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Cristina Has
Cristina Has
Dermatologist
Verified email at uniklinik-freiburg.de
Title
Cited by
Cited by
Year
Inherited epidermolysis bullosa: updated recommendations on diagnosis and classification
JD Fine, L Bruckner-Tuderman, RAJ Eady, EA Bauer, JW Bauer, C Has, ...
Journal of the American Academy of Dermatology 70 (6), 1103-1126, 2014
10452014
Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility
C Has, JW Bauer, C Bodemer, MC Bolling, L Bruckner‐Tuderman, A Diem, ...
British Journal of Dermatology 183 (4), 614-627, 2020
5342020
Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome
F Jobard, B Bouadjar, F Caux, S Hadj-Rabia, C Has, F Matsuda, ...
Human molecular genetics 12 (8), 925-935, 2003
2872003
Integrin α3 Mutations with Kidney, Lung, and Skin Disease
C Has, G Spartà, D Kiritsi, L Weibel, A Moeller, V Vega-Warner, A Waters, ...
New England Journal of Medicine 366 (16), 1508-1514, 2012
2762012
Epidermolysis bullosa
A Bardhan, L Bruckner-Tuderman, ILC Chapple, JD Fine, N Harper, ...
Nature reviews Disease primers 6 (1), 78, 2020
2562020
Kindlin-1 is a phosphoprotein involved in regulation of polarity, proliferation, and motility of epidermal keratinocytes
C Herz, M Aumailley, C Schulte, U Schlotzer-Schrehardt, ...
Journal of biological chemistry 281 (47), 36082-36090, 2006
1672006
Kindler syndrome: Extension of FERMT1 mutational spectrum and natural history
C Has, D Castiglia, M del Rio, M Garcia Diez, E Piccinni, D Kiritsi, ...
Human mutation 32 (11), 1204-1212, 2011
1432011
Laminin 332 in junctional epidermolysis bullosa
D Kiritsi, C Has, L Bruckner-Tuderman
Cell adhesion & migration 7 (1), 135-141, 2013
1422013
Expanding the COL7A1 mutation database: novel and recurrent mutations and unusual genotype–phenotype constellations in 41 patients with dystrophic epidermolysis bullosa
JS Kern, J Kohlhase, L Bruckner-Tuderman, C Has
Journal of investigative dermatology 126 (5), 1006-1012, 2006
1352006
Clinical practice guidelines for laboratory diagnosis of epidermolysis bullosa
C Has, L Liu, MC Bolling, AV Charlesworth, M El Hachem, MJ Escámez, ...
The British Journal of Dermatology 182 (3), 574, 2020
1182020
The Conradi–Hünermann–Happle syndrome (CDPX2) and emopamil binding protein: novel mutations, and somatic and gonadal mosaicism
C Has, L Bruckner-Tuderman, D Müller, M Floeth, E Folkers, D Donnai, ...
Human molecular genetics 9 (13), 1951-1955, 2000
1112000
Epidermolysis bullosa: Molecular pathology of connective tissue components in the cutaneous basement membrane zone
C Has, A Nyström, AH Saeidian, L Bruckner-Tuderman, J Uitto
Matrix Biology 71, 313-329, 2018
1082018
Lack of plakoglobin leads to lethal congenital epidermolysis bullosa: a novel clinico-genetic entity
M Pigors, D Kiritsi, S Krümpelmann, N Wagner, Y He, M Podda, ...
Human molecular genetics 20 (9), 1811-1819, 2011
1062011
The international dystrophic epidermolysis bullosa patient registry: An online database of dystrophic epidermolysis bullosa patients and their COL7A1 mutations
PC van den Akker, MF Jonkman, T Rengaw, L Bruckner‐Tuderman, ...
Human mutation 32 (10), 1100-1107, 2011
1052011
APOBEC mutation drives early-onset squamous cell carcinomas in recessive dystrophic epidermolysis bullosa
RJ Cho, LB Alexandrov, NY Den Breems, VS Atanasova, M Farshchian, ...
Science Translational Medicine 10 (455), eaas9668, 2018
1042018
Molecular basis of inherited skin-blistering disorders, and therapeutic implications
M Aumailley, C Has, L Tunggal, L Bruckner-Tuderman
Expert reviews in molecular medicine 8 (24), 1-21, 2006
1022006
Chronic colitis due to an epithelial barrier defect: the role of kindlin‐1 isoforms
JS Kern, C Herz, E Haan, D Moore, S Nottelmann, T Von Lilien, P Greiner, ...
The Journal of Pathology: A Journal of the Pathological Society of Great …, 2007
992007
Monoallelic mutations in the translation initiation codon of KLHL24 cause skin fragility
Y He, K Maier, J Leppert, I Hausser, A Schwieger-Briel, L Weibel, ...
The American Journal of Human Genetics 99 (6), 1395-1404, 2016
952016
Molecular mechanisms of phenotypic variability in junctional epidermolysis bullosa
D Kiritsi, JS Kern, H Schumann, J Kohlhase, C Has, L Bruckner-Tuderman
Journal of medical genetics 48 (7), 450-457, 2011
952011
Forty‐two novel COL7A1 mutations and the role of a frequent single nucleotide polymorphism in the MMP1 promoter in modulation of disease severity in a large …
JS Kern, G Grüninger, R Imsak, ML Müller, H Schumann, D Kiritsi, ...
British Journal of Dermatology 161 (5), 1089-1097, 2009
952009
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