"Siblings" 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.
Persons or animals having at least one parent in common. (American College Dictionary, 3d ed)
| Descriptor ID |
D035781
|
| MeSH Number(s) |
F01.829.263.500.490 I01.880.853.150.500.505 M01.781
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Siblings".
Below are MeSH descriptors whose meaning is more specific than "Siblings".
This graph shows the total number of publications written about "Siblings" by people in this website by year, and whether "Siblings" 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 |
|---|
| 2002 | 0 | 1 | 1 |
| 2003 | 0 | 4 | 4 |
| 2004 | 3 | 5 | 8 |
| 2005 | 2 | 4 | 6 |
| 2006 | 0 | 5 | 5 |
| 2007 | 0 | 5 | 5 |
| 2008 | 1 | 4 | 5 |
| 2009 | 2 | 0 | 2 |
| 2010 | 1 | 1 | 2 |
| 2011 | 1 | 4 | 5 |
| 2012 | 3 | 8 | 11 |
| 2013 | 2 | 3 | 5 |
| 2014 | 3 | 5 | 8 |
| 2015 | 4 | 4 | 8 |
| 2016 | 4 | 3 | 7 |
| 2017 | 2 | 3 | 5 |
| 2018 | 0 | 6 | 6 |
| 2019 | 2 | 8 | 10 |
| 2020 | 0 | 2 | 2 |
| 2021 | 1 | 2 | 3 |
| 2022 | 0 | 1 | 1 |
| 2023 | 2 | 2 | 4 |
| 2024 | 2 | 3 | 5 |
| 2025 | 1 | 4 | 5 |
| 2026 | 0 | 2 | 2 |
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Below are the most recent publications written about "Siblings" by people in Profiles.
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Small partial deletion of a highly GC-rich FOXF1 exon 1 in two deceased siblings with alveolar capillary dysplasia. Genomics. 2026 07; 118(4):111259.
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Optimizing Haploidentical Donor Selection for Pediatric Hematopoietic Cell Transplant. J Clin Oncol. 2026 Apr 10; 44(11):1003-1015.
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Chronic Health Conditions and Academic Achievement: A Childhood Cancer Survivor Study Report. JCO Oncol Pract. 2026 Jul; 22(7):1322-1330.
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Highly Variable Expressivity of a CNV Deletion Involving TBX4 in Three Deceased Siblings With Lung Developmental Disorder and Their Mildly Affected Mother and Grandfather. Clin Genet. 2026 01; 109(1):161-166.
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A family-based approach to cascade genetic testing in a pediatric cancer genetics clinic. Fam Cancer. 2024 11 20; 24(1):8.
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Genetic architecture reconciles linkage and association studies of complex traits. Nat Genet. 2024 Nov; 56(11):2352-2360.
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Recessive loss-of-function variants in DPH1 identified as the molecular cause in a sibling pair previously diagnosed with Fine-Lubinsky syndrome. Am J Med Genet A. 2025 01; 197(1):e63845.
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Multilocus pathogenic variants contribute to intrafamilial clinical heterogeneity: a retrospective study of sibling pairs with neurodevelopmental disorders. BMC Med Genomics. 2024 04 16; 17(1):85.
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Intrafamilial phenotypic heterogeneity in siblings with pseudohypoparathyroidism 1B due to maternal STX16 deletion. J Pediatr Endocrinol Metab. 2024 Jan 29; 37(1):84-89.
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"We are Family": Remembering Siblings of Youth with Psychiatric Concerns. Child Psychiatry Hum Dev. 2024 02; 55(1):1-2.