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1دورية أكاديمية
المؤلفون: Shan-Shan Zhang, Lance Larrabee, Andrew H. Chang, Sapna Desai, Lisa Sloan, Xin Wang, Yixuan Wu, Nazia Parvez, Karen Amaratunga, Allison C. Hartman, Abby Whitnall, Joseph Mason, Nicholas P. Barton, Audrey Y. Chu, Jonathan M. Davitte, Adam J. Csakai, Caitlin Vestal Tibbetts, Audrey E. Tolbert, Heather O’Keefe, Jessie Polanco, Joseph Foley, Casey Kmett, Jonathan Kehler, Gabriela Kozejova, Feng Wang, Andrew P. Mayer, Patrick Koenig, Davide Foletti, Steven J. Pitts, Christine G. Schnackenberg
المصدر: Scientific Reports, Vol 14, Iss 1, Pp 1-20 (2024)
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2045-2322
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2دورية أكاديمية
المؤلفون: Marina Sirota, Gonneke Willemsen, Purnima Sundar, Steven J Pitts, Shobha Potluri, Edi Prifti, Sean Kennedy, S Dusko Ehrlich, Jacoline Neuteboom, Cornelis Kluft, Karen E Malone, David R Cox, Eco J C de Geus, Dorret I Boomsma
المصدر: PLoS ONE, Vol 10, Iss 4, p e0120898 (2015)
وصف الملف: electronic resource
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المؤلفون: Karl Heilbron, Jingchunzi Shi, Wei Wang, Adrian M. Jubb, Steven J. Pitts, Sahar V. Mozaffari, Vladimir Vacic, Peng Yue, Xin Wang
المصدر: The Journal of Pathology
مصطلحات موضوعية: 0301 basic medicine, precision medicine, Big data, human genetics, Genome-wide association study, Context (language use), Population health, Pathology and Forensic Medicine, 03 medical and health sciences, 0302 clinical medicine, therapeutic discovery, direct‐to‐consumer, Drug Discovery, GWAS, Humans, Invited Reviews, Invited Review, Drug discovery, business.industry, Genome, Human, Precision medicine, drug development, humanities, Human genetics, 030104 developmental biology, Drug development, 030220 oncology & carcinogenesis, polygenic risk score, Engineering ethics, Psychology, business
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4دورية أكاديمية
المؤلفون: Pierre Fontanillas, Babak Alipanahi, Nicholas A. Furlotte, Michaela Johnson, Catherine H. Wilson, Steven J. Pitts, Robert Gentleman, Adam Auton
المصدر: Nature, Nature Communications. 12(1):1-13
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المؤلفون: Kristi Krebs, Jonas Bovijn, Neil Zheng, Maarja Lepamets, Jenny C. Censin, Tuuli Jürgenson, Dage Särg, Erik Abner, Triin Laisk, Yang Luo, Line Skotte, Frank Geller, Bjarke Feenstra, Wei Wang, Adam Auton, Soumya Raychaudhuri, Tõnu Esko, Andres Metspalu, Sven Laur, Dan M. Roden, Wei-Qi Wei, Michael V. Holmes, Cecilia M. Lindgren, Elizabeth J. Phillips, Reedik Mägi, Lili Milani, João Fadista, Michelle Agee, Stella Aslibekyan, Robert K. Bell, Katarzyna Bryc, Sarah K. Clark, Sarah L. Elson, Kipper Fletez-Brant, Pierre Fontanillas, Nicholas A. Furlotte, Pooja M. Gandhi, Karl Heilbron, Barry Hicks, David A. Hinds, Karen E. Huber, Ethan M. Jewett, Yunxuan Jiang, Aaron Kleinman, Keng-Han Lin, Nadia K. Litterman, Marie K. Luff, Jennifer C. McCreight, Matthew H. McIntyre, Kimberly F. McManus, Joanna L. Mountain, Sahar V. Mozaffari, Priyanka Nandakumar, Elizabeth S. Noblin, Carrie A.M. Northover, Jared O’Connell, Aaron A. Petrakovitz, Steven J. Pitts, G. David Poznik, J. Fah Sathirapongsasuti, Anjali J. Shastri, Janie F. Shelton, Suyash Shringarpure, Chao Tian, Joyce Y. Tung, Robert J. Tunney, Vladimir Vacic, Xin Wang, Amir S. Zare
المساهمون: Institute for Molecular Medicine Finland, University of Helsinki
المصدر: The American Journal of Human Genetics. 107:612-621
