Evidence for HNRNPH1 being another gene for Bain type syndromic mental retardation
Pilch, Jacek, Koppolu, Agnieszka A., Walczak, Anna, Murcia Pienkowski, Victor A., Biernacka, Anna, Skiba, Paweł, Machnik‐Broncel, Joanna, Gasperowicz, Piotr, Kosińska, Joanna, Rydzanicz, Małgorzata, Emich‐Widera, Ewa, Płoski, Rafał
Published in Clinical genetics (01.10.2018)
Published in Clinical genetics (01.10.2018)
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Rapid Whole-Exome Sequencing as a Diagnostic Tool in a Neonatal/Pediatric Intensive Care Unit
Śmigiel, Robert, Biela, Mateusz, Szmyd, Krzysztof, Błoch, Michal, Szmida, Elżbieta, Skiba, Paweł, Walczak, Anna, Gasperowicz, Piotr, Kosińska, Joanna, Rydzanicz, Małgorzata, Stawiński, Piotr, Biernacka, Anna, Zielińska, Marzena, Gołębiowski, Waldemar, Jalowska, Agnieszka, Ohia, Grażyna, Głowska, Bożena, Walas, Wojciech, Królak-Olejnik, Barbara, Krajewski, Paweł, Sykut-Cegielska, Jolanta, Sąsiadek, Maria M., Płoski, Rafał
Published in Journal of clinical medicine (13.07.2020)
Published in Journal of clinical medicine (13.07.2020)
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Polymorphisms in immune-inflammatory response genes and the risk of deficit schizophrenia
Mak, Monika, Misiak, Błażej, Frydecka, Dorota, Pełka-Wysiecka, Justyna, Kucharska-Mazur, Jolanta, Samochowiec, Agnieszka, Bieńkowski, Przemysław, Pawlak-Adamska, Edyta, Karabon, Lidia, Szmida, Elżbieta, Skiba, Paweł, Kotowicz, Kamila, Piotrowski, Patryk, Beszłej, Jan Aleksander, Samochowiec, Jerzy
Published in Schizophrenia research (01.03.2018)
Published in Schizophrenia research (01.03.2018)
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The Impact of the FKBP5 Gene Polymorphisms on the Relationship between Traumatic Life Events and Psychotic-Like Experiences in Non-Clinical Adults
Stramecki, Filip, Frydecka, Dorota, Gawęda, Łukasz, Prochwicz, Katarzyna, Kłosowska, Joanna, Samochowiec, Jerzy, Szczygieł, Krzysztof, Pawlak, Edyta, Szmida, Elżbieta, Skiba, Paweł, Cechnicki, Andrzej, Misiak, Błażej
Published in Brain sciences (28.04.2021)
Published in Brain sciences (28.04.2021)
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The Role of the Reanalysis of Genetic Test Results in the Diagnosis of Dysmorphic Syndrome Caused by Inherited xq24 Deletion including the UBE2A and CXorf56 Genes
Wolańska, Ewelina, Pollak, Agnieszka, Rydzanicz, Małgorzata, Pesz, Karolina, Kłaniewska, Magdalena, Rozensztrauch, Anna, Skiba, Paweł, Stawiński, Piotr, Płoski, Rafał, Śmigiel, Robert
Published in Genes (27.02.2021)
Published in Genes (27.02.2021)
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Journal Article
The Moderating Role of the FKBP5 Gene Polymorphisms in the Relationship between Attachment Style, Perceived Stress and Psychotic-like Experiences in Non-Clinical Young Adults
Stramecki, Filip, Misiak, Błażej, Gawęda, Łukasz, Prochwicz, Katarzyna, Kłosowska, Joanna, Samochowiec, Jerzy, Samochowiec, Agnieszka, Pawlak, Edyta, Szmida, Elżbieta, Skiba, Paweł, Cechnicki, Andrzej, Frydecka, Dorota
Published in Journal of clinical medicine (15.03.2022)
Published in Journal of clinical medicine (15.03.2022)
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Multiplex ligation-dependent probe amplification as a screening test in children with autism spectrum disorders
Łaczmańska, Izabela, Stembalska, Agnieszka, Złocińska, Magdalena, Kozłowska, Joanna, Skiba, Paweł, Pesz, Karolina, Ślęzak, Ryszard, Śmigiel, Robert, Jakubiak, Aleksandra, Misiak, Błażej, Sąsiadek, Maria M
Published in Advances in clinical and experimental medicine : official organ Wroclaw Medical University (01.01.2020)
Published in Advances in clinical and experimental medicine : official organ Wroclaw Medical University (01.01.2020)
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Rapid diagnosis of the most common fetal aneuploidies with the QF-PCR method--a study of 100 cases
Łaczmańska, Izabela, Gil, Justyna, Stembalska, Agnieszka, Makowska, Izabela, Kozłowska, Joanna, Skiba, Paweł, Czemarmazowicz, Halina, Pesz, Karolina, Slęzak, Ryszard, Smigiel, Robert, Jakubiak, Aleksandra, Doraczyńska-Kowalik, Anna, Sąsiadek, Maria M
