"Amniocentesis" 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.
Percutaneous transabdominal puncture of the uterus during pregnancy to obtain amniotic fluid. It is commonly used for fetal karyotype determination in order to diagnose abnormal fetal conditions.
| Descriptor ID |
D000649
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| MeSH Number(s) |
E01.370.225.500.384.050 E01.370.225.998.329.309 E01.370.378.630.050 E04.665.600.309 E05.200.500.384.050 E05.200.998.329.309 E05.242.384.050
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Amniocentesis".
Below are MeSH descriptors whose meaning is more specific than "Amniocentesis".
This graph shows the total number of publications written about "Amniocentesis" by people in this website by year, and whether "Amniocentesis" was a major or minor topic of these publications.
To see the data from this visualization as text,
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1996 | 0 | 1 | 1 |
| 1998 | 0 | 5 | 5 |
| 1999 | 0 | 4 | 4 |
| 2002 | 0 | 1 | 1 |
| 2004 | 2 | 2 | 4 |
| 2005 | 1 | 1 | 2 |
| 2007 | 0 | 1 | 1 |
| 2008 | 1 | 1 | 2 |
| 2009 | 0 | 2 | 2 |
| 2011 | 1 | 0 | 1 |
| 2012 | 2 | 0 | 2 |
| 2014 | 1 | 0 | 1 |
| 2016 | 1 | 1 | 2 |
| 2017 | 0 | 1 | 1 |
| 2019 | 1 | 5 | 6 |
| 2023 | 0 | 1 | 1 |
| 2024 | 1 | 0 | 1 |
| 2025 | 0 | 1 | 1 |
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Below are the most recent publications written about "Amniocentesis" by people in Profiles.
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Radial Ray Malformation. Am J Obstet Gynecol. 2019 12; 221(6):B16-B18.
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Congenital talipes equinovarus (clubfoot). Am J Obstet Gynecol. 2019 12; 221(6):B10-B12.
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The current and future impact of genome-wide sequencing on fetal precision medicine. Hum Genet. 2020 Sep; 139(9):1121-1130.
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Positive predictive value estimates for cell-free noninvasive prenatal screening from data of a large referral genetic diagnostic laboratory. Am J Obstet Gynecol. 2017 12; 217(6):691.e1-691.e6.
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Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases. Prenat Diagn. 2009 Jan; 29(1):29-39.
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Middle cerebral artery peak systolic velocity for the diagnosis of fetal anemia: the untold story. Ultrasound Obstet Gynecol. 2005 Apr; 25(4):323-30.
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Prenatal diagnosis and treatment of holocarboxylase synthetase deficiency. Prenat Diagn. 1999 Feb; 19(2):108-12.
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Mosaic trisomy 16 ascertained through amniocentesis: evaluation of 11 new cases. Am J Med Genet. 1998 Dec 28; 80(5):473-80.
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Prenatal diagnosis and carrier detection for glycogen storage disease type III using polymorphic DNA markers. Prenat Diagn. 1998 Jan; 18(1):61-4.
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The beta-core fragment of chorionic gonadotropin is not complexed to macromolecules in amniotic fluid. J Clin Endocrinol Metab. 1994 Jun; 78(6):1349-53.