"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 | 2 | 24 | 26 |
| 1995 | 0 | 21 | 21 |
| 1996 | 0 | 33 | 33 |
| 1997 | 0 | 32 | 32 |
| 1998 | 0 | 37 | 37 |
| 1999 | 0 | 38 | 38 |
| 2000 | 0 | 37 | 37 |
| 2001 | 0 | 33 | 33 |
| 2002 | 1 | 30 | 31 |
| 2003 | 1 | 30 | 31 |
| 2004 | 0 | 31 | 31 |
| 2005 | 1 | 28 | 29 |
| 2006 | 1 | 30 | 31 |
| 2007 | 1 | 39 | 40 |
| 2008 | 0 | 28 | 28 |
| 2009 | 0 | 26 | 26 |
| 2010 | 1 | 27 | 28 |
| 2011 | 1 | 23 | 24 |
| 2012 | 0 | 28 | 28 |
| 2013 | 3 | 30 | 33 |
| 2014 | 2 | 34 | 36 |
| 2015 | 0 | 39 | 39 |
| 2016 | 3 | 43 | 46 |
| 2017 | 1 | 30 | 31 |
| 2018 | 0 | 46 | 46 |
| 2019 | 0 | 48 | 48 |
| 2020 | 0 | 41 | 41 |
| 2021 | 2 | 33 | 35 |
| 2022 | 0 | 9 | 9 |
| 2023 | 0 | 4 | 4 |
| 2024 | 5 | 13 | 18 |
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Below are the most recent publications written about "Pedigree" by people in Profiles.
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ClC-Kb pore mutation disrupts glycosylation and triggers distal tubular remodeling. JCI Insight. 2024 Nov 22; 9(22).
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Homozygous variants in WDR83OS lead to a neurodevelopmental disorder with hypercholanemia. Am J Hum Genet. 2024 Nov 07; 111(11):2566-2581.
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Family Lore, a Variant of Uncertain Significance, and?CADASIL. Am J Med Genet C Semin Med Genet. 2024 Nov; 196(2-3):e32117.
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Germline mutations in a G protein identify signaling cross-talk in T cells. Science. 2024 Sep 20; 385(6715):eadd8947.
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Chromatin conformation capture in the clinic: 4C-seq/HiC distinguishes pathogenic from neutral duplications at the GPR101 locus. Genome Med. 2024 Sep 13; 16(1):112.
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Non-coding cause of congenital heart defects: Abnormal RNA splicing with multiple isoforms as a mechanism for heterotaxy. HGG Adv. 2024 Oct 10; 5(4):100353.
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Whole-exome sequencing uncovers the genetic complexity of bicuspid aortic valve in families with early-onset complications. Am J Hum Genet. 2024 Oct 03; 111(10):2219-2231.
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Detection of distant relatedness in biobanks to identify undiagnosed cases of Mendelian disease as applied to Long QT syndrome. Nat Commun. 2024 Aug 29; 15(1):7507.
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Recessive loss-of-function variants in DPH1 identified as the molecular cause in a sibling pair previously diagnosed with Fine-Lubinsky syndrome. Am J Med Genet A. 2025 Jan; 197(1):e63845.
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"The truth should not be hidden": Experiences and recommendations of individuals making NPE discoveries through genetic genealogy databases. Genet Med. 2024 Oct; 26(10):101210.