B. Lakkakula

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Role of renin-angiotensin-aldosterone system gene polymorphisms and hypertension-induced end-stage renal disease in autosomal dominant polycystic kidney disease.

Gnanasambandan Ramanathan, Ramprasad Elumalai, S. Periyasamy, 2014, Iranian journal of kidney diseases.

Insulin receptor gene polymorphisms modify the progression of kidney failure in diabetic nephropathy patients

Ramprasad Elumalai, S. Periyasamy, B. Lakkakula, 2017 .

Lack of association of EPHX1 genotypes and haplotypes with oral cancer in South Indians.

B. Lakkakula, Solomon F. D. Paul, L. Balaji, 2011, Genetic testing and molecular biomarkers.

SATB2 gene variants in non-syndromic cleft lip with or without cleft palate in Indian population.

B. Lakkakula, J. Murthy, V. B. Gurramkonda, 2015, Journal of oral biology and craniofacial research.

Sodium-glucose co-transporter 2 inhibitors (SGLT2i); as a preventive factor of kidney failure in patients with type 2 diabetes; a meta-analysis of randomized controlled trials

B. Lakkakula, H. Nasri, R. Valizadeh, 2021, Journal of Renal Injury Prevention.

Strive for kidney health for everyone during COVID-19; the possible theme for the world kidney day 2021

B. Lakkakula, B. Roshan, E. Mazaheri, 2020, Journal of Nephropharmacology.

Administration of metformin in type 2 diabetes mellitus patients with chronic kidney disease; facts and myths

B. Lakkakula, R. Valizadeh, Steven James Kellner, 2019 .

Renin gene rs1464816 polymorphism contributes to chronic kidney disease progression in ADPKD

Gnanasambandan Ramanathan, Ramprasad Elumalai, S. Periyasamy, 2016, Journal of Biomedical Science.

NOS3 tagSNPs does not modify the chronic kidney disease progression in autosomal dominant polycystic kidney disease

Gnanasambandan Ramanathan, S. Periyasamy, B. Lakkakula, 2014, Nephrology.

Angiotensinogen gene polymorphisms and progression of chronic kidney disease in ADPKD patients

Ramprasad Elumalai, B. Lakkakula, R. Gnanasambandan, 2016, Clinical and Experimental Nephrology.

Role of endothelial nitric oxide synthase VNTR (intron 4 a/b) polymorphism on the progression of renal disease in autosomal dominant polycystic kidney disease

Gnanasambandan Ramanathan, Ramprasad Elumalai, B. Lakkakula, 2014, Journal of renal injury prevention.

ECE1 gene variant shows tendency toward chronic kidney disease advancement among autosomal polycystic kidney disease patients

Gnanasambandan Ramanathan, Ramprasad Elumalai, S. Periyasamy, 2016 .

Retrospection of the effect of hydroxyurea treatment in patients with sickle cell disease

B. Lakkakula, H. Verma, Saikrishna Lakkakula, 2018 .

COVID-19 and the kidney; mechanisms of tubular injury by SARS-CoV-2

B. Lakkakula, H. Nasri, Z. Mojtahedi, 2020, Journal of Renal Injury Prevention.

Glomerulonephritis associated with SARS-CoV-2 infection

B. Lakkakula, B. Roshan, Banafsheh Yalameha, 2020, Journal of Nephropharmacology.

A novel polymorphism in codon 25 of the KRAS gene associated with gallbladder carcinoma patients of the eastern part of India.

B. Lakkakula, M. Kar, B. Sarkar, 2011, Genetic testing and molecular biomarkers.

Biomarkers of Oxidative Stress Tethered to Cardiovascular Diseases

B. Lakkakula, Mohammad Saffree Jeffree, Neha Merchant, 2022, Oxidative medicine and cellular longevity.

Functional PstI/RsaI polymorphisms in the CYP2E1 gene among south Indian populations.

