[Suggestions from Department of Health and Security's genetic screening advisory committee have been published]

Identification of C12orf4 as a gene for autosomal recessive intellectual disability.

Clinical genetics·2016

A genome-wide linkage and association study of musical aptitude identifies loci containing genes related to inner ear development and neurocognitive functions.

Molecular psychiatry·2014

Novel PORCN mutations in focal dermal hypoplasia.

Clinical genetics·2009

Complement factor H variant Y402H is not a risk factor for preeclampsia in the Finnish population.

Hypertension in pregnancy·2008

Genome-wide linkage scan for loci of musical aptitude in Finnish families: evidence for a major locus at 4q22.

Journal of medical genetics·2008

The T/G 13915 variant upstream of the lactase gene (LCT) is the founder allele of lactase persistence in an urban Saudi population.

Journal of medical genetics·2007

Update on Current Care Guideline: Psoriasis (skin and joints).

Duodecim; laaketieteellinen aikakauskirja·2017

FOUR score in monitoring the level of consciousness of an intensive care patient: first experience of the use of the Finnish language version.

Duodecim; laaketieteellinen aikakauskirja·2017

Discussing a serious illness with a patient and family.

Duodecim; laaketieteellinen aikakauskirja·2017

Invasive treatment of superficial veins of the lower extremities.

Duodecim; laaketieteellinen aikakauskirja·2017

When should a drain be left in the abdominal cavity upon surgery?

Duodecim; laaketieteellinen aikakauskirja·2017

Diagnostics and current care of myasthenia gravis.

Duodecim; laaketieteellinen aikakauskirja·2017

Burr Hole Microsurgical Transsylvian Approach for Insular Gliomas.

Operative neurosurgery (Hagerstown, Md.)·2026

ARTS-DB 2.0: an expanded database for target-directed genome mining across bacteria and fungi.

Database : the journal of biological databases and curation·2026

Vascularized glioblastoma-on-a-chip reveals microglia-mediated regulation of tumor invasion and stemness.

Lab on a chip·2026

Association Between Genetic Ancestry and Multiple Sclerosis Severity.

Annals of neurology·2026

GWAS studies and polygenic risk scores in organ transplantation.

Current opinion in organ transplantation·2026

[Corrigendum] High expression of hnRNPA1 promotes cell invasion by inducing EMT in gastric cancer.

Oncology reports·2026

Related Experiment Videos

[Suggestions from Department of Health and Security's genetic screening advisory committee have been published]

Related Concept Videos

Identification of C12orf4 as a gene for autosomal recessive intellectual disability.

A genome-wide linkage and association study of musical aptitude identifies loci containing genes related to inner ear development and neurocognitive functions.

Novel PORCN mutations in focal dermal hypoplasia.

Complement factor H variant Y402H is not a risk factor for preeclampsia in the Finnish population.

Genome-wide linkage scan for loci of musical aptitude in Finnish families: evidence for a major locus at 4q22.

The T/G 13915 variant upstream of the lactase gene (LCT) is the founder allele of lactase persistence in an urban Saudi population.

Update on Current Care Guideline: Psoriasis (skin and joints).

FOUR score in monitoring the level of consciousness of an intensive care patient: first experience of the use of the Finnish language version.

Discussing a serious illness with a patient and family.

Invasive treatment of superficial veins of the lower extremities.

When should a drain be left in the abdominal cavity upon surgery?

Diagnostics and current care of myasthenia gravis.

Burr Hole Microsurgical Transsylvian Approach for Insular Gliomas.

ARTS-DB 2.0: an expanded database for target-directed genome mining across bacteria and fungi.

Vascularized glioblastoma-on-a-chip reveals microglia-mediated regulation of tumor invasion and stemness.

Association Between Genetic Ancestry and Multiple Sclerosis Severity.

GWAS studies and polygenic risk scores in organ transplantation.

[Corrigendum] High expression of hnRNPA1 promotes cell invasion by inducing EMT in gastric cancer.

Related Experiment Videos

[Suggestions from Department of Health and Security's genetic screening advisory committee have been published]

Related Concept Videos

Related Articles