"Haplotypes" 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 genetic constitution of individuals with respect to one member of a pair of allelic genes, or sets of genes that are closely linked and tend to be inherited together such as those of the MAJOR HISTOCOMPATIBILITY COMPLEX.
| Descriptor ID |
D006239
|
| MeSH Number(s) |
G05.380.360
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Haplotypes".
Below are MeSH descriptors whose meaning is more specific than "Haplotypes".
This graph shows the total number of publications written about "Haplotypes" by people in this website by year, and whether "Haplotypes" 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 | 2 | 4 | 6 |
| 1995 | 0 | 5 | 5 |
| 1996 | 2 | 6 | 8 |
| 1997 | 1 | 1 | 2 |
| 1998 | 0 | 9 | 9 |
| 1999 | 2 | 12 | 14 |
| 2000 | 5 | 11 | 16 |
| 2001 | 3 | 11 | 14 |
| 2002 | 6 | 15 | 21 |
| 2003 | 4 | 15 | 19 |
| 2004 | 8 | 11 | 19 |
| 2005 | 4 | 26 | 30 |
| 2006 | 8 | 22 | 30 |
| 2007 | 6 | 24 | 30 |
| 2008 | 4 | 37 | 41 |
| 2009 | 5 | 29 | 34 |
| 2010 | 4 | 29 | 33 |
| 2011 | 4 | 30 | 34 |
| 2012 | 2 | 32 | 34 |
| 2013 | 5 | 21 | 26 |
| 2014 | 1 | 19 | 20 |
| 2015 | 4 | 13 | 17 |
| 2016 | 6 | 13 | 19 |
| 2017 | 2 | 11 | 13 |
| 2018 | 1 | 10 | 11 |
| 2019 | 1 | 16 | 17 |
| 2020 | 2 | 7 | 9 |
| 2021 | 1 | 8 | 9 |
| 2022 | 0 | 9 | 9 |
| 2023 | 0 | 2 | 2 |
| 2024 | 5 | 6 | 11 |
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Below are the most recent publications written about "Haplotypes" by people in Profiles.
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Association of common and rare variants with Alzheimer's disease in more than 13,000 diverse individuals with whole-genome sequencing from the Alzheimer's Disease Sequencing Project. Alzheimers Dement. 2024 Dec; 20(12):8470-8483.
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Long-read sequencing of an advanced cancer cohort resolves rearrangements, unravels haplotypes, and reveals methylation landscapes. Cell Genom. 2024 Nov 13; 4(11):100674.
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Mitochondrial genome analysis across different populations reveals the intraspecific variation and phylogeography of the Caucasian soft tick relapsing fever vector, Ornithodoros (Pavlovskyella) verrucosus (Ixodida: Argasidae). Infect Genet Evol. 2024 Nov; 125:105673.
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Impact and characterization of serial structural variations across humans and great apes. Nat Commun. 2024 Sep 13; 15(1):8007.
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Extended haplotype with rs41524547-G defines the ancestral origin of SCA10. Hum Mol Genet. 2024 09 03; 33(18):1567-1574.
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Detection of distant relatedness in biobanks to identify undiagnosed cases of Mendelian disease as applied to Long QT syndrome. Nat Commun. 2024 Aug 29; 15(1):7507.
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MethPhaser: methylation-based long-read haplotype phasing of human genomes. Nat Commun. 2024 Jun 22; 15(1):5327.
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Inverted triplications formed by iterative template switches generate structural variant diversity at genomic disorder loci. Cell Genom. 2024 Jul 10; 4(7):100590.
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Pharmacogenomic insights in psychiatric care: uncovering novel actionability, allele-specific CYP2D6 copy number variation, and phenoconversion in 15,000 patients. Mol Psychiatry. 2024 Nov; 29(11):3495-3502.
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MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study. Lancet Neurol. 2024 May; 23(5):487-499.