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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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".

Analytical, Diagnostic and Therapeutic Techniques and Equipment [E]
Diagnosis [E01]
Diagnostic Techniques and Procedures [E01.370]
Clinical Laboratory Techniques [E01.370.225]
Cytological Techniques [E01.370.225.500]
Cytogenetic Analysis [E01.370.225.500.385]
Karyotyping [E01.370.225.500.385.315]
Investigative Techniques [E05]
Clinical Laboratory Techniques [E05.200]
Cytological Techniques [E05.200.500]
Cytogenetic Analysis [E05.200.500.385]
Karyotyping [E05.200.500.385.315]
Cytological Techniques [E05.242]
Cytogenetic Analysis [E05.242.385]
Karyotyping [E05.242.385.315]
Genetic Techniques [E05.393]
Cytogenetic Analysis [E05.393.285]
Karyotyping [E05.393.285.475]

Below are MeSH descriptors whose meaning is related to "Karyotyping".

Below are MeSH descriptors whose meaning is more specific than "Karyotyping".

Karyotyping
Spectral Karyotyping

publications

Timeline | Most Recent

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.

Bar chart showing 99 publications over 28 distinct years, with a maximum of 10 publications in 1998

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
1995	0	5	5
1996	0	4	4
1997	1	3	4
1998	1	9	10
1999	0	4	4
2000	0	5	5
2001	0	3	3
2002	1	4	5
2003	0	4	4
2004	1	5	6
2005	0	6	6
2006	0	1	1
2007	0	2	2
2008	0	2	2
2009	0	3	3
2010	0	4	4
2011	0	3	3
2012	0	4	4
2013	0	2	2
2014	1	2	3
2015	0	3	3
2016	0	3	3
2017	1	3	4
2018	0	1	1
2019	0	3	3
2020	0	1	1
2021	1	1	2
2022	0	2	2

Below are the most recent publications written about "Karyotyping" by people in Profiles.

Powel JE, Sham CE, Spiliopoulos M, Ferreira CR, Rosenthal E, Sinkovskaya ES, Brown S, Jelin AC, Al-Kouatly HB. Genetics of non-isolated hemivertebra: A systematic review of fetal, neonatal, and infant cases. Clin Genet. 2022 10; 102(4):262-287.

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Spahn PN, Zhang X, Hu Q, Lu H, Hamaker NK, Hefzi H, Li S, Kuo CC, Huang Y, Lee JC, Davis AJ, Ly P, Lee KH, Lewis NE. Restoration of DNA repair mitigates genome instability and increases productivity of Chinese hamster ovary cells. Biotechnol Bioeng. 2022 03; 119(3):963-982.

View in: PubMed
Klimczak AM, Patel DP, Hotaling JM, Scott RT. Role of the sperm, oocyte, and embryo in recurrent pregnancy loss. Fertil Steril. 2021 03; 115(3):533-537.

View in: PubMed
Snyder EA, San Roman AK, Pi?a-Aguilar RE, Steeves MA, McNamara EA, Souter I, Hayes FJ, Levitsky LL, Lin AE. Genetic counseling for women with 45,X/46,XX mosaicism: Towards more personalized management. Eur J Med Genet. 2021 Mar; 64(3):104140.

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Levy AT, Berghella V, Al-Kouatly HB. Outcome of 45,X fetuses with cystic hygroma: A systematic review. Am J Med Genet A. 2021 01; 185(1):26-32.

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Lin AE, Santoro S, High FA, Goldenberg P, Gutmark-Little I. Congenital heart defects associated with aneuploidy syndromes: New insights into familiar associations. Am J Med Genet C Semin Med Genet. 2020 03; 184(1):53-63.

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Ross JL, Bloy L, Roberts TPL, Miller J, Xing C, Silverman LA, Zinn AR. Y chromosome gene copy number and lack of autism phenotype in a male with an isodicentric Y chromosome and absent NLGN4Y expression. Am J Med Genet B Neuropsychiatr Genet. 2019 10; 180(7):471-482.

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Blakey-Cheung S, Parker P, Schlaff W, Monseur B, Keppler-Noreuil K, Al-Kouatly HB. Diagnosis and clinical delineation of mosaic tetrasomy 5p. Eur J Med Genet. 2020 Jan; 63(1):103634.

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Marin D, Zimmerman R, Tao X, Zhan Y, Scott RT, Treff NR. Validation of a targeted next generation sequencing-based comprehensive chromosome screening platform for detection of triploidy in human blastocysts. Reprod Biomed Online. 2018 Apr; 36(4):388-395.

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Hurd LM, Thacker MM, Okenfuss E, Duker AL, Lou Y, Harty MP, Conard K, Lian JB, Bober MB. Aneurysmal bone cysts and pathologic fracture associated with supernumerary ring chromosome 6 in two unrelated patients. Am J Med Genet A. 2017 Dec; 173(12):3205-3210.

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