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| Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness C Zeitz, SG Jacobson, CP Hamel, K Bujakowska, M Neuillé, E Orhan, ... The American Journal of Human Genetics 92 (1), 67-75, 2013 | 147 | 2013 |
| Identification of African-specific admixture between modern and archaic humans JD Wall, A Ratan, E Stawiski, HL Kim, C Kim, R Gupta, K Suryamohan, ... The American Journal of Human Genetics 105 (6), 1254-1261, 2019 | 23 | 2019 |
| Next‐generation sequencing confirms the implication of SLC24A1 in autosomal‐recessive congenital stationary night blindness M Neuillé, S Malaichamy, M Vadalà, C Michiels, C Condroyer, ... Clinical genetics 89 (6), 690-699, 2016 | 22 | 2016 |
| Molecular profiling of complete congenital stationary night blindness: A pilot study on an Indian cohort S Malaichamy, P Sen, R Sachidanandam, T Arokiasamy, ME Lancelot, ... Molecular vision 20, 341, 2014 | 20 | 2014 |
| Prevalence of mutations in inherited retinal diseases: a comparison between the United States and India S Yohe, M Sivasankar, A Ghosh, A Ghosh, J Holle, S Murugan, R Gupta, ... Molecular Genetics & Genomic Medicine 8 (2), e1081, 2020 | 15 | 2020 |
| Retinoblastoma genetics screening and clinical management H Gupta, S Malaichamy, A Mallipatna, S Murugan, N Jeyabalan, ... BMC Medical Genomics 14, 1-9, 2021 | 13 | 2021 |
| Myoneuropathic presentation of limb girdle muscular dystrophy R8 with a novel TRIM32 mutation SV Chandrasekharan, S Sundaram, S Malaichamy, R Poyuran, SS Nair Neuromuscular Disorders 31 (9), 886-890, 2021 | 4 | 2021 |
| Retinoblastoma Mutational Screening in India: Opportunities and Challenges in Clinical Decisions and Genetic Counselling H Gupta, S Malaichamy, A Mallipatna, S Murugan, N Jeyabalan, ... | | 2021 |
| Überblick über die kongenitale stationäre Nachtblindheit mit überwiegend normalem Fundus C Zeitz, C Friedburg, MN Preising, B Lorenz Klinische Monatsblätter für Augenheilkunde 235 (03), 281-289, 2018 | | 2018 |
| Retinoblastoma and Next-Gen-Sequencing Era: Challenges and Opportunities at Clinics and Counseling in India G Kumaramanickavel, S Malaichamy, R Shetty, A Ghosh, S Seshagiri, ... Investigative Ophthalmology & Visual Science 58 (8), 854-854, 2017 | | 2017 |
| Novel mutations in SLC24A1 leading to congenital stationary night blindness (CSNB) M Neuille, S Malaichamy, M Vadala, R Sachidanandam, T Arokiasamy, ... Investigative Ophthalmology & Visual Science 57 (12), 658-658, 2016 | | 2016 |
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| NOVEL GENE DISCOVERIES M Neuillé, S Malaichamy, M Vadalà, C Michiels, C Condroyer, ... | | |
