Vesarat Wessagowit

Loss of Kindlin-1, a Human Homolog of the Caenorhabditis elegans Actin–Extracellular-Matrix Linker Protein UNC-112, Causes Kindler Syndrome

Dawn H. Siegel, G H S Ashton, Homero Penagos et al. · The American Journal of Human Genetics · 2003 · 344 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

Autoantibodies to extracellular matrix protein 1 in lichen sclerosus

Noritaka Oyama, Ien Chan, S. M. Neill et al. · The Lancet · 2003 · 313 citations

Life Sciences, Dermatology, Immunology +11

Extracellular Matrix Protein 1 Gene (ECM1) Mutations in Lipoid Proteinosis and Genotype-Phenotype Correlation

Takahiro Hamada, Vesarat Wessagowit, Andrew P. South et al. · Journal of Investigative Dermatology · 2003 · 146 citations · Full text

Life Sciences, Genetics, Molecular Biology +16

Complete Maternal Isodisomy of Chromosome 3 in a Child with Recessive Dystrophic Epidermolysis Bullosa but No Other Phenotypic Abnormalities

Hiva Fassihi, Lu Liu, Vesarat Wessagowit et al. · Journal of Investigative Dermatology · 2006 · 69 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Molecular Basis of Kindler Syndrome in Italy: Novel and Recurrent Alu/Alu Recombination, Splice Site, Nonsense, and Frameshift Mutations in the KIND1 Gene

Cristina Has, Vesarat Wessagowit, Monica Pascucci et al. · Journal of Investigative Dermatology · 2006 · 62 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13