المؤلفون: Salgado, Catarina, Gruis, Nelleke, Heijmans, Bastiaan T, Oosting, Jan, van Doorn, Remco, Pool, Renée, van Dongen, Jenny, Hottenga, Jouke Jan, Boomsma, Dorret

المساهمون: Human genetics, VU University medical center, Laboratory Medicine, Psychiatry, APH - Mental Health, Consortium, BIOS, van Duijn, C, APH - Personalized Medicine, APH - Health Behaviors & Chronic Diseases, Biological Psychology, APH - Methodology

المصدر: Clinical Epigenetics
Clinical epigenetics, 12(1):43. Springer Verlag
Clinical epigenetics, 12(1):43, 1-7. Springer Verlag
Salgado, C, Gruis, N, Heijmans, B T, Oosting, J, Van Doorn, R & r 2020, ' Genome-wide analysis of constitutional DNA methylation in familial melanoma ', Clinical epigenetics, vol. 12, no. 1, 43 . https://doi.org/10.1186/s13148-020-00831-7Test
Clinical epigenetics, 12(1):43. BioMed Central Ltd
Clinical Epigenetics, 12(1). BMC
Salgado, C, Gruis, N, Heijmans, B T, Oosting, J, van Doorn, R, BIOS Consortium, Pool, R, van Dongen, J, Hottenga, J J & Boomsma, D 2020, ' Genome-wide analysis of constitutional DNA methylation in familial melanoma ', Clinical epigenetics, vol. 12, no. 1, 43, pp. 1-7 . https://doi.org/10.1186/s13148-020-00831-7Test

مصطلحات موضوعية: Skin Neoplasms, VARIANT, 0302 clinical medicine, GERMLINE EPIMUTATION, Imprinting (psychology), Promoter Regions, Genetic, Melanoma, Genetics (clinical), Genetics, 0303 health sciences, Genome, DNA methylation, Loss of imprinting, MLH1, Methylation, Middle Aged, Familial melanoma, CpG site, 030220 oncology & carcinogenesis, Human, Adult, Short Report, Biology, INHERITANCE, Promoter Regions, Melanoma/genetics, CDKN2A, 03 medical and health sciences, Genetic, SDG 3 - Good Health and Well-being, Skin Neoplasms/genetics, medicine, Humans, Epimutation, Epigenetics, Molecular Biology, Gene, Aged, 030304 developmental biology, Genome, Human, MUTATIONS, DNA Methylation, medicine.disease, GENE, Human genetics, MSH2, CpG Islands, Developmental Biology

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24673e455d4a75c696f8a1f42b65ad23Test
https://doi.org/10.1186/s13148-020-00831-7Test

المؤلفون: Jordana T. Bell, Claudio D. Stern, Scott D. Gordon, Erik A. Ehli, Silvère M. van der Maarel, Jonathan Mill, Gibran Hemani, Hamdi Mbarek, Juan E. Castillo-Fernandez, Tim D. Spector, Allan F. McRae, Catharina E. M. van Beijsterveldt, Jouke-Jan Hottenga, Veronika V. Odintsova, Nicholas G. Martin, Jaakko Kaprio, Eilis Hannon, P. Eline Slagboom, Gonneke Willemsen, Bastiaan T. Heijmans, Sara N. Lundgren, Josine L. Min, Jenny van Dongen, Miina Ollikainen, Dorret I. Boomsma, Pei-Chien Tsai, Karen Sugden, Charles E. Breeze, Terrie E. Moffitt, Bruno Reversade, Lucia Daxinger, Franziska Paul, Fiona A. Hagenbeek, Eco J. C. de Geus, Grant W. Montgomery, T.D. Spector, Avshalom Caspi

