Galluccio Tiziana | Biologist Geneticist | Women Researcher Award

Mrs. Galluccio Tiziana | Biologist Geneticist | Women Researcher Award

DIRIGENTE at IRCCS Ospedale Pediatrico Bambino Gesù, Italy

Tiziana Galluccio is an accomplished biologist with extensive experience in immunogenetics and molecular diagnostics. She holds multiple positions, including her current role as a permanent biologist at OPBG Ospedalepediatrico Bambin Gesù in Rome. With a background in both research and clinical practice, she has contributed to several key research projects, particularly in the field of HLA typing and chimerism. Galluccio’s work spans across various prestigious institutions, such as the Mediterranean Institute of Hematology and the S. Lucia Hospital, contributing significantly to genetic research related to neurodegenerative diseases and genetic mutations. She has participated in groundbreaking studies focused on Duchenne muscular dystrophy and movement disorders. Over the years, she has earned recognition for her work in molecular diagnostics, gene research, and clinical applications, marking her as a leader in her field. Galluccio has consistently demonstrated her expertise in both research and diagnostics, making significant contributions to the understanding and treatment of genetic diseases, as well as to the development of novel diagnostic tools.

Professional Profile

Education

Tiziana Galluccio has a solid academic background with a degree in Biology obtained from the University of “Roma Tre” in 2002, where she focused on virology and the study of the transcription factor Ets-1 in erythroid differentiation. In addition to this, Galluccio pursued further academic qualifications, including a Ph.D. in Cellular and Molecular Biology from the University of Tor Vergata, which cemented her specialization in cellular biology. She also qualified as a medical geneticist with a specialization in Human Genetics from the University of “La Sapienza” in Rome. Her commitment to ongoing professional development led her to engage in specialized courses and competitions in medical genetics, further deepening her expertise in the field. Galluccio also holds qualifications as a registered biologist, and her academic journey reflects a deep commitment to exploring and understanding the genetic underpinnings of various diseases, particularly neurodegenerative disorders.

Professional Experience

Tiziana Galluccio’s professional career spans a wide range of roles across esteemed institutions in Italy, contributing to both research and clinical practices. Her most recent role has been as a biologist at OPBG Ospedalepediatrico Bambin Gesù, where she focuses on immunogenetics and transplant biology, specifically working on HLA typing and chimerism. Prior to this, she worked for nearly a decade at the Mediterranean Institute of Hematology in Rome, where she was responsible for various research tasks, including gene analysis for neurodegenerative diseases. Additionally, Galluccio has participated in research as a freelancer in various private organizations and institutions. Her role at the IRCCS Foundation Hospital Maggiore Polyclinic Mangiagalli and Regina Elena Hospital involved molecular diagnostics, including studies on complex genetic rearrangements, while her tenure at the CSS-Mendel Institute of Rome further bolstered her expertise in genetics related to movement disorders. Galluccio’s broad experience in both private and public sector roles highlights her multifaceted expertise in genetic research, molecular diagnostics, and laboratory management.

Research Interests

Tiziana Galluccio’s research interests lie primarily in the field of immunogenetics, particularly focusing on transplant biology, genetic diagnostics, and neurodegenerative diseases. Her work involves studying HLA typing and chimerism, which are vital for understanding immune compatibility in transplants. She has also made significant contributions to the genetic study of neurodegenerative conditions such as Parkinson’s disease and Joubert syndrome. Galluccio has explored candidate genes related to conditions such as Duchenne muscular dystrophy and tuberous sclerosis, aiming to uncover the genetic factors involved in these disorders. Her passion for understanding complex genetic diseases is reflected in her research efforts, which aim to improve diagnostic methods and therapeutic approaches. Additionally, Galluccio has shown a deep interest in using molecular techniques to investigate genetic mutations related to infertility, further demonstrating the breadth of her expertise.

Research Skills

Tiziana Galluccio’s research skills are extensive and include a solid command of molecular genetics and bioinformatics techniques. Her expertise in HLA typing and chimerism is central to her work in immunogenetics, where she applies cutting-edge laboratory methods to study transplant compatibility and immune responses. Galluccio is also highly skilled in molecular diagnostics, utilizing various laboratory tools to detect genetic mutations, especially in the context of neurodegenerative diseases and inherited disorders. Her ability to analyze complex genetic data through bioinformatics, coupled with her practical experience in experimental validation using model organisms, reflects her strong scientific and analytical abilities. Furthermore, her involvement in research related to neurodegenerative diseases and gene mutations demonstrates her deep understanding of molecular biology and genetics, equipping her to drive significant advancements in the field.

