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Advances in Experimental Medicine and Biology|February 21, 2009
Control of muscle synergies by cortical ensemblesMichelle M Morrow, Eric A Pohlmeyer, Lee E MillerJournal of Medical Genetics|March 20, 2024
A comparative medical genomics approach may facilitate the interpretation of rare missense variationBushra Haque, George Guirguis, Meredith Curtis, et al.Human Mutation|April 27, 2022
Mutation update: Variants of the ENPP1 gene in pathologic calcification, hypophosphatemic rickets, and cutaneous hypopigmentation with punctate keratodermaDouglas Ralph, Michael A Levine, Gabriele Richard, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 14, 2014
New roles for the external globus pallidus in basal ganglia circuits and behaviorAryn H Gittis, Joshua D Berke, Mark D Bevan, et al.HGG Advances|November 27, 2024
MGA-related syndrome: A proposed novel disorderBobbi McGivern, Michelle M Morrow, Erin Torti, et al.HGG Advances|January 22, 2025
Missense variants at the p.Arg225 residue in ARHGEF40 identified in individuals with multiple congenital anomalies and developmental delayMelanie P Napier, Erin Ryan, Adi Reich, et al.American Journal of Medical Genetics. Part A|February 16, 2023
TELO2-related syndrome (You-Hoover-Fong syndrome): Description of 14 new affected individuals and review of the literatureDaniah Albokhari, Amanda Barone Pritchard, Adelyn Beil, et al.Plos Genetics|January 6, 2025
Leveraging cancer mutation data to inform the pathogenicity classification of germline missense variantsBushra Haque, David Cheerie, Amy Pan, et al.HGG Advances|March 23, 2025
Identification of de novo variants in KCTD10 as a proposed cause for multiple congenital anomaliesMichelle M Morrow, Erin Torti, Bobbi McGivern, et al.Annals of Clinical and Translational Neurology|October 15, 2020
Novel NUDT2 variant causes intellectual disability and polyneuropathyFrank Diaz, Shaweta Khosa, Dmitriy Niyazov, et al.Pageof 3