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1دورية أكاديمية
المؤلفون: Lee, Young Lim, Bosse, Mirte, Takeda, Haruko, Moreira, Gabriel Costa Monteiro, Karim, Latifa, Druet, Tom, Oget-Ebrad, Claire, Coppieters, Wouter, Veerkamp, Roel F, Groenen, Martien A M, Georges, Michel, Bouwman, Aniek C, Charlier, Carole
المصدر: BMC Genomics, 24 (1), 225 (2023-05-01)
مصطلحات موضوعية: Cattle, Copy number variants, Linkage disequilibrium, Structural variants, Whole genome sequencing, eQTL, POPDC3 protein, human, Muscle Proteins, Cell Adhesion Molecules, Female, Humans, Animals, Genotype, DNA Copy Number Variations, Haplotypes, Polymorphism, Single Nucleotide, Muscle Proteins/genetics, Cell Adhesion Molecules/genetics, Genome, Genomics/methods, Genetics, Biotechnology, Life sciences, Genetics & genetic processes, Sciences du vivant, Génétique & processus génétiques
Relation: https://link.springer.com/content/pdf/10.1186/s12864-023-09259-8.pdf; urn:issn:1471-2164
URL الوصول: https://orbi.uliege.be/handle/2268/303481
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المؤلفون: Daniel J. Smith, Laura M. Lyall, Keira J.A. Johnston, Angela Silveira, Bruna Gigante, Joey Ward, Amy Ferguson, Hugh Watkins, Bengt Sennblad, Anuj Goel, Philippe Giral, Fabrizio Veglia, Breda Cullen, Damiano Baldassarre, Steve E. Humphries, Julia Morris, Anders Hamsten, Elena Tremoli, Donald M. Lyall, Rona J. Strawbridge, Ulf de Faire, Nicholas Graham, Mark E.S. Bailey, Andries J. Smit
المساهمون: University of Glasgow, Università degli Studi di Milano [Milano] (UNIMI), Centro Cardiologico Monzino [Milano], Dpt di Scienze Cliniche e di Comunità [Milano] (DISCCO), Università degli Studi di Milano [Milano] (UNIMI)-Università degli Studi di Milano [Milano] (UNIMI)-Istituti di Ricovero e Cura a Carattere Scientifico (IRCCS), The Institute of Environmental Medicine [Stockholm] (IMM), Karolinska Institutet [Stockholm], Service d’Endocrinologie, Métabolisme et Prévention des Risques Cardio-Vasculaires [CHU Pitié-Salpêtrière], CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Radcliffe Department of Medicine [Oxford], University of Oxford [Oxford], The Wellcome Trust Centre for Human Genetics [Oxford], University College of London [London] (UCL), University of Edinburgh, Stockholm Bioinformatics Center (SBC), Stockholm University, Uppsala University, University Medical Center Groningen [Groningen] (UMCG), University of Groningen [Groningen], Groningen Kidney Center (GKC)
المصدر: Scientific Reports, Vol 9, Iss 1, Pp 1-14 (2019)
Scientific Reports
Scientific Reports, Nature Publishing Group, 2019, 9 (1), ⟨10.1038/s41598-019-43861-9⟩
Scientific Reports, 9:7339. Nature Publishing Group
Morris, J, Bailey, M E S, Baldassarre, D, Cullen, B, de Faire, U, Ferguson, A, Gigante, B, Giral, P, Goel, A, Graham, N, Hamsten, A, Humphries, S E, Johnston, K J A, Lyall, D M, Lyall, L M, Sennblad, B, Silveira, A, Smit, A J, Tremoli, E, Veglia, F, Ward, J, Watkins, H, Smith, D J & Strawbridge, R J 2019, ' Genetic variation in CADM2 as a link between psychological traits and obesity ', Scientific Reports, vol. 9, no. 1, pp. 7339 . https://doi.org/10.1038/s41598-019-43861-9مصطلحات موضوعية: 0301 basic medicine, Male, Bipolar Disorder, [SDV]Life Sciences [q-bio], Obesity/genetics, LOCI, lcsh:Medicine, Genome-wide association study, Bioinformatics, 0302 clinical medicine, Genetics