Works by Rydzanicz, Malgorzata

Results: 106

Genotypowanie grup krwi dawców panelowych przy użyciu sekwencjonowania następnej generacji.

Published in:

Acta Haematologica Polonica, 2022, v. 53, n. A, p. 61

By:

Orzińska, Agnieszka;
Rydzanicz, Małgorzata;
Stawiński, Piotr;
Płoski, Rafał;
Purchla-Szepioła, Sylwia;
Krzemienowska, Magdalena;
Skulimowska, Joanna;
Smolarczyk-Wodzyńska, Justyna;
Pelc-Kłopotowska, Monika;
Guz, Katarzyna;
Głodkowska-Mrówka, Eliza

Publication type:

Article

Clinical heterogeneity of polish patients with KAT6B–related disorder.

Published in:

Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 12, p. 1, doi. 10.1002/mgg3.2265

By:

Magdalena, Klaniewska;
Anna, Bolanowska‐Tyszko;
Anna, Latos‐Bielenska;
Aleksandra, Jezela‐Stanek;
Krzysztof, Szczaluba;
Malgorzata, Krajewska‐Walasek;
Elzbieta, Ciara;
Magdalena, Pelc;
Dorota, Jurkiewicz;
Piotr, Stawinski;
Agnieszka, Zubkiewicz‐Kucharska;
Małgorzata, Rydzanicz;
Rafal, Ploski;
Robert, Smigiel

Publication type:

Article

FINCA syndrome—Defining neurobehavioral phenotype in survivors into late childhood.

Published in:

Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 4, p. 1, doi. 10.1002/mgg3.1899

By:

Badura‐Stronka, Magdalena;
Śmigiel, Robert;
Rutkowska, Karolina;
Szymańska, Krystyna;
Hirschfeld, Adam Sebastian;
Monkiewicz, Michał;
Kosińska, Joanna;
Wolańska, Ewelina;
Rydzanicz, Małgorzata;
Latos‐Bieleńska, Anna;
Płoski, Rafał

Publication type:

Article

Variants of ATP1A3 in residue 756 cause a separate phenotype of relapsing encephalopathy with cerebellar ataxia (RECA)—Report of two cases and literature review.

Published in:

Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 9, p. 1, doi. 10.1002/mgg3.1772

By:

Biela, Mateusz;
Rydzanicz, Malgorzata;
Szymanska, Krystyna;
Pieniawska‐Smiech, Karolina;
Lewandowicz‐Uszynska, Aleksandra;
Chruszcz, Joanna;
Benben, Lucyna;
Kuzior‐Plawiak, Malgorzata;
Szyld, Pawel;
Jakubiak, Aleksandra;
Szenborn, Leszek;
Ploski, Rafal;
Smigiel, Robert

Publication type:

Article

Variable degree of mosaicism for tetrasomy 18p in phenotypically discordant monozygotic twins—Diagnostic implications.

Published in:

Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 1, p. 1, doi. 10.1002/mgg3.1526

By:

Rydzanicz, Małgorzata;
Olszewski, Pawel;
Kedra, Darek;
Davies, Hanna;
Filipowicz, Natalia;
Bruhn‐Olszewska, Bozena;
Cavalli, Marco;
Szczałuba, Krzysztof;
Młynek, Marlena;
Machnicki, Marcin M.;
Stawiński, Piotr;
Kostrzewa, Grażyna;
Krajewski, Paweł;
Śladowski, Dariusz;
Chrzanowska, Krystyna;
Dumanski, Jan P.;
Płoski, Rafał

Publication type:

Article

Phenotypic expansion in Zhu‐Tokita‐Takenouchi‐Kim syndrome caused by de novo variants in the SON gene.

Published in:

Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 10, p. 1, doi. 10.1002/mgg3.1432

By:

Slezak, Ryszard;
Smigiel, Robert;
Rydzanicz, Malgorzata;
Pollak, Agnieszka;
Kosinska, Joanna;
Stawinski, Piotr;
Malgorzata Sasiadek, Maria;
Ploski, Rafal

Publication type:

Article

Non-allergic eye rubbing is a major behavioral risk factor for keratoconus.

