Current Management of Neurological Wilson's Disease. [PDF]
Ganaraja VH, Holla VV, Pal PK.
europepmc +1 more source
ABSTRACT The present study develops a finite element‐based numerical method for simulation of frictional rotational sliding induced damage and heating effects on rock. The method is applied to the Sievers’ J‐ miniature drill test, which is widely used for estimating the rock drillability and predicting the cutter life.
Timo Saksala+8 more
wiley +1 more source
Bioinformatic Analysis of Autism-Related miRNAs and Their PoTential as Biomarkers for Autism Epigenetic Inheritance. [PDF]
Acerbi da Silva LN, Stumpp T.
europepmc +1 more source
Knowledge Gradient Procedure to Select the Best System Under Pairwise Comparisons
ABSTRACT This article considers fixed‐budget ranking and selection (R&S) problems where the performance of alternative designs can only be assessed through pairwise comparisons, a setting encountered in many applications, including player ranking in games, sports tournaments, recommender systems, image‐based search, public choice models such as voting ...
Dongyang Li+4 more
wiley +1 more source
Advances in Cardiac Imaging and Genetic Testing for Diagnosis and Risk Stratification in Cardiomyopathies: 2024 Update. [PDF]
Gasior T.
europepmc +1 more source
Med Research: Building Interdisciplinary Bridges and Leading Global Medical Innovation
Med Research, EarlyView.
Quan Cheng+5 more
wiley +1 more source
An Exact Algorithm for the Hazardous Orienteering Problem
ABSTRACT The hazardous orienteering problem is the topic of this study. It is a variant of the well‐studied orienteering problem, where a vehicle, given a maximum mission time, has to select and visit customers out of a set of requests, aiming at maximizing the total profit associated with the customers selected. In the hazardous version of the problem
Roberto Montemanni, Derek H. Smith
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PNL: a software to build polygenic risk scores using a super learner approach based on PairNet, a Convolutional Neural Network. [PDF]
Chen TH+4 more
europepmc +1 more source
Abstract Variants in the CNGB3 gene, encoding the B3‐subunit of the cone photoreceptor cyclic nucleotide gated channel, are a major cause of autosomal recessive achromatopsia, a rare inherited retinal disease. The mutation spectrum of achromatopsia‐associated CNGB3 variants comprises all types of mutations, including those that are straightforward to ...
Katharina Rawnsley+3 more
wiley +1 more source
Identification of intragenic variants in pediatric patients with intellectual disability in Peru. [PDF]
Abarca-Barriga HH+4 more
europepmc +1 more source