H. Vahidnezhad

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Expanding genetics and phenotypic spectrum of epidermodysplasia verruciformis

J. Uitto, H. Vahidnezhad, 2016, The British journal of dermatology.

Molecular Genetics of Keratinization Disorders – What’s New About Ichthyosis

J. Uitto, H. Vahidnezhad, L. Youssefian, 2020, Acta dermato-venereologica.

Erythrokeratoderma: a manifestation associated with multiple types of ichthyoses with different gene defects

J. Uitto, S. Zeinali, H. Vahidnezhad, 2018, The British journal of dermatology.

Kindler syndrome, an orphan disease of cell/matrix adhesion in the skin – molecular genetics and therapeutic opportunities

J. Uitto, C. Has, H. Vahidnezhad, 2016 .

The matriptase‐prostasin proteolytic cascade in dermatologic diseases

J. Uitto, Sara Pajouhanfar, H. Vahidnezhad, 2020, Experimental dermatology.

Autosomal recessive congenital ichthyosis: CERS3 mutations identified by a next generation sequencing panel targeting ichthyosis genes

P. Fortina, J. Uitto, S. Zeinali, 2017, European Journal of Human Genetics.

Autozygosity Mapping by Genome-wide Single Nucleotide Polymorphism Array Identifies a Novel Homozygous HR Mutation in a Consanguineous Family with Universal Hereditary Hair Loss

J. Uitto, S. Zeinali, H. Vahidnezhad, 2021, International Journal of Dermatology and Venereology.

Genetic heterogeneity of heritable ectopic mineralization disorders in a large international cohort.

S. Terry, P. Fortina, J. Uitto, 2021, Genetics in medicine : official journal of the American College of Medical Genetics.

Applications of Spherical Nucleic Acid Nanoparticles as Delivery Systems.

J. Uitto, B. Baradaran, A. Mokhtarzadeh, 2019, Trends in molecular medicine.

Are Dyskeratosis Congenita patients at higher risk of symptomatic COVID-19?

H. Vahidnezhad, S. Dorgaleleh, Karim Naghipoor, 2022, Medical Hypotheses.

An Inherited Cancer Syndrome Due to a Germline Monoallelic EGFR Mutation with Loss of Heterozygosity in Lung and Breast Tumors

H. Vahidnezhad, H. Mirtavoos-Mahyari, Farbod Bahreini, 2021 .

Inherited non-alcoholic fatty liver disease and dyslipidemia due to monoallelic ABHD5 mutations.

K. Peris, J. Uitto, S. Zeinali, 2019, Journal of hepatology.

Klippel–Trenaunay syndrome belongs to the PIK3CA‐related overgrowth spectrum (PROS)

J. Uitto, H. Vahidnezhad, L. Youssefian, 2016, Experimental dermatology.

Phenotypic Spectrum of Epidermolysis Bullosa: The Paradigm of Syndromic versus Non-Syndromic Skin Fragility Disorders.

J. Uitto, H. Vahidnezhad, L. Youssefian, 2019, The Journal of investigative dermatology.

Ichthyosis, psoriasiform dermatitis, and recurrent fungal infections in patients with biallelic mutations in PERP

H. Vahidnezhad, S. Khodavaisy, H. Mahmoudi, 2021, Journal of the European Academy of Dermatology and Venereology : JEADV.

Management of symptomatic mucosal involvement in paediatric pachyonychia congenita

H. Vahidnezhad, L. Youssefian, 2020, The British journal of dermatology.

Genetic Predisposition to Numerous Large Ulcerating Basal Cell Carcinomas and Response to Immune Therapy

P. Fortina, J. Uitto, A. Ertel, 2021, International journal of dermatology and venereology.

Phenotypic spectrum of autosomal recessive congenital ichthyosis due to PNPLA1 mutation

J. Uitto, R. Lifton, A. Paller, 2017, The British journal of dermatology.

Association of MTHFR C677T polymorphism with elevated homocysteine level and disease development in vitiligo

J. Uitto, F. Abdollahimajd, H. Vahidnezhad, 2020, International Journal of Immunogenetics.

Autosomal recessive cutis laxa type 1C with a homozygous LTBP4 splicing variant: a case report and update of literature

M. Mazaheri, H. Vahidnezhad, Mahdieh Yavari, 2022, Molecular Biology Reports.

Pathomechanisms of epidermolysis bullosa: Beyond structural proteins.

