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Institute Of Genetics &
Hospital For Genetic Diseases

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Institute Of Genetics &
Hospital For Genetic Diseases

  1. Inapurapu SP, Pullakhandam R, Bodiga S, Yaduvanshi PS, Bodiga VL. Physicochemical studies of sunflower oil based vitamin D nanoemulsions. Journal of Dispersion Science and Technology. 2021 Dec 11:1-1. 
  1. Bodiga VL, Vemuri PK, Kudle MR, Bodiga S. Ellagic Acid from Terminalia arjuna Fruits Protects Against Chromium and Cobalt Toxicity in Primary Human Lymphocytes. Biological Trace Element Research. 2022 Jun;200(6):2698-708. 
  1. Bodiga VL, Vemuri PK, Kudle MR, Bodiga S. Zinc ionophores isolated from Terminalia bellirica fruit rind extract protect against cardiomyocyte hypoxia/reoxygenation injury. Bioorganic & Medicinal Chemistry. 2021 Sep 15;46:116394. 
  1. SD A, Pasumarthi D, Pasha A, Doneti R, Botlagunta M, Pawar SC. Identification of differentially expressed genes in cervical cancer patients by comparative transcriptome analysis. BioMed research international. 2021 Mar 20;2021. 
  1. Pasha A, Kumbhakar DV, Doneti R, Kumar K, Dharmapuri G, Poleboyina PK, SK H, Basavaraju P, Pasumarthi D, SD A, Soujanya P. Inhibition of inducible nitric oxide synthase (iNOS) by andrographolide and in vitro evaluation of its antiproliferative and proapoptotic effects on cervical cancer. Oxidative Medicine and Cellular Longevity. 2021 Mar 16;2021. 
  1. Boddakayala N, Bodiga S, Bodiga VL, Tummala PK, Vemuru S, Setti R, Manne AA, Veeravilli S, Vemuri PK. Conformational Epitope Prediction of Birch Betv 1 and Hazel Cor A1 Towards B-Cells. Journal of Pharmaceutical Research International. 2021:146-59. 
  1. Sanikommu A, Vaddi SA, Yeddula V, Manikyala LS, Kommineni CK, Sanikommu LP, Talla SR, Vemuri PK. Study on Molecular Basis of Cancer Induced Angiogenesis. Int. J. Life Sci. 11 102-106 2021, Pharma Res (ISSN: 2250-0480) 
  1. Bodiga VL, Kudle MR, Vemuri PK, Bodiga S. Crocin inhibits urea-induced amyloid formation by bovine β-lactoglobulin. New Journal of Chemistry. 2021;45(5):2589-96. 
  1. Velagapudi K, Jeevigunta NL, Bodiga VL. Zinc dyshomeostasis in azoxymethane-induced colonic precancerous and cancerous lesions in Fischer rats. Metallomics. 2021 Feb;13(2):mfaa009. 
  1. Bodiga VL, Bathula J, Kudle MR, Vemuri PK, Bodiga S. Andrographolide suppresses cisplatin-induced endothelial hyperpermeability through activation of PI3K/Akt and eNOS–derived nitric oxide. Bioorganic & Medicinal Chemistry. 2020 Dec 1;28(23):115809. 
  1. SP Inapurapu, A Ibrahim, SR Kona, SC Pawar, S Bodiga, VL Bodiga* Development and characterization of <omega>-3 fatty acid nanoemulsions with improved physicochemical stability and bioaccessibility Colloids Surf. A Physicochem. Eng. Asp. IF:3.990 
  1. Bodiga VL, Vemuri PK, Nimmagadda G, Bodiga S. Zinc-dependent changes in oxidative and endoplasmic reticulum stress during cardiomyocyte hypoxia/reoxygenation. Biological chemistry. 2020 Oct 1;401(11):1257-71. 
  1. Maddhuri S, Vemuri PK, Tatineni J, Puppala J, Bodiga VL. Association of Calcineurin B (PPP3R1) Functional Gene Polymorphism in South Indian Children with Idiopathic Mental Retardation. Research Journal of Pharmacy and Technology. 2020 Feb 15;13(2):599-603. 
