Author

Ilker Karaca

Observed names: I Karaca, I. Karaca, Karaca, Ilker

Institution: University of Bonn

Observed institutions: University of Bonn, University Hospital Bonn

OpenAlex ID: A5080179646

Cerebrospinal fluid and blood biomarkers for neurodegenerative dementias: An update of the Consensus of the Task Force on Biological Markers in Psychiatry of the World Federation of Societies of Biological Psychiatry

2017 · Piotr Lewczuk, Peter Riederer, et al. · The World Journal of Biological Psychiatry · 307

Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia

2017 · Martina Minnerop, Delia Kurzwelly, et al. · Brain · 120

Trehalose Alters Subcellular Trafficking and the Metabolism of the Alzheimer-associated Amyloid Precursor Protein

2016 · Nguyen T. Tien, Ilker Karaca, et al. · Journal of Biological Chemistry · 71

PLCG2 Protective Variant p.P522R Modulates Tau Pathology and Disease Progression in Patients with Mild Cognitive Impairment

2018 · Alzheimer’s Disease Neuroimaging Initiative (ADNI), Luca Kleineidam, et al. · Acta Neuropathologica · 62

Deficiency of Sphingosine-1-phosphate Lyase Impairs Lysosomal Metabolism of the Amyloid Precursor Protein

2014 · Ilker Karaca, Irfan Y. Tamboli, et al. · Journal of Biological Chemistry · 57

Sphingosine-1-Phosphate: Boon and Bane for the Brain

2014 · Gerhild van Echten-Deckert, Nadine Hagen-Euteneuer, et al. · Cellular Physiology and Biochemistry · 50

Caspase-8, association with Alzheimer’s Disease and functional analysis of rare variants

2017 · Jan Rehker, Johanna Rodhe, et al. · PLoS ONE · 47

Functional involvement of γ-secretase in signaling of the triggering receptor expressed on myeloid cells-2 (TREM2)

2016 · Konstantin Glebov, Patrick Wunderlich, et al. · Journal of Neuroinflammation · 43

A rare heterozygous TREM2 coding variant identified in familial clustering of dementia affects an intrinsically disordered protein region and function of TREM2

2019 · Meliha Karsak, Konstantin Glebov, et al. · Human Mutation · 6

No Association of the Variant rs11887120 in DNMT3A with Cognitive Decline in Individuals with Mild Cognitive Impairment

2016 · Katharina Bey, Steffen Wolfsgruber, et al. · Epigenomics · 6

CCL17 deficiency is associated with beneficial CNS immune responses and prevents cognitive decline in a mouse model of Alzheimer’s disease

2013 · Kim Neitzert, Önder Albayram, et al. · Brain Behavior and Immunity · 3

Suche nach Risikogenen bei der Alzheimer-Erkrankung

2017 · I. Karaca, H. Wagner, et al. · Der Nervenarzt · 2

3 .Neuropathologie und molekulare Mechanismen

2018 · Dietmar Rudolf Thal, Jochen Walter, et al. · De Gruyter eBooks · 1

CCL17-deficiency alters myeloid cell-responses and prevents cognitive decline in APP/PS1-mice

2015 · K Neitzert, Ö Albayram, et al. · Pharmacopsychiatry · 1

[P3–164]: FUNCTIONAL CHARACTERIZATION OF A RARE GENETIC VARIANT IN PHOSPHOLIPASE Cγ2 WHICH IS ASSOCIATED WITH A BENEFICIAL EFFECT ON THE PROGRESSION OF ALZHEIMER's DISEASE

2017 · Ilker Karaca, Claudia Walliser, et al. · Alzheimer s & Dementia

Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia

2017 · Martina Minnerop, Delia Kurzwelly, et al. · Newcastle University ePrints (Newcastle Univesity)

Works count: 19

Citation count: 776

H-index: 8

I10-index: 8