research, lcsh:Science, RISK, Multidisciplinary, Bipolar Disorder/genetics, Endocrine system and metabolic diseases, Middle Aged, Neuroticism, Anxiety Disorders, 3. Good health, INSIGHTS, Cardiovascular diseases, Medical genetics, Major depressive disorder, Female, Cell Adhesion Molecules/genetics, Depressive Disorder, Major/genetics, Medical Genetics, EXPRESSION, medicine.medical_specialty, Quantitative Trait Loci, Quantitative trait locus, Biology, Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, Risk-Taking, [SDV.MHEP.CSC]Life Sciences [q-bio]/Human health and pathology/Cardiology and cardiovascular system, Genetic variation, medicine, Humans, Genetic Predisposition to Disease, Bipolar disorder, Obesity, GENOME-WIDE ASSOCIATION, COMMON, METAANALYSIS, Medicinsk genetik, Aged, [SDV.GEN]Life Sciences [q-bio]/Genetics, Depressive Disorder, Major, ENERGY HOMEOSTASIS, lcsh:R, Genetic Variation, medicine.disease, BODY-MASS INDEX, Affect, 030104 developmental biology, VISUALIZATION, lcsh:Q, Psychiatric disorders, Anxiety Disorders/genetics, Cell Adhesion Molecules, 030217 neurology & neurosurgery
وصف الملف: application/pdf
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المؤلفون: Pasman, Joëlle A., Verweij, Karin J.H., Gerring, Zachary, Stringer, Sven, Sanchez-Roige, Sandra, Treur, Jorien L., Abdellaoui, Abdel, Nivard, Michel G., Baselmans, Bart M.L., Ong, Jue-Sheng, Ip, Hill F., van der Zee, Matthijs D., Bartels, Meike, Day, Felix R., Fontanillas, Pierre, Elson, Sarah L., de Wit, Harriet, Davis, Lea K., MacKillop, James, Derringer, Jaime L., Branje, Susan J.T., Hartman, Catharina A., Heath, Andrew C., van Lier, Pol A.C., Madden, Pamela A.F., Mägi, Reedik, Meeus, Wim, Montgomery, Grant W., Oldehinkel, A.J., Pausova, Zdenka, Ramos-Quiroga, Josep A., Paus, Tomas, Ribases, Marta, Kaprio, Jaakko, Boks, Marco P.M., Bell, Jordana T., Spector, Tim D., Gelernter, Joel, Boomsma, Dorret I., Martin, Nicholas G., MacGregor, Stuart, Perry, John R.B., Palmer, Abraham A., Posthuma, Danielle, Munafò, Marcus R., Gillespie, Nathan A., Derks, Eske M., Vink, Jacqueline M.
المساهمون: Leerstoel Branje, Adolescent development: Characteristics and determinants, Interdisciplinary Centre Psychopathology and Emotion regulation (ICPE)
المصدر: Pasman, J A, Verweij, K J H, Gerring, Z, Stringer, S, Sanchez-Roige, S, Treur, J L, Abdellaoui, A, Nivard, M G, Baselmans, B M L, Ong, J-S, Ip, H F, van der Zee, M D, Bartels, M, Day, F R, Fontanillas, P, Elson, S L, de Wit, H, Davis, L K, MacKillop, J, Derringer, J L, Branje, S J T, Hartman, C A, Heath, A C, van Lier, P A C, Madden, P A F, Mägi, R, Meeus, W, Montgomery, G W, Oldehinkel, A J, Pausova, Z, Ramos-Quiroga, J A, Paus, T, Ribases, M, Kaprio, J, Boks, M P M, Bell, J T, Spector, T D, Gelernter, J, Boomsma, D I, Martin, N G, MacGregor, S, Perry, J R B, Palmer, A A, Posthuma, D, Munafò, M R, Gillespie, N A & Derks, E M & Vink, J M 2018, ' GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal influence of schizophrenia ', Nature Neuroscience, vol. 21, no. 9, pp. 1161-1170 . https://doi.org/10.1038/s41593-018-0206-1
Pasman, JA; Verweij, KJH; Gerring, Z; Stringer, S; Sanchez-Roige, S; Treur, JL; et al.(2018). GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal influence of schizophrenia. Nature Neuroscience, 21(9), 1161-1170. doi: 10.1038/s41593-018-0206-1. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/4692767n
