| Genetic landscape of the people of India: a canvas for disease gene exploration Indian Genome Variation Consortium Journal of genetics 87 (1), 3-20, 2008 | 325 | 2008 |
| EGLN1 involvement in high-altitude adaptation revealed through genetic analysis of extreme constitution types defined in Ayurveda S Aggarwal, S Negi, P Jha, PK Singh, T Stobdan, MAQ Pasha, S Ghosh, ... Proceedings of the National Academy of Sciences 107 (44), 18961-18966, 2010 | 197 | 2010 |
| Role of cholesterol in APP metabolism and its significance in Alzheimer’s disease pathogenesis M Maulik, D Westaway, JH Jhamandas, S Kar Molecular neurobiology 47, 37-63, 2013 | 140 | 2013 |
| Primary role of CYP1B1 in Indian juvenile-onset POAG patients M Acharya, S Mookherjee, A Bhattacharjee, AK Bandyopadhyay, ... Mol Vis 12 (1), 399-404, 2006 | 130 | 2006 |
| Genomic insights into ayurvedic and western approaches to personalized medicine B Prasher, G Gibson, M Mukerji Journal of genetics 95, 209-228, 2016 | 71 | 2016 |
| Altered levels and distribution of amyloid precursor protein and its processing enzymes in Niemann‐Pick type C1‐deficient mouse brains A Kodam, M Maulik, K Peake, A Amritraj, KS Vetrivel, G Thinakaran, ... Glia 58 (11), 1267-1281, 2010 | 66 | 2010 |
| Molecular diagnosis of Wilson disease using prevalent mutations and informative single-nucleotide polymorphism markers A Gupta, M Maulik, P Nasipuri, I Chattopadhyay, SK Das, ... Clinical chemistry 53 (9), 1601-1608, 2007 | 62 | 2007 |
| Mutant human APP exacerbates pathology in a mouse model of NPC and its reversal by a β-cyclodextrin M Maulik, B Ghoshal, J Kim, Y Wang, J Yang, D Westaway, S Kar Human molecular genetics 21 (22), 4857-4875, 2012 | 41 | 2012 |
| APP overexpression in the absence of NPC1 exacerbates metabolism of amyloidogenic proteins of Alzheimer's disease M Maulik, K Peake, JY Chung, Y Wang, JE Vance, S Kar Human molecular genetics 24 (24), 7132-7150, 2015 | 34 | 2015 |
| A role for astrocyte‐derived amyloid β peptides in the degeneration of neurons in an animal model of temporal lobe epilepsy A Kodam, D Ourdev, M Maulik, J Hariharakrishnan, M Banerjee, Y Wang, ... Brain Pathology 29 (1), 28-44, 2019 | 30 | 2019 |
| Parkin polymorphisms: risk for Parkinson's disease in Indian population. A Biswas, M Maulik, SK Das, K Ray, J Ray Clinical genetics 72 (5), 484-486, 2007 | 27 | 2007 |
| Myocilin variants in Indian patients with open-angle glaucoma A Bhattacharjee, M Acharya, A Mukhopadhyay, S Mookherjee, ... Archives of Ophthalmology 125 (6), 823-829, 2007 | 27 | 2007 |
| Increased levels and activity of cathepsins B and D in kainate-induced toxicity M Banerjee, VA Sasse, Y Wang, M Maulik, S Kar Neuroscience 284, 360-373, 2015 | 22 | 2015 |
| Amyloid-β regulates gap junction protein connexin 43 trafficking in cultured primary astrocytes M Maulik, L Vasan, A Bose, SD Chowdhury, N Sengupta, JD Sarma Journal of Biological Chemistry 295 (44), 15097-15111, 2020 | 18 | 2020 |
| Loss of Cx43-mediated functional gap junction communication in meningeal fibroblasts following mouse hepatitis virus infection A Bose, R Basu, M Maulik, J Das Sarma Molecular Neurobiology 55, 6558-6571, 2018 | 18 | 2018 |
| Endosomal-lysosomal cholesterol sequestration by U18666A differentially regulates amyloid precursor protein (APP) metabolism in normal and APP-overexpressing cells J Chung, G Phukan, D Vergote, A Mohamed, M Maulik, M Stahn, ... Molecular and Cellular Biology 38 (11), e00529-17, 2018 | 15 | 2018 |
| Evaluation of genetic markers linked to hemophilia A locus: an Indian experience A Saha, S Mukherjee, M Maulik, GR Chandak, K Ray, ... Haematologica 92 (12), 1725-1726, 2007 | 13 | 2007 |
| Alterations in gene expression in mutant amyloid precursor protein transgenic mice lacking Niemann-Pick type C1 protein M Maulik, G Thinakaran, S Kar PloS one 8 (1), e54605, 2013 | 8 | 2013 |
| Haplotype-based genomic analysis reveals novel association of CNTNAP5 genic region with primary angle closure glaucoma S Chakraborty, A Sharma, A Sharma, R Sihota, S Bhattacharjee, ... Journal of Biosciences 46, 1-9, 2021 | 6 | 2021 |
| Indian Genome Variation C, Ray K (2007) Molecular diagnosis of Wilson disease using prevalent mutations and informative single-nucleotide polymorphism markers A Gupta, M Maulik, P Nasipuri, I Chattopadhyay, SK Das, ... Clin Chem 53 (9), 1601-1608, 0 | 6 | |
Satyabrata KarProfessor of University of AlbertaVerified email at ualberta.ca
