Supplemental material
Epigenetics
Volume 13, 2018 - Issue 2
Point of View
Recommendations for a nomenclature system for reporting methylation aberrations in imprinted domains
David MonkImprinting and Cancer group, Cancer Epigenetic and Biology Program, Bellvitge Biomedical Research Institute, Barcelona, Spain
http://orcid.org/0000-0001-8991-0497View further author information
http://orcid.org/0000-0001-8991-0497View further author information, , , , , , , , , & the Nomenclature group of the European Network for Human Congenital Imprinting Disorders show allRelated Research Data
Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment
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Cold Spring Harbor Laboratory
High-resolution analysis of germ cells from men with sex chromosomal aneuploidies reveals normal transcriptome but impaired imprinting
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Springer Science and Business Media LLC
Time for a standardized system of reporting sites of genomic methylation
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Springer Nature
Complex Tissue-Specific Epigenotypes in Russell-Silver Syndrome Associated with 11p15 ICR1 Hypomethylation
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Wiley-Blackwell
Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement
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Springer Science and Business Media LLC
Recommendations for a nomenclature system for reporting methylation aberrations in imprinted domains
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Figshare
Parental-origin-specific epigenetic modification of the mouse H19 gene
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Springer Nature
Recommendations for a nomenclature system for reporting methylation aberrations in imprinted domains
Source:
Figshare
Temple syndrome in a patient with variably methylated CpGs at the primary MEG3/DLK1:IG-DMR and severely hypomethylated CpGs at the secondary MEG3:TSS-DMR
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Springer Science and Business Media LLC
A case of intraplacental gestational choriocarcinoma; characterised by the methylation pattern of the early placenta and an absence of driver mutations
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Springer Science and Business Media LLC
Congenital imprinting disorders: Application of multilocus and high throughput methods to decipher new pathomechanisms and improve their management
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Elsevier BV
Locus Reference Genomic: reference sequences for the reporting of clinically relevant sequence variants
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Oxford University Press (OUP)
Genomic imprinting: The emergence of an epigenetic paradigm
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Springer Science and Business Media LLC
Causes and Consequences of Multi-Locus Imprinting Disturbances in Humans
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Elsevier BV
Standard mutation nomenclature in molecular diagnostics: practical and educational challenges.
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Elsevier BV
Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal
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Elsevier BV
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