עקוב אחר
Periyasamy Govindaraj
Periyasamy Govindaraj
Assistant Professor
כתובת אימייל מאומתת בדומיין nimhans.ac.in
כותרת
צוטט על ידי
צוטט על ידי
שנה
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
3522013
Genome-wide analysis correlates Ayurveda Prakriti
P Govindaraj, S Nizamuddin, A Sharath, V Jyothi, H Rotti, R Raval, ...
Scientific reports 5 (1), 15786, 2015
1652015
Mitochondrial disorders: challenges in diagnosis & treatment
NA Khan, P Govindaraj, AK Meena, K Thangaraj
Indian Journal of Medical Research 141 (1), 13-26, 2015
1212015
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
932014
RAF1 mutations in childhood-onset dilated cardiomyopathy
PS Dhandapany, MA Razzaque, U Muthusami, S Kunnoth, JJ Edwards, ...
Nature genetics 46 (6), 635-639, 2014
892014
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
842011
Mitochondrial dysfunction and genetic heterogeneity in chronic periodontitis
P Govindaraj, NA Khan, P Gopalakrishna, RV Chandra, A Vanniarajan, ...
Mitochondrion 11 (3), 504-512, 2011
692011
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
662015
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
482017
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
402014
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
352021
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
352011
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
332018
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
332010
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
322016
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
302018
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
302013
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
292014
Mitochondrial oxidative phosphorylation disorders in children: phenotypic, genotypic and biochemical correlations in 85 patients from South India
K Sonam, PS Bindu, MMS Bharath, P Govindaraj, N Gayathri, HR Arvinda, ...
Mitochondrion 32, 42-49, 2017
282017
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
272017
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מאמרים 1–20