Ally, M

Kamuzora, P

Mills, A

Mtei, G

Mulligan, J

Palmer, N

English

LSHTM Research Online

A genome-wide association study for diabetic nephropathy genes in African Americans. Kidney Int.

A genome-wide association study identifies novel risk loci for type 2 diabetes.

A genomewide association study of type 2 diabetes in Finns detects multiple susceptibility variants.

A new member of the Rho family, Rnd1, promotes disassembly of actin filament structures and loss of cell adhesion.

A second generation human haplotype map of over 3.1 million SNPs.

A variant in CDKAL1 influences insulin response and risk of type 2 diabetes.

A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk.

Advanced glycosylation end products induced tissue factor expression in human monocytelike U937 cells and increased tissue factor expression in monocytes from diabetic patients.

Association analysis in african americans of European-derived type 2 diabetes single nucleotide polymorphisms from whole-genome association studies.

Combining probability from independent tests: the weighted Z-method is superior to Fisher’s approach.

Common variant in MTNR1B associated with increased risk of type 2 diabetes and impaired early insulin secretion.

Common variants in WFS1 confer risk of type 2 diabetes.

diabetes: new genes, new understanding.

Estimation of individual admixture: analytical and study design considerations.

Evaluation of common variants in the six known maturity-onset diabetes of the young (MODY) genes for association with type 2 diabetes.

Exploration of the utility of ancestry informative markers for genetic association studies of African Americans with type 2 diabetes and end stage renal disease.

Genetic epidemiology of insulin resistance and visceral adiposity. The IRAS Family Study design and methods.

Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia.

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.

Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.

Genotypeimputation accuracy across worldwide human populations.

Global prevalence of diabetes: estimates for the year 2000 and projections for 2030. Diabetes Care

Identification of a novel human Rho protein with unusual properties: GTPase deficiency and in vivo farnesylation.

Identification of Barx2b, a serum response factor-associated homeodomain protein.

Largescale association studies of variants in genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that the KCNJ11 E23K variant is associated with type 2 diabetes.

Meta-analysis of genome-wide association data and large-scale replication

Multipoint quantitative-trait linkage analysis in general pedigrees.

MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis.

MYH9 is associated with nondiabetic end-stage renal disease in African Americans.

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.

Newly identified loci that influence lipid concentrations and risk of coronary artery disease.

Nonmuscle myosin heavy chain 9 gene MYH9 associations in African Americans with clinically diagnosed type 2 diabetes mellitus-associated ESRD.

PedCheck: a program for identification of genotype incompatibilities in linkage analysis.

Polymorphisms in the non-muscle myosin heavy chain 9 gene (MYH9) are strongly associated with end-stage renal disease historically attributed to hypertension in African Americans.

Population genomics of human gene expression.

Prevalence of diabetes and impaired fasting glucose in adults in the U.S. population: National Health And Nutrition Examination Survey 1999–2002.

Quantitative trait analysis of type 2 diabetes susceptibility loci identified from whole genome association studies in the Insulin Resistance Atherosclerosis Family Study.

Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes.

SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations.

Soluble CD40 ligand, soluble P-selectin, interleukin-6, and tissue factor in diabetes mellitus: relationships to cardiovascular disease and risk factor intervention.

The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes.

The effect of multifactorial intervention on plasma von Willebrand factor, soluble E-selectin and tissue factor in diabetes mellitus: implications for atherosclerotic vascular disease.

The Genetical Interpretation of Statistics of the Third Degree in the Study of Quantitative Inheritance.

The homeobox transcription factor Barx2 regulates chondrogenesis during limb development.

The homeodomain protein Barx2 promotes myogenic differentiation and is regulated by myogenic regulatory factors.

The insulin resistance atherosclerosis study (IRAS) objectives, design, and recruitment results.

The new type 2 diabetes gene TCF7L2.

The structure of haplotype blocks in the human genome.

Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.

Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes.

Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus.

Variants in MTNR1B influence fasting glucose levels.

Variants of the transcription factor 7-like 2 (TCF7L2) gene are associated with type 2 diabetes in an African-American population enriched for nephropathy.

An Assessment of the Health Financing System in Tanzania: Implications for Equity and Social Health Insurance: Report on Shield Work Package 1

http://researchonline.lshtm.ac.uk/4877/1/AN%20ASSESSMENT%20OF%20THE%20HEALTH%20FINANCING%20SYSTEM%20IN%20TANZANIA%20IMPLICATIONS%20FOR%20EQUITY%20AND%20SOCIAL%20HEALTH%20INSURANCE.pdf

An Assessment of the Health Financing System in Tanzania: Implications for Equity and Social Health Insurance: Report on Shield Work Package 1

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