M. Rotunno

发表

Gene Expression Signature of Cigarette Smoking and Its Role in Lung Adenocarcinoma Development and Survival

S. Wacholder, J. Jen, A. Bergen, 2008, PloS one.

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

S. Puig, S. Chanock, Jia Liu, 2018, Genome Medicine.

A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma.

Ying Wang, William Wheeler, Andres Metspalu, 2009, American journal of human genetics.

GPC5 rs2352028 variant and risk of lung cancer in never smokers.

D. Gudbjartsson, T. Thorgeirsson, K. Stefánsson, 2010, The Lancet. Oncology.

Tau PTM Profiles Identify Patient Heterogeneity and Stages of Alzheimer’s Disease

Christoph N Schlaffner, Amanda J. Guise, Christoph N. Schlaffner, 2020, Cell.

Control Selection Options for Genome-Wide Association Studies in Cohorts

S. Wacholder, M. Rotunno, 2009, Cancer Epidemiology Biomarkers & Prevention.

Post-translational modification by cysteine protects Cu/Zn-superoxide dismutase from oxidative damage.

Qian Liu, Gregory A Petsko, Dagmar Ringe, 2013, Biochemistry.

Amyotrophic Lateral Sclerosis inSuperoxide Dismutase 1 That Is Exposed Identification of a Misfolded Region in Molecular Bases of Disease

Jared R. Auclair, Jared R Auclair, D. A. Bosco, 2014 .

An emerging role for misfolded wild-type SOD1 in sporadic ALS pathogenesis

D. A. Bosco, M. Rotunno, Melissa Rotunno, 2013, Front. Cell. Neurosci..

GSTM1 and GSTT1 copy numbers and mRNA expression in lung cancer

T. Lam, J. Lubin, P. Bertazzi, 2012, Molecular carcinogenesis.

Chronic Obstructive Pulmonary Disease and Altered Risk of Lung Cancer in a Population-Based Case-Control Study

S. Wacholder, J. Lubin, A. Goldstein, 2009, PloS one.

Lower Risk of Lung Cancer after Multiple Pneumonia Diagnoses

S. Wacholder, J. Lubin, A. Goldstein, 2010, Cancer Epidemiology, Biomarkers & Prevention.

Environment And Genetics in Lung cancer Etiology (EAGLE) study: An integrative population-based case-control study of lung cancer

S. Wacholder, M. Tucker, J. Lubin, 2008, BMC public health.

T. Lam, M. Spitz, A. Pesatori, 2014, Molecular carcinogenesis.

Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma

X. Hua, Jianxin Shi, S. Chanock, 2014, Nature Genetics.

Germline mutations in Protection of Telomeres 1 in two families with Hodgkin lymphoma

S. Chanock, M. Tucker, A. Goldstein, 2018, British journal of haematology.

Cerebrospinal fluid proteomics implicates the granin family in Parkinson’s disease

S. Sardi, L. Shihabuddin, M. Lane, 2020, Scientific Reports.

A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma.

K. Stefánsson, M. Thun, J. Chang-Claude, 2011, American journal of human genetics.

A Gene Expression Signature from Peripheral Whole Blood for Stage I Lung Adenocarcinoma

Nan Hu, Maria Teresa Landi, Neil E Caporaso, 2011, Cancer Prevention Research.

Whole exome sequencing in families with CLL detects a variant in Integrin β 2 associated with disease susceptibility.

G. Marti, S. Chanock, M. Yeager, 2016, Blood.

Epidemiologic Research of Rare Cancers: Trends, Resources, and Challenges

E. Gillanders, T. Lam, A. Freedman, 2021, Cancer Epidemiology, Biomarkers & Prevention.

P. Meltzer, M. García-Closas, M. Sherman, 2014, Breast Cancer Research.

Whole‐exome sequencing of nevoid basal cell carcinoma syndrome families and review of Human Gene Mutation Database PTCH1 mutation data

A. Goldstein, L. Mirabello, K. Jones, 2018, Molecular genetics & genomic medicine.

Cerebrospinal fluid proteomics implicates the granin family in Parkinson’s disease

S. Sardi, L. Shihabuddin, M. Lane, 2020, Scientific Reports.

Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma

Jianxin Shi, Florence Demenais, Maria Teresa Landi, 2014, Nature Genetics.

A Systematic Literature Review of Whole Exome and Genome Sequencing Population Studies of Genetic Susceptibility to Cancer

Leah E. Mechanic, E. Gillanders, T. Lam, 2020, Cancer Epidemiology, Biomarkers & Prevention.

Rare germline variants in known melanoma susceptibility genes in familial melanoma

S. Chanock, Jiali Han, M. Yeager, 2017, Human molecular genetics.

Inherited variation at chromosome 12p13.33, including RAD52, influences the risk of squamous cell lung carcinoma.

Jianxin Shi, M. Thun, S. Chanock, 2012, Cancer discovery.

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

S. Chanock, H. Olsson, M. Yeager, 2016, Human Genetics.

Inherited polymorphisms in the RNA-mediated interference machinery affect microRNA expression and lung cancer survival

F. Marincola, L. Burdette, A. Bergen, 2010, British Journal of Cancer.

Characterization of T gene sequence variants and germline duplications in familial and sporadic chordoma

Jianxin Shi, S. Chanock, M. Yeager, 2014, Human Genetics.

ALS-linked FUS exerts a gain of toxic function involving aberrant p38 MAPK activation

D. A. Bosco, J. Landers, C. Fallini, 2017, Scientific Reports.

Identifying, Targeting, and Exploiting a Common Misfolded, Toxic Conformation of SOD1 in ALS: A Dissertation

M. Rotunno, Melissa Rotunno, 2015 .

Pathway analysis of breast cancer genome-wide association study highlights three pathways and one canonical signaling cascade.

