Developing Family Healthware, a Family History Screening Tool to Prevent Common Chronic Diseases

Por Yoon, Paula W., Scheuner, Maren T., Jorgensen, Cynthia, Khoury, Muin J.
Publicado em 2008

Relation of familial patterns of coronary heart disease, stroke, and diabetes to subclinical atherosclerosis: The Multi-Ethnic Study of Atherosclerosis

Por Scheuner, Maren T., Setodji, Claude Messan, Pankow, James S., Blumenthal, Roger S., Keeler, Emmett
Publicado em 2008

The General Cardiovascular Risk Profile Identifies Advanced Coronary Artery Calcium and is Improved by Family History. The Multi-Ethnic Study of Atherosclerosis

Por Scheuner, Maren T., Setodji, Claude Messan, Pankow, James S., Blumenthal, Roger S., Keeler, Emmett
Publicado em 2009

A graphical method for assessing risk factor threshold values using the generalized additive model: the multi-ethnic study of atherosclerosis

Por Setodji, Claude Messan, Scheuner, Maren, Pankow, James S., Blumenthal, Roger S., Chen, Haiying, Keeler, Emmett
Publicado em 2012

Integrating Germline Genetics Into Precision Oncology Practice in the Veterans Health Administration: Challenges and Opportunities

Por Scheuner, Maren T., Myrie, Kenute, Peredo, Jane, Hoffman-Hogg, Lori, Lundquist, Margaret, Guerra, Stephanie L., Ball, Douglas
Publicado no Fed Pract (2020)

Probable Diagnosis of a Patient with Niemann–Pick Disease Type C: Managing Pitfalls of Exome Sequencing

Por Zeiger, William A., Jamal, Nasheed I., Scheuner, Maren T., Pittman, Patricia, Raymond, Kimiyo M., Morra, Massimo, Mishra, Shri K.
Publicado no JIMD Rep (2018)

A Comparison of Basic versus more Complex Definitions of Family History in the Prediction of Coronary Heart Disease: The Multi-Ethnic Study of Atherosclerosis

Por Patel, Jaideep, Al Rifai, Mahmoud, Scheuner, Maren T., Shea, Steven, Blumenthal, Roger S., Nasir, Khurram, Blaha, Michael J., McEvoy, John W.
Publicado no Mayo Clin Proc (2018)

Multilevel Research and the Challenges of Implementing Genomic Medicine

Por Khoury, Muin J., Coates, Ralph J., Fennell, Mary L., Glasgow, Russell E., Scheuner, Maren T., Schully, Sheri D., Williams, Marc S., Clauser, Steven B.
Publicado em 2012

Systematic evidence-based review: outcomes from exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability

Por Malinowski, Jennifer, Miller, David T., Demmer, Laurie, Gannon, Jennifer, Pereira, Elaine Maria, Schroeder, Molly C., Scheuner, Maren T., Tsai, Anne Chun-Hui, Hickey, Scott E., Shen, Jun
Publicado no Genet Med (2020)

Pharmacogenetic testing in the Veterans Health Administration: Policy recommendations from the VHA Clinical Pharmacogenetics Subcommittee

Por Vassy, Jason L., Stone, Annjanette, Callaghan, John T., Mendes, Margaret, Meyer, Laurence J., Pratt, Victoria M., Przygodzki, Ronald M., Scheuner, Maren T., Wang-Rodriguez, Jessica, Schichman, Steven A.
Publicado no Genet Med (2018)

Gnathodiaphyseal dysplasia: report of a family with a novel mutation of the ANO5 gene

Por Duong, Hannah A., Le, Karen T., Soulema, Albert L., Yueh, Ronald H., Scheuner, Maren T., Holick, Michael F., Christensen, Russell, Tajima, Tracey L., Leung, Angela M., Mallya, Sanjay M.
Publicado no Oral Surg Oral Med Oral Pathol Oral Radiol (2016)

Electronic health record interventions at the point of care improve documentation of care processes and decrease orders for genetic tests commonly ordered by nongeneticists

Por Scheuner, Maren T., Peredo, Jane, Tangney, Kelly, Schoeff, Diane, Sale, Taylor, Lubick-Goldzweig, Caroline, Hamilton, Alison, Hilborne, Lee, Lee, Martin, Mittman, Brian, Yano, Elizabeth M., Lubin, Ira M.
Publicado no Genet Med (2016)

