Paria, Nandina
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1

RAB1A haploinsufficiency phenocopies the 2p14–p15 microdele..:

Rios, Jonathan J. ; Li, Yang ; Paria, Nandina...
The American Journal of Human Genetics.  110 (2023)  12 - p. 2103-2111 , 2023
 
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Molecular Dissection of Somatic Skeletal Disease in Neurofi..:

Paria, Nandina ; Khalid, Aysha ; Shen, Bo...
Journal of Bone and Mineral Research.  38 (2020)  2 - p. 288-299 , 2020
 
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Germline Saturation Mutagenesis Induces Skeletal Phenotypes..:

Rios, Jonathan J ; Denton, Kristin ; Russell, Jamie...
Journal of Bone and Mineral Research.  36 (2020)  8 - p. 1548-1565 , 2020
 
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8

Genetics of adolescent idiopathic scoliosis:

Paria, Nandina ; Wise, Carol A.
Seminars in Spine Surgery.  27 (2015)  1 - p. 9-15 , 2015
 
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9

Neurofibromin Deficiency-Associated Transcriptional Dysregu..:

Paria, Nandina ; Cho, Tae-Joon ; Choi, In Ho...
Journal of Bone and Mineral Research.  29 (2014)  12 - p. 2636-2642 , 2014
 
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