"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 | 22 | 24 |
1995 | 0 | 20 | 20 |
1996 | 0 | 29 | 29 |
1997 | 0 | 26 | 26 |
1998 | 0 | 32 | 32 |
1999 | 0 | 30 | 30 |
2000 | 0 | 31 | 31 |
2001 | 0 | 20 | 20 |
2002 | 1 | 19 | 20 |
2003 | 1 | 32 | 33 |
2004 | 0 | 30 | 30 |
2005 | 1 | 26 | 27 |
2006 | 1 | 28 | 29 |
2007 | 1 | 37 | 38 |
2008 | 0 | 27 | 27 |
2009 | 0 | 26 | 26 |
2010 | 1 | 26 | 27 |
2011 | 1 | 23 | 24 |
2012 | 0 | 29 | 29 |
2013 | 2 | 32 | 34 |
2014 | 2 | 33 | 35 |
2015 | 0 | 37 | 37 |
2016 | 3 | 43 | 46 |
2017 | 1 | 31 | 32 |
2018 | 0 | 45 | 45 |
2019 | 0 | 49 | 49 |
2020 | 0 | 42 | 42 |
2021 | 2 | 32 | 34 |
2022 | 0 | 10 | 10 |
2023 | 0 | 4 | 4 |
2024 | 0 | 1 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Pedigree" by people in Profiles.
-
IGG in the trenches: Results of an in-depth interview study on the practice, politics, and future of investigative genetic genealogy. Forensic Sci Int. 2024 Mar; 356:111946.
-
Genome-wide association study of thoracic aortic aneurysm and dissection in the Million Veteran Program. Nat Genet. 2023 07; 55(7):1106-1115.
-
FOXI3 pathogenic variants cause one form of craniofacial microsomia. Nat Commun. 2023 04 11; 14(1):2026.
-
Bi-allelic SNAPC4 variants dysregulate global alternative splicing and lead to neuroregression and progressive spastic paraparesis. Am J Hum Genet. 2023 04 06; 110(4):663-680.
-
A biallelic frameshift indel in PPP1R35 as a cause of primary microcephaly. Am J Med Genet A. 2023 03; 191(3):794-804.
-
Whole genome sequencing identifies candidate genes for familial essential tremor and reveals biological pathways implicated in essential tremor aetiology. EBioMedicine. 2022 Nov; 85:104290.
-
Biallelic variants in ADAMTS15 cause a novel form of distal arthrogryposis. Genet Med. 2022 10; 24(10):2187-2193.
-
Sporadic dilated cardiomyopathy is often familial. Cardiovasc Res. 2022 07 27; 118(10):e69-e71.
-
Significant familial clustering of Peyronie's disease in close and distant relatives. Andrology. 2022 10; 10(7):1361-1367.
-
Variants in genes coding for collagen type IV a-chains are frequent causes of persistent, isolated hematuria during childhood. Pediatr Nephrol. 2023 03; 38(3):687-695.