Denis A. Akkad

St. Josef Hospital
Bochum, NW, Germany

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 23 publications

Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients.

Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients.

Journal: G3 (Bethesda, Md.)

Published: May 20, 2016

Dietary Fatty Acids Directly Impact Central Nervous System Autoimmunity via the Small Intestine.

Dietary Fatty Acids Directly Impact Central Nervous System Autoimmunity via the Small Intestine.

Journal: Immunity

Published: April 21, 2016

A large deletion in RPGR causes XLPRA in Weimaraner dogs.

A large deletion in RPGR causes XLPRA in Weimaraner dogs.

Journal: Canine genetics and epidemiology

Published: March 23, 2016

Exome Sequencing Reveals AGBL5 as Novel Candidate Gene and Additional Variants for Retinitis Pigmentosa in Five Turkish Families.

Exome Sequencing Reveals AGBL5 as Novel Candidate Gene and Additional Variants for Retinitis Pigmentosa in Five Turkish Families.

Journal: Investigative ophthalmology & visual science

Published: January 01, 2016

Multiple sclerosis in families: risk factors beyond known genetic polymorphisms.

Multiple sclerosis in families: risk factors beyond known genetic polymorphisms.

Journal: Neurogenetics

Published: October 04, 2015

Left-Right Axis Differentiation and Functional Lateralization: a Haplotype in the Methyltransferase Encoding Gene SETDB2 Might Mediate Handedness in Healthy Adults.

Left-Right Axis Differentiation and Functional Lateralization: a Haplotype in the Methyltransferase Encoding Gene SETDB2 Might Mediate Handedness in Healthy Adults.

Journal: Molecular neurobiology

Published: September 08, 2015

Genome-wide significant association with seven novel multiple sclerosis risk loci.

Genome-wide significant association with seven novel multiple sclerosis risk loci.

Journal: Journal of medical genetics

Published: August 06, 2015

A rare P2X7 variant Arg307Gln with absent pore formation function protects against neuroinflammation in multiple sclerosis.

A rare P2X7 variant Arg307Gln with absent pore formation function protects against neuroinflammation in multiple sclerosis.

Journal: Human molecular genetics

Published: May 13, 2015

Investigation of sex-specific effects of apolipoprotein E on severity of EAE and MS.

Investigation of sex-specific effects of apolipoprotein E on severity of EAE and MS.

Journal: Journal of neuroinflammation

Published: April 08, 2015

Combinations of susceptibility genes are associated with higher risk for multiple sclerosis and imply disease course specificity.

Combinations of susceptibility genes are associated with higher risk for multiple sclerosis and imply disease course specificity.

Journal: PloS one

Published: January 05, 2015

Homozygosity mapping and sequencing identify two genes that might contribute to pointing behavior in hunting dogs.

Homozygosity mapping and sequencing identify two genes that might contribute to pointing behavior in hunting dogs.

Journal: Canine genetics and epidemiology

Published: December 20, 2014

Association of TNFAIP3 and TNFRSF1A variation with multiple sclerosis in a German case-control cohort.

Association of TNFAIP3 and TNFRSF1A variation with multiple sclerosis in a German case-control cohort.

Journal: International journal of immunogenetics

Published: December 19, 2014

Showing 1-12 of 23

Last Updated: 09/26/2026