| Confirmation of TTC8 as a disease gene for nonsyndromic autosomal recessive retinitis pigmentosa (RP51) S Goyal, M Jäger, PN Robinson, V Vanita Clinical Genetics 89 (4), 454-460, 2016 | 38 | 2016 |
| APOC3 genetic variation, serum triglycerides, and risk of coronary artery disease in Asian Indians, Europeans, and other ethnic groups. Lipids Health Dis 20 (1), 113, 2021 | 28* | 2021 |
| Genetics of diabetes S Goyal, J Rani, MA Bhat, V Vanita World journal of diabetes 14 (6), 656, 2023 | 19 | 2023 |
| A novel mutation in the PRPF31 in a North Indian adRP family with incomplete penetrance S Bhatia, S Goyal, IR Singh, D Singh, V Vanita Documenta Ophthalmologica 137, 103-119, 2018 | 19 | 2018 |
| Association of TNF-α gene alterations (c.-238G> A, c.-308G> A, c.-857C> T, c.-863C> A) with primary glaucoma in north Indian cohort S Passan, S Goyal, MA Bhat, D Singh, V Vanita Gene 709, 25-35, 2019 | 17 | 2019 |
| A Bidirectional Mendelian Randomization Study to evaluate the causal role of reduced blood vitamin D levels with type 2 diabetes risk in South Asians and Europeans CA Bejar, S Goyal, S Afzal, M Mangino, A Zhou, PJ van der Most, Y Bao, ... Nutrition journal 20, 1-11, 2021 | 14 | 2021 |
| Genetic and non-genetic determinants of cardiovascular disease in South Asians S Goyal, DK Sanghera Current diabetes reviews 17 (9), 63-73, 2021 | 4 | 2021 |
| Association of endothelial nitric oxide synthase gene polymorphisms with coronary artery disease in north Indian Punjabi population MA Bhat, J Singh, S Goyal Biochemical Genetics 60 (6), 2120-2136, 2022 | 2 | 2022 |
| Novel mutation in MKKS/BBS6 linked with arRP and polydactyly in a family of North Indian origin S Goyal, IR Singh, V Vanita Clinical & Experimental Ophthalmology 48 (3), 343-355, 2020 | 2 | 2020 |
| Mutation screening in autosomal dominant congenital cataract families from North India S Goyal, R Singh, JR Singh, V Vanita Molecular Genetics and Genomics 298 (6), 1279-1288, 2023 | 1 | 2023 |
| Molecular diagnosis of autosomal dominant congenital cataract in two families from North India reveals a novel and a known variant in GJA8 and GJA3 V Vanita, S Goyal, S Tibrewal, S Ganesh Frontiers in Pediatrics 10, 1003909, 2022 | 1 | 2022 |
| A missense mutation in TTC8/BBS8 affecting mRNA splicing in patients with non-syndromic retinitis pigmentosa S Goyal, V Vanita Molecular Genetics and Genomics 297 (5), 1439-1449, 2022 | 1 | 2022 |
| The Rise of Type 2 Diabetes in Children and Adolescents: An Emerging Pandemic S Goyal, V Vanita Diabetes/Metabolism Research and Reviews 41 (1), e70029, 2025 | | 2025 |
| Novel and known variants in GJA3 and LIM2 in congenital cataract families from North India S Goyal, R Singh, JR Singh, V Vanita BMC genomics 25 (1), 31, 2024 | | 2024 |
| A nonsense mutation in C8orf37 linked with retinitis pigmentosa, early macular degeneration, cataract, and myopia in an arRP family from North India S Goyal, K Singh, A Uppal, V Vanita BMC ophthalmology 23 (1), 210, 2023 | | 2023 |
| WJD S Goyal, J Rani, MA Bhat, V Vanita | | 2023 |
| Molecular diagnosis of autosomal dominant and autosomal recessive congenital cataract families from North India S Goyal, R Singh, JR Singh, V Vanita | | 2022 |
| Association of ApoCIII common variants with risk of coronary artery disease: A Mendelian randomization study S Goyal, Y Tanigawa, W Zhang, C Jin-Fang, M Almeida, X Sim, M Lerner, ... Atherosclerosis 331, e10-e11, 2021 | | 2021 |
| Multiethnic Study of Genetics of Dyslipidemia: No Evidence of Cardioprotective Role of Rare Variants in APOCIII S Goyal, C Bejar, WH Zhang, JF Chai, M Almeida, XL Sim, J Chainakul, ... Obesity 28 (2), 126, 2020 | | 2020 |
| Multiethnic study of genetics of dyslipidemia: No evidence of cardio-protective role of rare variants in the Apo CIII in non-European populations DK Sanghera, S Goyal, C Bejar GENETIC EPIDEMIOLOGY 44 (5), 514-515, 2020 | | 2020 |