Other Memberships/Affiliations
Indian Society of Human Genetics
Indian Academy of Paediatrics
Environmental Mutagen Society of India
Society of Biological Chemists of India
Degrees:
1990
Doctorate Medical and Health Sciences incl Neurosciences
Biological and Medical Sciences/Human Genetics
1990
Master Medical and Health Sciences incl Neurosciences
Publications resulting from Research
Publications in the last 5 years
1. M.Vidyadhari M.SUJATHA P.Krupa A.Jyothy PratibhaNallari A.VenkateshwariA functional polymorphism in the promoter region of interleukin-10 gene increases the risk for spontaneous abortions—a triad study. J of Assisted Reproduction and Genetics. 2015 Jul; 32(7): 1129–1134. (IF 1.718)
2. Vidyadhari M, SUJATHA M, Krupa P, Jyothy A, Nallari P, Venkateshwari A. Association of interleukin-10 gene promoter polymorphism in spontaneous abortions: a family-based triad study. Inflamm Res. 2015 Dec;64(12):963-9. doi: 10.1007/s00011-015-0879-9. Epub 2015 Oct 7. PMID:26445972. Impact Factor: 2.659.
3. A Pavani Sowjanya, Meera Rao, Hari Priya Vedantham and SUJATHA MADIREDDI.
Correlation of plasma nitrite/nitrate levels and inducible nitic oxide gene expression among women with cervical abnormalities and cancer. Jr.nitric oxide.Oct 2015
Venkateshwari Ananthapur, Srilekha Avvari, Veena Koka, SUJATHA MADIREDDI, Jyothy Akka . A Rare De Novo Balanced X; 1 Translocation in an Indian Female with Primary Amenorrhea. J Reprod Infertil. 2015;16(3):171-173.
4 Sreenivasa Rao Guggilla, Jalandhar Senagari, PN Rao and SUJATHA MADIREDDI. Spectrum of mutations in the ATP binding domain of ATP7B gene of Wilson Disease in a regional Indian cohorte. Gene, Volume, 569, issue 1, 10th Sept 2015, pages 83-87.
.M. Vidyadhari, M. SUJATHA, P. Krupa, Pratibha Nallari and A. Venkateshwari. Haplotype analysis of IL-10 gene polymorphism in couples with spontaneous abortions and aborted fetuses. Immunologic Research (2017) DOI 10.1007/s12026-017-8923-1.
Immunol Res (2017) 65:853–861 Impact Factor: 2.905.
5 M. Vidyadhari, M. SUJATHA, P. Krupa, Pratibha Nallari and A. Venkateshwari. A family based triad study evaluating the role of MTHFR gene polymorphisms in spontaneous abortions. Gene Reports 10 (2018); Dec 5. doi.org/10.1016/j.genrep.2017.12.001. 2452-0144/ © 2017 Published by Elsevier Inc.pgs-116-122. Impact Factor: 2.138.
6M. Vidyadhari , M. SUJATHA, P. Krupa, Pratibha Nallari, A. Venkateshwari. Association Of Genetic Polymorphism Of Vascular Endothelial Growth Factor In The Etiology Of Recurrent Pregnancy Loss – A Triad Study. Journal of Assisted Reproduction and Genetics (In press) 2019.
7.Avvari Srilekha, Akka Jyothy, MADIREDDI SUJATHA, Pratibha Nallari, Ananthapur Venkateshwari (2019.) An Inherited Balanced Translocation between Chromosomes 4 and 6 in Recurrent Pregnancy Loss: A Case Report. Journal of family medicine – 1(3):10-14.
8.Srilekha, A., Sowmya, S., Jyothy, A., SUJATHA, M. and Venkateshwari, A. A rare variant of turners syndrome with mosaic 46, X idic X /45, X karyotype: A case report. Journal of Cell and Tissue Research, 19(2) 6713-6716 (2019).
