All Stories

  1. Forensic genetics associated with hair analysis as a tool for jaguar (Panthera onca) identification

    Article • Global Ecology and Conservation, August 2024, Elsevier

    Cintia Fridman

  2. Multiple TP53 p.R337H haplotypes and implications for tumor susceptibility

    Article • Human Genetics and Genomics Advances, January 2024, Elsevier

    Cintia Fridman

  3. Analysis of genetic polymorphisms associated with the presence of freckles for phenotypic prediction

    Article • Forensic Science International Genetics Supplement Series, December 2022, Elsevier

    Cintia Fridman

  4. Analysis of isoalleles and flanking SNPs of STR markers by NGS to distinguish monozygotic twins

    Article • Forensic Science International Genetics Supplement Series, December 2022, Elsevier

    Cintia Fridman

  5. Perspective on the use of investigative genetic genealogy in Brazil

    Article • Forensic Science International Genetics Supplement Series, December 2022, Elsevier

    Cintia Fridman

  6. Casework direct kit as an alternative extraction method to enhance touch DNA samples analysis

    Article • Forensic Science International Genetics, July 2020, Elsevier

    Cintia Fridman

  7. Male lineages in Brazilian populations and performance of haplogroup prediction tools

    Article • Forensic Science International Genetics, January 2020, Elsevier

    Cintia Fridman

  8. DNA phenotyping

    Article • Research and Reports in Forensic Medical Science, February 2019, Dove Medical Press

    Cintia Fridman, Leonardo Marano

  9. Genetic characterization of four Brazilian states with 25 Yfiler®Plus markers

    Article • Forensic Science International Genetics Supplement Series, December 2017, Elsevier

    Cintia Fridman

  10. Polymorphisms of mitochondrial DNA control region are associated to endometriosis

    Article • Journal of Assisted Reproduction and Genetics, November 2017, Springer Science + Business Media

    Cintia Fridman

  11. Growth hormone insensitivity with immune dysfunction caused by a STAT5B mutation in the south of Brazil: evidence for a founder effect

    Article • Genetics and Molecular Biology, June 2017, FapUNIFESP (SciELO)

    Cintia Fridman

  12. CCDC22 gene polymorphism is associated with advanced stages of endometriosis in a sample of Brazilian women

    Article • Journal of Assisted Reproduction and Genetics, May 2017, Springer Science + Business Media

    Cintia Fridman

  13. Polymorphisms of ICAM-1 and IL-6 genes related to endometriosis in a sample of Brazilian women

    Article • Journal of Assisted Reproduction and Genetics, September 2016, Springer Science + Business Media

    Cintia Fridman

  14. Post-mortem cytogenomic investigations in patients with congenital malformations

    Article • Experimental and Molecular Pathology, August 2016, Elsevier

    Cintia Fridman

  15. Y haplotype variability in a population of SÃO Paulo state, Brazil

    Article • Forensic Science International Genetics, July 2016, Elsevier

    Cintia Fridman

  16. Corrigendum to “SLC24A5 and ASIP as phenotypic predictors in Brazilian population for forensic purposes” [Leg. Med. 17 (4) (2015) 261–266]

    Article • Legal Medicine, March 2016, Elsevier

    Cintia Fridman

  17. Is it possible to use Forensic DNA phenotyping in Brazilian population?

    Article • Forensic Science International Genetics Supplement Series, December 2015, Elsevier

    Cintia Fridman

  18. SLC24A5 and ASIP as phenotypic predictors in Brazilian population for forensic purposes

    Article • Legal Medicine, July 2015, Elsevier

    Cintia Fridman

  19. Mitochondrial and genomic ancestry are associated with etiology of heart failure in Brazilian patients

    Article • Journal of Human Hypertension, May 2015, Springer Science + Business Media

    Cintia Fridman

  20. Amerindian genetic ancestry is associated with higher survival rates compared to African and European ancestry in Brazilian patients with heart failure

    Article • International Journal of Cardiology, September 2014, Elsevier

    Cintia Fridman

  21. Haplotype diversity in mitochondrial DNA hypervariable region in a population of southeastern Brazil

    Article • International Journal of Legal Medicine, May 2014, Springer Science + Business Media

    Cintia Fridman

  22. The E180splice mutation in theGHRgene causing Laron syndrome: Witness of a Sephardic Jewish exodus from the Iberian Peninsula to the New World?

    Article • American Journal of Medical Genetics Part A, March 2014, Wiley

    Professor Alexander A L Jorge, Cintia Fridman

  23. MYH9 and APOL1 Gene Polymorphisms and the Risk of CKD in Patients with Lupus Nephritis from an Admixture Population

    Article • PLoS ONE, March 2014, PLOS

    Cintia Fridman

  24. Assessment of the Relationship between Self-Declared Ethnicity, Mitochondrial Haplogroups and Genomic Ancestry in Brazilian Individuals

    Article • PLoS ONE, April 2013, PLOS

    Cintia Fridman

  25. A new duplication in themitochondrially encoded tRNA prolinegene in a patient with dilated cardiomyopathy

    Article • Mitochondrial DNA, September 2012, Taylor & Francis

    Cintia Fridman

  26. Evaluation of the relationship between mitochondrial haplogroup and development of heart failure in Brazilian sample

    Article • Forensic Science International Genetics Supplement Series, December 2011, Elsevier

    Jose Krieger, Cintia Fridman

  27. The discrimination power of the hypervariable regions HV1, HV2 and HV3 of mitochondrial DNA in the Brazilian population

    Article • Forensic Science International Genetics Supplement Series, December 2011, Elsevier

    Jose Krieger, Cintia Fridman

  28. SNPs in mitochondrial DNA coding region used to discriminate common sequences in HV1–HV2–HV3 region

    Article • Forensic Science International Genetics Supplement Series, December 2011, Elsevier

