Wenqi Zeng
Hong Kong University of Science and Technology(HK)
Publications by Year
Research Areas
Metabolism and Genetic Disorders, Posttraumatic Stress Disorder Research, Mitochondrial Function and Pathology, Genetic Neurodegenerative Diseases, Genomics and Rare Diseases
Most-Cited Works
- → Enhanced utility of family-centered diagnostic exome sequencing with inheritance model–based analysis: results from 500 unselected families with undiagnosed genetic conditions(2014)464 cited
- → Biotin-Responsive Basal Ganglia Disease Maps to 2q36.3 and Is Due to Mutations in SLC19A3(2005)215 cited
- → Neurexin 1α structural variants associated with autism(2008)152 cited
- → ELP2 is a novel gene implicated in neurodevelopmental disabilities(2015)73 cited
- → Congenital lethal motor neuron disease with a novel defect in ribosome biogenesis(2014)61 cited
- → New Insights into the Genetics of Fetal Megacystis: ACTG2 Mutations, Encoding γ-2 Smooth Muscle Actin in Megacystis Microcolon Intestinal Hypoperistalsis Syndrome (Berdon Syndrome)(2015)56 cited
- → A human de novo mutation inMYH10phenocopies the loss of function mutation in mice(2013)50 cited
- → Diagnostic Exome Sequencing Identifies Two Novel IQSEC2 Mutations Associated with X‐Linked Intellectual Disability with Seizures: Implications for Genetic Counseling and Clinical Diagnosis(2013)46 cited
- → Expanding the clinical and mutational spectrum of Kaufman oculocerebrofacial syndrome with biallelic UBE3B mutations(2014)39 cited
- → Risk factors of post-traumatic stress disorder 10 years after Wenchuan earthquake: a population-based case–control study(2021)32 cited