"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 | 21 | 21 |
| 1997 | 0 | 22 | 22 |
| 1998 | 0 | 26 | 26 |
| 1999 | 0 | 32 | 32 |
| 2000 | 0 | 32 | 32 |
| 2001 | 0 | 25 | 25 |
| 2002 | 1 | 22 | 23 |
| 2003 | 0 | 27 | 27 |
| 2004 | 1 | 19 | 20 |
| 2005 | 1 | 20 | 21 |
| 2006 | 0 | 18 | 18 |
| 2007 | 0 | 21 | 21 |
| 2008 | 0 | 18 | 18 |
| 2009 | 1 | 19 | 20 |
| 2010 | 1 | 15 | 16 |
| 2011 | 0 | 20 | 20 |
| 2012 | 0 | 26 | 26 |
| 2013 | 2 | 28 | 30 |
| 2014 | 1 | 32 | 33 |
| 2015 | 0 | 36 | 36 |
| 2016 | 1 | 41 | 42 |
| 2017 | 0 | 28 | 28 |
| 2018 | 0 | 49 | 49 |
| 2019 | 0 | 53 | 53 |
| 2020 | 0 | 37 | 37 |
| 2021 | 1 | 36 | 37 |
| 2022 | 0 | 9 | 9 |
| 2023 | 0 | 4 | 4 |
| 2024 | 4 | 13 | 17 |
| 2025 | 2 | 21 | 23 |
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Below are the most recent publications written about "Pedigree" by people in Profiles.
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A novel homozygous frameshift mutation likely causing nonsense-mediated mRNA decay in an Algerian kindred with CD19 complex deficiency. Front Immunol. 2025; 16:1634146.
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De novo and inherited variants in DDX39B cause a novel neurodevelopmental syndrome. Brain. 2025 Aug 01; 148(8):2658-2670.
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Heterozygous RAB3A variants cause cerebellar ataxia by a partial loss-of-function mechanism. Brain. 2025 Aug 01; 148(8):2812-2826.
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Increased colorectal and endometrial cancer rates in a genomically ascertained Lynch syndrome cohort. JNCI Cancer Spectr. 2025 Jul 01; 9(4).
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Recurrent de novo variants in the spliceosomal factor CRNKL1 are associated with severe microcephaly and pontocerebellar hypoplasia with seizures. Am J Hum Genet. 2025 Jul 03; 112(7):1722-1732.
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Biallelic Loss-of-Function Variant in MINPP1 Causes Pontocerebellar Hypoplasia with Characteristic Severe Neurodevelopmental Disorder. Int J Mol Sci. 2025 May 29; 26(11).
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Loss of function of the zinc finger homeobox 4 gene, ZFHX4, underlies a neurodevelopmental disorder. Am J Hum Genet. 2025 Jun 05; 112(6):1388-1414.
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Deletion Testing of the DEGS1 Gene Should Be Part of the Diagnostic Pipeline for Hypomyelinating Leukodystrophy (HLD18). Hum Mutat. 2025; 2025:3531508.
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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.