J. Uitto, H. Vahidnezhad, L. Youssefian, 2022, Matrix biology : journal of the International Society for Matrix Biology.

A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome

J. Uitto, S. Zeinali, H. Vahidnezhad, 2017, Orphanet Journal of Rare Diseases.

Assessment of the risk and characterization of non-melanoma skin cancer in Kindler syndrome: study of a series of 91 patients

M. del Río, P. Itin, J. Uitto, 2019, Orphanet journal of rare diseases.

Advance trends in targeting homology-directed repair for accurate gene editing: An inclusive review of small molecules and modified CRISPR-Cas9 systems

A. Rahimpour, H. Vahidnezhad, Hadi Bayat, 2022, BioImpacts : BI.

Coronavirus disease 2019 and epidermolysis bullosa: Report of three cases

J. Uitto, F. Abdollahimajd, H. Vahidnezhad, 2020, Dermatologic Therapy.

Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathy.

P. Fortina, J. Uitto, J. McGrath, 2017, Matrix biology : journal of the International Society for Matrix Biology.

BMI1 and TWIST1 downregulated mRNA expression in basal cell carcinoma.

K. K. Hesari, P. Noormohammadpour, M. M. Shahshahani, 2014, Asian Pacific journal of cancer prevention : APJCP.

Phenotypic heterogeneity in PIK3CA‐related overgrowth spectrum

J. Uitto, S. Zeinali, H. Vahidnezhad, 2016, The British journal of dermatology.

Fibroadipose hyperplasia versus Proteus syndrome: segmental overgrowth with a mosaic mutation in the PIK3CA gene.

J. Uitto, Qiaoli Li, H. Vahidnezhad, 2015, The Journal of investigative dermatology.

Homozygous IL1RN Mutation in Siblings with Deficiency of Interleukin-1 Receptor Antagonist (DIRA)

J. Uitto, V. Ziaee, A. Jazayeri, 2020, Journal of Clinical Immunology.

Gene-Targeted Next-Generation Sequencing Identifies a Novel CLDN1 Mutation in a Consanguineous Family With NISCH Syndrome

J. Uitto, S. Zeinali, H. Vahidnezhad, 2017, The American Journal of Gastroenterology.

ENPP1 variants in patients with GACI and PXE expand the clinical and genetic heterogeneity of heritable disorders of ectopic calcification

S. Terry, J. Uitto, Qiaoli Li, 2022, PLoS genetics.

Inherited human ITK deficiency impairs IFN-γ immunity and underlies tuberculosis

J. Casanova, J. Uitto, L. Abel, 2022, The Journal of experimental medicine.

Genotypic Heterogeneity and the Mode of Inheritance in Epidermolysis Bullosa.

J. Uitto, H. Vahidnezhad, L. Youssefian, 2016, JAMA dermatology.

Clinical Characteristics of Coronavirus Disease 2019 in a Cohort of Iranian Patients: Olfactory Dysfunction as a Frequent Clinical Presentation

H. Vahidnezhad, M. Dalvandi, A. Kamali, 2021, Indian Journal of Forensic Medicine & Toxicology.

Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities.

J. Uitto, H. Vahidnezhad, Leila Yousseﬁan, 2016, The Journal of investigative dermatology.

Skin Manifestations in COVID-19 Patients: Are They Indicators for Disease Severity? A Systematic Review

M. Mirsaeidi, H. Vahidnezhad, M. Nasiri, 2021, Frontiers in Medicine.

Acquired ichthyosis, asteatotic dermatitis or xerosis? An update on pathoetiology and drug‐induced associations

H. Vahidnezhad, L. Youssefian, A. Saeidian, 2022, Journal of the European Academy of Dermatology and Venereology : JEADV.

De novo severe pemphigus vulgaris following SARS‐CoV‐2 vaccination with BBIBP‐CorV

H. Vahidnezhad, A. Ghanadan, Z. Saffarian, 2022, Dermatologic therapy.

Whole Genome Linkage Analysis Followed by Whole Exome Sequencing Identifies Nicastrin (NCSTN) as a Causative Gene in a Multiplex Family with γ-Secretase Spectrum of Autoinflammatory Skin Phenotypes.

