Nicola C. Ho

Structural and Functional Mutations of the Perlecan Gene Cause Schwartz-Jampel Syndrome, with Myotonic Myopathy and Chondrodysplasia

Eri Arikawa‐Hirasawa, Alexander H. Le, Ichizo Nishino et al. · The American Journal of Human Genetics · 2002 · 192 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +8

Mutations of CTSK Result in Pycnodysostosis via a Reduction in Cathepsin K Protein

Nicola C. Ho, Antonello Punturieri, Douglas J. Wilkin et al. · Journal of Bone and Mineral Research · 1999 · 55 citations · Full text

Gene Expression Profile of Human Bone Marrow Stromal Cells: High-Throughput Expressed Sequence Tag Sequencing Analysis

Libin Jia, Marian F. Young, John Powell et al. · Genomics · 2002 · 53 citations

Human Cell, Functional Genomics, Gene Expression Profile +11

A Skeletal Gene Database

Nicola C. Ho, Libin Jia, Catherine C. Driscoll et al. · Journal of Bone and Mineral Research · 2000 · 53 citations

Sclerostin, Engineering, Genetics +20

Living with achondroplasia: Quality of life evaluation following cervico‐medullary decompression

Nicola C. Ho, Michael Guarnieri, Larry J. Brant et al. · American Journal of Medical Genetics Part A · 2004 · 38 citations