Chromosomes, Human, Pair 4
"Chromosomes, Human, Pair 4" 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.
A specific pair of GROUP B CHROMOSOMES of the human chromosome classification.
MeSH Number(s)
A11.284.187.520.300.280.285
G05.360.162.520.300.280.285
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, Pair 4".
- Anatomy [A]
- Cells [A11]
- Cellular Structures [A11.284]
- Chromosomes [A11.284.187]
- Chromosomes, Mammalian [A11.284.187.520]
- Chromosomes, Human [A11.284.187.520.300]
- Chromosomes, Human, 4-5 [A11.284.187.520.300.280]
- Chromosomes, Human, Pair 4 [A11.284.187.520.300.280.285]
- Biological Sciences [G]
- Genetic Phenomena [G05]
- Genetic Structures [G05.360]
- Chromosomes [G05.360.162]
- Chromosomes, Mammalian [G05.360.162.520]
- Chromosomes, Human [G05.360.162.520.300]
- Chromosomes, Human, 4-5 [G05.360.162.520.300.280]
- Chromosomes, Human, Pair 4 [G05.360.162.520.300.280.285]
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, Pair 4".
This graph shows the total number of publications written about "Chromosomes, Human, Pair 4" by people in Harvard Catalyst Profiles by year, and whether "Chromosomes, Human, Pair 4" 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 |
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1993 | 3 | 4 | 7 |
1994 | 4 | 3 | 7 |
1995 | 2 | 2 | 4 |
1996 | 5 | 2 | 7 |
1997 | 5 | 3 | 8 |
1998 | 0 | 1 | 1 |
1999 | 3 | 4 | 7 |
2000 | 3 | 0 | 3 |
2001 | 3 | 1 | 4 |
2002 | 4 | 3 | 7 |
2003 | 3 | 4 | 7 |
2004 | 2 | 1 | 3 |
2005 | 2 | 3 | 5 |
2006 | 4 | 3 | 7 |
2007 | 9 | 1 | 10 |
2008 | 2 | 5 | 7 |
2009 | 5 | 5 | 10 |
2010 | 1 | 3 | 4 |
2011 | 3 | 5 | 8 |
2012 | 3 | 1 | 4 |
2013 | 0 | 1 | 1 |
2014 | 1 | 1 | 2 |
2015 | 3 | 2 | 5 |
2016 | 0 | 2 | 2 |
2017 | 0 | 3 | 3 |
2018 | 0 | 1 | 1 |
2019 | 0 | 3 | 3 |
2020 | 1 | 1 | 2 |
Below are the most recent publications written about "Chromosomes, Human, Pair 4" by people in Profiles.
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A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans. Hum Genet. 2021 Jun; 140(6):915-931.
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IgH translocation with undefined partners is associated with superior outcome in multiple myeloma patients. Eur J Haematol. 2020 Sep; 105(3):326-334.
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Genome sequencing identifies a homozygous inversion disrupting QDPR as a cause for dihydropteridine reductase deficiency. Mol Genet Genomic Med. 2020 04; 8(4):e1154.
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Clinical and molecular characterization of patients with acute myeloid leukemia and sole trisomies of chromosomes 4, 8, 11, 13 or 21. Leukemia. 2020 02; 34(2):358-368.
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Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies. Am J Hum Genet. 2019 02 07; 104(2):260-274.
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Detection of Large Structural Variants Causing Inherited Retinal Diseases. Adv Exp Med Biol. 2019; 1185:197-202.
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Increased Chromosome Aberrations in Cells Exposed Simultaneously to Simulated Microgravity and Radiation. Int J Mol Sci. 2018 Dec 22; 20(1).
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Facioscapulohumeral Muscular Dystrophy. Compr Physiol. 2017 Sep 12; 7(4):1229-1279.
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Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium. Sci Rep. 2017 09 12; 7(1):11303.
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Identification of six new genetic loci associated with atrial fibrillation in the Japanese population. Nat Genet. 2017 Jun; 49(6):953-958.