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■ Abbreviation / Long Form : LOD / log of the odds

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Total Number of Papers: 48
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Abbreviation:   LOD  (>> Co-occurring Abbreviation)
Long Form:   log of the odds
 Abbreviation Variation
 Long Form Variation
 Pair(Abbreviation/Long Form) Variation
No. Year Title Co-occurring Abbreviation
2021 Systems genetic analysis of binge-like eating in a C57BL/6J x DBA/2J-F2 cross. BLE, QTL
2019 C57BL/6 substrain differences in inflammatory and neuropathic nociception and genetic mapping of a major quantitative trait locus underlying acute thermal nociception. ---
2015 Dual-trait selection for ethanol consumption and withdrawal: genetic and transcriptional network effects. Chr, WGCNA
2014 Nonsense mutations in BAG3 are associated with early-onset dilated cardiomyopathy in French Canadians. DCM
2013 A genome-wide search for linkage of estimated glomerular filtration rate (eGFR) in the Family Investigation of Nephropathy and Diabetes (FIND). AA, AI, DN, EA, eGFR, FIND, MA, MDRD, QTL, SNPs
2013 A new genetic linkage map of the zygomycete fungus Phycomyces blakesleeanus. ---
2013 Susceptibility to lethal cerebral malaria is regulated by epistatic interaction between chromosome 4 (Berr6) and chromosome 1 (Berr7) loci in mice. ECM
2012 A variable age of onset segregation model for linkage analysis, with correction for ascertainment, applied to glioma. ---
2011 Identification of quantitative trait loci for diabetic nephropathy in KK-Ay/Ta mice. ACRs, FBW, G/B, QTL
10  2011 Significant linkage at chromosome 19q for otitis media with effusion and/or recurrent otitis media (COME/ROM). COME/ROM
11  2010 Clinical and genetic characterization of a Danish family with North Carolina macular dystrophy. NCMD
12  2009 Further evidence of genetic heterogeneity segregating with hereditary gingival fibromatosis. HGF, NPL
13  2009 Heritability and a genome-wide linkage analysis of a Type II/B cluster construct for cannabis dependence in an American Indian community. cM
14  2009 Novel loci interacting epistatically with bone morphogenetic protein receptor 2 cause familial pulmonary arterial hypertension. BMPR2, FPAH, SNP
15  2008 A genome-wide linkage scan identifies multiple chromosomal regions influencing serum lipid levels in the population on the Samoan islands. TC
16  2007 Evidence for a quantitative trait locus affecting low levels of apolipoprotein B and low density lipoprotein on chromosome 10 in Caucasian families. apoB, FHBL, SNPs
17  2007 Lumbar disc disease shows linkage to chromosome 19 overlapping with a QTL for hand OA. OA
18  2007 Novel locus for benign hereditary chorea with adult onset maps to chromosome 8q21.3 q23.3. BHC, DRPLA, HD, HDL1, HDL2, SCA17
19  2006 A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD. FTLD
20  2006 A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33-34. ---
21  2006 Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2-21.3. ALS, FTD, MAPT, SNP, SOD1
22  2006 Genome-wide linkage scan of common stroke in families from northern Sweden. ---
23  2006 Genomewide scans in North American families reveal genetic linkage of essential tremor to a region on chromosome 6p23. ET, NPL
24  2006 Quantitative trait loci influencing low density lipoprotein particle size in African Americans. cM, HDL-C
25  2005 A genome scan for all-cause end-stage renal disease in African Americans. BMI, ESRD, NPL, OSA
26  2005 A genome scan for linkage with aortic root diameter in hypertensive African Americans and whites in the Hypertension Genetic Epidemiology Network (HyperGEN) study. ARD, FBPP, HyperGEN
27  2005 Determinants of variation in serum paraoxonase enzyme activity in baboons. PON
28  2005 Fine mapping of the 5p13 locus linked to schizophrenia and schizotypal personality disorder in a Puerto Rican family. SALPR
29  2005 Genome-wide linkage analyses and candidate gene fine mapping for HDL3 cholesterol: the Framingham Study. cM, HDL-C, SNPs
30  2005 Genome-wide linkage study of erythrocyte sodium-lithium countertransport. RFHS, SLC
31  2005 Genome-wide scans for heritability of fasting serum insulin and glucose concentrations in hypertensive families. HyperGEN
32  2005 Genome-wide search for genes affecting serum uric acid levels: the Framingham Heart Study. BMI, cM
33  2004 Evidence of QTLs on chromosomes 1q42 and 8q24 for LDL-cholesterol and apoB levels in the HERITAGE family study. apoB, cM
34  2004 Genome scan for hypertension in nonobese African Americans: the National Heart, Lung, and Blood Institute Family Blood Pressure Program. FBPP
35  2004 Linkage of serum creatinine and glomerular filtration rate to chromosome 2 in Utah pedigrees. GFR
36  2004 PARK6-linked autosomal recessive early-onset parkinsonism in Asian populations. AR-EOPD
37  2004 Two quantitative trait loci affect ACE activities in Mexican-Americans. ACE
38  2003 A quantitative trait locus on chromosome 16q influences variation in plasma HDL-C levels in Mexican Americans. CETP, HDL-C, LCAT, QTL, SAFHS
39  2002 Fine mapping of an IgE-controlling gene on chromosome 2q: Analysis of CTLA4 and CD28. BHR, SNP
40  2002 Genome scan linkage results for heart rate variability (the Framingham Heart Study). HRV
41  2001 The impact of population admixture on traditional linkage analysis. HWE, LE
42  2000 Evidence for a gene influencing blood pressure on chromosome 17. Genome scan linkage results for longitudinal blood pressure phenotypes in subjects from the framingham heart study. BP, cM
43  2000 Identification of quantitative trait loci for serum cholesterol levels in stroke-prone spontaneously hypertensive rats. SHRSP, WKY
44  1999 Evidence that multiple genes influence baseline concentrations and diet response of Lp(a) in baboons. LDL-C
45  1997 Linkage of combined factors V and VIII deficiency to chromosome 18q by homozygosity mapping. STR
46  1995 Candidate gene studies in pedigrees with maturity-onset diabetes of the young not linked with glucokinase. MODY
47  1993 Linkage analysis of the glucokinase locus in familial type 2 (non-insulin-dependent) diabetic pedigrees. ---
48  1992 Identification of genetic markers flanking the locus for maturity-onset diabetes of the young on human chromosome 20. MODY