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American Journal of Medical Genetics. Part A|November 19, 2009
The phenotypic spectrum of contiguous deletion of CYP21A2 and tenascin XB: quadricuspid aortic valve and other midline defectsWuyan Chen, Mimi S Kim, Sujata Shanbhag, et al.
Molecules (Basel, Switzerland)|May 18, 2013
Virtual screening and structure-based discovery of indole acylguanidines as potent β-secretase (BACE1) inhibitorsYiquan Zou, Li Li, Wuyan Chen, et al.
Clinical Chemistry|December 14, 2011
Junction site analysis of chimeric CYP21A1P/CYP21A2 genes in 21-hydroxylase deficiencyWuyan Chen, Zhi Xu, Annie Sullivan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 26, 2017
Revisiting the prevalence of nonclassic congenital adrenal hyperplasia in US Ashkenazi Jews and CaucasiansFady Hannah-Shmouni, Rachel Morissette, Ninet Sinaii, et al.
Kidney360|April 4, 2022
Clinical Utility of Genetic Testing in the Precision Diagnosis and Management of Pediatric Patients with Kidney and Urinary Tract DiseasesNasim Bekheirnia, Kevin E Glinton, Linda Rossetti, et al.
Neuroscience Letters|July 6, 2004
No association between the genetic polymorphisms within RTN4 and schizophrenia in the Chinese populationWuyan Chen, Niufan Gu, Shiwei Duan, et al.
Journal of Investigative Medicine High Impact Case Reports|May 10, 2021
A Novel Intronic Pathogenic Variant in STAR With a Dominant Negative Mechanism Causes Attenuated Lipoid Congenital Adrenal HyperplasiaErin Finn, Kimberly Kripps, Christina Chambers, et al.
Human Mutation|June 15, 2016
Ehlers-Danlos Syndrome Caused by Biallelic TNXB Variants in Patients with Congenital Adrenal HyperplasiaWuyan Chen, Ashley F Perritt, Rachel Morissette, et al.
Biochemical and Biophysical Research Communications|February 15, 2005
Association of the carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase gene with schizophrenia in the Chinese Han populationYonglan Zheng, Huafang Li, Wei Qin, et al.
Biological Psychiatry|February 16, 2006
Significant association between the genetic variations in the 5' end of the N-methyl-D-aspartate receptor subunit gene GRIN1 and schizophreniaXinzhi Zhao, Huafang Li, Yongyong Shi, et al.
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