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1دورية أكاديمية
المؤلفون: Maria Derakhshan, Noah J. Kessler, Miho Ishida, Charalambos Demetriou, Nicolas Brucato, Gudrun E. Moore, Caroline Fall, Giriraj R. Chandak, François‐Xavier Ricaut, Andrew M. Prentice, Garrett Hellenthal, Matt J. Silver
مصطلحات موضوعية: Epigenetic Modifications and Their Functional Implications, Molecular Biology, Biochemistry, Genetics and Molecular Biology, Life Sciences, Genomic Imprinting and Parental Gene Expression Control, Genetics, FOS Biological sciences, Prenatal Aneuploidy Diagnosis and Screening Techniques, Pediatrics, Perinatology and Child Health, Medicine, Health Sciences, DNA Methylation, Biology, DNA methylation, Methylation, Epigenetics, Hypervariable region, Embryo, Epigenesis, DNA, Gene, Gene expression
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2دورية أكاديمية
المؤلفون: Maria Derakhshan, Noah J. Kessler, Miho Ishida, Charalambos Demetriou, Nicolas Brucato, Gudrun E. Moore, Caroline Fall, Giriraj Ratan Chandak, François‐Xavier Ricaut, Andrew M. Prentice, Garrett Hellenthal, Matt J. Silver
مصطلحات موضوعية: Epigenetic Modifications and Their Functional Implications, Molecular Biology, Biochemistry, Genetics and Molecular Biology, Life Sciences, Genomic Imprinting and Parental Gene Expression Control, Genetics, FOS Biological sciences, Developmental Origins of Adult Health and Disease, Pediatrics, Perinatology and Child Health, Medicine, Health Sciences, DNA Methylation, Transgenerational Inheritance, DNA methylation, Methylation, Epigenetics, Hypervariable region, Biology, Embryo, DNA, Gene, Gene expression
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المؤلفون: Maria Derakhshan, Noah J Kessler, Miho Ishida, Charalambos Demetriou, Nicolas Brucato, Gudrun E Moore, Caroline H D Fall, Giriraj R Chandak, Francois-Xavier Ricaut, Andrew M Prentice, Garrett Hellenthal, Matt J Silver
المساهمون: Evolution et Diversité Biologique (EDB), Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Université de Toulouse (UT)-Centre National de la Recherche Scientifique (CNRS), Medical Research Council, Human Genetics Division [Singapore], Genome Institute of Singapore (GIS), University College of London [London] (UCL)
المصدر: Nucleic Acids Research
Nucleic Acids Research, 2022, 50 (12), pp.6735-6752. ⟨10.1093/nar/gkac503⟩مصطلحات موضوعية: Tissue-and ethnicity-independent, Illumina 450K array, Hypervariable DNA methylation, Genetics, Early embryo, Humans, Reproducibility of Results, Systemic inter-individual variation, [SDE.BE]Environmental Sciences/Biodiversity and Ecology, DNA Methylation
وصف الملف: application/pdf; text
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bae458740f23f467577d189ea55c9238Test
https://pubmed.ncbi.nlm.nih.gov/35713545Test -
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المؤلفون: Emma Wakeling, Jenny Child, Deborah J G Mackay, Miho Ishida, Christopher D. Byrne, Justin H Davies, I. Karen Temple, Oluwakemi Lokulo-Sodipe, Hazel Inskip, Gudrun E. Moore, Angela Fenwick, Lisa Marie Ballard
المصدر: Journal of Medical Genetics
مصطلحات موضوعية: Adult, Male, Pediatrics, medicine.medical_specialty, Adolescent, uniparental disomy, Short stature, Epigenesis, Genetic, Impaired glucose tolerance, Genomic Imprinting, Young Adult, Insulin-Like Growth Factor II, parasitic diseases, Genetics, medicine, Humans, Genetics (clinical), Aged, Chromosome 7 (human), business.industry, Silver Russell syndrome, Silver–Russell syndrome, Genotype-Phenotype Correlations, Retrospective cohort study, DNA Methylation, Middle Aged, medicine.disease, Uniparental disomy, Growth hormone treatment, short stature, Silver-Russell Syndrome, Phenotype, Cohort, Quality of Life, Female, RNA, Long Noncoding, medicine.symptom, imprinting, business
وصف الملف: text; image
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4fcf40152ba1c5a1d9381d94b71adf0Test
https://eprints.soton.ac.uk/437350Test/ -
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المؤلفون: Joris A. M. van der Post, Charalambos Demetriou, Adi N Mul, Chela James, Faisal I. Rezwan, Emma Peskett, Susanne E Stalman, Frans B. Plötz, Nicole A Nibbering, Miho Ishida, Lia Knegt, Jan M. Wit, Carrie Ris-Stalpers, Lucas Alvizi, Cristina Alemán-Charlet, Marcel M.A.M. Mannens, Peter Henneman, Gudrun E. Moore, W. Baird, Philip Stanier, Nita Solanky, Sayeda Abu-Amero, Marielle Alders, Lydia J. Leon, Gerdine A Kamp, Raoul C.M. Hennekam
