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Genomic sequencing in diverse and underserved pediatric populations: Parent perspectives on understanding, uncertainty, psychosocial impact, and personal utility of results 在多样化和弱势儿童人群中的基因组测序：家长对结果的理解、不确定性、心理社会影响和个人效用观点 Biesecker, Barbara B.; Ackerman, Sara L.; Brothers, Kyle B.; East, Kelly M.; Foreman, Ann Katherine M.; Hindorff, Lucia A.; Horowitz, Carol R.; Jarvik, Gail P.; Knight, Sara J.; Leo, Michael C.; Patrick, Donald L.; Rini, Christine; Robinson, Jill O.; Sahin-Hodoglugil, Nuriye Nalan; Slavotinek, Anne; Suckiel, Sabrina A.; Veenstra, David L.; Zinberg, Randi E.; Hunter, Jessica Ezzell 分享 收藏
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SeqFirst: Building equity access to a precise genetic diagnosis in critically ill newborns Wenger, Tara L.; Scott, Abbey; Kruidenier, Lukas; Sikes, Megan; Keefe, Alexandra; Buckingham, Kati J.; Marvin, Colby T.; Shively, Kathryn M.; Bacus, Tamara; Sommerland, Olivia M.; Anderson, Kailyn; Gildersleeve, Heidi; Davis, Chayna J.; Love-Nichols, Jamie; Macduffie, Katherine E.; Miller, Danny E.; Yu, Joon-Ho; Snook, Amy; Johnson, Britt; Veenstra, David L.; Parish-Morris, Julia; Mcwalter, Kirsty; Retterer, Kyle; Copenheaver, Deborah; Friedman, Bethany; Juusola, Jane; Ryan, Erin; Varga, Renee; Doherty, Daniel A.; Dipple, Katrina; Chong, Jessica X.; Kruszka, Paul; Bamshad, Michael J. 分享 收藏
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Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations 十种慢性病多基因风险评分的选择，优化和验证，以在美国不同人群中进行临床实施 Lennon, Niall J.; Kottyan, Leah C.; Kachulis, Christopher; Abul-Husn, Noura S.; Arias, Josh; Belbin, Gillian; Below, Jennifer E.; Berndt, Sonja I.; Chung, Wendy K.; Cimino, James J.; Clayton, Ellen Wright; Connolly, John J.; Crosslin, David R.; Dikilitas, Ozan; Edwards, Digna R. Velez; Feng, Qiping; Fisher, Marissa; Freimuth, Robert R.; Ge, Tian; Berndt, Sonja; Hirschhorn, Joel; Loos, Ruth; Glessner, Joseph T.; Gordon, Adam S.; Patterson, Candace; Hakonarson, Hakon; Harden, Maegan; Harr, Margaret; Hirschhorn, Joel N.; Hoggart, Clive; Hsu, Li; Irvin, Marguerite R.; Jarvik, Gail P.; Karlson, Elizabeth W.; Khan, Atlas; Khera, Amit; Kiryluk, Krzysztof; Kullo, Iftikhar; Larkin, Katie; Limdi, Nita; Linder, Jodell E.; Loos, Ruth J. F.; Luo, Yuan; Malolepsza, Edyta; Manolio, Teri A.; Martin, Lisa J.; Mccarthy, Li; Mcnally, Elizabeth M.; Meigs, James B.; Mersha, Tesfaye B.; Mosley, Jonathan D.; Musick, Anjene; Namjou, Bahram; Pai, Nihal; Pesce, Lorenzo L.; Peters, Ulrike; Peterson, Josh F.; Prows, Cynthia A.; Puckelwartz, Megan J.; Rehm, Heidi L.; Roden, Dan M.; Rosenthal, Elisabeth A.; Rowley, Robb; Sawicki, Konrad Teodor; Schaid, Daniel J.; Smit, Roelof A. J.; Smith, Johanna L.; Smoller, Jordan W.; Thomas, Minta; Tiwari, Hemant; Toledo, Diana M.; Vaitinadin, Nataraja Sarma; Veenstra, David; Walunas, Theresa L.; Wang, Zhe; Wei, Wei-Qi; Weng, Chunhua; Wiesner, Georgia L.; Yin, Xianyong; Kenny, Eimear E. 分享 收藏
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Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing 临床测序可采取的单基因结果后医疗保健利用的前瞻性，多站点研究 Linder, Jodell E.; Tao, Ran; Chung, Wendy K.; Kiryluk, Krzysztof; Liu, Cong; Weng, Chunhua; Connolly, John J.; Hakonarson, Hakon; Harr, Margaret; Leppig, Kathleen A.; Jarvik, Gail P.; Veenstra, David L.; Aufox, Sharon; Chisholm, Rex L.; Gordon, Adam S.; Hoell, Christin; Rasmussen-Torvik, Laura J.; Smith, Maureen E.; Holm, Ingrid A.; Miller, Erin M.; Prows, Cynthia A.; Elskeally, Omar; Kullo, Iftikhar J.; Lee, Christopher; Jose, Sheethal; Manolio, Teri A.; Rowley, Robb; Padi-Adjirackor, Nana Addo; Wilmayani, Ni Ketut; City, Brittany; Wei, Wei-Qi; Wiesner, Georgia L.; Rahm, Alanna Kulchak; Williams, Janet L.; Williams, Marc S.; Peterson, Josh F. 分享 收藏