J. Uitto, A. Kariminejad, H. Najmabadi, 2016, The Journal of investigative dermatology.

Co-existence of phenylketonuria either with maple syrup urine disease or Sandhoff disease in two patients from Iran: emphasizing the role of consanguinity

J. Uitto, S. Zeinali, M. Abiri, 2016, Journal of Pediatric Endocrinology & Metabolism (JPEM).

The utility of dermal fibroblasts in treatment of skin disorders: A paradigm of recessive dystrophic epidermolysis bullosa

J. Uitto, F. Abdollahimajd, S. Hosseinzadeh, 2021, Dermatologic therapy.

Epidermolysis bullosa and the COVID-19 pandemic: challenges and recommendations

F. Abdollahimajd, H. Vahidnezhad, H. Moravvej, 2020, The Journal of dermatological treatment.

Genomics‐based treatment in a patient with two overlapping heritable skin disorders: Epidermolysis bullosa and acrodermatitis enteropathica

J. Uitto, J. McGrath, A. Kariminejad, 2020, Human mutation.

Humans with inherited T cell CD28 deficiency are susceptible to skin papillomaviruses but are otherwise healthy

Mark M. Davis, J. Casanova, L. Notarangelo, 2021, Cell.

Lipoid proteinosis: phenotypic heterogeneity in Iranian families with c.507delT mutation in ECM1

J. Uitto, S. Akhondzadeh, Qiaoli Li, 2015, Experimental dermatology.

Increased level of cathelicidin (LL‐37) in vitiligo: Possible pathway independent from vitamin D receptor gene polymorphism

J. Uitto, S. Younespour, F. Abdollahimajd, 2020, Experimental dermatology.

Knock-Down of SDR9C7 Impairs Epidermal Barrier Function.

J. Uitto, A. South, H. Vahidnezhad, 2021, Journal of Investigative Dermatology.

Genotype–phenotype correlation in a large English cohort of patients with autosomal recessive ichthyosis

M. Simpson, J. Uitto, J. McGrath, 2019, The British journal of dermatology.

Autosomal recessive congenital ichthyosis: Genomic landscape and phenotypic spectrum in a cohort of 125 consanguineous families

P. Fortina, J. Uitto, K. K. Hesari, 2019, Human mutation.

Gene-Targeted Next Generation Sequencing Identifies PNPLA1 Mutations in Patients with a Phenotypic Spectrum of Autosomal Recessive Congenital Ichthyosis: The Impact of Consanguinity.

P. Fortina, J. Uitto, S. Zeinali, 2017, The Journal of investigative dermatology.

Keratitis‐ichthyosis‐deafness syndrome: Phenotypic heterogeneity and treatment perspective of patients with p.Asp50Asn GJB2 mutation

J. Uitto, Z. Naraghi, S. Zeinali, 2020, Dermatologic therapy.

Expanding the Genotypic Spectrum of Bathing Suit Ichthyosis

J. Uitto, H. Kaymakçalan, A. Paller, 2017, JAMA dermatology.

Research Techniques Made Simple: Genome-Wide Homozygosity/Autozygosity Mapping Is a Powerful Tool for Identifying Candidate Genes in Autosomal Recessive Genetic Diseases.

J. Uitto, A. Jazayeri, H. Vahidnezhad, 2018, The Journal of investigative dermatology.

Whole‐transcriptome sequencing identifies postzygotic ATP2A2 mutations in a patient misdiagnosed with herpes zoster, confirming the diagnosis of very late‐onset segmental Darier disease

J. Uitto, H. Galehdari, H. Vahidnezhad, 2022, Experimental dermatology.

Whole-transcriptome sequencing–based concomitant detection of viral and human genetic determinants of cutaneous lesions

J. Casanova, P. Fortina, J. Uitto, 2022, JCI insight.

Recalcitrant Cutaneous Warts in a Family with Inherited ICOS Deficiency.