Nature neuroscience, 21(9), 1161-1170. NATURE AMERICA INCمصطلحات موضوعية: Adult, Male, Marijuana Abuse, Adolescent, Genotype, Gene Expression Regulation/genetics, Polymorphism, Single Nucleotide, 23andMe Research Team, Article, Schizophrenia/chemically induced, Marijuana Abuse/genetics, Young Adult, Risk-Taking, Databases, Genetic, Taverne, Humans, International Cannabis Consortium, Genetic Predisposition to Disease, Aged, Aged, 80 and over, Mendelian Randomization Analysis, Middle Aged, Mental Health, Gene Expression Regulation, Schizophrenia, Substance Use Disorders Working Group of the Psychiatric Genomics Consortium, Female, Cell Adhesion Molecules/genetics, Cell Adhesion Molecules, Genome-Wide Association Study
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المؤلفون: Y.V. Sanders, J.G. van der Bom, A. Isaacs, M.H. Cnossen, M.P.M. de Maat, B.A.P. Laros-van Gorkom, K. Fijnvandraat, K. Meijer, C.M. van Duijn, E.P. Mauser-Bunschoten, J. Eikenboom, F.W.G. Leebeek, M. Coppens, A. Kors, J. de Meris, M.R. Nijziel, R.Y.J. Tamminga, P.F. Ypma, F.J.W. Smiers, B. Granzen, K. Hamulyák, P. Brons
المساهمون: RS: CARIM - R1.06 - Genetic Epidemiology and Genomics of cardiovascular diseases, Biochemie, MUMC+: MA Heelkunde (9), Nutrition and Movement Sciences, RS: NUTRIM - R3 - Chronic inflammatory disease and wasting, Hematology, Epidemiology, Pediatrics, ACS - Amsterdam Cardiovascular Sciences, AII - Amsterdam institute for Infection and Immunity, Paediatric Infectious Diseases / Rheumatology / Immunology, Vascular Medicine, Vascular Ageing Programme (VAP), Cardiovascular Centre (CVC), Real World Studies in PharmacoEpidemiology, -Genetics, -Economics and -Therapy (PEGET)
المصدر: Journal of Thrombosis and Haemostasis, 13(6), 956-966
Journal of Thrombosis and Haemostasis, 13, 956-66
Journal of Thrombosis and Haemostasis, 13, 6, pp. 956-66
Journal of Thrombosis and Haemostasis, 13(6), 956. Wiley-Blackwell
Journal of Thrombosis and Haemostasis, 13(6), 956-66. Wiley
Journal of Thrombosis and Haemostasis, 13(6), 956-966. Wiley-Blackwell Publishing Ltd
Journal of thrombosis and haemostasis, 13(6), 956-966. Wiley-Blackwell
Journal of Thrombosis and Haemostasis, 13(6), 956-966. Wileyمصطلحات موضوعية: Receptors, Cell Surface/genetics, Male, single nucleotide, Vascular damage Radboud Institute for Health Sciences [Radboudumc 16], Von Willebrand factor, von Willebrand factor, PHENOTYPE, Gastroenterology, polymorphism, CLINICAL MARKERS, BLOOD-GROUP, 80 and over, Nerve Tissue Proteins/genetics, Child, von Willebrand Factor/analysis, Aged, 80 and over, Blood Coagulation/genetics, Pathophysiology, von Willebrand Disease, Type 1/blood, Child, Preschool, cardiovascular system, Blood Coagulation Tests, medicine.medical_specialty, Type 1/blood, Single-nucleotide polymorphism, Hemorrhage, Receptors, Cell Surface, Lectins, C-Type/genetics, DIAGNOSIS, ABO blood group system, Hemorrhage/blood, Humans, human, Blood Coagulation, Aged, Infant, von Willebrand Disease, Type 2/blood, medicine.disease, Cross-Sectional Studies, CLEC4M protein, Polymorphism, single nucleotide, Cell Adhesion Molecules, Biomarkers, STXBP5 protein, DETERMINANTS, C-Type/genetics, R-SNARE Proteins/genetics, R-SNARE Proteins, Gene Frequency, Risk Factors, Lectins, hemic and lymphatic diseases, Receptors, Non-U.S. Gov't, MCMDM-1VWD, Netherlands, Genetics, RISK, biology, Von