B. Lakkakula, A. K. Munirajan, R. Pathapati, 2013, Asian Pacific journal of cancer prevention : APJCP.

Compound Heterozygosity of β-Thalassemia and the Sickle Cell Hemoglobin in Various Populations of Chhattisgarh State, India

B. Lakkakula, Aditya N Jha, H. Verma, 2018, Hemoglobin.

CBS c.844ins68 Polymorphism Frequencies in Control Populations: Implications on Nonsyndromic Cleft Lip with or without Cleft Palate

B. Lakkakula, R. Pathapati, J. Murthy, 2015, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

Cyclic Guanosine Monophosphate-Dependent Protein Kinase I Stimulators and Activators Are Therapeutic Alternatives for Sickle Cell Disease

B. Lakkakula, Mohankrishna Ghanta, Elango Panchanathan, 2017, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Parathyroid hormone abnormities in sickle cell anemia patients

B. Lakkakula, A. Neral, 2018 .

Understanding kidney injury in COVID-19; a pressing priority

B. Lakkakula, R. Tolouian, Elham Ahmadipour, 2020, Journal of Nephropharmacology.

Perspectives on the relationship of urolithiatic markers and primary hyperparathyroidism

B. Lakkakula, Mohankrishna Ghanta, M. Ghanta, 2020 .

EPHX1 gene polymorphisms among south Indian populations

B. Lakkakula, A. K. Munirajan, R. Pathapati, 2013, Molecular & Cellular Toxicology.

Association Between the M268T Polymorphism in the Angiotensinogen Gene and Essential Hypertension in a South Indian Population

B. Lakkakula, V. Rao, Satish Kumar, 2011, Biochemical Genetics.

Molecular basis of β-thalassemia in Karnataka, India.

K. Thangaraj, B. Lakkakula, B. Kulkarni, 2012, Genetic testing and molecular biomarkers.

Endothelial nitric oxide synthase VNTR (intron 4 a/b) polymorphism association with nonsyndromic oral clefts

B. Lakkakula, R. Pathapati, J. Murthy, 2013 .

Genetic association of ACE gene I/D polymorphism with the risk of diabetic kidney disease; a meta-analysis

B. Lakkakula, H. Verma, S. Pattnaik, 2019, Journal of Nephropathology.

Significant association of MTHFD1 1958G>A single nucleotide polymorphism with nonsyndromic cleft lip and palate in Indian population

B. Lakkakula, J. Murthy, V. B. Gurramkonda, 2014, Medicina oral, patologia oral y cirugia bucal.

Presence of atypical beta globin (HBB) gene cluster haplotypes in sickle cell anemia patients of India

B. Lakkakula, P. Patra, H. Verma, 2017, Revista Brasileira de Hematologia e Hemoterapia.

The HBG2 rs7482144 (C > T) Polymorphism is Linked to HbF Levels but not to the Severity of Sickle Cell Anemia

B. Lakkakula, S. Pattnaik, 2021, Journal of Pediatric Genetics.

Association between MTHFR 677C>T polymorphism and vascular complications in sickle cell disease: A meta-analysis.

B. Lakkakula, 2019, Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine.

Pain Management Issues as Part of the Comprehensive Care of Patients with Sickle Cell Disease

B. Lakkakula, H. Verma, Saikrishna Lakkakula, 2018, Pain management nursing : official journal of the American Society of Pain Management Nurses.

Attitudes and beliefs among high- and low-risk population groups towards β-thalassemia prevention: a cross-sectional descriptive study from India

B. Lakkakula, R. Singh, Swati Chawla, 2017, Journal of Community Genetics.

NAT2 genetic variations among South Indian populations

G. Chaubey, B. Lakkakula, A. K. Munirajan, 2014, Human Genome Variation.

HLA class II SNP interactions and the association with type 1 diabetes mellitus in Bengali speaking patients of Eastern India

B. Lakkakula, P. Raychaudhuri, S. Chowdhury, 2013, Journal of Biomedical Science.

World Kidney Day 2021 with the theme of living well with kidney disease; a review of current concepts

B. Lakkakula, P. Peymani, F. Ahmadizar, 2021, Journal of Preventive Epidemiology.

Apelin gene polymorphism influences apelin expression and obesity phenotypes in Chinese women.

