المؤلفون: Lies H. Hoefsloot, P. Martin van Hagen, L. Ingeborgh van den Born, Carel B. Hoyng, Kornelia Neveling, Frans P.M. Cremers, Mieke Kipping-Geertsema, Anna M. Siemiatkowska, Anneke I. den Hollander, Rob W.J. Collin, Monique Stoffels, Anna Simon, Arjen Henkes

المساهمون: Immunology, Ophthalmology

المصدر: Ophthalmology, 120, 2697-705
Ophthalmology, 120(12), 2697-2705. Elsevier Inc.
Ophthalmology, 120, 12, pp. 2697-705

مصطلحات موضوعية: Adult, Male, Proband, Oncology, medicine.medical_specialty, Pathology, Genetics and epigenetic pathways of disease [NCMLS 6], DNA Mutational Analysis, Visual Acuity, Mevalonic Acid, Compound heterozygosity, Genomic disorders and inherited multi-system disorders [IGMD 3], Evaluation of complex medical interventions Genomic disorders and inherited multi-system disorders [NCEBP 2], Internal medicine, Retinitis pigmentosa, Electroretinography, medicine, Humans, Exome, Fluorescein Angiography, Exome sequencing, Mevalonate kinase deficiency, biology, business.industry, Genetic heterogeneity, Mevalonate kinase, Middle Aged, medicine.disease, Pedigree, Pathogenesis and modulation of inflammation [N4i 1], Phosphotransferases (Alcohol Group Acceptor), Ophthalmology, Mutation, biology.protein, Female, Genetics and epigenetic pathways of disease Genomic disorders and inherited multi-system disorders [NCMLS 6], business, Retinitis Pigmentosa, Tomography, Optical Coherence

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b23a34004ac4b791b1b83b121055c17Test
https://doi.org/10.1016/j.ophtha.2013.07.052Test

المؤلفون: Arjen R. Mensenkamp, Ron A. Wevers, Jyotsna U. Rao, Angelina G. Goudswaard, Henricus P.M. Kunst, Udo F. H. Engelke, Karel Pacak, Graeme Eisenhofer, Nan Qin, Ad Hermus, Jacques W. M. Lenders, Richard J. Rodenburg, Henri J. L. M. Timmers, Benno Kusters, Fred C.G.J. Sweep

المصدر: Clinical Cancer Research; Vol 19
Clinical Cancer Research, 19, 3787-95
Clinical Cancer Research, 19, 14, pp. 3787-95

مصطلحات موضوعية: Male, Cancer Research, SDHB, Adrenal Gland Neoplasms, Succinic Acid, DCN PAC - Perception action and control, Mitochondrion, Catecholamines, 0302 clinical medicine, Paraganglioma, Citrate synthase, 0303 health sciences, Cardiovascular diseases [NCEBP 14], Electron Transport Complex II, Succinate dehydrogenase, Middle Aged, Mitochondria, 3. Good health, Mitochondrial medicine [IGMD 8], Oncology, 030220 oncology & carcinogenesis, Female, medicine.drug, Adult, medicine.medical_specialty, Adolescent, Genotype, Pheochromocytoma, Biology, Article, Genomic disorders and inherited multi-system disorders [IGMD 3], Young Adult, 03 medical and health sciences, Internal medicine, ONCOL 3 - Translational research DCN MP - Plasticity and memory, medicine, Humans, Glycostation disorders [DCN PAC - Perception action and control IGMD 4], DCN NN - Brain networks and neuronal communication, 030304 developmental biology, Translational research Genomic disorders and inherited multi-system disorders [ONCOL 3], Hormonal regulation [IGMD 6], Glycostation disorders [IGMD 4], medicine.disease, Endocrinology, Hereditary cancer and cancer-related syndromes Genomic disorders and inherited multi-system disorders [ONCOL 1], biology.protein, Catecholamine, Hormonal regulation Aetiology, screening and detection [IGMD 6], SDHD, Energy Metabolism

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a8b55612d5f34a85347800592c9f568Test
https://doi.org/10.1158/1078-0432.ccr-12-3922Test

المؤلفون: S. H. Powis, Robert Kleta, Marieke J H Coenen, Anne Boland-Augé, Peter W. Mathieson, Paul Brenchley, Hanna Debiec, Jack F.M. Wetzels, Johanne M. Groothuismink, Bénédicte Stengel, Horia Stanescu, Alan Medlar, Julia M. Hofstra, Pierre Ronco, Detlef Bockenhauer

