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Noralane M. Lindor

Noralane M. Lindor

D-Index & Metrics

Medicine

D-Index
115
Citations
48416
World Ranking
4552
National Ranking
2473

Overview

Noralane M. Lindor is affiliated with the Mayo Clinic in the United States and has a significant body of work focused on the genetics and epidemiology of colorectal cancer. Their research spans multiple fields within medicine and molecular biology, with a particular emphasis on cancer research and pathology.

The scientist's main fields of study include:

  • Medicine
  • Biochemistry, Genetics and Molecular Biology

Subfields of study reflect a concentration on disease mechanisms and genetic factors associated with cancer:

  • Pathology and Forensic Medicine
  • Genetics
  • Oncology
  • Cancer Research
  • Molecular Biology

The main topics covered in their work are:

  • Genetic factors in colorectal cancer
  • Colorectal Cancer Screening and Detection
  • Colorectal Cancer Treatments and Studies
  • BRCA gene mutations in cancer
  • Genetic Associations and Epidemiology
  • Cancer Genomics and Diagnostics
  • Genomics and Rare Diseases

Frequent coauthors collaborating with Noralane M. Lindor include:

  • Polly A. Newcomb
  • Mark A. Jenkins
  • Loïc Le Marchand
  • Steven Gallinger
  • John L. Hopper

The scientist has published extensively in various venues, with the most frequent publication sources being:

  • UNC Libraries
  • Genetics in Medicine
  • Cancer Epidemiology Biomarkers & Prevention
  • Gastroenterology
  • bioRxiv (Cold Spring Harbor Laboratory)

Significant recent papers highlighting aspects of their research include:

  • "Physical activity and risks of breast and colorectal cancer: a Mendelian randomisation analysis," 2020, Nature Communications
  • "Genome-wide Modeling of Polygenic Risk Score in Colorectal Cancer Risk," 2020, The American Journal of Human Genetics
  • "Mortality 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," 2023, EClinicalMedicine
  • "Genetic architectures of proximal and distal colorectal cancer are partly distinct," 2021, Gut
  • "Circulating bilirubin levels and risk of colorectal cancer: serological and Mendelian randomization analyses," 2020, BMC Medicine

Best Publications

  • Revised Bethesda Guidelines for Hereditary Nonpolyposis Colorectal Cancer (Lynch Syndrome) and Microsatellite Instability

    Asad Umar;C. Richard Boland;Jonathan P. Terdiman;Sapna Syngal

  • Immunohistochemistry Versus Microsatellite Instability Testing in Phenotyping Colorectal Tumors

    Noralane M. Lindor;Lawrence J. Burgart;Olga Leontovich;Richard M. Goldberg

  • Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic review.

    Noralane M. Lindor;Gloria M. Petersen;Donald W. Hadley;Anita Y. Kinney

  • American Society of Clinical Oncology Policy Statement Update: Genetic and Genomic Testing for Cancer Susceptibility

    Mark E. Robson;Mark E. Robson;Angela R. Bradbury;Banu K Arun;Susan M. Domchek

  • Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome

    Saori Kitao;Akira Shimamoto;Makoto Goto;Robert W. Miller

  • Pathology of Breast and Ovarian Cancers among BRCA1 and BRCA2 Mutation Carriers: Results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA).

    Nasim Mavaddat;Daniel Barrowdale;Irene L. Andrulis;Susan M. Domchek

  • Hereditary diffuse gastric cancer syndrome: CDH1 mutations and beyond

    Samantha Hansford;Pardeep Kaurah;Hector Li-Chang;Michelle Woo

  • Lower Cancer Incidence in Amsterdam-I Criteria Families Without Mismatch Repair Deficiency: Familial Colorectal Cancer Type X

    Noralane M. Lindor;Kari Rabe;Gloria M. Petersen;Robert Haile

  • Altered Expression of hMSH2 and hMLH1 in Tumors with Microsatellite Instability and Genetic Alterations in Mismatch Repair Genes

    Stephen N. Thibodeau;Amy J. French;Patrick C. Roche;Julie M. Cunningham

  • The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations

    Leigha Senter;Mark Clendenning;Kaisa Sotamaa;Heather Hampel

  • Identification of Lynch syndrome among patients with colorectal cancer

    Leticia Moreira;Francesc Balaguer;Noralane Lindor;Albert De La Chapelle

  • Increased Risk for Cancer in Patients with the Peutz-Jeghers Syndrome

    Lisa A. Boardman;Stephen N. Thibodeau;Daniel J. Schaid;Noralane M. Lindor

  • Mutations in CD2BP1 disrupt binding to PTP PEST and are responsible for PAPA syndrome, an autoinflammatory disorder

    Carol A. Wise;Joseph D. Gillum;Christine E. Seidman;Noralane M. Lindor

  • Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer.

    Timothy R. Rebbeck;Nandita Mitra;Fei Wan;Olga M. Sinilnikova

  • Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

    Mev Dominguez-Valentin;Julian R. Sampson;Toni T. Seppälä;Sanne W. ten Broeke

  • Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database

    Bryony A Thompson;Bryony A Thompson;Amanda B Spurdle;John-Paul Plazzer;Marc S Greenblatt

  • Discovery of common and rare genetic risk variants for colorectal cancer

    Jeroen R. Huyghe;Stephanie A. Bien;Tabitha A. Harrison;Hyun Min Kang

  • Microduplication 22q11.2, an Emerging Syndrome: Clinical, Cytogenetic, and Molecular Analysis of Thirteen Patients

    Regina E. Ensenauer;Adewale Adeyinka;Heather C. Flynn;Virginia V. Michels

  • The spectrum, management and clinical outcome of Ehlers-Danlos syndrome type IV: a 30-year experience.

    Gustavo S. Oderich;Jean M. Panneton;Thomas C. Bower;Noralane M. Lindor

  • Prediction of Germline Mutations and Cancer Risk in the Lynch Syndrome

    Sining Chen;Wenyi Wang;Shing Lee;Khedoudja Nafa

Frequent Co-Authors

Polly A. Newcomb
Polly A. Newcomb Fred Hutchinson Cancer Research Center
John L. Hopper
John L. Hopper University of Melbourne
Mark A. Jenkins
Mark A. Jenkins University of Melbourne
John D. Potter
John D. Potter Massey University
Daniel D. Buchanan
Daniel D. Buchanan University of Melbourne
Robert W. Haile
Robert W. Haile Stanford University
Steven Gallinger
Steven Gallinger Ontario Institute for Cancer Research
Loic Le Marchand
Loic Le Marchand University of Hawaii at Manoa
Graham G. Giles
Graham G. Giles University of Melbourne

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