Publications by authors named "C. Has"

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Tissue and systemic inflammation in dystrophic epidermolysis bullosa: a systematic review and meta-analysis.
Meropi Karakioulaki, Nana-Adjoa Kwarteng, Adriani Nikolakopoulou, Hanning Yang, Moritz Hess, Cristina Has

Orphanet J Rare Dis· September 2025

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Effects of bcsE, luxS and rfaG genes on the physiology and pathogenicity of Salmonella Typhimurium.
Semra Soydam, Elif Gamze Has, Tuba Nur Sürkaç, Mustafa Akçelik, Nefise Akçelik

Arch Microbiol· February 2025

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An intronic variant in LAMB3 contributes to junctional epidermolysis bullosa and enamel hypoplasia via translational attenuation.
Yi Yang, Yao Wang, Man Qin, Yuming Zhao, Cristina Has

Arch Oral Biol· January 2025

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Biologics in congenital ichthyosis: are they effective?
Juliette Mazereeuw-Hautier, Céline Granier Tournier, Angela Hernandez-Martin, Sarah Milesi, Hélène Texier, Cristina Has

Br J Dermatol· January 2025

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Generation and genetic repair of two human induced pluripotent stem cell lines from patients with Epidermolysis Bullosa simplex associated with a heterozygous mutation in the translation initiation codon of KLHL24.
Spyridon T Pachis, Veronika Ramovs, Christian Freund, Cristina Has, Karine Raymond

Stem Cell Res· December 2024

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[
[Molecular pathology of skin fragility].
Cristina Has, Meropi Karakioulaki

Dermatologie (Heidelb)· December 2024

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[
[Skin fragility].
Meropi Karakioulaki, Cristina Has

Dermatologie (Heidelb)· December 2024

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Comparison of Left Ventricular Global Longitudinal Strain and Left Ventricular Ejection Fraction in Acute Respiratory Failure Patients Requiring Invasive Mechanical Ventilation.
Zubair Bashir, Feven Ataklte, Shuyuan Wang, Edward W Chen, Vishnu Kadiyala, Phinnara Has

J Cardiovasc Dev Dis· October 2024

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Invasive Mechanical Ventilation Is Associated with Worse Right Ventricular Strain in Acute Respiratory Failure Patients.
Shuyuan Wang, Zubair Bashir, Edward W Chen, Vishnu Kadiyala, Charles F Sherrod, Phinnara Has

J Cardiovasc Dev Dis· August 2024

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Proprotein convertase subtilisn/kexin type 9 inhibitors and small interfering RNA therapy for cardiovascular risk reduction: A systematic review and meta-analysis.
Tasnim F Imran, Ali A Khan, Phinnara Has, Alexis Jacobson, Stephanie Bogin

PLoS One· December 2023

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Amino Acid Substitution in the Cysteine-Rich Region of the Integrin β4 Subunit Causes Late-Onset Mild Junctional Epidermolysis Bullosa without Extracutaneous Involvement.
Yao Wang, Alrun Hotz, Philipp R Esser, Judith Fischer, Cristina Has

J Invest Dermatol· November 2023

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Acral lamellar ichthyosis with amino acid substitution in the C-terminus of keratin 2.
Leonie Frommherz, Katalin Komlosi, Charlotte Hewel, Julia Kopp, Malin Dewenter, Cristina Has

J Eur Acad Dermatol Venereol· April 2023

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Lipoid proteinosis: Novel ECM1 pathogenic variants and intrafamilial variability in four unrelated Arab families.
Mingfeng Li, Judith Fischer, Sylvia Safwat, Walaa Shoman, Yasmine El Chazli, Cristina Has

Pediatr Dermatol· January 2023

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Assessment of biventricular function with speckle tracking echocardiography in newly-diagnosed adult-onset asthma.
Sadettin Selçuk Baysal, Mehmet Has

J Asthma· February 2022

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Maternal Isodisomy of Chromosome 3 Combined with a Mutation in the Gene Causes Autosomal Recessive Chanarin-Dorfman Syndrome.
Julia Kopp, Cristina Has, Alrun Hotz, Sarah C Grünert, Judith Fischer

Genes (Basel)· July 2021

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Women's Empowerment and Determinants of Early Initiation of Breastfeeding: A Scoping Review.
Setho Hadisuyatmana, Eka Mishbahatul Marah Has, Susy Katikana Sebayang, Ferry Efendi, Erni Astutik

J Pediatr Nurs· April 2021

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Rothmund-Thomson syndrome type 1 caused by biallelic ANAPC1 gene mutations.
B Zirn, U Bernbeck, K Alt, F Oeffner, A Gerhardinger, C Has

Skin Health Dis· March 2021

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A
Aberrant splicing as potential modifier of the phenotype of junctional epidermolysis bullosa.
R Mittwollen, S Wohlfart, J Park, E Grosch, C Has

J Eur Acad Dermatol Venereol· September 2020

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Natural history of growth and anaemia in children with epidermolysis bullosa: a retrospective cohort study.
A Reimer, M Hess, A Schwieger-Briel, D Kiritsi, F Schauer, C Has

Br J Dermatol· June 2020

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Coping with the Unexpected: Patient Trust in Physicians following Delivery.
Martha B Kole, Nina K Ayala, Melissa A Clark, Phinnara Has, Erika F Werner

Am J Perinatol· June 2020

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Molecular Therapeutics in Development for Epidermolysis Bullosa: Update 2020.
Cristina Has, Andrew South, Jouni Uitto

Mol Diagn Ther· June 2020

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A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation.
Steffen Hörer, Slaheddine Marrakchi, Franz P W Radner, Gerd Zolles, Lisa Heinz, Cristina Has

J Invest Dermatol· October 2019

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Amino acid substitution in the C-terminal domain of collagen XVII reduces laminin-332 interaction causing mild skin fragility with atrophic scarring.
Jasmin Kroeger, Esther Hoppe, Célimène Galiger, Cristina Has, Claus-Werner Franzke

Matrix Biol· July 2019

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Kindler syndrome in a patient with colitis and primary sclerosing cholangitis: coincidence or association?
Ângela Roda, Ana Rita Travassos, Luís Soares-de-Almeida, Cristina Has

Dermatol Online J· March 2018

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Monoallelic Mutations in the Translation Initiation Codon of KLHL24 Cause Skin Fragility.
Yinghong He, Kristin Maier, Juna Leppert, Ingrid Hausser, Agnes Schwieger-Briel, Cristina Has

Am J Hum Genet· December 2016

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