مصطلحات موضوعية: 0301 basic medicine, Genome-wide association study, Human leukocyte antigen, HYPERSENSITIVITY REACTIONS, FREQUENCY, BIOBANK, MECHANISMS, PTPN22, 03 medical and health sciences, 0302 clinical medicine, MANAGEMENT, Genetics, medicine, SNP, Allele, METAANALYSIS, Genetics (clinical), business.industry, 1184 Genetics, developmental biology, physiology, ADVERSE DRUG-REACTIONS, POLYMORPHISM, HLA-B, 3. Good health, HLA, Penicillin, 030104 developmental biology, 030220 oncology & carcinogenesis, Pharmacogenomics, Immunology, T-CELLS, business, medicine.drug
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b449294124373a0265767122010de84
https://doi.org/10.1016/j .ajhg.2020.08.008 -
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المؤلفون: Nadia Litterman, Steven J. Micheletti, Janie F. Shelton, Joanna L. Mountain, Michelle Agee, Samantha G. Ancona Esselmann, Sayantan Das, Ethan M. Jewett, S. Clark, A. Petrakovitz, Karl Heilbron, Suyash Shringarpure, Jeffery R. O'Connell, G. David Poznik, Pierre Fontanillas, Kipper Fletez-Brant, Keng-Han Lin, Sahar V. Mozaffari, William A. Freyman, Joyce Y. Tung, Carrie Northover, Anjali J. Shastri, Kimberly F. McManus, Adam Auton, Aaron Kleinman, L. Noblin, P. Gandhi, Xin Wang, Vladimir Vacic, Chao Tian, Karen E. Huber, Jennifer C. McCreight, Yunxuan Jiang, R. Tunney, Robert K. Bell, Sarah L. Elson, Barry W. Hicks, A. Zare, Sandra Beleza, Stella Aslibekyan, David A. Hinds, Meghan E. Moreno, Steven J. Pitts, Kasia Bryc, Matthew H. McIntyre, P. Nandakumar
المصدر: American Journal of Human Genetics
مصطلحات موضوعية: Disembarkation, Variable survival, Present day, migration, identity by descent, Article, 03 medical and health sciences, 0302 clinical medicine, genetics, slave trade, Genetics (clinical), Historical record, 030304 developmental biology, 0303 health sciences, ancestry, Genetic data, population genetics, Forced migration, Geography, Africa, Ethnology, admixture, history, Americas, 030217 neurology & neurosurgery, Regional differences
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f08defb0a0eff823c05e153d1f0c5274
http://europepmc.org/articles/PMC7413858 -
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المؤلفون: Pierre Fontanillas, Babak Alipanahi, Nicholas A. Furlotte, Michaela Johnson, Catherine H. Wilson, 23andMe Research Team, Steven J. Pitts, Robert Gentleman, Adam Auton
المصدر: Nature Communications
Nature Communications, Vol 12, Iss 1, Pp 1-13 (2021)مصطلحات موضوعية: 0301 basic medicine, Oncology, Male, Percentile, Skin Neoplasms, General Physics and Astronomy, Datasets as Topic, Disease, 0302 clinical medicine, Risk Factors, Surveys and Questionnaires, Squamous cell carcinoma, Odds Ratio, Cancer genomics, Longitudinal Studies, Prospective Studies, Family history, Prospective cohort study, Medical History Taking, Melanoma, Skin, Aged, 80 and over, Multidisciplinary, Framingham Risk Score, integumentary system, Incidence, Middle Aged, 030220 oncology & carcinogenesis, Carcinoma, Squamous Cell, Female, Adult, medicine.medical_specialty, Ultraviolet Rays, Science, Risk Assessment, General Biochemistry, Genetics and Molecular Biology, White People, Article, Cancer screening, 03 medical and health sciences, Internal medicine, Direct-To-Consumer Screening and Testing, medicine, Humans, Basal cell carcinoma, Genetic Predisposition to Disease, Aged, Models, Statistical, business.industry, General Chemistry, Odds ratio, medicine.disease, 030104 developmental biology, Cross-Sectional Studies, Carcinoma, Basal Cell, Skin cancer, Neoplasm Recurrence, Local, business, Follow-Up Studies, Genome-Wide Association Study
