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Ingrid A. Holm

Harvard Medical School

65H指数
324论文数
1.5W被引数
收录论文 105
发表时间
Healthcare professionals’ experiences returning monogenic, polygenic, and integrated risk results in the eMERGE study医疗专业人员返馈单基因、多基因和综合风险结果在eMERGE研究中的经验
err2025-12-06
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errSabrina A. Suckiel; Laura Golfinopoulos; Courtney L. Scherr; Brenna M. Boyd; Wendy K. Chung; Hakon Hakonarson; Ingrid A. Holm; Iftikhar J. Kullo; Nita A. Limdi; Michael F. Murray; Melanie F. Myers; Cynthia A. Prows; Maya Sabatello; Georgia L. Wiesner; Eimear E. Kenny; Noura S. Abul-Husn
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Development of self-phenotyping tools to empower patients and improve diagnostics开发自表型工具以赋能患者并改善诊断
err2025-10-30
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errOAAI
errKent Shefchek; Sonja I. Ziniel; Julie A. McMurry; Catherine A. Brownstein; John S. Brownstein; Erin Rooney Riggs; Matthew Might; Damian Smedley; Amy Clugston; Alan H. Beggs; Heather Paterson; Peter N. Robinson; Nicole A. Vasilevsky; Ingrid A. Holm; Melissa A. Haendel
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Plasma proteomic markers of pain and emotional dysfunction in fibrous dysplasia/McCune-Albright syndrome纤维性骨 dysplasia/McCune-Albright 综合征中疼痛和情感功能障碍的血浆蛋白质组学标志物
errBone
IF3.6
err2025-09-03
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PREAI
errCamryn Berry; Evan E. Hsu; Courtney LeSon; Kailey E. Brodeur; Edin Randall; Julie Shulman; Catherine Stewart; Shealyn O'Donnell; Boyu Ren; Ingrid A. Holm; Alison M. Boyce; Zachary S. Peacock; Navil Sethna; Michael Mannstadt; Pui Y. Lee; Jaymin Upadhyay
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Growth Attenuation Therapy: Ongoing Ethical and Practical Challenges 20 Years Post Ashley生长抑制疗法:阿什利案例20年后的伦理与实践挑战
err2025-05-23
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PREAI
errStephen D. Brown; Kerri O. Kennedy; Faye F. Holder-Niles; Irina A. Anselm; Brian D. Snyder; David Fogelman; Margaret F. Kirber; Gal Kober; Ingrid Holm; Jonathan M. Marron
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Covering medical care costs for participants in the eMERGE Network: Challenges for equity and implementation为eMERGE Network参与者的医疗保健费用提供覆盖:公平性与实施方面的挑战
err2025-05-16
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PREAI
errLaura J. Rasmussen-Torvik; Katherine E. Bonini; Margaret H. Harr; Mohammad Ali Abbass; Hana Bangash; Harris T. Bland; Brenna M. Boyd; Wendy K. Chung; Ellen W. Clayton; Stuart J. Cohen; John J. Connolly; Catherine Gascoigne; Valentina Hernandez; Ingrid A. Holm; Martha Horike-Pyne; Gail P. Jarvik; Elizabeth W. Karlson; Iftikhar J. Kullo; Nita A. Limdi; Mary E. Maradik; Maya Sabatello
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Family genetic risk communication and reverse cascade testing in the BabySeq project家庭遗传风险沟通与BabySeq项目中的反向瀑布式检测
err2025-03-01
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PREAI
errUveges, Melissa K.; Smith, Hadley Stevens; Pereira, Stacey; Genetti, Casie; Mcguire, Amy L.; Beggs, Alan H.; Green, Robert C.; Holm, Ingrid A.; BabySeq Project Team
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Insights from the largest diverse ancestry sex-specific disease map for genetically predicted height基于遗传预测身高所得的最大异质性祖先别特异性疾病图谱的见解
err2025-02-27
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errOAAI
errPapadopoulou, A.; Litkowski, E. M.; Graff, M.; Wang, Z.; Smit, R. A. J.; Chittoor, G.; Dinsmore, I.; Josyula, N. S.; Lin, M.; Shortt, J.; Zhu, W.; Vedantam, S. L.; Yengo, L.; Wood, A. R.; Berndt, S. I.; Holm, I. A.; Mentch, F. D.; Hakonarson, H.; Kiryluk, K.; Weng, C.; Jarvik, G. P.; Crosslin, D.; Carrell, D.; Kullo, I. J.; Dikilitas, O.; Hayes, M. G.; Wei, W. Q.; Edwards, D. R. V.; Assimes, T. L.; Hirschhorn, J. N.; Below, J. E.; Gignoux, C. R.; Justice, A. E.; Loos, R. J. F.; Sun, Y. V.; Raghavan, S.; Deloukas, P.; North, K. E.; Marouli, E.
