Chromosomes, Human, Pair 5

"Chromosomes, Human, Pair 5" 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.

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One of the two pairs of human chromosomes in the group B class (CHROMOSOMES, HUMAN, 4-5).


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This graph shows the total number of publications written about "Chromosomes, Human, Pair 5" by people in this website by year, and whether "Chromosomes, Human, Pair 5" was a major or minor topic of these publications.
Below are the most recent publications written about "Chromosomes, Human, Pair 5" by people in Profiles.
  1. Genome-Wide Association Study Points to Novel Locus for Gilles de la Tourette Syndrome. Biol Psychiatry. 2024 Jul 15; 96(2):114-124.
    View in: PubMed
  2. Genome-wide DNA methylation analysis pre- and post-lenalidomide treatment in patients with myelodysplastic syndrome with isolated deletion (5q). Ann Hematol. 2021 Jun; 100(6):1463-1471.
    View in: PubMed
  3. 5q35 duplication presents with psychiatric and undergrowth phenotypes mediated by NSD1 overexpression and mTOR signaling downregulation. Hum Genet. 2021 Apr; 140(4):681-690.
    View in: PubMed
  4. Whole-Genome Sequencing Identifies Novel Functional Loci Associated with Lung Function in Puerto Rican Youth. Am J Respir Crit Care Med. 2020 10 01; 202(7):962-972.
    View in: PubMed
  5. Identification of a new genetic variant associated with cholecystitis: A multicenter genome-wide association study. J Trauma Acute Care Surg. 2020 07; 89(1):173-178.
    View in: PubMed
  6. Rare gain of chromosome 5 in a supratentorial hemispheric paediatric pilomyxoid astrocytoma. BMJ Case Rep. 2020 Mar 17; 13(3).
    View in: PubMed
  7. Mendelian Randomization and mediation analysis of leukocyte telomere length and risk of lung and head and neck cancers. Int J Epidemiol. 2019 06 01; 48(3):751-766.
    View in: PubMed
  8. Genome-wide meta-analysis of SNP-by9-ACEI/ARB and SNP-by-thiazide diuretic and effect on serum potassium in cohorts of European and African ancestry. Pharmacogenomics J. 2019 02; 19(1):97-108.
    View in: PubMed
  9. A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability. Elife. 2018 05 22; 7.
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  10. Genome-wide association studies for diabetic macular edema and proliferative diabetic retinopathy. BMC Med Genet. 2018 05 08; 19(1):71.
    View in: PubMed