| Genetic evidence for recent population mixture in India P Moorjani, K Thangaraj, N Patterson, M Lipson, PR Loh, P Govindaraj, ... The American Journal of Human Genetics 93 (3), 422-438, 2013 | 342 | 2013 |
| Genome-wide analysis correlates Ayurveda Prakriti P Govindaraj, S Nizamuddin, A Sharath, V Jyothi, H Rotti, R Raval, ... Scientific reports 5 (1), 15786, 2015 | 148 | 2015 |
| Mitochondrial disorders: challenges in diagnosis & treatment NA Khan, P Govindaraj, AK Meena, K Thangaraj Indian Journal of Medical Research 141 (1), 13-26, 2015 | 115 | 2015 |
| Determinants of prakriti, the human constitution types of Indian traditional medicine and its correlation with contemporary science H Rotti, R Raval, S Anchan, R Bellampalli, S Bhale, R Bharadwaj, ... Journal of Ayurveda and integrative medicine 5 (3), 167, 2014 | 87 | 2014 |
| RAF1 mutations in childhood-onset dilated cardiomyopathy PS Dhandapany, MA Razzaque, U Muthusami, S Kunnoth, JJ Edwards, ... Nature genetics 46 (6), 635-639, 2014 | 83 | 2014 |
| Indian siddis: African descendants with Indian admixture AM Shah, R Tamang, P Moorjani, DS Rani, P Govindaraj, G Kulkarni, ... The American Journal of Human Genetics 89 (1), 154-161, 2011 | 80 | 2011 |
| DNA methylation analysis of phenotype specific stratified Indian population H Rotti, S Mallya, SP Kabekkodu, S Chakrabarty, S Bhale, R Bharadwaj, ... Journal of translational medicine 13, 1-12, 2015 | 64 | 2015 |
| Mitochondrial dysfunction and genetic heterogeneity in chronic periodontitis P Govindaraj, NA Khan, P Gopalakrishna, RV Chandra, A Vanniarajan, ... Mitochondrion 11 (3), 504-512, 2011 | 62 | 2011 |
| Origin and spread of human mitochondrial DNA haplogroup U7 H Sahakyan, B Hooshiar Kashani, R Tamang, A Kushniarevich, A Francis, ... Scientific reports 7 (1), 46044, 2017 | 48 | 2017 |
| Mitochondrial DNA variations associated with hypertrophic cardiomyopathy P Govindaraj, NA Khan, B Rani, DS Rani, P Selvaraj, V Jyothi, A Bahl, ... Mitochondrion 16, 65-72, 2014 | 38 | 2014 |
| Contribution of muscle biopsy and genetics to the diagnosis of chronic progressive external opthalmoplegia of mitochondrial origin C Sundaram, AK Meena, MS Uppin, P Govindaraj, A Vanniarajan, ... Journal of Clinical Neuroscience 18 (4), 535-538, 2011 | 34 | 2011 |
| Mitochondrial DNA haplogroup ‘R’is associated with Noonan syndrome of south India DS Rani, PS Dhandapany, P Nallari, P Govindaraj, L Singh, K Thangaraj Mitochondrion 10 (2), 166-173, 2010 | 33 | 2010 |
| Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome S Chakrabarty, P Govindaraj, BP Sankaran, M Nagappa, SP Kabekkodu, ... Journal of neurology 268, 2192-2207, 2021 | 32 | 2021 |
| Mitochondrial leukoencephalopathies: a border zone between acquired and inherited white matter disorders in children? PS Bindu, K Sonam, S Chiplunkar, P Govindaraj, M Nagappa, ... Multiple sclerosis and related disorders 20, 84-92, 2018 | 31 | 2018 |
| Mitochondrial DNA variations in ova and blastocyst: implications in assisted reproduction MB Shamsi, P Govindaraj, L Chawla, N Malhotra, N Singh, S Mittal, ... Mitochondrion, 2013 | 30 | 2013 |
| Reconstructing the demographic history of the Himalayan and adjoining populations R Tamang, G Chaubey, A Nandan, P Govindaraj, VK Singh, N Rai, ... Human genetics 137, 129-139, 2018 | 29 | 2018 |
| Unravelling the distinct strains of Tharu ancestry G Chaubey, M Singh, F Crivellaro, R Tamang, A Nandan, K Singh, ... European Journal of Human Genetics 22 (12), 1404-1412, 2014 | 29 | 2014 |
| Huppke-Brendel syndrome in a seven months old boy with a novel 2-bp deletion in SLC33A1 S Chiplunkar, PS Bindu, M Nagappa, C Bineesh, P Govindaraj, ... Metabolic brain disease 31, 1195-1198, 2016 | 28 | 2016 |
| Magnetic resonance imaging correlates of genetically characterized patients with mitochondrial disorders: a study from south India PS Bindu, H Arvinda, AB Taly, C Govindaraju, K Sonam, S Chiplunkar, ... Mitochondrion 25, 6-16, 2015 | 27 | 2015 |
| Leber's hereditary optic neuropathy–specific mutation m. 11778G> A exists on diverse mitochondrial haplogroups in India NA Khan, P Govindaraj, N Soumittra, S Sharma, S Srilekha, S Ambika, ... Investigative ophthalmology & visual science 58 (10), 3923-3930, 2017 | 26 | 2017 |
Kumarasamy ThangarajCentre for Cellular and Molecular Biology在 ccmb.res.in 的电子邮件经过验证
