"Pedigree" 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 record of descent or ancestry, particularly of a particular condition or trait, indicating individual family members, their relationships, and their status with respect to the trait or condition.
| Descriptor ID |
D010375
|
| MeSH Number(s) |
E05.393.673
|
| Concept/Terms |
Identity, Genetic- Identity, Genetic
- Genetic Identities
- Identities, Genetic
- Genetic Identity
Family Tree- Family Tree
- Family Trees
- Tree, Family
- Trees, Family
- Genealogical Tree
- Genealogical Trees
- Tree, Genealogical
- Trees, Genealogical
- Genealogic Tree
- Genealogic Trees
- Tree, Genealogic
- Trees, Genealogic
|
Below are MeSH descriptors whose meaning is more general than "Pedigree".
Below are MeSH descriptors whose meaning is more specific than "Pedigree".
This graph shows the total number of publications written about "Pedigree" by people in this website by year, and whether "Pedigree" 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 |
|---|
| 1995 | 0 | 16 | 16 |
| 1996 | 0 | 19 | 19 |
| 1997 | 0 | 21 | 21 |
| 1998 | 0 | 26 | 26 |
| 1999 | 0 | 30 | 30 |
| 2000 | 0 | 29 | 29 |
| 2001 | 0 | 23 | 23 |
| 2002 | 1 | 20 | 21 |
| 2003 | 0 | 23 | 23 |
| 2004 | 0 | 19 | 19 |
| 2005 | 1 | 17 | 18 |
| 2006 | 0 | 20 | 20 |
| 2007 | 0 | 20 | 20 |
| 2008 | 0 | 19 | 19 |
| 2009 | 1 | 19 | 20 |
| 2010 | 1 | 14 | 15 |
| 2011 | 0 | 20 | 20 |
| 2012 | 0 | 26 | 26 |
| 2013 | 2 | 27 | 29 |
| 2014 | 1 | 29 | 30 |
| 2015 | 0 | 34 | 34 |
| 2016 | 2 | 37 | 39 |
| 2017 | 0 | 23 | 23 |
| 2018 | 0 | 43 | 43 |
| 2019 | 0 | 45 | 45 |
| 2020 | 0 | 37 | 37 |
| 2021 | 1 | 31 | 32 |
| 2022 | 0 | 9 | 9 |
| 2023 | 0 | 4 | 4 |
| 2024 | 5 | 12 | 17 |
| 2025 | 1 | 4 | 5 |
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Below are the most recent publications written about "Pedigree" by people in Profiles.
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Clinical characterization of Collagen XII-related disease caused by biallelic COL12A1 variants. Ann Clin Transl Neurol. 2025 Mar; 12(3):602-614.
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Unprecedented female mutation bias in the aye-aye, a highly unusual lemur from Madagascar. PLoS Biol. 2025 Feb; 23(2):e3003015.
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FIGG at 5: An update on U.S. public perspectives on forensic investigative genetic genealogy five years after its introduction to criminal investigations. Forensic Sci Int. 2025 Feb; 367:112372.
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Investigative genetic genealogy practices warranting policy attention: Results of a modified policy Delphi. PLoS Genet. 2025 Jan; 21(1):e1011520.
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A recurrent missense variant in ITPR3 causes demyelinating Charcot-Marie-Tooth with variable severity. Brain. 2025 Jan 07; 148(1):227-237.
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Phenotypic and Genetic Heterogeneity of a Pakistani Cohort of 15 Consanguineous Families Segregating Variants in Leber Congenital Amaurosis-Associated Genes. Genes (Basel). 2024 Dec 21; 15(12).
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ClC-Kb pore mutation disrupts glycosylation and triggers distal tubular remodeling. JCI Insight. 2024 Nov 22; 9(22).
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Homozygous variants in WDR83OS lead to a neurodevelopmental disorder with hypercholanemia. Am J Hum Genet. 2024 Nov 07; 111(11):2566-2581.
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Family Lore, a Variant of Uncertain Significance, and?CADASIL. Am J Med Genet C Semin Med Genet. 2024 Nov; 196(2-3):e32117.
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Compound heterozygous mutation of AFG3L2 causes autosomal recessive spinocerebellar ataxia through mitochondrial impairment and MICU1 mediated Ca2+ overload. Sci China Life Sci. 2025 Feb; 68(2):484-501.