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المؤلفون: Thomas Van Blarcom, Surabhi Srinivasan, Cendy Valle Oseguera, Sheng Ding, Arvind Rajpal, Purnima Sundar, Yu Yan, Dan McDonough, Zygy Roe-Zurz, Meri Galindo Casas, Wai Ling Cheung, Zea Melton, Shobha Potluri, Javier Chaparro-Riggers, Kevin Lindquist, Wagstrom Christopher R, Wenwu Zhai, Jaume Pons, Andrea Rossi, Steven J. Pitts, Jeffrey Jones, Marina Sirota
المصدر: mAbs, vol 10, iss 2
mAbsمصطلحات موضوعية: 0301 basic medicine, Bispecific antibody, medicine.drug_class, T cell, Immunology, Computational biology, Protein Engineering, Monoclonal antibody, Immunoglobulin light chain, Antibodies, Epitope, 4-1BB, Mice, 03 medical and health sciences, synthetic antibody library, 0302 clinical medicine, Antigen, Peptide Library, Report, Antibodies, Bispecific, medicine, Animals, Humans, Immunology and Allergy, Purification methods, biology, common light chain, Chemistry, high affinity, Pharmacology and Pharmaceutical Sciences, bispecific antibody, manufacturing, 030104 developmental biology, medicine.anatomical_structure, 030220 oncology & carcinogenesis, Public Health and Health Services, biology.protein, Bispecific, Immunoglobulin Light Chains, Immunization, Antibody, Biotechnology
وصف الملف: application/pdf
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المؤلفون: Sarah L. Elson, Joyce Y. Tung, Yunxuan Jiang, Kimberly F. McManus, Joanna L. Mountain, Nadia K. Litterman, Chao Tian, Karen E. Huber, Michelle Agee, G. David Poznik, Sohini Ramachandran, Keng-Han Lin, Pierre Fontanillas, J. Fah Sathirapongsasuti, Adam Auton, Elizabeth S. Noblin, Jennifer C. McCreight, Robert K. Bell, Matthew H. McIntyre, Xin Wang, Barry W. Hicks, Aaron Kleinman, Vladimir Vacic, Samuel Pattillo Smith, Suyash Shringarpure, Nicholas A. Furlotte, Ethan M. Jewett, Katarzyna Bryc, Carrie A.M. Northover, David A. Hinds, Priyanka Nakka, Janie F. Shelton, Steven J. Pitts, Anne H. O’Donnell-Luria
المصدر: American Journal of Human Genetics
مصطلحات موضوعية: 0301 basic medicine, Male, congenital, hereditary, and neonatal diseases and abnormalities, uniparental disomy, Population, Aneuploidy, 030105 genetics & heredity, Runs of Homozygosity, Biology, Identity by descent, Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, Genomic Imprinting, Genetics, medicine, Prevalence, Humans, education, Genetics (clinical), education.field_of_study, runs of homozygosity, Homozygote, medicine.disease, Uniparental disomy, 3. Good health, 030104 developmental biology, Phenotype, Nondisjunction, Autism, Female, identity-by-descent, Chromosome 22
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84b3745c1654fb180bf762c63aaf72d9
https://pubmed.ncbi.nlm.nih.gov/31607426 -
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المؤلفون: Elizabeth S. Noblin, Joanna L. Mountain, Michelle Agee, Sarah L. Elson, Angélica Salatino-Oliveira, Barbara Franke, Diego L. Rovaris, Josep Antoni Ramos-Quiroga, Vladimir Vacic, Tatyana Strekalova, Claiton H.D. Bau, Christian Fadeuilhe, Peter Almos, Mara H. Hutz, David A. Hinds, Henrik Larsson, Jonna Kuntsi, Olga Rivero, Anders D. Børglum, Laura Vilar, Lorena Arribas, Catherine H. Wilson, Marieke Klein, Adam Auton, Anke Hinney, Katarzyna Bryc, Mark A. Bellgrove, Christie L. Burton, J. Fah Sathirapongsasuti, Olga V. Sazonova, Luis Augusto Rohde, Edmund J.S. Sonuga-Barke, Andreas Reif, Ted Reichborn-Kjennerud, Sarah Kittel-Schneider, Anne Halmøy, Bru Cormand, Miquel Casas, Joyce Y. Tung, Robert D. Oades, Matthew H. McIntyre, Nicholas A. Furlotte, Janie F. Shelton, Alysa E. Doyle, Iris Garcia-Martínez, Marta Ribasés, Johannes Hebebrand, Søren Dalsgaard, Tetyana Zayats, María Soler Artigas, Carrie A.M. Northover, Steven J. Pitts, Ole