Results 211 to 220 of about 14,367 (319)
Robust causal inference for point exposures with missing confounders
Abstract Large observational databases are often subject to missing data. As such, methods for causal inference must simultaneously handle confounding and missingness; surprisingly little work has been done at this intersection. Motivated by this, we propose an efficient and robust estimator of the causal average treatment effect from cohort studies ...
Alexander W. Levis+3 more
wiley +1 more source
Abstract Cardiovascular disease is a leading complication after both liver and kidney transplantation. Factors associated with and rates of cardiovascular events (CVEs) after simultaneous liver–kidney transplant (SLKT) are unknown. This was a retrospective cohort study of adult SLKT recipients between 2002 and 2017 at six centers in six United Network ...
Jennifer Jo+19 more
wiley +1 more source
Secreto profesional y confidencialidad en la prestación de servicios de salud sexual y reproductiva [PDF]
Leonel Briozzo
openalex +1 more source
Salud sexual y reproductiva en la adolescencia
Pregnancy during adolescence period is a social and health problem. It has decreased over the years due to different prevention measures, such as access to reliable methods of contraception. Currently, the main cause of early pregnancy amongst adolescents is not the lack of these methods, as there is a great variety, which is adapted to the different ...
openaire +1 more source
Efficient and model‐agnostic parameter estimation under privacy‐preserving post‐randomization data
Abstract Balancing data privacy with public access is critical for sensitive datasets. However, even after de‐identification, the data are still vulnerable to, for example, inference attacks (by matching some keywords with external datasets). Statistical disclosure control (SDC) methods offer additional protection, and the post‐randomization method ...
Qinglong Tian, Jiwei Zhao
wiley +1 more source
de novo variant calling identifies cancer mutation signatures in the 1000 Genomes Project
Abstract Detection of de novo variants (DNVs) is critical for studies of disease‐related variation and mutation rates. To accelerate DNV calling, we developed a graphics processing units‐based workflow. We applied our workflow to whole‐genome sequencing data from three parent‐child sequenced cohorts including the Simons Simplex Collection (SSC), Simons
Jeffrey K. Ng+16 more
wiley +1 more source
Rare surfactant‐related variants in familial and sporadic pulmonary fibrosis
Abstract The role of constitutional genetic defects in idiopathic pulmonary fibrosis (IPF) is increasingly appreciated. Monogenic disorders associated with IPF affect two pathways: telomere maintenance, accounting for approximately 10% of all patients with IPF, and surfactant biology, responsible for 1%–3% of cases and often co‐occurring with lung ...
Rachel M. Sutton+10 more
wiley +1 more source
Imágenes de la mujer en la Política Nacional de Salud Sexual y Reproductiva de Colombia, 2003 – 2006 [PDF]
Claudia Milena Noguera Vargas
openalex +1 more source
El sistema de salud en Honduras ante la diversidad sexual
Pavlova María Polanco Alvarenga +1 more
doaj +1 more source
Tailoring pharmacogenomic (PGx) implementation to diverse populations is vital to promoting health equity. We assessed prescriptions for medications with potentially actionable PGx information to identify patient characteristics associated with differential PGx medication exposure.
Loren Saulsberry+5 more
wiley +1 more source