Published in Ginekologia polska (01.09.2015)
Published in Ginekologia polska (01.09.2015)
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Large patent ductus arteriosus and left ventricular non-compaction as cardiac manifestations of 1p36 monosomy
Mazurak, Magdalena, Kusa, Jacek, Skiba, Paweł, Śmigiel, Robert
Published in Pediatria polska (01.05.2017)
Published in Pediatria polska (01.05.2017)
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Journal Article
Rapid diagnostics of the most frequent fetal aneuploidies with QF-PCR method – study of 100 cases
Łaczmańska, Izabela, Gil, Justyna, Stembalska, Agnieszka, Makowska, Izabela, Kozłowska, Joanna, Skiba, Paweł, Czemarmazowicz, Halina, Pesz, Karolina, Ślęzak, Ryszard, Śmigiel, Robert, Jakubiak, Aleksandra, Doraczyńska-Kowalik, Anna, Sąsiadek, Maria
Published in Ginekologia polska (2015)
Published in Ginekologia polska (2015)
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OTC gene duplication as the possible cause of massive hyperammonaemia with a fatal prognosis
Natalia, Borkowska, Lukasz, Kaluzny, Dariusz, Rokicki, Elzbieta, Szmida, Pawel, Kowalski, Monika, Dus-Zuchowska, Pawel, Skiba, Elzbieta, Ciara, Mateusz, Biela, Malgorzata, Rydzanicz, Rafal, Ploski, Robert, Smigiel
Published in Molecular genetics and metabolism reports (01.12.2024)
Published in Molecular genetics and metabolism reports (01.12.2024)
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Epigenetic Findings in Twins with Esophageal Atresia
Błoch, Michal, Gasperowicz, Piotr, Gerus, Sylwester, Rasiewicz, Katarzyna, Lebioda, Arleta, Skiba, Pawel, Płoski, Rafal, Patkowski, Dariusz, Karpiński, Pawel, Śmigiel, Robert
Published in Genes (01.09.2023)
Published in Genes (01.09.2023)
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Broad phenotypic spectrum of germ line 7p12.1 microdeletions encompassing the IKZF1 gene includes predisposition to acute lymphoblastic leukemia
Pastorczak, Agata, Hogendorf, Anna, Urbanska, Zuzanna, Budzynska, Edyta, Jesionek‐Kupnicka, Dorota, Gach, Agnieszka, Hawula, Wanda, Smigiel, Robert, Skiba, Pawel, Sasiadek, Maria, Lejman, Monika, Constatinou, Maria, Lipska‐Ziętkiewicz, Beata S., Mlynarski, Wojciech
Published in Genes chromosomes & cancer (01.02.2021)
Published in Genes chromosomes & cancer (01.02.2021)
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Genome-wide analysis of gene expression after one year of venom immunotherapy
Karpinski, Pawel, Skiba, Pawel, Kosinska, Magdalena, Rosiek-Biegus, Marta, Królewicz, Emilia, Blin, Nikolaus, Meese, Eckart, Panaszek, Bernard, Nittner-Marszalska, Marita, Sasiadek, Maria Malgorzata
Published in Immunology letters (01.12.2018)
Published in Immunology letters (01.12.2018)
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The Role of the Reanalysis of Genetic Test Results in the Diagnosis of Dysmorphic Syndrome Caused by Inherited xq24 Deletion including the UBE2A and CXorf56 Genes
Wolańska, Ewelina, Pollak, Agnieszka, Rydzanicz, Małgorzata, Pesz, Karolina, Kłaniewska, Magdalena, Rozensztrauch, Anna, Skiba, Paweł, Stawiński, Piotr, Płoski, Rafał, Śmigiel, Robert
Published in Genes (27.02.2021)
Published in Genes (27.02.2021)
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Discovering Rules with Convolutional Neural Networks
Stankiewicz, Katarzyna, Skiba, Pawel, Chaber, Bartosz
Published in 2023 24th International Conference on Computational Problems of Electrical Engineering (CPEE) (10.09.2023)
Published in 2023 24th International Conference on Computational Problems of Electrical Engineering (CPEE) (10.09.2023)
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Conference Proceeding
Automated modeling of RNA 3D structure
Rother, Kristian, Rother, Magdalena, Skiba, Pawel, Bujnicki, Janusz M
Published in Methods in molecular biology (Clifton, N.J.) (01.01.2014)
Published in Methods in molecular biology (Clifton, N.J.) (01.01.2014)
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