Maria Styczyńska

Identification of a Novel LRRK2 Mutation Linked to Autosomal Dominant Parkinsonism: Evidence of a Common Founder across European Populations

Jennifer M. Kachergus, Ignácio F. Mata, Mary Hulihan et al. · The American Journal of Human Genetics · 2005 · 534 citations · Full text

Molecular Neuroscience, Mendelian Disorder, Genetic Disorder +7

The rate of conversion of mild cognitive impairment to dementia: predictive role of depression

Tomasz Gabryelewicz, Maria Styczyńska, E Łuczywek et al. · International Journal of Geriatric Psychiatry · 2006 · 198 citations

Prevalence of major and minor depression in elderly persons with mild cognitive impairment—MADRS factor analysis

Tomasz Gabryelewicz, Maria Styczyńska, A. Pfeffer et al. · International Journal of Geriatric Psychiatry · 2004 · 136 citations

Homocysteine, Apolipoproteine E and Methylenetetrahydrofolate Reductase in Alzheimer’s Disease and Mild Cognitive Impairment

Dorota Religa, Maria Styczyńska, Tomasz Gabryelewicz et al. · Dementia and Geriatric Cognitive Disorders · 2003 · 102 citations

Mutations in presenilin 1, presenilin 2 and amyloid precursor protein genes in patients with early-onset Alzheimer's disease in Poland

Cezary Żekanowski, Maria Styczyńska, Beata Pepłońska et al. · Experimental Neurology · 2003 · 97 citations

Alzheimer's Disease, Molecular Neuroscience, Genetics +12