Renata Suchanek-Raif

Dr. Renata Suchanek-Raif

orcid

Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 September 2017 in Biomedicine & Pharmacotherapy
Verified
Journal Article
Closed access
MPMarta Palacz-Wrobel
Marta Palacz-Wrobel
PBPaulina Borkowska
Paulina Borkowska
MPMonika Paul-Samojedny
Monika Paul-Samojedny
MKMalgorzata Kowalczyk
Malgorzata Kowalczyk
AFAnna Fila-Danilow
Anna Fila-Danilow
JKJan Kowalski
Jan Kowalski

15 April 2010 in Journal of Molecular Neuroscience
Verified
Journal Article
Closed access
PDF file
MPMonika Paul-Samojedny
Monika Paul-Samojedny
MKMalgorzata Kowalczyk
Malgorzata Kowalczyk
RSRenata Suchanek-Raif
Renata Suchanek-Raif
Aleksander Jerzy OwczarekAleksander Jerzy Owczarek
Aleksander Jerzy Owczarek
AFAnna Fila-Danilow
Anna Fila-Danilow
JKJan Kowalski
Jan Kowalski

5 April 2011 in Journal of Molecular Neuroscience
Verified
Journal Article
Open access
PDF file
PBPaulina Borkowska
Paulina Borkowska
KKKrzysztof Kucia
Krzysztof Kucia
SRSzymon Rzezniczek
Szymon Rzezniczek
MPMonika Paul-Samojedny
Monika Paul-Samojedny
MKMalgorzata Kowalczyk
Malgorzata Kowalczyk
JKJan Kowalski
Jan Kowalski
To elucidate a genetic predisposition to major depressive disorder, we investigated two polymorphisms (−31T/C and −511C/T) in the interleukin-1beta promoter region in patients who suffered from major recurrent depression. The aim of the current work was to compare alleles and genotype layout between patients with major recurrent depression and healthy people. We would like to indicate such combination of genotypes which corresponds with major recurrent depression. Correlations between genotypes for analyzed polymorphisms and number of episodes, number of points in Hamilton Depression Rating Scale, and age of onset were investigated as well. The study group consisted of 94 patients diagnosed with major recurrent depression. The control group included 206 healthy individuals. Both groups involved representatives of Caucasian population. Genotyping of polymorphisms was performed by using PCR-RFLP technique. A specific haplotype, composed of the C allele at −31 and the T allele at −511, has a tendency to have a statistically significant difference (p = 0.064) between patients and control group. Correspondence analysis revealed that genotype T/T at −31 and genotype C/C at −511 are associated with major recurrent depression. No association was found between genotypes for studied polymorphic sites and number of episodes, number of points in Hamilton Depression Rating Scale, and age of onset.

1 January 2013 in The Journal of Neuropsychiatry and Clinical Neurosciences
Verified
Journal Article
Closed access
PDF file
MPMonika Paul-Samojedny
Monika Paul-Samojedny
Aleksander Jerzy OwczarekAleksander Jerzy Owczarek
Aleksander Jerzy Owczarek
MKMalgorzata Kowalczyk
Malgorzata Kowalczyk
RSRenata Suchanek-Raif
Renata Suchanek-Raif
MPMarta Palacz
Marta Palacz
JKJan Kowalski
Jan Kowalski

1 January 2013 in The Journal of Neuropsychiatry and Clinical Neurosciences
Verified
Journal Article
Closed access
PDF file
RSRenata Suchanek-Raif
Renata Suchanek-Raif
Aleksander Jerzy OwczarekAleksander Jerzy Owczarek
Aleksander Jerzy Owczarek
MPMonika Paul-Samojedny
Monika Paul-Samojedny
MKMalgorzata Kowalczyk
Malgorzata Kowalczyk
KKKrzysztof Kucia
Krzysztof Kucia
JKJan Kowalski
Jan Kowalski

4 September 2010 in Journal of Molecular Neuroscience
Verified
Journal Article
Closed access
PDF file
MPMonika Paul-Samojedny
Monika Paul-Samojedny
Aleksander Jerzy OwczarekAleksander Jerzy Owczarek
Aleksander Jerzy Owczarek
RSRenata Suchanek-Raif
Renata Suchanek-Raif
MKMalgorzata Kowalczyk
Malgorzata Kowalczyk
AFAnna Fila-Danilow
Anna Fila-Danilow
JKJan Kowalski
Jan Kowalski