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Longitudinal adherence to breast cancer surveillance following cancer genetic testing in an integrated health care system Knerr, Sarah; Guo, Boya; Wernli, Karen J.; Mittendorf, Kathleen F. F.; Feigelson, Heather Spencer; Gilmore, Marian J. J.; Jarvik, Gail P. P.; Kauffman, Tia L. L.; Keast, Erin; Liles, Elizabeth G. G.; Lynch, Frances L. L.; Muessig, Kristin R. R.; Okuyama, Sonia; Veenstra, David L. L.; Zepp, Jamilyn M. M.; Wilfond, Benjamin S. S.; Devine, Beth; Goddard, Katrina A. B. 分享 收藏
Population Genomic Screening for Three Common Hereditary Conditions A Cost-Effectiveness Analysis 三种常见遗传条件的群体基因组筛查成本效益分析 Guzauskas, Gregory F.; Garbett, Shawn; Zhou, Zilu; Schildcrout, Jonathan S.; Graves, John A.; Williams, Marc S.; Hao, Jing; Jones, Laney K.; Spencer, Scott J.; Jiang, Shangqing; Veenstra, David L.; Peterson, Josh F. 分享 收藏
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Practical considerations for reinterpretation of individual genetic variants Appelbaum, Paul S.; Berger, Sara M.; Brokamp, Elly; Brown, Henry Shelton; Burke, Wylie; Clayton, Ellen Wright; Evans, Barbara J.; Hamid, Rizwan; Marchant, Gary E.; Martin, Donna M.; O'Connor, Bridget C.; Pagan, Jose A.; Parens, Erik; Roberts, Jessica L.; Rowe, John; Schneider, John; Siegel, Karolynn; Veenstra, David L.; Chung, Wendy K. 分享 收藏
Returning integrated genomic risk and clinical recommendations: The eMERGE study 回归综合基因组风险和临床建议: eMERGE研究 Linder, Jodell E.; Allworth, Aimee; Bland, Harris T.; Caraballo, Pedro J.; Chisholm, Rex L.; Clayton, Ellen Wright; Crosslin, David R.; Dikilitas, Ozan; DiVietro, Alanna; Esplin, Edward D.; Forman, Sophie; Freimuth, Robert R.; Gordon, Adam S.; Green, Richard; Harden, Maegan, V; Holm, Ingrid A.; Jarvik, Gail P.; Karlson, Elizabeth W.; Labrecque, Sofia; Lennon, Niall J.; Limdi, Nita A.; Mittendorf, Kathleen F.; Murphy, Shawn N.; Orlando, Lori; Prows, Cynthia A.; Rasmussen, Luke, V; Rasmussen-Torvik, Laura; Rowley, Robb; Sawicki, Konrad Teodor; Schmidlen, Tara; Terek, Shannon; Veenstra, David; Edwards, Digna R. Velez; Absher, Devin; Abul-Husn, Noura S.; Alsip, Jorge; Bangash, Hana; Beasley, Mark; Below, Jennifer E.; Berner, Eta S.; Booth, James; Chung, Wendy K.; Cimino, James J.; Connolly, John; Davis, Patrick; Devine, Beth; Fullerton, Stephanie M.; Guiducci, Candace; Habrat, Melissa L.; Hain, Heather; Hakonarson, Hakon; Harr, Margaret; Haverfield, Eden; Hernandez, Valentina; Hoell, Christin; Horike-Pyne, Martha; Hripcsak, George; Irvin, Marguerite R.; Kachulis, Christopher; Karavite, Dean; Kenny, Eimear E.; Khan, Atlas; Kiryluk, Krzysztof; Korf, Bruce; Kottyan, Leah; Kullo, Iftikhar J.; Larkin, Katie; Liu, Cong; Malolepsza, Edyta; Manolio, Teri A.; May, Thomas; McNally, Elizabeth M.; Mentch, Frank; Miller, Alexandra; Mooney, Sean D.; Murali, Priyanka; Mutai, Brenda; Muthu, Naveen; Namjou, Bahram; Perez, Emma F.; Puckelwartz, Megan J.; Rakhra-Burris, Tejinder; Roden, Dan M.; Rosenthal, Elisabeth A.; Saadatagah, Seyedmohammad; Sabatello, Maya; Schaid, Dan J.; Schultz, Baergen; Seabolt, Lynn; Shaibi, Gabriel Q.; Sharp, Richard R.; Shirts, Brian; Smith, Maureen E.; Smoller, Jordan W.; Sterling, Rene; Suckiel, Sabrina A.; Thayer, Jeritt; Tiwari, Hemant K.; Trinidad, Susan B.; Walunas, Theresa; Wei, Wei-Qi; Wells, Quinn S.; Weng, Chunhua; Wiesner, Georgia L.; Wiley, Ken; Peterson, Josh F. 分享 收藏
Screening Patterns of Mammography and Breast Magnetic Resonance Imaging Following Cancer Genetic Testing in an Integrated Health Care System Guo, Boya; Knerr, Sarah; Wernli, Karen; Mittendorf, Kathleen; Feigelson, Heather; Gilmore, Marian; Jarvik, Gail; Kauffman, Tia; Keast, Erin; Liles, Beth; Lynch, Frances; Muessig, Kristin; Sasaki, Sonia; Veenstra, David; Zepp, Jamilyn; Wilfond, Ben; Goddard, Katrina; Devine, Beth 分享 收藏
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