Associated Papers
Regional patterns of genetic variants in expanded carrier screening: a next-generation sequencing pilot study in Fujian Province, China.
Guo D et al.
Frontiers in Genetics, 2025
40421383 (PubMed )
Supplement: Table1.xlsx › Table_S3
Network expansion of genetic associations defines a pleiotropy map of human cell biology.
Barrio-Hernandez I et al.
Nature Genetics, 2023
36823319 (PubMed )
Supplement: EMS163741-supplement-Supplementary_Data_3.xlsx › ClinVar_evidence
Dental Phenotype with Minor Ectodermal Symptoms Suggestive of WNT10A Deficiency.
García-Martínez VE et al.
Children (basel, Switzerland), 2023
Prevalence of WNT10A gene mutations in non-syndromic oligodontia.
Ruiz-Heiland G et al.
Clinical Oral Investigations, 2019
Turkish Ectodermal Dysplasia Cohort: From Phenotype to Genotype in 17 Families.
Güven Y et al.
Cytogenetic and Genome Research, 2019
Case report of Schöpf-Schulz-Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in WNT10A.
Hsu TC et al.
The Journal of Dermatology, 2018
Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds.
Yang J et al.
Molecular Genetics & Genomic Medicine, 2015
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