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Author Details
Full Name
Melissa Rotunno
Affiliation
Boston Children's Hospital and Harvard Medical School
ORCID
Career Start Year
2004
Papers
48
H Index
22
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35073553
Urine Proteomics for Noninvasive Monitoring of Biomarkers in Bronchopulmonary Dysplasia.
Neonatology
2022
35460723
Prevalence of Americans reporting a family history of cancer indicative of increased cancer risk: Estimates from the 2015 National Health Interview Survey.
Prev Med
2022
33063887
On the application, reporting, and sharing of in silico simulations for genetic studies.
Genet Epidemiol
2021
33795213
Epidemiologic Research of Rare Cancers: Trends, Resources, and Challenges.
Cancer Epidemiol Biomarkers Prev
2021
33857240
Systems epidemiology and cancer: A review of the National Institutes of Health extramural grant portfolio 2013-2018.
PLoS One
2021
34972102
Facilitating cancer systems epidemiology research.
PLoS One
2021
34308104
Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in the Childhood Cancer Survivor Study.
JNCI Cancer Spectr
2021
32467344
A Systematic Literature Review of Whole Exome and Genome Sequencing Population Studies of Genetic Susceptibility to Cancer.
Cancer Epidemiol Biomarkers Prev
2020
33188775
Tau PTM Profiles Identify Patient Heterogeneity and Stages of Alzheimer's Disease.
Cell
2020
30101297
Genetic Simulation Resources and the GSR Certification Program.
Bioinformatics
2019
29693246
Germline mutations in Protection of Telomeres 1 in two families with Hodgkin lymphoma.
Br J Haematol
2018
30411536
Whole-exome sequencing of nevoid basal cell carcinoma syndrome families and review of Human Gene Mutation Database PTCH1 mutation data.
Mol Genet Genomic Med
2018
30583724
Prevalence of pathogenic/likely pathogenic variants in the 24 cancer genes of the ACMG Secondary Findings v2.0 list in a large cancer cohort and ethnicity-matched controls.
Genome Med
2018
29036293
Rare germline variants in known melanoma susceptibility genes in familial melanoma.
Hum Mol Genet
2017
27449771
Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations.
Hum Genet
2016
27629550
Whole exome sequencing in families with CLL detects a variant in Integrin β 2 associated with disease susceptibility.
Blood
2016
27365461
Whole exome sequencing in families at high risk for Hodgkin lymphoma: identification of a predisposing mutation in the KDR gene.
Haematologica
2016
25802059
Lung cancer prognosis before and after recurrence in a population-based setting.
J Natl Cancer Inst
2015
23681825
Heme-related gene expression signatures of meat intakes in lung cancer tissues.
Mol Carcinog
2014
25685612
Constitutive mitochondrial DNA copy number in peripheral blood of melanoma families with and without <i>CDKN2A</i> mutations.
J Carcinog Mutagen
2014
25005139
Parity-related molecular signatures and breast cancer subtypes by estrogen receptor status.
Breast Cancer Res
2014
24990759
Characterization of T gene sequence variants and germline duplications in familial and sporadic chordoma.
Hum Genet
2014
24762620
Constitutional promoter methylation and risk of familial melanoma.
Epigenetics
2014
24714516
Global changes in gene expression of Barrett's esophagus compared to normal squamous esophagus and gastric cardia tissues.
PLoS One
2014
24686846
Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma.
Nat Genet
2014
22392686
GSTM1 and GSTT1 copy numbers and mRNA expression in lung cancer.
Mol Carcinog
2012
22561519
Detectable clonal mosaicism and its relationship to aging and cancer.
Nat Genet
2012
22585858
Inherited variation at chromosome 12p13.33, including RAD52, influences the risk of squamous cell lung carcinoma.
Cancer Discov
2012
21293027
Assessment of human papillomavirus in lung tumor tissue.
J Natl Cancer Inst
2011
28472664
A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma.
Am J Hum Genet
2011
21742797
A gene expression signature from peripheral whole blood for stage I lung adenocarcinoma.
Cancer Prev Res (Phila)
2011
21654679
Epstein-Barr virus microRNAs and lung cancer.
Br J Cancer
2011
20044584
Dietary quercetin, quercetin-gene interaction, metabolic gene expression in lung tissue and lung cancer risk.
Carcinogenesis
2010
21102586
Inherited polymorphisms in the RNA-mediated interference machinery affect microRNA expression and lung cancer survival.
Br J Cancer
2010
20688270
GPC5 rs2352028 variant and risk of lung cancer in never smokers.
Lancet Oncol
2010
20460509
Pathway analysis of breast cancer genome-wide association study highlights three pathways and one canonical signaling cascade.
Cancer Res
2010
20663154
Evaluation of normalization methods for two-channel microRNA microarrays.
J Transl Med
2010
20200440
Lower risk of lung cancer after multiple pneumonia diagnoses.
Cancer Epidemiol Biomarkers Prev
2010
20068076
MicroRNA expression differentiates histology and predicts survival of lung cancer.
Clin Cancer Res
2010
19258469
Control selection options for genome-wide association studies in cohorts.
Cancer Epidemiol Biomarkers Prev
2009
19812684
Chronic obstructive pulmonary disease and altered risk of lung cancer in a population-based case-control study.
PLoS One
2009
19836008
A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma.
Am J Hum Genet
2009
19479063
Phase I metabolic genes and risk of lung cancer: multiple polymorphisms and mRNA expression.
PLoS One
2009
18297132
Gene expression signature of cigarette smoking and its role in lung adenocarcinoma development and survival.
PLoS One
2008
18538025
Environment And Genetics in Lung cancer Etiology (EAGLE) study: an integrative population-based case-control study of lung cancer.
BMC Public Health
2008
16907110
Memory effects in nematics with quenched disorder.
Phys Rev E Stat Nonlin Soft Matter Phys
2006
15784001
Nematics with quenched disorder: pinning out the origin of memory.
Phys Rev Lett
2005
15352849
Phase behavior of polarizable spherocylinders in external fields.
J Chem Phys
2004
1 - 48 of 48
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