List of works - Noralane Lindor

Identification and Management of Women With BRCA Mutations or Hereditary Predisposition for Breast and Ovarian Cancer

scientific article

American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers

scientific article

Interplay between BRCA1 and RHAMM regulates epithelial apicobasal polarization and may influence risk of breast cancer

scientific article

A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer

scientific article published on 20 May 2015

Germline E-cadherin gene mutations: is prophylactic total gastrectomy indicated?

scientific article

Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer

scientific article

A multifactorial likelihood model for MMR gene variant classification incorporating probabilities based on sequence bioinformatics and tumor characteristics: a report from the Colon Cancer Family Registry

scientific article published on 11 October 2012

A classification model for BRCA2 DNA binding domain missense variants based on homology-directed repair activity

scientific article published on 29 October 2012

Mutational Spectrum in a Worldwide Study of 29,700 Families with BRCA1 or BRCA2 Mutations

scientific article published on 15 February 2018

RECQL4 is essential for the transport of p53 to mitochondria in normal human cells in the absence of exogenous stress.

scientific article

Risk of colorectal cancer for carriers of mutations in MUTYH, with and without a family history of cancer

scientific article published on 17 January 2014

Clinical characteristics of ovarian cancer classified by BRCA1, BRCA2, and RAD51C status

scientific article

Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2.

scientific article published on 2 November 2011

Molecular Biomarkers for the Evaluation of Colorectal Cancer: Guideline From the American Society for Clinical Pathology, College of American Pathologists, Association for Molecular Pathology, and the American Society of Clinical Oncology.

scientific article

Risk of breast cancer in Lynch syndrome: a systematic review.

scientific article published on 19 March 2013

Lynch syndrome-associated breast cancers: clinicopathologic characteristics of a case series from the colon cancer family registry

scientific article published on 9 March 2010

Gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS): a new autosomal dominant syndrome

scientific article

Conversion analysis for mutation detection in MLH1 and MSH2 in patients with colorectal cancer

scientific article

A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age.

scientific article

Quality assessment and correlation of microsatellite instability and immunohistochemical markers among population- and clinic-based colorectal tumors results from the Colon Cancer Family Registry

scientific article

Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.

scientific article

Trans-ethnic genome-wide association study of colorectal cancer identifies a new susceptibility locus in VTI1A.

scientific article

Identification of constitutional MLH1 epimutations and promoter variants in colorectal cancer patients from the Colon Cancer Family Registry

scientific article published on 09 August 2012

Identification and Validation of an Anthracycline/Cyclophosphamide–Based Chemotherapy Response Assay in Breast Cancer

scientific article published on January 1, 2014

Risk of metachronous colon cancer following surgery for rectal cancer in mismatch repair gene mutation carriers

scientific article

Risks of colorectal and other cancers after endometrial cancer for women with Lynch syndrome

scientific article published on 5 February 2013

Association of the colorectal CpG island methylator phenotype with molecular features, risk factors, and family history

scientific article

BRCA1/2 Sequence Variants of Uncertain Significance: A Primer for Providers to Assist in Discussions and in Medical Management

scientific article published on April 24, 2013

Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers

scientific article

Refined histopathological predictors of BRCA1 and BRCA2 mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia

scientific article

Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer

scientific article published on 27 April 2016

Implementing individualized medicine into the medical practice

scientific article published on 10 March 2014

Tumor suppressor p53 represses transcription of RECQ4 helicase

scientific article

Increased cancer risks in myotonic dystrophy.

scientific article

Cancer risks for monoallelic MUTYH mutation carriers with a family history of colorectal cancer

scientific article

Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant

scientific article

Discovery of common and rare genetic risk variants for colorectal cancer

scientific article published on 03 December 2018

Frequency of deletions of EPCAM (TACSTD1) in MSH2-associated Lynch syndrome cases

scientific article

Familial colorectal cancer type X: the other half of hereditary nonpolyposis colon cancer syndrome

scientific article

Chronic intestinal pseudoobstruction associated with altered interstitial cells of cajal networks

scientific article published on 01 April 2003

Outcome of Whole Exome Sequencing for Diagnostic Odyssey Cases of an Individualized Medicine Clinic: The Mayo Clinic Experience

scientific article published on March 2016

Higher risk of mismatch repair-deficient colorectal cancer in alpha(1)-antitrypsin deficiency carriers and cigarette smokers

scientific article published on 01 December 2000

Prevalence of Alterations in DNA Mismatch Repair Genes in Patients With Young-Onset Colorectal Cancer

scientific article published on November 5, 2010

DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers

scientific article

Alpha1-antitrypsin deficiency allele carriers among lung cancer patients

scientific article published on 01 May 1999

Returning a Research Participant's Genomic Results to Relatives: Analysis and Recommendations

scientific article

Desmoid tumors -- a characterization of patients seen at Mayo Clinic 1976-1999.

