المؤلفون: Daniel Lancour, Josée Dupuis, Richard Mayeux, Jonathan L. Haines, Margaret A. Pericak-Vance, Gerard C. Schellenberg, Mark Crovella, Lindsay A. Farrer, Simon Kasif

المصدر: Alzheimer’s Research & Therapy, Vol 12, Iss 1, Pp 1-11 (2020)

مصطلحات موضوعية: Alzheimer disease, Gene network analysis, Brain regions, Genome-wide association study, EPS8, HSPA2, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

Relation: http://link.springer.com/article/10.1186/s13195-020-00674-7; https://doaj.org/toc/1758-9193

URL الوصول: https://doaj.org/article/a030cad76a4049c59eb4f3bca41ab8df

المؤلفون: Mark W. Logue, Daniel Lancour, John Farrell, Irina Simkina, M. Daniele Fallin, Kathryn L. Lunetta, Lindsay A. Farrer

المصدر: Frontiers in Neuroscience, Vol 12 (2018)

مصطلحات موضوعية: Alzheimer disease, sequencing, AKAP9, ABCA7, rare variant, African Americans, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/article/10.3389/fnins.2018.00592/full; https://doaj.org/toc/1662-453X

URL الوصول: https://doaj.org/article/899c255a48eb4d5a93b05869a441b32a

المؤلفون: Daniel Lancour, Adam Naj, Richard Mayeux, Jonathan L Haines, Margaret A Pericak-Vance, Gerard D Schellenberg, Mark Crovella, Lindsay A Farrer, Simon Kasif

المصدر: PLoS Genetics, Vol 14, Iss 4, p e1007306 (2018)

مصطلحات موضوعية: Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://europepmc.org/articles/PMC5933817?pdf=render; https://doaj.org/toc/1553-7390; https://doaj.org/toc/1553-7404

URL الوصول: https://doaj.org/article/239ce9c373814543a12a06c57a98aee4

المؤلفون: Richard Mayeux, Daniel Lancour, Jonathan L. Haines, Gerard C. Schellenberg, Mark Crovella, Lindsay A. Farrer, Margaret A. Pericak-Vance, Josée Dupuis, Simon Kasif

المصدر: Alzheimer's Research & Therapy
Alzheimer’s Research & Therapy, Vol 12, Iss 1, Pp 1-11 (2020)

مصطلحات موضوعية: 0301 basic medicine, Genome-wide association study, Cognitive Neuroscience, HSPA2, Gene regulatory network, Computational biology, Biology, EPS8, lcsh:RC346-429, lcsh:RC321-571, 03 medical and health sciences, 0302 clinical medicine, Alzheimer Disease, Gene expression, medicine, Cluster Analysis, Humans, Gene, lcsh:Neurosciences. Biological psychiatry. Neuropsychiatry, Gene knockout, lcsh:Neurology. Diseases of the nervous system, Adaptor Proteins, Signal Transducing, Gene Expression Profiling, Research, Neurodegeneration, Brain atlas, Brain, medicine.disease, Gene network analysis, 030104 developmental biology, Neurology, Neurology (clinical), Alzheimer's disease, 030217 neurology & neurosurgery, Brain regions

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9adeac079464c39ca5c0e2c3b4b29235
https://pubmed.ncbi.nlm.nih.gov/32878640

المؤلفون: Joshua C. Bis, Li-San Wang, Waleed Nasser, Giuseppe Tosto, Jean-Charles Lambert, Gary W. Beecham, Lucinda Fulton, Eric Boerwinkle, Reinhold Schmidt, Kara L. Hamilton-Nelson, Josée Dupuis, Cornelia M. van Duijn, Yuning Chen, Stéphanie Debette, Devanshi Patel, Philippe Amouyel, Gaël Nicolas, Farid Rajabli, Mark J. Daly, Richard Redon, Hilkka Soininen, Anita L. DeStefano, Aki S. Havulinna, Weixin Wang, Margaret A. Pericak-Vance, Chloé Sarnowski, Gerard D. Schellenberg, William S. Bush, Eden R. Martin, John J. Farrell, Richard A. Gibbs, Richard Mayeux, Emmanuelle Génin, Yi Zhao, Kwangsik Nho, Céline Bellenguez, Kari Mattila, Jean-François Deleuze, William J Salerno, Alzheimer’s Disease Sequencing, Brian W. Kunkle, Dominique Campion, Mikko Hiltunen, Richard K. Wilson, Sudha Seshadri, Paul K. Crane, Otto Valladares, Jennifer E. Below, Adam C. Naj, Timothy A. Thornton, Stacey Gabriel, Jan Konrad, Markus Perola, Mark Lathrop, Namrata Gupta, Badri N. Vardarajan, Bruce M. Psaty, Seppo Helisalmi, Jonathan L. Haines, Yiyi Ma, Honghuang Lin, Laura B. Cantwell, Carlos Cruchaga, Alan E. Renton, Terho Lehtimäki, Anne M. Remes, Michael A. Schmidt, Benjamin M. Neale, M. Arfan Ikram, Lindsay A. Farrer, Myriam Fornage, Daniel P. Howrigan, Ellen M. Wijsman, Mitja I. Kurki, Helena Schmidt, Aarno Palotie, Daniel Lancour, Camille Charbonnier, Daniela Witten, Liming Qu, Najaf Amin, Eric S. Lander, Alison Goate, Donna M. Muzny, Kathryn L. Lunetta, Jaakko Kaprio, Edoardo Marcora, Amanda B. Kuzma, Sven J. van der Lee, Shahzad Ahmad, Kim C. Worley, Christophe Tzourio, Benjamin Grenier-Boley, Jean-François Dartigues, L. Adrienne Cupples, Veikko Salomaa, Jaeyoon Chung, Christiane Reitz, Xueqiu Jian, Xiaoling Zhang, Olivier Quenez

