Temporal clustering of familial sarcoidosis in non-consanguineous relatives

Pretreatment absolute monocyte counts are associated with biological disease-modifying anti-rheumatic drug non-response in patients with rheumatoid arthritis.

Scandinavian journal of rheumatology·2025

Investigating CD11c expression as a potential genomic biomarker of response to TNF inhibitor biologics in whole blood rheumatoid arthritis samples.

Arthritis research & therapy·2015

Genome-wide association meta-analyses to identify common genetic variants associated with hallux valgus in Caucasian and African Americans.

Journal of medical genetics·2015

Identification of BACH2 and RAD51B as rheumatoid arthritis susceptibility loci in a meta-analysis of genome-wide data.

Arthritis and rheumatism·2013

Association of genetic variants in the IL4 and IL4R genes with the severity of joint damage in rheumatoid arthritis: a study in seven cohorts.

Arthritis and rheumatism·2013

Association of a complement receptor 1 gene variant with baseline erythrocyte sedimentation rate levels in patients starting anti-TNF therapy in a UK rheumatoid arthritis cohort: results from the Biologics in Rheumatoid Arthritis Genetics and Genomics Study Syndicate cohort.

The pharmacogenomics journal·2013

Apical pulmonary fibrosis in psoriasis.

British journal of diseases of the chest·1988

Progressive apical pleural fibrosis: a 'constrictive' ventilatory defect.

British journal of diseases of the chest·1988

Induction of bronchial hyperresponsiveness following smoke inhalation injury.

British journal of diseases of the chest·1988

Chronic beryllium disease in identical twins.

British journal of diseases of the chest·1988

Pleuropulmonary haemangiopericytoma masquerading as a post-infective encysted pleural effusion.

British journal of diseases of the chest·1988

Massive haemoptysis in the acquired immunodeficiency syndrome.

British journal of diseases of the chest·1988

iPSC neurodegenerative disease initiative isogenic CAG repeat iPSC line for Huntington's disease.

Journal of Huntington's disease·2026

Precision Medicine in Epilepsy: Diagnostic Yield by Next-Generation Sequencing and Genotype-Phenotype Findings in a Romanian Cohort.

International journal of molecular sciences·2026

NGAL as a Biomarker of Tubular Injury and Glomerular Dysfunction in Fabry Nephropathy.

Cells·2026

Towards a unified biology of vertebrate number sense.

Communications biology·2026

Liang-Wang syndrome-associated variants in the BK potassium channel KCNMA1 disrupt channel trafficking and gating.

The Journal of biological chemistry·2026

Different variants, different cellular outcomes: Balanced KIF1A activity shapes synapse development.

The Journal of cell biology·2026

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Temporal clustering of familial sarcoidosis in non-consanguineous relatives

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Pretreatment absolute monocyte counts are associated with biological disease-modifying anti-rheumatic drug non-response in patients with rheumatoid arthritis.

Investigating CD11c expression as a potential genomic biomarker of response to TNF inhibitor biologics in whole blood rheumatoid arthritis samples.

Genome-wide association meta-analyses to identify common genetic variants associated with hallux valgus in Caucasian and African Americans.

Identification of BACH2 and RAD51B as rheumatoid arthritis susceptibility loci in a meta-analysis of genome-wide data.

Association of genetic variants in the IL4 and IL4R genes with the severity of joint damage in rheumatoid arthritis: a study in seven cohorts.

Association of a complement receptor 1 gene variant with baseline erythrocyte sedimentation rate levels in patients starting anti-TNF therapy in a UK rheumatoid arthritis cohort: results from the Biologics in Rheumatoid Arthritis Genetics and Genomics Study Syndicate cohort.

Apical pulmonary fibrosis in psoriasis.

Progressive apical pleural fibrosis: a 'constrictive' ventilatory defect.

Induction of bronchial hyperresponsiveness following smoke inhalation injury.

Chronic beryllium disease in identical twins.

Pleuropulmonary haemangiopericytoma masquerading as a post-infective encysted pleural effusion.

Massive haemoptysis in the acquired immunodeficiency syndrome.

iPSC neurodegenerative disease initiative isogenic CAG repeat iPSC line for Huntington's disease.

Precision Medicine in Epilepsy: Diagnostic Yield by Next-Generation Sequencing and Genotype-Phenotype Findings in a Romanian Cohort.

NGAL as a Biomarker of Tubular Injury and Glomerular Dysfunction in Fabry Nephropathy.

Towards a unified biology of vertebrate number sense.

Liang-Wang syndrome-associated variants in the BK potassium channel KCNMA1 disrupt channel trafficking and gating.

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Temporal clustering of familial sarcoidosis in non-consanguineous relatives

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