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Interactions between the adducin 2 gene and antihypertensive drug therapies in determining blood pressure in people with hypertension.
- Published in:
- BMC Medical Genetics, 2007, v. 8, p. 61, doi. 10.1186/1471-2350-8-61
- Publication type:
- Article
Previously described sequence variant in CDK5RAP2 gene in a Pakistani family with autosomal recessive primary microcephaly.
- Published in:
- BMC Medical Genetics, 2007, v. 8, p. 58, doi. 10.1186/1471-2350-8-58
- Publication type:
- Article
The TCF7L2 locus and type 1 diabetes.
- Published in:
- BMC Medical Genetics, 2007, v. 8, p. 51, doi. 10.1186/1471-2350-8-51
- Publication type:
- Article
Resequencing PNMT in European hypertensive and normotensive individuals: no common susceptibilily variants for hypertension and purifying selection on intron 1.
- Published in:
- BMC Medical Genetics, 2007, v. 8, p. 47, doi. 10.1186/1471-2350-8-47
- Publication type:
- Article
Mechanistic role of a disease-associated genetic variant within the ADAM33 asthma susceptibility gene.
- Published in:
- BMC Medical Genetics, 2007, v. 8, p. 46, doi. 10.1186/1471-2350-8-46
- Publication type:
- Article
Multiplex SNaPshot for detection of BRCA1/2 common mutations in Spanish and Spanish related breast/ovarian cancer families.
- Published in:
- BMC Medical Genetics, 2007, v. 8, p. 40, doi. 10.1186/1471-2350-8-40
- Publication type:
- Article
The interactive role of type 2 diabetes mellitus and E-selectin S128R mutation on susceptibility to coronary heart disease.
- Published in:
- BMC Medical Genetics, 2007, v. 8, p. 35, doi. 10.1186/1471-2350-8-35
- Publication type:
- Article
Mutations in the 3'-untranslated region of GATA4 as molecular hotspots for congenital heart disease (CHD).
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- BMC Medical Genetics, 2007, v. 8, p. 38, doi. 10.1186/1471-2350-8-38
- Publication type:
- Article
High occurrence of BRCA1 intragenic rearrangements in hereditary breast and ovarian cancer syndrome in the Czech Republic.
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- BMC Medical Genetics, 2007, v. 8, p. 32, doi. 10.1186/1471-2350-8-32
- Publication type:
- Article
MRX87 family with Aristaless X dup24bp mutation and implication for polyAlanine expansions.
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- BMC Medical Genetics, 2007, v. 8, p. 25, doi. 10.1186/1471-2350-8-25
- Publication type:
- Article
Large genomic rearrangements in the CFTR gene contribute to CBAVD.
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- BMC Medical Genetics, 2007, v. 8, p. 22, doi. 10.1186/1471-2350-8-22
- Publication type:
- Article
Analysis of sequence variations in the suppressor of cytokine signaling (SOCS)-3 gene in extremely obese children and adolescents.
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- BMC Medical Genetics, 2007, v. 8, p. 21, doi. 10.1186/1471-2350-8-21
- Publication type:
- Article
Two novel missense mutations in the myostatin gene identified in Japanese patients with Duchenne muscular dystrophy.
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- BMC Medical Genetics, 2007, v. 8, p. 19, doi. 10.1186/1471-2350-8-19
- Publication type:
- Article
Novel APC mutations in Czech and Slovak FAP families: clinical and genetic aspects.
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- BMC Medical Genetics, 2007, v. 8, p. 16, doi. 10.1186/1471-2350-8-16
- Publication type:
- Article
Respiratory symptoms among infants at risk for asthma: association with surfactant protein A haplotypes.
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- BMC Medical Genetics, 2007, v. 8, p. 15, doi. 10.1186/1471-2350-8-15
- Publication type:
- Article
Incorporating medical interventions into carrier probability estimation for genetic counseling.
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- BMC Medical Genetics, 2007, v. 8, p. 13, doi. 10.1186/1471-2350-8-13
- Publication type:
- Article
Matrix Metalloproteinase-9 (MMP-9) polymorphisms in patients with cutaneous malignant melanoma.
