Architectural threats to security and privacy: a challenge for internet of things (IoT) applications

Y Khan, MBM Su'ud, MM Alam, SF Ahmad, NA Salim… - Electronics, 2022 - mdpi.com
The internet of things (IoT) is one of the growing platforms of the current era that has
encircled a large population into its domain, and life appears to be useless without adopting …

Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test

AC Lionel, G Costain, N Monfared, S Walker… - Genetics in …, 2018 - nature.com
Purpose Genetic testing is an integral diagnostic component of pediatric medicine. Standard
of care is often a time-consuming stepwise approach involving chromosomal microarray …

[HTML][HTML] Conceptual framework for precision cancer medicine in Germany: Consensus statement of the Deutsche Krebshilfe working group 'Molecular Diagnostics and …

CB Westphalen, C Bokemeyer, R Büttner… - European Journal of …, 2020 - Elsevier
Precision cancer medicine (PCM) holds great promises to offer more effective therapies to
patients based on molecular profiling of their individual tumours. Although the PCM …

[HTML][HTML] Genetic tests by next-generation sequencing in children with developmental delay and/or intellectual disability

JY Han, IG Lee - Clinical and experimental pediatrics, 2020 - ncbi.nlm.nih.gov
Developments in next-generation sequencing (NGS) techogies have assisted in clarifying
the diagnosis and treatment of developmental delay/intellectual disability (DD/ID) via …

Perceptions of students in health and molecular life sciences regarding pharmacogenomics and personalized medicine

L Mahmutovic, B Akcesme, C Durakovic, FB Akcesme… - Human Genomics, 2018 - Springer
Background Increasing evidence is demonstrating that a patient's unique genetic profile can
be used to detect the disease's onset, prevent its progression, and optimize its treatment …

Universal molecular screening does not effectively detect Lynch syndrome in clinical practice

B Brennan, CT Hemmings, I Clark… - Therapeutic …, 2017 - journals.sagepub.com
Background: Lynch syndrome (LS) due to an inherited damaging mutation in mismatch
repair (MMR) genes comprises 3% of all incident colorectal cancer (CRC). Molecular testing …

What's in a name? Justifying terminology for genomic findings beyond the initial test indication: A scoping review

S White, M Haas, KJ Laginha, K Laurendet, C Gaff… - Genetics in …, 2023 - Elsevier
Genome sequencing can generate findings beyond the initial test indication that may be
relevant to a patient or research participant's health. In the decade since the ACMG …

Understanding decisions to participate in genomic medicine in children's cancer care: A comparison of what influences parents, health care providers, and the general …

R De Abreu Lourenco, MC McCarthy… - Pediatric Blood & …, 2021 - Wiley Online Library
Background The emerging role of genomically guided precision medicine in pediatric
cancer care presents significant clinical, practical, and ethical challenges. We investigated …

Perception and knowledge of pharmacogenetics among Brazilian psychiatrists

BC Almeida, ED Gonçalves, MH de Sousa… - Psychiatry …, 2021 - Elsevier
Pharmacogenetics (PGx) can optimize drug therapy in psychiatry and is particularly
important in admixed populations. Here we developed and successfully validated a …

Precision medicine in the era of CRISPR-Cas9: evidence from Bosnia and Herzegovina

S Semiz, PC Aka - Palgrave Communications, 2019 - nature.com
This article explores the possibilities and challenges of genetic testing, genetic counseling,
and genome editing (collectively referred to in this piece as precision medicine) in Bosnia …