 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 |
|---|
| 1987 | 1 | 0 | 1 | | 1988 | 0 | 2 | 2 | | 1989 | 0 | 1 | 1 | | 1990 | 0 | 2 | 2 | | 1992 | 0 | 2 | 2 | | 1993 | 0 | 2 | 2 | | 1994 | 0 | 3 | 3 | | 1995 | 2 | 3 | 5 | | 1996 | 2 | 6 | 8 | | 1997 | 0 | 10 | 10 | | 1998 | 0 | 2 | 2 | | 1999 | 2 | 4 | 6 | | 2000 | 0 | 10 | 10 | | 2001 | 2 | 10 | 12 | | 2002 | 2 | 14 | 16 | | 2003 | 5 | 10 | 15 | | 2004 | 3 | 13 | 16 | | 2005 | 6 | 25 | 31 | | 2006 | 6 | 28 | 34 | | 2007 | 2 | 23 | 25 | | 2008 | 6 | 29 | 35 | | 2009 | 2 | 24 | 26 | | 2010 | 2 | 13 | 15 | | 2011 | 5 | 24 | 29 | | 2012 | 3 | 19 | 22 | | 2013 | 4 | 7 | 11 | | 2014 | 4 | 11 | 15 | | 2015 | 4 | 4 | 8 | | 2016 | 5 | 8 | 13 | | 2017 | 1 | 9 | 10 | | 2018 | 2 | 9 | 11 | | 2019 | 2 | 10 | 12 | | 2020 | 0 | 4 | 4 | | 2021 | 2 | 4 | 6 | | 2022 | 0 | 3 | 3 |
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Below are the most recent publications written about "Haplotypes" by people in Profiles.
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Sasani TA, Ashbrook DG, Beichman AC, Lu L, Palmer AA, Williams RW, Pritchard JK, Harris K. A natural mutator allele shapes mutation spectrum variation in mice. Nature. 2022 05; 605(7910):497-502.
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Biddanda A, Steinrücken M, Novembre J. Properties of 2-locus genealogies and linkage disequilibrium in temporally structured samples. Genetics. 2022 05 05; 221(1).
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Ortega-Del Vecchyo D, Lohmueller KE, Novembre J. Haplotype-based inference of the distribution of fitness effects. Genetics. 2022 04 04; 220(4).
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Ringbauer H, Novembre J, Steinrücken M. Parental relatedness through time revealed by runs of homozygosity in ancient DNA. Nat Commun. 2021 09 14; 12(1):5425.
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Quince C, Nurk S, Raguideau S, James R, Soyer OS, Summers JK, Limasset A, Eren AM, Chikhi R, Darling AE. STRONG: metagenomics strain resolution on assembly graphs. Genome Biol. 2021 07 26; 22(1):214.
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Sobreira DR, Joslin AC, Zhang Q, Williamson I, Hansen GT, Farris KM, Sakabe NJ, Sinnott-Armstrong N, Bozek G, Jensen-Cody SO, Flippo KH, Ober C, Bickmore WA, Potthoff M, Chen M, Claussnitzer M, Aneas I, Nóbrega MA. Extensive pleiotropism and allelic heterogeneity mediate metabolic effects of IRX3 and IRX5. Science. 2021 06 04; 372(6546):1085-1091.
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Creary LE, Sacchi N, Mazzocco M, Morris GP, Montero-Martin G, Chong W, Brown CJ, Dinou A, Stavropoulos-Giokas C, Gorodezky C, Narayan S, Periathiruvadi S, Thomas R, De Santis D, Pepperall J, ElGhazali GE, Al Yafei Z, Askar M, Tyagi S, Kanga U, Marino SR, Planelles D, Chang CJ, Fernández-Viña MA. High-resolution HLA allele and haplotype frequencies in several unrelated populations determined by next generation sequencing: 17th International HLA and Immunogenetics Workshop joint report. Hum Immunol. 2021 Jul; 82(7):505-522.
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Rhie A, McCarthy SA, Fedrigo O, Damas J, Formenti G, Koren S, Uliano-Silva M, Chow W, Fungtammasan A, Kim J, Lee C, Ko BJ, Chaisson M, Gedman GL, Cantin LJ, Thibaud-Nissen F, Haggerty L, Bista I, Smith M, Haase B, Mountcastle J, Winkler S, Paez S, Howard J, Vernes SC, Lama TM, Grutzner F, Warren WC, Balakrishnan CN, Burt D, George JM, Biegler MT, Iorns D, Digby A, Eason D, Robertson B, Edwards T, Wilkinson M, Turner G, Meyer A, Kautt AF, Franchini P, Detrich HW, Svardal H, Wagner M, Naylor GJP, Pippel M, Malinsky M, Mooney M, Simbirsky M, Hannigan BT, Pesout T, Houck M, Misuraca A, Kingan SB, Hall R, Kronenberg Z, Sovic I, Dunn C, Ning Z, Hastie A, Lee J, Selvaraj S, Green RE, Putnam NH, Gut I, Ghurye J, Garrison E, Sims Y, Collins J, Pelan S, Torrance J, Tracey A, Wood J, Dagnew RE, Guan D, London SE, Clayton DF, Mello CV, Friedrich SR, Lovell PV, Osipova E, Al-Ajli FO, Secomandi S, Kim H, Theofanopoulou C, Hiller M, Zhou Y, Harris RS, Makova KD, Medvedev P, Hoffman J, Masterson P, Clark K, Martin F, Howe K, Flicek P, Walenz BP, Kwak W, Clawson H, Diekhans M, Nassar L, Paten B, Kraus RHS, Crawford AJ, Gilbert MTP, Zhang G, Venkatesh B, Murphy RW, Koepfli KP, Shapiro B, Johnson WE, Di Palma F, Marques-Bonet T, Teeling EC, Warnow T, Graves JM, Ryder OA, Haussler D, O'Brien SJ, Korlach J, Lewin HA, Howe K, Myers EW, Durbin R, Phillippy AM, Jarvis ED. Towards complete and error-free genome assemblies of all vertebrate species. Nature. 2021 04; 592(7856):737-746.
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Sinnott-Armstrong N, Sousa IS, Laber S, Rendina-Ruedy E, Nitter Dankel SE, Ferreira T, Mellgren G, Karasik D, Rivas M, Pritchard J, Guntur AR, Cox RD, Lindgren CM, Hauner H, Sallari R, Rosen CJ, Hsu YH, Lander ES, Kiel DP, Claussnitzer M. A regulatory variant at 3q21.1 confers an increased pleiotropic risk for hyperglycemia and altered bone mineral density. Cell Metab. 2021 03 02; 33(3):615-628.e13.
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Dabitao D, Dembele M, Urbanowski M, Kone B, Wague M, Coulibaly N, Sarro YDS, Baya B, Goita D, Dao S, Belson M, Klein SL, Achenbach C, Holl JL, Diakite M, Doumbia S, Bream JH, Bishai WR, Diallo S, Murphy RL. Short Communication: Genetic Variation in Human IL10 Proximal Promoter and Susceptibility to HIV-1 Infection in Mali, West Africa. AIDS Res Hum Retroviruses. 2021 01; 37(1):57-61.
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