The incidence of pancreatic cancer in BRCA1 and BRCA2 mutation carriers

by IQBAL, J, RAGONE, A, SENTER, L, SINGER, C. F, AINSWORTH, P, KIM-SING, C, TUNG, N, FRIEDMAN, E, LLACUACHAQUI, M, PING, S, NAROD, S. A, LUBINSKI, J, LYNCH, H. T, MOLLER, P, GHADIRIAN, P, FOULKES, W. D, ARMEL, S, EISEN, A, NEUHAUSEN, S. L
Published in British journal of cancer

Germline and somatic testing for ovarian Cancer: An SGO clinical practice statement

by Gressel, G.M., Frey, M.K., Norquist, B., Senter, L., Blank, S.V., Urban, R.R.
Published in Gynecologic oncology

Incidence of colorectal cancer in BRCA1 and BRCA2 mutation carriers: results from a follow-up study

by PHELAN, C. M, IQBAL, J, NEUHAUSEN, S. L, SENTER, L, SINGER, C. F, AINSWORTH, P, KIM-SING, C, TUNG, N, LLACUACHAQUI, M, CHORNOKUR, G, PING, S, NAROD, S. A, LYNCH, H. T, LUBINSKI, J, GRONWALD, J, MOLLER, P, GHADIRIAN, P, FOULKES, W. D, ARMEL, S, EISEN, A
Published in British journal of cancer

Anti-thyroglobulin antibodies do not significantly increase the risk of finding iodine avid metastases on post-radioactive iodine ablation scan in low-risk thyroid cancer patients

by Nabhan, F., Porter, K., Senter, L., Ringel, M. D.
Published in Journal of endocrinological investigation

Change in genetics service model increases ovarian cancer patient referrals and decreases time to consultation: Improving compliance with guideline-based quality care

by Senter, L, O'Malley, D.M, Backes, F.J, Copeland, L.J, Fowler, J.M, Salani, R, Cohn, D.E
Published in Gynecologic oncology

Abstract P2-07-10: Breast health behaviors of women under 40 accessing the Avon breast health outreach program

by Gates-Ferris, K, Bauer, KM, Senter, L
Published in Cancer research (Chicago, Ill.)

Pathology of Breast and Ovarian Cancers among BRCA1 and BRCA2 Mutation Carriers: Results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)

by MAVADDAT, Nasim, BARROWDALE, Daniel, MULLIGAN, Anna Marie, COUCH, Fergus J, ENGEL, Christoph, MCGUFFOG, Lesley, HEALER, Sue, SINILNIKOVA, Olga M, SOUTHEY, Melissa C, TERRY, Mary Beth, GOLDGAR, David, O'MALLEY, Frances, ANDRULIS, Irene L, JOHN, Esther M, JANAVICIUS, Ramunas, TIHOMIROVA, Laima, HANSEN, Thomas V. O, NIELSEN, Finn C, OSORIO, Ana, STAVROPOULOU, Alexandra, BENITEZ, Javier, MANOUKIAN, Siranoush, PEISSEL, Bernard, DOMCHEK, Susan M, BARILE, Monica, VOLORIO, Sara, PASIN, Barbara, DOLCETTI, Riccardo, PUTIGNANO, Anna Laura, OTTINI, Laura, RADICE, Paolo, HAMANN, Ute, RASHID, Muhammad U, HOGERVORST, Frans B, ECCLES, Diana, KRIEGE, Mieke, VAN DER LUIJT, Rob B, HEBON, PEOCK, Susan, FROST, Debra, GARETH EVANS, D, BREWER, Carole, WALKER, Lisa, ROGERS, Mark T, SIDE, Lucy E, NEVANLINNA, Heli, HOUGHTON, Catherine, EMBRACE, WEAVER, Joellen, GODWIN, Andrew K, SCHMUTZLER, Rita K, WAPPENSCHMIDT, Barbara, MEINDL, Alfons, KAST, Karin, RAMUS, Susan J, SPURDLE, Amanda, ROBSON, Mark, SHERMAN, Mark
Published in Cancer epidemiology, biomarkers & prevention

Somatic and germline genetic testing in advanced ovarian/peritoneal/fallopian tube cancer and pathologic chemotherapy response score (pCRS) after neoadjuvant chemotherapy

by Cosgrove, C.M., Senter, L., Owda, R., Cohn, D.E., Suarez, A.A., Salani, R.
Published in Gynecologic oncology

Abstract P4-10-10: Withdrawn

by Gates-Ferris, K, Culler, TA, Senter, L, Ricci, C, Huber, D
Published in Cancer research (Chicago, Ill.)

Factors affecting the turnover of different groups of part-time workers

by Senter, Jenell L., Martin, James E.
Published in Journal of vocational behavior

Does using hormonal therapy after risk reducing salpingo-oophorectomy increase the incidence of malignancy in women with high risk genetic predisposition to cancer?

by Mills, K.A., Kuznicki, M., Kent, L., Hokenstad, A.N., Cripe, J.C., Woolfolk, C., Senter, L., Bakkum-Gamez, J.N., Wenham, R.M., Cohn, D.E., Thaker, P.H., Joshi, T.V.
Published in Gynecologic oncology

Paired tumor/germline testing for Lynch syndrome in endometrial cancers: A comprehensive testing approach

by Jasperson, K., Umali, M., Mason, C., Truelson, M., Fulk, K., Souders, B., Shah, S., Senter, L., Chen, D.
Published in Gynecologic oncology

Abstract P1-09-06: The effect of Hispanic nativity and ethnicity on mammography use through the Avon breast health outreach program

by Gates-Ferris, K, Senter, L, Aliaga, M, Hurlbert, M, Ricci, C
Published in Cancer research (Chicago, Ill.)