المساهمون: Medicum, Institute for Molecular Medicine Finland, Complex Disease Genetics, University of Helsinki, Centre of Excellence in Complex Disease Genetics, Research Programs Unit, Aarno Palotie / Principal Investigator, Genomics of Neurological and Neuropsychiatric Disorders, HUS Helsinki and Uusimaa Hospital District, Facteurs de Risque et Déterminants Moléculaires des Maladies liées au Vieillissement - U 1167 (RID-AGE), Institut Pasteur de Lille, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille), Génomique et Médecine Personnalisée du Cancer et des Maladies Neuropsychiatriques (GPMCND), Université de Rouen Normandie (UNIROUEN), Normandie Université (NU)-Normandie Université (NU)-Institut National de la Santé et de la Recherche Médicale (INSERM), CHU Rouen, Normandie Université (NU), Bordeaux population health (BPH), Université de Bordeaux (UB)-Institut de Santé Publique, d'Épidémiologie et de Développement (ISPED)-Institut National de la Santé et de la Recherche Médicale (INSERM), CHU Bordeaux [Bordeaux], Centre National de Recherche en Génomique Humaine (CNRGH), Commissariat à l'énergie atomique et aux énergies alternatives (CEA), Génétique, génomique fonctionnelle et biotechnologies (UMR 1078) (GGB), EFS-Université de Brest (UBO)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut Brestois Santé Agro Matière (IBSAM), Université de Brest (UBO), Unité de recherche de l'institut du thorax (ITX-lab), Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université de Nantes - UFR de Médecine et des Techniques Médicales (UFR MEDECINE), Université de Nantes (UN)-Université de Nantes (UN), Institut Brestois Santé Agro Matière (IBSAM), Université de Brest (UBO)-Université de Brest (UBO)-EFS-Institut National de la Santé et de la Recherche Médicale (INSERM), unité de recherche de l'institut du thorax UMR1087 UMR6291 (ITX), Université de Nantes - UFR de Médecine et des Techniques Médicales (UFR MEDECINE), Université de Nantes (UN)-Université de Nantes (UN)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Epidemiology

المصدر: Molecular psychiatry
Molecular Psychiatry
Molecular Psychiatry, 2018, 25 (8), pp.1859-1875. ⟨10.1038/s41380-018-0112-7⟩
Molecular Psychiatry, Nature Publishing Group, 2018, 25 (8), pp.1859-1875. ⟨10.1038/s41380-018-0112-7⟩
Molecular Psychiatry, 25(8), 1859-1875. Nature Publishing Group

مصطلحات موضوعية: Male, 0301 basic medicine, DYSBINDIN GENE DTNBP1, Transcription, Genetic, [SDV.NEU.NB]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]/Neurobiology, SORL1, PROTEIN, Diseases, Genome-wide association study, SUSCEPTIBILITY, [SDV.IMM.II]Life Sciences [q-bio]/Immunology/Innate immunity, DISEASE, ABCA7, 0302 clinical medicine, Exome sequencing, Aged, 80 and over, Genetics, RISK, 3. Good health, Psychiatry and Mental health, [SDV.IMM.IA]Life Sciences [q-bio]/Immunology/Adaptive immunology, Female, RNA, Long Noncoding, Alzheimer's disease, Immunoglobulin gene, EXPRESSION, Kruppel-Like Transcription Factors, Biology, Article, CODING MUTATIONS, 03 medical and health sciences, Cellular and Molecular Neuroscience, Apolipoproteins E, Alzheimer Disease, Exome Sequencing, medicine, Humans, GENOME-WIDE ASSOCIATION, Molecular Biology, Gene, Genotyping, Aged, Amyloid beta-Peptides, Polymorphism, Genetic, [SDV.GEN.GPO]Life Sciences [q-bio]/Genetics/Populations and Evolution [q-bio.PE], Haplotype, Immunity, 3112 Neurosciences, Correction, medicine.disease, 030104 developmental biology, Gene Expression Regulation, Haplotypes, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, Immunoglobulin G, 3111 Biomedicine, 030217 neurology & neurosurgery

