"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 | 1 | 3 | 4 |
| 1995 | 0 | 5 | 5 |
| 1996 | 1 | 5 | 6 |
| 1997 | 1 | 1 | 2 |
| 1998 | 0 | 7 | 7 |
| 1999 | 2 | 9 | 11 |
| 2000 | 3 | 6 | 9 |
| 2001 | 2 | 10 | 12 |
| 2002 | 6 | 8 | 14 |
| 2003 | 5 | 15 | 20 |
| 2004 | 8 | 9 | 17 |
| 2005 | 5 | 25 | 30 |
| 2006 | 8 | 21 | 29 |
| 2007 | 8 | 24 | 32 |
| 2008 | 5 | 36 | 41 |
| 2009 | 4 | 29 | 33 |
| 2010 | 4 | 31 | 35 |
| 2011 | 4 | 31 | 35 |
| 2012 | 3 | 29 | 32 |
| 2013 | 5 | 18 | 23 |
| 2014 | 1 | 18 | 19 |
| 2015 | 3 | 12 | 15 |
| 2016 | 4 | 13 | 17 |
| 2017 | 1 | 11 | 12 |
| 2018 | 1 | 11 | 12 |
| 2019 | 1 | 18 | 19 |
| 2020 | 2 | 8 | 10 |
| 2021 | 1 | 8 | 9 |
| 2022 | 0 | 9 | 9 |
| 2023 | 0 | 2 | 2 |
| 2024 | 0 | 2 | 2 |
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Below are the most recent publications written about "Haplotypes" by people in Profiles.
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Results of a phase I trial with Haploidentical mbIL-21 ex vivo expanded NK cells for patients with multiply relapsed and refractory AML. Am J Hematol. 2024 May; 99(5):890-899.
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Neuronal MAPT expression is mediated by long-range interactions with cis-regulatory elements. Am J Hum Genet. 2024 Feb 01; 111(2):259-279.
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Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation. Nat Methods. 2023 10; 20(10):1483-1492.
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Identification of Novel Associations and Localization of Signals in Idiopathic Inflammatory Myopathies Using Genome-Wide Imputation. Arthritis Rheumatol. 2023 06; 75(6):1021-1027.
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Detailed stratified GWAS analysis for severe COVID-19 in four European populations. Hum Mol Genet. 2022 11 28; 31(23):3945-3966.
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Diagnosis of Acute Chagas Disease in a Belizean Child with Evidence of a Multiclonal Trypanosoma cruzi Infection. Am J Trop Med Hyg. 2022 11 14; 107(5):992-995.
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Characterization of CYP2D6 Pharmacogenetic Variation in Sub-Saharan African Populations. Clin Pharmacol Ther. 2023 03; 113(3):643-659.
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A saturated map of common genetic variants associated with human height. Nature. 2022 10; 610(7933):704-712.
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Rare variants and HLA haplotypes associated in patients with neuromyelitis optica spectrum disorders. Front Immunol. 2022; 13:900605.
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Germline-somatic JAK2 interactions are associated with clonal expansion in myelofibrosis. Nat Commun. 2022 09 08; 13(1):5284.