| Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion E Klopocki, S Lohan, SC Doelken, S Stricker, CW Ockeloen, ... Journal of medical genetics 49 (2), 119-125, 2012 | 105 | 2012 |
| Analysis of the WISP3 gene in Indian families with progressive pseudorheumatoid dysplasia A Dalal, SL Bhavani G, PP Togarrati, T Bierhals, MR Nandineni, S Danda, ... American Journal of Medical Genetics Part A 158 (11), 2820-2828, 2012 | 80 | 2012 |
| Congenital pseudarthrosis of the tibia: Management and complications H Shah, M Rousset, F Canavese Indian journal of orthopaedics 46 (6), 616-626, 2012 | 70 | 2012 |
| Management of severe crouch gait in children and adolescents with cerebral palsy B Joseph, K Reddy, RA Varghese, H Shah, SN Doddabasappa Journal of Pediatric Orthopaedics 30 (8), 832-839, 2010 | 62 | 2010 |
| Perthes disease: evaluation and management H Shah Orthopedic Clinics 45 (1), 87-97, 2014 | 59 | 2014 |
| Congenital pseudarthrosis of the tibia treated with intramedullary rodding and cortical bone grafting: a follow-up study at skeletal maturity H Shah, SN Doddabasappa, B Joseph Journal of Pediatric Orthopaedics 31 (1), 79-88, 2011 | 59 | 2011 |
| Effect of prophylactic trochanteric epiphyseodesis in older children with Perthes' disease H Shah, ND Siddesh, B Joseph, SN Nair Journal of Pediatric Orthopaedics 29 (8), 889-895, 2009 | 54 | 2009 |
| Deletions in PITX1 cause a spectrum of lower-limb malformations including mirror-image polydactyly E Klopocki, C Kähler, N Foulds, H Shah, B Joseph, H Vogel, S Lüttgen, ... European journal of human genetics 20 (6), 705-708, 2012 | 51 | 2012 |
| Diagnostic strategies and genotype-phenotype correlation in a large Indian cohort of osteogenesis imperfecta J Mrosk, GSL Bhavani, H Shah, J Hecht, U Krüger, A Shukla, U Kornak, ... Bone 110, 368-377, 2018 | 44 | 2018 |
| Clinical utility of fetal autopsy and its impact on genetic counseling SS Nayak, A Shukla, L Lewis, R Kadavigere, M Mathew, PK Adiga, ... Prenatal Diagnosis 35 (7), 685-691, 2015 | 43 | 2015 |
| Mutations in patients with osteogenesis imperfecta from consanguineous Indian families J Stephen, KM Girisha, A Dalal, A Shukla, H Shah, P Srivastava, U Kornak, ... European journal of medical genetics 58 (1), 21-27, 2015 | 43 | 2015 |
| GALNS mutations in Indian patients with mucopolysaccharidosis IVA AM Bidchol, A Dalal, H Shah, S S, S Nampoothiri, M Kabra, N Gupta, ... American Journal of Medical Genetics Part A 164 (11), 2793-2801, 2014 | 43 | 2014 |
| Congenital posteromedial bowing of the tibia: a retrospective analysis of growth abnormalities in the leg HH Shah, SN Doddabasappa, B Joseph Journal of Pediatric Orthopaedics B 18 (3), 120-128, 2009 | 43 | 2009 |
| Quantitative measures for evaluating the radiographic outcome of Legg-Calvé-Perthes disease H Shah, ND Siddesh, H Pai, S Tercier, B Joseph JBJS 95 (4), 354-361, 2013 | 38 | 2013 |
| Environmental tobacco and wood smoke increase the risk of Legg-Calvé-Perthes disease AB Daniel, H Shah, A Kamath, V Guddettu, B Joseph Clinical Orthopaedics and Related Research® 470, 2369-2375, 2012 | 38 | 2012 |
| Clinical and mutation profile of multicentric osteolysis nodulosis and arthropathy GSL Bhavani, H Shah, A Shukla, N Gupta, K Gowrishankar, AP Rao, ... American journal of medical genetics Part A 170 (2), 410-417, 2016 | 37 | 2016 |
| Pre-axial mirror polydactyly associated with tibial deficiency: a study of the patterns of skeletal anomalies of the foot and leg R Verghese, H Shah, G Rebello, B Joseph Journal of children's orthopaedics 1 (1), 49-54, 2007 | 37 | 2007 |
| What factors influence union and refracture of congenital pseudarthrosis of the tibia? A multicenter long-term study H Shah, B Joseph, BVS Nair, DB Kotian, IH Choi, BS Richards, ... Journal of Pediatric Orthopaedics 38 (6), e332-e337, 2018 | 36 | 2018 |
| Mutation spectrum of COL1A1 and COL1A2 genes in Indian patients with osteogenesis imperfecta J Stephen, A Shukla, A Dalal, KM Girisha, H Shah, N Gupta, M Kabra, ... American journal of medical genetics Part A 164 (6), 1482-1489, 2014 | 35 | 2014 |
| Identification of a novel LRRK1 mutation in a family with osteosclerotic metaphyseal dysplasia L Guo, KM Girisha, A Iida, M Hebbar, A Shukla, H Shah, G Nishimura, ... Journal of human genetics 62 (3), 437-441, 2017 | 34 | 2017 |
