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Wen-Hann Tan

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Articles 85
Citations 1590
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Recent Articles
1.
Szenker-Ravi E, Ott T, Yusof A, Chopra M, Khatoo M, Pak B, et al.
Am J Hum Genet . 2025 Jan; 112(2):353-373. PMID: 39753129
Four genes-DAND5, PKD1L1, MMP21, and CIROP-form a genetic module that has specifically evolved in vertebrate species that harbor motile cilia in their left-right organizer (LRO). We find here that CIROZ...
2.
Kalanithy J, Mingardo E, Stegmann J, Dhakar R, Dakal T, Rosenfeld J, et al.
J Med Genet . 2024 Dec; 62(2):126-137. PMID: 39715634
Background: Previous studies in mouse, and zebrafish embryos show strong expression in progenitor cells of neuronal and neural crest tissues suggesting its involvement in neural crest specification. However, the role...
3.
Gomes A, Moore A, Cross M, Hardesty C, David K, Sampedro M, et al.
Am J Med Genet A . 2024 Dec; 197(4):e63961. PMID: 39679858
Angelman syndrome (AS) is a severe genetic neurodevelopmental disorder with an estimated prevalence of 1:20,000. Life expectancy appears to be normal, however, data regarding lifespan in AS are scarce. Until...
4.
Gong M, Li J, Qin Z, Machado Bressan Wilke M, Liu Y, Li Q, et al.
Am J Hum Genet . 2024 Oct; 111(11):2392-2410. PMID: 39419027
Microtubule affinity-regulating kinase 2 (MARK2) contributes to establishing neuronal polarity and developing dendritic spines. Although large-scale sequencing studies have associated MARK2 variants with autism spectrum disorder (ASD), the clinical features...
5.
Sadhwani A, Powers S, Wheeler A, Miller H, Potter S, Peters S, et al.
J Neurodev Disord . 2024 Jun; 16(1):32. PMID: 38879552
Background: Angelman syndrome (AS) is a neurodevelopmental disorder associated with severe global developmental delay. However, the ages at which different developmental skills are achieved in these individuals remain unclear. We...
6.
Russell B, Tan W
Hum Genet . 2024 Apr; 143(4):471-473. PMID: 38668862
No abstract available.
7.
Keary C, Bird L, de Wit M, Hatti S, Heimer G, Heussler H, et al.
Eur J Paediatr Neurol . 2023 Aug; 47:6-12. PMID: 37639777
Purpose: To evaluate efficacy and safety of gaboxadol for treatment of children with Angelman syndrome (AS). Method: In this international, double-blind, phase 3 trial, we randomized children 4-12 years old...
8.
Verscaj C, Velez-Bartolomei F, Bodle E, Chan K, Lyons M, Thorson W, et al.
Prenat Diagn . 2023 Aug; 44(2):237-246. PMID: 37632214
Objective: Recurrent deletions involving 17q12 are associated with a variety of clinical phenotypes, including congenital abnormalities of the kidney and urinary tract (CAKUT), maturity onset diabetes of the young, type...
9.
Terhal P, Venhuizen A, Lessel D, Tan W, Alswaid A, Grun R, et al.
Am J Hum Genet . 2023 Aug; 110(9):1470-1481. PMID: 37582359
Sclerosing skeletal dysplasias result from an imbalance between bone formation and resorption. We identified three homozygous, C-terminally truncating AXIN1 variants in seven individuals from four families affected by macrocephaly, cranial...
10.
Gwaltney A, Potter S, Peters S, Barbieri-Welge R, Horowitz L, Noll L, et al.
J Autism Dev Disord . 2023 Aug; 54(10):3863-3887. PMID: 37581718
In the current study, we examined adaptive skills and trajectories over time in 257 individuals with Angelman syndrome (AS) using the Vineland Adaptive Behavior Scales, 2nd Edition. Multilevel linear models...