"Genotype" 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 the individual, comprising the ALLELES present at each GENETIC LOCUS.
Descriptor ID |
D005838
|
MeSH Number(s) |
G05.380
|
Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Genotype".
Below are MeSH descriptors whose meaning is more specific than "Genotype".
This graph shows the total number of publications written about "Genotype" by people in this website by year, and whether "Genotype" 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 | 1 | 1 |
1998 | 0 | 2 | 2 |
2000 | 0 | 3 | 3 |
2001 | 0 | 1 | 1 |
2002 | 0 | 2 | 2 |
2003 | 0 | 2 | 2 |
2004 | 0 | 4 | 4 |
2005 | 0 | 1 | 1 |
2006 | 0 | 8 | 8 |
2007 | 1 | 9 | 10 |
2008 | 0 | 11 | 11 |
2009 | 0 | 13 | 13 |
2010 | 0 | 19 | 19 |
2011 | 0 | 18 | 18 |
2012 | 1 | 32 | 33 |
2013 | 1 | 17 | 18 |
2014 | 2 | 15 | 17 |
2015 | 1 | 20 | 21 |
2016 | 0 | 15 | 15 |
2017 | 0 | 13 | 13 |
2018 | 0 | 12 | 12 |
2019 | 1 | 15 | 16 |
2020 | 2 | 16 | 18 |
2021 | 0 | 8 | 8 |
2022 | 0 | 6 | 6 |
2023 | 0 | 8 | 8 |
To return to the timeline,
click here.
Below are the most recent publications written about "Genotype" by people in Profiles.
-
Clinical trio genome sequencing facilitates the interpretation of variants in cancer predisposition genes in paediatric tumour patients. Eur J Hum Genet. 2023 10; 31(10):1139-1146.
-
Pan-European study of genotypes and phenotypes in the Arabidopsis relative Cardamine hirsuta reveals how adaptation, demography, and development shape diversity patterns. PLoS Biol. 2023 07; 21(7):e3002191.
-
Reliable genotyping of recombinant genomes using a robust hidden Markov model. Plant Physiol. 2023 05 31; 192(2):821-836.
-
A clinical screening tool to detect genetic cancer predisposition in pediatric oncology shows high sensitivity but can miss a substantial percentage of affected children. Genet Med. 2023 08; 25(8):100875.
-
Haplotype sequence collection of ABO blood group alleles by long-read sequencing reveals putative A1-diagnostic variants. Blood Adv. 2023 03 28; 7(6):878-892.
-
Comprehensive neurological evaluation of a cohort of patients with neurofibromatosis type 1 from a single institution. Eur J Paediatr Neurol. 2023 Mar; 43:52-61.
-
Development and evaluations of the ancestry informative markers of the VISAGE Enhanced Tool for Appearance and Ancestry. Forensic Sci Int Genet. 2023 05; 64:102853.
-
Molecular characterisation of 36 multilocus imprinting disturbance (MLID) patients: a comprehensive approach. Clin Epigenetics. 2023 03 01; 15(1):35.
-
The serotonin receptor 3E variant is a risk factor for female IBS-D. J Mol Med (Berl). 2022 Nov; 100(11):1617-1627.
-
Variation in CFHR3 determines susceptibility to meningococcal disease by controlling factor H concentrations. Am J Hum Genet. 2022 Sep 01; 109(9):1680-1691.