المساهمون: Center for Reproductive Medicine, ACS - Heart failure & arrhythmias, Amsterdam Reproduction & Development, Reversade, Bruno, van Dongen, Jenny, Gordon, Scott D., McRae, Allan F., Odintsova, Veronika V., Mbarek, Hamdi, Breeze, Charles E., Sugden, Karen, Lundgren, Sara, Castillo-Fernandez, Juan E., Hannon, Eilis, Moffitt, Terrie E., Hagenbeek, Fiona A., van Beijsterveldt, Catharina E. M., Hottenga, Jouke Jan, Tsai, Pei-Chien, Min, Josine L., Hemani, Gibran, Ehli, Erik A., Paul, Franziska, Stern, Claudio D., Heijmans, Bastiaan T., Slagboom, P. Eline, Daxinger, Lucia, van der Maarel, Silvere M., de Geus, E. J. C., Willemsen, Gonneke, Montgomery, Grant W., Ollikainen, Miina, Kaprio, Jaakko, Spector, Tim D., Bell, Jordana T., Mill, Jonathan, Caspi, Avshalom, Martin, Nicholas G., Boomsma, Dorret, I., School of Medicine, APH - Personalized Medicine, APH - Mental Health, Biological Psychology, APH - Health Behaviors & Chronic Diseases, APH - Methodology, Breeze, Charles, Martin, Nicholas, Boomsma, Dorret, Institute for Molecular Medicine Finland, Epigenetics of Complex Diseases and Traits

المصدر: Nature communications, 12(1):5618. Nature Publishing Group
Nature Communications
Nature Communications, 12(1):5618, 1-14. Nature Publishing Group
Hemani, G 2021, ' Identical twins carry a persistent epigenetic signature of early genome programming ', Nature Communications, vol. 12, no. 1, 5618 . https://doi.org/10.1038/s41467-021-25583-7Test
Nature Communications, 12(1). NATURE PORTFOLIO
Nature Communications, Vol 12, Iss 1, Pp 1-14 (2021)
van Dongen, J, Gordon, S D, Odintsova, V V, Mbarek, H, Hagenbeek, F A, van Beijsterveldt, C E M, Jan Hottenga, J, de Geus, E J C, Willemsen, G, Boomsma, D I, Genetics of DNA Methylation Consortium & BIOS Consortium 2021, ' Identical twins carry a persistent epigenetic signature of early genome programming ', Nature Communications, vol. 12, no. 1, 5618, pp. 1-14 . https://doi.org/10.1038/s41467-021-25583-7Test, https://doi.org/10.1038/s41467-021-25583-7Test

مصطلحات موضوعية: Epigenomics, Somatic cell, General Physics and Astronomy, Monozygotic twin, PROBE DESIGN BIAS, Genome, Epigenesis, Genetic, NORMALIZATION, 0302 clinical medicine, Genetics research, Registries, Probe design bias, DNA methylation, Vanishing twin, Register, Cells, Normalization, Association, Ontology, Mothers, Family, 112 Statistics and probability, Science and technology, Finland, Netherlands, 0303 health sciences, Multidisciplinary, Zygote, Twinning, Monozygotic, MOTHERS, 1184 Genetics, developmental biology, physiology, VANISHING TWIN, ASSOCIATION, Middle Aged, 3142 Public health care science, environmental and occupational health, FAMILY, Multidisciplinary sciences, Embryogenesis, Adult, Genotype, Heterochromatin, Science, Quantitative Trait Loci, Biology, Polymorphism, Single Nucleotide, Article, General Biochemistry, Genetics and Molecular Biology, Young Adult, 03 medical and health sciences, SDG 3 - Good Health and Well-being, Centromere, Humans, Epigenetics, Genetic epigenesis, REGISTER, Retrospective Studies, 030304 developmental biology, 3112 Neurosciences, Twins, Monozygotic, General Chemistry, United Kingdom, 3141 Health care science, ONTOLOGY, Evolutionary biology, CELLS, 030217 neurology & neurosurgery

وصف الملف: pdf; application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c8782e417f5a11b5e6694746e20eb68Test
https://pure.amc.nl/en/publications/identical-twins-carry-a-persistent-epigenetic-signature-of-earlyTest-genome-programming(73725bc1-8f93-4e02-88e9-189d0ad79157).html