Willebrand disease, Research Support, Non-U.S. Gov't, Hematology, Middle Aged, Multicenter Study, Molecular Diagnostic Techniques, Female, Cell Adhesion Molecules/genetics, von Willebrand disease, circulatory and respiratory physiology, Adult, congenital, hereditary, and neonatal diseases and abnormalities, Adolescent, Nerve Tissue Proteins, von Willebrand Disease, Type 2, Research Support, von Willebrand Disease, Type 1, Young Adult, Internal medicine, Genetic variation, medicine, Journal Article, MANAGEMENT, Lectins, C-Type, Genetic Predisposition to Disease, Allele, Preschool, PLASMA-LEVELS, Genetic Association Studies, Cell Surface/genetics, Type 2/blood, business.industry, Confidence interval, THROMBOSIS, STXBP5 protein, human, biology.protein, CLEC4M protein, human, business, Biomarkers/blood
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المؤلفون: Christian Korff, Paul A. McGettigan, Thierry Deonna, Naisha Shah, Dara McCreary, Kevin Collins, Bronwyn Parry-Fielder, Sean Ennis, Sally Ann Lynch, Mary D. King, Judith Conroy, David Webb, Donncha Hanrahan, Margaret M. Moran
المصدر: Epilepsia, Vol. 55, No 6 (2014) pp. 858-65
مصطلحات موضوعية: Adult, Male, Candidate gene, Adolescent, Landau–Kleffner syndrome, Receptor, EphB2, Cell Adhesion Molecules, Neuronal, Serine Endopeptidases/genetics, Twins, Monozygotic/genetics, Nerve Tissue Proteins, Extracellular Matrix Proteins/genetics, Polymorphism, Single Nucleotide, Receptors, N-Methyl-D-Aspartate, Cell Adhesion Molecules, Neuronal/genetics, Young Adult, medicine, Landau-Kleffner Syndrome/genetics, Nerve Tissue Proteins/genetics, Humans, Genetic Predisposition to Disease, Child, Exome sequencing, Oligonucleotide Array Sequence Analysis, Genetics, Comparative Genomic Hybridization, Extracellular Matrix Proteins, Landau-Kleffner Syndrome, ddc:618, Receptors, N-Methyl-D-Aspartate/genetics, Genetic Predisposition to Disease/genetics, Calcium-Binding Proteins, Serine Endopeptidases, Twins, Monozygotic, medicine.disease, Polymorphism, Single Nucleotide/genetics, Receptor, EphB2/genetics, Rolandic epilepsy, Reelin Protein, Neurology, Female, Neurology (clinical), Psychology, Cell Adhesion Molecules/genetics, Cell Adhesion Molecules, Isolated cases
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المؤلفون: A. G. Uitterlinden, S. Y. Shin, Massimo Mangino, N. Dahmen, Lambertus A. Kiemeney, Dorret I. Boomsma, Arfan Ikram, B.A. Oostra, D. F. Gudbjartsson, Germaine C. Verwoert, Aravinda Chakravarti, Vilmundur Gudnason, Stefan Walter, J. C. Keers, Unnur Thorsteinsdottir, F. J.A. Van Rooij, Henning Tiemeier, Grant W. Montgomery, P. Sulem, Rajesh Rawal, Tim D. Spector, Erich Wichmann, Enda M. Byrne, Nicholas G. Martin, J. C. M. Witteman, Sebastian E. Baumeister, Najaf Amin, Christopher J Hammond, C.M. van Duijn, Astrid Petersmann, Julie Johnson, Aaron Isaacs, Georgia Chenevix-Trench, A. C. J. W. Janssens, Alexander Teumer, J. M. Vink, Ilja M. Nolte, Y S Aulchenko, Angela Doering, Linda Broer, A. C. Heath, B. H.R. Wolfenbuttel, Bruce M. Psaty, Harold Snieder, Fernando Rivadeneira, Kari Stefansson, Albert Hofman, Naomi R. Wray, J. J. Hottenga, Hans-Jörgen Grabe, Rainer Biffar, Daniel Levy