J. Casanova, J. Uitto, S. Zeinali, 2022, The Journal of investigative dermatology.

184 Whole-transcriptome analysis by RNA-Seq for genetic diagnosis of Mendelian skin disorders in the context of consanguinity

P. Fortina, J. Uitto, A. South, 2021 .

Research Techniques Made Simple: Whole-Transcriptome Sequencing by RNA-Seq for Diagnosis of Monogenic Disorders.

J. Uitto, H. Vahidnezhad, L. Youssefian, 2020, The Journal of investigative dermatology.

Ancestral patterns of recessive dystrophic epidermolysis bullosa mutations in Hispanic populations suggest sephardic ancestry

Christopher R. Gignoux, F. Montinaro, M. Metspalu, 2021, American journal of medical genetics. Part A.

Interpretation of genomic sequence variants in genetic skin diseases: A primer for clinicians.

J. Uitto, H. Vahidnezhad, L. Youssefian, 2021, Journal of the American Academy of Dermatology.

Homozygous ITGA3 Missense Mutation in Adults in a Family with Syndromic Epidermolysis Bullosa (ILNEB).

J. Uitto, N. Nagy, P. Degrell, 2021, The Journal of investigative dermatology.

Whole-Transcriptome Analysis by RNA Sequencing for Genetic Diagnosis of Mendelian Skin Disorders in the Context of Consanguinity.

P. Fortina, J. Uitto, F. Abdollahimajd, 2021, Clinical chemistry.

Next generation sequencing identifies double homozygous mutations in two distinct genes (EXPH5 and COL17A1) in a patient with concomitant simplex and junctional epidermolysis bullosa

J. Uitto, J. McGrath, A. Kariminejad, 2018, Human mutation.

KRT5 and KRT14 Mutations in Epidermolysis Bullosa Simplex with Phenotypic Heterogeneity, and Evidence of Semidominant Inheritance in a Multiplex Family.

J. Uitto, S. Zeinali, H. Vahidnezhad, 2016, The Journal of investigative dermatology.

Mutation update: The spectra of PLEC sequence variants and related plectinopathies

J. Uitto, S. Zeinali, H. Vahidnezhad, 2022, Human mutation.

Kindler epidermolysis bullosa-like skin phenotype and downregulated basement membrane zone gene expression in poikiloderma with neutropenia and a homozygous USB1 mutation.

J. Uitto, J. McGrath, A. Kariminejad, 2021, Matrix biology : journal of the International Society for Matrix Biology.

Modeling breast acini in tissue culture for detection of malignant phenotype reversion to non-malignant phenotype.

F. Shokri, H. Vahidnezhad, M. Akhondi, 2009, Iranian biomedical journal.

The human CIB1–EVER1–EVER2 complex governs keratinocyte-intrinsic immunity to β-papillomaviruses

J. Casanova, E. Fuchs, J. Franco, 2018, The Journal of experimental medicine.

Dystrophic Epidermolysis Bullosa: COL7A1 Mutation Landscape in a Multi-Ethnic Cohort of 152 Extended Families with High Degree of Customary Consanguineous Marriages.

P. Fortina, J. Uitto, A. Ertel, 2017, The Journal of investigative dermatology.

Elevated Serum Levels of Interleukin-15 in Pemphigus Vulgaris Patients: a Potential Therapeutic Target

S. Tavakolpour, H. Vahidnezhad, S. Dadkhahfar, 2022, Dermatology practical & conceptual.

Mutations in PLOD3, encoding lysyl hydroxylase 3, cause a complex connective tissue disorder including recessive dystrophic epidermolysis bullosa-like blistering phenotype with abnormal anchoring fibrils and type VII collagen deficiency.

J. Uitto, J. McGrath, A. Kariminejad, 2019, Matrix biology : journal of the International Society for Matrix Biology.

Autosomal recessive cutis laxa type 1C with a homozygous LTBP4 splicing variant: a case report and update of literature

M. Mazaheri, H. Vahidnezhad, Mahdieh Yavari, 2022, Molecular Biology Reports.

Using immunofluorescence (antigen) mapping in the diagnosis and classification of epidermolysis bullosa: a first report from Iran

A. Kariminejad, H. Vahidnezhad, P. Toossi, 2015, International journal of dermatology.

Biallelic KRT5 mutations in epidermolysis bullosa simplex, including a complete human keratin 5 "knock-out".

