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Author Details

Noralane M Lindor
Mayo Clinic
1992
380
82
PMIDPaper TitleJournal TitlePublished Year
36849229Update of penetrance estimates in Birt-Hogg-Dubé syndrome.J Med Genet2023
37181409Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database.EClinicalMedicine2023
36849229Update of penetrance estimates in Birt-Hogg-Dubé syndrome.J Med Genet2023
37181409Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database.EClinicalMedicine2023
35216901The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network.Genet Med2022
36344807Interactions between folate intake and genetic predictors of gene expression levels associated with colorectal cancer risk.Sci Rep2022
35616648Cancer Risk C (CR-C), a functional genomics test is a sensitive and rapid test for germline mismatch repair deficiency.Genet Med2022
35985511Quantitative Pathologic Analysis of Digitized Images of Colorectal Carcinoma Improves Prediction of Recurrence-Free Survival.Gastroenterology2022
35216901The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network.Genet Med2022
35616648Cancer Risk C (CR-C), a functional genomics test is a sensitive and rapid test for germline mismatch repair deficiency.Genet Med2022
35985511Quantitative Pathologic Analysis of Digitized Images of Colorectal Carcinoma Improves Prediction of Recurrence-Free Survival.Gastroenterology2022
36344807Interactions between folate intake and genetic predictors of gene expression levels associated with colorectal cancer risk.Sci Rep2022
33318029A Combined Proteomics and Mendelian Randomization Approach to Investigate the Effects of Aspirin-Targeted Proteins on Colorectal Cancer.Cancer Epidemiol Biomarkers Prev2021
33592611Experiences of Latino Participants Receiving Neutral Genomic Screening Results: A Qualitative Study.Public Health Genomics2021
33743481Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report.Eur J Cancer2021
33632709Genetic architectures of proximal and distal colorectal cancer are partly distinct.Gut2021
33524116Associations of Height With the Risks of Colorectal and Endometrial Cancer in Persons With Lynch Syndrome.Am J Epidemiol2021
33729042Integrating Genomic Screening into Primary Care: Provider Experiences Caring for Latino Patients at a Community-Based Health Center.J Prim Care Community Health2021
33667396Response to Li and Hopper.Am J Hum Genet2021
34203177No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in <i>MLH1</i> and <i>MSH2</i>: A Prospective Lynch Syndrome Database Study.J Clin Med2021
33824501Penetrance and outcomes at 1-year following return of actionable variants identified by genome sequencing.Genet Med2021
33653810Causal Effects of Lifetime Smoking on Breast and Colorectal Cancer Risk: Mendelian Randomization Study.Cancer Epidemiol Biomarkers Prev2021
33500569Increasing access to individualized medicine: a matched-cohort study examining Latino participant experiences of genomic screening.Genet Med2021
33318029A Combined Proteomics and Mendelian Randomization Approach to Investigate the Effects of Aspirin-Targeted Proteins on Colorectal Cancer.Cancer Epidemiol Biomarkers Prev2021
33257847Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report.Genet Med2021
34836419Salicylic Acid and Risk of Colorectal Cancer: A Two-Sample Mendelian Randomization Study.Nutrients2021
33743481Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report.Eur J Cancer2021
33653810Causal Effects of Lifetime Smoking on Breast and Colorectal Cancer Risk: Mendelian Randomization Study.Cancer Epidemiol Biomarkers Prev2021
33824501Penetrance and outcomes at 1-year following return of actionable variants identified by genome sequencing.Genet Med2021
33592611Experiences of Latino Participants Receiving Neutral Genomic Screening Results: A Qualitative Study.Public Health Genomics2021
33667396Response to Li and Hopper.Am J Hum Genet2021
33729042Integrating Genomic Screening into Primary Care: Provider Experiences Caring for Latino Patients at a Community-Based Health Center.J Prim Care Community Health2021
33500569Increasing access to individualized medicine: a matched-cohort study examining Latino participant experiences of genomic screening.Genet Med2021
33632709Genetic architectures of proximal and distal colorectal cancer are partly distinct.Gut2021
33524116Associations of Height With the Risks of Colorectal and Endometrial Cancer in Persons With Lynch Syndrome.Am J Epidemiol2021
