Physician
Medical Genetics
Dr. Noralane M. Lindor, MD
|
|
Give Review
Noralane Lindor works in the field of Medical Genetics. She went to medical school at Mayo Medical School. Mayo Medical School has a rank of 27 in research and a 42 in primary care Noralane Lindor is also a published doctor. She has 101 publication published. The most recent publication is: Knowledge and Uptake of Genetic Counseling and Colonoscopic Screening Among Individuals at Increased Risk for Lynch Syndrome and their Endoscopists from the Family Hea...
Publications
- Comparison of Prediction Models for Lynch Syndrome Among Individuals With Colorectal Cancer.
- Knowledge and Uptake of Genetic Counseling and Colonoscopic Screening Among Individuals at Increased Risk for Lynch Syndrome and their Endoscopists from the Family Hea...
- A genome-wide association study for colorectal cancer identifies a risk locus in 14q23.1.
- Mutation Spectrum and Risk of Colorectal Cancer in African American Families with Lynch Syndrome.
- American Society of Clinical Oncology Policy Statement Update: Genetic and Genomic Testing for Cancer Susceptibility.
- Preferences Regarding Return of Genomic Results to Relatives of Research Participants, Including after Participant Death: Empirical Results from a Cancer Biobank.
- Returning a Research Participant's Genomic Results to Relatives: Analysis and Recommendations.
- Association of aspirin and NSAID use with risk of colorectal cancer according to genetic variants.
- Public Perceptions of Disease Severity but Not Actionability Correlate with Interest in Receiving Genomic Results: Nonalignment with Current Trends in Practice.
- Association of the colorectal CpG island methylator phenotype with molecular features, risk factors, and family history.
- Genetic counselors' practices and confidence regarding variant of uncertain significance results and reclassification from BRCA testing.
- A preliminary investigation of genetic counselors' information needs when receiving a variant of uncertain significance result: a mixed methods study.
- A novel colorectal cancer risk locus at 4q32.2 identified from an international genome-wide association study.
- Genetic variation in prostaglandin synthesis and related pathways, NSAID use, and colorectal cancer risk in the Colon Cancer Family Registry.
- Characterisation of Familial Colorectal Cancer Type X, Lynch syndrome, and non-familial 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 ...
- American Society of Clinical Oncology Expert Statement: Collection and Use of a Cancer Family History for Oncology Providers.
- Appreciating the broad clinical features of SMAD4 mutation carriers: a multicenter chart review.
- A randomized trial to increase colonoscopy screening in members of high risk families in the Colorectal Cancer Family Registry and Cancer Genetics Network.
- Fragile X syndrome due to a missense mutation.
- Communication of genetic test results to family and health-care providers following disclosure of research results.
- Genetic Variation in the Inflammation and Innate Immunity Pathways and Colorectal Cancer Risk.
- Pleiotropic effects of genetic risk variants for other cancers on colorectal cancer risk: PAGE, GECCO and CCFR consortia.
- Colon and Rectal Cancer Survival by Tumor Location and Microsatellite Instability: The Colon Cancer Family Registry.
- Identification of Novel Variants in Colorectal Cancer Families by High-Throughput Exome Sequencing.
- Preserving personal autonomy in a genomic testing era.
- BRCA1/2 Sequence Variants of Uncertain Significance: A Primer for Providers to Assist in Discussions and in Medical Management.
- Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk.
- KRAS-mutation status in relation to colorectal cancer survival: the joint impact of correlated tumour markers.
- Comparison of the clinical prediction model PREMM(1,2,6) and molecular testing for the systematic identification of Lynch syndrome in colorectal cancer.
- Integrated analysis of genome-wide copy number alterations and gene expression in microsatellite stable, CpG island methylator phenotype-negative colon cancer.
- A classification model for BRCA2 DNA binding domain missense variants based on homology-directed repair activity.
- Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-wide Meta-analysis.
- Chronic tibial nonunion in a Rothmund-Thomson syndrome patient.
- Hereditary hemorrhagic telangiectasia and risks for adverse pregnancy outcomes.
- Colorectal Cancer Linkage on Chromosomes 4q21, 8q13, 12q24, and 15q22.
- Is colorectal surveillance indicated in patients with pten mutations?
- The Germline MLH1 K618A Variant and Susceptibility to Lynch Syndrome-Associated Tumors.
- Increased Cancer Risks in Myotonic Dystrophy.
- A population-based study of prevalence and adherence trends in average risk colorectal cancer screening, 1997-2008.
- A review of a multifactorial probability based model for classification of BRCA1 and BRCA2 variants of uncertain significance (VUS).
- Prophylactic and Therapeutic Mastectomy in BRCA Mutation Carriers: Can the Nipple Be Preserved?
- Pancreatic Cancer and a Novel MSH2 Germline Alteration.
- Hereditary hyperferritinemia-cataract syndrome in two large multigenerational American families.
- Meta-analysis of new genome-wide association studies of colorectal cancer risk.
- Determining the frequency of de novo germline mutations in DNA mismatch repair genes.
- Quality assessment and correlation of microsatellite instability and immunohistochemical markers among population- and clinic-based colorectal tumors results from the ...
- Body mass index in early adulthood and endometrial cancer risk for mismatch repair gene mutation carriers.
- Lynch Syndrome and MYH-Associated Polyposis: Review and Testing Strategy.
