| 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 | 328 | 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 | 132 | 2015 |
| Mitochondrial disorders: challenges in diagnosis & treatment NA Khan, P Govindaraj, AK Meena, K Thangaraj The Indian journal of medical research 141 (1), 13, 2015 | 108 | 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 | 80 | 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 | 77 | 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 | 72 | 2011 |
| Comparison of relative efficiency of genomic SSR and EST-SSR markers in estimating genetic diversity in sugarcane S Parthiban, P Govindaraj, S Senthilkumar 3 Biotech 8, 1-12, 2018 | 63 | 2018 |
| 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 | 59 | 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 | 54 | 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 | 40 | 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 | 36 | 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 |
| Collection, Characterization and Phenotypic Diversity of Saccharum spontaneum L. from Arid and Semi Arid Zones of Northwestern India P Govindaraj, VA Amalraj, K Mohanraj, NV Nair Sugar Tech 16, 36-43, 2014 | 31 | 2014 |
| 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 | 31 | 2010 |
| 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 |
| 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 | 28 | 2014 |
| 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 | 27 | 2018 |
| 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 |
| 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 | 26 | 2016 |
Kumarasamy ThangarajCentre for Cellular and Molecular Biology在 ccmb.res.in 的电子邮件经过验证