scientific article published in January 2006

GermlineTP53Mutations in Patients With Early-Onset Colorectal Cancer in the Colon Cancer Family Registry

scientific article published on May 1, 2015

Colon and rectal cancer survival by tumor location and microsatellite instability: the Colon Cancer Family Registry.

scientific article published on August 2013

Genetic testing in the diagnosis and management of multiple endocrine neoplasia type II.

scientific article published on January 1995

List of works by Noralane Lindor

Identification and Management of Women With BRCA Mutations or Hereditary Predisposition for Breast and Ovarian Cancer

American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers

Interplay between BRCA1 and RHAMM regulates epithelial apicobasal polarization and may influence risk of breast cancer

A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer

Germline E-cadherin gene mutations: is prophylactic total gastrectomy indicated?

Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer

A multifactorial likelihood model for MMR gene variant classification incorporating probabilities based on sequence bioinformatics and tumor characteristics: a report from the Colon Cancer Family Registry

A classification model for BRCA2 DNA binding domain missense variants based on homology-directed repair activity

Mutational Spectrum in a Worldwide Study of 29,700 Families with BRCA1 or BRCA2 Mutations

RECQL4 is essential for the transport of p53 to mitochondria in normal human cells in the absence of exogenous stress.

Risk of colorectal cancer for carriers of mutations in MUTYH, with and without a family history of cancer

Clinical characteristics of ovarian cancer classified by BRCA1, BRCA2, and RAD51C status

Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2.

Molecular Biomarkers for the Evaluation of Colorectal Cancer: Guideline From the American Society for Clinical Pathology, College of American Pathologists, Association for Molecular Pathology, and the American Society of Clinical Oncology.

Risk of breast cancer in Lynch syndrome: a systematic review.

Lynch syndrome-associated breast cancers: clinicopathologic characteristics of a case series from the colon cancer family registry

Gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS): a new autosomal dominant syndrome

Conversion analysis for mutation detection in MLH1 and MSH2 in patients with colorectal cancer

A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age.

Quality assessment and correlation of microsatellite instability and immunohistochemical markers among population- and clinic-based colorectal tumors results from the Colon Cancer Family Registry

Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.

Trans-ethnic genome-wide association study of colorectal cancer identifies a new susceptibility locus in VTI1A.

Identification of constitutional MLH1 epimutations and promoter variants in colorectal cancer patients from the Colon Cancer Family Registry

Identification and Validation of an Anthracycline/Cyclophosphamide–Based Chemotherapy Response Assay in Breast Cancer

Risk of metachronous colon cancer following surgery for rectal cancer in mismatch repair gene mutation carriers

Risks of colorectal and other cancers after endometrial cancer for women with Lynch syndrome

Association of the colorectal CpG island methylator phenotype with molecular features, risk factors, and family history

BRCA1/2 Sequence Variants of Uncertain Significance: A Primer for Providers to Assist in Discussions and in Medical Management

Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers

Refined histopathological predictors of BRCA1 and BRCA2 mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia

Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer

Implementing individualized medicine into the medical practice

Tumor suppressor p53 represses transcription of RECQ4 helicase

Increased cancer risks in myotonic dystrophy.

Cancer risks for monoallelic MUTYH mutation carriers with a family history of colorectal cancer

Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant

Discovery of common and rare genetic risk variants for colorectal cancer

Frequency of deletions of EPCAM (TACSTD1) in MSH2-associated Lynch syndrome cases

Familial colorectal cancer type X: the other half of hereditary nonpolyposis colon cancer syndrome

Chronic intestinal pseudoobstruction associated with altered interstitial cells of cajal networks

Outcome of Whole Exome Sequencing for Diagnostic Odyssey Cases of an Individualized Medicine Clinic: The Mayo Clinic Experience

Higher risk of mismatch repair-deficient colorectal cancer in alpha(1)-antitrypsin deficiency carriers and cigarette smokers

Prevalence of Alterations in DNA Mismatch Repair Genes in Patients With Young-Onset Colorectal Cancer

DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers

Alpha1-antitrypsin deficiency allele carriers among lung cancer patients

Returning a Research Participant's Genomic Results to Relatives: Analysis and Recommendations

Desmoid tumors -- a characterization of patients seen at Mayo Clinic 1976-1999.

GermlineTP53Mutations in Patients With Early-Onset Colorectal Cancer in the Colon Cancer Family Registry

Colon and rectal cancer survival by tumor location and microsatellite instability: the Colon Cancer Family Registry.

Genetic testing in the diagnosis and management of multiple endocrine neoplasia type II.