J. Uitto, J. McGrath, A. Kariminejad, 2019, Matrix biology : journal of the International Society for Matrix Biology.

Multigene Next-Generation Sequencing Panel Identifies Pathogenic Variants in Patients with Unknown Subtype of Epidermolysis Bullosa: Subclassification with Prognostic Implications.

P. Fortina, J. Uitto, S. Zeinali, 2017, The Journal of investigative dermatology.

Pathogenic DST sequence variants result in either epidermolysis bullosa simplex (EBS) or hereditary sensory and autonomic neuropathy type 6 (HSAN‐VI)

J. Uitto, M. Garshasbi, H. Vahidnezhad, 2022, Experimental dermatology.

Arrhythmogenic right ventricular cardiomyopathy in patients with biallelic JUP-associated skin fragility

J. Uitto, J. McGrath, Z. Sani, 2020, Scientific Reports.

Genome‐wide single nucleotide polymorphism‐based autozygosity mapping facilitates identification of mutations in consanguineous families with epidermolysis bullosa

H. Hakonarson, Cecilia Kim, J. Bradfield, 2019, Experimental dermatology.

Molecular pathology of the basement membrane zone in heritable blistering diseases:: The paradigm of epidermolysis bullosa.

J. Uitto, C. Has, L. Bruckner-Tuderman, 2017, Matrix biology : journal of the International Society for Matrix Biology.

Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous population

M. Alaei, S. Zeinali, M. Abiri, 2018, Journal of Inherited Metabolic Disease.

Novel splice mutation in CDSN gene causing type b peeling skin syndrome

J. Uitto, F. Mora-López, H. Vahidnezhad, 2022, Journal of the European Academy of Dermatology and Venereology : JEADV.

The Kindler syndrome: a spectrum of FERMT1 mutations in Iranian families.

J. Uitto, S. Zeinali, Qiaoli Li, 2015, The Journal of investigative dermatology.

Epidermodysplasia Verruciformis: Genetic Heterogeneity and EVER1 and EVER2 Mutations Revealed by Genome-Wide Analysis.

J. Casanova, J. Uitto, S. Zeinali, 2019, The Journal of investigative dermatology.

Homozygous MEFV Gene Variant and Pyrin-Associated Autoinflammation With Neutrophilic Dermatosis: A Family With a Novel Autosomal Recessive Mode of Inheritance.

J. Uitto, V. Ziaee, M. Yousefi, 2021, JAMA dermatology.

Hypotrichosis with juvenile macular dystrophy: Combination of whole‐genome sequencing and genome‐wide homozygosity mapping identifies a large deletion in CDH3 initially undetected by whole‐exome sequencing—A lesson from next‐generation sequencing

J. Uitto, S. Zeinali, H. Vahidnezhad, 2019, Molecular genetics & genomic medicine.

Potential functions of the human homeobox TGIFLX/Y genes in normal and abnormal development

H. Vahidnezhad, W. Greene, R. Raoofian, 2012 .

A novel autosomal recessive GJB2‐associated disorder: Ichthyosis follicularis, bilateral severe sensorineural hearing loss, and punctate palmoplantar keratoderma

P. Fortina, J. Uitto, A. Kariminejad, 2018, Human mutation.

The quality of life in epidermolysis bullosa (EB-QoL) questionnaire: Translation, cultural adaptation, and validation into the Farsi language

H. Vahidnezhad, H. Moravvej, K. Heidari, 2020, International journal of women's dermatology.

Self-Reported Hand Eczema: Assessment of Prevalence and Risk Factors in Health Care Versus Non-Health Care Workers During the COVID-19 Pandemic.

A. Talebi, Mohammad Shahidi Dadras, F. Abdollahimajd, 2020, Dermatitis : contact, atopic, occupational, drug.

Losartan treatment improves recessive dystrophic epidermolysis bullosa: A case series

J. Uitto, H. Vahidnezhad, B. Hajimoradi, 2022, Dermatologic therapy.

Very-Early-Onset Inflammatory Bowel Disease in a Patient With Junctional Epidermolysis Bullosa With a Homozygous Mutation in the α6 Integrin Gene (ITGA6).