Coronary Artery Calcium Improves Risk Assessment in Adults with a Family History of Premature Coronary Heart Disease: Results from MESA

Por Patel, Jaideep, Al Rifai, Mahmoud, Blaha, Michael J., Budoff, Matthew J., Post, Wendy S., Polak, Joseph F., Bluemke, David A., Scheuner, Maren T., Kronmal, Richard A., Blumenthal, Roger S., Nasir, Khurram, McEvoy, John W.
Publicado no Circ Cardiovasc Imaging (2015)

Identifying End Users' Preferences about Structuring Pharmacogenetic Test Orders in an Electronic Health Record System

Por Hull, Leland E., Vassy, Jason L., Stone, Annjanette, Chanfreau-Coffinier, Catherine C., Heise, Craig W., Pratt, Victoria M., Przygodzki, Ronald, Voils, Corrine I., Voora, Deepak, Wang-Rodriguez, Jessica, Schichman, Steven A., Scheuner, Maren T.
Publicado no J Mol Diagn (2020)

Examining the impact of genetic testing for type 2 diabetes on health behaviors: study protocol for a randomized controlled trial

Por Voils, Corrine I, Coffman, Cynthia J, Edelman, David, Maciejewski, Matthew L, Grubber, Janet M, Sadeghpour, Azita, Cho, Alex, McKenzie, Jamiyla, Blanpain, Francoise, Scheuner, Maren, Sandelowski, Margarete, Gallagher, M Patrick, Ginsburg, Geoffrey S, Yancy, William S
Publicado em 2012

An electronic family health history tool to identify and manage patients at increased risk for colorectal cancer: protocol for a randomized controlled trial

Por Goldstein, Karen M., Fisher, Deborah A., Wu, R. Ryanne, Orlando, Lori A., Coffman, Cynthia J., Grubber, Janet M., Rakhra-Burris, Tejinder, Wang, Virginia, Scheuner, Maren T., Sperber, Nina, Datta, Santanu K., Nelson, Richard E., Strawbridge, Elizabeth, Provenzale, Dawn, Hauser, Elizabeth R., Voils, Corrine I.
Publicado no Trials (2019)

Precision Medicine for CRC Patients in the Veteran Population: State-of-the-Art, Challenges and Research Directions

Por Mohapatra, Shyam S., Batra, Surinder K., Bharadwaj, Srinivas, Bouvet, Michael, Cosman, Bard, Goel, Ajay, Jogunoori, Wilma, Kelley, Michael J., Mishra, Lopa, Mishra, Bibhuti, Mohapatra, Subhra, Patel, Bhaumik, Pisegna, Joseph R., Raufman, Jean-Pierre, Rao, Shuyun, Roy, Hemant, Scheuner, Maren, Singh, Satish, Vidyarthi, Gitanjali, White, Jon
Publicado no Dig Dis Sci (2018)

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

Por 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., Pierre, Jeanette St., Westman, Judith, Wise, Paul, Yang, Vincent W., Khoury, Muin J.
Publicado em 2011

Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers

Por Qian, Frank, Rookus, Matti A., Leslie, Goska, Risch, Harvey A., Greene, Mark H., Aalfs, Cora M., Adank, Muriel A., Adlard, Julian, Agnarsson, Bjarni A., Ahmed, Munaza, Aittomäki, Kristiina, Andrulis, Irene L., Arnold, Norbert, Arun, Banu K., Ausems, Margreet G. E. M., Azzollini, Jacopo, Barrowdale, Daniel, Barwell, Julian, Benitez, Javier, Białkowska, Katarzyna, Bonadona, Valérie, Borde, Julika, Borg, Ake, Bradbury, Angela R., Brunet, Joan, Buys, Saundra S., Caldés, Trinidad, Caligo, Maria A., Campbell, Ian, Carter, Jonathan, Chiquette, Jocelyne, Chung, Wendy K., Claes, Kathleen B. M., Collée, J. Margriet, Collonge-Rame, Marie-Agnès, Couch, Fergus J., Daly, Mary B., Delnatte, Capucine, Diez, Orland, Domchek, Susan M., Dorfling, Cecilia M., Eason, Jacqueline, Easton, Douglas F., Eeles, Ros, Engel, Christoph, Evans, D. Gareth, Faivre, Laurence, Feliubadaló, Lidia, Foretova, Lenka, Friedman, Eitan, Frost, Debra, Ganz, Patricia A., Garber, Judy, Garcia-Barberan, Vanesa, Gehrig, Andrea, Glendon, Gord, Godwin, Andrew K., Gómez Garcia, Encarna B., Hamann, Ute, Hauke, Jan, Hopper, John L., Hulick, Peter J., Imyanitov, Evgeny N., Isaacs, Claudine, Izatt, Louise, Jakubowska, Anna, Janavicius, Ramunas, John, Esther M., Karlan, Beth Y., Kets, Carolien M., Laitman, Yael, Lázaro, Conxi, Leroux, Dominique, Lester, Jenny, Lesueur, Fabienne, Loud, Jennifer T., Lubiński, Jan, Łukomska, Alicja, McGuffog, Lesley, Mebirouk, Noura, Meijers-Heijboer, Hanne E. J., Meindl, Alfons, Miller, Austin, Montagna, Marco, Mooij, Thea M., Mouret-Fourme, Emmanuelle, Nathanson, Katherine L., Nehoray, Bita, Neuhausen, Susan L., Nevanlinna, Heli, Nielsen, Finn C., Offit, Kenneth, Olah, Edith, Ong, Kai-ren, Oosterwijk, Jan C., Ottini, Laura, Parsons, Michael T., Peterlongo, Paolo, Pfeiler, Georg, Pradhan, Nisha, Radice, Paolo, Ramus, Susan J., Rantala, Johanna, Rennert, Gad, Robson, Mark, Rodriguez, Gustavo C., Salani, Ritu, Scheuner, Maren T., Schmutzler, Rita K., Shah, Payal D., Side, Lucy E., Simard, Jacques, Singer, Christian F., Steinemann, Doris, Stoppa-Lyonnet, Dominique, Tan, Yen Yen, Teixeira, Manuel R., Terry, Mary Beth, Thomassen, Mads, Tischkowitz, Marc, Tognazzo, Silvia, Toland, Amanda E., Tung, Nadine, van Asperen, Christi J., van Engelen, Klaartje, van Rensburg, Elizabeth J., Venat-Bouvet, Laurence, Vierstraete, Jeroen, Wagner, Gabriel, Walker, Lisa, Weitzel, Jeffrey N., Yannoukakos, Drakoulis, Antoniou, Antonis C., Goldgar, David E., Olopade, Olufunmilayo I., Chenevix-Trench, Georgia, Rebbeck, Timothy R., Huo, Dezheng
Publicado no Br J Cancer (2019)

