1. A missense variant in SLC39A8 is associated with severe idiopathic scoliosis. Issue 1 (December 2018) Authors: Haller, Gabe; McCall, Kevin; Jenkitkasemwong, Supak; Sadler, Brooke; Antunes, Lilian; Nikolov, Momchil; Whittle, Julia; Upshaw, Zachary; Shin, Jimann; Baschal, Erin; Cruchaga, Carlos; Harms, Matthew; Raggio, Cathleen; Morcuende, Jose; Giampietro, Philip; Miller, Nancy; Wise, Carol; Gray, Ryan; So... Journal: Nature communications Issue: Volume 9:Issue 1(2018) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Rare and de novo duplications containing SHOX in clubfoot. Issue 12 (9th June 2020) Authors: Sadler, Brooke; Haller, Gabe; Antunes, Lilian; Nikolov, Momchil; Amarillo, Ina; Coe, Bradley; Dobbs, Matthew B.; Gurnett, Christina A. Journal: Journal of medical genetics Issue: Volume 57:Issue 12(2020) Page Start: 851 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Whole Exome Sequencing in Individuals with Idiopathic Clubfoot Reveals a Recurrent Filamin B (FLNB) Deletion. Issue 2 (February 2022) Authors: Quiggle, Ashley; Charng, Wu-Lin; Antunes, Lilian; Nikolov, Momchil; Bledsoe, Xavier; Hecht, Jacqueline T.; Dobbs, Matthew B.; Gurnett, Christina A. Journal: Clinical orthopaedics and related research Issue: Volume 480:Issue 2(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