المساهمون: Other departments, ACS - Amsterdam Cardiovascular Sciences, AGEM - Amsterdam Gastroenterology Endocrinology Metabolism, Other Research, Human Genetics, ARD - Amsterdam Reproduction and Development, Obstetrics and Gynaecology, APH - Quality of Care, Paediatric Genetics, ACS - Pulmonary hypertension & thrombosis
المصدر: Journal of Clinical Endocrinology and Metabolism, 103(3), 917-925
Journal of Clinical Endocrinology and Metabolism
Journal of clinical endocrinology and metabolism, 103(3), 917-925. The Endocrine Societyمصطلحات موضوعية: Male, 0301 basic medicine, medicine.medical_specialty, DNA Copy Number Variations, Endocrinology, Diabetes and Metabolism, Clinical Biochemistry, Gestational Age, Genome-wide association study, 030105 genetics & heredity, Bioinformatics, Biochemistry, 03 medical and health sciences, Endocrinology, Internal medicine, Exome Sequencing, medicine, Birth Weight, Humans, Genetic Predisposition to Disease, Prospective Studies, Copy-number variation, Prospective cohort study, Exome sequencing, Comparative Genomic Hybridization, Fetal Growth Retardation, Obstetrics, business.industry, Biochemistry (medical), Infant, Newborn, Gestational age, DNA Methylation, medicine.disease, 030104 developmental biology, Infant, Small for Gestational Age, DNA methylation, Cohort, Small for gestational age, Female, business, Genome-Wide Association Study
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::377172b894d2b2404edb3d80d245eee2Test
https://doi.org/10.1210/jc.2017-01843Test -
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المؤلفون: Gudrun E. Moore, Miho Ishida, Miguel Alsina Casanova, Julio Moreno Hernando, Franck Court, Ana Monteagudo-Sánchez, Luciana Rodiguez Guerineau, Elisenda Moliner Calderon, David Monk, Carlota Rovira Zurriaga, M. Castañón, Loreto Martorell, Isabel Gazquez Serrano
المصدر: Human Mutation. 38:615-620
مصطلحات موضوعية: 0301 basic medicine, Alveolar capillary dysplasia, Genetics, Non-Mendelian inheritance, Point mutation, Parenteral transmission, Methylation, Biology, medicine.disease, Molecular biology, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, DNA methylation, medicine, Allele, Genomic imprinting, 030217 neurology & neurosurgery, Genetics (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::292d054b18e4d55c1970645b03b46342Test
https://doi.org/10.1002/humu.23213Test -
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المؤلفون: Miho Ishida
المصدر: Epigenomics. 8:563-580
مصطلحات موضوعية: 0301 basic medicine, Proband, Chromosome 7 (human), Genetics, Cancer Research, Genetic heterogeneity, Chromosomes, Human, Pair 11, Silver–Russell syndrome, Locus (genetics), Review, DNA Methylation, Uniparental Disomy, Biology, medicine.disease, Genomic Imprinting, Silver-Russell Syndrome, 03 medical and health sciences, 030104 developmental biology, medicine, Humans, Epigenetics, Imprinting (psychology), Genomic imprinting, Chromosomes, Human, Pair 7
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7d33c2441cbbfa009d03be37671391aTest
https://doi.org/10.2217/epi-2015-0010Test -
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المؤلفون: Miguel, Alsina Casanova, Ana, Monteagudo-Sánchez, Luciana, Rodiguez Guerineau, Franck, Court, Isabel, Gazquez Serrano, Loreto, Martorell, Carlota, Rovira Zurriaga, Gudrun E, Moore, Miho, Ishida, Montserrat, Castañon, Elisenda, Moliner Calderon, David, Monk, Julio, Moreno Hernando
المصدر: Human mutation. 38(6)
مصطلحات موضوعية: Comparative Genomic Hybridization, Hypertension, Pulmonary, Infant, Newborn, Forkhead Transcription Factors, Twins, Monozygotic, DNA Methylation, Persistent Fetal Circulation Syndrome, Pulmonary Alveoli, Genomic Imprinting, Pregnancy, Mutation, Humans, Female, Maternal Inheritance
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::8a73fd270ab6dd9fb4515c52c9d84bd2Test
https://pubmed.ncbi.nlm.nih.gov/28256047Test -
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المؤلفون: Carlos Simón, Marta Sanchez-Delgado, Miho Ishida, Maria Eugenia Poo-Llanillo, David Monk, Jose V. Medrano, Isabel Iglesias-Platas, Gudrun E. Moore, Ana Monteagudo-Sánchez, Sonia Guara Ciurana
المصدر: OBM Genetics. 2:1-1
مصطلحات موضوعية: Genetics, CpG site, Allelic Imbalance, DNA methylation, Epigenetic Profile, Epigenetics, Methylation, Allele, Biology, Genomic imprinting
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::23ce01b3c0ace8da5f1e161f67e6f1e7Test
https://doi.org/10.21926/obm.genet.1803026Test
