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Denis A. Akkad

Observed names: Akkad, Denis, D A Akkad, D. A. Akkad, D.A. Akkad, Denis A Akkad, Denis Akkad, Denis Amer Akkad, Denis A. Akkad, Denis‐Amer Akkad
OpenAlex ID: A5111591135
Dietary Fatty Acids Directly Impact Central Nervous System Autoimmunity via the Small Intestine
2015 · Aiden Haghikia, Stefanie Jörg, et al. · Immunity · 952
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PGC-1alpha downstream transcription factors NRF-1 and TFAM are genetic modifiers of Huntington disease
2011 · Elahe Taherzadeh-Fard, Carsten Saft, et al. · Molecular Neurodegeneration · 140
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Dietary Fatty Acids Directly Impact Central Nervous System Autoimmunity via the Small Intestine
2016 · Aiden Haghikia, Stefanie Jörg, et al. · Immunity · 125
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The genetics of multiple sclerosis: An update 2010
2010 · Sabine Hoffjan, Denis A. Akkad · Molecular and Cellular Probes · 81
A rare P2X7 variant Arg307Gln with absent pore formation function protects against neuroinflammation in multiple sclerosis
2015 · Ben J. Gu, Judith Field, et al. · Human Molecular Genetics · 75
mtDNA nt13708A Variant Increases the Risk of Multiple Sclerosis
2008 · Xinhua Yu, Dirk Koczan, et al. · PLoS ONE · 75
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MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis
2013 · Christina M. Lill, Brit-Maren M. Schjeide, et al. · Brain · 74
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Mitochondrial haplogroup H correlates with ATP levels and age at onset in Huntington disease
2010 · Larissa Arning, Aiden Haghikia, et al. · Journal of Molecular Medicine · 60
Variation in the IL7RA and IL2RA genes in German multiple sclerosis patients
2009 · D.A. Akkad, S. Hoffjan, et al. · Journal of Autoimmunity · 58
ASK1 and MAP2K6 as modifiers of age at onset in Huntington’s disease
2008 · Larissa Arning, Didier Monté, et al. · Journal of Molecular Medicine · 51
Progressive retinal atrophy in Schapendoes dogs: mutation of the newly identified CCDC66 gene
2009 · Gabriele Dekomien, Conni Vollrath, et al. · Neurogenetics · 48
Exome Sequencing Reveals AGBL5 as Novel Candidate Gene and Additional Variants for Retinitis Pigmentosa in Five Turkish Families
2015 · Simone Kastner, Ina-Janine Thiemann, et al. · Investigative Ophthalmology & Visual Science · 44
Genome-wide significant association with seven novel multiple sclerosis risk loci
2015 · Christina M Lill, Felix Luessi, et al. · Journal of Medical Genetics · 43
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Ccdc66 null mutation causes retinal degeneration and dysfunction
2011 · Wanda M. Gerding, Sabrina Schreiber, et al. · Human Molecular Genetics · 43
Promoter polymorphism rs3087456 in the MHC class II transactivator gene is not associated with susceptibility for selected autoimmune diseases in German patient groups
2006 · D. A. Akkad, P. Jagiello, et al. · International Journal of Immunogenetics · 43
Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk
2013 · Christina M Lill, Brit-Maren M Schjeide, et al. · Journal of Medical Genetics · 36
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Generalized progressive retinal atrophy in the Irish Glen of Imaal Terrier is associated with a deletion in the ADAM9 gene
2010 · Regina Kropatsch, Elisabeth Petrasch-Parwez, et al. · Molecular and Cellular Probes · 36
Closing the case of APOE in multiple sclerosis: no association with disease risk in over 29 000 subjects: Figure 1
2012 · Christina M Lill, Tian Liu, et al. · Journal of Medical Genetics · 34
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Independent replication of STAT3 association with multiple sclerosis risk in a large German case–control sample
2011 · Christina M. Lill, Brit-Maren M. Schjeide, et al. · Neurogenetics · 30
Sex specifically associated promoter polymorphism in multiple sclerosis affects interleukin 4 expression levels
2007 · D A Akkad, L Arning, et al. · Genes and Immunity · 30
Association of age at onset in Huntington disease with functional promoter variations in NPY and NPY2R
2013 · Eugen Kloster, Carsten Saft, et al. · Journal of Molecular Medicine · 28
Electrophoresis of DNA in human genetic diagnostics – state‐of‐the‐art, alternatives and future prospects
2006 · René Gödde, Denis‐Amer Akkad, et al. · Electrophoresis · 26
Homozygosity mapping and sequencing identify two genes that might contribute to pointing behavior in hunting dogs
2015 · Denis A Akkad, Wanda M Gerding, et al. · Canine Genetics and Epidemiology · 25
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SOX9 Duplication Linked to Intersex in Deer
2013 · Regina Kropatsch, Gabriele Dekomien, et al. · PLoS ONE · 25
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A large deletion in RPGR causes XLPRA in Weimaraner dogs
2016 · Regina Kropatsch, Denis A. Akkad, et al. · Canine Genetics and Epidemiology · 24
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Works count: 44
Citation count: 2,436
H-index: 24
I10-index: 37
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