A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers

Por Coignard, Juliette, Lush, Michael, Beesley, Jonathan, O’Mara, Tracy A., Dennis, Joe, Tyrer, Jonathan P., Barnes, Daniel R., McGuffog, Lesley, Leslie, Goska, Bolla, Manjeet K., Adank, Muriel A., Agata, Simona, Ahearn, Thomas, Aittomäki, Kristiina, Andrulis, Irene L., Anton-Culver, Hoda, Arndt, Volker, Arnold, Norbert, Aronson, Kristan J., Arun, Banu K., Augustinsson, Annelie, Azzollini, Jacopo, Barrowdale, Daniel, Baynes, Caroline, Becher, Heiko, Bermisheva, Marina, Bernstein, Leslie, Białkowska, Katarzyna, Blomqvist, Carl, Bojesen, Stig E., Bonanni, Bernardo, Borg, Ake, Brauch, Hiltrud, Brenner, Hermann, Burwinkel, Barbara, Buys, Saundra S., Caldés, Trinidad, Caligo, Maria A., Campa, Daniele, Carter, Brian D., Castelao, Jose E., Chang-Claude, Jenny, Chanock, Stephen J., Chung, Wendy K., Claes, Kathleen B. M., Clarke, Christine L., Collée, J. Margriet, Conroy, Don M., Czene, Kamila, Daly, Mary B., Devilee, Peter, Diez, Orland, Ding, Yuan Chun, Domchek, Susan M., Dörk, Thilo, dos-Santos-Silva, Isabel, Dunning, Alison M., Dwek, Miriam, Eccles, Diana M., Eliassen, A. Heather, Engel, Christoph, Eriksson, Mikael, Evans, D. Gareth, Fasching, Peter A., Flyger, Henrik, Fostira, Florentia, Friedman, Eitan, Fritschi, Lin, Frost, Debra, Gago-Dominguez, Manuela, Gapstur, Susan M., Garber, Judy, Garcia-Barberan, Vanesa, García-Closas, Montserrat, García-Sáenz, José A., Gaudet, Mia M., Gayther, Simon A., Gehrig, Andrea, Georgoulias, Vassilios, Giles, Graham G., Godwin, Andrew K., Goldberg, Mark S., Goldgar, David E., González-Neira, Anna, Greene, Mark H., Guénel, Pascal, Haeberle, Lothar, Hahnen, Eric, Haiman, Christopher A., Håkansson, Niclas, Hall, Per, Hamann, Ute, Harrington, Patricia A., Hart, Steven N., He, Wei, Hogervorst, Frans B. L., Hollestelle, Antoinette, Hopper, John L., Horcasitas, Darling J., Hulick, Peter J., Hunter, David J., Imyanitov, Evgeny N., Jager, Agnes, Jakubowska, Anna, James, Paul A., Jensen, Uffe Birk, John, Esther M., Jones, Michael E., Kaaks, Rudolf, Kapoor, Pooja Middha, Karlan, Beth Y., Keeman, Renske, Khusnutdinova, Elza, Kiiski, Johanna I., Ko, Yon-Dschun, Kosma, Veli-Matti, Kraft, Peter, Kurian, Allison W., Laitman, Yael, Lambrechts, Diether, Le Marchand, Loic, Lester, Jenny, Lesueur, Fabienne, Lindstrom, Tricia, Lopez-Fernández, Adria, Loud, Jennifer T., Luccarini, Craig, Mannermaa, Arto, Manoukian, Siranoush, Margolin, Sara, Martens, John W. M., Mebirouk, Noura, Meindl, Alfons, Miller, Austin, Milne, Roger L., Montagna, Marco, Nathanson, Katherine L., Neuhausen, Susan L., Nevanlinna, Heli, Nielsen, Finn C., O’Brien, Katie M., Olopade, Olufunmilayo I., Olson, Janet E., Olsson, Håkan, Osorio, Ana, Ottini, Laura, Park-Simon, Tjoung-Won, Parsons, Michael T., Pedersen, Inge Sokilde, Peshkin, Beth, Peterlongo, Paolo, Peto, Julian, Pharoah, Paul D. P., Phillips, Kelly-Anne, Polley, Eric C., Poppe, Bruce, Presneau, Nadege, Pujana, Miquel Angel, Punie, Kevin, Radice, Paolo, Rantala, Johanna, Rashid, Muhammad U., Rennert, Gad, Rennert, Hedy S., Robson, Mark, Romero, Atocha, Rossing, Maria, Saloustros, Emmanouil, Sandler, Dale P., Santella, Regina, Scheuner, Maren T., Schmidt, Marjanka K., Schmidt, Gunnar, Scott, Christopher, Sharma, Priyanka, Soucy, Penny, Southey, Melissa C., Spinelli, John J., Steinsnyder, Zoe, Stone, Jennifer, Stoppa-Lyonnet, Dominique, Swerdlow, Anthony, Tamimi, Rulla M., Tapper, William J., Taylor, Jack A., Terry, Mary Beth, Teulé, Alex, Thull, Darcy L., Tischkowitz, Marc, Toland, Amanda E., Torres, Diana, Trainer, Alison H., Truong, Thérèse, Tung, Nadine, Vachon, Celine M., Vega, Ana, Vijai, Joseph, Wang, Qin, Wappenschmidt, Barbara, Weinberg, Clarice R., Weitzel, Jeffrey N., Wendt, Camilla, Wolk, Alicja, Yadav, Siddhartha, Yang, Xiaohong R., Yannoukakos, Drakoulis, Zheng, Wei, Ziogas, Argyrios, Zorn, Kristin K., Park, Sue K., Thomassen, Mads, Offit, Kenneth, Schmutzler, Rita K., Couch, Fergus J., Simard, Jacques, Chenevix-Trench, Georgia, Easton, Douglas F., Andrieu, Nadine, Antoniou, Antonis C.
Publicado no Nat Commun (2021)