPTION, Morning, biology, SERPINA6, Circadian Rhythm, Psychiatry and Mental health, SERPINA2, SERPINA1, Female, medicine.medical_specialty, Hypothalamo-Hypophyseal System, Globulin, 515 Psychology, PSYCHOSOCIAL STRESS, Stress, Polymorphism, Single Nucleotide, 03 medical and health sciences, HORMONE, CORTISOL RESPONSE, Internal medicine, Genetic variation, medicine, Humans, GLUCOCORTICOIDS, CORTICOSTEROID-BINDING GLOBULIN, Saliva, Genotyping, POLYMORPHISMS, Biological Psychiatry, Alleles, Endocrine and Autonomic Systems, Genetic Variation, GENE, 030227 psychiatry, Polygenic risk score (PRS), alpha 1-Antitrypsin, biology.protein, Polygenic risk score, 030217 neurology & neurosurgery, Stress, Psychological, Hormone, Genome-Wide Association Study

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65a77b978c87b0d810ce73800b96bb3c
https://www.pure.ed.ac.uk/ws/files/69369686/Polygenic_risk_score.pdf

المؤلفون: Eske M. Derks, Andries T. Marees, Hilde de Kluiver, Cynthia Marie-Claire, Florence Vorspan, Sven Stringer, Emmanuel Curis

المساهمون: Optimisation Thérapeutique en Neuropsychopharmacologie (VariaPsy - U1144), Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Diderot - Paris 7 (UPD7), Université Paris Descartes - Paris 5 (UPD5), Université Paris Diderot - Paris 7 (UPD7), Université Sorbonne Paris Cité (USPC), Groupe Hospitalier Saint Louis - Lariboisière - Fernand Widal [Paris], Assistance publique - Hôpitaux de Paris (AP-HP) (APHP), Université Paris Descartes - Faculté de Pharmacie de Paris (UPD5 Pharmacie), Service de biostatistique et information médicale de l’hôpital Saint Louis (Equipe ECSTRA) (SBIM), Université Paris Diderot - Paris 7 (UPD7)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut national du cancer [Boulogne] (INCA)-CHU Saint Louis [APHP], QIMR Berghofer Medical Research Institute, Variabilité de réponse aux Psychotropes (VariaPsy - U1144), Université Paris Diderot - Paris 7 (UPD7)-Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Hopital Saint-Louis [AP-HP] (AP-HP), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Institut national du cancer [Boulogne] (INCA)-Université Paris Diderot - Paris 7 (UPD7)-Institut National de la Santé et de la Recherche Médicale (INSERM), APH - Mental Health, Psychiatry, Amsterdam Neuroscience - Complex Trait Genetics, Graduate School, Adult Psychiatry, ANS - Complex Trait Genetics, Complex Trait Genetics, Biological Psychology

المصدر: International Journal of Methods in Psychiatric Research
International Journal of Methods in Psychiatric Research, Wiley, 2018, 27 (2), ⟨10.1002/mpr.1608⟩
Marees, A T, de Kluiver, H, Stringer, S, Vorspan, F, Curis, E, Marie-Claire, C & Derks, E M 2018, ' A tutorial on conducting genome-wide association studies: Quality control and statistical analysis ', International Journal of Methods in Psychiatric Research, vol. 27, no. 2, e1608 . https://doi.org/10.1002/mpr.1608
Marees, A T, de Kluiver, H, Stringer, S, Vorspan, F, Curis, E, Marie-Claire, C & Derks, E M 2018, ' A tutorial on conducting genome-wide association studies : Quality control and statistical analysis ', International Journal for Methods in Psychiatric Research, vol. 27, no. 2, e1608, pp. 1-10 . https://doi.org/10.1002/mpr.1608
International Journal of Methods in Psychiatric Research, 27(2):e1608. Wiley-Blackwell
International journal of methods in psychiatric research, 27(2):e1608. Wiley-Blackwell
International Journal for Methods in Psychiatric Research, 27(2):e1608, 1-10. Wiley

مصطلحات موضوعية: 0301 basic medicine, Quality Control, Multifactorial Inheritance, Computer science, polygenic risk score (PRS), media_common.quotation_subject, Control (management), Genome-wide association study, Guidelines as Topic, computer.software_genre, Polymorphism, Single Nucleotide, Risk Assessment, Field (computer science), GitHub, 03 medical and health sciences, tutorial, Software, [SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Genomics [q-bio.GN], Humans, PLINK, Statistical analysis, Quality (business), ComputingMilieux_MISCELLANEOUS, Genetic association, media_common, business.industry, genome-wide association study (GWAS), Data science, Psychiatry and Mental health, 030104 developmental biology, Scripting language, Data Interpretation, Statistical, business, computer, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff446dbd74e558767f269513c95a950f
https://hal.archives-ouvertes.fr/hal-01904753

