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List of works by Promita Bose

ATRX, DAXX or MEN1 mutant pancreatic neuroendocrine tumors are a distinct alpha-cell signature subgroup

scientific article published in Nature Communications

Atrx inactivation drives disease-defining phenotypes in glioma cells of origin through global epigenomic remodeling.

scientific article published on 13 March 2018

Author Correction: Atrx inactivation drives disease-defining phenotypes in glioma cells of origin through global epigenomic remodeling

correction of a scholarly article

Contribution of copy-number variation to Down syndrome-associated atrioventricular septal defects.

scientific article published on 23 October 2014

Dissecting Allele Architecture of Early Onset IBD Using High-Density Genotyping

scientific article published on 22 June 2015

EPIG-06ATRX DEFICIENCY PROMOTES MIGRATORY BEHAVIOR IN GLIOMA CELLS OF ORIGIN BY DYSREGULATING GENOME-WIDE CHROMATIN ACCESSIBILITY AND MODULATING TRANSCRIPTIONAL PROGRAMS.

scientific article

Evolution of the immune landscape during progression of pancreatic intraductal papillary mucinous neoplasms to invasive cancer

scientific article published on 04 April 2020

Excess variants in AFF2 detected by massively parallel sequencing of males with autism spectrum disorder ⬇️

scientific article published on July 5, 2012

Exome sequencing identifies a novel FOXP3 mutation in a 2-generation family with inflammatory bowel disease

scientific article

GENE-24. ATRX DEFICIENCY IN GLIOMA CELLS OF ORIGIN PROMOTES DISEASE-DEFINING PHENOTYPES BY WAY OF GLOBAL EPIGENOMIC REMODELING

Integrated Genomic Analysis of Hürthle Cell Cancer Reveals Oncogenic Drivers, Recurrent Mitochondrial Mutations, and Unique Chromosomal Landscapes

scientific article published on 01 August 2018

Integrated Genomics for Pinpointing Survival Loci within Arm-Level Somatic Copy Number Alterations.

scientific article published on May 2016

Noninvasive Discrimination of Low and High-risk Pancreatic Intraductal Papillary Mucinous Neoplasms

scientific article published on 07 July 2020

Tandem repeats and G-rich sequences are enriched at human CNV breakpoints

scientific article

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