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List of works by Joanna Siuda

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(Patho-)physiological relevance of PINK1-dependent ubiquitin phosphorylation

scientific article
Heterozygous PINK1 p.G411S increases risk of Parkinson's disease via a dominant-negative mechanism

scientific article
Parkinsonian syndrome in familial frontotemporal dementia

scientific article
Late-onset Alzheimer disease risk variants mark brain regulatory loci

scientific article published on 23 July 2015
A candidate regulatory variant at the TREM gene cluster associates with decreased Alzheimer's disease risk and increased TREML1 and TREM2 brain gene expression

scientific article published on 8 December 2016
Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders

scientific article
Cerebral white matter lesions in patients with dementia - from MCI to severe Alzheimer's disease.

scientific article published on 6 March 2009
Identification of genetic modifiers of age-at-onset for familial Parkinson's disease

scientific article
Role for the microtubule-associated protein tau variant p.A152T in risk of α-synucleinopathies

scientific article
ApoE variant p.V236E is associated with markedly reduced risk of Alzheimer's disease

scientific article published on 10 March 2014
Magnetic resonance spectroscopy as a predictor of conversion of mild cognitive impairment to dementia

scientific article published on 27 August 2013
Cognitive impairment and BDNF serum levels.

scientific article published on 21 October 2016
Early-onset Parkinson's disease due to PINK1 p.Q456X mutation--clinical and functional study

scientific article
Platelet phospholipase A2 activity in patients with Alzheimer's disease, vascular dementia and ischemic stroke.

scientific article published on 20 April 2007
Clinically meaningful parameters of progression and long-term outcome of Parkinson disease: An international consensus statement.

scientific article published on May 2015
Vascular risk factors and intensity of cognitive dysfunction in MCI.

scientific article published in March 2007
From mild cognitive impairment to Alzheimer's disease - influence of homocysteine, vitamin B12 and folate on cognition over time: results from one-year follow-up

scientific article published in July 2009
DNAJC13 p.Asn855Ser mutation screening in Parkinson's disease and pathologically confirmed Lewy body disease patients.

scientific article
Parkinsonism in chronic occupational metallic mercury intoxication

scientific article published in January 2003
Genetics of Parkinson's disease: a review of SNCA and LRRK2.

scientific article published in January 2016
Corrigendum to "Cognitive impairment and BDNF serum levels" [Polish J. Neurol. Neurosurg. 51 (2017) 24-32]

scientific article published on 14 July 2017
Inferior frontal region hypoperfusion in Parkinson disease with dementia

scientific article published in January 2003
Reply: Heterozygous PINK1 p.G411S in rapid eye movement sleep behaviour disorder

scientific article
PPM1M, a LRRK2-counteracting, phosphoRab12-preferring phosphatase with potential link to Parkinson’s disease

The Influence of Serum Uric Acid Level on Non-Motor Symptoms Occurrence and Severity in Patients with Idiopathic Parkinson’s Disease and Atypical Parkinsonisms—A Systematic Review

scientific article published in 2021
Exonic Re-Sequencing of the Chromosome 2q24.3 Parkinson's Disease Locus

scientific article published on 19 June 2015
Melkersson-Rosenthal syndrome as a rare cause of recurrent facial nerve palsy

scientific article published on 01 July 2005
Validation of the Polish version of the Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS)

scientific article published on 08 July 2020
Affective Disorder and Functional Status as well as Selected Sociodemographic Characteristics in Patients with Multiple Sclerosis, Parkinson's Disease and History of Stroke

scientific article published on 07 March 2020
Sensitive ELISA-based detection method for the mitophagy marker p-S65-Ub in human cells, autopsy brain, and blood samples

scientific article published on 28 October 2020
ALS-FTD complex disorder due to C9ORF72 gene mutation: description of first Polish family

scientific article

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