- Published in:
- BMC Medical Genetics, 2007, v. 8, p. 10, doi. 10.1186/1471-2350-8-10
- Publication type:
- Article
Detection of subtelomere imbalance using MLPA: validation, development of an analysis protocol, and application in a diagnostic centre.
- Published in:
- BMC Medical Genetics, 2007, v. 8, p. 9, doi. 10.1186/1471-2350-8-9
- Publication type:
- Article
SOD2 polymorphisms: unmasking the effect of polymorphism on splicing.
- Published in:
- BMC Medical Genetics, 2007, v. 8, p. 7, doi. 10.1186/1471-2350-8-7
- Publication type:
- Article
Effective quantitative real-time polymerase chain reaction analysis of the parkin gene (PARK2) exon 1-12 dosage.
- Published in:
- BMC Medical Genetics, 2007, v. 8, p. 6, doi. 10.1186/1471-2350-8-6
- Publication type:
- Article
The intron 4c allele of the NOS3 gene is associated with ischemicstroke in African Americans.
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- BMC Medical Genetics, 2007, v. 8, p. 76, doi. 10.1186/1471-2350-8-76
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- Article
CD209 in inflammatory bowel disease: a case-control study in theSpanish population.
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- BMC Medical Genetics, 2007, v. 8, p. 75, doi. 10.1186/1471-2350-8-75
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- Article
Association of autism with polymorphisms in the paired-likehomeodomain transcription factor 1 (PITX1) on chromosome 5q31:a candidate gene analysis.
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- BMC Medical Genetics, 2007, v. 8, p. 74, doi. 10.1186/1471-2350-8-74
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- Article
Impact of estrogen receptor gene polymorphisms and mRNA levelson obesity and lipolysis -a- cohort study.
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- BMC Medical Genetics, 2007, v. 8, p. 73, doi. 10.1186/1471-2350-8-73
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- Publication type:
- Article
Resequencing of genes for transforming growth factor β1 (TGFB1) type 1 and 2 receptors (TGFBR1, TGFBR2), and association analysis of variants with diabetic nephropathy.
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- BMC Medical Genetics, 2007, v. 8, p. 5, doi. 10.1186/1471-2350-8-5
- Publication type:
- Article
A comprehensive analysis of common genetic variation in prolactin(PRL) and PRL receptor (PRLR) genes in relation to plasmaprolactin levels and breast cancer risk: the Multiethnic Cohort.
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- BMC Medical Genetics, 2007, v. 8, p. 72, doi. 10.1186/1471-2350-8-72
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- Publication type:
- Article
Functional analysis of splicing mutations in exon 7 of NF1 gene.
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- BMC Medical Genetics, 2007, v. 8, p. 4, doi. 10.1186/1471-2350-8-4
- Publication type:
- Article
MRPS18CP2 alleles and DEFA3 absence as putative chromosome 8p23.1 modifiers of hearing loss due to mtDNA mutation A1555G in the 12S rRNA gene.
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- BMC Medical Genetics, 2007, v. 8, p. 81, doi. 10.1186/1471-2350-8-81
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- Publication type:
- Article
No evidence for association between tau gene haplotypic variants and susceptibility to Creutzfeldt-Jakob disease.
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- BMC Medical Genetics, 2007, v. 8, p. 77, doi. 10.1186/1471-2350-8-77
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- Article
Single nucleotide polymorphisms in bone turnover-related genes in Koreans: ethnic differences in linkage disequilibrium and haplotype.
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- BMC Medical Genetics, 2007, v. 8, p. 70, doi. 10.1186/1471-2350-8-70
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- Article
Missense mutations in Desmocollin-2 N-terminus, associated with arrhythmogenic right ventricular cardiomyopathy, affect intracellular localization of desmocollin-2 in vitro.
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- BMC Medical Genetics, 2007, v. 8, p. 65, doi. 10.1186/1471-2350-8-65
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- Article
A novel RUNX2 missense mutation predicted to disrupt DNAbinding causes cleidocranial dysplasia in a large Chinese family withhyperplastic nails.
