DNA damage contributes to neurotoxic inflammation in Aicardi-Goutières Syndrome astrocytes

Epigenetic reprogramming at estrogen-receptor binding sites alters 3D chromatin landscape in endocrine resistant breast cancer

Exhausted intratumoral Vδ2- γδ T cells in human kidney cancer retain effector function [bulk RNA-seq]

Multiplexed functional genomic analysis of somatic 5’ untranslated region mutations across the spectrum of human prostate cancer

Discovery of autism/intellectual disability somatic mutations in Alzheimer's brains: mutated ADNP cytoskeletal impairments and repair as a case study

Label-free single-cell RNA Multiplexing leveraging genetic variability [bulk RNA-seq]

Label-free single-cell RNA Multiplexing leveraging genetic variability

Patient-derived organoid cultures model human primary liver cancer in vitro

Dynamic interplay between structural variation and 3D chromosome organization in pancreatic cancer

Immunogenetic metabolomics revealed key enzymes that modulate CAR-T metabolism and function

Codon Specific Readthrough as a Mechanism of BRCA2 Restoration in Acquired PARP Inhibitor and Chemotherapy Resistance

Integrated -Omics Analyses Demonstrate that Patient-Derived Colon Organoids Faithfully Recapitulate the Tumor Tissue of Origin, Highlighting Altered Pathways in Colorectal Cancer Progression

High throughput single cell long-read sequencing analyses of same-cell genotypes and phenotypes in human tumors.

The relationship between regulatory changes in cis and trans and the evolution of gene expression in humans and chimpanzees

Gene expression responses to oxygen challenge in a panel of human brain organoids

Recruitment of ETS1 to activated accessible regions promotes cilia genes transcriptional program in ciliopathy

Longitudinal single-cell epitope and RNA-sequencing reveals the immunological impact of type 1 interferon autoantibodies in critical COVID-19

A germline mutation of CDKN2A and a novel RPLP1-C19MC fusion detected in a rare melanotic neuroectodermal tumor of infancy: a case report [Seq]

A germline mutation of CDKN2A and a novel RPLP1-C19MC fusion detected in a rare melanotic neuroectodermal tumor of infancy: a case report

Enhanced efficacy of aurora kinase inhibitors in G2/M checkpoint deficient TP53 mutant uterine carcinomas is linked to the summation of LKB1-AKT-p53 interactions