  1. Vemuri PK, Chowdary Lavu S, Dronavalli N, Nunna V, Nannapaneni S, Bodiga VL. Assessment of clinical-pharmacological activities of drugs and biopharmaceuticals. Drug Invention Today. 2020 Jan 1;13(1). 
  1. Pallem PV, Bodiga S, Bodiga VL. Dietary phytate lowers K-ras mutational frequency, decreases DNA-adduct and hydroxyl radical formation in azoxymethane-induced colon cancer. Iranian journal of basic medical sciences. 2020 Jan;23(1):20. 
  1. Veeravilli S, Nimmagadda G, Dondapati K, Naredla K, Bodiga VL. Cross-reactivity studies of Ligustrum robustum with Corylus avellana pollinosis for clinical significance. Drug Invention Today. 2020 Jan 1;13(1). 
  1. BK Panigrahi, S Das, FP Dumpala, R Vagicharla, SK Kunderu and VL Bodiga* Galectin-3 In Modulating Inflammation in Adipocytes and Macrophages Int. J. Adv. Res. ISSN 2320-5407 8(11) 285-290 2020 
  1. Thokala S, Bodiga VL, Kudle MR, Bodiga S. Comparative response of cardiomyocyte ZIPs and ZnTs to extracellular zinc and TPEN. Biological trace element research. 2019 Dec;192(2):297-307. 
  1. Kadali S, Naushad SM, Radha Rama Devi A, Bodiga VL. Biochemical, machine learning and molecular approaches for the differential diagnosis of Mucopolysaccharidoses. Molecular and Cellular Biochemistry. 2019 Aug;458(1):27-37. 
  1. Vemuri PK, Kollipara N, Nasika S, Kanneganti A, Bodiga VL, Veeravalli S. Touchdown PCR combined with semi degenerate primers for rapid amplification of HOXD9 loci in humans. Journal of Pharmaceutical Sciences and Research. 2019 May 1;11(5):1834-7. 
  1. PK Vemuri, A Kunta, R Challagulla, EA Jose, VL Bodiga Designing A Vaccine for Cancer: A Look into Dendritic Cell Cancer Vaccine Asian J Pharm Clin Res Online ISSN: 2455-3891 Print ISSN: 0974-2441 12 (6) 27-31 2019. 
  1. PVSP Pallem, S Bodiga, VL Bodiga. Dietary Phytate Lowers Iron Status, Suppresses Aberrant Crypt Foci and Inhibits Progression to Adenoma in Azoxymethane-Induced Colon Cancer Int. J Pharm. Biol. Sci IF:0.88 ISSN:2321-3272. 8 43-55 2018 
  1. PK Vemuri, S Madala , VL Bodiga, S Veeravalli, NC Kurra. Effect of Arabica and Canephora Coffee Bean Extracts Towards Modification of Red Blood Cell Surface Antigens Int. Res. J. Pharm. e-ISSN: 2230- 8407 9 (5) 91-95 2018 
  1. Prasanna JS, Aishwarya MD, Karunakar P, Rekharani K, Vijayalakshmi B, Jharna P. Evaluation of collagenase-3 matrix metalloproteinase-13 gene-associated polymorphisms 11A/12A and− 77A/G and its associated alleles with and without periodontitis. Journal of Indian Society of Periodontology. 2018 Nov;22(6):474. 
  1. Bodiga S, Vemuri PK, Bodiga VL. Low Ctr1p, due to lack of Sco1p results in lowered cisplatin uptake and mediates insensitivity of rho0 yeast to cisplatin. Journal of Inorganic Biochemistry. 2018 Oct 1;187:14-24. 
