Lack of plakoglobin leads to lethal congenital epidermolysis bullosa: a novel clinico-genetic entityManuela Pigors, Cristina Has, Dimitra Kiritsi et al.|Human Molecular Genetics|2011Cited by 86
Phenotypic spectrum of epidermolysis bullosa associated with α6β4 integrin mutationsHauke Schumann, Cristina Has, Dimitra Kiritsi et al.|British Journal of Dermatology|2013Cited by 60
Exome Sequencing and Rare Variant Analysis Reveals Multiple Filaggrin Mutations in Bangladeshi Families with Atopic Eczema and Additional Risk GenesManuela Pigors, David P. Kelsell, John Common et al.|Journal of Investigative Dermatology|2018Cited by 45
Poikiloderma with neutropenia: a novel<i>C16orf57</i>mutation and clinical diagnostic criteriaAndreas Arnold, Cristina Has, Peter Itin et al.|British Journal of Dermatology|2010Cited by 43
Desmoplakin Mutations with Palmoplantar Keratoderma, Woolly Hair and CardiomyopathyManuela Pigors, Cristina Has, Agnes Schwieger‐Briel et al.|Acta Dermato Venereologica|2015Cited by 40