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The neurodevelopmental and facial phenotype in individuals with a TRIP12 variant
Comparison of telemonitoring combined with intensive patient support with standard care in patients with chronic cardiovascular disease
Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology
Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology
Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss
Development, validation, and implementation of biomarker testing in cardiovascular medicine state-of-the-art
The CHD4-related syndrome
Automated urinalysis combining physicochemical analysis, on-board centrifugation, and digital imaging in one system: A multicenter performance evaluation of the cobas 6500 urine work area
Identical and Nonidentical Twins: Risk and Factors Involved in Development of Islet Autoimmunity and Type 1 Diabetes
Integrating new approaches to atrial fibrillation management: the 6th AFNET/EHRA Consensus Conference
Effect of Oral Insulin on Prevention of Diabetes in Relatives of Patients With Type 1 Diabetes A Randomized Clinical Trial
A roadmap to improve the quality of atrial fibrillation management: proceedings from the fifth Atrial Fibrillation Network/European Heart Rhythm Association consensus conference
Development and Validation of a Melanoma Risk Score Based on Pooled Data from 16 Case-Control Studies
FTO genotype is associated with phenotypic variability of body mass index
Association Between Chromosome 9p21 Variants and the Ankle-Brachial Index Identified by a Meta-Analysis of 21 Genome-Wide Association Studies
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
Hundreds of variants clustered in genomic loci and biological pathways affect human height