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Connection

Anna Biernacka to Female

This is a "connection" page, showing publications Anna Biernacka has written about Female.
Connection Strength

0.325
  1. Cytomorphologic and molecular characterization of spindle cell carcinoid tumors of the lung. Cancer Cytopathol. 2024 Oct; 132(10):656-665.
    View in: PubMed
    Score: 0.043
  2. Histopathologic and clinical outcomes of Milan System categories "non-diagnostic" and "non-neoplastic" of salivary gland fine needle aspirations. J Am Soc Cytopathol. 2021 Jul-Aug; 10(4):349-356.
    View in: PubMed
    Score: 0.034
  3. Fine-needle aspiration of dermatofibrosarcoma protuberans metastasizing to hemithorax with superior vena cava compression: Case report and literature review. Diagn Cytopathol. 2019 Aug; 47(8):797-802.
    View in: PubMed
    Score: 0.030
  4. Smad3 Signaling Promotes Fibrosis While Preserving Cardiac and Aortic Geometry in Obese Diabetic Mice. Circ Heart Fail. 2015 Jul; 8(4):788-98.
    View in: PubMed
    Score: 0.023
  5. [Urinary TGF-beta1 excretion in children with renal cysts]. Przegl Lek. 2006; 63 Suppl 3:94-6.
    View in: PubMed
    Score: 0.012
  6. High tumor glucocorticoid receptor expression in early-stage, triple-negative breast cancer is associated with increased T-regulatory cell infiltration. Breast Cancer Res Treat. 2025 Feb; 209(3):563-572.
    View in: PubMed
    Score: 0.011
  7. Platelet-derived growth factor and platelet profiles in childhood nephrotic syndrome. Pediatr Nephrol. 2005 Jan; 20(1):36-41.
    View in: PubMed
    Score: 0.011
  8. Fate of nondiagnostic thyroid fine needle aspirations. Diagn Cytopathol. 2024 Dec; 52(12):709-714.
    View in: PubMed
    Score: 0.011
  9. Lung adenocarcinomas with isolated TP53 mutation: A comprehensive clinical, cytopathologic and molecular characterization. Cancer Med. 2024 01; 13(1):e6873.
    View in: PubMed
    Score: 0.010
  10. AP4B1-associated hereditary spastic paraplegia: expansion of phenotypic spectrum related to homozygous p.Thr387fs variant. J Appl Genet. 2020 May; 61(2):213-218.
    View in: PubMed
    Score: 0.008
  11. Feasibility Study of a Novel Protease-Activated Fluorescent Imaging System for Real-Time, Intraoperative Detection of Residual Breast Cancer in Breast Conserving Surgery. Ann Surg Oncol. 2020 Jun; 27(6):1854-1861.
    View in: PubMed
    Score: 0.008
  12. Novel COL12A1 variant as a cause of mild familial extracellular matrix-related myopathy. Clin Genet. 2019 06; 95(6):736-738.
    View in: PubMed
    Score: 0.007
  13. Correlation of cytopathology with flow cytometry and histopathology for the diagnosis of hematologic malignancies in young adults presenting with cervical lymphadenopathy. Diagn Cytopathol. 2019 Jun; 47(6):579-583.
    View in: PubMed
    Score: 0.007
  14. Homozygous mutation in the Neurofascin gene affecting the glial isoform of Neurofascin causes severe neurodevelopment disorder with hypotonia, amimia and areflexia. Hum Mol Genet. 2018 11 01; 27(21):3669-3674.
    View in: PubMed
    Score: 0.007
  15. Mapping of breakpoints in balanced chromosomal translocations by shallow whole-genome sequencing points to EFNA5, BAHD1 and PPP2R5E as novel candidates for genes causing human Mendelian disorders. J Med Genet. 2019 02; 56(2):104-112.
    View in: PubMed
    Score: 0.007
  16. Evidence for HNRNPH1 being another gene for Bain type syndromic mental retardation. Clin Genet. 2018 10; 94(3-4):381-385.
    View in: PubMed
    Score: 0.007
  17. Phenotype of two Polish patients with Schaaf-Yang syndrome confirmed by identifying mutation in MAGEL2 gene. Clin Dysmorphol. 2018 Apr; 27(2):49-52.
    View in: PubMed
