"Karyotyping" 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.
Mapping of the KARYOTYPE of a cell.
| Descriptor ID |
D007621
|
| MeSH Number(s) |
E01.370.225.500.385.315 E05.200.500.385.315 E05.242.385.315 E05.393.285.475
|
| Concept/Terms |
Karyotyping- Karyotyping
- Karyotypings
- Karyotype Analysis Methods
- Analysis Method, Karyotype
- Analysis Methods, Karyotype
- Karyotype Analysis Method
- Method, Karyotype Analysis
- Methods, Karyotype Analysis
|
Below are MeSH descriptors whose meaning is more general than "Karyotyping".
Below are MeSH descriptors whose meaning is more specific than "Karyotyping".
This graph shows the total number of publications written about "Karyotyping" by people in this website by year, and whether "Karyotyping" 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 |
|---|
| 1994 | 0 | 14 | 14 |
| 1995 | 2 | 21 | 23 |
| 1996 | 0 | 15 | 15 |
| 1997 | 0 | 13 | 13 |
| 1998 | 1 | 23 | 24 |
| 1999 | 1 | 20 | 21 |
| 2000 | 0 | 20 | 20 |
| 2001 | 2 | 14 | 16 |
| 2002 | 0 | 15 | 15 |
| 2003 | 2 | 23 | 25 |
| 2004 | 0 | 14 | 14 |
| 2005 | 0 | 19 | 19 |
| 2006 | 1 | 22 | 23 |
| 2007 | 0 | 13 | 13 |
| 2008 | 0 | 20 | 20 |
| 2009 | 0 | 25 | 25 |
| 2010 | 0 | 21 | 21 |
| 2011 | 0 | 8 | 8 |
| 2012 | 1 | 11 | 12 |
| 2013 | 0 | 8 | 8 |
| 2014 | 1 | 10 | 11 |
| 2015 | 0 | 9 | 9 |
| 2016 | 0 | 8 | 8 |
| 2017 | 1 | 14 | 15 |
| 2018 | 1 | 5 | 6 |
| 2019 | 1 | 9 | 10 |
| 2020 | 0 | 6 | 6 |
| 2021 | 2 | 2 | 4 |
| 2022 | 0 | 2 | 2 |
| 2023 | 0 | 1 | 1 |
| 2024 | 0 | 2 | 2 |
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click here.
Below are the most recent publications written about "Karyotyping" by people in Profiles.
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Impact of prenatal genomics on clinical genetics practice. Best Pract Res Clin Obstet Gynaecol. 2024 Dec; 97:102545.
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Optical genome mapping improves the accuracy of classification, risk stratification, and personalized treatment strategies for patients with acute myeloid leukemia. Am J Hematol. 2024 Oct; 99(10):1959-1968.
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Chromosome-length genome assembly and karyotype of the endangered black-footed ferret (Mustela nigripes). J Hered. 2023 08 23; 114(5):539-548.
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Recurring germline mosaicism in a family due to reversion of an inherited derivative chromosome 8 from an 8;21 translocation with interstitial telomeric sequences. J Med Genet. 2023 06; 60(6):547-556.
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International Society for Prenatal Diagnosis Updated Position Statement on the use of genome-wide sequencing for prenatal diagnosis. Prenat Diagn. 2022 05; 42(6):796-803.
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RNAseqCNV: analysis of large-scale copy number variations from RNA-seq data. Leukemia. 2022 06; 36(6):1492-1498.
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Prognostic and therapeutic implications of measurable residual disease in acute myeloid leukemia. J Hematol Oncol. 2021 09 03; 14(1):137.
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Patient-derived cell lines and orthotopic mouse model of peritoneal carcinomatosis recapitulate molecular and phenotypic features of human gastric adenocarcinoma. J Exp Clin Cancer Res. 2021 Jun 23; 40(1):207.
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A rare description of pure partial trisomy of 16q12.2q24.3 and review of the literature. Am J Med Genet A. 2021 10; 185(10):2903-2912.
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Analytical and clinical performance of chromosomal microarrays compared with FISH panel and conventional karyotyping in patients with chronic lymphocytic leukemia. Leuk Res. 2021 09; 108:106616.