J. Uitto, S. Zeinali, H. Vahidnezhad, 2021, Inflammatory bowel diseases.

Losartan for treatment of epidermolysis bullosa: A new perspective

J. Uitto, H. Vahidnezhad, 2020, Dermatologic therapy.

Widespread aplasia cutis congenita in sibs with PLEC1 and ITGB4 variants

R. Hennekam, J. Uitto, A. Kariminejad, 2019, American journal of medical genetics. Part A.

Whole transcriptome–based skin virome profiling in typical epidermodysplasia verruciformis reveals α-, β-, and γ-HPV infections

J. Casanova, J. Uitto, E. Jouanguy, 2023, JCI insight.

Recalcitrant Warts, Epidermodysplasia Verruciformis, and the Tree-Man Syndrome: Phenotypic Spectrum of Cutaneous HPV Infections at the Intersection of Genetic Variability of Viral and Human Genomes.

J. Casanova, J. Uitto, E. Jouanguy, 2021, The Journal of investigative dermatology.

Molecular Dynamics Simulation of the Consequences of a PYCR1 Mutation (p.Ala189Val) in Patients with Complex Connective Tissue Disorder and Severe Intellectual Disability.

J. Uitto, M. Vasei, S. Zeinali, 2017, The Journal of investigative dermatology.

Hyaline Fibromatosis Syndrome: A Novel Mutation and Recurrent Founder Mutation in the CMG2/ANTXR2 Gene.

J. Uitto, V. Ziaee, S. Zeinali, 2017, Acta dermato-venereologica.

Ichthyosis follicularis syndromes in patients with mutations in GJB2

J. Uitto, S. Zeinali, F. Rajabi, 2022, Clinical and experimental dermatology.

CD147 inhibitors as a treatment for melanoma: Promising agents against SARS‐CoV‐2 infection

F. Abdollahimajd, H. Vahidnezhad, L. Youssefian, 2020, Dermatologic Therapy.

Mycophenolate mofetil treatment of an H syndrome patient with a SLC29A3 mutation

J. Uitto, H. Vahidnezhad, A. Goodarzi, 2020, Dermatologic therapy.

Linear basal cell nevus with a novel mosaic PTCH1 mutation

Jason B. Lee, J. Uitto, H. Vahidnezhad, 2020, Experimental dermatology.

Inherited Interleukin 2-Inducible T-Cell (ITK) Kinase Deficiency in Siblings With Epidermodysplasia Verruciformis and Hodgkin Lymphoma.

J. Casanova, P. Fortina, J. Uitto, 2019, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Infantile systemic hyalinosis in an Iranian family with a mutation in the CMG2/ANTXR2 gene

J. Uitto, V. Ziaee, H. Vahidnezhad, 2015, Clinical and experimental dermatology.

The genetic basis of hyaline fibromatosis syndrome in patients from a consanguineous background: a case series

J. Uitto, V. Ziaee, S. Zeinali, 2018, BMC Medical Genetics.

Digital

J. Uitto, V. Ziaee, S. Zeinali, 2015, Sales Excellence.

Expanding mutation landscape and phenotypic spectrum of autosomal recessive congenital ichthyosis

J. Uitto, H. Vahidnezhad, L. Youssefian, 2017, The British journal of dermatology.

Pachyonychia congenita: a case report of a successful treatment with rosuvastatin in a patient with a KRT6A mutation

J. Uitto, F. Abdollahimajd, F. Rajabi, 2018, British Journal of Dermatology.

Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients

M. Garshasbi, Shaghayegh Zokaei, M. Rohani, 2023, Orphanet Journal of Rare Diseases.

A CIB1 Splice-Site Founder Mutation in Families with Typical Epidermodysplasia Verruciformis.

J. Casanova, J. Uitto, M. Yousefi, 2019, The Journal of investigative dermatology.

Human Mutation

S. Zeinali, H. Vahidnezhad, P. Lovell, 2020 .

a including phenotype with abnormal anchoring and

A. Kariminejad, S. Zeinali, H. Vahidnezhad, 2018 .

FLT3L governs the development of partially overlapping hematopoietic lineages in humans and mice

S. Tangye, C. Deswarte, K. Claeys, 2024, Cell.