المؤلفون: Jenny van Dongen, Erik A. Ehli, Rick Jansen, Catharina E. M. van Beijsterveldt, Gonneke Willemsen, Jouke J. Hottenga, Noah A. Kallsen, Shanna A. Peyton, Charles E. Breeze, Cornelis Kluft, Bastiaan T. Heijmans, Meike Bartels, Gareth E. Davies, Dorret I. Boomsma

المصدر: Epigenetics & Chromatin, Vol 11, Iss 1, Pp 1-14 (2018)

مصطلحات موضوعية: DNA methylation, Epigenetics, Illumina, 450 k, EPIC, Array, Genetics, QH426-470

وصف الملف: electronic resource

العلاقة: http://link.springer.com/article/10.1186/s13072-018-0225-xTest; https://doaj.org/toc/1756-8935Test

الوصول الحر: https://doaj.org/article/5ee79e6350ae48e68e870e924ea93735Test

المؤلفون: Noah A. Kallsen, Charles G. Mullighan, Jun J. Yang, Karen R. Rabin, Jasmine Healy, Catherine Metayer, Michael E. Scheurer, Andrew J. Carroll, Jonathan M. Chernus, Nyla A. Heerema, Logan G. Spector, Andrew T. DeWan, Gareth E. Davies, Mignon L. Loh, Shanna A. Peyton, Eleanor Feingold, Philip J. Lupo, Naomi J. Winick, Daniel Sinnett, William L. Carroll, Lisa F. Barcellos, Stephen P. Hunger, Austin L. Brown, Stephanie L. Sherman, Libby M. Morimoto, Mary V. Relling, Maria S. Pombo-de-Oliveira, Erik A. Ehli, Beth A. Mueller, Xiaomei Ma, Ivan Smirnov, Ching-Hon Pui, Vincent U. Gant, Brent L. Wood, Helen M. Hansen, Elizabeth A. Raetz, Pamela D. Thompson, Jillian M. Birch, Alice Y. Kang, Kyle M. Walsh, Adam J. de Smith, Wenjian Yang, Meenakshi Devidas, Joseph L. Wiemels, Jeffrey W. Taub, Caroline Laverdière, Michael J. Borowitz, Michael E. Zwick

المصدر: Blood. 134:1227-1237

مصطلحات موضوعية: 0301 basic medicine, Immunology, Locus (genetics), Single-nucleotide polymorphism, Genome-wide association study, GATA3 Transcription Factor, Biology, Polymorphism, Single Nucleotide, Biochemistry, Ikaros Transcription Factor, 03 medical and health sciences, 0302 clinical medicine, Gene Frequency, Genetic predisposition, Humans, Genetic Predisposition to Disease, Allele, Child, Allele frequency, Cyclin-Dependent Kinase Inhibitor p16, Genetics, Cell Biology, Hematology, CEBPE, Precursor Cell Lymphoblastic Leukemia-Lymphoma, Penetrance, DNA-Binding Proteins, 030104 developmental biology, 030220 oncology & carcinogenesis, Down Syndrome, Genome-Wide Association Study, Transcription Factors

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac6411b8099270eef1ec45b424751b37Test
https://doi.org/10.1182/blood.2018890764Test

المؤلفون: Suzan L. Carmichael, Ismael Zamilpa, Philip J. Lupo, Shanna A. Peyton, Noah A. Kallsen, Austin L. Brown, Richard A. Wyatt, Stephen Canon, Erik A. Ehli, Pagna Sok, Erin C. Peckham-Gregory, Ashay Patel, Charlotte A. Hobbs, Michael E. Scheurer, Gareth E. Davies, Wendy N. Nembhard, Melissa A. Richard

