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D. Parsons · SciRah

Researcher profile · Semantic Scholar

D. Parsons

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D. Parsons — researcher profile on SciRah

h-index: 43
Works: 124
Citations: 27K

Most-cited papers

Molecular subgroups of medulloblastoma: the current consensus
Michael D. Taylor, P. Northcott, A. Korshunov, M. Remke +12 more
2011Acta Neuropathologica1,819 citations Open access
Semantic Scholar
Exomic Sequencing Identifies PALB2 as a Pancreatic Cancer Susceptibility Gene
Siân Jones, R. Hruban, Mihoko Kamiyama, Michael Borges +16 more
2009Science808 citations Open access
Semantic Scholar
The genetic landscape of the childhood cancer medulloblastoma
D. Parsons, M. Li, Xiaosong Zhang, Siân Jones +43 more
2010Science735 citations Open access
Semantic Scholar
Diagnostic Yield of Clinical Tumor and Germline Whole-Exome Sequencing for Children With Solid Tumors
D. Parsons, A. Roy, Ya-Ping Yang, Tao Wang +29 more
2016JAMA Oncology476 citations Open access
Semantic Scholar
Mutually exclusive recurrent somatic mutations in MAP2K1 and BRAF support a central role for ERK activation in LCH pathogenesis.
Rikhia Chakraborty, O. Hampton, Xiao-Yun Shen, S. Simko +21 more
2014Blood403 citations Open access
Semantic Scholar
SMAD4 Gene Mutations Are Associated With Poor Prognosis in Pancreatic Cancer
A. Blackford, O. Serrano, elliot k fishman, G. Parmigiani +21 more
2009Clinical Cancer Research365 citations Open access
Semantic Scholar
Somatic mutations in the chromatin remodeling gene ARID1A occur in several tumor types
Siân Jones, Meng Li, D. Parsons, Xiaosong Zhang +17 more
2011Human Mutation296 citations Open access
Semantic Scholar
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.
R. Green, K. Goddard, G. Jarvik, L. Amendola +60 more
2016American Journal of Human Genetics157 citations Open access
Semantic Scholar
Alternative genetic mechanisms of BRAF activation in Langerhans cell histiocytosis.
Rikhia Chakraborty, Thomas M. Burke, O. Hampton, Daniel J. Zinn +12 more
2016Blood151 citations Open access
Semantic Scholar
Genetic Mutations Associated With Cigarette Smoking in Pancreatic Cancer
A. Blackford, G. Parmigiani, T. Kensler, elliot k fishman +19 more
2009Cancer Research139 citations Open access
Semantic Scholar
Recurrent internal tandem duplications of BCOR in clear cell sarcoma of the kidney
A. Roy, Vijetha Kumar, B. Zorman, Erica Fang +18 more
2015Nature Communications135 citations Open access
Semantic Scholar
The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations.
L. Amendola, J. Berg, C. Horowitz, Frank A Angelo +34 more
2018American Journal of Human Genetics130 citations Open access
Semantic Scholar
CNS Langerhans Cell Histiocytosis: Common Hematopoietic Origin for LCH-Associated Neurodegeneration and Mass Lesions
K. McClain, J. Picarsic, Rikhia Chakraborty, Daniel J. Zinn +41 more
2018Cancer114 citations Open access
Semantic Scholar
Actionable Tumor Alterations and Treatment Protocol Enrollment of Pediatric and Young Adult Patients With Refractory Cancers in the National Cancer Institute–Children's Oncology Group Pediatric MATCH Trial
D. Parsons, Katherine A. Janeway, D. Patton, Cynthia L. Winter +17 more
2022Journal of Clinical Oncology101 citations Open access
Semantic Scholar
Germline Findings in Tumor-Only Sequencing: Points to Consider for Clinicians and Laboratories.
Victoria M. Raymond, S. Gray, S. Roychowdhury, S. Joffe +3 more
2016Journal of the National Cancer Institute96 citations Open access
Semantic Scholar
Tazemetostat for Tumors Harboring SMARCB1/SMARCA4 or EZH2 Alterations: Results from NCI-COG Pediatric MATCH APEC1621C.
S. Chi, Joanna S. Yi, P. Williams, S. Roy-Chowdhuri +18 more
2023Journal of the National Cancer Institute94 citations Open access
Semantic Scholar
Precision medicine in pediatric oncology: Lessons learned and next steps
R. Mody, J. Prensner, Jessica N. Everett, D. Parsons +1 more
2016Pediatric Blood & Cancer81 citations Open access
Semantic Scholar