  1. Deepa Switha Vishnubhotla, Shouni Niveditha Tenali , Mini Fernandez, Sujatha Madireddi.   ‘Evaluation of Prevalence of PCOS and Associated Depression’ Nutrition, and Family History: A Questionnaire‐based   Assessment, 2022 Indian Journal of Endocrinology and Metabolism | Published by Wolters Kluwer – Medknow 
  1. . Chaitany Sravanthi chillara, Aaji Pasha Shek, Madan Mohan Anuradha ,Sujatha Madireddi, ‘Status of Estrogen Receptor Beta Gene Polymorphisms rs1256049 and rs4986938 in a cohort of South Indian  women with Primary ovarian  insufৎiciency’; Int. J. Res. Pharm. Sci., 2021, 12(1), 357-365 
  1. Deepa Switha Vishnubotla, Aaji Pasha Shek, Sujatha Madireddi⁎; Pooled genetic analysis identifies variants that confer enhanced susceptibility to PCOS in Indian ethnicity.GENE 752 (2020) 144760 
  1. 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. 
  1. 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). 
  1. 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. 
  1. M. 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 . 2019 
  1. Tella, Sunitha, et al. “Epidermolysis bullosa: A report of three cases with novel heterozygous deletions in PLEC and homozygous non sense mutations in COL7A1 genes.” Indian Journal of Dermatology 67.1 (2022): 45. 
  1. Deepika, M. L. N., et al. “A Rare Case of Dysmorphism with Duplication in Chromosome 22.” Indian Journal of Clinical Biochemistry 37.4 (2022): 504-506. Ganasyam SR, Namilakonda M, Madireddy S, Ananthapur V, Buragadda S, Tella S. Study of KIAA0319, DYXIC1 and DCDC2 Gene Polymorphisms in Children with Dyslexia in Indian Population. 
  1. Sehrish I, Sunitha T, Srilekha A, Gupta A, Nallari P, Venkateshwari A. A Novel Familial Case Report of Genetic Syndrome Mimicking Congenital TORCH infections; Pseudo-TORCH Syndrome 2. Journal of Reproduction & Infertility. 2022 Mar 17;23(2):135-8 
  1. Naga DM, Bhuwalka R, Sunitha T, Nallari P, Ananthapur V. Peroxisomal acyl CoA oxidase deficiency: a rare inherited disorder of nervous system. European Journal of Medical Case Reports. 2021;5(9):256-9. 
  1. Tella S, Sultana S, Ananthapur V, Rao N, Akka J. Maternal TCN1 (rs526934) G> A Gene Polymorphism and its Association with Congenital Heart Disease (CHD). Journal of Womens Health and Development. 2020;3(4):432-6. K. Rebekah, Prasoona, et al. “Interaction between Maternal and Paternal SHMT1 C1420T Predisposes to Neural Tube Defects in the Fetus:  Evidence from Case–Control and Family‐Based Trial. 
  1. K. Rebekah, P., Tella, S., Buragadda, S., Tiruvatturu, M. K., & Akka, J. (2017). Interaction between Maternal and Paternal SHMT1 C1420T Predisposes to Neural Tube Defects in the Fetus: Evidence from Case–Control and Family‐Based Triad Approaches. Birth defects research, 109(13), 1020-1029.iad Approaches.” Birth defects research 109.13 (2017): 1020-1029 
  1. Srilekha, Avvari, M. L. N. Deepika, Tella Sunitha, and Ananthapur Venkateshwari. “A novel de novo autosomal translocation 46, XX, t (5; 8) in a female with primary amenorrhea.” European Journal of Obstetrics and Gynecology and Reproductive Biology 221 (2018): 201-203. 
  1. Tella, Sunitha, et al. “Joubert Syndrome with Homozygous Duplication in Exon 7 of SMN2 Gene and c. 746G> A (p. R249H) Variant of Uncertain Significance in TRPV4 Gene: A Case Report.” Journal of Pediatrics, Perinatology and Child Health 4.4 (2020): 126-129 
  1. K. Rebekah, Prasoona, et al. “Interaction between Maternal and Paternal SHMT1 C1420T Predisposes to Neural Tube Defects in the Fetus: Evidence from Case–Control and Family‐Based Triad Approaches.” Birth defects research 109.13 (2017): 1020-1029  
  1. Sunitha, T., Prasoona, K. R., Kumari, T. M., Srinadh, B., Deepika, M. L. N., Aruna, R., & Jyothy, A. (2017). Risk factors for congenital anomalies in high risk pregnant women: a large study from South India. Egyptian Journal of Medical Human Genetics, 18(1), 79-85. 
