| A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome CE Sadowski, S Lovric, S Ashraf, WL Pabst, HY Gee, S Kohl, ... Journal of the American society of nephrology 26 (6), 1279-1289, 2015 | 652 | 2015 |
| Whole-exome sequencing identifies causative mutations in families with congenital anomalies of the kidney and urinary tract AT Van Der Ven, DM Connaughton, H Ityel, N Mann, M Nakayama, ... Journal of the American Society of Nephrology 29 (9), 2348-2361, 2018 | 189 | 2018 |
| Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment S Ashraf, H Kudo, J Rao, A Kikuchi, E Widmeier, JA Lawson, W Tan, ... Nature communications 9 (1), 1960, 2018 | 121 | 2018 |
| Exome sequencing discerns syndromes in patients from consanguineous families with congenital anomalies of the kidneys and urinary tract A Vivante, DY Hwang, S Kohl, J Chen, S Shril, J Schulz, A Van Der Ven, ... Journal of the American Society of Nephrology 28 (1), 69-75, 2017 | 102 | 2017 |
| Mutations of the transcriptional corepressor ZMYM2 cause syndromic urinary tract malformations DM Connaughton, R Dai, DJ Owen, J Marquez, N Mann, ... The American Journal of Human Genetics 107 (4), 727-742, 2020 | 29 | 2020 |
| A mutation in POLR3E impairs antiviral immune response and RNA polymerase III A Ramanathan, M Weintraub, N Orlovetskie, R Serruya, D Mani, O Marcu, ... Proceedings of the National Academy of Sciences 117 (36), 22113-22121, 2020 | 21 | 2020 |
| WT1 and NPHS2 gene mutation analysis and clinical management of steroid-resistant nephrotic syndrome ASK Ramanathan, M Vijayan, S Rajagopal, P Rajendiran, P Senguttuvan Molecular and cellular biochemistry 426, 177-181, 2017 | 21 | 2017 |
| Association of HLA‐DR/DQ alleles and haplotypes with nephrotic syndrome ASK Ramanathan, P Senguttuvan, R Chinniah, M Vijayan, ... Nephrology 21 (9), 745-752, 2016 | 21 | 2016 |
| Coordination of transcription and processing of tRNA N Jarrous, D Mani, A Ramanathan The FEBS Journal 289 (13), 3630-3641, 2022 | 19 | 2022 |
| Phenotype expansion of heterozygous FOXC1 pathogenic variants toward involvement of congenital anomalies of the kidneys and urinary tract (CAKUT) CHW Wu, N Mann, M Nakayama, DM Connaughton, R Dai, ... Genetics in Medicine 22 (10), 1673-1681, 2020 | 19 | 2020 |
| Hsp70 Is an Independent Stress Marker Among Frequent Users of Mobile Phones K Balakrishnan, V Murali, C Rathika, T Manikandan, RP Malini, ... Journal of Environmental Pathology, Toxicology and Oncology 33 (4), 2014 | 11 | 2014 |
| A homozygous missense variant in VWA2, encoding an interactor of the Fraser-complex, in a patient with vesicoureteral reflux AT van der Ven, B Kobbe, S Kohl, S Shril, HM Pogoda, T Imhof, H Ityel, ... Plos one 13 (1), e0191224, 2018 | 9 | 2018 |
| Wilms’ tumour 1 gene mutations in south Indian children with steroid-resistant nephrotic syndrome AS Kumar, R Srilakshmi, SMK Karthickeyan, K Balakrishnan, R Padmaraj, ... Indian Journal of Medical Research 144 (2), 276-280, 2016 | 8 | 2016 |
| Budding adult hypertensives with modifiable risk factors:“Catch them young” ASK Ramanathan, P Senguttuvan, V Prakash, A Vengadesan, ... Journal of Family and Community Medicine 23 (1), 38-42, 2016 | 8 | 2016 |
| Copy number variation analysis facilitates identification of genetic causation in patients with congenital anomalies of the kidney and urinary tract CHW Wu, TY Lim, C Wang, S Seltzsam, B Zheng, L Schierbaum, ... European Urology Open Science 44, 106-112, 2022 | 7 | 2022 |
| Effect of angiotensin converting enzyme gene I/D polymorphism in South Indian children with nephrotic syndrome ASK Ramanathan, B Karuppiah, M Vijayan, K Raju, D Mani, R Chinniah, ... Journal of Biomedical Research 33 (3), 201, 2019 | 1 | 2019 |
| Comment on" Budding adult hypertensives with modifiable risk factors: Catch them young" Reply ASK Ramanathan, P Senguttuvan, V Prakash, A Vengadesan, ... JOURNAL OF FAMILY AND COMMUNITY MEDICINE 24 (1), 56-56, 2017 | | 2017 |
| Identification of functional single nucleotide polymorphism of multidrug resistance gene-1 among nephrotic syndrome children in south India’ VP GANESAN A, MINI JACOB S , ARVIND SELVIN KUMAR R , PADMARAJ R , ANANDAN B ... asian journal of pharmaceutical and clinical research 10 (2), 418-422, 2016 | | 2016 |
| WT1 Mutation in Steroid Resistant Nephrotic Syndrome-Frasier syndrome ASK Ramanathan, P Senguttuvan, S Rajagopal PEDIATRIC NEPHROLOGY 28 (8), 1462-1463, 2013 | | 2013 |
| A fatal case of nocardiosis in a child with systemic lupus rythematosus PR Kalpana, AS Kumar, S Mathivanan, P Senguttuvan Pediatric Infectious Disease 2 (2), 109-111, 2010 | | 2010 |
