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List of works by Wen-Hann Tan

A Neurodevelopmental Survey of Angelman Syndrome With Genotype-Phenotype Correlations ⬇️

scientific article published on September 1, 2010

A homozygous mutation in the tight-junction protein JAM3 causes hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts

scientific article

A randomized controlled trial of levodopa in patients with Angelman syndrome.

scientific article published on 25 September 2017

CHMP1A encodes an essential regulator of BMI1-INK4A in cerebellar development

scientific article published on 30 September 2012

Clinical diversity of MYH7-related cardiomyopathies: Insights into genotype-phenotype correlations

scientific article published on 27 December 2018

Developmental and degenerative features in a complicated spastic paraplegia.

scientific article

Disruption of MBD5 contributes to a spectrum of psychopathology and neurodevelopmental abnormalities ⬇️

scientific article published on April 16, 2013

Exome sequencing identifies novel missense and deletion variants in RTN4IP1 associated with optic atrophy, global developmental delay, epilepsy, ataxia, and choreoathetosis

scientific article published on 09 October 2020

Expanding the neurodevelopmental phenotype of PURA syndrome.

scientific article published on 17 November 2017

Expanding the phenotypic spectrum of TP63-related disorders including the first set of monozygotic twins

scientific article published on 12 November 2017

Genetic diagnoses and associated anomalies in fetuses prenatally diagnosed with esophageal atresia

scientific article published on 23 June 2020

Healthcare burden among individuals with Angelman syndrome: Findings from the Angelman Syndrome Natural History Study

scientific article published on 14 May 2019

Maladaptive behaviors in individuals with Angelman syndrome

scientific article published on 03 April 2019

Neurodevelopmental profile of siblings with Angelman syndrome due to pathogenic UBE3A variants

scientific article published on 19 December 2019

Two Angelman families with unusually advanced neurodevelopment carry a start codon variant in the most highly expressed UBE3A isoform

scientific article published on 07 May 2018

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