"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 |
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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 |
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1996 | 0 | 1 | 1 |
1999 | 0 | 1 | 1 |
2000 | 1 | 0 | 1 |
2001 | 0 | 2 | 2 |
2002 | 0 | 1 | 1 |
2003 | 0 | 3 | 3 |
2005 | 2 | 3 | 5 |
2006 | 0 | 1 | 1 |
2007 | 0 | 3 | 3 |
2008 | 1 | 1 | 2 |
2009 | 0 | 1 | 1 |
2010 | 2 | 4 | 6 |
2011 | 0 | 1 | 1 |
2012 | 0 | 1 | 1 |
2015 | 1 | 0 | 1 |
2017 | 1 | 0 | 1 |
2022 | 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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Family Health Research. West J Nurs Res. 2022 10; 44(10):903.
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Caregiver subjective and physiological markers of stress and patient heart failure severity in family care dyads. Psychoneuroendocrinology. 2021 11; 133:105399.
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Polygenic risk scores in familial Alzheimer disease. Neurology. 2017 Mar 21; 88(12):1180-1186.
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Clustering of Toxoplasma gondii Infections Within Families of Congenitally Infected Infants. Clin Infect Dis. 2015 Dec 15; 61(12):1815-24.
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Genome-wide linkage analysis of obsessive-compulsive disorder implicates chromosome 1p36. Biol Psychiatry. 2012 Oct 15; 72(8):629-36.
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Genomewide linkage analysis in Costa Rican families implicates chromosome 15q14 as a candidate region for OCD. Hum Genet. 2011 Dec; 130(6):795-805.
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Neuropsychological Profile of Parkin Mutation Carriers with and without Parkinson Disease: The CORE-PD Study. J Int Neuropsychol Soc. 2011 Jan; 17(1):91-100.
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Seizures in fragile X syndrome: characteristics and comorbid diagnoses. Am J Intellect Dev Disabil. 2010 Nov; 115(6):461-72.
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Maternal depressive history, teen 5HTTLPR genotype, and the processing of emotional faces: Exploring mechanisms of risk. Behav Res Ther. 2011 Jan; 49(1):80-4.
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Directions for refining a school nursing intervention for Mexican immigrant families. J Sch Nurs. 2010 Dec; 26(6):430-5.