المصدر: Birth Defects Res

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Diacylglycerol Kinase, Embryology, medicine.medical_specialty, Genotype, Health, Toxicology and Mutagenesis, 030105 genetics & heredity, Toxicology, Population stratification, Logistic regression, Polymorphism, Single Nucleotide, Article, White People, Diacylglycerol kinase kappa, 03 medical and health sciences, Risk Factors, Internal medicine, Genetic variation, Odds Ratio, medicine, Humans, Genetic Predisposition to Disease, Genetic association, Hypospadias, Arkansas, business.industry, Genetic Variation, Infant, Odds ratio, medicine.disease, 030104 developmental biology, Case-Control Studies, Pediatrics, Perinatology and Child Health, Female, business, Genome-Wide Association Study, Developmental Biology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c25ac880c4d8b7dc0094045fe311c111Test
https://doi.org/10.1002/bdr2.1522Test

المؤلفون: Noah A. Kallsen, Yasushi Yatabe, Humam Kadara, Junya Fukuoka, Junya Fujimoto, Shanna A. Peyton, Erik A. Ehli, F. Anthony San Lucas, P. Andrew Futreal, Gareth E. Davies, Ignacio I. Wistuba, Paul Scheet, Smruthy Sivakumar, Ernest T. Hawk, Yasminka A. Jakubek, Tina McDowell, Jianjun Zhang, Wenhua Lang, Jerry Fowler

المصدر: EBioMedicine. 42:296-303

مصطلحات موضوعية: 0301 basic medicine, Genome instability, Research paper, Hyperplasia, Point mutation, Haplotype, Adenocarcinoma of Lung, Genomics, General Medicine, Allelic Imbalance, Biology, General Biochemistry, Genetics and Molecular Biology, Pathogenesis, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, 030220 oncology & carcinogenesis, Chromosome instability, Genotype, Cancer research, Humans, Atypical adenomatous hyperplasia, Precancerous Conditions

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a8b5d03d448139d30c064f9a7d053f9Test
https://doi.org/10.1016/j.ebiom.2019.03.020Test

المؤلفون: Ashay Patel, Minh Ton, Erin C. Peckham-Gregory, Shanna A. Peyton, Gareth E. Davies, Ismael Zamilpa, Austin L. Brown, Erik A. Ehli, Philip J. Lupo, Michael E. Scheurer, Charlotte A. Hobbs, Pagna Sok, Noah A. Kallsen, Wendy N. Nembhard, Melissa A. Richard, Stephen Canon

المصدر: Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-12 (2020)

مصطلحات موضوعية: Male, Candidate gene, lcsh:Medicine, Biology, Article, Epigenesis, Genetic, KLK7, Mendelian randomization, medicine, Humans, Gene Regulatory Networks, lcsh:Science, Gene, Genetic association, Genetics, Hypospadias, Multidisciplinary, DNA methylation, Gene Expression Profiling, lcsh:R, Infant, Methylation, medicine.disease, Gene Expression Regulation, Case-Control Studies, lcsh:Q, CpG Islands, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02bbc4c2e9b33f1e80f572511a299500Test
https://pubmed.ncbi.nlm.nih.gov/32728162Test

المؤلفون: Meike Bartels, Rick Jansen, Charles E. Breeze, Catharina E.M. van Beijsterveldt, Jouke J. Hottenga, Erik A. Ehli, Bastiaan T. Heijmans, Jenny van Dongen, Noah A. Kallsen, Gonneke Willemsen, Gareth E. Davies, Dorret I. Boomsma, Cornelis Kluft, Shanna A. Peyton

المساهمون: Division 6, Psychiatry, APH - Mental Health, Amsterdam Neuroscience - Complex Trait Genetics, Biological Psychology, APH - Personalized Medicine, APH - Health Behaviors & Chronic Diseases, Amsterdam Neuroscience - Mood, Anxiety, Psychosis, Stress & Sleep, APH - Methodology

