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

od Yoon, Paula W., Scheuner, Maren T., Jorgensen, Cynthia, Khoury, Muin J.
Izdano 2008

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

od Scheuner, Maren T., Setodji, Claude Messan, Pankow, James S., Blumenthal, Roger S., Keeler, Emmett
Izdano 2008

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

od Scheuner, Maren T., Setodji, Claude Messan, Pankow, James S., Blumenthal, Roger S., Keeler, Emmett
Izdano 2009

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

od Setodji, Claude Messan, Scheuner, Maren, Pankow, James S., Blumenthal, Roger S., Chen, Haiying, Keeler, Emmett
Izdano 2012

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

od Scheuner, Maren T., Myrie, Kenute, Peredo, Jane, Hoffman-Hogg, Lori, Lundquist, Margaret, Guerra, Stephanie L., Ball, Douglas
izdano v Fed Pract (2020)

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

od Zeiger, William A., Jamal, Nasheed I., Scheuner, Maren T., Pittman, Patricia, Raymond, Kimiyo M., Morra, Massimo, Mishra, Shri K.
izdano v 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

od Patel, Jaideep, Al Rifai, Mahmoud, Scheuner, Maren T., Shea, Steven, Blumenthal, Roger S., Nasir, Khurram, Blaha, Michael J., McEvoy, John W.
izdano v Mayo Clin Proc (2018)

Multilevel Research and the Challenges of Implementing Genomic Medicine

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

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

od 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
izdano v Genet Med (2020)

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

od 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.
izdano v Genet Med (2018)

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

od 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.
izdano v 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

od 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.
izdano v Genet Med (2016)

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

od 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.
izdano v Circ Cardiovasc Imaging (2015)

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

od 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.
izdano v J Mol Diagn (2020)

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

od 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
Izdano 2012

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

od 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.
izdano v Trials (2019)

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

od 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
izdano v Dig Dis Sci (2018)

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

od 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.
Izdano 2011

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

od 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
izdano v Br J Cancer (2019)

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

od 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.
izdano v Nat Commun (2021)