"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 |
|---|
| 1994 | 0 | 3 | 3 |
| 1995 | 0 | 2 | 2 |
| 1996 | 1 | 1 | 2 |
| 1997 | 1 | 1 | 2 |
| 1998 | 0 | 6 | 6 |
| 1999 | 1 | 10 | 11 |
| 2000 | 0 | 11 | 11 |
| 2001 | 0 | 12 | 12 |
| 2002 | 2 | 14 | 16 |
| 2003 | 2 | 11 | 13 |
| 2004 | 3 | 9 | 12 |
| 2005 | 3 | 9 | 12 |
| 2006 | 4 | 9 | 13 |
| 2007 | 4 | 14 | 18 |
| 2008 | 4 | 8 | 12 |
| 2009 | 5 | 10 | 15 |
| 2010 | 5 | 6 | 11 |
| 2011 | 4 | 5 | 9 |
| 2012 | 2 | 6 | 8 |
| 2013 | 2 | 7 | 9 |
| 2014 | 4 | 6 | 10 |
| 2015 | 1 | 4 | 5 |
| 2016 | 2 | 2 | 4 |
| 2017 | 1 | 3 | 4 |
| 2018 | 1 | 2 | 3 |
| 2019 | 2 | 5 | 7 |
| 2020 | 1 | 1 | 2 |
| 2021 | 0 | 1 | 1 |
| 2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "Family Health" by people in Profiles.
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Key drivers of family-level utility of pediatric genomic sequencing: a qualitative analysis to support preference research. Eur J Hum Genet. 2023 04; 31(4):445-452.
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Bi-allelic variants in OGDHL cause a neurodevelopmental spectrum disease featuring epilepsy, hearing loss, visual impairment, and ataxia. Am J Hum Genet. 2021 12 02; 108(12):2368-2384.
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The synergy of germline C634Y and V292M RET mutations in a northern Chinese family with multiple endocrine neoplasia type 2A. J Cell Mol Med. 2020 11; 24(22):13163-13170.
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Evidence for Household Transmission of Rotavirus in the United States, 2011-2016. J Pediatric Infect Dis Soc. 2020 Apr 30; 9(2):181-187.
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Parents' Perceptions of Internalizing and Externalizing Features in Childhood OCD. Child Psychiatry Hum Dev. 2019 08; 50(4):692-701.
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Enhancing an HIV index case testing passive referral model through a behavioural skills-building training for healthcare providers: a pre-/post-assessment in Mangochi District, Malawi. J Int AIDS Soc. 2019 07; 22 Suppl 3:e25292.
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Radiologist's Primer on Imaging of Common Hereditary Cancer Syndromes. Radiographics. 2019 May-Jun; 39(3):759-778.
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Variants in KIAA0825 underlie autosomal recessive postaxial polydactyly. Hum Genet. 2019 Jun; 138(6):593-600.
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Identifying Important Outcomes for Young People With CKD and Their Caregivers: A Nominal Group Technique Study. Am J Kidney Dis. 2019 07; 74(1):82-94.
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Spanish Version of the Family Health Behavior Scale: Adaptation and Validation. Int J Environ Res Public Health. 2019 03 06; 16(5).