 Haplotypes
"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
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| MeSH Number(s) |
G05.380.360
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| Concept/Terms |
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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 |
|---|
| 1997 | 0 | 2 | 2 | | 1998 | 0 | 1 | 1 | | 1999 | 1 | 1 | 2 | | 2000 | 0 | 1 | 1 | | 2001 | 1 | 4 | 5 | | 2002 | 2 | 5 | 7 | | 2003 | 0 | 8 | 8 | | 2004 | 4 | 6 | 10 | | 2005 | 3 | 14 | 17 | | 2006 | 6 | 20 | 26 | | 2007 | 5 | 19 | 24 | | 2008 | 1 | 20 | 21 | | 2009 | 5 | 9 | 14 | | 2010 | 3 | 13 | 16 | | 2011 | 4 | 16 | 20 | | 2012 | 2 | 20 | 22 | | 2013 | 2 | 20 | 22 | | 2014 | 3 | 10 | 13 | | 2015 | 2 | 17 | 19 | | 2016 | 2 | 12 | 14 | | 2017 | 2 | 10 | 12 | | 2018 | 1 | 11 | 12 | | 2019 | 2 | 11 | 13 | | 2020 | 1 | 4 | 5 | | 2021 | 1 | 16 | 17 | | 2022 | 0 | 5 | 5 | | 2023 | 0 | 3 | 3 | | 2024 | 4 | 5 | 9 | | 2025 | 1 | 8 | 9 | | 2026 | 2 | 5 | 7 |
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Below are the most recent publications written about "Haplotypes" by people in Profiles.
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Edington SL, Al-Hindi DR, Font-Porterias N, Surowiec A, Palmer WJ, Myrick JW, Norman PJ, Uren C, Möller M, Henn BM, Reynolds AW. Recovering the precolonial population structure of Khoe-San descendant populations. Sci Adv. 2026 Sep 04; 12(36):eadz7115.
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da Silva FV, Hoch VB, Auer ED, Dos Santos PI, Cline N, Oliveira LC, Hundt JE, Wittig M, Franke A, Norman PJ, Boldt ABW. Genetics of Celiac Disease in Southern Brazil: High-Resolution HLA Haplotypes and Non-HLA Polymorphisms. HLA. 2026 Sep; 108(3):e70972.
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Nieuwenhuis LM, Loza BL, Berger SP, Jansen BH, Blokzijl H, Daha MR, Lammerts RGM, Shaked A, Asrani S, Lisman T, Weersma RK, Festen EAM, de Meijer VE, Poppelaars F. Extended haplotypes at the complement factor H gene locus are associated with liver transplant rejection. Hepatol Commun. 2026 Aug 01; 10(8).
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Murphy JI, Barnard R, Null M, Hendricks AE. RAREsim2: flexible simulation of rare variant genetic data using real haplotypes. Bioinformatics. 2026 May 03; 42(5).
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Sapin E, Kelly KM, Keller MC. A novel method for across-chromosome phasing without relative data. Bioinformatics. 2026 May 03; 42(5).
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Aydemir O, Bailey JA, Agardh D, Lernmark Å, Noble JA, Andersson Svärd A, Blankenhorn EP, Parikh HM, Ziegler AG, Toppari J, Akolkar B, Hagopian WA, Rewers MJ, Mordes JP. Polymorphisms in intron 1 of HLA-DRA differentially associate with type 1 diabetes and celiac disease and implicate involvement of complement system genes C4A and C4B. Elife. 2026 Feb 02; 12.
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Steck AK, Parikh HM, Triolo TM, Ferrat L, You L, Gottlieb PA, Oram RA, Onengut-Gumuscu S, Krischer JP, Rich SS, Redondo MJ. Genetic Risk and Transition Through Preclinical Stages of Type 1 Diabetes. J Clin Endocrinol Metab. 2026 Jan 21; 111(2):e493-e499.
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Ramadan DJ, Kichula KM, Tao S, Porfilio T, Lande A, Fluge Ø, Mella O, Strand EB, Saugstad OD, Norman PJ, Lie BA, Viken MK. Killer cell immunoglobulin-like receptor (KIR) alleles suggested to be associated with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). Brain Behav Immun. 2025 Nov; 130:106098.
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Williams CM, Scelza BA, Slack SD, Font-Porterias N, Al-Hindi DR, Mathias RA, Watson H, Barnes KC, Lange E, Johnson RK, Gignoux CR, Ramachandran S, Henn BM. A rapid accurate approach to inferring pedigrees in endogamous populations. Genetics. 2025 08 06; 230(4).
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Logsdon GA, Ebert P, Audano PA, Loftus M, Porubsky D, Ebler J, Yilmaz F, Hallast P, Prodanov T, Yoo D, Paisie CA, Harvey WT, Zhao X, Martino GV, Henglin M, Munson KM, Rabbani K, Chin CS, Gu B, Ashraf H, Scholz S, Austine-Orimoloye O, Balachandran P, Bonder MJ, Cheng H, Chong Z, Crabtree J, Gerstein M, Guethlein LA, Hasenfeld P, Hickey G, Hoekzema K, Hunt SE, Jensen M, Jiang Y, Koren S, Kwon Y, Li C, Li H, Li J, Norman PJ, Oshima KK, Paten B, Phillippy AM, Pollock NR, Rausch T, Rautiainen M, Song Y, Söylev A, Sulovari A, Surapaneni L, Tsapalou V, Zhou W, Zhou Y, Zhu Q, Zody MC, Mills RE, Devine SE, Shi X, Talkowski ME, Chaisson MJP, Dilthey AT, Konkel MK, Korbel JO, Lee C, Beck CR, Eichler EE, Marschall T. Complex genetic variation in nearly complete human genomes. Nature. 2025 08; 644(8076):430-441.
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