المساهمون: Department of Human Genetics [Nijmegen], Radboud University Medical Center [Nijmegen], Department of Nephrology [Nijmegen, The Netherlands], Des Maladies Rénales Rares aux Maladies Fréquentes, Remodelage et Réparation, Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM), CHU Tenon [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Centre for Nephrology [London, UK], University College of London [London] (UCL), Centre de recherche en épidémiologie et santé des populations (CESP), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Université Paris-Sud - Paris 11 (UP11)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Paul Brousse-Institut National de la Santé et de la Recherche Médicale (INSERM), Centre National de Génotypage (CNG), Commissariat à l'énergie atomique et aux énergies alternatives (CEA), Academic Renal Unit [Bristol, UK], University of Bristol [Bristol], School of Biomedicine [Manchester, UK], University of Manchester [Manchester], The research leading to these results has received funding from the European Community’s Seventh Framework Programme under grant agreement 2012-305608 'European Consortium for High-Throughput Research in Rare Kidney Diseases' (EURenOmics)' (to P.W.M., P.E.B., R.K., J.F.M.W., P.R.), by the David and Elaine Potter Charitable Foundation (to S.H.P., R.K.), by the Dutch Kidney Foundation (J.M.H., grant KJPB11.021), and by the FrenchFoundation for Medical Research (H.D., P.R., grant 2012). The French Gn-Progress cohort was supported by grants from the French Ministry of Health (PHRC AOM 00022), the Ministry of Research (Decision d’aide 01P0513), and the Biomedicine Agency (AO Recherche et Greffes 2005)., Department of Human Genetics, Department of nephrology, Remodelage et Reparation du Tissu Renal, Centre for Nephrology, Equipe 10, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Université Paris-Sud - Paris 11 (UP11)-Hôpital Paul Brousse-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Université Paris-Sud - Paris 11 (UP11)-Hôpital Paul Brousse-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Academic Renal Unit, School of Biomedicine, Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), The research leading to these results has received funding from the European Community's Seventh Framework Programme under grant agreement 2012-305608 'European Consortium for High-Throughput Research in Rare Kidney Diseases' (EURenOmics)'(to P.W.M., P.E.B., R.K., J.F.M.W., P.R.), by the David and Elaine Potter Charitable Foundation (to S.H.P., R.K.), by the Dutch Kidney Foundation (J.M.H., grant KJPB11.021), and by the French Foundation for Medical Research (H.D., P.R., grant 2012). The French Gn-Progress cohort was supported by grants from the French Ministry of Health (PHRC AOM 00022), the Ministry of Research (Decision d'aide 01P0513), and the Biomedicine Agency (AO Recherche et Greffes 2005)., RONCO, Pierre, Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Université Paris-Sud - Paris 11 (UP11)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Paul Brousse-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Université Paris-Sud - Paris 11 (UP11)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Paul Brousse-Institut National de la Santé et de la Recherche Médicale (INSERM), Service de Département de Néphrologie = Service de Néphrologie et Dialyses [CHU Tenon], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Radboud University Medical Centre [Nijmegen, The Netherlands], Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Pierre et Marie Curie - Paris 6 (UPMC), Service de Néphrologie et Dialyses [CHU Tenon], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-CHU Tenon [AP-HP], Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Université Paris-Sud - Paris 11 (UP11)-Hôpital Paul Brousse-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)

المصدر: Journal of the American Society of Nephrology
Journal of the American Society of Nephrology, 2013, 24 (4), pp.677-683. ⟨10.1681/ASN.2012070730⟩
Journal of the American Society of Nephrology, American Society of Nephrology, 2013, 24 (4), pp.677-83. ⟨10.1681/ASN.2012070730⟩
Journal of the American Society of Nephrology, 2013, 24 (4), pp.677-83. ⟨10.1681/ASN.2012070730⟩
Journal of the American Society of Nephrology, American Society of Nephrology, 2013, 24 (4), pp.677-683. ⟨10.1681/ASN.2012070730⟩
Journal of the American Society of Nephrology, 24, 4, pp. 677-83
Journal of the American Society of Nephrology; Vol 24
Journal of the American Society of Nephrology, 24, 677-83

