 Karyotyping
"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
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| MeSH Number(s) |
E01.370.225.500.385.315 E05.200.500.385.315 E05.242.385.315 E05.393.285.475
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| Concept/Terms |
Karyotyping- Karyotyping
- Karyotypings
- Karyotype Analysis Methods
- Analysis Method, Karyotype
- Analysis Methods, Karyotype
- Karyotype Analysis Method
- Method, Karyotype Analysis
- Methods, Karyotype Analysis
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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 UAMS Profiles 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 |
|---|
| 2022 | 0 | 1 | 1 | | 2021 | 1 | 0 | 1 | | 2019 | 0 | 1 | 1 | | 2017 | 0 | 3 | 3 | | 2016 | 1 | 1 | 2 | | 2015 | 0 | 1 | 1 | | 2014 | 0 | 2 | 2 | | 2013 | 0 | 3 | 3 | | 2012 | 0 | 4 | 4 | | 2011 | 0 | 3 | 3 | | 2010 | 0 | 1 | 1 | | 2009 | 0 | 1 | 1 | | 2008 | 0 | 5 | 5 | | 2007 | 0 | 2 | 2 | | 2006 | 0 | 2 | 2 | | 2005 | 0 | 9 | 9 | | 2004 | 0 | 4 | 4 | | 2003 | 0 | 3 | 3 | | 2002 | 0 | 5 | 5 | | 2001 | 0 | 1 | 1 | | 1999 | 0 | 1 | 1 | | 1998 | 0 | 2 | 2 | | 1996 | 0 | 1 | 1 | | 1993 | 0 | 1 | 1 | | 1992 | 0 | 1 | 1 | | 1990 | 0 | 1 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Karyotyping" by people in Profiles over the past ten years.
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Malaga ML, Carrillo LF. FISH-negative, karyotype-negative acute promyelocytic leukemia. Blood. 2023 10 12; 142(15):1328.
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Binz RL, Pathak R. Molecular Cytogenetics Reveals Mosaicism in Human Umbilical Vein Endothelial Cells. Genes (Basel). 2022 06 03; 13(6).
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Song S, Xu Y, Huo L, Zhao S, Wang R, Li Y, Scott AW, Pizzi MP, Wang Y, Fan Y, Harada K, Jin J, Ma L, Yao X, Shanbhag ND, Gan Q, Roy-Chowdhuri S, Badgwell BD, Wang Z, Wang L, Ajani JA. 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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Stambough K, Magistrado L, Perez-Milicua G. Evaluation of ambiguous genitalia. Curr Opin Obstet Gynecol. 2019 10; 31(5):303-308.
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Knez V, Liu X, Schowinsky J, Pan Z, Wang D, Lorsbach R, Lu C, Luedke C, Haag M, Carstens B, Swisshelm K, Yang LH, Jug R, Wang E, Liang X. Clinicopathologic and genetic spectrum of infantile B-lymphoblastic leukemia: a multi-institutional study. Leuk Lymphoma. 2019 04; 60(4):1006-1013.
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Kubendran S, Duong J, Dong F, Lueking A, Farley D. Implementing a Protocol to Optimize Detection of Chromosome Abnormalities in Cases of Miscarriage or Stillbirth at a Midwestern Teaching Hospital. Perm J. 2018; 22:17-204.
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McKelvey KD, Trana CJ, Kelsay J, Sawyer J, Clothier J. Phelan-McDermid syndrome and cancer predisposition: The value of a karyotype. Am J Med Genet A. 2018 01; 176(1):144-145.
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Trpkov K, Abou-Ouf H, Hes O, Lopez JI, Nesi G, Comperat E, Sibony M, Osunkoya AO, Zhou M, Gokden N, Leroy X, Berney DM, Werneck Cunha I, Musto ML, Athanazio DA, Yilmaz A, Donnelly B, Hyndman E, Gill AJ, McKenney JK, Bismar TA. Eosinophilic Solid and Cystic Renal Cell Carcinoma (ESC RCC): Further Morphologic and Molecular Characterization of ESC RCC as a Distinct Entity. Am J Surg Pathol. 2017 Oct; 41(10):1299-1308.
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Sun M, Zhang H, Li G, Guy CJ, Wang X, Lu X, Gong F, Lee J, Hassed S, Li S. Molecular characterization of 20 small supernumerary marker chromosome cases using array comparative genomic hybridization and fluorescence in situ hybridization. Sci Rep. 2017 09 04; 7(1):10395.
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Sawyer JR, Tian E, Shaughnessy JD, Epstein J, Swanson CM, Stangeby C, Hale CL, Parr L, Lynn M, Sammartino G, Lukacs JL, Stein C, Bailey C, Zangari M, Davies FE, Van Rhee F, Barlogie B, Morgan GJ. Hyperhaploidy is a novel high-risk cytogenetic subgroup in multiple myeloma. Leukemia. 2017 03; 31(3):637-644.
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Montgomery ND, Coward WB, Johnson S, Yuan J, Gulley ML, Mathews SP, Kaiser-Rogers K, Rao KW, Sanger WG, Sanmann JN, Fedoriw Y. Karyotypic abnormalities associated with Epstein-Barr virus status in classical Hodgkin lymphoma. Cancer Genet. 2016 09; 209(9):408-416.
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Rush ET, Schaefer GB, Sanger WG, Coccia PF. Aplastic Anemia in Two Patients with Sex Chromosome Aneuploidies. Cytogenet Genome Res. 2015; 147(1):31-4.
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