"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 |
|---|
| 1996 | 0 | 21 | 21 |
| 1997 | 0 | 21 | 21 |
| 1998 | 0 | 26 | 26 |
| 1999 | 0 | 31 | 31 |
| 2000 | 0 | 32 | 32 |
| 2001 | 0 | 24 | 24 |
| 2002 | 1 | 22 | 23 |
| 2003 | 0 | 26 | 26 |
| 2004 | 1 | 20 | 21 |
| 2005 | 1 | 18 | 19 |
| 2006 | 0 | 18 | 18 |
| 2007 | 0 | 21 | 21 |
| 2008 | 0 | 18 | 18 |
| 2009 | 1 | 19 | 20 |
| 2010 | 1 | 14 | 15 |
| 2011 | 0 | 20 | 20 |
| 2012 | 0 | 27 | 27 |
| 2013 | 2 | 25 | 27 |
| 2014 | 1 | 32 | 33 |
| 2015 | 0 | 39 | 39 |
| 2016 | 1 | 41 | 42 |
| 2017 | 0 | 31 | 31 |
| 2018 | 0 | 49 | 49 |
| 2019 | 0 | 53 | 53 |
| 2020 | 0 | 36 | 36 |
| 2021 | 1 | 37 | 38 |
| 2022 | 0 | 9 | 9 |
| 2023 | 0 | 5 | 5 |
| 2024 | 4 | 14 | 18 |
| 2025 | 3 | 25 | 28 |
| 2026 | 1 | 3 | 4 |
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Below are the most recent publications written about "Pedigree" by people in Profiles.
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Interpretable Active Learning for Pedigree Data Deduplication in Cancer Genetics. JCO Clin Cancer Inform. 2026 Mar; 10:e2500252.
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Biallelic Novel SKOR2 Variants in Individuals With Cerebellar Hypoplasia and Intellectual Disability, Expanding the Phenotypic Spectrum of Valence-Farazi Cerebellar Ataxia Syndrome. Am J Med Genet A. 2026 07; 200(7):1725-1739.
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Bi-allelic variants in NRDC cause a neurodevelopmental disorder characterized by neonatal lethality, microcephaly, and brain abnormalities. Am J Hum Genet. 2026 03 05; 113(3):548-561.
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Bi-allelic variants in neuronal adhesion molecule astrotactin 1 gene ASTN1 cause diverse neurodevelopmental disorders. Am J Hum Genet. 2026 Feb 05; 113(2):362-379.
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Genetic variants in ESRRG are associated with a dominant non-progressive congenital movement disorder with ataxia. Am J Hum Genet. 2025 12 04; 112(12):2961-2972.
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A clinical and genotype-phenotype analysis of MACF1 variants. Am J Hum Genet. 2025 10 02; 112(10):2363-2380.
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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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Forensic investigative genetic genealogy and public trust. J Forensic Sci. 2025 Nov; 70(6):2113-2116.
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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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De novo and inherited variants in DDX39B cause a novel neurodevelopmental syndrome. Brain. 2025 Aug 01; 148(8):2658-2670.