"Family" 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.
A social group consisting of parents or parent substitutes and children.
Descriptor ID |
D005190
|
MeSH Number(s) |
F01.829.263 I01.880.853.150
|
Concept/Terms |
Family Life Cycles- Family Life Cycles
- Life Cycle, Family
- Life Cycles, Family
- Family Life Cycle
Family, Reconstituted- Family, Reconstituted
- Families, Reconstituted
- Reconstituted Families
- Reconstituted Family
Kinship Networks- Kinship Networks
- Kinship Network
- Network, Kinship
- Networks, Kinship
Extended Family- Extended Family
- Extended Families
- Families, Extended
- Family, Extended
|
Below are MeSH descriptors whose meaning is more general than "Family".
Below are MeSH descriptors whose meaning is more specific than "Family".
This graph shows the total number of publications written about "Family" by people in this website by year, and whether "Family" 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 |
---|
2007 | 0 | 2 | 2 |
2008 | 0 | 2 | 2 |
2009 | 0 | 2 | 2 |
2010 | 0 | 3 | 3 |
2011 | 0 | 1 | 1 |
2012 | 0 | 2 | 2 |
2013 | 0 | 2 | 2 |
2014 | 0 | 4 | 4 |
2015 | 1 | 0 | 1 |
2017 | 0 | 3 | 3 |
2018 | 0 | 4 | 4 |
2020 | 0 | 2 | 2 |
To return to the timeline,
click here.
Below are the most recent publications written about "Family" by people in Profiles.
-
Comprehensive molecular analysis of 61 Egyptian families with hereditary nonsyndromic hearing loss. Clin Genet. 2020 07; 98(1):32-42.
-
Bi-allelic Variants in RALGAPA1 Cause Profound Neurodevelopmental Disability, Muscular Hypotonia, Infantile Spasms, and Feeding Abnormalities. Am J Hum Genet. 2020 02 06; 106(2):246-255.
-
Recessive mutations in the neuronal isoforms of DST, encoding dystonin, lead to abnormal actin cytoskeleton organization and HSAN type VI. Hum Mutat. 2019 01; 40(1):106-114.
-
Exome sequencing in large, multiplex bipolar disorder families from Cuba. PLoS One. 2018; 13(10):e0205895.
-
Family-based germline sequencing in children with cancer. Oncogene. 2019 02; 38(9):1367-1380.
-
Genetics of intellectual disability in consanguineous families. Mol Psychiatry. 2019 07; 24(7):1027-1039.
-
Genetic predisposition in children with cancer - affected families' acceptance of Trio-WES. Eur J Pediatr. 2018 Jan; 177(1):53-60.
-
[Monilethrix is a hereditary hair shaft disorder]. Ugeskr Laeger. 2017 Sep 11; 179(37).
-
STAT3 gain-of-function mutations associated with autoimmune lymphoproliferative syndrome like disease deregulate lymphocyte apoptosis and can be targeted by BH3 mimetic compounds. Clin Immunol. 2017 08; 181:32-42.
-
Cancer susceptibility syndromes in children in the area of broad clinical use of massive parallel sequencing. Eur J Pediatr. 2015 Aug; 174(8):987-97.