Correcting Differential Gene Expression Analysis for Cyto—Architectural Alterations in Substantia Nigra of Parkinson’s Disease Patients Reveals Known and Potential Novel Disease—Associated Genes and Pathways

Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease

A hidden layer of structural variation in transposable elements reveals potential genetic modifiers in human disease-risk loci

A framework for employing longitudinally collected multicenter electronic health records to stratify heterogeneous patient populations on disease history

pmTR database: Population matched (pm) germline allelic variants of T-cell receptor (TR) loci

Dynamic prediction of mortality in COVID-19 patients in the intensive care unit: A retrospective multi-center cohort study

The Effect of Phenotype and Genotype on the Plasma Proteome in Patients with Inflammatory Bowel Disease

Resilience and resistance to the accumulation of amyloid plaques and neurofibrillary tangles in centenarians: An age-continuous perspective

Proving compliance of satellite InSAR technology with geotechnical design codes

Longitudinal Dynamics of Human B-Cell Response at the Single-Cell Level in Response to Tdap Vaccination

Differential analysis of binarized single-cell RNA sequencing data captures biological variation

Augmented satellite inSAR for assessing short-term and long-term surface deformation due to shield tunnelling

SnpXplorer: A web application to explore human SNP-associations and annotate SNP-sets

Polygenic Risk Score of Longevity Predicts Longer Survival across an Age Continuum

Evaluation of InSAR data for measuring the surface settlement during shield tunnel construction of the North-South Line in Amsterdam

Transcriptomic Signatures Associated With Regional Cortical Thickness Changes in Parkinson’s Disease

Robust deep learning model for prognostic stratification of pancreatic ductal adenocarcinoma patients

Population matched (pm) germline allelic variants of immunoglobulin (IG) loci: Relevance in infectious diseases and vaccination studies in human populations

Genetics Contributes to Concomitant Pathology and Clinical Presentation in Dementia with Lewy Bodies

Genome-wide association study of frontotemporal dementia identifies a C9ORF72 haplotype with a median of 12-G4C2 repeats that predisposes to pathological repeat expansions