Reliable tumor detection by whole-genome methylation sequencing of cell-free DNA in cerebrospinal fluid of pediatric medulloblastoma
Jia Li, Si-Bo Zhao, Minjung Lee, Yue Yin +10 more
2020Science Advances78 citations Open access
Semantic Scholar
The Challenge of Informed Consent and Return of Results in Translational Genomics: Empirical Analysis and Recommendations
G. Henderson, S. Wolf, K. Kuczynski, S. Joffe +5 more
2014Journal of Law, Medicine & Ethics74 citations Open access
Semantic Scholar
Obtaining informed consent for clinical tumor and germline exome sequencing of newly diagnosed childhood cancer patients
S. Scollon, Katie Bergstrom, Robin A. Kerstein, Tao Wang +10 more
2014Genome Medicine74 citations Open access
Semantic Scholar
ZFTA-RELA Dictates Oncogenic Transcriptional Programs to Drive Aggressive Supratentorial Ependymoma
A. Arabzade, Yan-Hua Zhao, S. Varadharajan, Hsiao-Chi Chen +37 more
2021Cancer Discovery70 citations Open access
Semantic Scholar
IDH1 and IDH2: Not Your Typical Oncogenes
Z. Reitman, D. Parsons, Hai Yan
2010Cancer Cell69 citations Open access
Semantic Scholar
Sodium ion channel mutations in glioblastoma patients correlate with shorter survival
A. Joshi, D. Parsons, V. Velculescu, G. Riggins
2011Molecular Cancer65 citations Open access
Semantic Scholar
Somatic cancer variant curation and harmonization through consensus minimum variant level data
D. Ritter, S. Roychowdhury, A. Roy, Shruti Rao +14 more
2016Genome Medicine61 citations Open access
Semantic Scholar
Biological and clinical significance of somatic mutations in Langerhans cell histiocytosis and related histiocytic neoplastic disorders.
Carl E. Allen, D. Parsons
2015Hematology. American Society of Hematology. Education Program61 citations Open access
Semantic Scholar
Current State of Pediatric Sarcoma Biology and Opportunities for Future Discovery: A Report from the Sarcoma Translational Research Workshop
P. Hingorani, Katherine A. Janeway, Brian D. Crompton, C. Kadoch +25 more
2016Cancer Genetics50 citations Open access
Semantic Scholar
Parental Perspectives on Whole Exome Sequencing in Pediatric Cancer: A Typology of Perceived Utility
Janet Malek, M. J. Slashinski, J. Robinson, A. Gutierrez +4 more
2017JCO Precision Oncology45 citations Open access
Semantic Scholar
Pediatric oncology enters an era of precision medicine.
N. Seibel, Katherine A. Janeway, C. Allen, S. Chi +8 more
2017Current Problems in Cancer43 citations
Semantic Scholar
Is Whole Exome Sequencing an Ethically Disruptive Technology? Perspectives of Pediatric Oncologists and Parents of Pediatric Patients with Solid Tumors
L. McCullough, M. J. Slashinski, Amy L. McGuire, Richard L. Street +4 more
2015Pediatric Blood & Cancer42 citations Open access
Semantic Scholar
Phase II Study of Selumetinib in Children and Young Adults With Tumors Harboring Activating Mitogen-Activated Protein Kinase Pathway Genetic Alterations: Arm E of the NCI-COG Pediatric MATCH Trial
O. Eckstein, C. Allen, P. Williams, S. Roy-Chowdhuri +18 more
2022Journal of Clinical Oncology41 citations Open access
Semantic Scholar
Clinical tumor sequencing: an incidental casualty of the American College of Medical Genetics and Genomics recommendations for reporting of incidental findings.
D. Parsons, A. Roy, S. Plon, S. Roychowdhury +1 more
2014Journal of Clinical Oncology36 citations Open access
Semantic Scholar
Activating MAPK1 (ERK2) mutation in an aggressive case of disseminated juvenile xanthogranuloma
Rikhia Chakraborty, O. Hampton, H. Abhyankar, Daniel J. Zinn +15 more
2017OncoTarget33 citations Open access
Semantic Scholar
Responsibility, Culpability, and Parental Views on Genomic Testing for Seriously Ill Children
Janet Malek, Stacey Pereira, J. Robinson, A. Gutierrez +4 more
2019Genetics in Medicine30 citations Open access
Semantic Scholar
Germline POLE mutation in a child with hypermutated medulloblastoma and features of constitutional mismatch repair deficiency
H. Lindsay, S. Scollon, J. Reuther, Horatiu Voicu +8 more