Published in:

PLoS ONE, 2023, v. 18, n. 4, p. 1, doi. 10.1371/journal.pone.0284454

By:

Jaskiewicz, Katarzyna;
Maleszka-Kurpiel, Magdalena;
Michalski, Andrzej;
Ploski, Rafal;
Rydzanicz, Malgorzata;
Gajecka, Marzena

Publication type:

Article

A novel KEL c.1414-1G>T allele in a polish patient with anti-Ku antibody.

Published in:

2022

By:

Pelc‐Kłopotowska, Monika;
Płoski, Rafał;
Szczałuba, Krzysztof;
Szymańska, Krystyna;
Rydzanicz, Małgorzata;
Purchla‐Szepioła, Sylwia;
Kolasińska, Katarzyna;
Lewicka, Małgorzata;
Thornton, Nicole;
Crew, Vanja Karamatic;
Orzińska, Agnieszka;
Guz, Katarzyna;
Pelc-Kłopotowska, Monika;
Purchla-Szepioła, Sylwia

Publication type:

journal article

Clinico-pathological correlation in case of BRAT1 mutation.

Published in:

Folia Neuropathologica, 2018, v. 56, n. 4, p. 362, doi. 10.5114/fn.2018.80870

By:

Szymańska, Krystyna;
Laure-Kamionowska, Milena;
Szczałuba, Krzysztof;
Koppolu, Agnieszka;
Furmanek, Mariusz;
Kuśmierska, Katarzyna;
Boniel, Snir;
Płoski, Rafał;
Rydzanicz, Małgorzata

Publication type:

Article

A novel de novo COL6A1 mutation emphasizes the role of intron 14 donor splice site defects as a cause of moderate-progressive form of ColVI myopathy - a case report and review of the genotype-phenotype correlation.

Published in:

Folia Neuropathologica, 2017, v. 55, n. 3, p. 214, doi. 10.5114/fn.2017.70486

By:

Koppolu, Agnieszka A.;
Madej-Pilarczyk, Agnieszka;
Rydzanicz, Małgorzata;
Kosińska, Joanna;
Gasperowicz, Piotr;
Dorszewska, Jolanta;
Kozubski, Wojciech;
Steinborn, Barbara;
Kochański, Andrzej M.;
Płoski, Rafał

Publication type:

Article

Bilateral striatal necrosis caused by ADAR mutations in two siblings with dystonia and freckles-like skin changes that should be differentiated from Leigh syndrome.

Published in:

Folia Neuropathologica, 2016, v. 54, n. 4, p. 405, doi. 10.5114/fn.2016.64819

By:

Piekutowska-Abramczuk, Dorota;
Mierzewska, Hanna;
Bekiesińska-Figatowska, Monika;
Ciara, Elżbieta;
Trubicka, Joanna;
Pronicki, Maciej;
Rokicki, Dariusz;
Rydzanicz, Małgorzata;
Płoski, Rafał;
Pronicka, Ewa

Publication type:

Article

SDF1-3'A Gene Polymorphism is Associated with Laryngeal Cancer.

Published in:

Pathology & Oncology Research, 2010, v. 16, n. 2, p. 223, doi. 10.1007/s12253-009-9214-5

By:

Kruszyna, Łukasz;
Lianeri, Margarita;
Rydzanicz, Małgorzata;
Szyfter, Krzysztof;
Jagodziński, Paweł

Publication type:

Article

Tracking Clonal Evolution of Multiple Myeloma Using Targeted Next-Generation DNA Sequencing.

