Found: 120
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Folliculin mutations are not associated with severe COPD.
- Published in:
- BMC Medical Genetics, 2008, v. 9, p. 120, doi. 10.1186/1471-2350-9-120
- Publication type:
- Article
Genome wide association for substance dependence: convergent results from epidemiologic and research volunteer samples.
- Published in:
- BMC Medical Genetics, 2008, v. 9, p. 113, doi. 10.1186/1471-2350-9-113
- Publication type:
- Article
Association between Ngb polymorphisms and ischemic stroke in the Southern Chinese Han population.
- Published in:
- BMC Medical Genetics, 2008, v. 9, p. 110, doi. 10.1186/1471-2350-9-110
- Publication type:
- Article
A new 500 kb haplotype associated with high CD8+ T-lymphocyte numbers predicts a less severe expression of hereditary hemochromatosis.
- Published in:
- BMC Medical Genetics, 2008, v. 9, p. 97, doi. 10.1186/1471-2350-9-97
- Publication type:
- Article
Selecting a BRCA risk assessment model for use in a familial cancer clinic.
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- BMC Medical Genetics, 2008, v. 9, p. 116, doi. 10.1186/1471-2350-9-116
- Publication type:
- Article
DNA methylation and mRNA expression of SYN III, a candidate gene for schizophrenia.
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- BMC Medical Genetics, 2008, v. 9, p. 115, doi. 10.1186/1471-2350-9-115
- Publication type:
- Article
An intronic alteration of the fibroblast growth factor 10 gene causing ALSG-(aplasia of lacrimal and salivary glands) syndrome.
- Published in:
- BMC Medical Genetics, 2008, v. 9, p. 114, doi. 10.1186/1471-2350-9-114
- Publication type:
- Article
Genetic polymorphisms are associated with serum levels of sex hormone binding globulin in postmenopausal women.
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- BMC Medical Genetics, 2008, v. 9, p. 112, doi. 10.1186/1471-2350-9-112
- Publication type:
- Article
Investigation of Gamma-aminobutyric acid (GABA) A receptors genes and migraine susceptibility.
- Published in:
- BMC Medical Genetics, 2008, v. 9, p. 109, doi. 10.1186/1471-2350-9-109
- Publication type:
- Article
No germline mutations in supposed tumour suppressor genes SAFB1 and SAFB2 in familial breast cancer with linkage to 19p.
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- BMC Medical Genetics, 2008, v. 9, p. 108, doi. 10.1186/1471-2350-9-108
- Publication type:
- Article
Genomic NGFB variation and multiple sclerosis in a case control study.
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- BMC Medical Genetics, 2008, v. 9, p. 107, doi. 10.1186/1471-2350-9-107
- Publication type:
- Article
TCF7L2 variant genotypes and type 2 diabetes risk in Brazil: significant association, but not a significant tool for risk stratification in the general population.
- Published in:
- BMC Medical Genetics, 2008, v. 9, p. 106, doi. 10.1186/1471-2350-9-106
- Publication type:
- Article
Assessment of the feasibility of exon 45-55 multiexon skipping for duchenne muscular dystrophy.
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- BMC Medical Genetics, 2008, v. 9, p. 105, doi. 10.1186/1471-2350-9-105
- Publication type:
- Article
Human genetic selection on the MTHFR 677C>T polymorphism.
- Published in:
- BMC Medical Genetics, 2008, v. 9, p. 104, doi. 10.1186/1471-2350-9-104
- Publication type:
- Article
QTLs of factors of the metabolic syndrome and echocardiographic phenotypes: the hypertension genetic epidemiology network study.
- Published in:
- BMC Medical Genetics, 2008, v. 9, p. 103, doi. 10.1186/1471-2350-9-103
- Publication type:
- Article
A novel insertion mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene underlies Grebe-type chondrodysplasia in a consanguineous Pakistani family.
- Published in:
- BMC Medical Genetics, 2008, v. 9, p. 102, doi. 10.1186/1471-2350-9-102
- Publication type:
- Article
Broad phenotypic spectrum in familial adenomatous polyposis; from early onset and severe phenotypes to late onset of attenuated polyposis with the first manifestation at age 72.
- Published in:
- BMC Medical Genetics, 2008, v. 9, p. 101, doi. 10.1186/1471-2350-9-101
- Publication type:
- Article
SIRT1 genetic variants associate with the metabolic response of Caucasians to a controlled lifestyle intervention--the TULIP Study.
- Published in:
- BMC Medical Genetics, 2008, v. 9, p. 100, doi. 10.1186/1471-2350-9-100
- Publication type:
- Article
A novel HSF4 gene mutation (p.R405X) causing autosomal recessive congenital cataracts in a large consanguineous family from Pakistan.
- Published in:
- BMC Medical Genetics, 2008, v. 9, p. 99, doi. 10.1186/1471-2350-9-99
- Publication type:
- Article
Birth weight and blood lipid levels in Spanish adolescents: Influence of selected APOE, APOC3 and PPARgamma2 gene polymorphisms. The AVENA Study.
- Published in:
- BMC Medical Genetics, 2008, v. 9, p. 98, doi. 10.1186/1471-2350-9-98
- Publication type:
- Article
Non-synonymous sequence variants within the oxygen-dependent degradation domain of the HIF1A gene are not associated with pre-eclampsia in the Finnish population.
- Published in:
- BMC Medical Genetics, 2008, v. 9, p. 96, doi. 10.1186/1471-2350-9-96
- Publication type:
- Article
Adverse events in families with hypertrophic or dilated cardiomyopathy and mutations in the MYBPC3 gene.