- A Novel Mutation of LAMB2 in a Multigenerational Mennonite Family Reveals a New Phenotypic Variant of Pierson Syndrome.
- Frequency of deletions of EPCAM (TACSTD1) in MSH2-associated lynch syndrome cases.
- The PREMM(1,2,6) model predicts risk of MLH1, MSH2, and MSH6 germline mutations based on cancer history.
- Metachronous colorectal cancer risk for mismatch repair gene mutation carriers: the advantage of more extensive colon surgery.
- Cancer risks for monoallelic MUTYH mutation carriers with a family history of colorectal cancer.
- Risk of endometrial cancer for women diagnosed with HNPCC-related colorectal carcinoma.
- Identification and Management of Women With BRCA Mutations or Hereditary Predisposition for Breast and Ovarian Cancer.
- Lower gastrointestinal tract cancer predisposition syndromes.
- Prevalence of Alterations in DNA Mismatch Repair Genes in Patients With Young-Onset Colorectal Cancer.
- Parent of origin effects on age at colorectal cancer diagnosis.
- A case of Down syndrome with mirror-image duplication of chromosome 21.
- Hereditary disorders of connective tissue: a guide to the emerging differential diagnosis.
- Lynch syndrome-associated breast cancers: clinicopathologic characteristics of a case series from the colon cancer family registry.
- Germline TGF-beta receptor mutations and skeletal fragility: a report on two patients with Loeys-Dietz syndrome.
- Smoking and colorectal cancer in Lynch syndrome: results from the Colon Cancer Family Registry and the University of Texas M.D. Anderson Cancer Center.
- Alpha-1-antitrypsin deficiency and smoking as risk factors for mismatch repair deficient colorectal cancer: a study from the colon cancer family registry.
- Left ventricular noncompaction cardiomyopathy: what do we know?
- Familial colorectal cancer type X: the other half of hereditary nonpolyposis colon cancer syndrome.
- LAPS syndrome and Myhre syndrome: two disorders or one?
- Slender bone dysplasia (gracile).
- Commentary: Making a case for surveillance colonoscopy in Lynch Syndrome.
- Germline duplication of chromosomes 10p15.3 and Yp11.32 in a man with learning disability and early onset cutaneous malignant melanoma.
- The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations.
- Premutations in the FMR1 gene are uncommon in men undergoing genetic testing for spinocerebellar ataxia.
- Ready reference to common segmental aneusomies by syndromic names, major features and chromosomal locations.
- Colorectal cancer risks in relatives of young-onset cases: is risk the same across all first-degree relatives?
- Higher frequency of diploidy in young-onset microsatellite-stable colorectal cancer.
- Multiple primary tumors associated with chromosome 9p deletion.
- Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic review.
- Genetic testing in an ethnically diverse cohort of high-risk women: a comparative analysis of BRCA1 and BRCA2 mutations in American families of European and African an...
- Isolated loss of PMS2 expression in colorectal cancers: frequency, patient age, and familial aggregation.
- The spectrum, management and clinical outcome of Ehlers-Danlos syndrome type IV: a 30-year experience.
- Tenascin-X deficiency in autosomal recessive Ehlers-Danlos syndrome.
- Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type X.
- Heterozygous Niemann-Pick disease type C presenting with tremor.
- Nonmosaic smallest duplication of 12q24.31-qter: the first reported case.
- MYH mutations in patients with attenuated and classic polyposis and with young-onset colorectal cancer without polyps.
- Recognition of genetic syndromes in families with suspected hereditary colon cancer syndromes.
- LEOPARD syndrome: a new polyaneurysm association and an update on the molecular genetics of the disease.
- Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability.
- Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients.
- Pelvic primitive neuroectodermal tumor associated with a cluster of small round cell tumors: case report and review of current literature.
- Chronic intestinal pseudoobstruction associated with altered interstitial cells of cajal networks.
- Unilateral Lisch nodules in the absence of other features of neurofibromatosis 1.
- Frequency of loss of hMLH1 expression in colorectal carcinoma increases with advancing age.
- Bilateral hip dislocation and pubic diastasis in familial nail-patella syndrome.
- Confirmation of existence of a new syndrome: LAPS syndrome.
- Immunohistochemistry versus microsatellite instability testing in phenotyping colorectal tumors.
- Colorectal cancer and self-reported tooth agenesis.
- Genetic Variations in SMAD7 Are Associated with Colorectal Cancer Risk in the Colon Cancer Family Registry.
- Clinical Characteristics of Ovarian Cancer Classified by BRCA1, BRCA2, and RAD51C Status.
Schools
Mayo Medical School
Wake Forest University Baptist Med Center
Doctors Specialties
- Geriatric Medicine
- Medical Genetics
Accepted Insurances
Education
-
Wake Forest University -
Mayo Medical School
Hospital
-
Mayo Clinic - Phoenix/Scottsdale, Arizona
Helpful Reviews
Similar Doctors
|
|
Dr. Sarah J. Crane, MD
 This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Ericka E. Tung, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Marcelo P. Vargas, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Aimee C. Yu-Ballard, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Shahzad K. Siddique, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Neel B. Shah, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Jay W. Ellison, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Pavel N. Pichurin, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Mohammad Albaba, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Neha S. Gupta, MD |
|
|
Dr. Xiangling Wang, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Hua Wang, MD |