Polycystic Kidney, Autosomal Dominant
"Polycystic Kidney, Autosomal Dominant" 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.
Kidney disorders with autosomal dominant inheritance and characterized by multiple CYSTS in both KIDNEYS with progressive deterioration of renal function.
MeSH Number(s)
C12.777.419.403.875.500
C13.351.968.419.403.875.500
Concept/Terms
Polycystic Kidney, Autosomal Dominant- Polycystic Kidney, Autosomal Dominant
- Adult Polycystic Kidney Disease
- Kidney, Polycystic, Autosomal Dominant
- ADPKD
- Polycystic Kidney Disease, Autosomal Dominant
- Autosomal Dominant Polycystic Kidney
Below are MeSH descriptors whose meaning is more general than "Polycystic Kidney, Autosomal Dominant".
Below are MeSH descriptors whose meaning is more specific than "Polycystic Kidney, Autosomal Dominant".
This graph shows the total number of publications written about "Polycystic Kidney, Autosomal Dominant" by people in Harvard Catalyst Profiles by year, and whether "Polycystic Kidney, Autosomal Dominant" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1994 | 0 | 1 | 1 |
| 1995 | 3 | 0 | 3 |
| 1996 | 2 | 0 | 2 |
| 1997 | 3 | 1 | 4 |
| 1998 | 2 | 1 | 3 |
| 1999 | 1 | 0 | 1 |
| 2000 | 7 | 0 | 7 |
| 2001 | 3 | 1 | 4 |
| 2002 | 2 | 1 | 3 |
| 2003 | 3 | 0 | 3 |
| 2004 | 2 | 1 | 3 |
| 2005 | 3 | 1 | 4 |
| 2006 | 3 | 0 | 3 |
| 2007 | 2 | 1 | 3 |
| 2008 | 4 | 2 | 6 |
| 2009 | 3 | 0 | 3 |
| 2010 | 2 | 2 | 4 |
| 2011 | 3 | 0 | 3 |
| 2012 | 3 | 0 | 3 |
| 2013 | 7 | 2 | 9 |
| 2014 | 5 | 1 | 6 |
| 2015 | 3 | 0 | 3 |
| 2016 | 6 | 0 | 6 |
| 2017 | 9 | 0 | 9 |
| 2018 | 3 | 0 | 3 |
| 2019 | 5 | 2 | 7 |
| 2020 | 8 | 0 | 8 |
| 2021 | 2 | 0 | 2 |
| 2022 | 3 | 0 | 3 |
Below are the most recent publications written about "Polycystic Kidney, Autosomal Dominant" by people in Profiles.
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Association of autosomal dominant polycystic kidney disease with cardiovascular disease: a US-National Inpatient Perspective. Clin Exp Nephrol. 2022 Jul; 26(7):659-668.
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Volume Progression and Imaging Classification of Polycystic Liver in Early Autosomal Dominant Polycystic Kidney Disease. Clin J Am Soc Nephrol. 2022 03; 17(3):374-384.
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The utility of a genetic kidney disease clinic employing a broad range of genomic testing platforms: experience of the Irish Kidney Gene Project. J Nephrol. 2022 07; 35(6):1655-1665.
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Monoallelic IFT140 pathogenic variants are an important cause of the autosomal dominant polycystic kidney-spectrum phenotype. Am J Hum Genet. 2022 01 06; 109(1):136-156.
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Somatostatin analog therapy effectiveness on the progression of polycystic kidney and liver disease: A systematic review and meta-analysis of randomized clinical trials. PLoS One. 2021; 16(9):e0257606.
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A Rare Kidney Disease To Cure Them All? Towards Mechanism-Based Therapies for Proteinopathies. Trends Mol Med. 2021 04; 27(4):394-409.
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Proteomics and metabolomics studies exploring the pathophysiology of renal dysfunction in autosomal dominant polycystic kidney disease and other ciliopathies. Nephrol Dial Transplant. 2020 11 01; 35(11):1853-1861.
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Mineral bone disease in autosomal dominant polycystic kidney disease. Kidney Int. 2021 04; 99(4):977-985.
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The value of genotypic and imaging information to predict functional and structural outcomes in ADPKD. JCI Insight. 2020 08 06; 5(15).
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Interactions between FGF23 and Genotype in Autosomal Dominant Polycystic Kidney Disease. Kidney360. 2020 Jul; 1(7):648-656.