[New and old genetic markers of childhood diabetes]

Season of birth is associated with multiple sclerosis and disease severity.

Multiple sclerosis journal - experimental, translational and clinical·2022

Technological readiness and implementation of genomic-driven precision medicine for complex diseases.

Journal of internal medicine·2021

Epstein-Barr virus infection after adolescence and human herpesvirus 6A as risk factors for multiple sclerosis.

European journal of neurology·2020

Stressful life events are associated with the risk of multiple sclerosis.

European journal of neurology·2020

The immunogenetics of narcolepsy associated with A(H1N1)pdm09 vaccination (Pandemrix) supports a potent gene-environment interaction.

Genes and immunity·2017

VAV1 regulates experimental autoimmune arthritis and is associated with anti-CCP negative rheumatoid arthritis.

Genes and immunity·2017

[Longer medical certificates do not improve the quality of physicians' assessments].

Lakartidningen·2026

[Upper tract urothelial carcinoma - regional differences observed in several quality indicators].

Lakartidningen·2026

[Rare manifestations of giant cell arteritis].

Lakartidningen·2026

[Neoehrlichiosis in rituximab-treated patients with MS in Sweden].

Lakartidningen·2026

[The Swedish Neonatal Quality Register (SNQ) - a complete register for a complex chain of events].

Lakartidningen·2026

[Postoperative atrial fibrillation after open heart surgery].

Lakartidningen·2026

Dominant truncating variants in KAT6A cause two neurodevelopmental disorders with opposite gene regulatory and metabolic changes.

medRxiv : the preprint server for health sciences·2026

GIRK Channel Loss of Function Increases Dendritic Excitability in a Mouse Model of GNB1 Encephalopathy.

bioRxiv : the preprint server for biology·2026

First Prenatal Report of Ververi-Brady Syndrome: From Fetal Clues to Genetic Truth!

Journal of clinical ultrasound : JCU·2026

A Regulator SNP Affecting the Transcription Factor SP1 Binding Site in the PIK3R3 Gene Contributes to Noise-Induced Hearing Loss Risk.

Human mutation·2026

Neuropsychiatry genetics in Africa.

Nature communications·2026

Genetic findings in a Turkish clinical cohort with hereditary Parkinson's disease.

Neurogenetics·2026

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[New and old genetic markers of childhood diabetes]

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Season of birth is associated with multiple sclerosis and disease severity.

Technological readiness and implementation of genomic-driven precision medicine for complex diseases.

Epstein-Barr virus infection after adolescence and human herpesvirus 6A as risk factors for multiple sclerosis.

Stressful life events are associated with the risk of multiple sclerosis.

The immunogenetics of narcolepsy associated with A(H1N1)pdm09 vaccination (Pandemrix) supports a potent gene-environment interaction.

VAV1 regulates experimental autoimmune arthritis and is associated with anti-CCP negative rheumatoid arthritis.

[Longer medical certificates do not improve the quality of physicians' assessments].

[Upper tract urothelial carcinoma - regional differences observed in several quality indicators].

[Rare manifestations of giant cell arteritis].

[Neoehrlichiosis in rituximab-treated patients with MS in Sweden].

[The Swedish Neonatal Quality Register (SNQ) - a complete register for a complex chain of events].

[Postoperative atrial fibrillation after open heart surgery].

Dominant truncating variants in KAT6A cause two neurodevelopmental disorders with opposite gene regulatory and metabolic changes.

GIRK Channel Loss of Function Increases Dendritic Excitability in a Mouse Model of GNB1 Encephalopathy.

First Prenatal Report of Ververi-Brady Syndrome: From Fetal Clues to Genetic Truth!

A Regulator SNP Affecting the Transcription Factor SP1 Binding Site in the PIK3R3 Gene Contributes to Noise-Induced Hearing Loss Risk.

Neuropsychiatry genetics in Africa.

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[New and old genetic markers of childhood diabetes]

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