| ptk7 mutant zebrafish models of congenital and idiopathic scoliosis implicate dysregulated Wnt signalling in disease M Hayes, X Gao, LX Yu, N Paria, RM Henkelman, CA Wise, B Ciruna Nature communications 5 (1), 4777, 2014 | 165 | 2014 |
| Somatic gain-of-function mutations in PIK3CA in patients with macrodactyly JJ Rios, N Paria, DK Burns, BA Israel, R Cornelia, CA Wise, M Ezaki Human molecular genetics 22 (3), 444-451, 2013 | 156 | 2013 |
| Stallion sperm transcriptome comprises functionally coherent coding and regulatory RNAs as revealed by microarray analysis and RNA-seq PJ Das, F McCarthy, M Vishnoi, N Paria, C Gresham, G Li, P Kachroo, ... PloS one 8 (2), e56535, 2013 | 108 | 2013 |
| Total RNA isolation from stallion sperm and testis biopsies PJ Das, N Paria, A Gustafson-Seabury, M Vishnoi, SP Chaki, CC Love, ... Theriogenology 74 (6), 1099-1106. e2, 2010 | 95 | 2010 |
| DNA polymerase epsilon deficiency causes IMAGe syndrome with variable immunodeficiency CV Logan, JE Murray, DA Parry, A Robertson, R Bellelli, Ž Tarnauskaitė, ... The American Journal of Human Genetics 103 (6), 1038-1044, 2018 | 80 | 2018 |
| Horse Y chromosome assembly displays unique evolutionary features and putative stallion fertility genes JE Janečka, BW Davis, S Ghosh, N Paria, PJ Das, L Orlando, M Schubert, ... Nature communications 9 (1), 1-15, 2018 | 77 | 2018 |
| A gene catalogue of the euchromatic male-specific region of the horse Y chromosome: comparison with human and other mammals N Paria, T Raudsepp, AJ Pearks Wilkerson, PCM O'Brien, ... PLoS One 6 (7), e21374, 2011 | 73 | 2011 |
| Glutathione S-transferase M1 and T1 null genotype frequency in chronic myeloid leukaemia BC Mondal, N Paria, S Majumdar, S Chandra, A Mukhopadhyay, ... European journal of cancer prevention 14 (3), 281-284, 2005 | 44 | 2005 |
| Genome-wide meta-analysis and replication studies in multiple ethnicities identify novel adolescent idiopathic scoliosis susceptibility loci AM Khanshour, I Kou, Y Fan, E Einarsdottir, N Makki, YH Kidane, J Kere, ... Human molecular genetics 27 (22), 3986-3998, 2018 | 43 | 2018 |
| Potential applications of equine genomics in dissecting diseases and fertility BP Chowdhary, N Paria, T Raudsepp Animal reproduction science 107 (3-4), 208-218, 2008 | 36 | 2008 |
| Equine genomics BP Chowdhary John Wiley & Sons, 2013 | 33 | 2013 |
| Neurofibromin deficiency‐associated transcriptional dysregulation suggests a novel therapy for tibial pseudoarthrosis in NF1 N Paria, TJ Cho, IH Choi, N Kamiya, K Kayembe, R Mao, RL Margraf, ... Journal of Bone and Mineral Research 29 (12), 2636-2642, 2014 | 27 | 2014 |
| Mutations preventing regulated exon skipping in MET cause osteofibrous dysplasia MJ Gray, P Kannu, S Sharma, C Neyt, D Zhang, N Paria, PB Daniel, ... The American Journal of Human Genetics 97 (6), 837-847, 2015 | 25 | 2015 |
| The reduced osteogenic potential of Nf1-deficient osteoprogenitors is EGFR-independent SE Tahaei, G Couasnay, Y Ma, N Paria, J Gu, BF Lemoine, X Wang, ... Bone 106, 103-111, 2018 | 22 | 2018 |
| Whole-exome sequencing: discovering genetic causes of orthopaedic disorders N Paria, LA Copley, JA Herring, HKW Kim, BS Richards, DJ Sucato, ... JBJS 95 (23), e185, 2013 | 9 | 2013 |
| Genetics of adolescent idiopathic scoliosis N Paria, CA Wise Seminars in Spine Surgery 27 (1), 9-15, 2015 | 8 | 2015 |
| Genetic association and characterization of FSTL5 in isolated clubfoot AM Khanshour, YH Kidane, J Kozlitina, R Cornelia, A Rafipay, V De Mello, ... Human molecular genetics 29 (22), 3717-3728, 2020 | 7 | 2020 |
| Germline saturation mutagenesis induces skeletal phenotypes in mice JJ Rios, K Denton, J Russell, J Kozlitina, CR Ferreira, AF Lewanda, ... Journal of Bone and Mineral Research 36 (8), 1548-1565, 2020 | 6 | 2020 |
| Discovery of candidate genes for stallion fertility N Paria College of Veterinary Medicine, 223, 2009 | 6 | 2009 |
| ptk7 mutant zebrafish models of congenital and idiopathic scoliosis implicate dysregulated Wnt signalling in disease. Nat Commun. 2014; 5 M Hayes, X Gao, LX Yu, N Paria, RM Henkelman, CA Wise, B Ciruna Pedro A. Rubio Belmar, 0 | 6 | |
