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M. Barcikowska · SciRah

Researcher profile · Semantic Scholar

M. Barcikowska

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M. Barcikowska — researcher profile on SciRah

h-index: 43
Works: 259
Citations: 7,357

Most-cited papers

Common variants in ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer’s disease
P. Hollingworth, D. Harold, R. Sims, A. Gerrish +168 more
2011Nature Genetics1,946 citations Open access
Semantic Scholar
neurodegeneration : evidence for association of the p . R 47 H variant with frontotemporal dementia and Parkinson ¿ s disease Permalink
Sruti Rayaprolu, Bianca Mullen, M. Baker, T. Lynch +29 more
2013264 citations
Semantic Scholar
Sigma nonopioid intracellular receptor 1 mutations cause frontotemporal lobar degeneration–motor neuron disease
A. Luty, John B. Kwok, C. Dobson-Stone, C. Loy +15 more
2010Annals of Neurology210 citations
Semantic Scholar
TREM2 in neurodegeneration: evidence for association of the p.R47H variant with frontotemporal dementia and Parkinson’s disease
Sruti Rayaprolu, Bianca Mullen, M. Baker, Timothy Lynch +29 more
2013Molecular Neurodegeneration115 citations Open access
Semantic Scholar
A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants
Manu Sharma, J. Ioannidis, J. Aasly, G. Annesi +59 more
2012Journal of Medical Genetics110 citations Open access
Semantic Scholar
Glutathione S-transferase omega genes in Alzheimer and Parkinson disease risk, age-at-diagnosis and brain gene expression: an association study with mechanistic implications
M. Allen, F. Zou, H. Chai, C. Younkin +30 more
2012Molecular Neurodegeneration92 citations Open access
Semantic Scholar
DNA methylation in ELOVL2 and C1orf132 correctly predicted chronological age of individuals from three disease groups
M. Spólnicka, E. Pośpiech, B. Pepłońska, R. Zbieć-Piekarska +11 more
2017Zeitschrift für Rechtsmedizin90 citations Open access
Semantic Scholar
Mitochondrial haplogroup H and Alzheimer's disease--is there a connection?
A. Maruszak, J. A. Canter, M. Styczyńska, C. Żekanowski +1 more
2009Neurobiology of Aging89 citations
Semantic Scholar
Guideline on the clinical investigation of medicines for the treatment of Alzheimer’s disease
M. Barcikowska
201888 citations
Semantic Scholar
Conformationally altered p53: a novel Alzheimer's disease marker?
C. Lanni, M. Racchi, G. Mazzini, A. Ranzenigo +10 more
2008Molecular Psychiatry84 citations
Semantic Scholar
Conformational Altered p53 as an Early Marker of Oxidative Stress in Alzheimer's Disease
L. Buizza, Giovanna Cenini, C. Lanni, G. Ferrari-Toninelli +10 more
2012PLoS ONE80 citations Open access
Semantic Scholar
ApoE variant p.V236E is associated with markedly reduced risk of Alzheimer’s disease
C. Medway, Samer O. Abdul-Hay, Tynickwa Mims, Li Ma +17 more
2014Molecular Neurodegeneration74 citations Open access
Semantic Scholar
Replication of EPHA1 and CD33 associations with late-onset Alzheimer's disease: a multi-centre case-control study
M. Carrasquillo, O. Belbin, T. Hunter, Li Ma +14 more
2011Molecular Neurodegeneration74 citations Open access
Semantic Scholar
Replication of BIN1 association with Alzheimer’s disease and evaluation of genetic interactions
M. Carrasquillo, O. Belbin, T. Hunter, Li Ma +13 more
2011Journal of Alzheimer's Disease70 citations Open access
Semantic Scholar
Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders
Kotaro Ogaki, Shunsuke Koga, M. Heckman, Fabienne C. Fiesel +28 more
2015Neurology67 citations Open access
Semantic Scholar
The Role of Matrix Metalloproteinases and Tissue Inhibitors of Metalloproteinases in the Pathophysiology of Neurodegeneration: A Literature Study
B. Mroczko, Magdalena Groblewska, M. Barcikowska
2013Journal of Alzheimer's Disease61 citations
Semantic Scholar
TOMM40 rs10524523 Polymorphism's Role in Late-Onset Alzheimer's Disease and in Longevity
A. Maruszak, B. Pepłońska, K. Safranow, M. Chodakowska-Żebrowska +2 more
2012Journal of Alzheimer's Disease56 citations
Semantic Scholar