A. Andreassen, Chao Tian, Karen E. Huber, Josephine Elia, Montserrat Corrales, Jennifer C. McCreight, Benjamin M. Neale, Aribert Rothenberger, Sandra K. Loo, Cristina Sánchez-Mora, Stefan Johansson, Hakon Hakonarson, Christian Jacob, Mireia Pagerols, Jan Haavik, Joseph Biederman, Paula Rovira, Rosa Bosch, Alejandro Arias-Vasquez, Stephen V. Faraone, Catharina A. Hartman, Vanesa Richarte, Oliver Grimm, Irwin D. Waldman, Heike Weber, Martine Hoogman, Per M. Knappskog, Aaron Kleinman, Suyash Shringarpure, Jan K. Buitelaar, Philip Asherson, James J. McGough, Emma Sprooten, Russell Schachar, Ditte Demontis, Klaus-Peter Lesch, Nadia K. Litterman, Gemma Martín, Xin Wang, Evgeniy Svirin, Babak Alipanahi, Ziarih Hawi, Tobias Banaschewski, Bruna Santos da Silva, Robert K. Bell, Eugenio H. Grevet, Pierre Fontanillas, Nina Roth Mota, Jennifer Crosbie, Astri J. Lundervold
المساهمون: Psychiatrie & Neuropsychologie, RS: MHeNs - R3 - Neuroscience
المصدر: Rovira, P, Demontis, D, Sánchez-Mora, C, Zayats, T, Klein, M, Mota, N R, Weber, H, Garcia-Martínez, I, Pagerols, M, Vilar-Ribó, L, Arribas, L, Richarte, V, Corrales, M, Fadeuilhe, C, Bosch, R, Martin, G E, Almos, P, Doyle, A E, Grevet, E H, Grimm, O, Halmøy, A, Hoogman, M, Hutz, M, Jacob, C P, Kittel-Schneider, S, Knappskog, P M, Lundervold, A J, Rivero, O, Rovaris, D L, Salatino-Oliveira, A, da Silva, B S, Svirin, E, Sprooten, E, Strekalova, T, Arias-Vasquez, A, Sonuga-Barke, E J S, Asherson, P, Bau, C H D, Buitelaar, J K, Cormand, B, Faraone, S V, Haavik, J, Johansson, S E, Kuntsi, J, Larsson, H, Lesch, K P, Reif, A, Rohde, L A, Casas, M, Børglum, A D, ADHD Working Group of the Psychiatric Genomics Consortium & 23andMe Research Team 2020, ' Shared genetic background between children and adults with attention deficit/hyperactivity disorder ', Neuropsychopharmacology, vol. 45, no. 10, pp. 1617-1626 . https://doi.org/10.1038/s41386-020-0664-5
Neuropsychopharmacology, 45, 1617-1626
Neuropsychopharmacology, 45, 10, pp. 1617-1626
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Neuropsychopharmacology
Dipòsit Digital de la UB
Universidad de Barcelona
Neuropsychopharmacology, 45(10), 1617-1626. Nature Publishing Groupمصطلحات موضوعية: Persistence (psychology), Trastorns per dèficit d'atenció amb hiperactivitat en els infants, SYMPTOMS, LD SCORE REGRESSION, Stress-related disorders Donders Center for Medical Neuroscience [Radboudumc 13], CHILDHOOD, Genome-wide association study, Attention deficit disorder with hyperactivity in children, CA2+-DEPENDENT ACTIVATOR PROTEIN, 0302 clinical medicine, Neurodevelopmental disorder, Child, SECRETION 2, 0303 health sciences, HERITABILITY, 220 Statistical Imaging Neuroscience, Psychiatry and Mental health, Phenotype, Trastorns per dèficit d'atenció amb hiperactivitat en els adults, medicine.symptom, Genetic Background, Clinical psychology, Adult, DEFICIT HYPERACTIVITY DISORDER, Impulsivity, behavioral disciplines and activities, Genetic correlation, Article, 03 medical and health sciences, mental disorders, medicine, Humans, ADHD, Attention deficit hyperactivity disorder, GENOME-WIDE ASSOCIATION, METAANALYSIS, 030304 developmental biology, Genetic association, Pharmacology, Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7], business.industry, medicine.disease, Genetic architecture, Attention Deficit Disorder with Hyperactivity, Impulsive Behavior, Attention deficit, Genetic markers, Attention deficit disorder with hyperactivity in adults, business, 030217 neurology & neurosurgery, Genome-Wide Association Study
وصف الملف: application/pdf
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