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Journal Articles

Whole Exome Analysis Reveals Key Genomic Differences between Sporadic and Endemic Pediatric Burkitt Lymphoma

Denice Mae Palmos, BS, Rikhia Chakraborty, PhD, Harshal Abhyankar, MS, Joy C. Jayaseelan, MS, Maria F. Cardenas, BS, Joyce Kambugu, MBChB, Jeff Otiti, MBChB, Fadhil Geriga, MBChB, Pietro Pala, MD, John Sekabira, MBChB, MMed, Peter Wasswa, MBChB, Joseph Ssenyondwa, MBChB, Jackson Orem, MBChB, MMed, PhD, David A. Wheeler, PhD, Joseph Lubega, MBChB, MPH, Carl E. Allen, MD PhD, Donald Williams Parsons, MD PhD

Blood (2018) 132 (Supplement 1): 4117.

https://doi.org/10.1182/blood-2018-99-110762

Published: 2018

Journal Articles

Integrated Genomic Analysis of Down Syndrome Acute Lymphoblastic Leukemia Reveals Recurrent Cancer Gene Alterations and Evidence of Frequent Subclonal Driver Events

Blood (2016) 128 (22): 4083.

https://doi.org/10.1182/blood.V128.22.4083.4083

Published: 2016

Journal Articles

Alternative genetic mechanisms of BRAF activation in Langerhans cell histiocytosis

Rikhia Chakraborty, Thomas M. Burke, Oliver A. Hampton, Daniel J. Zinn, Karen Phaik Har Lim, Harshal Abhyankar, Brooks Scull, Vijetha Kumar, Nipun Kakkar, David A. Wheeler, Angshumoy Roy, Poulikos I. Poulikakos, Miriam Merad, Kenneth L. McClain, D. Williams Parsons, Carl E. Allen

Blood (2016) 128 (21): 2533–2537.

https://doi.org/10.1182/blood-2016-08-733790

Published: 2016

Includes: Supplemental data

Journal Articles

Coexistence of gain-of-function JAK2 germ line mutations with JAK2 V617F in polycythemia vera

Lucie Lanikova, Olga Babosova, Sabina Swierczek, Linghua Wang, David A. Wheeler, Vladimir Divoky, Vladimir Korinek, Josef T. Prchal

Blood (2016) 128 (18): 2266–2270.

https://doi.org/10.1182/blood-2016-04-711283

Published: 2016

Includes: Supplemental data

Journal Articles

Mixed Phenotype Acute Leukemia (MPAL) Has a High Frequency of Mutations in Epigenetic Regulatory Genes: Results from Whole Exome Sequencing

Olive S. Eckstein, MD, Linghua Wang, MD PhD, Jyotinder N. Punia, MD, Steven M. Kornblau, MD, Michael Andreef, MD PhD, David A. Wheeler, PhD, Margaret A. Goodell, PhD

Blood (2014) 124 (21): 3560.

https://doi.org/10.1182/blood.V124.21.3560.3560

Published: 2014

Journal Articles

Mutually exclusive recurrent somatic mutations in MAP2K1 and BRAF support a central role for ERK activation in LCH pathogenesis

Blood (2014) 124 (19): 3007–3015.

https://doi.org/10.1182/blood-2014-05-577825

Published: 2014

Includes: Supplemental data

Journal Articles

Whole Exome Sequencing and Analysis Of Mutations In Sézary Syndrome

David A. Wheeler, PhD, Lui Xi, Xiao Ni, MD, PhD, Misha Koshelev, MD, PhD, Jennifer Drummond, Donna M. Muzny, Xiang Zhang, MD, MS, Madeleine Duvic, MD

Blood (2013) 122 (21): 2558.

https://doi.org/10.1182/blood.V122.21.2558.2558

Published: 2013

Journal Articles

Molecular Characterization Of Polycythemia Vera Based On The Relationship Of JAK2 V617F and 9pUPD

Linghua Wang, MD, PhD, Sabina Swierczek, PhD, Kimberly Hickman, Soo-Jin Kim, David A. Wheeler, PhD, Josef Prchal, MD

Blood (2013) 122 (21): 1607.

https://doi.org/10.1182/blood.V122.21.1607.1607

Published: 2013

Journal Articles

Comparison Of Mutational Profiles Of Diagnosis and Relapsed Pediatric B-Acute Lymphoblastic Leukemia: A Report From The COG ALL Target Project

Blood (2013) 122 (21): 824.

https://doi.org/10.1182/blood.V122.21.824.824

Published: 2013

Journal Articles

Clinically Significant Mutations, Deletions and Translocations Involving ETV6 Identified by Whole Genome and Whole Exome Sequencing; Report From NCI/COG Target AML Initiative

Heather L. Helton, MD, Rhonda E. Ries, MA, Todd A. Alonzo, PhD, Robert B. Gerbing, M.A., Lisa R. Trevino, PhD, Jason Farrar, M.D., Jaime M. Guidry Auvil, Ph.D., Tanja M. Davidsen, PhD, Patee Gesuwan, Ph.D., Donna M. Muzny, Alan S. Gamis, MD, MPH, Janet Franklin, MD, MPH, David A. Wheeler, PhD, Malcolm A. Smith, MD, PhD, Daniela S. Gerhard, Ph.D., Robert J. Arceci, MD, PhD, Soheil Meshinchi, MD, PhD

