Wen‐Hann Tan
Boston Children's Hospital(US)Harvard University(US)Baylor College of Medicine(US)Capital Medical University(CN)Cornell University(US)University of Malaya(MY)Boston Children's Museum(US)Beijing Shijitan Hospital(CN)
Publications by Year
Research Areas
Genetic Syndromes and Imprinting, Genetics and Neurodevelopmental Disorders, Epigenetics and DNA Methylation, Genomics and Rare Diseases, Prenatal Screening and Diagnostics
Most-Cited Works
- → Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders(2008)430 cited
- → Deletions of NRXN1 (neurexin‐1) predispose to a wide spectrum of developmental disorders(2010)309 cited
- → The spectrum of vascular anomalies in patients with PTEN mutations: implications for diagnosis and management(2007)294 cited
- → GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects(2017)252 cited
- → Polymorphisms of Death Pathway Genes FAS and FASL in Esophageal Squamous-Cell Carcinoma(2004)198 cited
- → De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability(2017)197 cited