 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 |
|---|
| 1995 | 1 | 0 | 1 | | 1996 | 1 | 0 | 1 | | 1997 | 0 | 1 | 1 | | 2000 | 1 | 0 | 1 | | 2001 | 1 | 0 | 1 | | 2002 | 0 | 1 | 1 | | 2004 | 0 | 2 | 2 | | 2005 | 0 | 3 | 3 | | 2007 | 0 | 2 | 2 | | 2009 | 1 | 1 | 2 | | 2010 | 0 | 2 | 2 | | 2011 | 0 | 1 | 1 | | 2012 | 0 | 2 | 2 | | 2013 | 0 | 1 | 1 | | 2014 | 0 | 2 | 2 |
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Below are the most recent publications written about "Haplotypes" by people in Profiles.
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Waid DM, Schreiner T, Vaitaitis G, Carter JR, Corboy JR, Wagner DH. Defining a new biomarker for the autoimmune component of Multiple Sclerosis: Th40 cells. J Neuroimmunol. 2014 May 15; 270(1-2):75-85.
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Elhaik E, Tatarinova TV, Klyosov AA, Graur D. The 'extremely ancient' chromosome that isn't: a forensic bioinformatic investigation of Albert Perry's X-degenerate portion of the Y chromosome. Eur J Hum Genet. 2014 Sep; 22(9):1111-6.
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Campbell D, Bick J, Yrigollen CM, Lee M, Joseph A, Chang JT, Grigorenko EL. Schooling and variation in the COMT gene: the devil is in the details. J Child Psychol Psychiatry. 2013 Oct; 54(10):1056-65.
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Spellicy CJ, Northrup H, Fletcher JM, Cirino PT, Dennis M, Morrison AC, Martinez CA, Au KS. Folate metabolism gene 5,10-methylenetetrahydrofolate reductase (MTHFR) is associated with ADHD in myelomeningocele patients. PLoS One. 2012; 7(12):e51330.
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Zufall RA, Dimond KL, Doerder FP. Restricted distribution and limited gene flow in the model ciliate Tetrahymena thermophila. Mol Ecol. 2013 Feb; 22(4):1081-91.
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Donnelly MP, Paschou P, Grigorenko E, Gurwitz D, Barta C, Lu RB, Zhukova OV, Kim JJ, Siniscalco M, New M, Li H, Kajuna SL, Manolopoulos VG, Speed WC, Pakstis AJ, Kidd JR, Kidd KK. A global view of the OCA2-HERC2 region and pigmentation. Hum Genet. 2012 May; 131(5):683-96.
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Grigorenko EL, De Young CG, Eastman M, Getchell M, Haeffel GJ, Klinteberg Ba, Koposov RA, Oreland L, Pakstis AJ, Ponomarev OA, Ruchkin VV, Singh JP, Yrigollen CM. Aggressive behavior, related conduct problems, and variation in genes affecting dopamine turnover. Aggress Behav. 2010 May-Jun; 36(3):158-76.
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DeYoung CG, Getchell M, Koposov RA, Yrigollen CM, Haeffel GJ, af Klinteberg B, Oreland L, Ruchkin VV, Pakstis AJ, Grigorenko EL. Variation in the catechol-O-methyltransferase Val 158 Met polymorphism associated with conduct disorder and ADHD symptoms, among adolescent male delinquents. Psychiatr Genet. 2010 Feb; 20(1):20-4.
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Zhang JE, Jorgensen AL, Alfirevic A, Williamson PR, Toh CH, Park BK, Pirmohamed M. Effects of CYP4F2 genetic polymorphisms and haplotypes on clinical outcomes in patients initiated on warfarin therapy. Pharmacogenet Genomics. 2009 Oct; 19(10):781-9.
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Chang W, Winder TL, LeDuc CA, Simpson LL, Millar WS, Dungan J, Ginsberg N, Plaga S, Moore SA, Chung WK. Founder Fukutin mutation causes Walker-Warburg syndrome in four Ashkenazi Jewish families. Prenat Diagn. 2009 Jun; 29(6):560-9.
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