Blood (2012) 120 (21): 125.

https://doi.org/10.1182/blood.V120.21.125.125

Published: 2012

Journal Articles

Whole Genome Sequencing of Four CD34+-Derived iPSC Polycythemia Vera Clones From a Single Female

Lifeng Tian, PhD., Lucie Piterkova, PhD, Linghua Wang, PhD, Zhaohui Ye, PhD, Linzhao Cheng, PhD, David A. Wheeler, PhD, Hakon Hakonarson, MD, PhD, Josef T Prchal, MD

Blood (2012) 120 (21): 1755.

https://doi.org/10.1182/blood.V120.21.1755.1755

Published: 2012

Journal Articles

Identification of Novel Somatic Mutations, Regions of Recurrent Loss of Heterozygosity (LOH) and Significant Clonal Evolution From Diagnosis to Relapse in Childhood AML Determined by Exome Capture Sequencing – an NCI/COG Target AML Study

Soheil Meshinchi, MD, PhD, Rhonda E. Ries, MA, Lisa R. Trevino, PhD, Oliver A. Hampton, PhD, Todd Alonzo, PhD, Jason E. Farrar, MD, Jaime M. Guidry Auvil, PhD, Tanja M. Davidsen, PhD, Patee Gesuwan, PhD, Donna M. Muzny, Alan S. Gamis, MD, MPH, Heather L. Helton, MD, David A. Wheeler, PhD, Malcolm A. Smith, MD, PhD, Daniela S. Gerhard, Ph.D., Robert J. Arceci, MD, PhD

Blood (2012) 120 (21): 123.

https://doi.org/10.1182/blood.V120.21.123.123

Published: 2012

Journal Articles

Genome Wide Promoter Methylation Patterns Predict AML Subtype Outcomes and Identify Novel Pathways Characterizing Diagnostic and Relapsed Disease in Children

Michael Ochs, Ph.D., Jason Farrar, M.D., Michael Considine, M.S., Rhonda E. Ries, MA, Lisa R. Trevino, PhD, Todd A. Alonzo, PhD, Jaime Guidry-Auvil, Ph.D., Tanja M. Davidsen, PhD, Patee Gesuwan, Ph.D., Donna M. Muzny, Alan S. Gamis, MD, MPH, David A. Wheeler, PhD, Heather L. Helton, MD, Malcolm A. Smith, MD, PhD, Daniela S. Gerhard, Ph.D., Soheil Meshinchi, MD, PhD, Robert J. Arceci, MD, PhD

Blood (2012) 120 (21): 1287.

https://doi.org/10.1182/blood.V120.21.1287.1287

Published: 2012

Journal Articles

Whole Exome Sequencing of Polycythemia Vera Reveals Novel Recurrent Somatic and Germline Variation

Linghua Wang, PhD, Sabina Swierczek, PhD, Lucie Piterkova, PhD, Kimberly Hickman, David A. Wheeler, PhD, Josef T. Prchal, MD

Blood (2012) 120 (21): 705.

https://doi.org/10.1182/blood.V120.21.705.705

Published: 2012

NARROW

Whole Exome Analysis Reveals Key Genomic Differences between Sporadic and Endemic Pediatric Burkitt Lymphoma

Integrated Genomic Analysis of Down Syndrome Acute Lymphoblastic Leukemia Reveals Recurrent Cancer Gene Alterations and Evidence of Frequent Subclonal Driver Events

Alternative genetic mechanisms of BRAF activation in Langerhans cell histiocytosis

Coexistence of gain-of-function JAK2 germ line mutations with JAK2 V617F in polycythemia vera

Mixed Phenotype Acute Leukemia (MPAL) Has a High Frequency of Mutations in Epigenetic Regulatory Genes: Results from Whole Exome Sequencing

Mutually exclusive recurrent somatic mutations in MAP2K1 and BRAF support a central role for ERK activation in LCH pathogenesis

Whole Exome Sequencing and Analysis Of Mutations In Sézary Syndrome

Molecular Characterization Of Polycythemia Vera Based On The Relationship Of JAK2 V617F and 9pUPD

Comparison Of Mutational Profiles Of Diagnosis and Relapsed Pediatric B-Acute Lymphoblastic Leukemia: A Report From The COG ALL Target Project

Clinically Significant Mutations, Deletions and Translocations Involving ETV6 Identified by Whole Genome and Whole Exome Sequencing; Report From NCI/COG Target AML Initiative

Whole Genome Sequencing of Four CD34+-Derived iPSC Polycythemia Vera Clones From a Single Female

Identification of Novel Somatic Mutations, Regions of Recurrent Loss of Heterozygosity (LOH) and Significant Clonal Evolution From Diagnosis to Relapse in Childhood AML Determined by Exome Capture Sequencing – an NCI/COG Target AML Study

Genome Wide Promoter Methylation Patterns Predict AML Subtype Outcomes and Identify Novel Pathways Characterizing Diagnostic and Relapsed Disease in Children

Whole Exome Sequencing of Polycythemia Vera Reveals Novel Recurrent Somatic and Germline Variation

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American Society of Hematology

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ASH Publications

American Society of Hematology

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