-
1
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
-
2
المؤلفون: Kathrin Ks Grassme, Ralf H. Adams, Benoit Vanhollebeke, Heinz-Georg Belting, Stefan Guenther, Rodrigo Diéguez-Hurtado, Markus Affolter, Cora Wiesner, Kathleen Hübner, Pauline Cabochette, Marvin Hubert, Wiebke Herzog, Yuki Wakayama
المصدر: Nature Communications, Vol 9, Iss 1, Pp 1-17 (2018)
Nature Communications
Nature communications, 9 (1مصطلحات موضوعية: 0301 basic medicine, Embryo, Nonmammalian, Antigens, CD -- genetics -- metabolism, Angiogenesis, Regulator, General Physics and Astronomy, Animals, Genetically Modified, Neovascularization, 0302 clinical medicine, Genes, Reporter, Zebrafish Proteins -- genetics -- metabolism, lcsh:Science, Wnt Signaling Pathway, Zebrafish, beta Catenin, S1PR1, Cadherins -- genetics -- metabolism, Regulation of gene expression, Multidisciplinary, Chemistry, Wnt signaling pathway, Brain, Gene Expression Regulation, Developmental, Sciences bio-médicales et agricoles, Cadherins, Cell biology, Receptors, Lysosphingolipid, medicine.anatomical_structure, Blood-Brain Barrier, Cerebrovascular Circulation, cardiovascular system, beta Catenin -- genetics -- metabolism, medicine.symptom, Science, Central nervous system, Brain -- blood supply -- growth & development -- metabolism, Luminescent Proteins -- genetics -- metabolism, Neovascularization, Physiologic, Blood-Brain Barrier -- growth & development -- metabolism, Article, General Biochemistry, Genetics and Molecular Biology, 03 medical and health sciences, Antigens, CD, Receptors, Lysosphingolipid -- genetics -- metabolism, medicine, Animals, Cerebrovascular Circulation -- genetics, Neovascularization, Physiologic -- genetics, Cell Adhesion Molecules -- genetics -- metabolism, General Chemistry, Zebrafish Proteins, Zebrafish -- genetics -- growth & development -- metabolism, Capillaries, Luminescent Proteins, 030104 developmental biology, lcsh:Q, VE-cadherin, Cell Adhesion Molecules, 030217 neurology & neurosurgery, Capillaries -- growth & development -- metabolism
وصف الملف: 1 full-text file(s): application/pdf
-
3دورية أكاديمية
المؤلفون: Anttila, Verneri, Stefansson, Hreinn, Kallela, Mikko, Todt, Unda, Terwindt, Gisela M, Calafato, M Stella, Nyholt, Dale R, Dimas, Antigone S, Freilinger, Tobias, Muller-Myhsok, Bertram, Artto, Ville, Inouye, Michael, Alakurtti, Kirsi, Kaunisto, Mari A, Hamalainen, Eija, de Vries, Boukje, Stam, Anine H, Weller, Claudia M, Heinze, Axel, Heinze-Kuhn, Katja, Goebel, Ingrid, Borck, Guntram, Gobel, Hartmut, Steinberg, Stacy, Wolf, Christiane, Bjornsson, Asgeir, Gudmundsson, Gretar, Kirchmann, Malene, Hauge, Anne, Werge, Thomas, Schoenen, Jean, Eriksson, Johan G, Hagen, Knut, Stovner, Lars, Wichmann, H*-Erich, Meitinger, Thomas, Alexander, Michael, Moebus, Susanne, Schreiber, Stefan, Aulchenko, Yurii S, Breteler, Monique M B, Uitterlinden, Andre G, Hofman, Albert, van Duijn, Cornelia M, Tikka-Kleemola, Paivi, Vepsalainen, Salli, Lucae, Susanne, Tozzi, Federica, Muglia, Pierandrea, Barrett, Jeffrey, Kaprio, Jaakko, Farkkila, Markus, Peltonen, Leena, Stefansson, Kari, Zwart, John*-Anker, Ferrari, Michel D, Olesen, Jes, Daly, Mark, Wessman, Maija, van den Maagdenberg, Arn M J M, Dichgans, Martin, Kubisch, Christian, Dermitzakis, Emmanouil T, Frants, Rune R, Palotie, Aarno
المصدر: Nature Genetics, 42 (10), 869-73 (2010)
مصطلحات موضوعية: Antigens, Surface/genetics, Calcium-Binding Proteins/genetics, Case-Control Studies, Cell Adhesion Molecules/genetics, Cells, Cultured, Chromosomes, Human, Pair 8/genetics, Female, Genetic Predisposition to Disease, Genome, Human, Genome-Wide Association Study, Genotype, Glutamate Carboxypeptidase II/genetics, Humans, Lymphocytes/metabolism, Male, Microsatellite Repeats/genetics, Migraine Disorders/genetics, Quantitative Trait Loci, Social & behavioral sciences, psychology, Neurosciences & behavior, Human health sciences, Neurology, Sciences sociales & comportementales, psychologie, Neurosciences & comportement, Sciences de la santé humaine, Neurologie
Relation: urn:issn:1061-4036; urn:issn:1546-1718
URL الوصول: https://orbi.uliege.be/handle/2268/89836
-
4مورد إلكتروني
المصدر: European Journal of Human Genetics
مصطلحات الفهرس: Genome-Wide Association Study, Cell Adhesion Molecules/*genetics, Genetic Predisposition to Disease, Glutamic Acid/biosynthesis, Iceland, Migraine Disorders/*genetics, Nerve Growth Factor/genetics, Nerve Tissue Proteins/genetics, Netherlands, Polymorphism, Receptors, Single Nucleotide, Contribution to Journal
URL: doi:10.1038/ejhg.2011.48
Ligthart, Lannie, de Vries, Boukje, Smith, Albert, Ikram, M. Arfan, Amin, Najaf, Hottenga, Jouke-Jan, Koelewijn, Stephany, Kattenberg, V. Mathijs, de Moor, Marleen, Nyholt, Dale, & other, and (2011) Meta-analysis of genome-wide association for migraine in six population-based European cohorts. European Journal of Human Genetics, 19(8), pp. 901-907. -
5مورد إلكتروني
المصدر: Nature Genetics
مصطلحات الفهرس: Genetic Predisposition to Disease, Genome, Genome-Wide Association Study, Antigens, Calcium-Binding Proteins/genetics, Case-Control Studies, Cell Adhesion Molecules/genetics, Cells, Chromosomes, Cultured, Female, Genotype, Glutamate Carboxypeptidase II/genetics, Human, Humans, Lymphocytes/metabolism, Male, Microsatellite Repeats/*genetics, Migraine Disorders/*genetics, Pair 8/*genetics, Quantitative Trait Loci, Surface/genetics, Contribution to Journal
URL: doi:10.1038/ng.652
Anttila, Verneri, Stefansson, Hreinn, Kallela, Mikko, Todt, Unda, Terwindt, Gisela, Calafato, Maria, Nyholt, Dale, Dimas, Antigone, Freilinger, Tobias, Müller-Myhsok, Bertram, & other, and (2010) Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1. Nature Genetics, 42(10), pp. 869-873.