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- BMC Medical Genetics, 2007, v. 8, p. 82, doi. 10.1186/1471-2350-8-82
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- Article
Association between the -455T>C promoter polymorphism of theAPOC3 gene and the metabolic syndrome in a multi-ethnic sample.
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- BMC Medical Genetics, 2007, v. 8, p. 80, doi. 10.1186/1471-2350-8-80
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- Article
Sphingomyelin phosphodiesterase-1 (SMPD1) coding variants donot contribute to low levels of high-density lipoprotein cholesterol.
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- BMC Medical Genetics, 2007, v. 8, p. 79, doi. 10.1186/1471-2350-8-79
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- Article
Synpolydactyly and HOXD13 polyalanine repeat: addition of 2alanine residues is without clinical consequences.
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- BMC Medical Genetics, 2007, v. 8, p. 78, doi. 10.1186/1471-2350-8-78
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- Article
Framingham Heart Study genome-wide association: results for pulmonary function measures.
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- BMC Medical Genetics, 2007, v. 8, p. S8, doi. 10.1186/1471-2350-8-S1-S8
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- Article
Genome-wide association with bone mass and geometry in the Framingham Heart Study.
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- BMC Medical Genetics, 2007, v. 8, p. S14, doi. 10.1186/1471-2350-8-S1-S14
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- Article
CADASIL in Arabs: clinical and genetic findings.
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- BMC Medical Genetics, 2007, v. 8, p. 67, doi. 10.1186/1471-2350-8-67
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- Article
The candidate genes TAF5L, TCF7, PDCD1, IL6 and ICAM1 cannot beexcluded from having effects in type 1 diabetes.
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- BMC Medical Genetics, 2007, v. 8, p. 71, doi. 10.1186/1471-2350-8-71
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- Article
Prevalence of H63D, S65C and C282Y hereditary hemochromatosisgene mutations in Slovenian population by an improvedhigh-throughput genotyping assay.
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- BMC Medical Genetics, 2007, v. 8, p. 69, doi. 10.1186/1471-2350-8-69
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- Article
Genome-wide association of sleep and circadian phenotypes.
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- BMC Medical Genetics, 2007, v. 8, p. S9, doi. 10.1186/1471-2350-8-S1-S9
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- Article
Mutation analysis of the NSD1 gene in patients with autismspectrum disorders and macrocephaly.
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- BMC Medical Genetics, 2007, v. 8, p. 68, doi. 10.1186/1471-2350-8-68
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- Article
Metabolic phenotype of methylmalonic acidemia in mice andhumans: the role of skeletal muscle.
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- BMC Medical Genetics, 2007, v. 8, p. 64, doi. 10.1186/1471-2350-8-64
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- Article
Exploring the functional role of the CHRM2 gene in humancognition: results from a dense genotyping and brain expressionstudy.
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- BMC Medical Genetics, 2007, v. 8, p. 66, doi. 10.1186/1471-2350-8-66
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- Publication type:
- Article
Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham study.
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- BMC Medical Genetics, 2007, v. 8, p. S15, doi. 10.1186/1471-2350-8-S1-S15
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- Article
The Framingham Heart Study, on its way to becoming the goldstandard for Cardiovascular Genetic Epidemiology?
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- BMC Medical Genetics, 2007, v. 8, p. 63, doi. 10.1186/1471-2350-8-63
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- Article
The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports.
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- BMC Medical Genetics, 2007, v. 8, p. S1, doi. 10.1186/1471-2350-8-S1-S1
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- Publication type:
- Article
Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study.
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- BMC Medical Genetics, 2007, v. 8, p. S7, doi. 10.1186/1471-2350-8-S1-S7
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- Publication type:
- Article
Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes.
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- BMC Medical Genetics, 2007, v. 8, p. S5, doi. 10.1186/1471-2350-8-S1-S5
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- Publication type:
- Article
A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study.
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- BMC Medical Genetics, 2007, v. 8, p. S6, doi. 10.1186/1471-2350-8-S1-S6
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- Article