"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 |
|---|
| 1994 | 1 | 19 | 20 |
| 1995 | 0 | 17 | 17 |
| 1996 | 0 | 32 | 32 |
| 1997 | 0 | 37 | 37 |
| 1998 | 0 | 22 | 22 |
| 1999 | 1 | 17 | 18 |
| 2000 | 0 | 27 | 27 |
| 2001 | 2 | 18 | 20 |
| 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 | 23 | 25 |
| 2009 | 1 | 15 | 16 |
| 2010 | 1 | 15 | 16 |
| 2011 | 1 | 19 | 20 |
| 2012 | 2 | 18 | 20 |
| 2013 | 1 | 15 | 16 |
| 2014 | 1 | 11 | 12 |
| 2015 | 1 | 13 | 14 |
| 2016 | 2 | 16 | 18 |
| 2017 | 1 | 7 | 8 |
| 2018 | 0 | 11 | 11 |
| 2019 | 2 | 10 | 12 |
| 2020 | 1 | 13 | 14 |
| 2021 | 0 | 3 | 3 |
| 2023 | 0 | 1 | 1 |
| 2024 | 0 | 5 | 5 |
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Below are the most recent publications written about "Pedigree" by people in Profiles.
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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.
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Severe neurodevelopmental phenotype, diagnostic, and treatment challenges in patients with SECISBP2 deficiency. Genet Med. 2024 Dec; 26(12):101280.
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Evaluation of the genetic basis of familial-associated early-onset hematologic cancers in an ancestral/ethnically diverse population. Haematologica. 2024 07 01; 109(7):2085-2091.
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STR mutations on chromosome 15q cause thyrotropin resistance by activating a primate-specific enhancer of MIR7-2/MIR1179. Nat Genet. 2024 May; 56(5):877-888.
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Implications of methodologies for integrating empirical kinships into ex situ population management using PMx: A case study of Baer's Pochard (Aythya baeri) in North America. J Hered. 2024 Feb 03; 115(1):19-31.
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Insulin Deficiency From Insulin Gene Mutation Leads to Smaller Pancreas. Diabetes Care. 2023 04 01; 46(4):773-776.
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Immunodeficiency and bone marrow failure with mosaic and germline TLR8 gain of function. Blood. 2021 05 06; 137(18):2450-2462.
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Ancestral haplotype reconstruction in endogamous populations using identity-by-descent. PLoS Comput Biol. 2021 02; 17(2):e1008638.
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Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations. J Clin Immunol. 2021 05; 41(4):756-768.
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Lifelong Reduction in LDL (Low-Density Lipoprotein) Cholesterol due to a Gain-of-Function Mutation in LDLR. Circ Genom Precis Med. 2021 02; 14(1):e003029.