"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.
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 Harvard Catalyst Profiles by year, and whether "Haplotypes" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
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1994 | 3 | 15 | 18 |
1995 | 3 | 12 | 15 |
1996 | 4 | 14 | 18 |
1997 | 2 | 26 | 28 |
1998 | 2 | 16 | 18 |
1999 | 3 | 9 | 12 |
2000 | 2 | 26 | 28 |
2001 | 6 | 25 | 31 |
2002 | 2 | 35 | 37 |
2003 | 13 | 39 | 52 |
2004 | 18 | 55 | 73 |
2005 | 14 | 69 | 83 |
2006 | 24 | 90 | 114 |
2007 | 17 | 93 | 110 |
2008 | 17 | 89 | 106 |
2009 | 7 | 91 | 98 |
2010 | 15 | 71 | 86 |
2011 | 12 | 74 | 86 |
2012 | 10 | 50 | 60 |
2013 | 8 | 34 | 42 |
2014 | 9 | 42 | 51 |
2015 | 9 | 40 | 49 |
2016 | 12 | 48 | 60 |
2017 | 7 | 38 | 45 |
2018 | 5 | 44 | 49 |
2019 | 3 | 24 | 27 |
2020 | 10 | 31 | 41 |
2021 | 5 | 32 | 37 |
2022 | 0 | 13 | 13 |
2023 | 0 | 14 | 14 |
Below are the most recent publications written about "Haplotypes" by people in Profiles.
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Haplotype-based inference of recent effective population size in modern and ancient DNA samples. Nat Commun. 2023 Dec 01; 14(1):7945.
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Association of APOE Haplotypes With Common Age-Related Ocular Diseases in 412,171 Individuals. Invest Ophthalmol Vis Sci. 2023 Nov 01; 64(14):33.
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Multiple TP53 p.R337H haplotypes and implications for tumor susceptibility. HGG Adv. 2024 Jan 11; 5(1):100244.
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µ- PBWT: a lightweight r-indexing of the PBWT for storing and querying UK Biobank data. Bioinformatics. 2023 09 02; 39(9).
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Extremely sparse models of linkage disequilibrium in ancestrally diverse association studies. Nat Genet. 2023 09; 55(9):1494-1502.
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Haplotype-specific MAPK3 expression in 16p11.2 deletion contributes to variable neurodevelopment. Brain. 2023 08 01; 146(8):3347-3363.
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Tutorial: a statistical genetics guide to identifying HLA alleles driving complex disease. Nat Protoc. 2023 09; 18(9):2625-2641.
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Accurate rare variant phasing of whole-genome and whole-exome sequencing data in the UK Biobank. Nat Genet. 2023 07; 55(7):1243-1249.
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A non-coding variant linked to metabolic obesity with normal weight affects actin remodelling in subcutaneous adipocytes. Nat Metab. 2023 05; 5(5):861-879.
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Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome. Nat Commun. 2023 04 29; 14(1):2481.