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Membership type: full

Sujatha Madireddi

Country of origin: India Currently in: India, Secunderabad General field of specialization: Medical and Health Sciences incl Neurosciences
Academic Background

Degrees

1990 Doctorate Medical and Health Sciences incl Neurosciences
1990 Master Medical and Health Sciences incl Neurosciences
Research and Profession

Current Research Activities

Medical and Health Sciences incl Neurosciences

1.Genetic and molecular assessment of polycystic ovarian disease in South Indian population. 2. Genetic and Molecular studies in Primary Ovarian Insufficiency 3. Chromosomal abormalities in Infertlity Principal Co- Investigator of the following DBT projects PG Diploma Programme in Medical Biotechnology on Genetic Counselling with special emphasis on Pre-natal and Post –natal Diagnosis (Project Subcordinator) A Multicentric effort towards understanding a High Resolution Genetic Architecture of Congenital Non-syndromic Deafness in India


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



Current profession

Current professional activities type: 
Research
Teaching
Other
 Clinical diagnosis of genetic disorders, Genetic Counseling., Maintenance of genetic registers, Interpretation of Karyograms , DNA analysis,NGSand inborn errors of metabolism. Teaching and Research.

Workshop and Conference Attended

2015 Washington USA American Society of Human Genetics Annual Meeting
December 2018 Hyderabad, Telangana State,INDIA Seminar on Clinical Genomics in Every Day Medical Practice,by Board of Genetic Counselling
September 2019 Hyderabad, Telangana State, INDIA Sixth Annual National Conference of the Society for Indian Academy of Medical Genetics &Indo-US symposium on Genetic Neuromuscular disorders
November 2019 KIMS Hospitals,Dept. of Bone Marrow transplantation,Hyderabad,Telangana State,INDIA CME-All about Bone Marrow Transplant for Paediatricians
December 2019 Hyderabad, Telangana State,INDIA 25th Silver Jubilee Annual Convention TWIN Cities Branch of IAP

Affiliations

Indian Society of Human Genetics
Indian Academy of Paediatrics
Environmental Mutagen Society of India
Society of Biological Chemists of India

Presentation given

2015
Screening for Mutations and Variants in FSHR gene in Women with Pemature Ovarian Failureon Clini ilure in a South
Washington DC USA
Event: American Society of Human Genetics
Prizes, Grants and Awards

Other Awards

Sep 2018
Principal Co- Investigator of the DBT projects
1) PG Diploma Programme in Medical Biotechnology on Genetic Counselling with special emphasis on Pre-natal and Post –natal Diagnosis (Project Subcordinator) 2) A Multicentric effort towards understanding a High Resolution Genetic Architecture of Congenital Non-syndromic Deafness in India

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