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- BMC Medical Genetics, 2008, v. 9, p. 95, doi. 10.1186/1471-2350-9-95
- Publication type:
- Article
Significant association of SREBP-2 genetic polymorphisms with avascular necrosis in the Korean population.
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- BMC Medical Genetics, 2008, v. 9, p. 94, doi. 10.1186/1471-2350-9-94
- Publication type:
- Article
Multiple interactions between the alpha<sub>2C</sub>- and beta<sub>1</sub>-adrenergic receptors influence heart failure survival.
- Published in:
- BMC Medical Genetics, 2008, v. 9, p. 93, doi. 10.1186/1471-2350-9-93
- Publication type:
- Article
Extending the spectrum of Ellis van Creveld syndrome: a large family with a mild mutation in the EVC gene.
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- BMC Medical Genetics, 2008, v. 9, p. 92, doi. 10.1186/1471-2350-9-92
- Publication type:
- Article
Lack of association between the CALM1 core promoter polymorphism (-16C/T) and susceptibility to knee osteoarthritis in a Chinese Han population.
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- BMC Medical Genetics, 2008, v. 9, p. 91, doi. 10.1186/1471-2350-9-91
- Publication type:
- Article
Diabetes-specific genetic effects on obesity traits in American Indian populations: the Strong Heart Family Study.
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- BMC Medical Genetics, 2008, v. 9, p. 90, doi. 10.1186/1471-2350-9-90
- Publication type:
- Article
Association analyses of the interaction between the ADSS and ATMgenes with schizophrenia in a Chinese population.
- Published in:
- BMC Medical Genetics, 2008, v. 9, p. 119, doi. 10.1186/1471-2350-9-119
- Publication type:
- Article
Lack of association between PKLR rs3020781 and NOS1APrs7538490 and type 2 diabetes, overweight, obesity and relatedmetabolic phenotypes in a Danish large-scale study: case-controlstudies and analyses of quantitative traits.
- Published in:
- BMC Medical Genetics, 2008, v. 9, p. 118, doi. 10.1186/1471-2350-9-118
- Publication type:
- Article
INSIG2 gene polymorphism is associated with increasedsubcutaneous fat in women and poor response to resistancetraining in men.
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- BMC Medical Genetics, 2008, v. 9, p. 117, doi. 10.1186/1471-2350-9-117
- Publication type:
- Article
Prevalence of variations in melanoma susceptibility genes among Slovenian melanoma families.
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- BMC Medical Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2350-9-86
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- Article
Common variants of the TCF7L2 gene are associated with increased risk of type 2 diabetes mellitus in a UK-resident South Asian population.
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- BMC Medical Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2350-9-8
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- Article
Polymorphisms in the interleukin-10 gene cluster are possiblyinvolved in the increased risk for major depressive disorder.
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- BMC Medical Genetics, 2008, v. 9, p. 111, doi. 10.1186/1471-2350-9-111
- Publication type:
- Article
Functional analysis of the novel TBX5 c.1333delC mutation resulting in an extended TBX5 protein.
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- BMC Medical Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2350-9-88
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- Publication type:
- Article
Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2 mutations.
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- BMC Medical Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2350-9-87
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- Article
'Fat mass and obesity associated' gene (FTO): No significant association of variant rs9939609 with weight loss in a lifestyle intervention and lipid metabolism markers in German obese children and adolescents.
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- BMC Medical Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2350-9-85
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- Publication type:
- Article
Association between variations in the TLR4 gene and incident type 2 diabetes is modified by the ratio of total cholesterol to HDL-cholesterol.
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- BMC Medical Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2350-9-9
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- Publication type:
- Article
French database of children and adolescents with Prader-Willi syndrome.
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- BMC Medical Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2350-9-89
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- Publication type:
- Article
Five recurrent BRCA1/2 mutations are responsible for cancer predisposition in the majority of Slovenian breast cancer families.
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- BMC Medical Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2350-9-83
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- Publication type:
- Article
Lack of evidence for association of primary sclerosing cholangitis and primary biliary cirrhosis with risk alleles for Crohn's disease in Polish patients.
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- BMC Medical Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2350-9-81
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- Publication type:
- Article
Association of ADAM33 gene polymorphisms with adult allergic asthma and rhinitis in a Chinese Han population.
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- BMC Medical Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2350-9-82
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- Publication type:
- Article
TCF7L2 gene polymorphisms do not predict susceptibility to diabetes in tropical calcific pancreatitis but may interact with SPINK1 and CTSB mutations in predicting diabetes.
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- BMC Medical Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2350-9-80
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- Article
The APOA5 Trp19 allele is associated with metabolic syndrome via its association with plasma triglycerides.
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- BMC Medical Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2350-9-84
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- Publication type:
- Article
Association of narcolepsy-cataplexy with HLA-DRB1 and DQB1 in Mexican patients: A relationship between HLA and gender is suggested.
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- BMC Medical Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2350-9-79
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- Publication type:
- Article
Methionine synthase A2756G polymorphism may predict ulcerative colitis and methylenetetrahydrofolate reductase C677T pancolitis, in Central China.
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- BMC Medical Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2350-9-78
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- Article
Linkage study of fibrinogen levels: the Strong Heart Family Study.
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- BMC Medical Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2350-9-77
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- Publication type:
- Article
Lack of association between serotonin transporter gene polymorphism 5-HTTLPR and smoking among Polish population: a case-control study.
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- BMC Medical Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2350-9-76
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- Article
Mutation study of Spanish patients with Hereditary Hemorrhagic Telangiectasia.
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- BMC Medical Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2350-9-75
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- Article
R497K polymorphism in epidermal growth factor receptor gene is associated with the risk of acute coronary syndrome.
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- BMC Medical Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2350-9-74
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- Article
The value of some Corsican sub-populations for genetic association studies.
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- BMC Medical Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2350-9-73
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- Article