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

PloS one, 2014-07, Vol.9 (7), p.e101607-e101607

2014

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

Cancer cell, 2018-08, Vol.34 (2), p.256-270.e5

2018

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

Nature communications, 2018-10, Vol.9 (1), p.4158-10, Article 4158

2018

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

Nature communications, 2018-03, Vol.9 (1), p.1057-15, Article 1057

2018

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

Nature communications, 2022-01, Vol.13 (1), p.190-190, Article 190

2022

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Prenatal alcohol exposure is associated with changes in placental gene co-expression networks

Scientific reports, 2024-02, Vol.14 (1), p.2687-2687, Article 2687

2024

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

Cancer cell, 2016-05, Vol.29 (5), p.737-750

2016

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

EBioMedicine, 2020-04, Vol.54, p.102714-102714, Article 102714

2020

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Genomic landscape of early-stage prostate adenocarcinoma in Mexican patients: an exploratory study

Discover. Oncology, 2024-08, Vol.15 (1), p.378-13, Article 378

2024

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

Genetics in medicine, 2015-07, Vol.17 (7), p.554-560

2015

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

Annals of surgery, 2021-06, Vol.273 (6), p.e273-e275

2021

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Prenatal Trace Metal Exposures and Genetic Variants Inform Birth Weight-related Placental Isoform Expression

Environmental health perspectives. Supplements, 2022-09, Vol.2022 (1)

2022

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GENT-21. ATRX DEFICIENCY PROMOTES INVASION AND ALTERS THE DIFFERENTIATION CAPACITY OF GLIOMA CELLS OF ORIGIN BY DYSREGULATING GENOME-WIDE CHROMATIN ACCESSIBILITY AND MODULATING TRANSCRIPTIONAL PROGRAMS

Neuro-oncology (Charlottesville, Va.), 2016-11, Vol.18 (suppl_6), p.vi78-vi78

2016

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Circulating small molecules are associated with exposure to uranium and radon in people living near a former uranium processing site

Environmental health perspectives. Supplements, 2024-08, Vol.2024 (1)

2024

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Abstract 1799: ATRX, DAXX or MEN1 mutant pancreatic neuroendocrine tumors are a distinct “alpha-cell signature” subgroup

Cancer research (Chicago, Ill.), 2018-07, Vol.78 (13_Supplement), p.1799-1799

2018

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Abstract 4322: Atrx inactivation drives motility and dysregulates differentiation in glioma cells of origin through global epigenomic remodeling

Cancer research (Chicago, Ill.), 2018-07, Vol.78 (13_Supplement), p.4322-4322

2018

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Exome Sequencing Identifies a Novel FOXP3 Mutation in a 2‐Generation Family With Inflammatory Bowel Disease

Journal of pediatric gastroenterology and nutrition, 2014-05, Vol.58 (5), p.561-568

2014

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A diagnostic algorithm to predict malignant potential of pancreatic intraductal papillary mucinous neoplasms

Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.], 2019-06, Vol.19, p.S121-S121

2019

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Abstract LB-169: Multidimensional genomic dissection of chromosome 9p in glioma

Cancer research (Chicago, Ill.), 2015-08, Vol.75 (15_Supplement), p.LB-169-LB-169

2015

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Exposure to uranium and its decay products is associated with plasma metabolome of people living near former uranium processing site

Environmental health perspectives. Supplements, 2023-09, Vol.2023 (1)

2023

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

Neuro-oncology (Charlottesville, Va.), 2015-11, Vol.17 (suppl 5), p.v87.2-v87

2015

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

Human molecular genetics, 2012-10, Vol.21 (19), p.4356-4364

2012

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

Neuro-oncology (Charlottesville, Va.), 2017-11, Vol.19 (suppl_6), p.vi97-vi97

2017

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976 Early Onset Crohn's Disease Exhibit Distinct Allele Architecture Differences and Reveal New IBD Loci

Gastroenterology (New York, N.Y. 1943), 2013-05, Vol.144 (5), p.S-178-S-178

2013

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

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

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

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

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

Prenatal alcohol exposure is associated with changes in placental gene co-expression networks

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

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

Genomic landscape of early-stage prostate adenocarcinoma in Mexican patients: an exploratory study

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

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

Prenatal Trace Metal Exposures and Genetic Variants Inform Birth Weight-related Placental Isoform Expression

GENT-21. ATRX DEFICIENCY PROMOTES INVASION AND ALTERS THE DIFFERENTIATION CAPACITY OF GLIOMA CELLS OF ORIGIN BY DYSREGULATING GENOME-WIDE CHROMATIN ACCESSIBILITY AND MODULATING TRANSCRIPTIONAL PROGRAMS

Circulating small molecules are associated with exposure to uranium and radon in people living near a former uranium processing site

Abstract 1799: ATRX, DAXX or MEN1 mutant pancreatic neuroendocrine tumors are a distinct “alpha-cell signature” subgroup

Abstract 4322: Atrx inactivation drives motility and dysregulates differentiation in glioma cells of origin through global epigenomic remodeling

Exome Sequencing Identifies a Novel FOXP3 Mutation in a 2‐Generation Family With Inflammatory Bowel Disease

A diagnostic algorithm to predict malignant potential of pancreatic intraductal papillary mucinous neoplasms

Abstract LB-169: Multidimensional genomic dissection of chromosome 9p in glioma

Exposure to uranium and its decay products is associated with plasma metabolome of people living near former uranium processing site

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

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

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

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

976 Early Onset Crohn's Disease Exhibit Distinct Allele Architecture Differences and Reveal New IBD Loci

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