مصطلحات موضوعية: Male, MESH: Sequence Analysis, DNA, MESH: Glomerulonephritis, Membranous, 030232 urology & nephrology, Glomerulonephritis, Membranous, Exon, 0302 clinical medicine, Coding region, MESH: Genomic Structural Variation, Renal disorder [IGMD 9], MESH: Aged, Genetics, Sanger sequencing, 0303 health sciences, MESH: Middle Aged, MESH: Polymorphism, Single Nucleotide, MESH: Genetic Predisposition to Disease, General Medicine, Middle Aged, 3. Good health, Nephrology, symbols, [SDV.BBM.GTP] Life Sciences [q-bio]/Biochemistry, Molecular Biology/Genomics [q-bio.GN], Female, Adult, dbSNP, Sequence analysis, Biology, Polymorphism, Single Nucleotide, Mental health [NCEBP 9], Genomic disorders and inherited multi-system disorders [IGMD 3], 03 medical and health sciences, symbols.namesake, [SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Genomics [q-bio.GN], MESH: Receptors, Phospholipase A2, Humans, Genetic Predisposition to Disease, Allele, 1000 Genomes Project, Genomic disorders and inherited multi-system disorders Molecular epidemiology [IGMD 3], Gene, Aged, 030304 developmental biology, MESH: Humans, Receptors, Phospholipase A2, MESH: Adult, Sequence Analysis, DNA, Molecular biology, MESH: Male, Genomic Structural Variation, MESH: Female

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b192b20a06677d3bf650e3bd66ad35fTest
https://doi.org/10.1681/asn.2012070730Test

المؤلفون: Camiel J. F. Boon, Thomas Theelen, Yara T. E. Lechanteur, Dzenita Smailhodzic, Carel B. Hoyng, Johannes P. H. van de Ven, Anneke I. den Hollander

المصدر: American Journal of Ophthalmology, 154, 3, pp. 560-7
American Journal of Ophthalmology, 154, 560-7

مصطلحات موضوعية: Male, medicine.medical_specialty, genetic structures, Visual Acuity, Retinal Drusen, Spectral domain, Retinal Pigment Epithelium, Drusen, Evaluation of complex medical interventions Functional imaging [NCEBP 2], Basement Membrane, Optics, Optical coherence tomography, Evaluation of complex medical interventions Genomic disorders and inherited multi-system disorders [NCEBP 2], Ophthalmology, Odds Ratio, Humans, Medicine, Prospective Studies, Prospective cohort study, Aged, Aged, 80 and over, Retinal pigment epithelium, medicine.diagnostic_test, business.industry, Odds ratio, Middle Aged, medicine.disease, eye diseases, Confidence interval, Extracellular Matrix, Phenotype, medicine.anatomical_structure, Basal Laminar Drusen, Female, Bruch Membrane, sense organs, Genetics and epigenetic pathways of disease Genomic disorders and inherited multi-system disorders [NCMLS 6], business, Tomography, Optical Coherence

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b699448957048b8c15d0f5c46866ce35Test
https://doi.org/10.1016/j.ajo.2012.03.012Test

المؤلفون: Carel B. Hoyng, Shazia Micheal, Anneke I. den Hollander, Bjorn Bakker, Barend F. Hogewind

المصدر: Ophthalmic Genetics, 33, 4, pp. 221-4
Ophthalmic Genetics, 33, 221-4

مصطلحات موضوعية: Male, Intraocular pressure, medicine.medical_specialty, Triamcinolone acetonide, Genotype, genetic structures, medicine.drug_class, Ocular hypertension, Single-nucleotide polymorphism, Pharmacology, Polymerase Chain Reaction, Polymorphism, Single Nucleotide, Triamcinolone Acetonide, Gastroenterology, Tacrolimus Binding Proteins, Tonometry, Ocular, Gene Frequency, Evaluation of complex medical interventions Genomic disorders and inherited multi-system disorders [NCEBP 2], Internal medicine, medicine, Humans, Glucocorticoids, Intraocular Pressure, Genetics (clinical), Aged, Retrospective Studies, Serine-Arginine Splicing Factors, business.industry, RNA-Binding Proteins, Intravitreal administration, Middle Aged, medicine.disease, Acetonide, eye diseases, Ophthalmology, Case-Control Studies, Intravitreal Injections, Pediatrics, Perinatology and Child Health, Cohort, Corticosteroid, Female, Ocular Hypertension, Genetics and epigenetic pathways of disease Genomic disorders and inherited multi-system disorders [NCMLS 6], business, medicine.drug

