D. Merino

发表

Genome Sequencing of Pediatric Medulloblastoma Links Catastrophic DNA Rearrangements with TP53 Mutations

David T. W. Jones, V. Beneš, R. Eils, 2012, Cell.

Spatial heterogeneity in medulloblastoma

Steven J. M. Jones, Gary D Bader, Richard A. Moore, 2017, Nature Genetics.

Establishing guidelines to harmonize tumor mutational burden (TMB): in silico assessment of variation in TMB quantification across diagnostic platforms: phase I of the Friends of Cancer Research TMB Harmonization Project

A. Stenzinger, M. Dietel, Mingchao Xie, 2020, Journal for ImmunoTherapy of Cancer.

Spatial and temporal heterogeneity of panel-based tumor mutational burden (TMB) in pulmonary adenocarcinoma: separating biology from technical artifacts.

S. Fröhling, M. Kriegsmann, A. Warth, 2019, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

Harmonization and Standardization of Panel-Based Tumor Mutational Burden (TMB) Measurement: Real-World Results and Recommendations of the QuIP Study.

S. Fröhling, M. Tiemann, W. Weichert, 2020, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

How Oncologists Perceive the Availability and Quality of Information Generated From Patient-Reported Outcomes (PROs)

D. Merino, B. Gentile, E. Sigal, 2019, Journal of Patient Experience.

Basic Science of Pediatric Brain Tumors

P. Sin-Chan, M. Remke, Michael D. Taylor, 2015 .

Tumor mutational burden standardization initiatives: Recommendations for consistent tumor mutational burden assessment in clinical samples to guide immunotherapy treatment decisions

A. Stenzinger, M. Dietel, D. Merino, 2019, Genes, chromosomes & cancer.

Polymorphisms in FADS1 and FADS2 alter desaturase activity in young Caucasian and Asian adults.

A. El-Sohemy, A. Badawi, D. Mutch, 2011, Molecular genetics and metabolism.

Risk of Second Primary Bone and Soft-Tissue Sarcomas Among Young Adulthood Cancer Survivors.

M. Tucker, A. D. de González, S. Savage, 2019, JNCI cancer spectrum.

Advocacy and Patient Involvement in Clinical Trials

D. Merino, E. Sigal, Diana M Merino, 2020 .

International liquid biopsy standardization alliance white paper.

Lauren C Leiman, T. Schlange, K. Pantel, 2020, Critical reviews in oncology/hematology.

Abstract 5671: Alignment of TMB measured on clinical samples: Phase IIB of the Friends of Cancer Research TMB Harmonization Project

Brett J. Kennedy, Lisa M Haley, Mingchao Xie, 2020 .

Improving attribution of adverse events in oncology clinical trials.

G. Y. Wong, L. Minasian, J. Sloan, 2019, Cancer Treatment Reviews.

Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers

Roland Arnold, Richard G Grundy, Daniele Merico, 2015, Nature Genetics.

Subsequent Neoplasm Risk Associated With Rare Variants in DNA Damage Response and Clinical Radiation Sensitivity Syndrome Genes in the Childhood Cancer Survivor Study.

Stephen W. Hartley, S. Chanock, D. Karyadi, 2020, JCO precision oncology.

Methylation of the TERT promoter and risk stratification of childhood brain tumours: an integrative genomic and molecular study.

David T. W. Jones, R. Weksberg, N. Alon, 2013, The Lancet. Oncology.

Chapter 1 p 53 and Hereditary Cancer

D. Malkin, D. Merino, Diana M Merino, 2014 .

p53 and hereditary cancer.

D. Malkin, D. Merino, Diana M Merino, 2014, Sub-cellular biochemistry.

Myc and Loss of p53 Cooperate to Drive Formation of Choroid Plexus Carcinoma.

Andrew P. Hodges, S. Vandenberg, M. Roussel, 2019, Cancer research.

MycandLossofp53Cooperate toDriveFormation of Choroid Plexus Carcinoma

Andrew P. Hodges, S. Vandenberg, M. Roussel, 2019 .

Molecular Characterization of Choroid Plexus Tumors Reveals Novel Clinically Relevant Subgroups

Nada Jabado, Uri Tabori, Sanaa Choufani, 2014, Clinical Cancer Research.

Genome-Wide DNA Methylation Analysis Reveals Epigenetic Dysregulation of MicroRNA-34A in TP53-Associated Cancer Susceptibility.

R. Weksberg, A. Paterson, T. Hudson, 2016, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Alternative lengthening of telomeres is enriched in, and impacts survival of TP53 mutant pediatric malignant brain tumors

D. Johnston, N. Alon, J. Rutka, 2014, Acta Neuropathologica.

Genome-Wide Association Study to Identify Susceptibility Loci That Modify Radiation-Related Risk for Breast Cancer After Childhood Cancer

Carmen L. Wilson, S. Chanock, L. Strong, 2017, Journal of the National Cancer Institute.

Genetic variation in lipid desaturases and its impact on the development of human disease

D. Mutch, D. Ma, D. Merino, 2010, Lipids in Health and Disease.

DNA methylation signature is prognostic of choroid plexus tumor aggressiveness

Andrei L. Turinsky, R. Weksberg, M. Brudno, 2019, Clinical Epigenetics.

TMB standardization by alignment to reference standards: Phase II of the Friends of Cancer Research TMB Harmonization Project.

Mingchao Xie, L. Macconaill, V. Weigman, 2019, Journal of Clinical Oncology.

Cross-Species Genomics Identifies TAF12, NFYC, and RAD54L as Choroid Plexus Carcinoma Oncogenes.

D. Ellison, R. Gilbertson, D. Finkelstein, 2015, Cancer cell.

Molecular Targeted Therapies of Childhood Choroid Plexus Carcinoma

D. Malkin, D. Merino, 2011 .

Correction to: DNA methylation signature is prognostic of choroid plexus tumor aggressiveness

Andrei L. Turinsky, R. Weksberg, M. Brudno, 2019, Clinical Epigenetics.

Proteomic analysis of common bean seed with storage protein deficiency reveals up-regulation of sulfur-rich proteins and starch and raffinose metabolic enzymes, and down-regulation of the secretory pathway.

A. Pająk, D. Merino, J. Rivoal, 2010, Journal of proteomics.

Access to CAR T-cell Clinical Trials in Underrepresented Populations: a Multicenter Cohort Study of Pediatric and Young Adult ALL Patients.

Tumaini R. Coker, D. Merino, Julie R. Park, 2023, Transplantation and cellular therapy.