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Nature Communications|October 11, 2018
A missense variant in SLC39A8 is associated with severe idiopathic scoliosisGabe Haller, Kevin McCall, Supak Jenkitkasemwong, et al.The Lancet. Planetary Health|July 10, 2021
Integrating solutions to adapt cities for climate changeBrenda B Lin, Alessandro Ossola, Marina Alberti, et al.Nature Cell Biology|February 3, 2026
DOT1L provides transcriptional memory through PRC1.1 antagonismDaniel Neville, Daniel T Ferguson, Emily B Heikamp, et al.Trials|March 3, 2011
Impact on mortality and cancer incidence rates of using random invitation from population registers for recruitment to trialsMatthew Burnell, Aleksandra Gentry-Maharaj, Andy Ryan, et al.Frontiers in Immunology|August 8, 2014
Next generation sequencing reveals skewing of the T and B cell receptor repertoires in patients with wiskott-Aldrich syndromeAmy E O'Connell, Stefano Volpi, Kerry Dobbs, et al.Human Molecular Genetics|May 17, 2014
Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosisJillian G Buchan, David M Alvarado, Gabe E Haller, et al.Spine|November 23, 2023
BrAIST-Calc: Prediction of Individualized Benefit From Bracing for Adolescent Idiopathic ScoliosisLori A Dolan, Stuart L Weinstein, Matthew B Dobbs, et al.Blood|April 15, 2018
Patients with CD3G mutations reveal a role for human CD3γ in Treg diversity and suppressive functionJared H Rowe, Ottavia M Delmonte, Sevgi Keles, et al.BMJ (Clinical Research Ed.)|November 15, 2008
Recruitment to multicentre trials--lessons from UKCTOCS: descriptive studyUsha Menon, Aleksandra Gentry-Maharaj, Andy Ryan, et al.Human Mutation|December 31, 2020
Mutations in KIF7 implicated in idiopathic scoliosis in humans and axial curvatures in zebrafishElizabeth A Terhune, Melissa T Cuevas, Anna M Monley, et al.Pageof 188