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Awards

September 2018 Principal Co- Investigator of the DBT projects
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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

American Society of Human Genetics
2025
icon-pin-location Washington DC USA

American Society of Human Genetics Annual Meeting
2025
icon-pin-location Washington USA
Seminar on Clinical Genomics in Every Day Medical Practice,by Board of Genetic Counselling
2025
icon-pin-location Hyderabad, Telangana State,INDIA
Sixth Annual National Conference of the Society for Indian Academy of Medical Genetics &Indo-US symposium on Genetic Neuromuscular disorders
2025
icon-pin-location Hyderabad, Telangana State, INDIA
CME-All about Bone Marrow Transplant for Paediatricians
2025
icon-pin-location KIMS Hospitals,Dept. of Bone Marrow transplantation,Hyderabad,Telangana State,INDIA
25th Silver Jubilee Annual Convention TWIN Cities Branch of IAP
2025
icon-pin-location Hyderabad, Telangana State,INDIA