Published in:

Biomedicines, 2022, v. 10, n. 7, p. N.PAG, doi. 10.3390/biomedicines10071674

By:

Salomon-Perzyński, Aleksander;
Barankiewicz, Joanna;
Machnicki, Marcin;
Misiewicz-Krzemińska, Irena;
Pawlak, Michał;
Radomska, Sylwia;
Krzywdzińska, Agnieszka;
Bluszcz, Aleksandra;
Stawiński, Piotr;
Rydzanicz, Małgorzata;
Jakacka, Natalia;
Solarska, Iwona;
Borg, Katarzyna;
Spyra-Górny, Zofia;
Szpila, Tomasz;
Puła, Bartosz;
Grosicki, Sebastian;
Stokłosa, Tomasz;
Płoski, Rafał;
Lech-Marańda, Ewa

Publication type:

Article

Sudden cardiac arrest in patients without overt heart disease: a limited value of next generation sequencing.

Published in:

Polish Archives of Internal Medicine, 2018, v. 128, n. 12, p. 721, doi. 10.20452/pamw.4366

By:

Stępień-Wojno, Małgorzata;
Ponińska, Joanna;
Rydzanicz, Małgorzata;
Bilińska, Maria;
Truszkowska, Grażyna;
Baranowski, Rafał;
Lutyńska, Anna;
Biernacka, Elżbieta K.;
Stępińska, Janina;
Kowalik, Ilona;
Płoski, Rafał;
Bilińska, Zofia T.

Publication type:

Article

The Cys326 Allele of the 8-Oxoguanine DNA N-Glycosylase 1 Gene as a Risk Factor in Smoking- and Drinking-Associated Larynx Cancer.

Published in:

Tohoku Journal of Experimental Medicine, 2009, v. 219, n. 4, p. 269, doi. 10.1620/tjem.219.269

By:

Pawlowska, Elsbieta;
Janik-Papis, Katarzyna;
Rydzanicz, Malgorzata;
Zuk, Karolina;
Kaczmarczyk, Dariusz;
Olszewski, Jurek;
Szyfter, Krzysztof;
Blasiak, Janusz;
Morawiec-Sztandera, Alina

Publication type:

Article

New perspective in diagnostics of mitochondrial disorders: two years' experience with whole-exome sequencing at a national paediatric centre.

Published in:

2016

By:

Pronicka, Ewa;
Piekutowska-Abramczuk, Dorota;
Ciara, Elżbieta;
Trubicka, Joanna;
Rokicki, Dariusz;
Karkucińska-Więckowska, Agnieszka;
Pajdowska, Magdalena;
Jurkiewicz, Elżbieta;
Halat, Paulina;
Kosińska, Joanna;
Pollak, Agnieszka;
Rydzanicz, Małgorzata;
Stawinski, Piotr;
Pronicki, Maciej;
Krajewska-Walasek, Małgorzata;
Płoski, Rafał

Publication type:

journal article

The MRN protein complex genes: MRE11 and RAD50 and susceptibility to head and neck cancers.

Published in:

Molecular Cancer, 2013, v. 12, n. 1, p. 1, doi. 10.1186/1476-4598-12-113

By:

Ziółkowska-Suchanek, Iwona;
Mosor, Maria;
Wierzbicka, Małgorzata;
Rydzanicz, Małgorzata;
Baranowska, Marta;
Nowak, Jerzy

Publication type:

Article

THE MED13L HAPLOINSUFFICIENCY SYNDROME ASSOCIATED WITH DE NOVO NONSENSE VARIANT (P.GLN1981*).

Published in:

Journal of Mother & Child, 2020, v. 24, n. 3, p. 32, doi. 10.34763/jmotherandchild.20202403.2021.d-20-00003

By:

Dawidziuk, Mateusz;
Kutkowska-Kaźmierczak, Anna;
Gawliński, Paweł;
Wiszniewski, Wojciech;
Gos, Monika;
Stawiński, Piotr;
Rydzanicz, Małgorzata;
Kosińska, Joanna;
Własienko, Paweł;
Malinowska (Kordowska), Olga;
Bartnik-Głaska, Magdalena;
Bernaciak, Joanna;
Szczałuba, Krzysztof;
Bekiesińska-Figatowska, Monika;
Płoski, Rafał;
Bal, Jerzy;
Rzońca-Niewczas, Sylwia Olimpia

Publication type:

Article

Differences in the composition of the bacterial element of the urinary tract microbiome in patients undergoing dialysis and patients after kidney transplantation.

