Zobrazeno 1 - 10
of 174
pro vyhledávání: '"Hui-Qi Qu"'
Autor:
Yichuan Liu, Hui‐Qi Qu, Xiao Chang, Frank D Mentch, Haijun Qiu, Kenny Nguyen, Kayleigh Ostberg, Tiancheng Wang, Joseph Glessner, Hakon Hakonarson
Publikováno v:
Cancer Communications, Vol 44, Iss 11, Pp 1374-1378 (2024)
Externí odkaz:
https://doaj.org/article/bc3392c761ea4a18bff6b28ffbd1d9e2
Autor:
Yichuan Liu, Hui‐Qi Qu, Xiao Chang, Frank D Mentch, Haijun Qiu, Kenny Nguyen, Xiang Wang, Amir Hossein Saeidian, Deborah Watson, Joseph Glessner, Hakon Hakonarson
Publikováno v:
Cancer Communications, Vol 43, Iss 11, Pp 1271-1274 (2023)
Externí odkaz:
https://doaj.org/article/fac5fa64e384499d8b772adb37e217a7
Autor:
Hui-Qi Qu, Hakon Hakonarson
Publikováno v:
Biomedicines, Vol 12, Iss 8, p 1911 (2024)
Postural Orthostatic Tachycardia Syndrome (POTS) affects up to 1% of the US population, predominantly women, and is characterized by a complex, elusive etiology and heterogeneous phenotypes. This review delves into the intricate physiology and etiolo
Externí odkaz:
https://doaj.org/article/3057b2d853ed48c68c9551f17b5fd702
Autor:
Yichuan Liu, Hui-Qi Qu, Xiao Chang, Frank D Mentch, Haijun Qiu, Xiang Wang, Amir Hossein Saeidian, Deborah Watson, Joseph Glessner, Hakon Hakonarson
Publikováno v:
Molecular Cancer, Vol 22, Iss 1, Pp 1-6 (2023)
Abstract Children with birth defects (BD) express distinct clinical features that often have various medical consequences, one of which is predisposition to the development of cancers. Identification of the underlying genetic mechanisms related to th
Externí odkaz:
https://doaj.org/article/20b97dee967c415aae8902ffd39dacfc
Autor:
Yichuan Liu, Hui-Qi Qu, Xiao Chang, Frank D Mentch, Haijun Qiu, Kenny Nguyen, Xiang Wang, Amir Hossein Saeidian, Deborah Watson, Joseph Glessner, Hakon Hakonarson
Publikováno v:
Biomarker Research, Vol 10, Iss 1, Pp 1-9 (2022)
Abstract Background Children with birth defects (BD) are more likely to develop cancer and the increased risk of cancer persists into adulthood. Prior population-based assessments have demonstrated that even non-chromosomal BDs are associated with at
Externí odkaz:
https://doaj.org/article/7e3940e024534ddab5294bf4eae709a5
Publikováno v:
Clinical and Translational Discovery, Vol 3, Iss 4, Pp n/a-n/a (2023)
Abstract Background Obesity is a complex trait caused by a combination of genetic, environmental and lifestyle factors that contributes to the risks of numerous serious diseases. Predictive measures of body mass index (BMI) hold significant promise,
Externí odkaz:
https://doaj.org/article/da118f66772e43b79297db9d5198e7c2
Autor:
Hui‐Qi Qu, John J Connolly, Peter Kraft, Jirong Long, Alexandre Pereira, Christopher Flatley, Constance Turman, Bram Prins, Frank Mentch, Paulo A Lotufo, Per Magnus, Meir J Stampfer, Rulla Tamimi, A Heather Eliassen, Wei Zheng, Gun Peggy Stromstad Knudsen, Oyvind Helgeland, Adam S. Butterworth, Hakon Hakonarson, Patrick M. Sleiman, the IHCC consortium
Publikováno v:
Clinical and Translational Medicine, Vol 13, Iss 6, Pp n/a-n/a (2023)
Abstract Background While polygenic risk scores hold significant promise in estimating an individual's risk of developing a complex trait such as obesity, their application in the clinic has, to date, been limited by a lack of data from non‐Europea
Externí odkaz:
https://doaj.org/article/f91a9b2167ce492faa7f00c547b8a133
Autor:
Wentao Zhou, Jun Jia, Hui-Qi Qu, Feier Ma, Junyi Li, Xiaohui Qi, Xinyi Meng, Zhiyong Ding, Gang Zheng, Hakon Hakonarson, Xiantie Zeng, Jin Li, Qianghua Xia
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Hallux valgus is a common form of foot deformity, and genetic factors contribute substantially to the pathogenesis of hallux valgus deformity. We conducted a genetic study on the structural variants underlying familial hallux valgus using whole exome
Externí odkaz:
https://doaj.org/article/a9c972c4adde44ababc48d258b219adb
Autor:
Yichuan Liu, Hui-Qi Qu, Jingchun Qu, Xiao Chang, Frank D. Mentch, Kenny Nguyen, Lifeng Tian, Joseph Glessner, Patrick M. A. Sleiman, Hakon Hakonarson
Publikováno v:
Respiratory Research, Vol 23, Iss 1, Pp 1-6 (2022)
Abstract Background Asthma is a complex condition largely attributed to the interactions among genes and environments as a heterogeneous phenotype. Obesity is significantly associated with asthma development, and genetic studies on obese vs. non-obes
Externí odkaz:
https://doaj.org/article/84e0f1c57f91478296a976802fd7faf5
Autor:
Christopher J. Cardinale, Xiao Chang, Zhi Wei, Hui-Qi Qu, Jonathan P. Bradfield, Constantin Polychronakos, Hakon Hakonarson
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
IntroductionType 1 diabetes, a disorder caused by autoimmune destruction of pancreatic insulin-producing cells, is more difficult to manage when it presents at a younger age. We sought to identify genetic correlates of the age of onset by conducting
Externí odkaz:
https://doaj.org/article/9d52458b245040239cac7c9f831930a9