S. Juo, B. Lakkakula, Y. Liao, 2011, The American journal of clinical nutrition.

Genetic variant in MTRR A66G, but not MTR A2756G, is associated with risk of non-syndromic cleft lip and palate in Indian population☆

B. Lakkakula, J. Murthy, V. B. Gurramkonda, 2015 .

The M235T polymorphism in the angiotensinogen gene is not a major risk factor for diabetic nephropathy; a meta-analysis

B. Lakkakula, H. Verma, S. Pattnaik, 2021, Journal of Preventive Epidemiology.

PPARG genotypes are not a major modifiers of chronic kidney disease progression among the diabetic nephropathy patients

Periyasamy, Ramprasad Elumalai, B. Lakkakula, 2018 .

Lack of association between IRF6 polymorphisms and nonsyndromic oral clefts in South Indian population

B. Lakkakula, J. Murthy, V. B. Gurramkonda, 2013 .

Interleukin-10 gene promoter variants and susceptibility to diabetic nephropathy; a meta-analysis

B. Lakkakula, S. Gautam, G. Mishra, 2020, Journal of Nephropathology.

Metformin induced acute kidney injury; a systematic review

B. Lakkakula, M. Momenzadeh, 2020, Journal of Nephropharmacology.

Lack of Association Between the IL-10 Gene Polymorphisms and Features of the Metabolic Syndrome

P. Tsai, S. Juo, B. Lakkakula, 2011, Journal of Investigative Medicine.

International Journal for Pharmaceutical Research Scholars (IJPRS)

B. Lakkakula, S. Chidambaram, Harivanzan Vijayakumar, 2014 .

Two promoter polymorphisms in TBX22 are associated with the risk of NSCLP in Indian women

B. Lakkakula, J. Murthy, S. Hussain, 2015, Clinical dysmorphology.

Maternal and infant MTHFR gene polymorphisms and non-syndromic oral cleft susceptibility: An updated meta-analysis

B. Lakkakula, G. Nagaraju, Priyank Shukla, 2020 .

Association between PPARG Pro 12 Ala polymorphism and diabetic nephropathy risk ; an updated meta-analysis of 27 studies

B. Lakkakula, Punita Gupta, H. Verma, 2018 .

Endothelin 1 gene is not a major modifier of chronic kidney disease advancement among the autosomal dominant polycystic kidney disease patients

Gnanasambandan Ramanathan, Ramprasad Elumalai, B. Lakkakula, 2015, Journal of nephropharmacology.

Influence of angiotensin converting enzyme (ACE) gene rs4362 polymorphism on the progression of kidney failure in patients with autosomal dominant polycystic kidney disease (ADPKD)

Santu Ghosh, Gnanasambandan Ramanathan, Ramprasad Elumalai, 2016, The Indian journal of medical research.

Potential of renin-angiotensin system inhibition to improve metabolic bone disorders

B. Lakkakula, M. Momenzadeh, M. Khosravian, 2020, Journal of Nephropharmacology.

Gene Frequencies of the Human GSTT1 (Null Allele) and GSTP1 (Ile105Val) Polymorphisms among South Indian Populations

B. Lakkakula, R. Pathapati, V. B. Gurramkonda, 2013 .

MTHFR C677T and A1298C polymorphisms and risk of nonsyndromic orofacial clefts in a south Indian population.

B. Lakkakula, J. Murthy, V. B. Gurramkonda, 2014, International journal of pediatric otorhinolaryngology.

Lack of association between IRF 6 polymorphisms and nonsyndromic oral clefts in South Indian population

B. Lakkakula, J. Murthy, V. B. Gurramkonda, 2013 .

IRF6 rs2235375 single nucleotide polymorphism is associated with isolated non-syndromic cleft palate but not with cleft lip with or without palate in South Indian population

B. Lakkakula, J. Murthy, V. B. Gurramkonda, 2017, Brazilian journal of otorhinolaryngology.

Relationship between reduced folate carrier gene polymorphism and non-syndromic cleft lip and palate in Indian population

B. Lakkakula, J. Murthy, V. B. Gurramkonda, 2015, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Renin gene rs1464816 polymorphism contributes to chronic kidney disease progression in ADPKD

Gnanasambandan Ramanathan, Ramprasad Elumalai, B. Lakkakula, 2016, Journal of Biomedical Science.

Evidence of the involvement of the polymorphisms near MSX1 gene in non-syndromic cleft lip with or without cleft palate.

B. Lakkakula, J. Murthy, V. B. Gurramkonda, 2015, International journal of pediatric otorhinolaryngology.