"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 | 31 | 31 |
| 1997 | 0 | 37 | 37 |
| 1998 | 0 | 20 | 20 |
| 1999 | 1 | 17 | 18 |
| 2000 | 0 | 27 | 27 |
| 2001 | 2 | 17 | 19 |
| 2002 | 2 | 20 | 22 |
| 2003 | 2 | 25 | 27 |
| 2004 | 2 | 30 | 32 |
| 2005 | 0 | 24 | 24 |
| 2006 | 0 | 19 | 19 |
| 2007 | 2 | 23 | 25 |
| 2008 | 2 | 22 | 24 |
| 2009 | 1 | 16 | 17 |
| 2010 | 1 | 15 | 16 |
| 2011 | 1 | 20 | 21 |
| 2012 | 2 | 17 | 19 |
| 2013 | 1 | 15 | 16 |
| 2014 | 1 | 12 | 13 |
| 2015 | 1 | 16 | 17 |
| 2016 | 2 | 16 | 18 |
| 2017 | 1 | 8 | 9 |
| 2018 | 0 | 11 | 11 |
| 2019 | 2 | 13 | 15 |
| 2020 | 1 | 13 | 14 |
| 2021 | 0 | 5 | 5 |
| 2022 | 0 | 1 | 1 |
| 2023 | 0 | 1 | 1 |
| 2024 | 1 | 5 | 6 |
| 2025 | 1 | 8 | 9 |
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Below are the most recent publications written about "Pedigree" by people in Profiles.
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Pathogenic Variants, Family History, and Cumulative Risk of Breast Cancer in US Women. JAMA Oncol. 2025 Dec 01; 11(12):1458-1469.
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Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition. Nat Commun. 2025 Nov 10; 16(1):9875.
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Prevalence of pendrin defects in sudanese families with congenital hypothyroidism. Endocrine. 2025 12; 90(3):1339-1349.
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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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Clinical and Pathologic Phenotyping of Mesotheliomas Developing in Carriers of Germline BAP1 Mutations. J Thorac Oncol. 2025 11; 20(11):1683-1698.
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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 07 03; 112(7):1722-1732.
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Germline mutation rates and fine-scale recombination parameters in zebra finch. PLoS Genet. 2025 Apr; 21(4):e1011661.
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Overall cancer risk in people with deleterious germline DDX41 variants. Haematologica. 2025 09 01; 110(9):2076-2090.
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Whole Genome Sequencing of Pedigrees With High Density of Substance Use and Psychiatric Disorders: A Meeting Report. Genes Brain Behav. 2025 02; 24(1):e70017.
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Germ line ERG haploinsufficiency defines a new syndrome with cytopenia and hematological malignancy predisposition. Blood. 2024 10 24; 144(17):1765-1780.