المصدر: Epigenetics and Chromatin
Epigenetics and Chromatin, 11
Van Dongen, J, Ehli, E A, Jansen, R, Van Beijsterveldt, C E M, Willemsen, G, Hottenga, J J, Kallsen, N A, Peyton, S A, Breeze, C E, Kluft, C, Heijmans, B T, Bartels, M, Davies, G E & Boomsma, D I 2018, ' Genome-wide analysis of DNA methylation in buccal cells : A study of monozygotic twins and mQTLs ', Epigenetics and Chromatin, vol. 11, no. 1, 54 . https://doi.org/10.1186/s13072-018-0225-xTest
Epigenetics & Chromatin, Vol 11, Iss 1, Pp 1-14 (2018)
Van Dongen, J, Ehli, E A, Jansen, R, Van Beijsterveldt, C E M, Willemsen, G, Hottenga, J J, Kallsen, N A, Peyton, S A, Breeze, C E, Kluft, C, Heijmans, B T, Bartels, M, Davies, G E & Boomsma, D I 2018, ' Genome-wide analysis of DNA methylation in buccal cells : A study of monozygotic twins and mQTLs ', Epigenetics and Chromatin, vol. 11, 54, pp. 1-14 . https://doi.org/10.1186/s13072-018-0225-xTest
Epigenetics and Chromatin, 11(1):54. BioMed Central
Epigenetics and Chromatin, 11:54, 1-14. BioMed Central

مصطلحات موضوعية: Netherlands Twin Register (NTR), Male, 0301 basic medicine, lcsh:QH426-470, QTL, Quantitative Trait Loci, Buccal swab, Quantitative trait locus, Biology, Buccal, 03 medical and health sciences, chemistry.chemical_compound, 450 k, 0302 clinical medicine, Illumina, Genetics, Humans, Epigenetics, Child, Children, Molecular Biology, DNA methylation, Mouth Mucosa, Array, Infant, Twin study, Twins, Monozygotic, Methylation, lcsh:Genetics, 030104 developmental biology, Histone, chemistry, Child, Preschool, biology.protein, Female, EPIC, 030217 neurology & neurosurgery, DNA, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23f544aef0daf9c0508add6fa0c8fdfbTest
https://doi.org/10.1186/s13072-018-0225-xTest

المؤلفون: Reuven J. Schore, Maria S. Pombo-de-Oliveira, Helen M. Hansen, Beth A. Mueller, Ching-Hon Pui, Elizabeth A. Raetz, Austin L. Brown, Erik A. Ehli, Jillian M. Birch, Michael E. Zwick, Brent L. Wood, Xiaomei Ma, Mignon L. Loh, Shanna A. Peyton, Elanor Feingold, Jeffrey W. Taub, Meenakshi Devidas, Catherine Metayer, Stephanie L. Sherman, Naomi J. Winick, Jun J. Yang, Kyle M. Walsh, Daniel Sinnett, Jasmine Healy, Michael E. Scheurer, William L. Carroll, Michael J. Borowitz, Stephen P. Hunger, Noah A. Kallsen, Karen R. Rabin, Andrew J. Carroll, Philip J. Lupo, Gareth E. Davies, Lisa F. Barcellos, Kelly W. Maloney, Charles G. Mullighan, Ivan Smirnov, Mary V. Relling, Michael M. Burke, Nyla A. Heerema, Wanda L. Salzer, Joseph L. Wiemels, Anne L. Angiolillo, Adam J. de Smith, Wenjian Yang, Andrew T. DeWan

المصدر: Cancer Research. 78:222-222

مصطلحات موضوعية: 0301 basic medicine, Cancer Research, Down syndrome, Lymphoblastic Leukemia, Single-nucleotide polymorphism, Genome-wide association study, medicine.disease, Minor allele frequency, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, Oncology, 030220 oncology & carcinogenesis, medicine, Etiology, Childhood all, Genetic association, Demography

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::87d7a5c8f16701657b05ad13b5e8c57fTest
https://doi.org/10.1158/1538-7445.am2018-222Test