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Multidimensional and Longitudinal Impact of a Genetic Diagnosis for Critically Ill Infants
err2024-11-08
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errWojcik, Monica H.; del Rosario, Maya C.; Feldman, Henry A.; Smith, Hadley Stevens; Holm, Ingrid A.
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The BabySeq Project: A clinical trial of genome sequencing in a diverse cohort of infants
err2024-10-01
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PREAI
errSmith, Hadley Stevens; Zettler, Bethany; Genetti, Casie A.; Hickingbotham, Madison R.; Coleman, Tanner F.; Lebo, Matthew; Nagy, Anna; Zouk, Hana; Mahanta, Lisa; Christensen, Kurt D.; Pereira, Stacey; Shah, Nidhi D.; Gold, Nina B.; Walmsley, Sheyenne; Edwards, Sarita; Homayouni, Ramin; Krasan, Graham P.; Hakonarson, Hakon; Horowitz, Carol R.; Gelb, Bruce D.; Korf, Bruce R.; McGuire, Amy L.; Holm, Ingrid A.; Green, Robert C.
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Expanding the genetic and phenotypic landscape of replication factor C complex-related disorders: RFC4 deficiency is linked to a multisystemic disorder
err2024-09-01
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PREAI
errMorimoto, Marie; Ryu, Eunjin; Steger, Benjamin J.; Dixit, Abhijit; Saito, Yoshihiko; Yoo, Juyeong; van der Ven, Amelie T.; Hauser, Natalie; Steinbach, Peter J.; Oura, Kazumasa; Huang, Alden Y.; Kortum, Fanny; Ninomiya, Shinsuke; Rosenthal, Elisabeth A.; Robinson, Hannah K.; Guegan, Katie; Denecke, Jonas; Subramony, Sankarasubramoney H.; Diamonstein, Callie J.; Ping, Jie; Fenner, Mark; Balton, Elsa, V; Strohbehn, Sam; Allworth, Aimee; Bamshad, Michael J.; Gandhi, Mahi; Dipple, Katrina M.; Blue, Elizabeth E.; Jarvik, Gail P.; Lau, C. Christopher; Holm, Ingrid A.; Weisz-Hubshman, Monika; Solomon, Benjamin D.; Nelson, Stanley F.; Nishino, Ichizo; Adams, David R.; Kang, Sukhyun; Gahl, William A.; Toro, Camilo; Myung, Kyungjae; Malicdan, May Christine V.
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Genetic predictors of blood pressure traits are associated with preeclampsia
err2024-07-30
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errJasper, Elizabeth A.; Hellwege, Jacklyn N.; Breeyear, Joseph H.; Xiao, Brenda; Jarvik, Gail P.; Stanaway, Ian B.; Leppig, Kathleen A.; Chittoor, Geetha; Hayes, M. Geoffrey; Dikilitas, Ozan; Kullo, Iftikhar J.; Holm, Ingrid A.; Verma, Shefali Setia; Edwards, Todd L.; Edwards, Digna R. Velez
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Managing differential performance of polygenic risk scores across groups: Real-world experience of the eMERGE Network管理跨组多基因风险评分的差异表现: eMERGE网络的现实经验
err2024-06-01
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PREAI
errLewis, Anna C. F.; Chisholm, Rex L.; Connolly, John J.; Esplin, Edward D.; Glessner, Joe; Gordon, Adam; Green, Robert C.; Hakonarson, Hakon; Harr, Margaret; Holm, Ingrid A.; Jarvik, Gail P.; Karlson, Elizabeth; Kenny, Eimear E.; Kottyan, Leah; Lennon, Niall; Linder, Jodell E.; Luo, Yuan; Martin, Lisa J.; Perez, Emma; Puckelwartz, Megan J.; Rasmussen-Torvik, Laura J.; Sabatello, Maya; Sharp, Richard R.; Smoller, Jordan W.; Sterling, Rene; Terek, Shannon; Wei, Wei-Qi; Fullerton, Stephanie M.