  1. Prasoona, Kattekola R., Tella Sunitha, Buragadda Srinadh, Madireddy LN Deepika, Tiruvatturu M. Kumari, and Akka Jyothy. “Paternal transmission of MTHFD 1 G1958A variant predisposes to neural tube defects in the offspring.” Developmental Medicine & Child Neurology 58, no. 6 (2016): 625-631 
  1. G.Shilpa Reddy, M.Sujatha, A.Jyothy. A Rare case Short-Chain Acyl- CoA Dehydrogenase Deficiency The Apparent Rarity of the Disorder Results in under Diagnosis. Indian Journal of Clinical Biochemistry ISSN 0970-1915 Ind J Clin Biochem DOI 10.1007/s12291-011-0139. 
  1. Association Of Estrogen Receptor- α Gene & Metallothionein-1 Gene Polymorphisms In Type 2 Diabetic Women Of Indian Population..Dr .Shilpa.Reddy.Ganasyam, , Talluri Bhaskar Rao, Y.S.R. Murthy, A. Jyothy, and M.Sujatha. Ind J Clin Biochem 2011 .Indian J Clin Biochem. 2012 January; 27(1): 69–73. Published online 2012 January 6. doi: 10.1007/s12291-011-0179-2 PMCID: PMC3286578. 
  1. Shilpa Reddy, Sujatha Madireddy and Pooja Nair Association of Genetic Markers Contributing to Dyslexia Susceptibility in Indian Population. Journal of Neurology and      Neuroscience. Received date: April 26, 2016; Accepted date: May 25, 2016; Published date: May 30, 2016. 
  1. ShilpaReddy, Sujatha Madireddy and Pooja Nair Evaluation of the single Nucleotide polymorphism’s in KIAA Gene contributing to Dyslexia susceptibility in south Indian population, International Journal of Humanities and Social Sciences (IJHSS) Vol 5.Issue 3 April-May 2016,75-96 
  1. Association of ABCC8 and KCNJ11 gene variants with type 1 diabetes in south Indians .Reddy et al. Egyptian Journal of Medical Human Genetics (2021) 22:27 
  1. Reddy GS, Sultana S, Madireddy S, Nallari P, Ananthapur V. Wiedemann-Steiner Syndrome with Variants of Uncertain Significance in Spermatogenesis Associated 5 and Lysine Methyltransferase 2A Genes. Focus On Medical Sciences Journal. 2019;5(4). 
  1. Association of FOXP3 rs3761548 polymorphism and its reduced expression with unexplained recurrent spontaneous abortions: A South Indian study.  Kethura Dirsipam, Deepika Ponnala, Dhatri Madduru, Rajeswari Bonu, Parveen Jahan; American Journal of Reproductive Immunology. 2021 
  1. Study of Anti-Apoptotic mechanism of Ruthenium(II) Polypyridyl Complexes via RT-PCR and DNA binding. Satyanarayana S, Ravi Kumar Vuradia , Navaneetha Nambigaria, Pushpanjali Pendyala , Srinivas Gopu , Kotha Laxma Reddy , G. Deepika , M. Vinoda Rani., Applied Organometallic Chemistry. 23 December 2019 
  1. Srilekha Avvari, Neelu Mishra, Sujatha Madireddy, Venkateshwari Ananthapur. Inherited Robertsonian translocation (13;14) in a child with Down’s syndrome., Journal of Biochemical and Clinical Genetics 2020;3(2):113–117. https://doi.org/10.24911/JBCGenetics/183-1592993055. 
  1. Deepika, M., Tella, S., Avvari, S. Nallari, N and Ananthapur,V. A Rare Case of Dysmorphism with Duplication in Chromosome 22. Ind J Clin Biochem (2021). https://doi.org/10.1007/s12291-020-00945-y  
  1. Banala Ashok Reddy, Shehnaz Sultana, Pratibha Nallari, Sujatha Madireddi , Venkateshwari Ananthapur. A Case Report of Family with Congenital Non-Syndromic Hearing Loss (NSHL) with Variants of Uncertain Significance (VUS) in GATA3 and COLA43 Genes . Annals of Review and Research2021; 6(2): 555681. 