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb00bf58897e303f91ff849b56261c05Test
https://doi.org/10.3109/13816810.2012.716488Test

المؤلفون: Ernie M.H.F. Bongers, Rolph Pfundt, Marjolijn C.J. Jongmans, Eugène T P Verwiel, Koen L.I. van Gassen, Eveline J. Kamping, Yvonne F. Heijdra, Roland P. Kuiper, Frank N. van Leeuwen, Nicoline Hoogerbrugge, Ad Geurts van Kessel, Tom Vulliamy, Jayne Y. Hehir-Kwa, Marjolijn J L Ligtenberg, Liesbeth van Emst, Inderjeet Dokal

المصدر: American Journal of Human Genetics, 90, 426-33
American Journal of Human Genetics, 90, 3, pp. 426-33

مصطلحات موضوعية: Male, Telomerase, Germline, Cohort Studies, Genetics(clinical), Child, Genetics (clinical), Renal disorder [IGMD 9], Genetics, Recombination, Genetic, Mosaicism, Homozygote, Middle Aged, Age-related aspects of cancer Immune Regulation [ONCOL 2], Pedigree, Pathogenesis and modulation of inflammation [N4i 1], Child, Preschool, Female, Adult, Mitotic crossover, Adolescent, Hereditary cancer and cancer-related syndromes Genetics and epigenetic pathways of disease [ONCOL 1], Mitosis, Biology, Polymorphism, Single Nucleotide, Dyskeratosis Congenita, Article, Genomic disorders and inherited multi-system disorders [IGMD 3], Telomerase RNA component, Young Adult, Germline mutation, Translational research [ONCOL 3], medicine, Humans, Cell Lineage, Allele, Genetics and epigenetic pathways of disease Translational research [NCMLS 6], Alleles, Germ-Line Mutation, Aged, Hereditary cancer and cancer-related syndromes [ONCOL 1], Chromosome, Sequence Analysis, DNA, medicine.disease, Molecular biology, RNA, Genetics and epigenetic pathways of disease Genomic disorders and inherited multi-system disorders [NCMLS 6], Dyskeratosis congenita

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b45f601ddb4f5674f953d3c22b0ecc29Test

المؤلفون: Richard C. Oude Voshaar, Boudewijn A.A. Bus, Alejandro Arias-Vasquez, Jacqueline de Graaf, Barbara Franke, Jos Prickaerts

المساهمون: Psychiatrie & Neuropsychologie, RS: MHeNs School for Mental Health and Neuroscience, Faculteit Medische Wetenschappen/UMCG, Interdisciplinary Centre Psychopathology and Emotion regulation (ICPE)

المصدر: Neuropsychobiology, 65, 4, pp. 183-7
Neuropsychobiology, 65, 183-7
Neuropsychobiology, 65(4), 183-187. S. Karger AG
Neuropsychobiology, 65(4), 183-187. KARGER

مصطلحات موضوعية: Male, Serum, medicine.medical_specialty, STRESS, Genotype, DCN MP - Plasticity and memory, Val66met polymorphism, DCN PAC - Perception action and control, Mental health [NCEBP 9], Community Health Planning, Brain-derived neurotrophic factor, Genomic disorders and inherited multi-system disorders DCN MP - Plasticity and memory [IGMD 3], Sex interaction, Methionine, Val66Met, Neurotrophic factors, Internal medicine, medicine, Humans, Allele, Alleles, Health aging / healthy living Cardiovascular diseases [IGMD 5], Biological Psychiatry, Depression (differential diagnoses), Aged, Genetic association, Genetics, Sex Characteristics, Chi-Square Distribution, Polymorphism, Genetic, Valine, Middle Aged, Genomic disorders and inherited multi-system disorders [DCN PAC - Perception action and control IGMD 3], DEPRESSION, Psychiatry and Mental health, Neuropsychology and Physiological Psychology, Endocrinology, Female, Psychology

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0221bdb9a99a8dbd795926d56b5e9c76Test
https://doi.org/10.1159/000336997Test

