"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 |
|---|
| 1997 | 0 | 1 | 1 |
| 2002 | 0 | 2 | 2 |
| 2003 | 0 | 1 | 1 |
| 2006 | 0 | 3 | 3 |
| 2009 | 0 | 1 | 1 |
| 2010 | 0 | 2 | 2 |
| 2011 | 0 | 4 | 4 |
| 2012 | 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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Gragnoli C. Proteasome modulator 9 is linked to microvascular pathology of T2D. J Cell Physiol. 2012 Aug; 227(8):3116-8.
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Gragnoli C. Proteasome modulator 9 and carpal tunnel syndrome. Diabetes Res Clin Pract. 2011 Nov; 94(2):e47-9.
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Gragnoli C. PSMD9 is linked to type 2 diabetes neuropathy. J Diabetes Complications. 2011 Sep-Oct; 25(5):329-31.
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Gragnoli C. Hypercholesterolemia and a candidate gene within the 12q24 locus. Cardiovasc Diabetol. 2011; 10:38.
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Gragnoli C. Proteasome modulator 9 and macrovascular pathology of T2D. Cardiovasc Diabetol. 2011; 10:32.
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Tanaka A, Morice-Picard F, Lacombe D, Nagy N, Hide M, Ta?eb A, McGrath J. Identification of a homozygous deletion mutation in C16orf57 in a family with Clericuzio-type poikiloderma with neutropenia. Am J Med Genet A. 2010 Jun; 152A(6):1347-8.
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Gragnoli C. PSMD9 gene in the NIDDM2 locus is linked to type 2 diabetes in Italians. J Cell Physiol. 2010 Feb; 222(2):265-7.
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Feldman G, Dalsey C, Fertala K, Azimi D, Fortina P, Devoto M, Pacifici M, Parvizi J. The Otto Aufranc Award: Identification of a 4 Mb region on chromosome 17q21 linked to developmental dysplasia of the hip in one 18-member, multigeneration family. Clin Orthop Relat Res. 2010 Feb; 468(2):337-44.
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Gouya L, Muzeau F, Robreau AM, Letteron P, Couchi E, Lyoumi S, Deybach JC, Puy H, Fleming R, Demant P, Beaumont C, Grandchamp B. Genetic study of variation in normal mouse iron homeostasis reveals ceruloplasmin as an HFE-hemochromatosis modifier gene. Gastroenterology. 2007 Feb; 132(2):679-86.
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Lugassy J, Itin P, Ishida-Yamamoto A, Holland K, Huson S, Geiger D, Hennies HC, Indelman M, Bercovich D, Uitto J, Bergman R, McGrath JA, Richard G, Sprecher E. Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: two allelic ectodermal dysplasias caused by dominant mutations in KRT14. Am J Hum Genet. 2006 Oct; 79(4):724-30.