 Paternal Inheritance
"Paternal Inheritance" 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.
A form of inheritance where the traits of the offspring are paternal in origin due to the expression of extra-nuclear genetic material such as MITOCHONDRIAL DNA or Y chromosome genes. CENTRIOLES are also paternally inherited.
| Descriptor ID |
D000072740
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| MeSH Number(s) |
G05.420.623
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| Concept/Terms |
Paternal Inheritance- Paternal Inheritance
- Inheritance, Paternal
- Paternal Effect
- Effect, Paternal
- Effects, Paternal
- Paternal Effects
- Inherited Paternally
- Paternally, Inherited
- Paternally Inherited
- Inherited, Paternally
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Below are MeSH descriptors whose meaning is more general than "Paternal Inheritance".
Below are MeSH descriptors whose meaning is more specific than "Paternal Inheritance".
This graph shows the total number of publications written about "Paternal Inheritance" by people in this website by year, and whether "Paternal Inheritance" 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 |
|---|
| 2020 | 1 | 1 | 2 | | 2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Paternal Inheritance" by people in Profiles.
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Balbona JV, Kim Y, Keller MC. Estimation of Parental Effects Using Polygenic Scores. Behav Genet. 2021 05; 51(3):264-278.
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Kim Y, Balbona JV, Keller MC. Bias and Precision of Parameter Estimates from Models Using Polygenic Scores to Estimate Environmental and Genetic Parental Influences. Behav Genet. 2021 05; 51(3):279-288.
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Granot-Hershkovitz E, Wu P, Karasik D, Peter I, Peloso GM, Levy D, Vasan RS, Adrienne Cupples L, Liu CT, Meigs JB, Siscovick DS, Dupuis J, Friedlander Y, Hochner H. Searching for parent-of-origin effects on cardiometabolic traits in imprinted genomic regions. Eur J Hum Genet. 2020 05; 28(5):646-655.
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Karolak JA, Vincent M, Deutsch G, Gambin T, Cogn? B, Pichon O, Vetrini F, Mefford HC, Dines JN, Golden-Grant K, Dipple K, Freed AS, Leppig KA, Dishop M, Mowat D, Bennetts B, Gifford AJ, Weber MA, Lee AF, Boerkoel CF, Bartell TM, Ward-Melver C, Besnard T, Petit F, Bache I, T?mer Z, Denis-Musquer M, Joubert M, Martinovic J, B?n?teau C, Molin A, Carles D, Andr? G, Bieth E, Chassaing N, Devisme L, Chalabreysse L, Pasquier L, Secq V, Don M, Orsaria M, Missirian C, Mortreux J, Sanlaville D, Pons L, K?ry S, B?zieau S, Liet JM, Joram N, Bihou?e T, Scott DA, Brown CW, Scaglia F, Tsai AC, Grange DK, Phillips JA, Pfotenhauer JP, Jhangiani SN, Gonzaga-Jauregui CG, Chung WK, Schauer GM, Lipson MH, Mercer CL, van Haeringen A, Liu Q, Popek E, Coban Akdemir ZH, Lupski JR, Szafranski P, Isidor B, Le Caignec C, Stankiewicz P. Complex Compound Inheritance of Lethal Lung Developmental Disorders Due to Disruption of the TBX-FGF Pathway. Am J Hum Genet. 2019 02 07; 104(2):213-228.
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