日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Covering medical care costs for participants in the eMERGE Network: Challenges for equity and implementation

为eMERGE网络参与者支付医疗保健费用:公平性和实施方面的挑战

Rasmussen-Torvik, Laura J; Bonini, Katherine E; Harr, Margaret H; Abbass, Mohammad Ali; Bangash, Hana; Bland, Harris T; Boyd, Brenna M; Chung, Wendy K; Clayton, Ellen W; Cohen, Stuart J; Connolly, John J; Gascoigne, Catherine; Hernandez, Valentina; Holm, Ingrid A; Horike-Pyne, Martha; Jarvik, Gail P; Karlson, Elizabeth W; Kullo, Iftikhar J; Limdi, Nita A; Maradik, Mary E; McNally, Elizabeth M; Perez, Emma; Prows, Cynthia A; Shaibi, Gabriel Q; Weng, Chunhua; Rowley, Robb K; Peterson, Josh F; Linder, Jodell E; Sabatello, Maya

Implementing integrated genomic risk assessments for breast cancer: lessons learned from the Electronic Medical Records and Genomics study

实施乳腺癌综合基因组风险评估:从电子病历和基因组学研究中汲取的经验教训

Liu, Cong; Crew, Katherine D; Morse, Jennifer; Linder, Jodell E; Antoniou, Antonis C; Carver, Tim; Cortopassi, Josh; Peterson, Josh F; Ta, Casey N; Hoell, Christin; Prows, Cynthia; Kenny, Eimear E; Miller, Emily; Perez, Emma; Jarvik, Gail P; Bland, Harris T; Odgis, Jacqueline A; Mittendorf, Kathleen F; Bonini, Katherine E; McGuffin, Kyle; Kottyan, Leah C; Maradik, Mary; Limdi, Nita; Abul-Husn, Noura S; Marathe, Priya N; Suckiel, Sabrina A; Aguilar, Sienna; Lewis, Toni J; Wei, Wei-Qi; Luo, Yuan; Freimuth, Robert R; Hakonarson, Hakon; Weng, Chunhua; Chung, Wendy K; Wiesner, Georgia L

Family history and cancer risk study (FOREST): A clinical trial assessing electronic patient-directed family history input for identifying patients at risk of hereditary cancer

家族史与癌症风险研究(FOREST):一项评估电子化患者自主输入家族史信息在识别遗传性癌症高危患者方面的临床试验

Mittendorf, Kathleen F; Bland, Harris T; Andujar, Justin; Celaya-Cobbs, Natasha; Edwards, Clasherrol; Gerhart, Meredith; Hooker, Gillian; Hubert, Mryia; Jones, Sarah H; Marshall, Dana R; Myers, Rachel A; Pratap, Siddharth; Rosenbloom, S Trent; Sadeghpour, Azita; Wu, R Ryanne; Orlando, Lori A; Wiesner, Georgia L

A rare case of acute liver failure due to disseminated Varicella-Zoster Virus (VZV) infection

一例罕见的由播散性水痘-带状疱疹病毒(VZV)感染引起的急性肝功能衰竭病例

Feldman, Harris T; Neale, Matthew; Batra, Ajay; Mangano, Mark; Newstein, Michael C

Corrigendum to 'A rare case of acute liver failure due to disseminated Varicella-Zoster Virus (VZV) infection' [IDCases 2025;40:e02224]

对“一例因播散性水痘-带状疱疹病毒(VZV)感染引起的罕见急性肝衰竭”的更正[IDCases 2025;40:e02224]

Feldman, Harris T; Neale, Matthew; Batra, Ajay; Mangano, Mark; Newstein, Michael C

Implementing Integrated Genomic Risk Assessments for Breast Cancer: Lessons Learned from the eMERGE Study

实施乳腺癌综合基因组风险评估:eMERGE 研究的经验教训

Liu, Cong; Crew, Katherine; Morse, Jennifer; Linder, Jodell E; Antoniou, Antonis C; Carver, Tim; Cortopassi, Josh; Peterson, Josh F; Ta, Casey N; Hoell, Christin; Prows, Cynthia; Kenny, Eimear E; Miller, Emily; Perez, Emma; Jarvik, Gail P; Bland, Harris T; Odgis, Jacqueline A; Mittendorf, Kathleen F; Bonini, Katherine E; McGuffin, Kyle; Kottyan, Leah C; Maradik, Mary; Limdi, Nita; Abul-Husn, Noura S; Marathe, Priya N; Suckiel, Sabrina A; Aguilar, Sienna; Lewis, Toni J; Wei, Wei-Qi; Luo, Yuan; Freimuth, Robert R; Hakonarson, Hakon; Weng, Chunhua; Chung, Wendy K; Wiesner, Georgia L

Conducting inclusive research in genetics for transgender, gender-diverse, and sex-diverse individuals: Case analyses and recommendations from a clinical genomics study

为跨性别者、性别多元者和性取向多元者开展包容性遗传学研究:一项临床基因组学研究的案例分析和建议

Bland, Harris T; Gilmore, Marian J; Andujar, Justin; Martin, Makenna A; Celaya-Cobbs, Natasha; Edwards, Clasherrol; Gerhart, Meredith; Hooker, Gillian W; Kraft, Stephanie A; Marshall, Dana R; Orlando, Lori A; Paul, Natalie A; Pratap, Siddharth; Rosenbloom, S Trent; Wiesner, Georgia L; Mittendorf, Kathleen F

Genetic sex validation for sample tracking in next-generation sequencing clinical testing

下一代测序临床检测中样本追踪的基因性别验证

Hu, Jianhong; Korchina, Viktoriya; Zouk, Hana; Harden, Maegan V; Murdock, David; Macbeth, Alyssa; Harrison, Steven M; Lennon, Niall; Kovar, Christie; Balasubramanian, Adithya; Zhang, Lan; Chandanavelli, Gauthami; Pasham, Divya; Rowley, Robb; Wiley, Ken; Smith, Maureen E; Gordon, Adam; Jarvik, Gail P; Sleiman, Patrick; Kelly, Melissa A; Bland, Harris T; Murugan, Mullai; Venner, Eric; Boerwinkle, Eric; Prows, Cynthia; Mahanta, Lisa; Rehm, Heidi L; Gibbs, Richard A; Muzny, Donna M

Returning integrated genomic risk and clinical recommendations: The eMERGE study

整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; Velez Edwards, Digna R; 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

Education and electronic medical records and genomics network, challenges, and lessons learned from a large-scale clinical trial using polygenic risk scores

教育、电子病历和基因组学网络:一项使用多基因风险评分的大规模临床试验面临的挑战和经验教训

Connolly, John J; Berner, Eta S; Smith, Maureen; Levy, Samuel; Terek, Shannon; Harr, Margaret; Karavite, Dean; Suckiel, Sabrina; Holm, Ingrid A; Dufendach, Kevin; Nelson, Catrina; Khan, Atlas; Chisholm, Rex L; Allworth, Aimee; Wei, Wei-Qi; Bland, Harris T; Clayton, Ellen Wright; Soper, Emily R; Linder, Jodell E; Limdi, Nita A; Miller, Alexandra; Nigbur, Scott; Bangash, Hana; Hamed, Marwan; Sherafati, Alborz; Lewis, Anna C F; Perez, Emma; Orlando, Lori A; Rakhra-Burris, Tejinder K; Al-Dulaimi, Mustafa; Cifric, Selma; Scherr, Courtney Lynam; Wynn, Julia; Hakonarson, Hakon; Sabatello, Maya