Published in:

Frontiers in Microbiology, 2023, p. 01, doi. 10.3389/fmicb.2023.1187625

By:

Jaworska, Marcelina M.;
Pecyna, Paulina;
Jaskiewicz, Katarzyna;
Rydzanicz, Małgorzata;
Kaluzna, Malgorzata;
Pawlaczyk, Krzysztof;
Ploski, Rafal;
Nowak-Malczewska, Dorota M.;
Karolak, Justyna A.;
Gajecka, Marzena

Publication type:

Article

A novel de novo FEM1C variant is linked to neurodevelopmental disorder with absent speech, pyramidal signs and limb ataxia.

Published in:

Human Molecular Genetics, 2023, v. 32, n. 7, p. 1152, doi. 10.1093/hmg/ddac276

By:

Dubey, Abhishek Anil;
Krygier, Magdalena;
Szulc, Natalia A;
Rutkowska, Karolina;
Kosińska, Joanna;
Pollak, Agnieszka;
Rydzanicz, Małgorzata;
Kmieć, Tomasz;
Mazurkiewicz-Bełdzińska, Maria;
Pokrzywa, Wojciech;
Płoski, Rafał

Publication type:

Article

Homozygous mutation in the Neurofascin gene affecting the glial isoform of Neurofascin causes severe neurodevelopment disorder with hypotonia, amimia and areflexia.

Published in:

Human Molecular Genetics, 2018, v. 27, n. 21, p. 3669, doi. 10.1093/hmg/ddy277

By:

Smigiel, Robert;
Sherman, Diane L;
Rydzanicz, Małgorzata;
Walczak, Anna;
Mikolajkow, Dorota;
Krolak-Olejnik, Barbara;
Kosińska, Joanna;
Gasperowicz, Piotr;
Biernacka, Anna;
Stawinski, Piotr

Publication type:

Article

CLOVES syndrome caused by mosaic mutation in the PIK3CA gene identified in fibroblasts.

Published in:

Polish Journal of Pediatrics / Pediatria Polska, 2021, v. 96, n. 2, p. 148, doi. 10.5114/POLP.2021.107401

By:

Kłaniewska, Magdalena;
Rydzanicz, Małgorzata;
Kosińska, Joanna;
Biela, Mateusz;
Walczak, Anna;
Szmida, Elżbieta;
Rozensztrauch, Anna;
Płoski, Rafał;
Śmigiel, Robert

Publication type:

Article

Titin Truncating Variants in Dilated Cardiomyopathy – Prevalence and Genotype-Phenotype Correlations.

Published in:

PLoS ONE, 2017, v. 12, n. 1, p. 1, doi. 10.1371/journal.pone.0169007

By:

Franaszczyk, Maria;
Chmielewski, Przemyslaw;
Truszkowska, Grazyna;
Stawinski, Piotr;
Michalak, Ewa;
Rydzanicz, Malgorzata;
Sobieszczanska-Malek, Malgorzata;
Pollak, Agnieszka;
Szczygieł, Justyna;
Kosinska, Joanna;
Parulski, Adam;
Stoklosa, Tomasz;
Tarnowska, Agnieszka;
Machnicki, Marcin M.;
Foss-Nieradko, Bogna;
Szperl, Malgorzata;
Sioma, Agnieszka;
Kusmierczyk, Mariusz;
Grzybowski, Jacek;
Zielinski, Tomasz

Publication type:

Article

Novel and De Novo Mutations Extend Association of POU3F4 with Distinct Clinical and Radiological Phenotype of Hearing Loss.