2019Cold Spring Harbor molecular case studies29 citations Open access
Semantic Scholar
Agents of Empathy: How Medical Interpreters Bridge Sociocultural Gaps in Genomic Sequencing Disclosures with Spanish-Speaking Families
A. Gutierrez, Emily E Statham, J. Robinson, M. J. Slashinski +6 more
2018Patient Education and Counseling29 citations Open access
Semantic Scholar
Identification of targetable molecular alterations in the NCI-COG Pediatric MATCH trial.
D. Parsons, Katherine A. Janeway, D. Patton, Brent Coffey +16 more
2019Journal of Clinical Oncology26 citations
Semantic Scholar
Xenotransplantation of pediatric low grade gliomas confirms the enrichment of BRAF V600E mutation and preservation of CDKN2A deletion in a novel orthotopic xenograft mouse model of progressive pleomorphic xanthoastrocytoma
M. Kogiso, Lin Qi, H. Lindsay, Yu-Lun Huang +24 more
2017OncoTarget24 citations Open access
Semantic Scholar
Erdafitinb in patients with FGFR-altered tumors: Results from the NCI-COG Pediatric MATCH trial arm B (APEC1621B).
Alice Lee, Alexander Chou, P. Williams, S. Roy-Chowdhuri +16 more
2023Journal of Clinical Oncology22 citations Open access
Semantic Scholar
Portero versus Portador: Spanish Interpretation of Genomic Terminology during Whole Exome Sequencing Results Disclosure
A. Gutierrez, J. Robinson, Emily E Statham, S. Scollon +6 more
2017Personalized Medicine22 citations Open access
Semantic Scholar
Novel PDGFRB rearrangement in multifocal infantile myofibromatosis is tumorigenic and sensitive to imatinib
Mohammed Hassan, E. Butler, Raphael A. Wilson, A. Roy +12 more
2019Cold Spring Harbor molecular case studies21 citations Open access
Semantic Scholar
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.
R. Green, Katrina A. B. Goddard, G. Jarvik, L. Amendola +237 more
2016American Journal of Human Genetics20 citations Open access
Semantic Scholar
Exome Sequencing Disclosures in Pediatric Cancer Care: Patterns of Communication among Oncologists, Genetic Counselors, and Parents
S. Scollon, M. Majumder, Katie Bergstrom, Tao Wang +8 more
2018Patient Education and Counseling19 citations Open access
Semantic Scholar
A genome-wide association study of LCH identifies a variant in SMAD6 associated with susceptibility.
Erin C. Peckham-Gregory, Rikhia Chakraborty, M. Scheurer, J. Belmont +12 more
2017Blood19 citations Open access
Semantic Scholar
Fixing the leaky pipeline: identifying solutions for improving pediatrician-scientist training during pediatric residency
Audrea M Burns, K. Ackerman, S. Thammasitboon, Caroline E. Rassbach +17 more
2020Pediatric Research14 citations
Semantic Scholar
Renal cell carcinoma harboring somatic TSC2 mutations in a child with methylmalonic acidemia
Samara L. Potter, R. Venkatramani, S. Wenderfer, B. Graham +10 more
2016Pediatric Blood & Cancer11 citations Open access
Semantic Scholar
The Pharmacogenomics of Vincristine-Induced Neuropathy: On Pins and Needles.
S. Berg, D. Parsons
2015JAMA Oncology10 citations Open access
Semantic Scholar
A Validation Framework for Somatic Copy Number Detection in Targeted Sequencing Panels.
Raghu Chandramohan, J. Reuther, Ilavarasi Gandhi, Horatiu Voicu +6 more
2022Journal of Molecular Diagnostics9 citations Open access
Semantic Scholar
Applications of Genomic Sequencing in Pediatric CNS Tumors.
A. Bavle, F. Lin, D. Parsons
2016Oncology9 citations
Semantic Scholar
Circulating tumor DNA sequencing of pediatric solid and brain tumor patients: An institutional feasibility study
Ross Mangum, J. Reuther, Koel Sen Baksi, Ilavarasi Gandhi +21 more
2023Pediatric Hematology & Oncology8 citations Open access
Semantic Scholar
Synergistic anti-tumor efficacy of mutant isocitrate dehydrogenase 1 inhibitor SYC-435 with standard therapy in patient-derived xenograft mouse models of glioma
M. Kogiso, Lin Qi, Yu-Chen Du, F. Braun +20 more
2022Translational Oncology8 citations Open access
Semantic Scholar

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N. Takebe — researcher profile on SciRah

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