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Deepti Anand, PhD
Deepti Anand, PhD
Research Scientist at Nemours Children's Health/ Alfred I. duPont Hospital for Children
Verified email at nemours.org
Title
Cited by
Cited by
Year
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
2082011
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
2082010
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
982018
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
872017
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
772018
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
742016
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
672018
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
662019
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
542018
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
522017
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
522015
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
502021
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
482019
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
452017
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
372017
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
362015
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
312018
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
292020
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
292019
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
282018
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