المؤلفون: Sultan Chaudhury, Tulsi Patel, Imelda S. Barber, Tamar Guetta-Baranes, Keeley J. Brookes, Sally Chappell, James Turton, Rita Guerreiro, Jose Bras, Dena Hernandez, Andrew Singleton, John Hardy, David Mann, Kevin Morgan, Peter Passmore, David Craig, Janet Johnston, Bernadette McGuinness, Stephen Todd, Reinhard Heun, Heike Kölsch, Patrick G. Kehoe, Emma R.L.C. Vardy, Nigel M. Hooper, Stuart Pickering-Brown, Julie Snowden, Anna Richardson, Matthew Jones, David Neary, Jennifer Harris, James Lowe, A. David Smith, Gordon Wilcock, Donald Warden, Clive Holmes

المصدر: Chaudhury, S, Patel, T, Barber, I S, Guetta-Baranes, T, Brookes, K, Chappell, S, Turton, J, Guerreiro, R, Bras, J M, Hernandez, D G, Singleton, A B, Hardy, J, Mann, D & Morgan, K & Kehoe, P 2017, ' Polygenic risk score in postmortem diagnosed sporadic early-onset Alzheimer's disease ', Neurobiology of Aging . https://doi.org/10.1016/j.neurobiolaging.2017.09.035

مصطلحات موضوعية: Male, 0301 basic medicine, Oncology, Apolipoprotein E, Multifactorial Inheritance, Aging, Genotyping Techniques, Disease, Bioinformatics, Cohort Studies, 0302 clinical medicine, Early-onset Alzheimer's disease, education.field_of_study, General Neuroscience, Middle Aged, Sporadic early-onset Alzheimer's disease (sEOAD), Phenotype, Cohort, Female, Risk, medicine.medical_specialty, Genotyping, Population, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, Apolipoproteins E, Alzheimer Disease, Internal medicine, medicine, Humans, Dementia, Allele, education, Alleles, Aged, NeuroChip, Genome, Human, medicine.disease, Polygenic risk score (PRS), NeuroX, Logistic Models, 030104 developmental biology, Gene-Environment Interaction, Neurology (clinical), Geriatrics and Gerontology, 030217 neurology & neurosurgery, Genome-Wide Association Study, Developmental Biology, Sporadic early-onset Alzheimer's disease

وصف الملف: application/pdf; PDF

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c7e73a90a9bdd86d0680c418d8f2939
https://eprints.nottingham.ac.uk/46892/3/2017_PRS_NoA_Revised%20version.pdf

المؤلفون: Hannon, Eilis, Dempster, Emma, Viana, Joana, Burrage, Joe, Smith, Adam R., Macdonald, Ruby, St Clair, David, Mustard, Colette, Breen, Gerome, Therman, Sebastian, Kaprio, Jaakko, Toulopoulou, Timothea, Pol, Hilleke E. Hulshoff, Bohlken, Marc M., Kahn, Rene S., Nenadic, Igor, Hultman, Christina M., Murray, Robin M., Collier, David A., Bass, Nick, Gurling, Hugh, McQuillin, Andrew, Schalkwyk, Leonard, Mill, Jonathan

المساهمون: Clinicum, Jaakko Kaprio / Principal Investigator, Department of Public Health, Institute for Molecular Medicine Finland, Genetic Epidemiology

المصدر: Genome Biology
Hannon, E, Dempster, E, Viana, J, Burrage, J, Smith, A R, Macdonald, R, St Clair, D, Mustard, C, Breen, G, Therman, S, Kaprio, J, Toulopoulou, T, Pol, H E H, Bohlken, M M, Kahn, R S, Nenadic, I, Hultman, C M, Murray, R M, Collier, D A, Bass, N, Gurling, H, McQuillin, A, Schalkwyk, L & Mill, J 2016, ' An integrated genetic-epigenetic analysis of schizophrenia : Evidence for co-localization of genetic associations and differential DNA methylation ', Genome Biology, vol. 17, no. 1, 176 . https://doi.org/10.1186/s13059-016-1041-x
Genome Biology, 17. BioMed Central

مصطلحات موضوعية: DISORDER, Epigenomics, Multifactorial Inheritance, BLOOD, Quantitative Trait Loci, LOCI, GENOTYPE IMPUTATION, DISEASE, 3124 Neurology and psychiatry, INFECTION, Journal Article, Genetics, Humans, GENOME-WIDE ASSOCIATION, CELL-TYPES, RISK, DNA methylation, Genome-wide association study (GWAS), Research, Bayes Theorem, Twins, Monozygotic, 3142 Public health care science, environmental and occupational health, Polygenic risk score (PRS), Phenotype, Epigenome-wide association study (EWAS), Schizophrenia, HUMAN BRAIN-TISSUE, Epigenetics, CpG Islands, 3111 Biomedicine, Genome-Wide Association Study

وصف الملف: image/pdf; application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::2a15611c058416ebf20e21386536747c
http://europepmc.org/articles/PMC5004279