Published in:

PLoS ONE, 2016, v. 11, n. 12, p. 1, doi. 10.1371/journal.pone.0166618

By:

Pollak, Agnieszka;
Lechowicz, Urszula;
Kędra, Anna;
Stawiński, Piotr;
Rydzanicz, Małgorzata;
Furmanek, Mariusz;
Brzozowska, Małgorzata;
Mrówka, Maciej;
Skarżyński, Henryk;
Skarżyński, Piotr H.;
Ołdak, Monika;
Płoski, Rafał

Publication type:

Article

Association of polymorphisms and haplotypes of the NBN gene with laryngeal cancer and multiple primary tumors of the head and neck.

Published in:

Head & Neck, 2012, v. 34, n. 3, p. 376, doi. 10.1002/hed.21741

By:

Ziółkowska-Suchanek, Iwona;
Mosor, Maria;
Wierzbicka, Małgorzata;
Fichna, Marta;
Rydzanicz, Małgorzata;
Nowak, Jerzy

Publication type:

Article

Simple technique for RNA purification from mouse inner ear hair cells.

Published in:

Molecular Biology Reports, 2012, v. 39, n. 6, p. 6467, doi. 10.1007/s11033-012-1465-7

By:

Szaumkessel, Marcin;
Brauze, Damian;
Rydzanicz, Małgorzata;
Karlik, Michał;
Szyfter, Krzysztof;
Szyfter, Witold;
Maciej, Wróbel

Publication type:

Article

Erratum to: Simple technique for RNA purification from mouse inner ear hair cells.

Published in:

2012

By:

Szaumkessel, Marcin;
Brauze, Damian;
Rydzanicz, Małgorzata;
Karlik, Michał;
Szyfter, Krzysztof;
Szyfter, Witold;
Wróbel, Maciej

Publication type:

Correction Notice

Effects of maternal type 1 diabetes and confounding factors on neonatal microbiomes.

Published in:

Diabetologia, 2024, v. 67, n. 2, p. 312, doi. 10.1007/s00125-023-06047-7

By:

Gajecka, Marzena;
Gutaj, Pawel;
Jaskiewicz, Katarzyna;
Rydzanicz, Malgorzata;
Szczapa, Tomasz;
Kaminska, Dorota;
Kosewski, Grzegorz;
Przyslawski, Juliusz;
Ploski, Rafal;
Wender-Ozegowska, Ewa

Publication type:

Article

Case report: Variants in the ERCC4 gene as a rare cause of cerebellar ataxia with chorea.

Published in:

Frontiers in Genetics, 2023, v. 14, p. 1, doi. 10.3389/fgene.2023.1107460

By:

Kulikowska, Joanna;
Jakubiuk-Tomaszuk, Anna;
Rydzanicz, Małgorzata;
Płoski, Rafał;
Kochanowicz, Jan;
Kulakowska, Alina;
Kapica-Topczewska, Katarzyna

Publication type:

Article

The most frequent Polish mutations are not susceptibility factors for tobacco-related cancers.

Published in:

2021

By:

Podralska, Marta;
Dzikiewicz-Krawczyk, Agnieszka;
Mosor, Maria;
Żurawek, Magdalena;
Iżykowska, Katarzyna;
Słomski, Ryszard;
Rydzanicz, Małgorzata;
Gabryel, Piotr;
Dyszkiewicz, Wojciech;
Ziółkowska-Suchanek, Iwona

Publication type:

journal article

Postzygotic mosaicism of a novel PTPN11 mutation in monozygotic twins discordant for metachondromatosis.

Published in:

American Journal of Medical Genetics. Part A, 2022, v. 188, n. 5, p. 1482, doi. 10.1002/ajmg.a.62670

By:

Rydzanicz, Małgorzata;
Glinkowski, Wojciech;
Walczak, Anna;
Koppolu, Agnieszka;
Kostrzewa, Grażyna;
Gasperowicz, Piotr;
Pollak, Agnieszka;
Stawiński, Piotr;
Płoski, Rafał

Publication type:

Article

Germline missense NF1 mutation in an elderly patient with a blastic plasmacytoid dendritic cell neoplasm.

