Wen‐Hann Tan

Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders

David T. Miller, Yiping Shen, Lauren A. Weiss et al. · Journal of Medical Genetics · 2008 · 429 citations

Deletions of <i>NRXN1</i> (neurexin‐1) predispose to a wide spectrum of developmental disorders

Michael S. Ching, Yiping Shen, Wen‐Hann Tan et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2010 · 308 citations · Full text

Brain Development, Genetics, Genetic Epidemiology +21

<i>GRIN2B</i> encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects

Konrad Platzer, Hongjie Yuan, Hannah M. Schutz et al. · Journal of Medical Genetics · 2017 · 249 citations · Full text

Polymorphisms of Death Pathway Genes FAS and FASL in Esophageal Squamous-Cell Carcinoma

Tong Sun, Xiaoping Miao, Xun Zhang et al. · JNCI Journal of the National Cancer Institute · 2004 · 198 citations · Full text

De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability

Sébastien Küry, Geeske M. van Woerden, Thomas Besnard et al. · The American Journal of Human Genetics · 2017 · 193 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +5