Genetic Carrier Screening
"Genetic Carrier Screening" 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.
Identification of individuals who are heterozygous at a GENETIC LOCUS for a recessive PHENOTYPE.
| Descriptor ID |
D006580
|
| MeSH Number(s) |
E01.370.225.562.250 E05.200.562.250 E05.393.435.250 N02.421.308.200 N02.421.726.233.221.250
|
| Concept/Terms |
Genetic Carrier Screening- Genetic Carrier Screening
- Carrier Screening, Genetic
- Screening, Genetic Carrier
- Screenings, Genetic Carrier
- Carrier Detection, Genetic
- Heterozygote Detection
- Detection, Heterozygote
- Genetic Carrier Detection
- Carriers, Genetic, Detection
- Genetic Carriers, Detection
- Heterozygote Screening
- Screening, Heterozygote
- Detection, Genetic Carrier
|
Below are MeSH descriptors whose meaning is more general than "Genetic Carrier Screening".
Below are MeSH descriptors whose meaning is more specific than "Genetic Carrier Screening".
This graph shows the total number of publications written about "Genetic Carrier Screening" by people in this website by year, and whether "Genetic Carrier Screening" 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 | 0 | 1 | 1 |
| 1998 | 0 | 2 | 2 |
| 2004 | 1 | 1 | 2 |
| 2006 | 0 | 1 | 1 |
| 2009 | 0 | 1 | 1 |
| 2010 | 0 | 1 | 1 |
| 2013 | 1 | 0 | 1 |
| 2015 | 0 | 1 | 1 |
| 2016 | 1 | 0 | 1 |
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Below are the most recent publications written about "Genetic Carrier Screening" by people in Profiles.
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Wood SL, Brewer F, Ellison R, Biggio JR, Edwards RK. Prenatal Carrier Screening for Spinal Muscular Atrophy. Am J Perinatol. 2016 10; 33(12):1211-7.
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Hayes B, Hassed S, Chaloner JL, Aston CE, Guy C. Duchenne Muscular Dystrophy: a Survey of Perspectives on Carrier Testing and Communication Within the Family. J Genet Couns. 2016 06; 25(3):443-53.
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Howard EW, Been LF, Lerner M, Brackett D, Lightfoot S, Bullen EC, Sanghera DK. Carriers of a novel frame-shift insertion in WNT16a possess elevated pancreatic expression of TCF7L2. BMC Genet. 2013 Apr 23; 14:28.
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Little SE, Janakiraman V, Kaimal A, Musci T, Ecker J, Caughey AB. The cost-effectiveness of prenatal screening for spinal muscular atrophy. Am J Obstet Gynecol. 2010 Mar; 202(3):253.e1-7.
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Alonso ME, Ochoa A, Sosa AL, Rodríguez Y, Chávez M, Boll C, Yescas P, Macías R, Rasmussen A. Presymptomatic diagnosis in Huntington's disease: the Mexican experience. Genet Test Mol Biomarkers. 2009 Dec; 13(6):717-20.
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Locker GY, Kaul K, Weinberg DS, Gatalica Z, Gong G, Peterman A, Lynch J, Klatzco L, Olopade OI, Bomzer CA, Newlin A, Keenan E, Tajuddin M, Knezetic J, Coronel S, Lynch HT. The I1307K APC polymorphism in Ashkenazi Jews with colorectal cancer: clinical and pathologic features. Cancer Genet Cytogenet. 2006 Aug; 169(1):33-8.
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Sharma R, De Biase I, Gómez M, Delatycki MB, Ashizawa T, Bidichandani SI. Friedreich ataxia in carriers of unstable borderline GAA triplet-repeat alleles. Ann Neurol. 2004 Dec; 56(6):898-901.
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Ellerhorst JA, Hildebrand WH, Cavett JW, Fernandez-Vina MA, Hodges S, Poindexter N, Fischer H, Grimm EA. HLA class II haplotypes predict favorable outcomes for patients with metastatic RCC. Urologe A. 2004 Sep; 43 Suppl 3:S137.
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Machkhas H, Bidichandani SI, Patel PI, Harati Y. A mild case of Friedreich ataxia: lymphocyte and sural nerve analysis for GAA repeat length reveals somatic mosaicism. Muscle Nerve. 1998 Mar; 21(3):390-3.
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Kamboh MI, Aston CE, Dekosky ST. Association between ACT polymorphism and Alzheimer's disease. Neurology. 1998 Feb; 50(2):574-6.