Published in:

2019

By:

Szczepaniak, Andrzej;
Machnicki, Marcin;
Gniot, Michał;
Pępek, Monika;
Rydzanicz, Małgorzata;
Płoski, Rafał;
Kaźmierczak, Maciej;
Stokłosa, Tomasz;
Lewandowski, Krzysztof

Publication type:

journal article

A study in Polish patients with cardiomyopathy emphasizes pathogenicity of phospholamban (PLN) mutations at amino acid position 9 and low penetrance of heterozygous null PLN mutations.

Published in:

BMC Medical Genetics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12881-015-0167-0

By:

Truszkowska, Grażyna T.;
Bilińska, Zofia T.;
Kosińska, Joanna;
Śleszycka, Justyna;
Rydzanicz, Małgorzata;
Sobieszczańska-Małek, Małgorzata;
Franaszczyk, Maria;
Bilińska, Maria;
Stawiński, Piotr;
Michalak, Ewa;
Małek, Łukasz A.;
Chmielewski, Przemysław;
Foss-Nieradko, Bogna;
Machnicki, Marcin M.;
Stokłosa, Tomasz;
Ponińska, Joanna;
Szumowski, Łukasz;
Grzybowski, Jacek;
Piwoński, Jerzy;
Drygas, Wojciech

Publication type:

Article

Non-syndromic inherited retinal diseases in Poland: Genes, mutations, and phenotypes.

Published in:

Molecular Vision, 2021, v. 27, p. 457

By:

Tracewska, Anna M.;
Kocyła-Karczmarewicz, Beata;
Rafalska, Agnieszka;
Murawska, Joanna;
Jakubaszko-Jabłońska, Joanna;
Rydzanicz, Małgorzata;
Stawiński, Piotr;
Ciara, Elżbieta;
Lipska-Ziętkiewicz, Beata S.;
Khan, Muhammad Imran;
Cremers, Frans P. M.;
Płoski, Rafał;
Chrzanowska, Krystyna H.

Publication type:

Article

Increased risk of larynx cancer in heterozygous carriers of the I171V mutation of the NBS1 gene.

Published in:

Cancer Science, 2007, v. 98, n. 11, p. 1701, doi. 10.1111/j.1349-7006.2007.00594.x

By:

Ziólkowska, Iwona;
Mosor, Maria;
Wierzbicka, Malgorzata;
Rydzanicz, Malgorzata;
Pernak-Schwarz, Monika;
Nowak, Jerzy

Publication type:

Article

Comparison of rehabilitation results in deaf patients with and without genetically related hearing loss.

Published in:

Cochlear Implants International: An Interdisciplinary Journal, 2008, v. 9, n. 3, p. 132, doi. 10.1179/cim.2008.9.3.132

By:

WRÓBEL, MACIEJ;
MAGIERSKA-KRZYSZTON, MAGDALENA;
SZYFTER, KRZYSZTOF;
MIȨTKIEWSKA, DOROTA;
SZYFTER, WITOLD;
RYDZANICZ, MAŁGORZATA;
KARLIK, MICHAŁ

Publication type:

Article

Genetyka słuchu - co nowego?

Published in:

Advances in Head & Neck Surgery / Postępy w Chirurgii Głowy i Szyi, 2015, v. 14, n. 2, p. 25

By:

Szyfter, Krzysztof;
Rydzanicz, Małgorzata;
Gawęcki, Wojciech;
Wróbel, Maciej;
Szyfter-Harris, Joanna

Publication type:

Article

Predictive significance of selected gene mutations in relapsed and refractory chronic lymphocytic leukemia patients treated with ibrutinib.

