Familial Colorectal Cancer Type X: the other half of Hereditary Non-Polyposis Colon Cancer Syndrome

Por Lindor, Noralane M
Publicado em 2009

Genetics of colorectal cancer

Por Potter, John D., Lindor, Noralane M.
Publicado em 2009

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

Por Pruthi, Sandhya, Gostout, Bobbie S., Lindor, Noralane M.
Publicado em 2010

Estimating cumulative risks for breast cancer for carriers of variants in uncommon genes

Por Lindor, Noralane M., Hopper, John, Dowty, James
Publicado no Fam Cancer (2016)

Risk of breast cancer in Lynch syndrome: a systematic review

Por Win, Aung Ko, Lindor, Noralane M, Jenkins, Mark A
Publicado em 2013

Birt-Hogg-Dube syndrome presenting as multiple oncocytic parotid tumors

Por Lindor, Noralane M, Kasperbauer, Jan, Lewis, Jean E, Pittelkow, Mark
Publicado em 2012

The Germline MLH1 K618A Variant and Susceptibility to Lynch Syndrome-Associated Tumors

Por Medeiros, Fabiola, Lindor, Noralane M., Couch, Fergus J., Highsmith, W. Edward
Publicado no J Mol Diagn (2012)

Pyogenic Arthritis, Pyoderma Gangrenosum, and Acne Syndrome Maps to Chromosome 15q

Por Yeon, Howard B., Lindor, Noralane M., Seidman, J. G., Seidman, Christine E.
Publicado em 2000

Mutation screening of RAD51C in high-risk breast and ovarian cancer families

Por Lu, Wenping, Wang, Xianshu, Lin, Hongsheng, Lindor, Noralane M., Couch, Fergus J.
Publicado em 2012

Primary appendiceal mucinous adenocarcinoma in two first-degree relatives: case report and review

Por Racek, Adrianne R, Rabe, Kari G, Wick, Myra J, Psychogios, Apostolos, Lindor, Noralane M
Publicado em 2011

Increased Cancer Risks in Myotonic Dystrophy

Por Win, Aung Ko, Perattur, Promilla G., Pulido, Jose S., Pulido, Christine M., Lindor, Noralane M.
Publicado em 2012

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

Por Ward, Robyn L., Dobbins, Timothy, Lindor, Noralane M., Rapkins, Robert W., Hitchins, Megan P.
Publicado em 2013

A preliminary investigation of genetic counselors’ information needs when receiving a variant of uncertain significance result: a mixed methods study

Por Scherr, Courtney L., Lindor, Noralane M., Malo, Teri L., Couch, Fergus J., Vadaparampil, Susan T.
Publicado no Genet Med (2015)

Genetic counselors' practices and confidence regarding variant of uncertain significance results and reclassification from BRCA testing

Por Scherr, Courtney L., Lindor, Noralane M., Malo, Teri L., Couch, Fergus J., Vadaparampil, Susan T.
Publicado no Clin Genet (2015)

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

Por Lindor, Noralane M., Goldgar, David E., Tavtigian, Sean V., Plon, Sharon E., Couch, Fergus J.
Publicado em 2013

Fragile X syndrome due to a missense mutation

Por Myrick, Leila K, Nakamoto-Kinoshita, Mika, Lindor, Noralane M, Kirmani, Salman, Cheng, Xiaodong, Warren, Stephen T
Publicado em 2014

Pancreatic cancer and a novel MSH2 germline alteration

Por Lindor, Noralane M., Petersen, Gloria M., Spurdle, Amanda B., Thompson, Bryony, Goldgar, David E., Thibodeau, Stephen N.
Publicado em 2011

Colorectal cancer and self-reported tooth agenesis

Por Lindor, Noralane M, Win, Aung Ko, Gallinger, Steven, Daftary, Darshana, Thibodeau, Stephen N, Silva, Renato, Letra, Ariadne
Publicado em 2014

Pre-Diagnostic Alcohol Consumption and Colorectal Cancer Survival: The Colon Cancer Family Registry

Por Phipps, Amanda I., Robinson, Jamaica R., Campbell, Peter T., Win, Aung Ko, Figueiredo, Jane, Lindor, Noralane M., Newcomb, Polly A.
Publicado no Cancer (2016)

Genetic variants in the cell cycle control pathways contribute to early onset colorectal cancer in Lynch syndrome

Por Chen, Jinyun, Etzel, Carol J., Amos, Christopher I., Zhang, Qing, Viscofsky, Nancy, Lindor, Noralane M., Lynch, Patrick M., Frazier, Marsha L.
Publicado em 2009