Items where Subject is "Genetics"

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Number of items at this level: 20.

Article

UNSPECIFIED (2021) A RARE CAUSE OF AORTIC STENOSIS IN A SIBLING - MORQUIO SYNDROME - A CASE REPORT. Journal of Cardiovascular Disease Research, 12 (1). ISSN 09762833

Alshatwi, Ali A. and Hasan, Tarique N. and Syed, Naveed A. and Shafi, Gowhat and Grace, B. Leena (2012) Identification of Functional SNPs in BARD1 Gene and In Silico Analysis of Damaging SNPs: Based on Data Procured from dbSNP Database. PLoS ONE, 7 (10). e43939. ISSN 1932-6203

Anjum, Asra and Senthil Kumar, B. (2025) The Influence of AMHR II Polymorphisms on Infertility: A Comprehensive Study of A10G/rs11170555 and G4952A/rs3741664 in South Indian Women. Research Journal of Biotechnology, 20 (10). 29 - 34. ISSN 09736263; 22784535

Arbind Kumar Choudhary, R. (57283846200) and Manivannan, E. (6603237852) and Rajeswari, P. (57520390200) and Sivasankari, V. (55485997800) and Arul Kothai Chandrashekar, R. (57284725400) and Ravi, Indla (57226675265) (2021) Determination and evaluation of ellagic acid in terminalia chebula fruit extract by RP-HPLC.

Dhanalakshmi, Y. and Feula, Jothi Marie and Pal, Gopal Krushna (2021) Association of Matrix Metalloproteinase 9 Polymorphism with Pulmonary Functions in South Indian Population -A cross sectional study. Indian Journal of Physiology and Pharmacology, 65. pp. 69-73. ISSN 0019-5499

Divahar, R. (56352569700) and Aravind Raj, P. S. (55006023900) and Siva, M. (58107264700) and Xavier, S. Ispara (57462847900) (2021) Durability Performance Of Self-Healing Bacterial Impregnated Concrete With M-Sand For Sustainable Environment.

Ganesh, Irisappan and Karthiga, Ilangovan and Murugan, Manoranjani and Rangarajalu, Kumar and Ballambattu, Vishnu Bhat and Ravikumar, Sambandam (2025) CRISPR/Cas-Based Prenatal Screening for Aneuploidy: Challenges and Opportunities for Early Diagnosis. Medicina (Lithuania), 61 (4). ISSN 1010660X; 16489144

Govindhasamy, Rekha and Govindhasamy, Paramesh and Vanga, Rajitha and Burute, Pushpa (2021) Role of TP53 Gene Polymorphism in Male Infertility. International Journal of Infertility & Fetal Medicine, 12 (2). pp. 44-48. ISSN 2229-3817

Gurugubelli, Krishna Rao and Ballambattu, Vishnu Bhat and Bobby, Zacheriah (2020) Global DNA Methylation in Cord Blood and Neurodevelopmental Outcome at 18 Months of Age among Intrauterine Growth Restricted and Appropriate for Gestational Age Infants. Journal of Tropical Pediatrics, 67 (1). ISSN 0142-6338

Ignasimuthu, Arockiamary and Hait, Anamitra and null, null and Santhi, P. and Periasamy, Panneerselvam and Choudhary, R. Arbind Kumar (2025) PRECISION FRONTIERS IN FAMILIAL HYPERCHOLESTEROLEMIA: INTEGRATING PHARMACOGENOMICS AND AI FOR NEXT-GEN CARE � A SYSTEMATIC REVIEW. Opera Medica et Physiologica, 12 (3). 28 - 48. ISSN 25002287; 25002295

Maheswari, Uma and Ninawe, Swapnil S. and Pokkuluri, Kiran Sree and Pandit, Shraddha V. and Hariram, Venkatesan and Shankar, R Shiva (2024) Scaling AI With Quantum Network Models for Back Pain Genetic Architecture. Springer. pp. 307-320. ISSN 2327-0411

Murugan, Durga and Babu, Senthil Kumar and Kalaimamani, Ezhil Vendhan and Raju, Kamaraj (2024) Corneal microstructural changes of precise CHST6 gene mutation: a case series. Egyptian Journal of Medical Human Genetics, 25 (1). ISSN 2090-2441

Murugan, Manoranjani and Musib, Sourav and Vetriselvan, Yogesh and Karthiga, Ilangovan and Soccalingam, Artchoudane and Samuel, Melissa Shaelyn and Ganesh, Irisappan and Ravikumar, Sambandam (2025) Genetic variants of leptin receptor gene (rs1137101) and obesity risk in prakriti individuals and its pathogenicity prediction using in silico approaches. Egyptian Journal of Medical Human Genetics, 26 (1). ISSN 11108630; 20902441

Murugan, Manoranjani and Sadasivam, Ilakkia Priya and Manoharan, Aarthi and Jayakumar, Swetha and Vetriselvan, Yogesh and Samuel, Melissa Shaelyn and Ravikumar, Sambandam (2025) Association between PITX2 polymorphism and androgenetic alopecia in the Indian population. Indian Journal of Dermatology, Venereology and Leprology, 91 (2). 158 - 162. ISSN 03786323; 09733922

Nelaturi, Prabhudas and Ravikumar, Sambandam and P Kademani, Sangeetha (2024) Long Non-Coding RNAs as Emerging Role in Prognosis of Alcohol Related Liver Disease. International Research Journal of Multidisciplinary Scope, 05 (02). pp. 345-453. ISSN 2582631X

Ramesh, V. and Lakshmiprabha, S. and Ponnudhali, D. and Jeyachandran, G. and Sridevi, M. (2024) Leucine repeat polymorphism in CNDP1 gene (D18S880) and Type 2 Diabetic kidney disease in South Indians. Research Journal of Biotechnology, 19 (12). pp. 85-92. ISSN 22784535

Suresh, Padmanaban S. and Venkatesh, Thejaswini and Rajan, Thangarasu (2012) Single nucleotide polymorphisms in genes that are common targets of luteotropin and luteolysin in primate corpus luteum: Computational exploration. Gene, 511 (2). pp. 353-357. ISSN 03781119

Swetha, Jayakumar and Sakthignanavel, Arulmozhi and Manoharan, Aarthi and Rangarajalu, Jayakumar and Arunagiri, Priyadharshini and Govindasamy, Chandramohan and Ravikumar, Sambandam (2025) A 250-kb Microdeletion Identified in Chromosome 16 Is Associated With Non-Syndromic Sensorineural Hearing Loss in a South Indian Consanguineous Family. Journal of Audiology and Otology, 29 (1). 31 - 37. ISSN 23841621; 23841710

Vasudevan and Nur Afiqah and Mohd Nazil and Wan Aliaa, WS and Liyana Najwa, IM and Mohd Hazmi and Siew Mooi and Abdul Hanif Khan, YK and Hamidon and Pannerselvam and Suganthi and Narenkumar (2024) Genetic Susceptibility Variants of Vascular Dementia among Asians: A Systematic Review and Meta-Analysis. Dementia and Geriatric Cognitive Disorders, 53 (4). pp. 200-216. ISSN 1420-8008

Velmurugan, Saranya and Ganesan, Karthikeyan and Rajendran, Ramya and Gowtham Kumar, Subbaraj Kumar (2025) The X-ray repair cross-completing gene 1 (XRCC1) polymorphisms and lung cancer incidence – a confirmatory umbrella review of observational evidence. European Journal of Clinical and Experimental Medicine, 23 (1). 245 - 256. ISSN 25442406; 25441361

This list was generated on Thu Dec 11 21:03:55 2025 IST.