9.Srilekha Avvari, SUJATHA MADIREDDI, Pratibha Nallari, Jyothy Akka, Venkateshwari Ananthapur. A case of Hematometra with a chromosomal abnormality: A case report. J of Genet Disord and Genet Med Vol.3 No.1 2019.
Conferences
1. A Venkateshwari, A.Srilekha, Ashrafunnisa Begum, M.SUJATHA, T.Sunitha, Pratibha Nallari and A Jyothy. “A rare variant of Turner syndrome with mosaic 46, X, dic X / 45, XO, karyotype.” TWOWS Fourth general Assembly and International conference: Women scientists in a changing world. June 27-30, 2010 Beijing, China.
2. A. Jyothy, Sharma V, Venkateshwari. A, Munshi A, SUJATHA M, Singh R, Thangaraj K. Xenoantiandrogens: Risk factiors for androgen receptor mutation in Hypospadias. 41st Annual meeting of Environmental Mutagen Society, October 23-27, 2010, Fort Worth, Texas, USA.
3. K. Rebekah Prasoona, Anjana Munshi, T. Sunitha, B. Srinadh, M. SUJATHA, T. M. Kumari, A. Venkateshwari, A. Jyothy. Association of MTHFD1 gene G1958A polymorphism as a maternal risk factor for neural tube defects. AP Science Congress – 2013, “Innovations in Science and technology for emerging knowledge society”, held at 14th – 16th November, 2013, University of Hyderabad, Hyderabad.
4. K. Sri Manjari, KSPS. Teja, M. SUJATHA, A. Jyothy, PratibhaNallari, A. Venkateshwari. Transferrin (rs3811647) gene polymorphism in Iron Deficiency Anemia. ISHG-2014. “Healthy Genes - Healthy Life”, International Conference on Human Genetics and 39th Annual Meeting of the Indian Society of Human Genetics. Ahmedabad Management Association, Ahmedabad, India, from 22nd - 25th Jan
1. M.Vidyadhari M.SUJATHA P.Krupa A.Jyothy PratibhaNallari A.VenkateshwariA functional polymorphism in the promoter region of interleukin-10 gene increases the risk for spontaneous abortions—a triad study. J of Assisted Reproduction and Genetics. 2015 Jul; 32(7): 1129–1134. (IF 1.718)
2. Vidyadhari M, SUJATHA M, Krupa P, Jyothy A, Nallari P, Venkateshwari A. Association of interleukin-10 gene promoter polymorphism in spontaneous abortions: a family-based triad study. Inflamm Res. 2015 Dec;64(12):963-9. doi: 10.1007/s00011-015-0879-9. Epub 2015 Oct 7. PMID:26445972. Impact Factor: 2.659.
3. A Pavani Sowjanya, Meera Rao, Hari Priya Vedantham and SUJATHA MADIREDDI.
Correlation of plasma nitrite/nitrate levels and inducible nitic oxide gene expression among women with cervical abnormalities and cancer. Jr.nitric oxide.Oct 2015
Venkateshwari Ananthapur, Srilekha Avvari, Veena Koka, SUJATHA MADIREDDI, Jyothy Akka . A Rare De Novo Balanced X; 1 Translocation in an Indian Female with Primary Amenorrhea. J Reprod Infertil. 2015;16(3):171-173.
4 Sreenivasa Rao Guggilla, Jalandhar Senagari, PN Rao and SUJATHA MADIREDDI. Spectrum of mutations in the ATP binding domain of ATP7B gene of Wilson Disease in a regional Indian cohorte. Gene, Volume, 569, issue 1, 10th Sept 2015, pages 83-87.
.M. Vidyadhari, M. SUJATHA, P. Krupa, Pratibha Nallari and A. Venkateshwari. Haplotype analysis of IL-10 gene polymorphism in couples with spontaneous abortions and aborted fetuses. Immunologic Research (2017) DOI 10.1007/s12026-017-8923-1.
