| Androgen receptor CAG repeats length polymorphism and the risk of polycystic ovarian syndrome (PCOS) S Rajender, SJ Carlus, SK Bansal, MPS Negi, N Sadasivam, ... PLoS one 8 (10), e75709, 2013 | 39 | 2013 |
| Genotype-phenotype study of the middle Gangetic plain in India shows association of rs2470102 with skin pigmentation A Mishra, S Nizammuddin, CB Mallick, S Singh, S Prakash, NA Siddiqui, ... Journal of Investigative Dermatology 137 (3), 670-677, 2017 | 31 | 2017 |
| MTHFR 677C> T polymorphism and the risk of breast cancer: evidence from an original study and pooled data for 28031 cases and 31880 controls S Pooja, J Carlus, D Sekhar, A Francis, N Gupta, R Konwar, S Kumar, ... PLoS One 10 (3), e0120654, 2015 | 31 | 2015 |
| Digenic Inheritance of LAMA4 and MYH7 Mutations in Patient with Infantile Dilated Cardiomyopathy AM Abdallah, SJ Carlus, AH Al-Mazroea, M Alluqmani, Y Almohammadi, ... Medicina 55 (1), 17, 2019 | 29 | 2019 |
| Mitochondrial DNA variations associated with recurrent pregnancy loss among Indian women A Vanniarajan, P Govindaraj, SJ Carlus, M Aruna, P Aruna, A Kumar, ... Mitochondrion 11 (3), 450-456, 2011 | 27 | 2011 |
| Is MTHFR 677 C>T Polymorphism Clinically Important in Polycystic Ovarian Syndrome (PCOS)? A Case-Control Study, Meta-Analysis and Trial Sequential Analysis SJ Carlus, S Sarkar, SK Bansal, V Singh, K Singh, RK Jha, N Sadasivam, ... PLoS One 11 (3), e0151510, 2016 | 26 | 2016 |
| Targeted next-generation sequencing of 406 genes identified genetic defects underlying congenital heart disease in Down syndrome patients KM Alharbi, AH Al-Mazroea, AM Abdallah, Y Almohammadi, SJ Carlus, ... Pediatric Cardiology 39, 1676-1680, 2018 | 24 | 2018 |
| CAG repeat variation in the mtDNA polymerase γ is not associated with oligoasthenozoospermia DS Rani, SJ Carlus, J Poongothai, A Jyothi, K Pavani, NJ Gupta, ... International journal of andrology 32 (6), 647-655, 2009 | 24 | 2009 |
| The MTHFR C677T polymorphism is associated with mitral valve rheumatic heart disease SJ Carlus, AM Abdallah, LV Bhaskar, MM Morsy, GS Al-Harbi, ... European Review for Medical and Pharmacological Sciences 20 (1), 109, 2016 | 17 | 2016 |
| SRD5A2 gene polymorphisms and the risk of benign prostatic hyperplasia but not prostate cancer VK Choubey, SN Sankhwar, SJ Carlus, AN Singh, D Dalela, K Thangaraj, ... Asian Pacific Journal of Cancer Prevention 16 (3), 1033-1036, 2015 | 14 | 2015 |
| The peopling of Lakshadweep archipelago MS Mustak, N Rai, MR Naveen, S Prakash, SJ Carlus, N Pasupuleti, ... Scientific Reports 9 (1), 6968, 2019 | 13 | 2019 |
| Transforming Growth Factor-β1 gene polymorphism and osteoporosis in postmenopausal egyptian women IM Taha, AMA Allah, MAF Hamoudah, SJ Carlus Cellular and Molecular Biology 63 (11), 53-57, 2017 | 12 | 2017 |
| A novel homozygous TPM1 mutation in familial pediatric hypertrophic cardiomyopathy and in silico screening of potential targeting drugs. SJ Carlus, IS Almuzaini, M Karthikeyan, L Loganathan, GS Al-Harbi, ... European Review for Medical and Pharmacological Sciences, 2020 | 10 | 2020 |
| Next-generation sequencing identifies a homozygous mutation in ACADVL associated with pediatric familial dilated cardiomyopathy SJ Carlus, IS Almuzaini, M Karthikeyan, L Loganathan, GS Al-Harbi, ... European Review for Medical and Pharmacological Sciences 23 (4), 1710-1721, 2019 | 5 | 2019 |
| An in silico analysis of the impact of POLE mutations on cladribine docking. L Loganathan, A Al-Haidose, AG Kumar, LB Sujatha, FH Carlus, A Alharbi, ... European Review for Medical & Pharmacological Sciences 26 (20), 2022 | 4 | 2022 |
| In Silico Analysis of Drug Repurposing Strategy for the Identification of Potential NS3 Helicase Inhibitors Against Zika Virus KM Lakshmanan Loganathan, Justin Carlus Current Chinese Science 1 (3), 373 - 385, 2021 | 3 | 2021 |
| The Polymorphism at the microRNA-155 binding site in the AGTR1 gene is not significantly associated with rheumatic heart disease in Saudi Arabia Population SJ Carlus, FH Carlus, MK Al-Harbi, AH Al-Mazroea, KM Al-Harbi, ... Microrna 9 (4), 266-270, 2020 | 2 | 2020 |
| Interaction between MTHFR Polymorphisms and Maternal Age Increases the Risk of Congenital Heart Defects in Down Syndrome SJ Carlus, AM Abdallah, AH Al-Mazroea, MK Al-Harbi, KM Al-Harbi Pakistan Journal of Zoology 51 (3), 865, 2019 | 2 | 2019 |
| Gene database for the development of genetic testing for hypertrophic cardiomyopathy JC Silas, KM Al Harbi BMC Genomics 15 (Suppl 2), P65, 2014 | 2 | 2014 |
| Renin and CYP P450 gene variations significantly associated with essential hypertension: A prospective pharmacogenomics study L Loganathan, SJ Carlus, K Muthusamy Gene Reports 37, 102023, 2024 | | 2024 |
