AnnaBiernackaMD

PubMed

• Lung adenocarcinomas with isolated TP53 mutation: A comprehensive clinical, cytopathologic and molecular characterization.
  Mendoza, R., Wanjari, P., Johnson, D., Chen-Yost, H., Wang, P., Reeves, W., Mueller, J., Antic, T., Biernacka, A., Symes, E.> ;Cancer Medicine. 2024 Jan 2
• 3 citations
  Brain Tissue Low-Level Mosaicism for MTOR Mutation Causes Smith-Kingsmore Phenotype with Recurrent Hypoglycemia-A Novel Phenotype and a Further Proof for Testing of an...
  Krzysztof Szczałuba, Małgorzata Rydzanicz, Anna Walczak, Joanna Kosińska, Agnieszka Koppolu, Anna Biernacka, Katarzyna Iwanicka-Pronicka, Wiesława Grajkowska, Elżbieta...> ;Diagnostics. 2021 Jul 15
• 3 citations
  Histopathologic and clinical outcomes of Milan System categories "non-diagnostic" and "non-neoplastic" of salivary gland fine needle aspirations.
  Daniel Johnson, Tatjana Antic, Ward Reeves, Jeffrey Mueller, Ricardo R. Lastra, Nicole A. Cipriani, Anna Biernacka> ;Journal of the American Society of Cytopathology. 2021 Mar 19
• 1 citations
  Accuracy of Subclassification and Grading of Renal Tumors on Fine Needle Aspiration Cytology Alone.
  Heather Chen, Razvan Lapadat, Ricardo R. Lastra, Anna Biernacka, Ward Reeves, Jeffrey Mueller, Stefan E. Pambuccian, Güliz A. Barkan, Eva M. Wojcik, Tatjana Antic> ;Acta Cytologica. 2021 Feb 3
• 1 citations
  High-resolution, ultrasensitive and quantitative DNA double-strand break labeling in eukaryotic cells using i-BLESS
  Anna Biernacka, Magdalena Skrzypczak, Yingjie Zhu, Philippe Pasero, Maga Rowicka, Krzysztof Ginalski> ;Nature Protocols. 2021 Feb 1
• Correction to: Feasibility Study of a Novel Protease-Activated Fluorescent Imaging System for Real-Time, Intraoperative Detection of Residual Breast Cancer in Breast C...
  Barbara L. Smith, Conor R. Lanahan, Michelle C. Specht, Bridget N. Kelly, Carson Brown, David B. Strasfeld, Jorge Ferrer, Upahvan Rai, Rong Tang, Travis Rice-Stitt, An...> ;Annals of Surgical Oncology. 2020 Dec 1
• 80 citations
  Topoisomerase 1 prevents replication stress at R-loop-enriched transcription termination sites.
  Alexy Promonet, Ismael Padioleau, Yaqun Liu, Lionel A. Sanz, Anna Biernacka, Anne Lyne Schmitz, Magdalena Skrzypczak, Amélie Sarrazin, Clément Mettling, Maga Rowicka, ...> ;Nature Communications. 2020 Aug 7
• 43 citations
  Rapid Whole-Exome Sequencing as a Diagnostic Tool in a Neonatal/Pediatric Intensive Care Unit.
  Robert Śmigiel, Mateusz Biela, Krzysztof Szmyd, Michał Błoch, Elżbieta Szmida, Paweł Skiba, Anna Walczak, Piotr Gasperowicz, Joanna Kosińska, Małgorzata Rydzanicz, Pio...> ;Journal of Clinical Medicine. 2020 Jul 13
• 11 citations
  Feasibility Study of a Novel Protease-Activated Fluorescent Imaging System for Real-Time, Intraoperative Detection of Residual Breast Cancer in Breast Conserving Surgery.
  Barbara L Smith, Conor R Lanahan, Michelle C Specht, Bridget N Kelly, Carson Brown, David B Strasfeld, Jorge M Ferrer, Upahvan Rai, Rong Tang, Travis Rice-Stitt, Anna ...> ;Annals of Surgical Oncology. 2020 Jun 1
• 5 citations
  AP4B1 -associated hereditary spastic paraplegia: expansion of phenotypic spectrum related to homozygous p.Thr387fs variant
  Krzysztof Szczałuba, Hanna Mierzewska, Robert Śmigiel, Joanna Kosińska, Agnieszka Koppolu, Anna Biernacka, Piotr Stawiński, Agnieszka Pollak, Małgorzata Rydzanicz, Raf...> ;Journal of Applied Genetics. 2020 Mar 12
• 10 citations
  Analysis of De Novo Mutations in Sporadic Cardiomyopathies Emphasizes Their Clinical Relevance and Points to Novel Candidate Genes.
  Maria Franaszczyk, Grażyna Truszkowska, Przemysław Chmielewski, Małgorzata Rydzanicz, Joanna Kosińska, Tomasz Rywik, Anna Biernacka, Mateusz Spiewak, Grażyna Kostrzewa...> ;Journal of Clinical Medicine. 2020 Jan 29
• 5 citations
  Novel COL12A1 variant as a cause of mild familial extracellular matrix-related myopathy.
