"Lod Score" 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 total relative probability, expressed on a logarithmic scale, that a linkage relationship exists among selected loci. Lod is an acronym for "logarithmic odds."
Concept/Terms
Lod Score- Lod Score
- Lod Scores
- Score, Lod
- Scores, Lod
Below are MeSH descriptors whose meaning is more general than "Lod Score".
Below are MeSH descriptors whose meaning is more specific than "Lod Score".
This graph shows the total number of publications written about "Lod Score" by people in Harvard Catalyst Profiles by year, and whether "Lod Score" 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 |
|---|
| 1993 | 0 | 9 | 9 |
| 1994 | 0 | 12 | 12 |
| 1995 | 0 | 20 | 20 |
| 1996 | 0 | 14 | 14 |
| 1997 | 0 | 18 | 18 |
| 1998 | 2 | 17 | 19 |
| 1999 | 0 | 20 | 20 |
| 2000 | 1 | 22 | 23 |
| 2001 | 0 | 24 | 24 |
| 2002 | 0 | 21 | 21 |
| 2003 | 2 | 32 | 34 |
| 2004 | 1 | 24 | 25 |
| 2005 | 1 | 15 | 16 |
| 2006 | 0 | 19 | 19 |
| 2007 | 2 | 9 | 11 |
| 2008 | 2 | 19 | 21 |
| 2009 | 0 | 7 | 7 |
| 2010 | 0 | 12 | 12 |
| 2011 | 0 | 7 | 7 |
| 2012 | 0 | 10 | 10 |
| 2013 | 0 | 6 | 6 |
| 2014 | 0 | 1 | 1 |
| 2015 | 0 | 3 | 3 |
| 2016 | 0 | 1 | 1 |
| 2018 | 0 | 2 | 2 |
| 2020 | 0 | 1 | 1 |
Below are the most recent publications written about "Lod Score" by people in Profiles.
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Detecting sample swaps in diverse NGS data types using linkage disequilibrium. Nat Commun. 2020 07 29; 11(1):3697.
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GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes. Nat Commun. 2018 12 03; 9(1):5141.
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Analysis of pedigree data in populations with multiple ancestries: Strategies for dealing with admixture in Caribbean Hispanic families from the ADSP. Genet Epidemiol. 2018 09; 42(6):500-515.
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Homomorphic ZW chromosomes in a wild strawberry show distinctive recombination heterogeneity but a small sex-determining region. New Phytol. 2016 09; 211(4):1412-23.
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Genome-wide linkage on chromosome 10q26 for a dimensional scale of major depression. J Affect Disord. 2016 Feb; 191:123-31.
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T (brachyury) is linked to a Mendelian form of neural tube defects in humans. Hum Genet. 2015 Oct; 134(10):1139-41.
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Ecological and Genetic Barriers Differentiate Natural Populations of Saccharomyces cerevisiae. Mol Biol Evol. 2015 Sep; 32(9):2317-27.
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Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export. Nat Genet. 2015 Jun; 47(6):579-81.
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Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening. Nat Genet. 2015 May; 47(5):512-7.
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Whole-exome sequencing identifies rare, functional CFH variants in families with macular degeneration. Hum Mol Genet. 2014 Oct 01; 23(19):5283-93.