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

por Lindor, Noralane M., Hopper, John, Dowty, James
Publicado 2016

Risk of breast cancer in Lynch syndrome: a systematic review

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

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

por Lindor, Noralane M, Kasperbauer, Jan, Lewis, Jean E, Pittelkow, Mark
Publicado 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 2011

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 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 2015

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 2014

Targeted sequencing of established and candidate colorectal cancer genes in the Colon Cancer Family Registry Cohort

por Raskin, Leon, Guo, Yan, Du, Liping, Clendenning, Mark, Rosty, Christophe, Lindor, Noralane M., Gruber, Stephen B., Buchanan, Daniel D.
Publicado 2017

Actionable Variants Identified by Genome Sequencing: Penetrance and Outcomes at 1-year Following Return to Participants

por Lee, Christopher, Elsekaily, Omar, Kochan, David C., Alhalabi, Lubna, Faizee, Faizan, Sharp, Richard, Lindor, Noralane M., Kullo, Iftikhar J.
Publicado 2021

Metachronous colorectal cancer risk for mismatch repair gene mutation carriers – the advantage of more extensive surgery

por Parry, Susan, Win, Aung K, Macrae, Finlay A, Parry, Bryan, Gurrin, Lyle C, Lindor, Noralane M, Gallinger, Steven, Hopper, John L, Jenkins, Mark A
Publicado 2011

Clinical verification of genetic results returned to research participants: findings from a Colon Cancer Family Registry

por Laurino, Mercy Y., Truitt, Anjali R., Tenney, Lederle, Fisher, Douglass, Lindor, Noralane M., Veenstra, David, Jarvik, Gail P., Newcomb, Polly A., Fullerton, Stephanie M.
Publicado 2017

Colorectal Tumour Microsatellite Instability Test Results: Perspectives from Patients

por Lindor, Noralane M, Sloan, Jeff, Goldberg, Richard, Bowen, Deborah, Nigon, Sandra, Roche, Amber, Petersen, Gloria, Thibodeau, Stephen N, Burgart, Laurence, Leontovich, Olga, Morlan, Bruce W
Publicado 2004

Contribution of mRNA Splicing to Mismatch Repair Gene Sequence Variant Interpretation

por Thompson, Bryony A., Walters, Rhiannon, Parsons, Michael T., Dumenil, Troy, Drost, Mark, Tiersma, Yvonne, Lindor, Noralane M., Tavtigian, Sean V., de Wind, Niels, Spurdle, Amanda B.
Publicado 2020

How well do whole exome sequencing results correlate with medical findings? A study of 89 Mayo Clinic Biobank samples

por Middha, Sumit, Lindor, Noralane M., McDonnell, Shannon K., Olson, Janet E., Johnson, Kiley J., Wieben, Eric D., Farrugia, Gianrico, Cerhan, James R., Thibodeau, Stephen N.
Publicado 2015

Integrating Genomic Screening into Primary Care: Provider Experiences Caring for Latino Patients at a Community-Based Health Center

por Srinivasan, Tarika, Sutton, Erica J., Beck, Annika T., Cuellar, Idali, Hernandez, Valentina, Pacyna, Joel E., Shaibi, Gabriel Q., Kullo, Iftikhar J., Lindor, Noralane M., Singh, Davinder, Sharp, Richard R.
Publicado 2021

Increasing access to individualized medicine: A matched-cohort study examining Latino participant experiences of genomic screening

por Pacyna, Joel E., Shaibi, Gabriel Q., Lee, Alex, O Byrne, Jamie, Cuellar, Idali, Sutton, Erica J., Hernandez, Valentina, Lindor, Noralane M., Singh, Davinder, Kullo, Iftikhar J., Sharp, Richard R.
Publicado 2021

Comprehensive annotation of BRCA1 and BRCA2 missense variants by functionally validated sequence-based computational prediction models

por Hart, Steven N., Hoskin, Tanya, Shimelis, Hermela, Moore, Raymond M., Feng, Bingjian, Thomas, Abigail, Lindor, Noralane M., Polley, Eric C., Goldgar, David E., Iversen, Edwin, Monteiro, Alvaro N.A., Suman, Vera J., Couch, Fergus J.
Publicado 2018

Returning Genomic Results in a Federally Qualified Health Center: The intersection of precision medicine and social determinants of health.

por Shaibi, Gabriel Q., Kullo, Iftikhar J., Singh, Davinder P., Hernandez, Valentina, Sharp, Richard R., Cuellar, Idali, De Filippis, Eleanna, Levey, Sharon, Breitkopf, Carmen Radecki, Mandarino, Lawrence J., Yang, Ping, Thibodeau, Stephen N., Lindor, Noralane M.
Publicado 2020

Risks of cancers for carriers of monoallelic MUTYH mutation with a family history of colorectal cancer

por Win, Aung K, Cleary, Sean P, Dowty, James G, Lindor, Noralane M, Newcomb, Polly A, Haile, Robert W, Young, Joanne P, Buchanan, Daniel D, Le Marchand, Loïc, Green, Roger, Hopper, John L, Gallinger, Steven, Jenkins, Mark A
Publicado 2011

Associations of Height With the Risks of Colorectal and Endometrial Cancer in Persons With Lynch Syndrome

por Brouwer, Jesca G M, Newcomb, Polly A, Bisseling, Tanya M, Figueiredo, Jane C, Hopper, John L, Jenkins, Mark A, Koornstra, Jan J, Lindor, Noralane M, Vasen, Hans F A, Win, Aung K, Kampman, Ellen, van Duijnhoven, Fränzel J B
Publicado 2020