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Genetics of disease

Single nucleus RNA sequencing of the cerebral cortex from genetically diverse inbred mouse strains reveals differences in pericyte and endothelial cell composition

Jieun Park, Bonnie Taylor-Blake, James L. Krantz, Mark J. Zylka

Integrative molecular network analysis of genetic risk factors to infer biomarkers and therapeutic targets for rheumatoid arthritis

Sakhaa Alsaedi, Katsuhiko Mineta, [ ... ], Michihiro Ogasawara

Characterization of congenital hyperinsulinism in Argentina: Clinical features, genetic findings, and treatment outcomes

Gabriela Pacheco, Maria G. Bastida, [ ... ], Ana Tangari-Saredo

Genetic structure of different ethnic populations at the frontotemporal dementia risk loci

Volodymyr Mavrych, Maryam Alamil, Olena Bolgova, Volodymyr Dvornyk

DNA sequence classification for diabetes mellitus using NuSVC and XGBoost: A comparative

Said A. Salloum, Khaled Mohammad Alomari, Ayham Salloum

Certain vs. uncertain actionable secondary findings in a cohort of 500 Lebanese participants: What to report to the patient?

Eileen Marie Hanna, Cybel Mehawej, [ ... ], Eliane Chouery

Genetic markers for knee osteoarthritis presence are not associated with disease progression - data from the IMI-APPROACH cohort

Mieke L. M. Bentvelzen, Paco M.J. Welsing, [ ... ], Said el Bouhaddani

Genomic profiling in hidradenitis suppurativa: InterOmics pipeline for DNA-RNA sequencing highlights HLA variants, keratin-associated mutations and extracellular matrix alterations as contributing factors to HS pathogenesis

Lucas André Cavalcanti Brandão, Ronald Rodrigues de Moura, [ ... ], Sergio Crovella

AD-GCN: A novel graph convolutional network integrating multi-omics data for enhanced Alzheimer’s disease diagnosis

Zilu Li, Qingyun Li, [ ... ], Yangfan Guo

Bidirectional genetic links between chronic obstructive pulmonary disease and frailty: Genome-wide association study insights

Fuhui Yan, Tong Wu, Qiang Meng, Feng Qu

Estimating multiplicity of infection, haplotype frequencies, and linkage disequilibria from multi-allelic markers for molecular disease surveillance

Henri Christian Junior Tsoungui Obama, Kristan Alexander Schneider

The impact of VUS reclassification on reproductive decision making

Alexandra Peyser, Kenan Onel, Avner Hershlag

Unraveling genetic etiologies in complex pediatric neurological diseases: A genetic investigation using whole exome sequencing

Zainab Gaouzi, Aziza Belkhayat, [ ... ], Yamna Kriouile

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