Papadopoulou, 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.

Multidimensional and Longitudinal Impact of a Genetic Diagnosis for Critically Ill Infants

PEDIATRICS

IF6.4

2024-11-080

The BabySeq Project: A clinical trial of genome sequencing in a diverse cohort of infants

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2024-10-013

PRE

Expanding the genetic and phenotypic landscape of replication factor C complex-related disorders: RFC4 deficiency is linked to a multisystemic disorder

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2024-09-011

PRE

Morimoto, 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.

Genetic predictors of blood pressure traits are associated with preeclampsia

SCIENTIFIC REPORTS

IF3.9

2024-07-300

OAAI

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

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2024-06-013

PRE

Lewis, 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.

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

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2023-11-012

OAAI

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.

NBSTRN Tools to Advance Newborn Screening Research and Support Newborn Screening Stakeholders

NBSTRN工具推进新生儿筛查研究并支持新生儿筛查利益相关者

INTERNATIONAL JOURNAL OF NEONATAL SCREENING

IF4

2023-10-309

OAAI

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

GENETICS IN MEDICINE

IF6.2

2023-09-015

OAAI

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

Advancing Understanding of Inequities in Rare Disease Genomics

CLINICAL THERAPEUTICS

IF3.6

2023-08-0110

OAAI

Actionability of unanticipated monogenic disease risks in newborn genomic screening: Findings from the BabySeq Project

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2023-07-0121

OAAI

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

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2023-07-016

OAAI

The fundamental need for unifying phenotypes in sudden unexpected pediatric deaths

FRONTIERS IN MEDICINE

IF3

2023-06-023

OAAI

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

AMERICAN JOURNAL OF BIOETHICS

IF20.8

2023-05-0813

OAAI

Shen, 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.

Ingrid A. Holm

个人简介

教育背景

工作经历

荣誉奖项

研究方向