Published in:

European Journal of Haematology, 2021, v. 106, n. 3, p. 320, doi. 10.1111/ejh.13550

By:

Machnicki, Marcin M.;
Górniak, Patryk;
Pępek, Monika;
Szymczyk, Agnieszka;
Iskierka‐Jażdżewska, Elżbieta;
Steckiewicz, Paweł;
Bluszcz, Aleksandra;
Rydzanicz, Małgorzata;
Hus, Marek;
Płoski, Rafał;
Makuch‐Łasica, Hanna;
Nowak, Grażyna;
Juszczyński, Przemysław;
Jamroziak, Krzysztof;
Stokłosa, Tomasz;
Puła, Bartosz

Publication type:

Article

A Rare Mutation in a Rare Tumor--SMARCB1- Deficient Malignant Glomus Tumor.

Published in:

Genes, Chromosomes & Cancer, 2016, v. 55, n. 1, p. 107, doi. 10.1002/gcc.22296

By:

Dabek, Bartosz;
Kram, Andrzej;
Kubrak, Jadwiga;
Kurzawski, Mateusz;
Wojcik, Piotr;
Machnicki, Marcin M.;
Stoklosa, Tomasz;
Rydzanicz, Malgorzata;
Ploski, Rafal;
Debiec ‐ Rychter, Maria

Publication type:

Article

Author Correction: Hybrid de novo whole-genome assembly and annotation of the model tapeworm Hymenolepis diminuta.

Published in:

2020

By:

Nowak, Robert M.;
Jastrzębski, Jan P.;
Kuśmirek, Wiktor;
Sałamatin, Rusłan;
Rydzanicz, Małgorzata;
Sobczyk-Kopcioł, Agnieszka;
Sulima-Celińska, Anna;
Paukszto, Łukasz;
Makowczenko, Karol G.;
Płoski, Rafał;
Tkach, Vasyl V.;
Basałaj, Katarzyna;
Młocicki, Daniel

Publication type:

Correction Notice

Hybrid de novo whole-genome assembly and annotation of the model tapeworm Hymenolepis diminuta.

Published in:

Scientific Data, 2019, v. 6, n. 1, p. N.PAG, doi. 10.1038/s41597-019-0311-3

By:

Nowak, Robert M.;
Jastrzębski, Jan P.;
Kuśmirek, Wiktor;
Sałamatin, Rusłan;
Rydzanicz, Małgorzata;
Sobczyk-Kopcioł, Agnieszka;
Sulima-Celińska, Anna;
Paukszto, Łukasz;
Makowczenko, Karol G.;
Płoski, Rafał;
Tkach, Vasyl V.;
Basałaj, Katarzyna;
Młocicki, Daniel

Publication type:

Article

Whole-exome sequencing in patients with protein aggregate myopathies reveals causative mutations associated with novel atypical phenotypes.

Published in:

Neurological Sciences, 2021, v. 42, n. 7, p. 2819, doi. 10.1007/s10072-020-04876-7

By:

Machnicki, Marcin M.;
Guglielmi, Valeria;
Pancheri, Elia;
Gualandi, Francesca;
Verriello, Lorenzo;
Pruszczyk, Katarzyna;
Kosinska, Joanna;
Sangalli, Antonella;
Rydzanicz, Malgorzata;
Romanelli, Maria Grazia;
Neri, Marcella;
Ploski, Rafal;
Tonin, Paola;
Tomelleri, Giuliano;
Stoklosa, Tomasz;
Vattemi, Gaetano

Publication type:

Article

Characterization of Ocular Surface Microbial Profiles Revealed Discrepancies between Conjunctival and Corneal Microbiota.

Published in:

Pathogens, 2021, v. 10, n. 4, p. 405, doi. 10.3390/pathogens10040405

By:

Matysiak, Anna;
Kabza, Michal;
Karolak, Justyna A.;
Jaworska, Marcelina M.;
Rydzanicz, Malgorzata;
Ploski, Rafal;
Szaflik, Jacek P.;
Gajecka, Marzena

Publication type:

Article

Non-infectious mixed cryoglobulinemia as a new clinical presentation of mutation in the gene encoding coatomer subunit alpha: a case report of two adult sisters.