  1. Sunitha Tella, Shehnaz Sultana, Pratibha Nallari, Sujatha Madireddy, Venkateshwari Ananthapur. Joubert Syndrome with Homozygous Duplication in Exon 7 of SMN2 Gene and c.746G>A (p.R249H) Variant of Uncertain Significance in TRPV4 Gene: A Case Report. J Pediatr Perinatol Child Health 2020; 4 (4): 126-129. DOI: 10.26502/jppch.74050052. 
  1.  Sunitha Tella, Shehnaz Sultana, Venkateshwari Ananthapur, Nageshwar Rao K, Jyothy Akka, Satyanarayana U. Maternal TCN1 (rs526934) G>A Gene Polymorphism and its Association with Congenital Heart Disease (CHD) J Women’s Health Dev 2020; 3 (4): 432-436. 
  1. Shehnaz Sultana, Pratibha Nallari, Venkateshwari Ananthapur. Role of Genetic Factors in the Causation of Non-Syndromic Hearing Loss (NSHL) in Indian Population. Arch Clin Biomed Res 2020; 4 (6): 775-793. DOI: 10.26502/acbr.50170143  
  1. Amar chand Bayal, Shehnaz Sultana, Pratibha Nallari and Venkateshwari Ananthapur. Genetic Polymorphisms of Vascular Endothelial Growth Factor (VEGF) -2549 I/D and +405G/C in the susceptibility to Gastric Cancer. Arch Clin Gastroenterol 7(1): 001-006. DOI: https://dx.doi.org/10.17352/2455-2283.000088  
  1. Shilpa Reddy; Sailaja Maddhuri; Pratiba Nallari; Venkateshwari Ananthapur; Srinivas Kalyani; Murali Krishna; Nirmala Cherkuri; Sireesha Patibandala. Association of ABCC8 and KCNJ11 gene variants with Type 1 Diabetes in South Indians. Egyptian Journal of Medical Human Genetics. an Genetics (2021) 22:27 https://doi.org/10.1186/s43042-021-00149-w 
  1. Shaile Sudha Bandla, Avvari Srilekha, Poojita Karchalkar, Sowmya Gayatri, Ananthapur Venkateshwari. A Case Report an a Novel Pink1 Gene Mutation In A Female with  Neurodegenerative  Disorder.  EMJ Neurol.2022;DOI/10.33590/emjneurol/2100206.https:/doi.org/10.33590/emjn eurol/21-00206. With  
  1. Iram Sehrish, Tella Sunitha, Avvari Srilekha, Aayushi Gupta, Pratibha Nallari, Ananthapur Venkateshwari. A Novel Familial Case Report of Genetic Syndrome Mimicking Congenital TORCH infections; Pseudo-TORCH Syndrome Journal of Reproduction and Infertility 2022: 23(2): 135-38 https://doi.org/ (IF: 1.63)  
  1. Tella S, Sultana S, Madireddy S, Nallari P, Ananthapur V. Epidermolysis bullosa: A report of three cases with novel heterozygous deletions in PLEC and homozygous non sense mutations in COL7A1 genes. Indian J Dermatol 2022 Jan-Feb;67(1):45-49. (IF:1.757). 
  1. Shehnaz Sultana, Samuel Abraham, Joshi Davala, Venkateshwari Ananthapur, Penagaluru Pardhananda Reddy. Covid 19 Infection and its adverse effects on Multiorgan. Arch Intern Med Res. 2022; 5(1): 56-70  
  1. Avvari Srilekha, Madireddy Sujatha, Akka Jyothy and Venkateshwari Ananthapur. Developmental delay with dysmorphism in a child with ring chromosome 6. European Journal of Biomedical and Pharmaceutical Sciences 2022 ; 9(8) :352-254. 
  1. The insertion/deletion (i/d) polymorphism in the angiotensin converting enzyme gene and recurrent pregnancy loss. Srinivas Rao P1., Apurva Shrivastava2., Srilekha Avvari2., Deepika G and Deepika MLN; International Journal of Recent Scientific Research Vol. 9, Issue, 5(D), pp. 26769-26772, May, 2018. 
