Search Results - "Murray, J. C."
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1
Global burden of depressive disorders in the year 2000
Published in British journal of psychiatry (01-05-2004)“…The initial Global Burden of Disease study found that depression was the fourth leading cause of disease burden, accounting for 3.7% of total disability…”
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2
Gene/environment causes of cleft lip and/or palate
Published in Clinical genetics (01-04-2002)“…Craniofacial anomalies, and in particular cleft lip and palate, are major human birth defects with a worldwide frequency of 1 in 700 and substantial clinical…”
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3
Folic acid and orofacial clefts: a review of the evidence
Published in Oral diseases (01-01-2010)“…Orofacial clefts are common and burdensome birth defects with a complex genetic and environmental etiology. The contribution of nutritional factors and…”
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4
PI(3) kinase is associated with a mechanism of immunoresistance in breast and prostate cancer
Published in Oncogene (15-01-2009)“…Immune escape describes a critical event whereby tumor cells adopt an immunoresistant phenotype to escape adaptive surveillance. We show that expression of a…”
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5
Evaluating rare coding variants as contributing causes to non-syndromic cleft lip and palate
Published in Clinical genetics (01-11-2013)“…Rare coding variants are a current focus in studies of complex disease. Previously, at least 68 rare coding variants were reported from candidate gene…”
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6
A framework for assessing the performance of health systems: Health Systems
Published in Bulletin of the World Health Organization (01-06-2000)“…Health systems vary widely in performance, and countries with similar levels of income, education and health expenditure differ in their ability to attain key…”
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7
Confirming genes influencing risk to cleft lip with/without cleft palate in a case–parent trio study
Published in Human genetics (01-07-2013)“…A collection of 1,108 case–parent trios ascertained through an isolated, nonsyndromic cleft lip with or without cleft palate (CL/P) was used to replicate the…”
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8
Clinical findings in patients with GLI2 mutations - phenotypic variability
Published in Clinical genetics (01-01-2012)“…Bertolacini CDP, Ribeiro‐Bicudo LA, Petrin A, Richieri‐Costa A, Murray JC. Clinical findings in patients with GLI2 mutations – phenotypic variability…”
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Risk of pre‐eclampsia in patients with a maternal genetic predisposition to common medical conditions: a case–control study
Published in BJOG : an international journal of obstetrics and gynaecology (01-01-2021)“…Objective To assess whether women with a genetic predisposition to medical conditions known to increase pre‐eclampsia risk have an increased risk of…”
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10
Peptide Templates for Nanoparticle Synthesis Derived from Polymerase Chain Reaction-Driven Phage Display
Published in Advanced functional materials (01-01-2004)“…Phage peptide display libraries are commonly used to select peptides that bind to inorganic surfaces (metals, metal oxides, and semiconductors). These binding…”
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11
MSX1, PAX9, and TGFA Contribute to Tooth Agenesis in Humans
Published in Journal of dental research (01-09-2004)“…In this study, we sought to determine the association between tooth agenesis and DNA sequence variation in the genes MSX1 and PAX9 in an ethnically diverse…”
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12
Armed conflict as a public health problem
Published in BMJ (09-02-2002)“…Given the necessary caveats about the accuracy of epidemiological assessment table 2 puts the potential size of mortality directly related to conflict in…”
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13
Synthetic lethal screening reveals FGFR as one of the combinatorial targets to overcome resistance to Met-targeted therapy
Published in Oncogene (26-02-2015)“…Met is a receptor tyrosine kinase that promotes cancer progression. In addition, Met has been implicated in resistance of tumors to various targeted therapies…”
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14
The effect of malaria control on Plasmodium falciparum in Africa between 2000 and 2015
Published in Nature (London) (08-10-2015)“…Since the year 2000, a concerted campaign against malaria has led to unprecedented levels of intervention coverage across sub-Saharan Africa. Understanding the…”
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15
A novel mutation in the PHF8 gene is associated with X-linked mental retardation with cleft lip/cleft palate
Published in Clinical genetics (01-07-2007)“…Recently, two truncating mutations in the PHF8 (plant homeodomain finger protein 8) gene have been found to cause X‐linked mental retardation associated with…”
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16
DNA methylation differences in monozygotic twins with Van der Woude syndrome
Published in Frontiers in dental medicine (2023)“…Van der Woude Syndrome (VWS) is an autosomal dominant disorder responsible for 2% of all syndromic orofacial clefts (OFCs) with being the primary causal gene…”
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17
Global Burden of Untreated Caries: A Systematic Review and Metaregression
Published in Journal of Dental Research (01-05-2015)“…We aimed to consolidate all epidemiologic data about untreated caries and subsequently generate internally consistent prevalence and incidence estimates for…”
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18
Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate
Published in Journal of medical genetics (01-06-2003)“…MSX1 has been proposed as a gene in which mutations may contribute to non-syndromic forms of cleft lip and/or cleft palate. Support for this comes from human…”
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19
Quantifying the burden of disease: the technical basis for disability-adjusted life years
Published in Bulletin of the World Health Organization (01-05-1994)“…Detailed assumptions used in constructing a new indicator of the burden of disease, the disability-adjusted life year (DALY), are presented. Four key social…”
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Measuring Quality of Health Care from the User's Perspective in 41 Countries: Psychometric Properties of WHO's Questions on Health Systems Responsiveness
Published in Quality of life research (01-09-2007)“…Objective To evaluate, for different populations, psychometric properties of questions on "health systems responsiveness", a concept developed by World Health…”
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