The Impact of Mitochondrial and Nuclear DNA Variants on Late-Onset Alzheimer's Disease Risk
A. Maruszak, K. Safranow, W. Branicki, K. Gaweda-Walerych +5 more
2011Journal of Alzheimer's Disease54 citations Open access
Semantic Scholar
Mitochondrial transcription factor A variants and the risk of Parkinson's disease.
K. Gaweda-Walerych, K. Safranow, A. Maruszak, M. Białecka +12 more
2010Neuroscience Letters48 citations Open access
Semantic Scholar
GWAS risk factors in Parkinson's disease: LRRK2 coding variation and genetic interaction with PARK16.
A. Soto-Ortolaza, M. Heckman, C. Labbé, D. Serie +12 more
2013American Journal of Neurodegenerative Disease43 citations
Semantic Scholar
Role for the microtubule-associated protein tau variant p.A152T in risk of α-synucleinopathies
C. Labbé, Kotaro Ogaki, O. Lorenzo-Betancor, A. Soto-Ortolaza +32 more
2015Neurology42 citations Open access
Semantic Scholar
Plasma leptin levels and free leptin index in women with Alzheimer's disease.
A. Baranowska-Bik, W. Bik, M. Styczyńska, M. Chodakowska-Żebrowska +5 more
2015Neuropeptides41 citations
Semantic Scholar
Human leukocyte antigen variation and Parkinson’s disease
A. Puschmann, Christophe Verbeeck, M. Heckman, A. Soto-Ortolaza +8 more
2011Parkinsonism & Related Disorders41 citations Open access
Semantic Scholar
Association between genetic and environmental factors and the risk of Alzheimer's disease.
M. Styczyńska, J. Strosznajder, D. Religa, M. Chodakowska-Żebrowska +6 more
2008Folia Neuropathologica39 citations
Semantic Scholar
Increased CD44 Gene Expression in Lymphocytes Derived from Alzheimer Disease Patients
D. Uberti, Giovanna Cenini, S. Bonini, M. Barcikowska +3 more
2010Neurodegenerative Diseases35 citations
Semantic Scholar
Variation in NPC1, the gene encoding Niemann-Pick C1, a protein involved in intracellular cholesterol transport, is associated with Alzheimer disease and/or aging in the Polish Population
R. Erickson, Katherine Larson-Thomé, Lyndon Weberg, A. Szybińska +4 more
2008Neuroscience Letters35 citations Open access
Semantic Scholar
Cell cycle regulation distinguishes lymphocytes from sporadic and familial Alzheimer's disease patients.
E. Białopiotrowicz, B. Kuźniewska, N. Kachamakova-Trojanowska, M. Barcikowska +2 more
2011Neurobiology of Aging34 citations Open access
Semantic Scholar
A Patient with Posterior Cortical Atrophy Possesses a Novel Mutation in the Presenilin 1 Gene
E. Sitek, E. Narożańska, B. Pepłońska, S. Filipek +9 more
2013PLoS ONE31 citations Open access
Semantic Scholar
DNAJC13 p.Asn855Ser mutation screening in Parkinson’s disease and pathologically confirmed Lewy body disease patients
O. Lorenzo-Betancor, Kotaro Ogaki, A. Soto-Ortolaza, C. Labbé +26 more
2015European Journal of Neurology27 citations Open access
Semantic Scholar
A Novel MAPT Mutation, G55R, in a Frontotemporal Dementia Patient Leads to Altered Tau Function
A. Iyer, N. Lapointe, Krzysztof Zielke, M. Berdyński +6 more
2013PLoS ONE27 citations Open access
Semantic Scholar
Genetic variation of the retromer subunits VPS26A/B-VPS29 in Parkinson’s disease
Barbara Shannon, A. Soto-Ortolaza, Sruti Rayaprolu, Heather D. Cannon +14 more
2014Neurobiology of Aging26 citations Open access
Semantic Scholar
Association between Cerebrospinal Fluid Biomarkers for Alzheimer’s Disease, APOE Genotypes and Auditory Verbal Learning Task in Subjective Cognitive Decline, Mild Cognitive Impairment, and Alzheimer’s Disease
Monika Mandecka, M. Budziszewska, A. Barczak, B. Pepłońska +6 more
2016Journal of Alzheimer's Disease25 citations
Semantic Scholar
Writing in Richardson variant of progressive supranuclear palsy in comparison to progressive non-fluent aphasia.
E. Sitek, A. Barczak, Klaudia Kluj-Kozłowska, Marcin Kozlowski +5 more
2015Neurologia i Neurochirurgia Polska25 citations
Semantic Scholar
N-acetylaspartate, choline, myoinositol, glutamine and glutamate (glx) concentration changes in proton MR spectroscopy (1H MRS) in patients with mild cognitive impairment (MCI)
J. Walecki, M. Barcikowska, J. Cwikła, T. Gabryelewicz