  1. Deepika Madireddy Lakshmi Naga, Rashmi Bhuwalka, Tella Sunitha, Pratibha Nallari, Venkateshwari Ananthapur. Peroxisomal acyl CoA oxidase deficiency: a rare inherited disorder of nervous system EJMCR. 2021; 5(9): 256-259. 
  1. Deepika, M., Tella, S., Avvari, S. et al. A Rare Case of Dysmorphism with Duplication in Chromosome 22. Ind J Clin Biochem (2021). https://doi.org/10.1007/s12291-020-00945-y. 
  1. Dr. P. Srinivas Rao, Gandla Radhika, Deepak Raghava, K. Kavya Priya, Sowmya Bairavi, Dr.Deepika M. L. N. Prevalence And Patterns Of Dyslipidemia Among Type 2 Diabetic Patients In The City Of Hyderabad: An Observational Study. EJPMR. 2020; 7(3): 300-303. 
  1. Joddie Cresswell, Deepika MLN. Is screening of thyroid, TORCH, APL, ACL, cytogenetic and MTHFR analysis is of mandate in women with bad obstetric history: An observational study from Hyderabad. ANNQUEST. 2018; 7(5): 23-28. 
  1. Tella Sunitha, Deepika MLN, K Nageshwar Rao, Akka Jyothy, U Satyanarayana. Do Abnormal Levels Of Serum Folate, Vitaminb12, Homocysteine In Maternal Serum Serve As A Predictive Marker For Congenital Heart efects? International Journal Of Scientific Research. 2018;7(2):41-43. 
  1. Shrivastava A, Deepika MLN (2018) Journey of Women: Puberty to Post-menopause. Gynecol Women’s Health Res 1(1): dx.doi.org/10.16966/gwhr.107. 
  1. Avvari Srilekha, MLN Deepika, Tella Sunitha, Ananthapur Venkateshwari. A novel de novo autosomal translocation 46, XX, t (5; 8) in a female with primary amenorrhea. European Journal of Obstetrics and Gynecology and Reproductive Biology 2018; 221:201-203  
  1. SailajaMaddhuri ,SrinivasBandaru , ChaitanyaBhukya , VinodCingeetham , Amaresh Rao Malempati , M.L.N. Deepikaa, PratibhaNallari , Hema Prasad Mundluru .”Association of CnB 5I/5D promoter gene polymorphism and serum calcineurin levels in early onset of coronary artery disease of south Indian cohort”. Gene 632 (2017) 1–6 Published by Elsevier B.V. (ImapctFcator -2.9) 
  1. Shilpa Reddy ,SailajaMaddhuri , PratibhaNallari , VenkateshwariAnanthapur, Srinivas Kalyani , Murali Krishna , Nirmala Cherkuri and SireeshaPatibandala “Association of ABCC8 and KCNJ11 gene variants with type 1 diabetes in south Indians” Egyptian Journal of Medical Human Genetics (2021) 22:27 Springeropen 
  1. SailajaMaddhuri , Suresh Gudala , ChandanaLakkaraju , Amaresh Rao Malempati ,N. PratibhaNallari , Hema Prasad Mundluru “Association of Mef2a gene polymorphisms in early onset of coronary artery disease of south Indian cohort “.Meta Gene 15 (2018) 16–22 PublishedbyElsevierB.V. 
  1. SailajaMaddhuri , PriyankaPallapolu , SrinivasBandaru , Gudlla Suresh , Amaresh Rao Malempati , Akka Jyothy1 , Hema Prasad Mundluru Analysis of Myeloperoxidase Functional Gene -463G >A & -129 G >A Polymorphisms with Early Onset of Coronary Artery Disease in South Indian Population Folia Cardiologica 2016 DOI: 10.5603/FC.2016.0047 2016 Via Medica ISSN 2353–7752. 
