"Family Health" 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 health status of the family as a unit including the impact of the health of one member of the family on the family as a unit and on individual family members; also, the impact of family organization or disorganization on the health status of its members.
| Descriptor ID |
D005192
|
| MeSH Number(s) |
N01.400.300
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Family Health".
Below are MeSH descriptors whose meaning is more specific than "Family Health".
This graph shows the total number of publications written about "Family Health" by people in this website by year, and whether "Family Health" 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 |
|---|
| 1995 | 0 | 1 | 1 |
| 1996 | 0 | 1 | 1 |
| 1997 | 0 | 3 | 3 |
| 1998 | 2 | 1 | 3 |
| 1999 | 0 | 4 | 4 |
| 2000 | 1 | 5 | 6 |
| 2001 | 0 | 7 | 7 |
| 2002 | 0 | 4 | 4 |
| 2003 | 1 | 7 | 8 |
| 2004 | 1 | 6 | 7 |
| 2005 | 3 | 5 | 8 |
| 2006 | 1 | 6 | 7 |
| 2007 | 1 | 4 | 5 |
| 2008 | 4 | 6 | 10 |
| 2009 | 0 | 5 | 5 |
| 2010 | 2 | 4 | 6 |
| 2011 | 2 | 2 | 4 |
| 2012 | 1 | 5 | 6 |
| 2013 | 3 | 2 | 5 |
| 2014 | 0 | 1 | 1 |
| 2015 | 1 | 1 | 2 |
| 2016 | 1 | 1 | 2 |
| 2017 | 1 | 4 | 5 |
| 2018 | 0 | 4 | 4 |
| 2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "Family Health" by people in Profiles.
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Large, three-generation human families reveal post-zygotic mosaicism and variability in germline mutation accumulation. Elife. 2019 09 24; 8.
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Congenital Hypothyroidism due to Oligogenic Mutations in Two Sudanese Families. Thyroid. 2019 02; 29(2):302-304.
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Homozygous Mutation in Human Serum Albumin and Its Implication on Thyroid Tests. Thyroid. 2018 06; 28(6):811-814.
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Hangover in Post-College-Aged Drinkers: Psychometric Properties of the Hangover Symptom Scale (HSS) and the Hangover Symptom Scale-Short Form (HSS-5). Alcohol Clin Exp Res. 2018 06; 42(6):1122-1131.
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De novo mutations in GRIN1 cause extensive bilateral polymicrogyria. Brain. 2018 03 01; 141(3):698-712.
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Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees. Proc Natl Acad Sci U S A. 2018 01 09; 115(2):379-384.
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TIA1 Mutations in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Promote Phase Separation and Alter Stress Granule Dynamics. Neuron. 2017 Aug 16; 95(4):808-816.e9.
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Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach. Eur Arch Psychiatry Clin Neurosci. 2018 Apr; 268(3):301-316.
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Fever-Induced Paroxysmal Weakness and Encephalopathy, a New Phenotype of ATP1A3 Mutation. Pediatr Neurol. 2017 Aug; 73:101-105.
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Population- and individual-specific regulatory variation in Sardinia. Nat Genet. 2017 May; 49(5):700-707.