Prevalence of BRCA1 and BRCA2 mutations in women with carcinoma in situ of the breast referred for genetic testing

Tekijä Hall, Michael J., Reid, Julia E., Wenstrup, Richard J.
Julkaistu 2010

The Nf1 Tumor Suppressor Regulates Mouse Skin Wound Healing, Fibroblast Proliferation, and Collagen Deposited by Fibroblasts

Tekijä Atit, Radhika P., Crowe, Maria J., Greenhalgh, David G., Wenstrup, Richard J., Ratner, Nancy
Julkaistu 1999

Prevalence and Phenotypes of APC and MUTYH Mutations in Patients with Multiple Colorectal Adenomas

Tekijä Grover, Shilpa, Kastrinos, Fay, Steyerberg, Ewout W., Cook, E. Francis, Dewanwala, Akriti, Burbidge, Lynn Anne, Wenstrup, Richard J., Syngal, Sapna
Julkaistu 2012

Targeted Deletion of Collagen V in Tendons and Ligaments Results in a Classic Ehlers-Danlos Syndrome Joint Phenotype

Tekijä Sun, Mei, Connizzo, Brianne K., Adams, Sheila M., Freedman, Benjamin R., Wenstrup, Richard J., Soslowsky, Louis J., Birk, David E.
Julkaisussa Am J Pathol (2015)

Collagen V is a dominant regulator of collagen fibrillogenesis: dysfunctional regulation of structure and function in a corneal-stroma-specific Col5a1-null mouse model

Tekijä Sun, Mei, Chen, Shoujun, Adams, Sheila M., Florer, Jane B., Liu, Hongshan, Kao, Winston W.-Y., Wenstrup, Richard J., Birk, David E.
Julkaistu 2011

Regulation of Collagen Fibril Nucleation and Initial Fibril Assembly Involves Coordinate Interactions with Collagens V and XI in Developing Tendon

Tekijä Wenstrup, Richard J., Smith, Simone M., Florer, Jane B., Zhang, Guiyun, Beason, David P., Seegmiller, Robert E., Soslowsky, Louis J., Birk, David E.
Julkaistu 2011

Clinical significance of large rearrangements in BRCA1 and BRCA2

Tekijä Judkins, Thaddeus, Rosenthal, Eric, Arnell, Christopher, Burbidge, Lynn Anne, Geary, Wade, Barrus, Toby, Schoenberger, Jeremy, Trost, Jeffrey, Wenstrup, Richard J, Roa, Benjamin B
Julkaistu 2012

Comparison of locus-specific databases for BRCA1 and BRCA2 variants reveals disparity in variant classification within and among databases

Tekijä Vail, Paris J., Morris, Brian, van Kan, Aric, Burdett, Brianna C., Moyes, Kelsey, Theisen, Aaron, Kerr, Iain D., Wenstrup, Richard J., Eggington, Julie M.
Julkaisussa J Community Genet (2015)

Frequency of Germline Mutations in 25 Cancer Susceptibility Genes in a Sequential Series of Patients With Breast Cancer

Tekijä Tung, Nadine, Lin, Nancy U., Kidd, John, Allen, Brian A., Singh, Nanda, Wenstrup, Richard J., Hartman, Anne-Renee, Winer, Eric P., Garber, Judy E.
Julkaisussa J Clin Oncol (2016)

Implementation of Pharmacogenetics at Cincinnati Children’s Hospital Medical Center: Lessons learned over 14 years of personalizing medicine

Tekijä Ramsey, Laura B., Prows, Cynthia A., Zhang, Kejian, Saldaña, Shannon N., Sorter, Michael T., Pestian, John P., Wenstrup, Richard J., Vinks, Alexander A., Glauser, Tracy A.
Julkaisussa Clin Pharmacol Ther (2018)

Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients with Suspected Lynch Syndrome

Tekijä Yurgelun, Matthew B., Allen, Brian, Kaldate, Rajesh R., Bowles, Karla R., Judkins, Thaddeus, Kaushik, Praveen, Roa, Benjamin B., Wenstrup, Richard J., Hartman, Anne-Renee, Syngal, Sapna
Julkaisussa Gastroenterology (2015)

BRCA1 and BRCA2 mutations in women of different ethnicities undergoing testing for hereditary breast-ovarian cancer

Tekijä Hall, Michael J., Reid, Julia E., Burbidge, Lynn A., Pruss, Dmitry, Deffenbaugh, Amie M., Frye, Cynthia, Wenstrup, Richard J., Ward, Brian E., Scholl, Thomas A., Noll, Walter W.
Julkaistu 2009

