scholarly article | Q13442814 |
P356 | DOI | 10.1038/S41588-018-0232-7 |
P2888 | exact match | https://scigraph.springernature.com/pub.10.1038/s41588-018-0232-7 |
P698 | PubMed publication ID | 30349119 |
P50 | author | Kári Stefánsson | Q6453246 |
Unnur Þorsteinsdóttir | Q28050158 | ||
Daníel F. Guðbjartsson | Q30348313 | ||
Thorunn Rafnar | Q30430661 | ||
Páll Melsted | Q56420205 | ||
P2093 | author name string | Asgeir Sigurdsson | |
Gisli Masson | |||
Julius Gudmundsson | |||
Gudmundur Ingi Eyjolfsson | |||
Hilma Holm | |||
Isleifur Olafsson | |||
Florian Zink | |||
Anna Helgadottir | |||
Olof Sigurdardottir | |||
Ingileif Jonsdottir | |||
Bjarni V. Halldorsson | |||
Droplaug N. Magnusdottir | |||
Simon N. Stacey | |||
Gisli H. Halldorsson | |||
Helga Ingimundardottir | |||
Snædis Kristmundsdottir | |||
Olafur T. Magnusson | |||
Sigurjon A. Gudjonsson | |||
Kristjan F. Alexandersson | |||
Nicolas J. Walker | |||
Tiffany J. Morris | |||
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Locally disordered methylation forms the basis of intratumor methylome variation in chronic lymphocytic leukemia | Q34997508 | ||
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DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome | Q37231371 | ||
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease | Q37634534 | ||
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P433 | issue | 11 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | transcriptome | Q252857 |
P304 | page(s) | 1542-1552 | |
P577 | publication date | 2018-10-22 | |
P1433 | published in | Nature Genetics | Q976454 |
P1476 | title | Insights into imprinting from parent-of-origin phased methylomes and transcriptomes | |
P478 | volume | 50 |
Q97559181 | Alteration of methylation status in archival DNA samples: A qualitative assessment by methylation specific polymerase chain reaction |
Q93063992 | Assisted reproductive technologies are associated with limited epigenetic variation at birth that largely resolves by adulthood |
Q100433819 | Clinically and biologically relevant subgroups of Wilms tumour defined by genomic and epigenomic analyses |
Q64990350 | Epigenetic therapy of Prader-Willi syndrome. |
Q90595517 | Genome-wide allele-specific methylation is enriched at gene regulatory regions in a multi-generation pedigree from the Norfolk Island isolate |
Q91063421 | Genomic imprinting disorders: lessons on how genome, epigenome and environment interact |
Q91619136 | Loss of p57KIP2 expression confers resistance to contact inhibition in human androgenetic trophoblast stem cells |
Q99415614 | Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance |
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Q64066289 | Novel parent-of-origin-specific differentially methylated loci on chromosome 16 |
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Q90179394 | The Role of microRNAs, Long Non-coding RNAs, and Circular RNAs in Cervical Cancer |
Q93192447 | Twin Registries Moving Forward and Meeting the Future: A Review |
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