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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
err2023-11-01
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errLinder, 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.
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NBSTRN Tools to Advance Newborn Screening Research and Support Newborn Screening StakeholdersNBSTRN工具推进新生儿筛查研究并支持新生儿筛查利益相关者
err2023-10-30
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errChan, Kee; Hu, Zhanzhi; Bush, Lynn W.; Cope, Heidi; Holm, Ingrid A.; Kingsmore, Stephen F.; Wilhelm, Kevin; Scharfe, Curt; Brower, Amy
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Education and electronic medical records and genomics network, challenges, and lessons learned from a large-scale clinical trial using polygenic risk scores教育和电子病历和基因组学网络,挑战和从使用多基因风险评分的大规模临床试验中吸取的教训
err2023-09-01
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errConnolly, 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
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Advancing Understanding of Inequities in Rare Disease Genomics
err2023-08-01
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errSerrano, Jillian G.; O'Leary, Melanie; VanNoy, Grace E.; Mangilog, Brian E.; Holm, Ingrid A.; Fraiman, Yarden S.; Rehm, Heidi L.; O'Donnell-Luria, Anne; Wojcik, Monica H.
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Actionability of unanticipated monogenic disease risks in newborn genomic screening: Findings from the BabySeq Project
err2023-07-01
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errGreen, Robert C.; Shah, Nidh; Genetti, Casie A.; Yu, Timothy; Zettler, Bethany; Uveges, Melissa K.; Ceyhan-Birsoy, Ozge; Lebo, Matthew S.; Pereira, Stacey; Agrawal, Pankaj B.; Parad, Richard B.; McGuire, Amy L.; Christensen, Kurt D.; Schwartz, Talia S.; Rehm, Heidi L.; Holm, Ingrid A.; Beggs, Alan H.
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Studying the impact of translational genomic research: Lessons from eMERGE研究转化基因组研究的影响: 来自emerging的经验教训
err2023-07-01
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errClayton, Ellen Wright; Smith, Maureen E.; Anderson, Katherine C.; Chung, Wendy K.; Connolly, John J.; Fullerton, Stephanie M.; McGowan, Michelle L.; Peterson, Josh F.; Prows, Cynthia A.; Sabatello, Maya; Holm, Ingrid A.
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The fundamental need for unifying phenotypes in sudden unexpected pediatric deaths
err2023-06-02
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errOAAI
errWojcik, Monica H.; Poduri, Annapurna H.; Holm, Ingrid A.; MacRae, Calum A.; Goldstein, Richard D.
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Returning Individual Research Results from Digital Phenotyping in Psychiatry从精神病学的数字表型中返回个人研究结果
err2023-05-08
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errShen, Francis X.; Baum, Matthew L.; Martinez-Martin, Nicole; Miner, Adam S.; Abraham, Melissa; Brownstein, Catherine A.; Cortez, Nathan; Evans, Barbara J.; Germine, Laura T.; Glahn, David C.; Grady, Christine; Holm, Ingrid A.; Hurley, Elisa A.; Kimble, Sara; Lazaro-Munoz, Gabriel; Leary, Kimberlyn; Marks, Mason; Monette, Patrick J.; Onnela, Jukka-Pekka; O'Rourke, P. Pearl; Rauch, Scott L.; Shachar, Carmel; Sen, Srijan; Vahia, Ipsit; Vassy, Jason L.; Baker, Justin T.; Bierer, Barbara E.; Silverman, Benjamin C.
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