"Phenotype" 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.
The outward appearance of the individual. It is the product of interactions between genes, and between the GENOTYPE and the environment.
| Descriptor ID |
D010641
|
| MeSH Number(s) |
G05.695
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Phenotype".
Below are MeSH descriptors whose meaning is more specific than "Phenotype".
This graph shows the total number of publications written about "Phenotype" by people in this website by year, and whether "Phenotype" 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 |
|---|
| 1994 | 0 | 19 | 19 |
| 1995 | 0 | 15 | 15 |
| 1996 | 1 | 22 | 23 |
| 1997 | 0 | 22 | 22 |
| 1998 | 0 | 20 | 20 |
| 1999 | 0 | 25 | 25 |
| 2000 | 0 | 38 | 38 |
| 2001 | 0 | 36 | 36 |
| 2002 | 0 | 36 | 36 |
| 2003 | 3 | 53 | 56 |
| 2004 | 2 | 38 | 40 |
| 2005 | 4 | 47 | 51 |
| 2006 | 5 | 33 | 38 |
| 2007 | 3 | 36 | 39 |
| 2008 | 2 | 63 | 65 |
| 2009 | 2 | 52 | 54 |
| 2010 | 5 | 54 | 59 |
| 2011 | 12 | 66 | 78 |
| 2012 | 5 | 67 | 72 |
| 2013 | 11 | 64 | 75 |
| 2014 | 5 | 82 | 87 |
| 2015 | 8 | 82 | 90 |
| 2016 | 8 | 89 | 97 |
| 2017 | 3 | 63 | 66 |
| 2018 | 10 | 73 | 83 |
| 2019 | 7 | 75 | 82 |
| 2020 | 5 | 66 | 71 |
| 2021 | 8 | 62 | 70 |
| 2022 | 2 | 43 | 45 |
| 2023 | 2 | 41 | 43 |
| 2024 | 8 | 23 | 31 |
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Below are the most recent publications written about "Phenotype" by people in Profiles.
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Body composition and muscle composition phenotypes in patients on waitlist and shortly after liver transplant - results from a pilot study. BMC Gastroenterol. 2024 Oct 09; 24(1):356.
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Two distinct phenotypes of calcium oxalate stone formers could imply different long-term risks for renal function. Urolithiasis. 2024 Sep 28; 52(1):133.
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Severe neurodevelopmental phenotype, diagnostic, and treatment challenges in patients with SECISBP2 deficiency. Genet Med. 2024 Dec; 26(12):101280.
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Distribution of MRI-derived T2 values as a biomarker for in vivo rapid screening of phenotype severity in mdx mice. PLoS One. 2024; 19(9):e0310551.
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The simplicity of protein sequence-function relationships. Nat Commun. 2024 Sep 11; 15(1):7953.
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Emerin deficiency drives MCF7 cells to an invasive phenotype. Sci Rep. 2024 08 28; 14(1):19998.
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Genetic determinants and phenotypic consequences of blood T-cell proportions in 207,000 diverse individuals. Nat Commun. 2024 Aug 07; 15(1):6732.
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Patent Ductus Arteriosus and Lung Magnetic Resonance Imaging Phenotype in Moderate and Severe Bronchopulmonary Dysplasia-Pulmonary Hypertension. Am J Respir Crit Care Med. 2024 08 01; 210(3):318-328.
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Symptoms of Lower Urinary Tract Dysfunction Research Network (LURN): An introduction to the Urinary Urgency Phenotyping Protocol LURN II. Neurourol Urodyn. 2024 Nov; 43(8):1800-1808.
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Gyrification across psychotic disorders: A bipolar-schizophrenia network of intermediate phenotypes study. Schizophr Res. 2024 Sep; 271:169-178.