 Lod Score
"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
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| MeSH Number(s) |
G05.540.750
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| Concept/Terms |
Lod Score- Lod Score
- Lod Scores
- Score, Lod
- Scores, Lod
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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 |
|---|
| 1980 | 0 | 1 | 1 | | 1983 | 0 | 2 | 2 | | 1985 | 0 | 1 | 1 | | 1988 | 0 | 1 | 1 | | 1989 | 0 | 2 | 2 | | 1990 | 0 | 2 | 2 | | 1991 | 0 | 1 | 1 | | 1992 | 0 | 5 | 5 | | 1993 | 1 | 4 | 5 | | 1994 | 0 | 10 | 10 | | 1995 | 0 | 2 | 2 | | 1996 | 0 | 5 | 5 | | 1997 | 1 | 6 | 7 | | 1998 | 0 | 3 | 3 | | 1999 | 0 | 5 | 5 | | 2000 | 1 | 4 | 5 | | 2001 | 0 | 10 | 10 | | 2002 | 0 | 4 | 4 | | 2003 | 1 | 2 | 3 | | 2004 | 1 | 9 | 10 | | 2005 | 0 | 3 | 3 | | 2006 | 2 | 3 | 5 | | 2007 | 0 | 4 | 4 | | 2008 | 0 | 5 | 5 | | 2009 | 0 | 2 | 2 | | 2010 | 0 | 2 | 2 | | 2012 | 0 | 1 | 1 | | 2013 | 0 | 1 | 1 | | 2014 | 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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Sanders AR, Beecham GW, Guo S, Badner JA, Bocklandt S, Mustanski BS, Hamer DH, Martin ER. Genome-Wide Linkage Study Meta-Analysis of Male Sexual Orientation. Arch Sex Behav. 2021 11; 50(8):3371-3375.
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Carbonetto P, Cheng R, Gyekis JP, Parker CC, Blizard DA, Palmer AA, Lionikas A. Discovery and refinement of muscle weight QTLs in B6 × D2 advanced intercross mice. Physiol Genomics. 2014 Aug 15; 46(16):571-82.
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Rubicz R, Zhu J, Laston S, Cole SA, Voruganti VS, Ebbesson SO, Howard BV, Maccluer JW, Davidson M, Umans JG, Comuzzie AG, Göring HH. Statistical genetic analysis of serological measures of common, chronic infections in Alaska Native participants in the GOCADAN study. Genet Epidemiol. 2013 Nov; 37(7):751-7.
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Sun X, Vengoechea J, Elston R, Chen Y, Amos CI, Armstrong G, Bernstein JL, Claus E, Davis F, Houlston RS, Il'yasova D, Jenkins RB, Johansen C, Lai R, Lau CC, Liu Y, McCarthy BJ, Olson SH, Sadetzki S, Schildkraut J, Shete S, Yu R, Vick NA, Merrell R, Wrensch M, Yang P, Melin B, Bondy ML, Barnholtz-Sloan JS. A variable age of onset segregation model for linkage analysis, with correction for ascertainment, applied to glioma. Cancer Epidemiol Biomarkers Prev. 2012 Dec; 21(12):2242-51.
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Ferreira CM, Chen JL, Li J, Shimomura K, Yang X, Lussier YA, Pinto LH, Solway J. Genetic interactions between chromosomes 11 and 18 contribute to airway hyperresponsiveness in mice. PLoS One. 2012; 7(1):e29579.
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Ross J, Badner J, Garrido H, Sheppard B, Chavira DA, Grados M, Woo JM, Doo P, Umaña P, Fournier E, Murray SS, Mathews CA. Genomewide linkage analysis in Costa Rican families implicates chromosome 15q14 as a candidate region for OCD. Hum Genet. 2011 Dec; 130(6):795-805.
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Xu H, Cheng R, Juo SH, Liu J, Loth JE, Endicott J, Gilliam C, Baron M. Fine mapping of candidate regions for bipolar disorder provides strong evidence for susceptibility loci on chromosomes 7q. Am J Med Genet B Neuropsychiatr Genet. 2011 Mar; 156(2):168-76.
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Samocha KE, Lim JE, Cheng R, Sokoloff G, Palmer AA. Fine mapping of QTL for prepulse inhibition in LG/J and SM/J mice using F(2) and advanced intercross lines. Genes Brain Behav. 2010 Oct; 9(7):759-67.
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Zhao C, Bellur DL, Lu S, Zhao F, Grassi MA, Bowne SJ, Sullivan LS, Daiger SP, Chen LJ, Pang CP, Zhao K, Staley JP, Larsson C. Autosomal-dominant retinitis pigmentosa caused by a mutation in SNRNP200, a gene required for unwinding of U4/U6 snRNAs. Am J Hum Genet. 2009 Nov; 85(5):617-27.
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Rajab A, Aldinger KA, El-Shirbini HA, Dobyns WB, Ross ME. Recessive developmental delay, small stature, microcephaly and brain calcifications with locus on chromosome 2. Am J Med Genet A. 2009 Feb; 149A(2):129-37.
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