PREVALENCE OF GERMLINE MUTATIONS IN CANCER GENES AMONG PANCREATIC CANCER PATIENTS WITH POSITIVE FAMILY HISTORY

Tekijä Chaffee, Kari G., Oberg, Ann L., McWilliams, Robert R., Majithia, Neil, Allen, Brian A., Kidd, John, Singh, Nanda, Hartman, Anne-Renee, Wenstrup, Richard J., Petersen, Gloria M.
Julkaisussa Genet Med (2017)

A Systematic Genetic Assessment of 1,433 Sequence Variants of Unknown Clinical Significance in the BRCA1 and BRCA2 Breast Cancer–Predisposition Genes

Tekijä Easton, Douglas F. , Deffenbaugh, Amie M. , Pruss, Dmitry , Frye, Cynthia , Wenstrup, Richard J. , Allen-Brady, Kristina , Tavtigian, Sean V. , Monteiro, Alvaro N. A. , Iversen, Edwin S. , Couch, Fergus J. , Goldgar, David E. 
Julkaistu 2007

The PREMM(1,2,6) Model Predicts Risk of MLH1, MSH2, and MSH6 Germline Mutations Based on Cancer History

Tekijä Kastrinos, Fay, Steyerberg, Ewout W., Mercado, Rowena, Balmaña, Judith, Holter, Spring, Gallinger, Steven, Siegmund, Kimberly D., Church, James M., Jenkins, Mark A., Lindor, Noralane M., Thibodeau, Stephen N., Burbidge, Lynn Anne, Wenstrup, Richard J., Syngal, Sapna
Julkaistu 2010

Validation of a Molecular and Pathological Model for Five-Year Mortality Risk in Patients with Early Stage Lung Adenocarcinoma

Tekijä Bueno, Raphael, Hughes, Elisha, Wagner, Susanne, Gutin, Alexander S., Lanchbury, Jerry S., Zheng, Yifan, Archer, Michael A., Gustafson, Corinne, Jones, Joshua T., Rushton, Kristen, Saam, Jennifer, Kim, Edward, Barberis, Massimo, Wistuba, Ignacio, Wenstrup, Richard J., Wallace, William A., Hartman, Anne-Renee, Harrison, David J.
Julkaisussa J Thorac Oncol (2015)

Community Practice Implementation of a Self-administered Version of PREMM(1,2,6) to Assess Risk for Lynch Syndrome

Tekijä Luba, Daniel G., DiSario, James A., Rock, Colleen, Saraiya, Devki, Moyes, Kelsey, Brown, Krystal, Rushton, Kristen, Ogara, Maydeen M., Raphael, Mona, Zimmerman, Dayna, Garrido, Kimmie, Silguero, Evelyn, Nelson, Jonathan, Yurgelun, Matthew B., Kastrinos, Fay, Wenstrup, Richard J., Syngal, Sapna
Julkaisussa Clin Gastroenterol Hepatol (2017)

Functional evaluation of BRCA2 variants mapping to the PALB2-binding and C-terminal DNA-binding domains using a mouse ES cell-based assay

Tekijä Biswas, Kajal, Das, Ranabir, Eggington, Julie M., Qiao, Huanyu, North, Susan L., Stauffer, Stacey, Burkett, Sandra S., Martin, Betty K., Southon, Eileen, Sizemore, Scott C., Pruss, Dmitry, Bowles, Karla R., Roa, Benjamin B., Hunter, Neil, Tessarollo, Lino, Wenstrup, Richard J., Byrd, R. Andrew, Sharan, Shyam K.
Julkaistu 2012

Assessment of in silico protein sequence analysis in the clinical classification of variants in cancer risk genes

Tekijä Kerr, Iain D., Cox, Hannah C., Moyes, Kelsey, Evans, Brent, Burdett, Brianna C., van Kan, Aric, McElroy, Heather, Vail, Paris J., Brown, Krystal L., Sumampong, Dechie B., Monteferrante, Nicholas J., Hardman, Kennedy L., Theisen, Aaron, Mundt, Erin, Wenstrup, Richard J., Eggington, Julie M.
Julkaisussa J Community Genet (2017)

Clinical validation of a gene expression signature that differentiates benign nevi from malignant melanoma

Tekijä Clarke, Loren E., Warf, M.B., Flake, Darl D., Hartman, Anne‐Renee, Tahan, Steven, Shea, Christopher R., Gerami, Pedram, Messina, Jane, Florell, Scott R., Wenstrup, Richard J., Rushton, Kristen, Roundy, Kirstin M., Rock, Colleen, Roa, Benjamin, Kolquist, Kathryn A., Gutin, Alexander, Billings, Steven, Leachman, Sancy
Julkaisussa J Cutan Pathol (2015)