Acute lymphoblastic leukemia with myeloid mutations is a high-risk disease associated with clonal hematopoiesis December 27, 2023
Predicting outcomes in esophageal adenocarcinoma following neoadjuvant chemoradiation: Interactions between tumor response and survival December 25, 2023
Diagnostic exome identifies a novel PRKG2 mutation in a proband with skeletal dysplasia. December 13, 2023
Neonatal Ichthyosis and sclerosing cholangitis (NISCH) syndrome with a novel Claudin-1 (CLDN1) mutation: A report from India December 5, 2023
The Genetic Drivers of Juvenile, Young, and Early-Onset Parkinson’s Disease in India November 29, 2023
Clinical Utility of Proband Only Clinical Exome Sequencing in Neurodevelopmental Disorders November 9, 2023
Identification of a shared, common haplotype segregating with an SGCB c.544 T > G mutation in Indian patients affected with sarcoglycanopathy September 12, 2023
Intervention of next-generation sequencing in diagnosis of Alzheimer’s disease: challenges and future prospects August 7, 2023
