Marker assisted selection: a paradigm shift in Basmati breeding AK Singh, S Gopalakrishnan, VP Singh, KV Prabhu, T Mohapatra, ... Indian Journal of Genetics and Plant Breeding 71 (2), 120, 2011 | 209 | 2011 |
Marker-assisted improvement of bacterial blight resistance in parental lines of Pusa RH10, a superfine grain aromatic rice hybrid SH Basavaraj, VK Singh, A Singh, A Singh, A Singh, D Anand, S Yadav, ... Molecular breeding 26, 293-305, 2010 | 209 | 2010 |
Mutations in the epithelial cadherin-p120-catenin complex cause mendelian non-syndromic cleft lip with or without cleft palate LL Cox, TC Cox, LMM Uribe, Y Zhu, CT Richter, N Nidey, JM Standley, ... The American Journal of Human Genetics 102 (6), 1143-1157, 2018 | 101 | 2018 |
Novel phenotypes and loci identified through clinical genomics approaches to pediatric cataract N Patel, D Anand, D Monies, S Maddirevula, AO Khan, T Algoufi, ... Human genetics 136, 205-225, 2017 | 87 | 2017 |
iSyTE 2.0: a database for expression-based gene discovery in the eye A Kakrana, A Yang, D Anand, D Djordjevic, D Ramachandruni, A Singh, ... Nucleic acids research 46 (D1), D875-D885, 2018 | 81 | 2018 |
Prox1 and fibroblast growth factor receptors form a novel regulatory loop controlling lens fiber differentiation and gene expression DS Audette, D Anand, T So, TB Rubenstein, SA Lachke, FJ Lovicu, ... Development 143 (2), 318-328, 2016 | 74 | 2016 |
Genomic analyses in African populations identify novel risk loci for cleft palate A Butali, PA Mossey, WL Adeyemo, MA Eshete, LJJ Gowans, TD Busch, ... Human molecular genetics 28 (6), 1038-1051, 2019 | 67 | 2019 |
Mutation update of transcription factor genes FOXE3, HSF4, MAF, and PITX3 causing cataracts and other developmental ocular defects D Anand, SA Agrawal, A Slavotinek, SA Lachke Human mutation 39 (4), 471-494, 2018 | 67 | 2018 |
The RNA-binding protein Celf1 post-transcriptionally regulates p27Kip1 and Dnase2b to control fiber cell nuclear degradation in lens development AD Siddam, C Gautier-Courteille, L Perez-Campos, D Anand, A Kakrana, ... PLoS genetics 14 (3), e1007278, 2018 | 54 | 2018 |
A large multiethnic GWAS meta-analysis of cataract identifies new risk loci and sex-specific effects H Choquet, RB Melles, D Anand, J Yin, G Cuellar-Partida, W Wang, ... Nature communications 12 (1), 3595, 2021 | 53 | 2021 |
Exome sequencing provides additional evidence for the involvement of ARHGAP29 in Mendelian orofacial clefting and extends the phenotypic spectrum to isolated cleft palate H Liu, T Busch, S Eliason, D Anand, S Bullard, LJJ Gowans, N Nidey, ... Birth defects research 109 (1), 27-37, 2017 | 53 | 2017 |
Compound mouse mutants of bZIP transcription factors Mafg and Mafk reveal a regulatory network of non-crystallin genes associated with cataract SA Agrawal, D Anand, AD Siddam, A Kakrana, S Dash, DA Scheiblin, ... Human genetics 134, 717-735, 2015 | 52 | 2015 |
A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signals JC Carlson, D Anand, A Butali, CJ Buxo, K Christensen, F Deleyiannis, ... Genetic epidemiology 43 (6), 704-716, 2019 | 48 | 2019 |
Systems biology of lens development: A paradigm for disease gene discovery in the eye D Anand, SA Lachke Experimental eye research 156, 22-33, 2017 | 46 | 2017 |
N-myc regulates growth and fiber cell differentiation in lens development GR Cavalheiro, GE Matos-Rodrigues, Y Zhao, AL Gomes, D Anand, ... Developmental biology 429 (1), 105-117, 2017 | 37 | 2017 |
Molecular characterization of mouse lens epithelial cell lines and their suitability to study RNA granules and cataract associated genes AM Terrell, D Anand, SF Smith, CA Dang, SM Waters, M Pathania, ... Experimental eye research 131, 42-55, 2015 | 36 | 2015 |
RNA sequencing-based transcriptomic profiles of embryonic lens development for cataract gene discovery D Anand, A Kakrana, AD Siddam, H Huang, I Saadi, SA Lachke Human genetics 137, 941-954, 2018 | 32 | 2018 |
The Tudor-domain protein TDRD7, mutated in congenital cataract, controls the heat shock protein HSPB1 (HSP27) and lens fiber cell morphology CE Barnum, S Al Saai, SD Patel, C Cheng, D Anand, X Xu, S Dash, ... Human molecular genetics 29 (12), 2076-2097, 2020 | 29 | 2020 |
Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humans TC Cox, AC Lidral, JC McCoy, H Liu, LL Cox, Y Zhu, RD Anderson, ... Human mutation 40 (10), 1813-1825, 2019 | 29 | 2019 |
A zebrafish model of foxe3 deficiency demonstrates lens and eye defects with dysregulation of key genes involved in cataract formation in humans M Krall, S Htun, D Anand, D Hart, SA Lachke, AM Slavotinek Human genetics 137, 315-328, 2018 | 29 | 2018 |