Publications by authors named "Jonathan D Labonne"

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Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autism.
Hyung-Goo Kim, Jill A Rosenfeld, Daryl A Scott, Gerard Bénédicte, Jonathan D Labonne

Mol Autism· June 2020

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Steric Clash in the SET Domain of Histone Methyltransferase NSD1 as a Cause of Sotos Syndrome and Its Genetic Heterogeneity in a Brazilian Cohort.
Kyungsoo Ha, Priya Anand, Jennifer A Lee, Julie R Jones, Chong Ae Kim, Jonathan D J Labonne

Genes (Basel)· November 2016

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A microdeletion at Xq22.2 implicates a glycine receptor GLRA4 involved in intellectual disability, behavioral problems and craniofacial anomalies.
Jonathan D J Labonne, Tyler D Graves, Yiping Shen, Julie R Jones, Il-Keun Kong

BMC Neurol· August 2016

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An atypical 12q24.31 microdeletion implicates six genes including a histone demethylase KDM2B and a histone methyltransferase SETD1B in syndromic intellectual disability.
Jonathan D J Labonne, Kang-Han Lee, Shigeki Iwase, Il-Keun Kong, Michael P Diamond

Hum Genet· July 2016

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Comparative deletion mapping at 1p31.3-p32.2 implies NFIA responsible for intellectual disability coupled with macrocephaly and the presence of several other genes for syndromic intellectual disability.
Jonathan D J Labonne, Yiping Shen, Il-Keun Kong, Michael P Diamond, Lawrence C Layman

Mol Cytogenet· March 2016

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Concomitant partial exon skipping by a unique missense mutation of RPS6KA3 causes Coffin-Lowry syndrome.
Jonathan D J Labonne, Min Ji Chung, Julie R Jones, Priya Anand, Wolfgang Wenzel

Gene· January 2016

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A microdeletion encompassing PHF21A in an individual with global developmental delay and craniofacial anomalies.
Jonathan D J Labonne, Julie Vogt, Lisa Reali, Il-Keun Kong, Lawrence C Layman

Am J Med Genet A· December 2015

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Differential nuclease sensitivity profiling of chromatin reveals biochemical footprints coupled to gene expression and functional DNA elements in maize.
Daniel L Vera, Thelma F Madzima, Jonathan D Labonne, Mohammad P Alam, Gregg G Hoffman

Plant Cell· October 2014

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Changes in nucleosome position at transcriptional start sites of specific genes in Zea mays mediator of paramutation1 mutants.
Jonathan D J Labonne, Jane E Dorweiler, Karen M McGinnis

Epigenetics· April 2013

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Positional cloning of the s haplotype determining the floral and incompatibility phenotype of the long-styled morph of distylous Turnera subulata.
Jonathan D J Labonne, Joel S Shore

Mol Genet Genomics· February 2011

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