Researchclopedia

Research Researchers Institutions Topics Submit About

Command Palette

Search for a command to run...

Researchclopedia

Research Researchers Institutions About

© 2026 Researchclopedia. Powered by OpenAlex under CC0 license.

Wen‐Hann Tan | Researchclopedia

Back to researchers

Wen‐Hann Tan

Boston Children's Hospital ORCID

157

Works

6,076

Citations

42

h-index

84

i10-index

Research Topics

Genetic Syndromes and Imprinting Genetics and Neurodevelopmental Disorders Epigenetics and DNA Methylation

Affiliations

Boston University2020–2021

Rush University Medical Center2020–2023

Boston Children's Hospital2005–2025

Academy of Medical Sciences2002–2005

Howard Hughes Medical Institute2010–2010

Top Works

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

David T. Miller,Yiping Shen,et al.

2008430 citations

Genomics and Rare Diseases

Prenatal Screening and Diagnostics

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

Michael S. Ching,Yiping Shen,et al.

2010309 citations

The spectrum of vascular anomalies in patients with <i>PTEN</i> mutations: implications for diagnosis and management

Wen‐Hann Tan,Hagit Baris,et al.

2007294 citations

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

Konrad Platzer,Hongjie Yuan,et al.

2017253 citations

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

Tong Sun,Xiaoping Miao,et al.

2004198 citations

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

Sébastien Küry,Geeske M. van Woerden,et al.

2017198 citations

Copy number variation plays an important role in clinical epilepsy

Heather E. Olson,Yiping Shen,et al.

2014172 citations

A Neurodevelopmental Survey of Angelman Syndrome With Genotype-Phenotype Correlations

Jennifer Gentile,Wen‐Hann Tan,et al.

2010166 citations

Update of PAX2 mutations in renal coloboma syndrome and establishment of a locus-specific database

Matthew Bower,Rémi Salomon,et al.

2011154 citations