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Dramatic resurgence of malaria after 7 years of intensive vector control interventions in Eastern Uganda.

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Multi-trait Analysis of GWAS for circulating FGF23 Identifies Novel Network Interactions Between HRG-HMGB1 and Cardiac Disease in CKD.

  • Read more about Multi-trait Analysis of GWAS for circulating FGF23 Identifies Novel Network Interactions Between HRG-HMGB1 and Cardiac Disease in CKD.

Selection of artemisinin partial resistance Kelch13 mutations in Uganda in 2016-22 was at a rate comparable to that seen previously in South-East Asia.

  • Read more about Selection of artemisinin partial resistance Kelch13 mutations in Uganda in 2016-22 was at a rate comparable to that seen previously in South-East Asia.

Unveiling the crucial neuronal role of the proteasomal ATPase subunit gene PSMC5 in neurodevelopmental proteasomopathies.

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Risk Factors for Pediatric Critical COVID-19: A Systematic Review and Meta-Analysis.

  • Read more about Risk Factors for Pediatric Critical COVID-19: A Systematic Review and Meta-Analysis.

Interstitial Fibrosis and Arrhythmic Mitral Valve Prolapse: Unravelling Sex-Based Differences.

  • Read more about Interstitial Fibrosis and Arrhythmic Mitral Valve Prolapse: Unravelling Sex-Based Differences.

Unveiling the autoreactome: Proteome-wide immunological fingerprints reveal the promise of plasma cell depleting therapy.

  • Read more about Unveiling the autoreactome: Proteome-wide immunological fingerprints reveal the promise of plasma cell depleting therapy.

Pulmonary microbiome and transcriptome signatures reveal distinct pathobiologic states associated with mortality in two cohorts of pediatric stem cell transplant patients.

  • Read more about Pulmonary microbiome and transcriptome signatures reveal distinct pathobiologic states associated with mortality in two cohorts of pediatric stem cell transplant patients.

Noninvasive molecular subtyping of pediatric low-grade glioma with self-supervised transfer learning.

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Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic disease.

  • Read more about Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic disease.

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