Peter Kraft, Nilanjan Chatterjee, Jonine D Figueroa, 2010, Cancer research.

GPC5 rs2352028 variant and risk of lung cancer in never smokers.

D. Gudbjartsson, T. Thorgeirsson, K. Stefánsson, 2010, The Lancet. Oncology.

MicroRNA Expression Differentiates Histology and Predicts Survival of Lung Cancer

Yingdong Zhao, Neil E. Caporaso, Maria Teresa Landi, 2010, Clinical Cancer Research.

Phase I Metabolic Genes and Risk of Lung Cancer: Multiple Polymorphisms and mRNA Expression

Nilanjan Chatterjee, Neil E. Caporaso, Maria Teresa Landi, 2009, PloS one.

Detectable clonal mosaicism and its relationship to aging and cancer

William Wheeler, Nan Hu, Peter Kraft, 2012, Nature Genetics.

Global Changes in Gene Expression of Barrett's Esophagus Compared to Normal Squamous Esophagus and Gastric Cardia Tissues

N. Hu, C. Abnet, P. Taylor, 2014, PloS one.

Lung cancer prognosis before and after recurrence in a population-based setting.

M. Gail, S. Wacholder, M. Tucker, 2015, Journal of the National Cancer Institute.

Assessment of Human Papillomavirus in Lung Tumor Tissue

S. Wacholder, A. Goldstein, P. Taylor, 2011, Journal of the National Cancer Institute.

Whole exome sequencing in families at high risk for Hodgkin lymphoma: identification of a predisposing mutation in the KDR gene

S. Chanock, M. Yeager, M. Tucker, 2016, Haematologica.

On the application, reporting, and sharing of in silico simulations for genetic studies

Bo Peng, Naoko I Simonds, Huann-Sheng Chen, 2020, Genetic epidemiology.

Anti-SOD1 Nanobodies That Stabilize Misfolded SOD1 Proteins Also Promote Neurite Outgrowth in Mutant SOD1 Human Neurons

D. A. Bosco, D. Golebiowski, M. Sena-Esteves, 2022, International journal of molecular sciences.

Epstein–Barr virus microRNAs and lung cancer

F. Marincola, M. Gulley, A. Goldstein, 2011, British Journal of Cancer.

Constitutional promoter methylation and risk of familial melanoma

M. Tucker, A. Goldstein, R. Pfeiffer, 2014, Epigenetics.

Evaluation of normalization methods for two-channel microRNA microarrays

F. Marincola, L. McShane, E. Wang, 2010, Journal of Translational Medicine.

Glucosylceramide in cerebrospinal fluid of patients with GBA-associated and idiopathic Parkinson’s disease enrolled in PPMI

J. Locascio, Ganqiang Liu, S. Sardi, 2021, NPJ Parkinson's disease.

Facilitating cancer systems epidemiology research

Leah E. Mechanic, E. Gillanders, L. Mechanic, 2021, PloS one.

Glucosylceramide in cerebrospinal fluid of patients with GBA-associated and idiopathic Parkinson’s disease enrolled in PPMI

J. Locascio, Ganqiang Liu, S. Sardi, 2021, npj Parkinson's Disease.

Dietary quercetin, quercetin-gene interaction, metabolic gene expression in lung tissue and lung cancer risk.

S. Chanock, T. Lam, S. Wacholder, 2010, Carcinogenesis.

Identification of a Misfolded Region in Superoxide Dismutase 1 That Is Exposed in Amyotrophic Lateral Sclerosis*

Jared R. Auclair, D. A. Bosco, S. Shaffer, 2014, The Journal of Biological Chemistry.

Constitutive mitochondrial DNA copy number in peripheral blood of melanoma families with and without CDKN2A mutations.

M. Tucker, A. Goldstein, J. Yuenger, 2014, Journal of carcinogenesis & mutagenesis.

Genetic Simulation Resources and the GSR Certification Program

Bo Peng, John Clarke, Huann-Sheng Chen, 2018, Bioinform..

Urine Proteomics for Noninvasive Monitoring of Biomarkers in Bronchopulmonary Dysplasia

J. Steen, H. Steen, R. Parad, 2022, Neonatology.

Characterization of T gene sequence variants and germline duplications in familial and sporadic chordoma

Jianxin Shi, S. Chanock, M. Yeager, 2014, Human Genetics.

Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in the Childhood Cancer Survivor Study.

Stephen W. Hartley, S. Chanock, D. Karyadi, 2021, JNCI cancer spectrum.

Prevalence of Americans reporting a family history of cancer indicative of increased cancer risk: Estimates from the 2015 National Health Interview Survey.

S. Dai, M. Rotunno, L. Peipins, 2022, Preventive medicine.

Table 2 . ORs and 95 % CIs for associations of lung cancer with pneumonia and tuberculosis diagnosed at least 1 y prior to entry into the EAGLE case-control study , both overall and stratified by smoking status

S. Wacholder, J. Lubin, A. Goldstein, 2010 .

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

S. Puig, S. Chanock, M. Greene, 2018, Genome Medicine.

Discovery of novel predisposing coding and noncoding variants in familial Hodgkin lymphoma.

Jia Liu, M. Tucker, E. Rampersaud, 2022, Blood.

Evaluation of normalization methods for two-channel microRNA microarrays

F. Marincola, L. McShane, E. Wang, 2010, Journal of Translational Medicine.