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Tej D. Azad

Researcher at Johns Hopkins University School of Medicine

Publications -  141
Citations -  5723

Tej D. Azad is an academic researcher from Johns Hopkins University School of Medicine. The author has contributed to research in topics: Medicine & Population. The author has an hindex of 28, co-authored 106 publications receiving 3590 citations. Previous affiliations of Tej D. Azad include Washington University in St. Louis & Johns Hopkins University.

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Early Detection of Molecular Residual Disease in Localized Lung Cancer by Circulating Tumor DNA Profiling

TL;DR: This study shows that ctDNA analysis can robustly identify posttreatment MRD in patients with localized lung cancer, identifying residual/recurrent disease earlier than standard-of-care radiologic imaging, and thus could facilitate personalized adjuvant treatment at early time points when disease burden is lowest.
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Estimate of the global volume of surgery in 2012: an assessment supporting improved health outcomes.

TL;DR: Surgical volume is large and continues to grow in all economic environments, yet many low-income countries fail to achieve basic levels of service and a correlation between increased life expectancy and increased surgical rates is noted.
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Relationship Between Cesarean Delivery Rate and Maternal and Neonatal Mortality

TL;DR: A cross-sectional, ecological study estimating annual cesarean delivery rates from data collected during 2005 to 2012 for all 194 WHO member states to estimate the contemporary relationship between national levels of cesAREan delivery and maternal and neonatal mortality.
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Size and distribution of the global volume of surgery in 2012.

TL;DR: Surgical volume is large and growing, with caesarean delivery comprising nearly a third of operations in most resource-poor settings, Nonetheless, there remains disparity in the provision of surgical services globally.
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Integrating genomic features for non-invasive early lung cancer detection

TL;DR: It is shown that, although levels are very low in early-stage lung cancers, ctDNA is present prior to treatment in most patients and its presence is strongly prognostic, and a machine-learning method termed ‘lung cancer likelihood in plasma’ (Lung-CLiP) is developed, which can robustly discriminate early-Stage lung cancer patients from risk-matched controls.