Publications by authors named "Devon Haynes"

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Rare de novo gain-of-function missense variants in DOT1L are associated with developmental delay and congenital anomalies.
Zelha Nil, Ashish R Deshwar, Yan Huang, Scott Barish, Xi Zhang, Devon Haynes

Am J Hum Genet· November 2023

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Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and mice.
Sarah E Sheppard, Laura Bryant, Rochelle N Wickramasekara, Courtney Vaccaro, Brynn Robertson, Devon Haynes

Sci Adv· March 2023

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Clinical, biochemical and genetic characteristics of MOGS-CDG: a rare congenital disorder of glycosylation.
Shino Shimada, Bobby G Ng, Amy L White, Kim K Nickander, Coleman Turgeon, Devon Haynes

J Med Genet· July 2022

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Haploinsufficiency of PRR12 causes a spectrum of neurodevelopmental, eye, and multisystem abnormalities.
Fuad Chowdhury, Lei Wang, Mohammed Al-Raqad, David J Amor, Alice Baxová, Devon Haynes

Genet Med· July 2021

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Phenotypic expansion of the BPTF-related neurodevelopmental disorder with dysmorphic facies and distal limb anomalies.
Kevin E Glinton, Anna C E Hurst, Kevin M Bowling, Ingrid Cristian, Devon Haynes

Am J Med Genet A· May 2021

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Germline mutation in : a heterogeneous, multi-systemic developmental disorder characterized by transcriptional dysregulation.
Adam W Hansen, Payal Arora, Michael M Khayat, Leah J Smith, Andrea M Lewis, Devon Haynes

HGG Adv· January 2021

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De Novo Variants in the ATPase Module of MORC2 Cause a Neurodevelopmental Disorder with Growth Retardation and Variable Craniofacial Dysmorphism.
Maria J Guillen Sacoto, Iva A Tchasovnikarova, Erin Torti, Cara Forster, E Hallie Andrew, Devon Haynes

Am J Hum Genet· August 2020

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Further delineation of Basel-Vanagaite-Smirin-Yosef syndrome: Report of three patients.
Devon Haynes, Lynda Pollack, Chitra Prasad, Sharan Goobie, Samantha Colaiacovo

Am J Med Genet A· July 2020

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Correction: A homozygous KAT2B variant modulates the clinical phenotype of ADD3 deficiency in humans and flies.
Sara Gonçalves, Julie Patat, Maria Clara Guida, Noelle Lachaussée, Christelle Arrondel, Devon Haynes

PLoS Genet· October 2018

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A homozygous KAT2B variant modulates the clinical phenotype of ADD3 deficiency in humans and flies.
Sara Gonçalves, Julie Patat, Maria Clara Guida, Noelle Lachaussée, Christelle Arrondel, Devon Haynes

PLoS Genet· May 2018

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