34836419Salicylic Acid and Risk of Colorectal Cancer: A Two-Sample Mendelian Randomization Study.Nutrients2021
34203177No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in <i>MLH1</i> and <i>MSH2</i>: A Prospective Lynch Syndrome Database Study.J Clin Med2021
33257847Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report.Genet Med2021
31337882Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database.Genet Med2020
32377377Challenges in returning results in a genomic medicine implementation study: the Return of Actionable Variants Empirical (RAVE) study.NPJ Genom Med2020
32371921Returning genomic results in a Federally Qualified Health Center: the intersection of precision medicine and social determinants of health.Genet Med2020
32307706Potential impact of family history-based screening guidelines on the detection of early-onset colorectal cancer.Cancer2020
32001714Physical activity and risks of breast and colorectal cancer: a Mendelian randomisation analysis.Nat Commun2020
32349224Returning Results in the Genomic Era: Initial Experiences of the eMERGE Network.J Pers Med2020
32107660Do the risks of Lynch syndrome-related cancers depend on the parent of origin of the mutation?Fam Cancer2020
31932410A New Comprehensive Colorectal Cancer Risk Prediction Model Incorporating Family History, Personal Characteristics, and Environmental Factors.Cancer Epidemiol Biomarkers Prev2020
31866242Cumulative Burden of Colorectal Cancer-Associated Genetic Variants Is More Strongly Associated With Early-Onset vs Late-Onset Cancer.Gastroenterology2020
32207560Functional informed genome-wide interaction analysis of body mass index, diabetes and colorectal cancer risk.Cancer Med2020
32651213Exploratory Genome-Wide Interaction Analysis of Nonsteroidal Anti-inflammatory Drugs and Predicted Gene Expression on Colorectal Cancer Risk.Cancer Epidemiol Biomarkers Prev2020
32878631Circulating bilirubin levels and risk of colorectal cancer: serological and Mendelian randomization analyses.BMC Med2020
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Collaborators

Steven Gallinger
Lunenfeld Tanenbaum Research Institute, Mount Sinai Hospital, University of Toronto
Co-authored papers 127
Stephen N Thibodeau
Mayo Clinic
Co-authored papers 118
Loic Le Marchand
Co-authored papers 111
Robert W Haile
Co-authored papers 95
John A Baron
University of North Carolina at Chapel Hill
Co-authored papers 61
Graham G Giles
Co-authored papers 55
Fergus J Couch
Mayo Clinic
Co-authored papers 47
Jenny Chang-Claude
German Cancer Research Center (DKFZ)
Co-authored papers 40
Douglas F Easton
University of Cambridge
Co-authored papers 40
Ulrike Peters
Co-authored papers 36
Andrew T Chan
Massachusetts General Hospital and Harvard Medical School
Co-authored papers 34
Sonja I Berndt
Co-authored papers 34
Georgia Chenevix-Trench
QIMR Berghofer Medical Research Institute
Co-authored papers 33
Susan M Domchek
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Katherine L Nathanson
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Amanda B Spurdle
QIMR Berghofer Medical Research Institute
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Fredrick R Schumacher
Case Comprehensive Cancer Center, Case Western Reserve University School of Medicine
Co-authored papers 31
David E Goldgar
University of Utah
Co-authored papers 30
David V Conti
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Paul D P Pharoah
Center for Cancer Genetic Epidemiology, University of Cambridge
Co-authored papers 29
Sue Healey
QIMR Berghofer Medical Research Institute
Co-authored papers 28
Irene L Andrulis
University of Toronto
Co-authored papers 28
Javier Ben??tez
Instituto de Salud Carlos III
Co-authored papers 27
Ana Osorio
Familial Cancer Clinical Unit, Spanish National Cancer Research Centre
Co-authored papers 26
Paolo Radice
Ospedale Circolo e Fondazione Macchi
Co-authored papers 26
Daniela Seminara
National Cancer Institute, 9609 Medical Center Dr
Co-authored papers 26
Rosalind A Eeles
The Institute of Cancer Research
Co-authored papers 24
Jan Lubinski
Pomeranian Medical University
Co-authored papers 24
Timothy R Rebbeck
Center for Cancer Equity and Engagement, Dana-Farber/Harvard Cancer Center
Co-authored papers 23
Beth Y Karlan
David Geffen School of Medicine, University of California los angeles
Co-authored papers 22
Release 1.2