"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 | 24 | 24 |
| 2004 | 0 | 19 | 19 |
| 2005 | 1 | 17 | 18 |
| 2006 | 0 | 19 | 19 |
| 2007 | 0 | 20 | 20 |
| 2008 | 0 | 17 | 17 |
| 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 | 42 | 42 |
| 2019 | 0 | 45 | 45 |
| 2020 | 0 | 34 | 34 |
| 2021 | 1 | 30 | 31 |
| 2022 | 0 | 9 | 9 |
| 2023 | 0 | 4 | 4 |
| 2024 | 5 | 12 | 17 |
| 2025 | 1 | 9 | 10 |
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Below are the most recent publications written about "Pedigree" by people in Profiles.
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Identification of Hepatic-like EPO as a Cause of Polycythemia. N Engl J Med. 2025 May 01; 392(17):1684-1697.
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Bi-allelic UGGT1 variants cause a congenital disorder of glycosylation. Am J Hum Genet. 2025 May 01; 112(5):1139-1157.
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De novo variants in CDKL1 and CDKL2 are associated with neurodevelopmental symptoms. Am J Hum Genet. 2025 Apr 03; 112(4):846-862.
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RNA methyltransferase SPOUT1/CENP-32 links mitotic spindle organization with the neurodevelopmental disorder SpADMiSS. Nat Commun. 2025 Feb 17; 16(1):1703.
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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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TFAP2E is implicated in central nervous system, orofacial and maxillofacial anomalies. J Med Genet. 2025 Jan 27; 62(2):126-137.
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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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Monoallelic expression can govern penetrance of inborn errors of immunity. Nature. 2025 Jan; 637(8048):1186-1197.