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Tella Sunitha

Observed names: Sunitha T., Sunitha Tella, Sunitha, T., T Sunitha, T. Sunitha
OpenAlex ID: A5023878656
Seroprevalence and Influence of Torch Infections in High Risk Pregnant Women: A Large Study from South India
2014 · K. Rebekah Prasoona, B. Srinadh, et al. · The Journal of Obstetrics and Gynecology of India · 33
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Risk factors for congenital anomalies in high risk pregnant women: A large study from South India
2016 · Tella Sunitha, Kattekola Rebekah Prasoona, et al. · Egyptian Journal of Medical Human Genetics · 30
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Interleukin 10 gene promoter polymorphisms in women with early-onset pre-eclampsia
2014 · S Sowmya, K Sri Manjari, et al. · Clinical & Experimental Immunology · 26
Role of IL-10 -819(T/C) Promoter Polymorphism in Preeclampsia
2014 · Sabnavis Sowmya, Aruna Ramaiah, et al. · Inflammation · 19
A Robertsonian Translocation rob (14;15) (q10:q10) in a Patient with Recurrent Abortions: A Case Report.
2010 · Venkateshwari Ananthapur, Srilekha Avvari, et al. · Europe PMC (PubMed Central) · 16
Evaluation of Interleukin-10 (G-1082A) Promoter Polymorphism in Preeclampsia.
2013 · Sabnavis Sowmya, Aruna Ramaiah, et al. · Europe PMC (PubMed Central) · 15
LRP2 gene variants and their haplotypes strongly influence the risk of developing neural tube defects in the fetus: a family-triad study from South India
2018 · Rebekah Prasoona K., Sunitha T., et al. · Metabolic Brain Disease · 12
Interaction between Maternal and Paternal SHMT1 C1420T Predisposes to Neural Tube Defects in the Fetus: Evidence from Case–Control and Family‐Based Triad Approaches
2017 · Prasoona K. Rebekah, Sunitha Tella, et al. · Birth Defects Research · 12
Paternal transmission of MTHFD 1 G1958A variant predisposes to neural tube defects in the offspring
2015 · Kattekola R Prasoona, Tella Sunitha, et al. · Developmental Medicine & Child Neurology · 10
Clinical and behavioural profile of a rare variant of Klinefelter syndrome-48, XXXY
2010 · A. Venkateshwari, A. Srilekha, et al. · The Indian Journal of Pediatrics · 10
Maternal association and influence of DHFR 19 bp deletion variant predisposes foetus to anencephaly susceptibility: a family-based triad study
2018 · K. R. Prasoona, T. Sunitha, et al. · Biomarkers · 8
De novo chromosomal translocation t(3;5)(q13;q35) in an infertile man
2011 · A. Venkateshwari, A. Srilekha, et al. · Andrologia · 6
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Mosaic triple X syndrome in a female with primary amenorrhea
2012 · A Venkateshwari, A Srilekha, et al. · Indian journal of human genetics · 5
Epidermolysis Bullosa
2022 · Sunitha Tella, Shehnaz Sultana, et al. · Indian Journal of Dermatology · 4
Variants of DHFR, MTHFD1, and MTHFR Genes: Relation to CNS Malformations
2013 · Anjana Munshi, Prasoona Rebekah, et al. · The Journal of Obstetrics and Gynecology of India · 2
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Association between Maternal FUT2 204A>G (rs492602) Genetic Polymorphism and Congenital Heart Disease in the Indian Population: A Study in Maternal-fetal Dyads
2023 · Sunitha Tella, Sowmya Gayatri Chukkayapalli, et al. · Molecular and Cellular Biomedical Sciences · 1
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A Novel Familial Case Report of Genetic Syndrome Mimicking Congenital TORCH infections; Pseudo-TORCH Syndrome 2
2022 · Iram Sehrish, Tella Sunitha, et al. · Journal of Reproduction & Infertility · 1
A Rare Case of Dysmorphism with Duplication in Chromosome 22
2021 · MLN Deepika, Sunitha Tella, et al. · Indian Journal of Clinical Biochemistry · 1
Maternal TCN1 (rs526934) G>A Gene Polymorphism and its Association with Congenital Heart Disease (CHD)
2020 · Sunitha Tella, Shehnaz Sultana, et al. · Journal of Women s Health and Development · 1
A novel de novo autosomal translocation 46, XX, t (5; 8) in a female with primary amenorrhea
2017 · Avvari Srilekha, Deepika MLN, et al. · European Journal of Obstetrics & Gynecology and Reproductive Biology · 1
Interaction between Maternal and Paternal SHMT1 C1420T Predisposes to Neural Tube Defects in the Fetus: Evidence from Case-Control and Family-Based Triad Approaches
2017 · Prasoona K. Rebekah, Sunitha Tella, et al. · Birth Defects Research · 1
A rare occurrence of concordant neural tube defects in monozygotic twins of an epileptic woman
2012 · Akka Jyothy, Tella Sunitha, et al. · Neurology India · 1
A Rare Balanced Translocation between Chromosome 1 and 10 in a Female with a History of Recurrent Pregnancy Loss: A Case report
2026 · Venkateshwari Ananthapur, Shehnaz Sultana, et al. · Journal of Human Reproductive Sciences
Study of KIAA0319, DYXIC1 and DCDC2 Gene Polymorphisms in Children with Dyslexia in Indian Population
2022 · Shilpa Reddy Ganasyam, Manaswini Namilakonda, et al. · Basic and Clinical Neuroscience Journal
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Maternal Gene Polymorphisms of Vitamin B12 Metabolic Pathway and Their Association With Congenital Heart Diseases
2021 · Sunitha, T., Sowmya Gayatri, C., et al. · Zenodo (CERN European Organization for Nuclear Research)
Works count: 32
Citation count: 215
H-index: 10
I10-index: 10
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