A common IL-1 complex haplotype is associated with an increased risk of atopy

Glucose exchange parameters in a subset of physiological conditions.

Physical chemistry chemical physics : PCCP·2023

Validation of the Finnish version of the food allergy quality of life questionnaire-parent form (F-FAQLQ-PF).

Acta paediatrica (Oslo, Norway : 1992)·2023

Mono- and biallelic variant effects on disease at biobank scale.

Nature·2023

Self-rated health in individuals with and without disease is associated with multiple biomarkers representing multiple biological domains.

Scientific reports·2021

Circulating cell-free DNA level predicts all-cause mortality independent of other predictors in the Health 2000 survey.

Scientific reports·2020

The rs2516839 variation of USF1 gene is associated with 4-year mortality of nonagenarian women: The Vitality 90+ study.

Annals of human genetics·2018

Exploring the clinical and mutational spectrum of MORC2-associated disorders.

Journal of medical genetics·2026

Founder variant in OTOG causing non-syndromic sensorineural hearing loss in Irish traveller population.

Journal of medical genetics·2026

Risk of breast cancer after ovarian cancer in germline BRCA1/2 heterozygotes.

Journal of medical genetics·2026

Rapid minigene workflow for functional reclassification of splicing variants in hereditary cancer diagnostics.

Journal of medical genetics·2026

Childhood-onset neurodegeneration and brain atrophy: defining UBTF-related developmental regression and progressive ataxia.

Journal of medical genetics·2026

BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.

Journal of medical genetics·2026

Concerted changes in the pediatric single-cell intestinal ecosystem before and after anti-TNF blockade.

eLife·2026

Hyper-IgE syndromes in pediatrics: clinical spectrum, differential diagnosis, and management.

Folia medica·2026

Immune Cell-Specific Regulatory Gene Prioritization in Low Back Pain Using Single-Cell eQTL-Informed Mendelian Randomization and Colocalization.

Journal of pain research·2026

Temporal windowing of recurrent sinusitis improves EHR-based immunodeficiency classification.

Journal of human immunity·2026

Screening and management of systemic sclerosis-associated pulmonary complications in Iraq: insights from a national survey of rheumatologists and pulmonologists.

Reumatologia·2026

Related Experiment Videos

A common IL-1 complex haplotype is associated with an increased risk of atopy

Related Concept Videos

Glucose exchange parameters in a subset of physiological conditions.

Validation of the Finnish version of the food allergy quality of life questionnaire-parent form (F-FAQLQ-PF).

Mono- and biallelic variant effects on disease at biobank scale.

Self-rated health in individuals with and without disease is associated with multiple biomarkers representing multiple biological domains.

Circulating cell-free DNA level predicts all-cause mortality independent of other predictors in the Health 2000 survey.

The rs2516839 variation of USF1 gene is associated with 4-year mortality of nonagenarian women: The Vitality 90+ study.

Exploring the clinical and mutational spectrum of MORC2-associated disorders.

Founder variant in OTOG causing non-syndromic sensorineural hearing loss in Irish traveller population.

Risk of breast cancer after ovarian cancer in germline BRCA1/2 heterozygotes.

Rapid minigene workflow for functional reclassification of splicing variants in hereditary cancer diagnostics.

Childhood-onset neurodegeneration and brain atrophy: defining UBTF-related developmental regression and progressive ataxia.

BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.

Concerted changes in the pediatric single-cell intestinal ecosystem before and after anti-TNF blockade.

Hyper-IgE syndromes in pediatrics: clinical spectrum, differential diagnosis, and management.

Immune Cell-Specific Regulatory Gene Prioritization in Low Back Pain Using Single-Cell eQTL-Informed Mendelian Randomization and Colocalization.

Temporal windowing of recurrent sinusitis improves EHR-based immunodeficiency classification.

Screening and management of systemic sclerosis-associated pulmonary complications in Iraq: insights from a national survey of rheumatologists and pulmonologists.

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A common IL-1 complex haplotype is associated with an increased risk of atopy

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