Implementing screening for Lynch syndrome among patients with newly diagnosed colorectal cancer: summary of a public health/clinical collaborative meeting

by Bellcross, Cecelia A, Bedrosian, Sara R, Daniels, Elvan, Duquette, Debra, Hampel, Heather, Jasperson, Kory, Joseph, Djenaba A, Kaye, Celia, Lubin, Ira, Meyer, Laurence J, Reyes, Michele, Scheuner, Maren T, Schully, Sheri D, Senter, Leigha, Stewart, Sherri L, St Pierre, Jeanette, Westman, Judith, Wise, Paul, Yang, Vincent W, Khoury, Muin J
Published in Genetics in medicine

Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium

by Møller, Pål, Seppälä, Toni, Dowty, James G, Haupt, Saskia, Dominguez-Valentin, Mev, Bernstein, Inge, Engel, Christoph, Aretz, Stefan, Nielsen, Maartje, Evans, Dafydd Gareth, Bertario, Lucio, Bonanni, Bernardo, Levi, Zohar, Winship, Ingrid, Plazzer, John-Paul, Sijmons, Rolf, Laghi, Luigi, Valle, Adriana Della, Heinimann, Karl, Half, Elizabeth, Lopez-Koestner, Francisco, Scott, Rodney J, Laish, Ido, Carraro, Dirce Maria, Gluck, Nathan, Greenblatt, Marc, Bohorquez, Mabel, Sheth, Harsh, Lino-Silva, Leonardo S, Portenkirchner, Carmen, Nascimento, Ivana, da Silva, Leandro Apolinário, Thomas, Huw, Mecklin, Jukka-Pekka, Pylvänäinen, Kirsi, Renkonen-Sinisalo, Laura, Peltomäki, Päivi, Thorlacius-Ussing, Ole, Rahner, Nils, Steinke-Lange, Verena, Schmiegel, Wolff, Hüneburg, Robert, de Vargas, Aída Falcón, Backman, Ann-Sofie, Guillén-Ponce, Carmen, Snyder, Carrie, Lautrup, Charlotte K, Amor, David, Palmero, Edenir, Stoffel, Elena, Duijkers, Floor, Hall, Michael J, Hampel, Heather, Okkels, Henrik, Lubiński, Jan, Guillem, Jose G, Monahan, Kevin, Rasmussen, Lene J, Ricciardiello, Luigi, Aronson, Melyssa, Zahary, Mohd N, Samadder, N Jewel, Hoogerbrugge, Nicoline, Morrison, Patrick J, Lee, Grant, Chen-Shtoyerman, Rakefet, Ankathil, Ravindran, Ward, Robyn, Dębniak, Tadeusz, John, Thomas, van Overeem Hansen, Thomas, Caldés, Trinidad, Yamaguchi, Tatsuro, Garre, Pilar, Cavestro, Giulia Martina, Redler, Silke, Büttner, Reinhard, Heuveline, Vincent, Win, Aung Ko, Lindor, Noralane, Gallinger, Steven, Le Marchand, Loïc, Figueiredo, Jane, Buchanan, Daniel D, Thibodeau, Stephen N, Ten Broeke, Sanne W, Hovig, Eivind, Brunet, Joan, Newton, Katie, Crosbie, Emma J, Mints, Miriam, Tjandra, Douglas, Kariv, Revital, Kalfayan, Pablo, Bassaneze, Thiago, Moslein, Gabriela, Ahadova, Aysel, Kloor, Matthias, Sampson, Julian R, Jenkins, Mark A
Published in Hereditary cancer in clinical practice

Long-range PCR facilitates the identification of PMS2-specific mutations

by Clendenning, Mark, Hampel, Heather, LaJeunesse, Jennifer, Lindblom, Annika, Lockman, Jan, Nilbert, Mef, Senter, Leigha, Sotamaa, Kaisa, de la Chapelle, Albert
Published in Human mutation

Abstract P4-13-02: Comparing data quality of client intake forms by interview mode: results of a pilot study on the use of audio computer-assisted self-interview (ACASI) in the Avo...

by Hallum-Montes, R, Senter, L, D'Souza, R, Hurlbert, M, Gates-Ferris, K, Anastario, M
Published in Cancer research (Chicago, Ill.)

Phosphorylation of Dystrophin: Effects on Actin Binding

by Senter, L., Ceoldo, S., Petrusa, M.M., Salviati, G.
Published in Biochemical and biophysical research communications

Does the age of breast cancer diagnosis in first-degree relatives impact on the risk of breast cancer in BRCA1 and BRCA2 mutation carriers?

by Semple, John, Metcalfe, Kelly A., Lubinski, Jan, Huzarski, Tomasz, Gronwald, Jacek, Armel, Susan, Lynch, Henry T., Karlan, Beth, Foulkes, William, Singer, Christian F., Neuhausen, Susan L., Eng, Charis, Iqbal, Javaid, Narod, Steven A.
Published in Breast cancer research and treatment

In rare acute myeloid leukemia patients harboring both RUNX1 and NPM1 mutations, RUNX1 mutations are unusual in structure and present in the germline

by Mendler, Jason H, Maharry, Kati, Becker, Heiko, Eisfeld, Ann-Kathrin, Senter, Leigha, Mrózek, Krzysztof, Kohlschmidt, Jessica, Metzeler, Klaus H, Schwind, Sebastian, Whitman, Susan P, Khalife, Jihane, Caligiuri, Michael A, Klisovic, Rebecca B, Moore, Joseph O, Carter, Thomas H, Marcucci, Guido, Bloomfield, Clara D
Published in Haematologica (Roma)