"Consanguinity" 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 magnitude of INBREEDING in humans.
Descriptor ID |
D003241
|
MeSH Number(s) |
G05.090.403.180 G05.180
|
Concept/Terms |
Consanguinous Mating- Consanguinous Mating
- Consanguinous Matings
- Mating, Consanguinous
- Matings, Consanguinous
- Inbreeding, Human
- Human Inbreeding
- Human Inbreedings
- Inbreedings, Human
Consanguineous Marriage- Consanguineous Marriage
- Consanguineous Marriages
- Marriage, Consanguineous
- Marriages, Consanguineous
|
Below are MeSH descriptors whose meaning is more general than "Consanguinity".
Below are MeSH descriptors whose meaning is more specific than "Consanguinity".
This graph shows the total number of publications written about "Consanguinity" by people in this website by year, and whether "Consanguinity" 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 |
---|
2008 | 0 | 1 | 1 |
2009 | 0 | 1 | 1 |
2010 | 1 | 1 | 2 |
2011 | 0 | 2 | 2 |
2012 | 0 | 3 | 3 |
2013 | 0 | 5 | 5 |
2014 | 0 | 4 | 4 |
2015 | 1 | 5 | 6 |
2016 | 2 | 8 | 10 |
2017 | 1 | 1 | 2 |
2018 | 0 | 3 | 3 |
2019 | 0 | 5 | 5 |
2021 | 0 | 4 | 4 |
2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "Consanguinity" by people in Profiles.
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Monoallelic and biallelic variants in LEF1 are associated with a new syndrome combining ectodermal dysplasia and limb malformations caused by altered WNT signaling. Genet Med. 2022 08; 24(8):1708-1721.
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A novel missense variant of SCN4A co-segregates with congenital essential tremor in a consanguineous Kurdish family. Am J Med Genet A. 2022 04; 188(4):1251-1258.
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Biallelic variants in YRDC cause a developmental disorder with progeroid features. Hum Genet. 2021 Dec; 140(12):1679-1693.
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A Novel Missense Mutation in TNNI3K Causes Recessively Inherited Cardiac Conduction Disease in a Consanguineous Pakistani Family. Genes (Basel). 2021 08 21; 12(8).
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An identical-by-descent novel splice-donor variant in PRUNE1 causes a neurodevelopmental syndrome with prominent dystonia in two consanguineous Sudanese families. Ann Hum Genet. 2021 09; 85(5):186-195.
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Distinct genetic variation and heterogeneity of the Iranian population. PLoS Genet. 2019 09; 15(9):e1008385.
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UV-sensitive syndrome: Whole exome sequencing identified a nonsense mutation in the gene UVSSA in two consanguineous pedigrees from Pakistan. J Dermatol Sci. 2019 Sep; 95(3):113-118.
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Mutated SON putatively causes a cancer syndrome comprising high-risk medulloblastoma combined with caf?-au-lait spots. Fam Cancer. 2019 07; 18(3):353-358.
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Biallelic loss-of-function LACC1/FAMIN Mutations Presenting as Rheumatoid Factor-Negative Polyarticular Juvenile Idiopathic Arthritis. Sci Rep. 2019 03 14; 9(1):4579.
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PDE10A mutation in two sisters with a hyperkinetic movement disorder - Response to levodopa. Parkinsonism Relat Disord. 2019 06; 63:240-242.