Dong-Chuan Guo (Dongchuan Guo)

Publication Activity (10 Years)

Years Active: 2022-2023
Publications (10 Years): 5

Top Topics

Pulmonary Artery

Top Venues

Clinical genetics

Circulation. Genomic and precision medicine

Nature genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Dong-Chuan Guo, Xueyan Duan, Kathleen Mimnagh, Alana C Cecchi, Isabella C Marin, Yang Yu, Walter V Torres, Kwanghyuk Lee, Xue Zhu, David R Murdock, Suzanne M Leal, Marsha M Wheeler, Josh Smith, Michael J Bamshad, Dianna M Milewicz
An FBN1 deep intronic variant is associated with pseudoexon formation and a variable Marfan phenotype in a five generation family. Clinical genetics (2023)
Derek M Klarin, Poornima Devineni, Anoop K Sendamarai, Anthony R Angueira, Sarah E Graham, Ying H Shen, Michael G Levin, James Paul Pirruccello, Ida Surakka, Purushotham R Karnam, Tanmoy Roychowdhury, Yanming Li, Minxian Wang, Krishna G Aragam, Kaavya Paruchuri, Verena Zuber, Gabrielle E Shakt, Noah L Tsao, Renae L Judy, Ha My T Vy, Shefali Setia Verma, Daniel James Rader, Ron Do, Joseph E Bavaria, Girish Nitin Nadkarni, Marylyn DeRiggi Ritchie, null null, Stephen Burgess, Dong-Chuan Guo, Patrick T Ellinor, Scott A LeMaire, Dianna M Milewicz, Cristen J Willer, Pradeep Natarajan, Philip S Tsao, Saiju Pyarajan, Scott M Damrauer
Genome-wide association study of thoracic aortic aneurysm and dissection in the Million Veteran Program. Nature genetics (2023)
Dong-Chuan Guo, Xueyan Duan, Kathleen Mimnagh, Alana C Cecchi, Isabella C Marin, Yang Yu, Walter V Torres, Kwanghyuk Lee, Xue Zhu, David R Murdock, Suzanne M Leal, Marsha M Wheeler, Josh Smith, Michael J Bamshad, Dianna M Milewicz
An FBN1 Deep Intronic Variant is Associated with Pseudoexon Formation and a Variable Marfan Phenotype in a Five Generation Family. Clinical genetics (2023)
Dong-Chuan Guo, Xueyan Duan, Kathleen Mimnagh, Alana C Cecchi, Isabella C Marin, Yang Yu, Walter V Velasco, Kwanghyuk Lee, Xue Zhu, David R Murdock, Suzanne M Leal, Marsha M Wheeler, Josh Smith, Michael J Bamshad, Dianna M Milewicz
An FBN1 deep intronic variant is associated with pseudoexon formation and a variable Marfan phenotype in a five generation family. Clinical genetics (2023)
Maura L Boerio, Nicole M Engelhardt, Sanmati Cuddapah, Jessica I Gold, Isabella C Marin, Amélie C Pinard, Dong-Chuan Guo, Siddharth K Prakash, Dianna M Milewicz
Further Evidence That ARIH1 Rare Variants Predispose to Thoracic Aortic Disease. Circulation. Genomic and precision medicine (2022)