Ms. Mandeep Kaur, Guru Nanak Dev University, India
Ms. Mandeep Kaur is a dedicated academic and researcher at Guru Nanak Dev University, India. With a passion for advancing knowledge and fostering educational growth, she has contributed significantly to her field through both teaching and research. Her work often focuses on [mention specific research interests or academic areas if known], reflecting her commitment to addressing contemporary challenges and enhancing academic understanding. Ms. Kaur’s dedication to her profession is evident through her involvement in various academic initiatives and her active engagement in the university community.
Profile
Scopus
Education Qualification
Ph.D. in the Department of Human Genetics, Biology Block, Guru Nanak Dev University, Amritsar.
M.Sc. (H.S.) Human genetics (2017-2019) Guru Nanak Dev University, Amritsar.
B.Sc. (H.S.) Human genetics (2014-2017) Guru Nanak Dev University, Amritsar.
Professional Experience
Research Scholar (Ph.D.)
Department of Human Genetics, Guru Nanak Dev University, Amritsar
February 2021 – Present
- Conducting advanced research on [specific research topic or area, if known], focusing on [specific aspects, methodologies, or technologies used].
- Utilizing various techniques such as [mention any specialized techniques or equipment used] to analyze and interpret genetic data.
- Collaborating with fellow researchers and faculty members on [mention any collaborative projects or research groups].
- Presenting research findings at academic conferences and seminars, contributing to the academic community and staying updated with the latest developments in the field.
- Publishing research articles in peer-reviewed journals, enhancing the visibility and impact of the research conducted.
Junior Research Fellow (CSIR-JRF)
Guru Nanak Dev University, Amritsar
February 2021 – February 2023
- Assisted in [specific research projects or areas] under the guidance of senior researchers and faculty.
- Engaged in literature review, experimental design, data collection, and analysis.
- Contributed to the preparation of research reports and manuscripts for publication.
- Provided support in the lab, including [mention any specific lab duties or techniques learned].
Intern / Research Assistant (if applicable)
Institution or Organization Name
Dates
- Gained hands-on experience in [mention specific tasks or projects].
- Assisted in [mention specific responsibilities or research tasks].
- Developed skills in [mention any specific techniques or tools used].
Research Contribution
- Genetic Studies: Extensive research on genetic variants related to PCOS and reproductive disorders, including polymorphisms in FSHR, LHCGR, CYP11B2, CYP1A1, and TNF-alpha, contributing to a deeper understanding of their roles in these conditions.
- Methodologies: Utilized advanced techniques such as ATR-FTIR spectroscopy, case-control studies, and meta-analyses to explore genetic factors and their impact on health conditions.
- Impact: Findings from her research have contributed to the scientific community’s understanding of genetic influences on PCOS and recurrent miscarriage, providing insights that could inform future research and clinical practices.
Publication Top Notes
- Kaur, M., Singh, S., & Kaur, A. (2024). Structural changes in amide I and amide II regions of PCOS women analyzed by ATR-FTIR spectroscopy. Heliyon, 10(13).
- Investigates structural changes in protein regions associated with Polycystic Ovary Syndrome (PCOS) using ATR-FTIR spectroscopy.
- Kaur, M., Singh, S., Kaur, R., Beri, A., & Kaur, A. (2023). Analyzing the impact of FSHR variants on polycystic ovary syndrome—a case-control study in Punjab. Reproductive Sciences, 30(8), 2563-2572.
- Examines the effect of FSHR gene variants on PCOS susceptibility in a Punjabi population.
- Kaur, M., Singh, S., & Kaur, A. (2023). Polymorphisms in FSHR modulating susceptibility to polycystic ovary syndrome: an updated meta-analysis. Journal of Ovarian Research, 16(1), 183.
- Provides a meta-analysis of FSHR gene polymorphisms and their influence on PCOS risk.
- Singh, S., Kaur, M., Kaur, R., Beri, A., & Kaur, A. (2022). Association analysis of LHCGR variants and polycystic ovary syndrome in Punjab: a case–control approach. BMC Endocrine Disorders, 22(1), 335.
- Explores the link between LHCGR gene variants and PCOS in a Punjabi cohort.
- Kaur, R., Kaur, M., Singh, S., Kaur, T., & Kaur, A. (2022). Genetic Variants of CYP11B2 and CYP1A1 Among the North-Indian Punjabi Females with Polycystic Ovary Syndrome. Korean Journal of Clinical Laboratory Science, 54(4), 316-324.
- Investigates the genetic variants of CYP11B2 and CYP1A1 associated with PCOS in North-Indian Punjabi women.
- Sudhir, N., Kaur, M., Singh, S., Beri, A., Kaur, T., & Kaur, A. (2023). Impact of Interleukin-10 Promoter Region Polymorphisms on Recurrent Miscarriage: A Case–Control Approach. Journal of Human Reproductive Sciences, 16(2), 156-165.
- Analyzes the influence of IL-10 promoter polymorphisms on recurrent miscarriage.
- Sudhir, N., Kaur, M., Singh, S., Beri, A., Kaur, T., Badaruddoza, & Kaur, A. (2023). Role of tumor necrosis factor‐alpha‐238 G> A promoter region polymorphism on recurrent miscarriage: An association study and meta‐analysis. American Journal of Reproductive Immunology, 90(4), e13775.
- Examines the TNF-alpha-238 G>A polymorphism’s role in recurrent miscarriage through association studies and meta-analysis.
- Rayat, A. K., Thapar, P., Kaur, M., Singh, S., & Kaur, A. (2023). Association of CYP11A1 Polymorphisms with Recurrent Pregnancy Loss in the Female Population of Punjab. Journal of Human Reproductive Sciences, 16(3), 242-245.
- Investigates the association between CYP11A1 gene polymorphisms and recurrent pregnancy loss in Punjabi women.
- Singh, S., Kaur, M., Beri, A., & Kaur, A. (2023). Significance of LHCGR polymorphisms in polycystic ovary syndrome: an association study. Scientific Reports, 13(1), 22841.
- Analyzes the impact of LHCGR gene polymorphisms on PCOS susceptibility.