Awards and Honors

Tiziana Galluccio has received multiple recognitions throughout her career, highlighting her contributions to genetic research and molecular diagnostics. One of her significant achievements includes winning competitive research grants, such as those from the IRCCS Foundation Hospital Maggiore Polyclinic Mangiagalli and Regina Elena, where she conducted pioneering studies on Duchenne muscular dystrophy. Galluccio has also earned specialized research awards in molecular diagnostics, as well as scholarships for her research in human genetics and neurodegenerative diseases. Her dedication to advancing scientific knowledge has earned her acknowledgment within the scientific community, particularly for her work on the genetics of movement disorders. These honors reflect her commitment to excellence in research and her continued efforts to improve understanding and treatment options for genetic diseases.

Conclusion

Tiziana Galluccio is a highly skilled biologist whose career spans research, diagnostics, and genetic studies, particularly in the fields of immunogenetics and neurodegenerative diseases. Her extensive professional experience and academic background demonstrate a deep commitment to scientific advancement. Galluccio’s research contributions, particularly in the areas of HLA typing and chimerism, as well as her work on genetic disorders, position her as an invaluable contributor to the field. Her research skills, particularly in molecular genetics and diagnostics, have made a lasting impact on the understanding of complex diseases. Despite her achievements, further strengthening her collaborative efforts and exploring international research partnerships could enhance the global impact of her work. Galluccio’s proven track record of scientific inquiry, coupled with her recognition within the medical and scientific communities, solidifies her as a top contender for the Best Researcher Award.

Publication Top Notes

  1. Publication: Characterisation of the novel HLA-DQA1*01:02:24 allele by sequencing-based typing
    Authors: Cargou, M., Andreani, M., Galluccio, T., Ralazamahaleo, M., Visentin, J.
    Year: 2024
    Citations: 2
  2. Publication: Identification of the novel HLA-C*07:1132 allele by next-generation sequencing
    Authors: Galluccio, T., Cerretti, R., Battarra, M., Giustiniani, P., Andreani, M.
    Year: 2024
    Citations: 2
  3. Publication: Identification of the novel HLA-B*27:276 allele by next-generation sequencing
    Authors: Tiziana, G., Paola, G., Annalisa, G., Francesca, B., Marco, A.
    Year: 2024
    Citations: 2
  4. Publication: Identification of the novel HLA-A*30:221 allele by next-generation sequencing
    Authors: Galluccio, T., Giustiniani, P., Di Luzio, A., Testa, G., Andreani, M.
    Year: 2024
    Citations: 2
  5. Publication: Identification of the novel HLA-DPA1*01:130 allele by next-generation sequencing
    Authors: Galluccio, T., Cerretti, R., Guagnano, A., Troiano, M., Andreani, M.
    Year: 2024
    Citations: 2
  6. Publication: Identification of the novel HLA-DPA1*02:110:02 allele by next-generation sequencing
    Authors: Galluccio, T., Battarra, M., Bianculli, A.G., Besi, F., Andreani, M.
    Year: 2023
    Citations: 2
  7. Publication: Identification of the novel HLA-DPA1*01:149 allele by next-generation sequencing
    Authors: Galluccio, T., Cerretti, R., Guagnano, A., Bianculli, A.G., Andreani, M.
    Year: 2023
    Citations: 2
  8. Publication: Identification of a robust DNA methylation signature for Fanconi anemia
    Authors: Pagliara, D., Ciolfi, A., Pedace, L., Locatelli, F., Tartaglia, M.
    Year: 2023
    Citations: 1
  9. Publication: Characterization of the novel HLA-DPA1*01:159 allele by sequencing-based typing
    Authors: Cargou, M., Andreani, M., Galluccio, T., Wojciechowski, E., Visentin, J.
    Year: 2023
    Citations: 2
  10. Publication: Identification of the novel HLA-DPB1*1328:01 allele by next-generation sequencing
    Authors: Tiziana, G., Franco, C., Paola, G., Antonio Giuseppe, B., Marco, A.
    Year: 2023
    Citations: 2