"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."
| Descriptor ID |
D008126
|
| MeSH Number(s) |
G05.348.750
|
| 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 this website by year, and whether "Lod Score" 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 |
|---|
| 1995 | 0 | 6 | 6 |
| 1996 | 0 | 3 | 3 |
| 1997 | 0 | 4 | 4 |
| 1998 | 0 | 5 | 5 |
| 1999 | 0 | 10 | 10 |
| 2000 | 0 | 6 | 6 |
| 2001 | 0 | 12 | 12 |
| 2002 | 0 | 5 | 5 |
| 2003 | 0 | 9 | 9 |
| 2004 | 1 | 5 | 6 |
| 2005 | 2 | 13 | 15 |
| 2006 | 1 | 9 | 10 |
| 2007 | 0 | 6 | 6 |
| 2008 | 0 | 4 | 4 |
| 2009 | 0 | 4 | 4 |
| 2010 | 0 | 4 | 4 |
| 2011 | 0 | 3 | 3 |
| 2012 | 0 | 1 | 1 |
| 2015 | 0 | 2 | 2 |
| 2018 | 0 | 2 | 2 |
| 2019 | 0 | 1 | 1 |
| 2021 | 0 | 1 | 1 |
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Below are the most recent publications written about "Lod Score" by people in Profiles.
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Genetic Variation and Recurrent Haplotypes on Chromosome 6q23-25 Risk Locus in Familial Lung Cancer. Cancer Res. 2021 06 15; 81(12):3162-3173.
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Whole Exome Sequencing of Highly Aggregated Lung Cancer Families Reveals Linked Loci for Increased Cancer Risk on Chromosomes 12q, 7p, and 4q. Cancer Epidemiol Biomarkers Prev. 2020 02; 29(2):434-442.
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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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Bi-allelic Loss-of-Function Variants in DNMBP Cause Infantile Cataracts. Am J Hum Genet. 2018 10 04; 103(4):568-578.
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Molecular Genetic Analysis of Pakistani Families With Autosomal Recessive Congenital Cataracts by Homozygosity Screening. Invest Ophthalmol Vis Sci. 2017 04 01; 58(4):2207-2217.
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Autosomal-Recessive Hearing Impairment Due to Rare Missense Variants within S1PR2. Am J Hum Genet. 2016 Feb 04; 98(2):331-8.
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A family-specific linkage analysis of blood lipid response to fenofibrate in the Genetics of Lipid Lowering Drug and Diet Network. Pharmacogenet Genomics. 2015 Oct; 25(10):511-4.
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COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritis. Nat Genet. 2015 Jun; 47(6):654-60.
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Genetic linkage analysis in the age of whole-genome sequencing. Nat Rev Genet. 2015 May; 16(5):275-84.
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Genome-wide genetic investigation of serological measures of common infections. Eur J Hum Genet. 2015 Nov; 23(11):1544-8.