  1. SailajaMaddhuri, Praveen Kumar Vemuri, JahnaviTatineni, JharnaPuppala, Vijaya Lakshmi Bodiga “Association of Calcineurin B (PPP3R1) Functional Gene Polymorphism in South Indian Children with Idiopathic Mental Retardation”.Research Journal of Pharmacy and TechnologyVolume13Issue2Pages599-603PublisherA & V Publications (Imapct Factor-1.2) 
  1. PriyankaPallapolu ,Chaitanya Kumar Bhukya , SailajaMaddhuri  , SunithaTella , JyothyAkka , Pardhanandana Reddy Penagaluru  , PratibhaNallari and Hema Prasad Mundluru Pon1 Gene Polymorphism and Serum Paraoxonase Levels In Women Occupationally Exposed to Organophosphate Pesticides In South India. Int. J. Adv. Res. 4(9), 539-546 ISSN: 2320-5407. 
  1. ChandanaLakkaraju,VidyullathaPeddireddy,SrinivasBandaru,SureshGudala,SailajaMaddhuri,PallapoluPriyanka., DeepikaMLN and Hema Prasad Mundluru “Xrcc1 arg399gln and arg194trp polymorphisms in welder occupationally exposed to welding fumes dwelling in industrial area of Hyderabad,telangana “ International Journal of Recent Scientific Research Vol. 9, Issue, 3(F), pp. 25041-25044, March, 2018. 
  1. SailajaMaddhuri, M.Amareshrao, Priyanka.P, AkkaJyothy&MunduluruHemaPrasad Role of Transcription factor Mef2A gene in Coronary Artery Disease. International Journal of MedicineandPharmaceuticalsciencesvol.3,79-88(2013). 

Articles 

  • Shehnaz sultana, Pratibha Nallari and A. Venkateshwari. Recurrent Pregnancy Loss (RPL): An overview. Journal of Women’s Health and Development (2020), 3:259-272. 
  • Ganesh Kumar Rauta, Sairam Manchineela, Moumita Chakrabartia,,Chaitanya Kumar Bhukya, Raju Naini, A. Venkateshwari, V.D. Reddy,Jolly Janette Mendonza, Y. Suresha, Pratibha Nallari,∗∗, Manika Pal Bhadra.  Imine stilbene analog ameliorate isoproterenol-induced cardiac hypertrophy and hydrogen peroxide-induced apoptosis Free Radical Biology Medicine 153 (2020) 80–88. 
  • Shehnaz Sultana,Venkateshwari  Ananthapur COVID-19 and its impact on neurological manifestations and mental health: the present scenario. Neurological Sciences, https://doi.org/10.1007/s10072-020-04695-w 31 Aug,2020 

Books chapters  

  1. Bodiga VL, Bodiga S. Ascorbic acid is a potential inhibitor of collagenases—In Silico and In Vitro biological studies. InIn Silico Drug Design 2019 Jan 1 (pp. 649-677). Academic Press. 
  1. K. Sri Manjari, Srilekha Avvari, Imran Ali Khan, and DKV Prasad, MicroRNAs and Cancer Signaling Pathways. D. Prasad, P. Santosh Sushma (eds.), Role of  MicroRNAs in Cancers, pg.no 13-36. The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2022.  https://doi.org/10.1007/978-981-16-9186-7_1. 
  1. Srilekha Avvari, DKV Prasad, and Imran Ali Khan. Role of MicroRNAs in Cell Growth Proliferation and Tumorigenesis. D. Prasad, P. Santosh Sushma (eds.), Role of MicroRNAs in Cancers, pg.no 37- 73.. The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2022. https://doi.org/10.1007/978-981-16-9186-7_1 
  1. Srilekha Avvari, M. Rishitha, K. Sri Manjari, Subhadra Poornima, and Imran Ali Khan. Oxidative Stress Modulation with MicroRNAs in Cancers. Role of MicroRNAs in Cancers, pg.no 73-92. The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2022.  https://doi.org/10.1007/978-981-16-9186-7_1 
  1. Advances in Science, Technology, Commerce and Management.  Chapter 16 : Ligninolytic peroxidases in Bioremediation and Biofuel production ;B.Y.Kavitha, Shruti Joshi, C. Swetha and Dr .G. Deepika 
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