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef68fac14439c7451be809c415a34cbd
http://europepmc.org/articles/PMC6375806

المؤلفون: Gerard D. Schellenberg, Alejandro Q. Nato, Daniel C. Koboldt, Kara L. Hamilton-Nelson, Honghuang Lin, Badri N. Vardarajan, Seung Hoan Choi, Alzheimer’s Disease Sequencing, Harkirat Sohi, Cornelia M. van Duijn, John Malamon, Michael A. Schmidt, Daniel Lancour, Fangui Sun, Simon White, Anita L. DeStefano, William J Salerno, Eden R. Martin, Sven J. van der Lee, Bowen Wang, Josée Dupuis, Joshua C. Bis, Li-San Wang, William S. Bush, Sudha Seshadri, Ellen M. Wijsman, Brian W. Kunkle, Adam C. Naj, Namrata Gupta, Amanda B. Kuzma, Najaf Amin, L. Adrienne Cupples, Mohamad Saad, Eric Boerwinkle, Yiyi Ma, Mariusz Butkiewicz

المساهمون: Neurology, Amsterdam Neuroscience - Neurodegeneration, Epidemiology

المصدر: Naj, A C, Lin, H, Vardarajan, B N, White, S, Lancour, D, Ma, Y, Schmidt, M, Sun, F, Butkiewicz, M, Bush, W S, Kunkle, B W, Malamon, J, Amin, N, Choi, S H, Hamilton-Nelson, K L, van der Lee, S J, Gupta, N, Koboldt, D C, Saad, M, Wang, B, Nato, A Q, Sohi, H K, Kuzma, A, Wang, L S, Cupples, L A, van Duijn, C, Seshadri, S, Schellenberg, G D, Boerwinkle, E, Bis, J C, Dupuis, J, Salerno, W J, Wijsman, E M, Martin, E R, DeStefano, A L & Alzheimer's Disease Sequencing Project (ADSP) 2019, ' Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project ', Genomics, vol. 111, no. 4, pp. 808-818 . https://doi.org/10.1016/j.ygeno.2018.05.004
Genomics, 111(4), 808-818. Academic Press Inc.
Genomics, 111(4), 808-818. Academic Press

مصطلحات موضوعية: 0106 biological sciences, Male, Quality Control, Genotype, Genotyping Techniques, Disease, Computational biology, Biology, 01 natural sciences, Article, 03 medical and health sciences, symbols.namesake, Alzheimer Disease, Genetics, Humans, Multiplex, Indel, 030304 developmental biology, Whole genome sequencing, 0303 health sciences, Variant Call Format, Polymorphism, Genetic, Whole Genome Sequencing, Mendelian inheritance, symbols, Female, Algorithms, 010606 plant biology & botany, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::493a2a982f239b630b656e067f1fbc20

المؤلفون: Lindsay A. Farrer, Gerard C. Schellenberg, Jonathan L. Haines, Daniel Lancour, Simon Kasif, Adam C. Naj, Mark Crovella, Margaret A. Pericak-Vance, Richard Mayeux

المصدر: PLoS Genetics
PLoS Genetics, Vol 14, Iss 4, p e1007306 (2018)

مصطلحات موضوعية: 0301 basic medicine, Proteomics, Cancer Research, Support Vector Machine, Gene Identification and Analysis, Datasets as Topic, Genome-wide association study, Genetic Networks, Alzheimer's Disease, Pathology and Laboratory Medicine, Genome, Biochemistry, Risk Factors, Medicine and Health Sciences, Protein Interaction Maps, Immune Response, Genetics (clinical), Neurodegenerative Diseases, Genomics, Neurology, Meta-analysis, Protein Interaction Networks, Alzheimer's disease, Network Analysis, Research Article, Prioritization, Computer and Information Sciences, lcsh:QH426-470, Gene prediction, Immunology, Computational biology, Biology, 03 medical and health sciences, Signs and Symptoms, Diagnostic Medicine, Alzheimer Disease, Mental Health and Psychiatry, medicine, Genetics, Genome-Wide Association Studies, Humans, Gene Prediction, Protein Interactions, Molecular Biology, Gene, Ecology, Evolution, Behavior and Systematics, Inflammation, Biology and Life Sciences, Computational Biology, Proteins, Reproducibility of Results, Human Genetics, medicine.disease, Genome Analysis, Replication (computing), lcsh:Genetics, 030104 developmental biology, Genetics of Disease, Dementia, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::849d57a584ceb70b9d2eea341d1aa083
http://europepmc.org/articles/PMC5933817