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Nandina Paria
Nandina Paria
未知所在单位机构
在 tsrh.org 的电子邮件经过验证
标题
引用次数
引用次数
年份
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
1742014
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
1612013
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
1112013
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
962010
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
862018
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
822018
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
752011
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
452018
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
442005
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
362008
Equine genomics
BP Chowdhary
John Wiley & Sons, 2013
342013
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
282014
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
262015
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
242018
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
112020
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
102013
Genetics of adolescent idiopathic scoliosis
N Paria, CA Wise
Seminars in Spine Surgery 27 (1), 9-15, 2015
82015
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
72020
Ptk7 mutant zebrafish models of congenital and idiopathic scoliosis impli‑cate dysregulated Wnt signalling in disease. Nat Commun. 2014; 5: 1–11
M Hayes, X Gao, LX Yu, N Paria, RM Henkelman, CA Wise, B Ciruna
Pedro A. Rubio Belmar, 0
7
Discovery of candidate genes for stallion fertility
N Paria
College of Veterinary Medicine, 223, 2009
62009
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