    Score: 0.007
  18. Novel GNB1 de novo mutation in a patient with neurodevelopmental disorder and cutaneous mastocytosis: Clinical report and literature review. Eur J Med Genet. 2018 Mar; 61(3):157-160.
    View in: PubMed
    Score: 0.007
  19. New evidence for association of recessive IARS gene mutations with hepatopathy, hypotonia, intellectual disability and growth retardation. Clin Genet. 2017 12; 92(6):671-673.
    View in: PubMed
    Score: 0.007
  20. Homozygous truncating mutation in NRAP gene identified by whole exome sequencing in a patient with dilated cardiomyopathy. Sci Rep. 2017 06 13; 7(1):3362.
    View in: PubMed
    Score: 0.007
  21. Cytoplasmic Cyclin E Predicts Recurrence in Patients with Breast Cancer. Clin Cancer Res. 2017 Jun 15; 23(12):2991-3002.
    View in: PubMed
    Score: 0.006
  22. Cytoplasmic Cyclin E and Phospho-Cyclin-Dependent Kinase 2 Are Biomarkers of Aggressive Breast Cancer. Am J Pathol. 2016 07; 186(7):1900-1912.
    View in: PubMed
    Score: 0.006
  23. [Use of salazopyrin in Schonlein-Henoch disease]. Wiad Lek. 1995 Jan-Jun; 48(1-12):63-5.
    View in: PubMed
    Score: 0.006
  24. Thrombospondin-1 induction in the diabetic myocardium stabilizes the cardiac matrix in addition to promoting vascular rarefaction through angiopoietin-2 upregulation. Circ Res. 2013 Dec 06; 113(12):1331-44.
    View in: PubMed
    Score: 0.005
  25. Hbo1 is a cyclin E/CDK2 substrate that enriches breast cancer stem-like cells. Cancer Res. 2013 Sep 01; 73(17):5556-68.
    View in: PubMed
    Score: 0.005
  26. Endogenous thrombospondin 1 protects the pressure-overloaded myocardium by modulating fibroblast phenotype and matrix metabolism. Hypertension. 2011 Nov; 58(5):902-11.
    View in: PubMed
    Score: 0.004
  27. Cyclin E deregulation impairs mitotic progression through premature activation of Cdc25C. Cancer Res. 2010 Jun 15; 70(12):5085-95.
    View in: PubMed
    Score: 0.004
  28. Low molecular weight cyclin E overexpression shortens mitosis, leading to chromosome missegregation and centrosome amplification. Cancer Res. 2010 Jun 15; 70(12):5074-84.
    View in: PubMed
    Score: 0.004
  29. Low-molecular-weight cyclin E can bypass letrozole-induced G1 arrest in human breast cancer cells and tumors. Clin Cancer Res. 2010 Feb 15; 16(4):1179-90.
    View in: PubMed
    Score: 0.004
  30. Assessment of serum cystatin C in children with congenital solitary kidney. Pediatr Nephrol. 2006 May; 21(5):688-93.
    View in: PubMed
    Score: 0.003
  31. Serum and urine leptin concentration in children with nephrotic syndrome. Pediatr Nephrol. 2005 May; 20(5):597-602.
    View in: PubMed
    Score: 0.003
  32. [Reference values of 24-hour ambulatory blood pressure in healthy children by height]. Pol Merkur Lekarski. 2004 Nov; 17(101):451-6.
    View in: PubMed
    Score: 0.003
  33. [Reference values of arterial pressure depending on age, assessed by 24-hour ambulatory monitoring]. Pol Merkur Lekarski. 2003 Jul; 15(85):29-33.
    View in: PubMed
    Score: 0.003
  34. [The course of post-streptococcal glomerulonephritis depending on methods of treatment for the preceding respiratory tract infection]. Wiad Lek. 2001; 54(1-2):56-63.
    View in: PubMed
    Score: 0.002
  35. [Anomalies of the cervical spine in children]. Wiad Lek. 1993 Sep; 46(17-18):714-7.
    View in: PubMed
    Score: 0.001
  36. [Primary hyperlipoproteinemia type V]. Pol Tyg Lek. 1992 Nov 16-30; 47(46-48):1067-8.
    View in: PubMed
    Score: 0.001
  37. [Familial occurrence of central diabetes insipidus]. Wiad Lek. 1990 Jun 15; 43(12):619-21.
    View in: PubMed
    Score: 0.001
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.