    Cintia Fridman

  29. The GHEP–EMPOP collaboration on mtDNA population data—A new resource for forensic casework

    Article • Forensic Science International Genetics, March 2011, Elsevier

    Cintia Fridman

  30. Establishment and characterization of androgen-independent human prostate cancer cell lines, PcBra1, PcBra2, and PcBra3

    Article • In Vitro Cellular & Developmental Biology - Animal, December 2009, Springer Science + Business Media

    Cintia Fridman

  31. HVIII discrimination power to distinguish HVI and HVII common sequences

    Article • Forensic Science International Genetics Supplement Series, December 2009, Elsevier

    Cintia Fridman

  32. Establishment and characterization of human bladder cancer cell lines BexBra1, BexBra2, and BexBra4

    Article • In Vitro Cellular & Developmental Biology - Animal, November 2009, Springer Science + Business Media

    Cintia Fridman

  33. Potential Effect of Using ABO-Compatible Living-Donor Liver Transplantation

    Article • Transplantation Proceedings, November 2009, Elsevier

    Cintia Fridman

  34. Erratum to “Brazilian population profile of 15 STR markers” [Forensic Science International: Genetics 2/2 (2008) e1–e4]

    Article • Forensic Science International Genetics, September 2008, Elsevier

    Cintia Fridman

  35. Genetic profile from the DNA databank of a Brazilian missing kids program

    Article • Forensic Science International Genetics Supplement Series, August 2008, Elsevier

    Cintia Fridman

  36. Mitochondrial HVI and HVII polymorphisms and heteroplasmies inheritance in Brazilian pairs of mother/child

    Article • Forensic Science International Genetics Supplement Series, August 2008, Elsevier

    Cintia Fridman

  37. DNA polymorphisms as tools for spinal cord injury research

    Article • Spinal Cord, May 2008, Springer Science + Business Media

    Cintia Fridman

  38. Brazilian population profile of 15 STR markers

    Article • Forensic Science International Genetics, March 2008, Elsevier

    Cintia Fridman

  39. “Projeto Caminho de Volta”: A Brazilian DNA program for missing kids

    Article • International Congress Series, April 2006, Elsevier

    Cintia Fridman

  40. Inv dup (15): Is the electroclinical phenotype helpful for this challenging clinical diagnosis?

    Article • Clinical Neurophysiology, April 2006, Elsevier

    Cintia Fridman

  41. Epilepsy in Patients With Angelman Syndrome Caused by Deletion of the Chromosome 15q11-13

    Article • Archives of Neurology, January 2006, American Medical Association (AMA)

    Cintia Fridman

  42. Angelman syndrome: Uniparental paternal disomy 15 determines mild epilepsy, but has no influence on EEG patterns

    Article • Epilepsy Research, December 2005, Elsevier

    Cintia Fridman

  43. Human genome and the perspectives for schizophrenia

    Article • January 2004, Springer Science + Business Media

    Cintia Fridman

  44. Angelman Syndrome: Difficulties in EEG Pattern Recognition and Possible Misinterpretations

    Article • Epilepsia, July 2003, Wiley

    Cintia Fridman

  45. Angelman syndrome associated with oculocutaneous albinism due to an intragenic deletion of the P gene

    Article • American Journal of Medical Genetics Part A, May 2003, Wiley

    Cintia Fridman

  46. Association of a new polymorphism in ALOX12 gene with bipolar disorder

    Article • European Archives of Psychiatry and Clinical Neuroscience, February 2003, Springer Science + Business Media

    Cintia Fridman

  47. Diagnosis of patients with Prader-Willi and Angelman Syndromes: the importance of an overall investigation

    Article • Genetics and Molecular Biology, January 2002, FapUNIFESP (SciELO)

    Cintia Fridman

  48. Article • Journal of Autism and Developmental Disorders, January 2002, Springer Science + Business Media

    Cintia Fridman

  49. Phenotypic and behavioral variability within Angelman Syndrome group with UPD

    Article • Genetics and Molecular Biology, January 2002, FapUNIFESP (SciELO)

    Cintia Fridman

  50. Prader-Willi Syndrome: Genetic Tests and Clinical Findings

    Article • Genetic Testing, December 2000, Mary Ann Liebert Inc

    Cintia Fridman

  51. Genomic imprinting: genetic mechanisms and phenotypic consequences in Prader-Willi and Angelman syndromes

    Article • Genetics and Molecular Biology, December 2000, FapUNIFESP (SciELO)

    Cintia Fridman

  52. A further Angelman syndrome patient with UPD15 due to paternal meiosis II nondisjunction

    Article • Clinical Genetics, January 2000, Wiley

    Cintia Fridman

  53. Origin of uniparental disomy 15 in patients with Prader-Willi or Angelman syndrome

    Article • American Journal of Medical Genetics, January 2000, Wiley

    Cintia Fridman

  54. Paternal UPD15: Further genetic and clinical studies in four Angelman syndrome patients

    Article • American Journal of Medical Genetics, January 2000, Wiley

    Cintia Fridman

  55. Rett Syndrome in a Boy with a 47,XXY Karyotype

    Article • The American Journal of Human Genetics, June 1999, Elsevier

    Cintia Fridman

  56. Unusual clinical features in an Angelman syndrome patient with uniparental disomy due to a translocation 15q15q

    Article • Clinical Genetics, October 1998, Wiley

    Cintia Fridman

  57. Síndrome de Angelman: causa frequentemente não reconhecida de deficiência mental e epilepsia. relato de caso

    Article • Arquivos de Neuro-Psiquiatria, June 1997, FapUNIFESP (SciELO)

    Cintia Fridman