"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 |
|---|
| 1997 | 0 | 1 | 1 |
| 2002 | 1 | 0 | 1 |
| 2005 | 1 | 1 | 2 |
| 2006 | 1 | 1 | 2 |
| 2008 | 0 | 1 | 1 |
| 2009 | 1 | 0 | 1 |
| 2013 | 1 | 0 | 1 |
| 2015 | 1 | 0 | 1 |
| 2020 | 2 | 0 | 2 |
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Below are the most recent publications written about "Genomic Imprinting" by people in Profiles.
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Prasasya R, Grotheer KV, Siracusa LD, Bartolomei MS. Temple syndrome and Kagami-Ogata syndrome: clinical presentations, genotypes, models and mechanisms. Hum Mol Genet. 2020 09 30; 29(R1):R107-R116.
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van Bosse HJP, Butler MG. Clinical Observations and Treatment Approaches for Scoliosis in Prader-Willi Syndrome. Genes (Basel). 2020 02 28; 11(3).
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Gripp KW, Robbins KM, Sheffield BS, Lee AF, Patel MS, Yip S, Doyle D, Stabley D, Sol-Church K. Paternal uniparental disomy 11p15.5 in the pancreatic nodule of an infant with Costello syndrome: Shared mechanism for hyperinsulinemic hypoglycemia in neonates with Costello and Beckwith-Wiedemann syndrome and somatic loss of heterozygosity in Costello syndrome driving clonal expansion. Am J Med Genet A. 2016 Mar; 170(3):559-64.
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Jacobs DI, Mao Y, Fu A, Kelly WK, Zhu Y. Dysregulated methylation at imprinted genes in prostate tumor tissue detected by methylation microarray. BMC Urol. 2013 Jul 26; 13:37.
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Manipalviratn S, DeCherney A, Segars J. Imprinting disorders and assisted reproductive technology. Fertil Steril. 2009 Feb; 91(2):305-15.
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Siracusa LD, Buchberg AM. The noncoding RNAs: a genomic symphony of transcripts. Mamm Genome. 2008 Aug; 19(7-8):449-53.
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Feuk L, Kalervo A, Lipsanen-Nyman M, Skaug J, Nakabayashi K, Finucane B, Hartung D, Innes M, Kerem B, Nowaczyk MJ, Rivlin J, Roberts W, Senman L, Summers A, Szatmari P, Wong V, Vincent JB, Zeesman S, Osborne LR, Cardy JO, Kere J, Scherer SW, Hannula-Jouppi K. Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia. Am J Hum Genet. 2006 Nov; 79(5):965-72.
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Fares F, David M, Lerner A, Diukman R, Lerer I, Abeliovich D, Rivlin J. Paternal isodisomy of chromosome 7 with cystic fibrosis and overgrowth. Am J Med Genet A. 2006 Aug 15; 140(16):1785-8.
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Polan HJ. Guidance and differentiation of maternally directed orienting behaviors: probing the origins of filial attachment. Dev Psychobiol. 2005 Nov; 47(3):278-87.
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Corradi JP, Ravyn V, Robbins AK, Hagan KW, Peters MF, Bostwick R, Buono RJ, Berrettini WH, Furlong ST. Alternative transcripts and evidence of imprinting of GNAL on 18p11.2. Mol Psychiatry. 2005 Nov; 10(11):1017-25.