2011Medical Science Monitor25 citations Open access
Semantic Scholar
An independent replication of PARK16 in Asian samples
C. Vilariño-Güell, O. Ross, J. Aasly, L. White +13 more
2010Neurology25 citations Open access
Semantic Scholar
PIN1 gene variants in Alzheimer's disease
A. Maruszak, K. Safranow, K. Gustaw, Beata Kijanowska-Haładyna +9 more
2009BMC Medical Genetics25 citations Open access
Semantic Scholar
Earlier Onset of Alzheimer's Disease: Risk Polymorphisms Within PRNP, PRND, CYP46, and APOE Genes
E. Golańska, K. Hułas-Bigoszewska, M. Sieruta, I. Zawlik +8 more
2009Journal of Alzheimer's Disease23 citations
Semantic Scholar
Intra-Familial Clinical Heterogeneity due to FTLD-U with TDP-43 Proteinopathy Caused by a Novel Deletion in Progranulin Gene (PGRN)
T. Gabryelewicz, M. Masellis, M. Berdyński, J. Bilbao +8 more
2011Journal of Alzheimer's Disease22 citations Open access
Semantic Scholar
TOMM40 and APOE common genetic variants are not Parkinson's disease risk factors.
B. Pepłońska, K. Safranow, K. Gaweda-Walerych, A. Maruszak +4 more
2013Neurobiology of Aging21 citations Open access
Semantic Scholar
Combined use of biochemical and volumetric biomarkers to assess the risk of conversion of mild cognitive impairment to Alzheimer's disease.
M. Nesteruk, T. Nesteruk, M. Styczyńska, Monika Mandecka +2 more
2016Folia Neuropathologica20 citations Open access
Semantic Scholar
TREM2 variants in neurodegenerative disorders in the Polish population. Homozygosity and compound heterozygosity in FTD patients
B. Pepłońska, M. Berdyński, Monika Mandecka, A. Barczak +3 more
2018Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration19 citations
Semantic Scholar
Identification of a Late Onset Alzheimer's Disease Candidate Risk Variant at 9q21.33 in Polish Patients
P. Gaj, A. Paziewska, W. Bik, Michalina Dąbrowska +7 more
2012Journal of Alzheimer's Disease19 citations
Semantic Scholar
LRRTM3 Interacts with APP and BACE1 and Has Variants Associating with Late-Onset Alzheimer’s Disease (LOAD)
S. Lincoln, M. Allen, Claire L. Cox, Louise P. Walker +24 more
2013PLoS ONE18 citations Open access
Semantic Scholar
Agraphia in patients with frontotemporal dementia and parkinsonism linked to chromosome 17 with P301L MAPT mutation: dysexecutive, aphasic, apraxic or spatial phenomenon?
E. Sitek, E. Narożańska, A. Barczak, B. Jasińska-Myga +14 more
2012Neurocase18 citations Open access
Semantic Scholar
Interleukin-1 Gene –511 CT Polymorphism and the Risk of Alzheimer’s Disease in a Polish Population
A. Klimkowicz-Mrowiec, M. Marona, P. Wołkow, A. Maruszak +5 more
2009Dementia and Geriatric Cognitive Disorders18 citations
Semantic Scholar
Cathepsin B p.Gly284Val Variant in Parkinson’s Disease Pathogenesis
L. Milanowski, Xu Hou, Jenny M. Bredenberg, Fabienne C. Fiesel +34 more
2022International Journal of Molecular Sciences15 citations Open access
Semantic Scholar
APBB2 genetic polymorphisms are associated with severe cognitive impairment in centenarians.
E. Golańska, M. Sieruta, S. Grešner, A. Pfeffer +7 more
2013Experimental Gerontology15 citations
Semantic Scholar
Frequency of Mutations in PRKN, PINK1, and DJ1 in Patients With Early-Onset Parkinson Disease From Neighboring Countries in Central Europe
Lukasz Milanowski, Jennifer A. Lindemann, D. Hoffman-Zacharska, A. Soto-Beasley +26 more
2021Parkinsonism & Related Disorders14 citations Open access
Semantic Scholar
Interleukin-6 gene (-174 C/G ) and apolipoprotein E gene polymorphisms and the risk of Alzheimer disease in a Polish population.
A. Klimkowicz-Mrowiec, Paweł Wotkow, Karolina Spisak, A. Maruszak +4 more
2010Neurologia i Neurochirurgia Polska14 citations Open access
Semantic Scholar
Assessment of Olfactory Function in MAPT-Associated Neurodegenerative Disease Reveals Odor-Identification Irreproducibility as a Non-Disease-Specific, General Characteristic of Olfactory Dysfunction
K. Markopoulou, B. Chase, P. Robowski, A. Strongosky +11 more
2016PLoS ONE13 citations Open access
Semantic Scholar

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