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Transcriptomic crossroads: Decoding genes and pathways that connect alopecia areata with chronic inflammatory skin disorders.

JID innovations : skin science from molecules to population health·2026

Do Alopecia Areata and Hair Colour Have a Shared Genetic Component?

Experimental dermatology·2026

Multicytokine-based transcriptome-wide association study for 7 inflammatory skin disorders identifies candidate causal genes in keratinocytes.

The Journal of allergy and clinical immunology·2026

Genome-wide association study of atopic and autoimmune comorbidities in alopecia areata.

Frontiers in immunology·2026

Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot.

Human genome variation·2026

Classification of angioedema types using decision tree modeling.

Frontiers in immunology·2026

[Mosaicism as a cause of Cowden syndrome].

Ugeskrift for laeger·2026

[Thyrotoxic crisis with cardiogenic shock].

Ugeskrift for laeger·2026

[Mindfulness-based cognitive therapy in the treatment of depression].

Ugeskrift for laeger·2026

[Fitness].

Ugeskrift for laeger·2026

[Risk of developing cataract related to fluoroscopy].

Ugeskrift for laeger·2026

[Obturator hernia with small bowel ileus presenting as hip pain in an elderly woman].

Ugeskrift for laeger·2026

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

Scientific reports·2026

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

The Lancet. Microbe·2026

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

Frontiers in genetics·2026

A Novel <i>FN1</i> Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

Journal of clinical medicine·2026

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

HLA·2026

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

Molecular syndromology·2026

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Transcriptomic crossroads: Decoding genes and pathways that connect alopecia areata with chronic inflammatory skin disorders.

Do Alopecia Areata and Hair Colour Have a Shared Genetic Component?

Multicytokine-based transcriptome-wide association study for 7 inflammatory skin disorders identifies candidate causal genes in keratinocytes.

Genome-wide association study of atopic and autoimmune comorbidities in alopecia areata.

Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot.

Classification of angioedema types using decision tree modeling.

[Mosaicism as a cause of Cowden syndrome].

[Thyrotoxic crisis with cardiogenic shock].

[Mindfulness-based cognitive therapy in the treatment of depression].

[Fitness].

[Risk of developing cataract related to fluoroscopy].

[Obturator hernia with small bowel ileus presenting as hip pain in an elderly woman].

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

A Novel <i>FN1</i> Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

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