Published in:

2024

By:

Leśniak, Ksymena;
Płoski, Rafał;
Rydzanicz, Małgorzata;
Rymarz, Aleksandra;
Lubas, Arkadiusz;
Syryło, Tomasz;
Niemczyk, Stanisław

Publication type:

Case Study

Metagenomic search of viral coinfections in herpes simplex encephalitis patients.

Published in:

Journal of NeuroVirology, 2023, v. 29, n. 5, p. 588, doi. 10.1007/s13365-023-01157-9

By:

Perlejewski, Karol;
Radkowski, Marek;
Rydzanicz, Małgorzata;
Dzieciątkowski, Tomasz;
Silling, Steffi;
Wieczorek, Magdalena;
Makowiecki, Michał;
Horban, Andrzej;
Laskus, Tomasz

Publication type:

Article

Cryptic MYC insertions in Burkitt lymphoma: New data and a review of the literature.

Published in:

PLoS ONE, 2022, v. 17, n. 2, p. 1, doi. 10.1371/journal.pone.0263980

By:

Woroniecka, Renata;
Rymkiewicz, Grzegorz;
Szafron, Lukasz M.;
Blachnio, Katarzyna;
Szafron, Laura A.;
Bystydzienski, Zbigniew;
Pienkowska-Grela, Barbara;
Borkowska, Klaudia;
Rygier, Jolanta;
Kotyl, Aleksandra;
Malawska, Natalia;
Wojtkowska, Katarzyna;
Parada, Joanna;
Borysiuk, Anita;
Murcia Pienkowski, Victor;
Rydzanicz, Malgorzata;
Grygalewicz, Beata

Publication type:

Article

Torque teno virus (TTV) Infection in Patients with Encephalitis.

Published in:

International Journal of Molecular Sciences, 2024, v. 25, n. 20, p. 11177, doi. 10.3390/ijms252011177

By:

Jurasz, Henryk;
Bukowska-Ośko, Iwona;
Rydzanicz, Małgorzata;
Popiel, Marta;
Dzieciątkowski, Tomasz;
Bakuła-Grządka, Karolina;
Paciorek, Marcin;
Makowiecki, Michał;
Horban, Andrzej;
Laskus, Tomasz;
Radkowski, Marek;
Perlejewski, Karol

Publication type:

Article

Gender Influences Gut Microbiota among Patients with Irritable Bowel Syndrome.

Published in:

International Journal of Molecular Sciences, 2023, v. 24, n. 13, p. 10424, doi. 10.3390/ijms241310424

By:

Pecyna, Paulina;
Gabryel, Marcin;
Mankowska-Wierzbicka, Dorota;
Nowak-Malczewska, Dorota M.;
Jaskiewicz, Katarzyna;
Jaworska, Marcelina M.;
Tomczak, Hanna;
Rydzanicz, Malgorzata;
Ploski, Rafal;
Grzymislawski, Marian;
Dobrowolska, Agnieszka;
Gajecka, Marzena

Publication type:

Article

Gene Expression Profile of Human Mesenchymal Stromal Cells Exposed to Hypoxic and Pseudohypoxic Preconditioning—An Analysis by RNA Sequencing.

Published in:

International Journal of Molecular Sciences, 2021, v. 22, n. 15, p. 8160, doi. 10.3390/ijms22158160

By:

Zielniok, Katarzyna;
Burdzinska, Anna;
Murcia Pienkowski, Victor;
Koppolu, Agnieszka;
Rydzanicz, Malgorzata;
Zagozdzon, Radoslaw;
Paczek, Leszek

Publication type:

Article

Higher Mutation Burden in High Proliferation Compartments of Heterogeneous Melanoma Tumors.

Published in:

International Journal of Molecular Sciences, 2021, v. 22, n. 8, p. 3886, doi. 10.3390/ijms22083886

By:

Grzywa, Tomasz M.;
Koppolu, Agnieszka A.;
Paskal, Wiktor;
Klicka, Klaudia;
Rydzanicz, Małgorzata;
Wejman, Jarosław;
Płoski, Rafał;
Włodarski, Paweł K.

Publication type:

Article