Immunol Res (2017) 65:853–861 Impact Factor: 2.905.
5 M. Vidyadhari, M. SUJATHA, P. Krupa, Pratibha Nallari and A. Venkateshwari. A family based triad study evaluating the role of MTHFR gene polymorphisms in spontaneous abortions. Gene Reports 10 (2018); Dec 5. doi.org/10.1016/j.genrep.2017.12.001. 2452-0144/ © 2017 Published by Elsevier Inc.pgs-116-122. Impact Factor: 2.138.
6M. Vidyadhari , M. SUJATHA, P. Krupa, Pratibha Nallari, A. Venkateshwari. Association Of Genetic Polymorphism Of Vascular Endothelial Growth Factor In The Etiology Of Recurrent Pregnancy Loss – A Triad Study. Journal of Assisted Reproduction and Genetics (In press) 2019.
7.Avvari Srilekha, Akka Jyothy, MADIREDDI SUJATHA, Pratibha Nallari, Ananthapur Venkateshwari (2019.) An Inherited Balanced Translocation between Chromosomes 4 and 6 in Recurrent Pregnancy Loss: A Case Report. Journal of family medicine – 1(3):10-14.
8.Srilekha, A., Sowmya, S., Jyothy, A., SUJATHA, M. and Venkateshwari, A. A rare variant of turners syndrome with mosaic 46, X idic X /45, X karyotype: A case report. Journal of Cell and Tissue Research, 19(2) 6713-6716 (2019).
9.Srilekha Avvari, SUJATHA MADIREDDI, Pratibha Nallari, Jyothy Akka, Venkateshwari Ananthapur. A case of Hematometra with a chromosomal abnormality: A case report. J of Genet Disord and Genet Med Vol.3 No.1 2019.
Conferences
1. A Venkateshwari, A.Srilekha, Ashrafunnisa Begum, M.SUJATHA, T.Sunitha, Pratibha Nallari and A Jyothy. “A rare variant of Turner syndrome with mosaic 46, X, dic X / 45, XO, karyotype.” TWOWS Fourth general Assembly and International conference: Women scientists in a changing world. June 27-30, 2010 Beijing, China.
2. A. Jyothy, Sharma V, Venkateshwari. A, Munshi A, SUJATHA M, Singh R, Thangaraj K. Xenoantiandrogens: Risk factiors for androgen receptor mutation in Hypospadias. 41st Annual meeting of Environmental Mutagen Society, October 23-27, 2010, Fort Worth, Texas, USA.
3. K. Rebekah Prasoona, Anjana Munshi, T. Sunitha, B. Srinadh, M. SUJATHA, T. M. Kumari, A. Venkateshwari, A. Jyothy. Association of MTHFD1 gene G1958A polymorphism as a maternal risk factor for neural tube defects. AP Science Congress – 2013, “Innovations in Science and technology for emerging knowledge society”, held at 14th – 16th November, 2013, University of Hyderabad, Hyderabad.
4. K. Sri Manjari, KSPS. Teja, M. SUJATHA, A. Jyothy, PratibhaNallari, A. Venkateshwari. Transferrin (rs3811647) gene polymorphism in Iron Deficiency Anemia. ISHG-2014. “Healthy Genes - Healthy Life”, International Conference on Human Genetics and 39th Annual Meeting of the Indian Society of Human Genetics. Ahmedabad Management Association, Ahmedabad, India, from 22nd - 25th Jan
American Society of Human Genetics
2025
American Society of Human Genetics Annual Meeting
2025
Seminar on Clinical Genomics in Every Day Medical Practice,by Board of Genetic Counselling
2025
Sixth Annual National Conference of the Society for Indian Academy of Medical Genetics &Indo-US symposium on Genetic Neuromuscular disorders
2025
CME-All about Bone Marrow Transplant for Paediatricians
2025
25th Silver Jubilee Annual Convention TWIN Cities Branch of IAP
2025