المؤلفون: Erik-Jan Kamsteeg, Vítor Tedim Cruz, Ruth Geraldes, Paula Coutinho, Jorge Pinto-Basto, Georgina Neves, Ana Margarida Lopes, Han G. Brunner, Pureza Dias, Eva Brandão, Jorge Sequeiros, Isabel Pavão Martins, Isabel Alonso, Maria Conceição Pereira, José Leal Loureiro

المصدر: Genetics in Medicine, 14, 1, pp. 143-51
Genetics in Medicine, 14, 143-51

مصطلحات موضوعية: Adult, Male, Genome evolution, Adolescent, Genotype, Hereditary spastic paraplegia, Molecular Sequence Data, Alu element, Locus (genetics), Biology, Genomic disorders and inherited multi-system disorders [IGMD 3], Chromosome Breakpoints, Young Adult, Exon, Alu Elements, Gene Order, Spastic, medicine, Humans, Amino Acid Sequence, Allele, Child, Alleles, Genetics (clinical), Sequence Deletion, Genetics, Base Sequence, Spastic Paraplegia, Hereditary, Genetic heterogeneity, Infant, Proteins, Exons, Middle Aged, medicine.disease, Pedigree, nervous system diseases, Child, Preschool, Mutation, Female, Genetics and epigenetic pathways of disease Genomic disorders and inherited multi-system disorders [NCMLS 6]

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee1673c4a78ebefb8ad3cc7e21bb613cTest
https://doi.org/10.1038/gim.2011.7Test

المؤلفون: Albert Tenesa, Michael A. Horan, Igor Rudan, Barbara Franke, Caroline Hayward, Sita H. Vermeulen, Michelle Luciano, Christel M. Middeldorp, Nicholas D. Hastie, Jennifer E. Huffman, Dorret I. Boomsma, Harry Campbell, Pieter E. Vos, Annette M. Hartmann, David J. Porteous, John M. Starr, Bettina Konte, Jan K. Buitelaar, Tessel E. Galesloot, Gail Davies, William E R Ollier, Dan Rujescu, James F. Wilson, Andrew C. Heath, Pamela A. F. Madden, Lina Zgaga, Alejandro Arias-Vásquez, Nicholas G. Martin, Xiayi Ke, Joost G. E. Janzing, Anna A. E. Vinkhuyzen, Ina Giegling, Grant W. Montgomery, Antony Payton, Ian J. Deary, Maaike Verhagen, Veronique Vitart, Jouke-Jan Hottenga, Alan F. Wright, Sanja Belak Kovačević, Ozren Polasek, Neil Pendleton, H. Konnerth, Gonneke Willemsen

المساهمون: Child Psychiatry, Biological Psychology, Neuroscience Campus Amsterdam - Anxiety & Depression, EMGO+ - Mental Health

المصدر: American journal of medical genetics. Part B, Neuropsychiatric genetics, 159(6), 684-695. Wiley-Liss Inc.
Luciano, M, Huffman, J E, Arias-Vásquez, A, Vinkhuyzen, A A E, Middeldorp, C M, Giegling, I, Payton, A, Davies, G, Zgaga, L, Janzing, J, Ke, X, Galesloot, T, Hartmann, A M, Ollier, W, Tenesa, A, Hayward, C, Verhagen, M, Montgomery, G W, Hottenga, J-J, Konte, B, Starr, J M, Vitart, V, Vos, P E, Madden, P A F, Willemsen, G, Konnerth, H, Horan, M A, Porteous, D J, Campbell, H, Vermeulen, S H, Heath, A C, Wright, A, Polasek, O, Kovacevic, S B, Hastie, N D, Franke, B, Boomsma, D I, Martin, N G, Rujescu, D, Wilson, J F, Buitelaar, J, Pendleton, N, Rudan, I & Deary, I J 2012, ' Genome-wide association uncovers shared genetic effects among personality traits and mood states ', American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol. 159B, no. 6, pp. 684-695 . https://doi.org/10.1002/ajmg.b.32072Test
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 159B, 684-95
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 159B, 6, pp. 684-695
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 159B(6), 684-695. Wiley-Liss Inc.
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 159B, 684-695
Luciano, M, Huffman, J E, Arias-Vasquez, A, Vinkhuyzen, A A E, Middeldorp, C M, Giegling, I, Payton, A, Davies, G E, Zgaga, L, Janzing, J G, Ke, X Y, Galesloot, T, Hartmann, A M, Ollier, W, Tenesa, A, Hayward, C, Verhagen, M, Montgomery, G W, Hottenga, J J, Konte, B, Starr, J M, Vitart, V, Vos, P E, Madden, P A F, Willemsen, G, Konnerth, H, Horan, M A, Porteous, D J, Campbell, H, Vermeulen, S H, Heath, A C, Wright, A, Polasek, O, Kovacevic, S B, Hastie, N, Franke, B, Boomsma, D I, Martin, N G, Rujescu, D, Wilson, J F, Buitelaar, J, Pendleton, N, Rudan, I & Deary, I J 2012, ' Genome-Wide Association Uncovers Shared Genetic Effects Among Personality Traits and Mood States ', American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol. 159B, no. 6, pp. 684-695 . https://doi.org/10.1002/ajmg.b.32072Test
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 159B, 6, pp. 684-95