المساهمون: Science in Healthy Ageing & healthcaRE (SHARE), Life Course Epidemiology (LCE), Faculteit Medische Wetenschappen/UMCG, Lifestyle Medicine (LM), Center for Liver, Digestive and Metabolic Diseases (CLDM), Biological Psychology, Neuroscience Campus Amsterdam - Addictive Behavior, EMGO+ - Lifestyle, Overweight and Diabetes, Epidemiology, Public Health, Hematology, Internal Medicine, Department of Strategic Management and Entrepreneurship, Child and Adolescent Psychiatry / Psychology, Clinical Genetics
المصدر: Molecular Psychiatry
Molecular Psychiatry, 17(11), 1116-1129. Nature Publishing Group
Amin, N, Byrne, E, Johnson, J, Chenevix-Trench, G, Walter, S, Nolte, I M, Vink, J M, Rawal, R, Mangino, M, Teumer, A, Keers, J C, Verwoert, G, Baumeister, S, Biffar, R, Petersmann, A, Dahmen, N, Doering, A, Isaacs, A, Broer, L, Wray, N R, Montgomery, G W, Levy, D, Psaty, B M, Gudnason, V, Chakravarti, A, Sulem, P, Gudbjartsson, D F, Kiemeney, L A, Thorsteinsdottir, U, Stefansson, K, van Rooij, F J A, Aulchenko, Y S, Rivadeneira, F, Hofman, A, Uitterlinden, A G, Hammond, C J, Shin, S Y, Arfan Ikram, M, Witteman, J C M, Janssens, A C J W, Snieder, H, Tiemeier, H, Wolfenbuttel, B H R, Oostra, B A, Heath, A C, Wichmann, E, Spector, T D, Grabe, H J, Boomsma, D I, Martin, N G & van Duijn, C M 2012, ' Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM ', Molecular Psychiatry, vol. 17, no. 11, pp. 1116-1129 . https://doi.org/10.1038/mp.2011.101
Molecular Psychiatry, 17, 11, pp. 1116-29
Molecular Psychiatry, 17(11), 1116-29. Nature Publishing Group
Molecular Psychiatry, 17, 1116-29
Molecular Psychiatry; Vol 17مصطلحات موضوعية: Netherlands Twin Register (NTR), PSYCHOMOTOR PERFORMANCE, Male, Linkage disequilibrium, Parkinson's disease, Gene Expression, Genome-wide association study, BLOOD-PRESSURE, Aetiology, screening and detection [ONCOL 5], CAFFEINE CONSUMPTION, Caffeine/pharmacology, chemistry.chemical_compound, 0302 clinical medicine, PARKINSONS-DISEASE, Polymorphism (computer science), CYP1A2 GENOTYPE, European Continental Ancestry Group/genetics, Parkinson Disease/genetics, NRCAM, GENE-EXPRESSION, Genetics, 0303 health sciences, Genetic Predisposition to Disease/genetics, Parkinson Disease, Single Nucleotide, HUMAN BRAIN, 3. Good health, Drinking/genetics, Antigens, Neoplasm/genetics, Psychiatry and Mental health, Genome-Wide Association Study/methods, Female, Original Article, Caffeine, Cell Adhesion Molecules/genetics, MESSENGER-RNA, Protein-Serine-Threonine Kinases/genetics, coffee, Drinking, TYPE-2 DIABETES-MELLITUS, Single-nucleotide polymorphism, Gene Expression/drug effects, Biology, Protein Serine-Threonine Kinases, Polymorphism, Single Nucleotide, White People, Cell Line, 03 medical and health sciences, Cellular and Molecular Neuroscience, Cytochrome P-450 CYP1A2/genetics, Antigens, Neoplasm, Cytochrome P-450 CYP1A2, CAB39L, Cytochrome P-450 CYP1A1, CYP1A1/CYP1A2, Humans, Genetic Predisposition to Disease, Antigens, Polymorphism, Molecular Biology, Gene, Molecular epidemiology Aetiology, screening and detection [NCEBP 1], 030304 developmental biology, Genetic association, Neoplasm/genetics, Cytochrome P-450 CYP1A1/genetics, Coffee/genetics, Gene Expression Profiling, Gene expression profiling, chemistry, Apoptosis Regulatory Proteins/genetics, Gene Expression Profiling/methods, Apoptosis Regulatory Proteins, AGED FINNISH MEN, Cell Adhesion Molecules, 030217 neurology & neurosurgery, Genome-Wide Association Study, P450
وصف الملف: application/pdf
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