Occurrence of cancer in Marfan syndrome: Report of two patients with neuroblastoma and review of the literature.

Diagnosing Monogenic Stroke at Younger Age.

Loss of Chromosome Y in Neuroblastoma Is Associated With High-Risk Disease, 11q-Deletion, and Telomere Maintenance.

Implementing data on targeted therapy from the INFORM registry platform for children with relapsed cancer in Sweden.

Genetic insights into resting heart rate and its role in cardiovascular disease.

Genome sequencing with comprehensive variant calling identifies structural variants and repeat expansions in a large fraction of individuals with ataxia and/or neuromuscular disorders.

Retrospective Pediatric Cohort Study Validates NEOS Score and Demonstrates Applicability in Children With Anti-NMDAR Encephalitis.

Loci for insulin processing and secretion provide insight into type 2 diabetes risk.

Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease.

Low numbers of COVID-19 in Swedish pediatric oncology patients during the first pandemic year despite an open society.

A saturated map of common genetic variants associated with human height.

Microbial and human transcriptome in vaginal fluid at midgestation: Association with spontaneous preterm delivery.

Clinical and biological impact of SAMHD1 expression in mantle cell lymphoma.

Development and validation of an ICU-specific pressure injury risk assessment scale.

MAP3K6 Mutations in a Neurovascular Disease Causing Stroke, Cognitive Impairment, and Tremor.