  Aleksandra Jezela-Stanek, Anna Walczak, Michał Łaźniewski, Joanna Kosińska, Piotr Stawiński, Victor Murcia Pienkowski, Anna Biernacka, Małgorzata Rydzanicz, Grażyna Ko...> ;Clinical Genetics. 2019 Jun 1
• 3 citations
  Correlation of cytopathology with flow cytometry and histopathology for the diagnosis of hematologic malignancies in young adults presenting with cervical lymphadenopathy
  Bonnie Choy, Girish Venkataraman, Anna Biernacka, Ricardo R. Lastra, Jeffery Mueller, Namrata Setia, Ward Reeves, Tatjana Antic> ;Diagnostic Cytopathology. 2019 Jun 1
• 34 citations
  qDSB-Seq is a general method for genome-wide quantification of DNA double-strand breaks using sequencing.
  Yingjie Zhu, Anna Biernacka, Benjamin Pardo, Norbert Dojer, Romain Forey, Magdalena Skrzypczak, Bernard Fongang, Jules Nde, Razie Yousefi, Philippe Pasero, Krzysztof G...> ;Nature Communications. 2019 May 24
• Fine-needle aspiration of dermatofibrosarcoma protuberans metastasizing to hemithorax with superior vena cava compression: Case report and literature review.
  Bridget Banach, Tatjana Antic, Julia A. Bridge, Nicole A. Cipriani, Laura Frye, Thomas Krausz, Anna Biernacka> ;Diagnostic Cytopathology. 2019 Mar 27
• 12 citations
  Mapping of breakpoints in balanced chromosomal translocations by shallow whole-genome sequencing points to EFNA5, BAHD1 and PPP2R5E as novel candidates for genes causi...
  Victor Murcia Pienkowski, Marzena Kucharczyk, Marlena Młynek, Krzysztof Szczałuba, Małgorzata Rydzanicz, Barbara Poszewiecka, Agata Skórka, Maciej Sykulski, Anna Biern...> ;Journal of Medical Genetics. 2019 Feb 1
• 12 citations
  Neurodevelopmental phenotype caused by a de novo PTPN4 single nucleotide variant disrupting protein localization in neuronal dendritic spines.
  Krzysztof Szczałuba, Joanna J. Chmielewska, Olga Sokolowska, Małgorzata Rydzanicz, Krystyna Szymańska, Wojciech Feleszko, Paweł Włodarski, Anna Biernacka, Victor Murci...> ;Clinical Genetics. 2018 Dec 1
• 25 citations
  Homozygous mutation in the Neurofascin gene affecting the glial isoform of Neurofascin causes severe neurodevelopment disorder with hypotonia, amimia and areflexia.
  Robert Smigiel, Diane L. Sherman, Małgorzata Rydzanicz, Anna Walczak, Dorota Mikolajkow, Barbara Królak-Olejnik, Joanna Kosińska, Piotr Gasperowicz, Anna Biernacka, Pi...> ;Human Molecular Genetics. 2018 Nov 1
• 31 citations
  i-BLESS is an ultra-sensitive method for detection of DNA double-strand breaks
  Anna Biernacka, Yingjie Zhu, Magdalena Skrzypczak, Romain Forey, Benjamin Pardo, Marta Grzelak, Jules Nde, Abhishek Mitra, Andrzej Kudlicki, Nicola Crosetto, Philippe ...> ;Communications Biology. 2018 Oct 31
• 179 citations
  Comprehensive Mapping of Histone Modifications at DNA Double-Strand Breaks Deciphers Repair Pathway Chromatin Signatures
  Thomas Clouaire, Vincent Rocher, Anahita Lashgari, Coline Arnould, Marion Aguirrebengoa, Anna Biernacka, Magdalena Skrzypczak, François Aymard, Bernard Fongang, Norber...> ;Molecular Cell. 2018 Oct 18
• 26 citations
  Evidence for HNRNPH1 being another gene for Bain type syndromic mental retardation.
  Jacek Pilch, Agnieszka Koppolu, Anna Walczak, Victor Murcia Pienkowski, Anna Biernacka, Paweł Skiba, Joanna Machnik-Broncel, Piotr Gasperowicz, Joanna Kosińska, Małgor...> ;Clinical Genetics. 2018 Oct 1
• 11 citations
  Predicting proteome dynamics using gene expression data.
  Krzysztof Kuchta, Joanna Towpik, Anna Biernacka, Jan Kutner, Andrzej Kudlicki, Krzysztof Ginalski, Maga Rowicka> ;Scientific Reports. 2018 Sep 14
• 3 citations
  Indeterminate diagnoses in EUS-guided FNA of the pancreas: analysis of cytologist and clinician perceptions, cytologic features, and clinical outcomes.
  Andrea M. Olofson, Anna Biernacka, Zhigang Li, Thanapoom Boonipat, Edward J. Gutmann, Kerrington D. Smith, Timothy B. Gardner, Stuart R. Gordon, Vijayalakshmi Padmanab...> ;Journal of the American Society of Cytopathology. 2018 Sep 1
• 3 citations
  A de novo loss-of-function DYNC1H1 mutation in a patient with parkinsonian features and a favourable response to levodopa.
  Krzysztof Szczałuba, Krystyna Szymańska, Małgorzata Rydzanicz, Elżbieta Ciara, Anna Walczak, Dorota Piekutowska-Abramczuk, Joanna Kosińska, A Jacoszek, K Czerska, Anna...> ;Clinical Genetics. 2018 May 1
• 11 citations
  Phenotype of two Polish patients with Schaaf-Yang syndrome confirmed by identifying mutation in MAGEL2 gene.
  Karolina Matuszewska, Magdalena Badura-Stronka, Robert Śmigiel, Magdalena Cabała, Anna Biernacka, Joanna Kosińska, Małgorzata Rydzanicz, Anna Winczewska-Wiktor, Maria ...> ;Clinical Dysmorphology. 2018 Apr 1
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