"Genomic Imprinting" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
The variable phenotypic expression of a GENE depending on whether it is of paternal or maternal origin, which is a function of the DNA METHYLATION pattern. Imprinted regions are observed to be more methylated and less transcriptionally active. (Segen, Dictionary of Modern Medicine, 1992)
| Descriptor ID |
D018392
|
| MeSH Number(s) |
G05.308.203.500
|
| Concept/Terms |
Genomic Imprinting- Genomic Imprinting
- Imprinting, Genomic
- Parental Imprinting
- Imprinting, Parental
- Imprinting, Genetic
- Genetic Imprinting
|
Below are MeSH descriptors whose meaning is more general than "Genomic Imprinting".
Below are MeSH descriptors whose meaning is more specific than "Genomic Imprinting".
This graph shows the total number of publications written about "Genomic Imprinting" by people in this website by year, and whether "Genomic Imprinting" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1994 | 1 | 0 | 1 |
| 1997 | 1 | 2 | 3 |
| 1998 | 1 | 5 | 6 |
| 1999 | 2 | 0 | 2 |
| 2000 | 6 | 2 | 8 |
| 2001 | 1 | 0 | 1 |
| 2002 | 1 | 2 | 3 |
| 2003 | 4 | 6 | 10 |
| 2004 | 2 | 5 | 7 |
| 2005 | 5 | 0 | 5 |
| 2006 | 3 | 3 | 6 |
| 2007 | 3 | 4 | 7 |
| 2008 | 4 | 1 | 5 |
| 2009 | 3 | 2 | 5 |
| 2010 | 1 | 3 | 4 |
| 2011 | 2 | 1 | 3 |
| 2012 | 5 | 4 | 9 |
| 2013 | 3 | 2 | 5 |
| 2014 | 0 | 4 | 4 |
| 2015 | 2 | 0 | 2 |
| 2016 | 3 | 3 | 6 |
| 2017 | 1 | 3 | 4 |
| 2019 | 4 | 3 | 7 |
| 2020 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
| 2023 | 0 | 1 | 1 |
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click here.
Below are the most recent publications written about "Genomic Imprinting" by people in Profiles.
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Genetic and epigenetic features of bilateral Wilms tumor predisposition in patients from the Children's Oncology Group AREN18B5-Q. Nat Commun. 2023 Dec 18; 14(1):8006.
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DNA Methylation Dynamics in the Female Germline and Maternal-Effect Mutations That Disrupt Genomic Imprinting. Genes (Basel). 2021 08 06; 12(8).
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The effect of laser-assisted hatching on the methylation and expression pattern of imprinted gene IGF2/H19 in mouse blastocysts and offspring. J Assist Reprod Genet. 2020 Dec; 37(12):3057-3067.
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Joint modeling of eQTLs and parent-of-origin effects using an orthogonal framework with RNA-seq data. Hum Genet. 2020 Aug; 139(8):1107-1117.
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Association of rare non-coding SNVs in the lung-specific FOXF1 enhancer with a mitigation of the lethal ACDMPV phenotype. Hum Genet. 2019 Dec; 138(11-12):1301-1311.
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High-resolution analysis of germ cells from men with sex chromosomal aneuploidies reveals normal transcriptome but impaired imprinting. Clin Epigenetics. 2019 08 28; 11(1):127.
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Epigenome-wide association study of DNA methylation and microRNA expression highlights novel pathways for human complex traits. Epigenetics. 2020 Jan - Feb; 15(1-2):183-198.
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SETD2 regulates the maternal epigenome, genomic imprinting and embryonic development. Nat Genet. 2019 05; 51(5):844-856.
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Interchromosomal template-switching as a novel molecular mechanism for imprinting perturbations associated with Temple syndrome. Genome Med. 2019 04 23; 11(1):25.
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Novel parent-of-origin-specific differentially methylated loci on chromosome 16. Clin Epigenetics. 2019 04 08; 11(1):60.