مصطلحات موضوعية: Male, Netherlands Twin Register (NTR), Neurotic Disorders, Genome-wide association study, DCN PAC - Perception action and control, Anxiety, Neuropsychological Tests, Cohort Studies, Extraversion, Psychological, 0302 clinical medicine, Big Five personality traits, Genetics (clinical), media_common, Aged, 80 and over, 0303 health sciences, Depression, Genomic disorders and inherited multi-system disorders [DCN PAC - Perception action and control IGMD 3], Middle Aged, Neuroticism, Psychiatry and Mental health, Major depressive disorder, Female, Personality, Adult, Adolescent, DCN MP - Plasticity and memory, media_common.quotation_subject, Biology, Molecular epidemiology Iron metabolism [NCEBP 1], Mental health [NCEBP 9], Polymorphism, Single Nucleotide, Article, Genomic disorders and inherited multi-system disorders DCN MP - Plasticity and memory [IGMD 3], Molecular epidemiology [NCEBP 1], Young Adult, 03 medical and health sciences, Cellular and Molecular Neuroscience, medicine, Humans, Genetic Predisposition to Disease, DCN PAC - Perception action and control NCEBP 9 - Mental health, Bipolar disorder, DCN NN - Brain networks and neuronal communication, Molecular epidemiology Aetiology, screening and detection [NCEBP 1], Aged, 030304 developmental biology, Extraversion and introversion, Mood Disorders, Reproducibility of Results, medicine.disease, Mood, Developmental Psychopathology, 030217 neurology & neurosurgery, Genome-Wide Association Study, Demography

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::713899f9e6aca20699bc5bf2c6831272Test
https://hdl.handle.net/2066/116809Test

المؤلفون: Bernd Kirchhof, Johannes P. H. van de Ven, Carel B. Hoyng, Robert K. Koenekoop, Amer Omar, Dzenita Smailhodzic, Alice Yang Zhang, Sascha Fauser, Anneke I. den Hollander, Angela Kwestro, Philipp S. Muether, John C. Chen, Jan E.E. Keunen, B. Jeroen Klevering

المصدر: Ophthalmology, 119, 2304-11
Ophthalmology, 119, 11, pp. 2304-11

مصطلحات موضوعية: Male, Vascular Endothelial Growth Factor A, medicine.medical_specialty, Genotype, genetic structures, Visual Acuity, Angiogenesis Inhibitors, Single-nucleotide polymorphism, Antibodies, Monoclonal, Humanized, Polymerase Chain Reaction, Polymorphism, Single Nucleotide, Cohort Studies, Risk Factors, Ranibizumab, Ophthalmology, Evaluation of complex medical interventions Genomic disorders and inherited multi-system disorders [NCEBP 2], medicine, Humans, Age of Onset, Fluorescein Angiography, Alleles, Aged, Aged, 80 and over, business.industry, Standard treatment, Proteins, Diabetic retinopathy, Middle Aged, Macular degeneration, medicine.disease, Vascular Endothelial Growth Factor Receptor-2, Frizzled Receptors, eye diseases, Low Density Lipoprotein Receptor-Related Protein-5, Pharmacogenetics, Complement Factor H, Intravitreal Injections, Wet Macular Degeneration, Female, sense organs, Age of onset, business, Genetics and epigenetic pathways of disease Genomic disorders and inherited multi-system disorders [NCMLS 6], Tomography, Optical Coherence, Cohort study, medicine.drug

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3af55bef306a2d2f3ffcf78d698eafbTest
https://hdl.handle.net/2066/110749Test