المؤلفون: Antoniol, Giuliano^Aff7, Ceccarelli, Michele^Aff7, Rollo, Fabio^Aff7, Longo, Wanda^Aff8, Nutile, Teresa^Aff8, Ciullo, Marina^Aff8, Colonna, Enza^Aff8, Calabria, Antonietta^Aff8, Astore, Maria^Aff8, Lembo, Anna^Aff8, Toriello, Paola^Aff8, Persico, M. Grazia^Aff8

المساهمون: Goos, Gerhard, editor^Aff1, Hartmanis, Juris, editor^Aff2, van Leeuwen, Jan, editor^Aff3, Apolloni, Bruno, editor^Aff4, Marinaro, Maria, editor^Aff5, Tagliaferri, Roberto, editor^Aff6

المصدر: Neural Nets : 14th Italian Workshop on Neural Nets, WIRN VIETRI 2003, Vietri sul Mare, Italy, June 4-7, 2003. Revised Papers. 2859:258-268

المؤلفون: Li Sun, Jing Jin, Linhua Zhang, Hui Chen, Chunwu Zhang, Xiaoru Xia, Zhenni Zhou, Zhen‑Ji Chen

المصدر: International Journal of Molecular Medicine

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Candidate gene, Adolescent, Gout, large pedigrees, Genome-wide association study, Biology, medicine.disease_cause, Urate transport, 03 medical and health sciences, 0302 clinical medicine, Exome Sequencing, Genetics, medicine, Humans, Family, Genetic Predisposition to Disease, whole-exome sequencing, Exome sequencing, Aged, Genetic association, Mutation, Genetic heterogeneity, genetic variants, Articles, bioinformatics, General Medicine, Middle Aged, Nucleoside monophosphate biosynthetic process, Pedigree, 030104 developmental biology, 030220 oncology & carcinogenesis, Female, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f582c7a6be02b0467caf0a8997e2a95
https://doi.org/10.3892/ijmm.2020.4501

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المؤلفون: A. Cecile J.W. Janssens, Anu Realo, Yurii S. Aulchenko, Nicholas G. Martin, Margaret J. Wright, Ben A. Oostra, Marleen H. M. de Moor, Andres Metspalu, Gonneke Willemsen, Andrew C. Heath, Tõnu Esko, Laura J. Bierut, Katri Räikkönen, Eco J. C. de Geus, Gonçalo R. Abecasis, Toshiko Tanaka, Gu Zhu, Narelle K. Hansell, Grant W. Montgomery, Michelle Luciano, Anatoly V. Kirichenko, Cornelia M. van Duijn, Paul T. Costa, Michele L. Pergadia, Jouke-Jan Hottenga, Aaron Isaacs, Irina V. Zorkoltseva, Ian J. Deary, Brenda W.J.H. Penninx, Pamela A. F. Madden, Tatiana I. Axenovich, Gail Davies, Viatcheslav Saviouk, Manuela Uda, Antonio Terracciano, Dorret I. Boomsma, Sarah E. Medland, Najaf Amin, Luigi Ferrucci

المساهمون: Psychiatry, EMGO - Mental health, Epidemiology, Immunology, Clinical Genetics, Biological Psychology, Clinical Child and Family Studies, EMGO+ - Mental Health

المصدر: European Journal of Human Genetics, 21(8), 876-882. Nature Publishing Group
European Journal of Human Genetics, 21(8), 876-882
Amin, N, Hottenga, J J, Hansell, N K, Janssens, A C J W, de Moor, M H M, Madden, P A F, Zorkoltseva, I V, Penninx, B W J H, Terracciano, A, Uda, M, Tanaka, T, Esko, T, Realo, A, Ferrucci, L, Luciano, M, Davies, G, Metspalu, A, Abecasis, G R, Deary, I J, Raikkonen, K, Bierut, L J, Costa, P T, Savyuk, V, Zhu, G, Kirichenko, A V, Isaacs, A, Aulchenko, Y S, Willemsen, G, Heath, A C, Pergadia, M L, Medland, S E, Axenovich, T I, de Geus, E J C, Montgomery, G W, Wright, M J, Oostra, B A, Martin, N G, Boomsma, D I & van Duijn, C M 2013, ' Refining genome-wide linkage intervals using a meta-analysis of genome-wide association studies identifies loci influencing personality dimensions ', European Journal of Human Genetics, vol. 21, no. 8, pp. 876-882 . https://doi.org/10.1038/ejhg.2012.263
European Journal of Human Genetics, 21(8), 876-82. Nature Publishing Group

مصطلحات موضوعية: Netherlands Twin Register (NTR), Candidate gene, Potassium Channels, Personality Inventory, A BEHAVIOR PATTERN, Genome-wide association study, Chromosomes, Human, Pair 11/genetics, LARGE PEDIGREES, 0302 clinical medicine, NEUROTICISM, Big Five personality traits, Genetics (clinical), POPULATION, media_common, Genetics, 0303 health sciences, education.field_of_study, Genome, Human/genetics, Inwardly Rectifying/genetics, Chromosome Mapping, Single Nucleotide, ALZHEIMERS-DISEASE, Phenotype, Genome-Wide Association Study/methods, linkage, TRAITS, Human, Agreeableness, media_common.quotation_subject, Population, Locus (genetics), Biology, Polymorphism, Single Nucleotide, Article, Chromosomes, Pair 11/genetics, 03 medical and health sciences, Personality/genetics, Personality, Humans, KCNJ1, Potassium Channels, Inwardly Rectifying, Polymorphism, education, 030304 developmental biology, Genetic association, GENDER-DIFFERENCES, Genome, Human, Chromosomes, Human, Pair 11, SEARCH METAANALYSIS, MAJOR DEPRESSION, NEO, COGNITIVE IMPAIRMENT, personality, Genome, Human/genetics, Potassium Channels, Inwardly Rectifying/genetics, GSMA, Lod Score, Chromosome Mapping/methods, 030217 neurology & neurosurgery, Genome-Wide Association Study

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd1322fafce4ef96c8876d441de4f4bf
https://research.vumc.nl/en/publications/48d728ef-83d3-48f1-8c3f-6d9972be4420

المؤلفون: Simon Heath, Ellen M. Wijsman, E. Warwick Daw

المصدر: American journal of human genetics. 64(3)

مصطلحات موضوعية: Monte Carlo Markov chain, Pedigree chart, Computational biology, Quantitative trait locus, Biology, Quantitative Trait, Heritable, Gene Frequency, Genetic linkage, Alzheimer Disease, medicine, Genetics, Humans, Genetics(clinical), Genetic Testing, Age of Onset, Genetics (clinical), Genetic testing, Linkage (software), Chromosomes, Human, Pair 14, medicine.diagnostic_test, Models, Genetic, Genetic heterogeneity, Inheritance (genetic algorithm), Age Factors, Age at onset, Markov Chains, Pedigree, Multipoint linkage analysis, Chromosomes, Human, Pair 1, Chromosomes, Human, Pair 5, Oligogenic, Age of onset, Large pedigrees, Research Article

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b144ea283e363c926ccfa71e4757749
https://pubmed.ncbi.nlm.nih.gov/10053019

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