Pages that link to "Q28039310"
Jump to navigation
Jump to search
The following pages link to Thomas Meitinger (Q28039310):
Displaying 50 items.
- Lifelong reduction of LDL-cholesterol related to a common variant in the LDL-receptor gene decreases the risk of coronary artery disease--a Mendelian Randomisation study (Q21090089) (← links)
- Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations (Q21092458) (← links)
- Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution (Q21092459) (← links)
- Mitochondrial genetic variants identified to be associated with BMI in adults (Q21131961) (← links)
- Genetic structure of Europeans: a view from the North-East (Q21143785) (← links)
- Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum (Q21145030) (← links)
- Discovery of sexual dimorphisms in metabolic and genetic biomarkers (Q21563382) (← links)
- The association of a SNP upstream of INSIG2 with body mass index is reproduced in several but not all cohorts (Q21563458) (← links)
- The DNA sequence of the human X chromosome (Q21735931) (← links)
- The retinitis pigmentosa GTPase regulator, RPGR, interacts with the delta subunit of rod cyclic GMP phosphodiesterase (Q22001446) (← links)
- Analysis of the human GDNF gene reveals an inducible promoter, three exons, a triplet repeat within the 3'-UTR and alternative splice products (Q22007985) (← links)
- Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein (Q22008011) (← links)
- Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis (Q22253273) (← links)
- Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy (Q24288778) (← links)
- Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance (Q24294967) (← links)
- The Parkinson disease causing LRRK2 mutation I2020T is associated with increased kinase activity (Q24297634) (← links)
- Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial disease (Q24308200) (← links)
- A gene (SRPX) encoding a sushi-repeat-containing protein is deleted in patients with X-linked retinitis pigmentosa (Q24312152) (← links)
- An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness (Q24315182) (← links)
- Mutations in FBXL4, encoding a mitochondrial protein, cause early-onset mitochondrial encephalomyopathy (Q24321305) (← links)
- Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia (Q24323876) (← links)
- Molecular modelling of the Norrie disease protein predicts a cystine knot growth factor tertiary structure (Q24337005) (← links)
- Analysis of a terminal Xp22.3 deletion in a patient with six monogenic disorders: implications for the mapping of X linked ocular albinism (Q24514987) (← links)
- Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language (Q24538957) (← links)
- Genes predict village of origin in rural Europe (Q24597340) (← links)
- Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (Q24609915) (← links)
- Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data (Q24612121) (← links)
- Biological, clinical and population relevance of 95 loci for blood lipids (Q24622541) (← links)
- Genome-wide association analysis identifies multiple loci related to resting heart rate (Q24624928) (← links)
- Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk (Q24630394) (← links)
- Hundreds of variants clustered in genomic loci and biological pathways affect human height (Q24630979) (← links)
- Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia (Q24631992) (← links)
- A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease (Q24633417) (← links)
- Common variants near MC4R are associated with fat mass, weight and risk of obesity (Q24641880) (← links)
- Natriuretic peptide system gene variants are associated with ventricular dysfunction after coronary artery bypass grafting (Q24644704) (← links)
- Six new loci associated with body mass index highlight a neuronal influence on body weight regulation (Q24646434) (← links)
- Narcolepsy is strongly associated with the T-cell receptor alpha locus (Q24649513) (← links)
- A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project (Q24653943) (← links)
- Genomewide association analysis of coronary artery disease (Q24658344) (← links)
- Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosis (Q24678616) (← links)
- Integrative analysis of the mitochondrial proteome in yeast (Q24793149) (← links)
- Systematic mutation analysis of KIAA0767 and KIAA1646 in chromosome 22q-linked periodic catatonia (Q24812307) (← links)
- MitoP2: the mitochondrial proteome database--now including mouse data (Q25256675) (← links)
- Impairment of Drosophila orthologs of the human orphan protein C19orf12 induces bang sensitivity and neurodegeneration (Q27320817) (← links)
- MTO1-deficient mouse model mirrors the human phenotype showing complex I defect and cardiomyopathy (Q27320993) (← links)
- TRMT5 Mutations Cause a Defect in Post-transcriptional Modification of Mitochondrial tRNA Associated with Multiple Respiratory-Chain Deficiencies (Q28115863) (← links)
- Molecular cloning of a novel human UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase, GalNAc-T8, and analysis as a candidate autosomal dominant hypophosphatemic rickets (ADHR) gene (Q28117021) (← links)
- Sudden Cardiac Death Due to Deficiency of the Mitochondrial Inorganic Pyrophosphatase PPA2 (Q28118605) (← links)
- Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology (Q28131833) (← links)
- The autosomal dominant hypophosphatemic rickets (ADHR) gene is a secreted polypeptide overexpressed by tumors that cause phosphate wasting (Q28142759) (← links)