Publications

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A
Lutz P-E, Tanti A, Gasecka A, Barnett-Burns S, Kim JJ, Zhou Y, Chen GG, Wakid M, Shaw M, Almeida D et al..  2017.  Association of a History of Child Abuse With Impaired Myelination in the Anterior Cingulate Cortex: Convergent Epigenetic, Transcriptional, and Morphological Evidence.. Am J Psychiatry. :appiajp201716111286.
Nagy C, Suderman M, Yang J, Szyf M, Mechawar N, Ernst C, Turecki G.  2015.  Astrocytic abnormalities and global DNA methylation patterns in depression and suicide.. Mol Psychiatry. 20(3):320-8.
B
Lopez JPablo, Diallo A, Cruceanu C, Fiori LM, Laboissiere S, Guillet I, Fontaine J, Ragoussis J, Benes V, Turecki G et al..  2015.  Biomarker discovery: quantification of microRNAs and other small non-coding RNAs using next generation sequencing.. BMC Med Genomics. 8:35.
Chen GG, Diallo AB, Poujol R, Nagy C, Staffa A, Vaillancourt K, Lutz P-E, Ota VK, Mash DC, Turecki G et al..  2014.  BisQC: an operational pipeline for multiplexed bisulfite sequencing.. BMC Genomics. 15:290.
C
Gross JA, Pacis A, Chen GG, Barreiro LB, Ernst C, Turecki G.  2015.  Characterizing 5-hydroxymethylcytosine in human prefrontal cortex at single base resolution.. BMC Genomics. 16:672.
Crapper L, Ernst C.  2015.  Comparative analysis of self-injury in people with psychopathology or neurodevelopmental disorders.. Pediatr Clin North Am. 62(3):619-31.
Maussion G, Cruceanu C, Rosenfeld JA, Bell SC, Jollant F, Szatkiewicz J, Collins RL, Hanscom C, Kolobova I, de Champfleur NMenjot et al..  2017.  Cover Image, Volume 173A, Number 2, February 2017.. Am J Med Genet A. 173(2):i.
D
Merner N, d'Arc BForgeot, Bell SC, Maussion G, Peng H, Gauthier J, Crapper L, Hamdan FF, Michaud JL, Mottron L et al..  2016.  A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature review.. Am J Med Genet A. 170A(5):1225-35.
Vaillancourt K, Ernst C, Mash D, Turecki G.  2017.  DNA Methylation Dynamics and Cocaine in the Brain: Progress and Prospects.. Genes (Basel). 8(5)
I
Maussion G, Cruceanu C, Rosenfeld JA, Bell SC, Jollant F, Szatkiewicz J, Collins RL, Hanscom C, Kolobova I, de Champfleur NMenjot et al..  2017.  Implication of LRRC4C and DPP6 in neurodevelopmental disorders.. Am J Med Genet A. 173(2):395-406.
Maussion G, Diallo AB, Gigek CO, Chen ES, Crapper L, Théroux J-F, Chen GG, Vasuta C, Ernst C.  2015.  Investigation of genes important in neurodevelopment disorders in adult human brain.. Hum Genet. 134(10):1037-53.
L
Bell S, Kolobova I, Crapper L, Ernst C.  2016.  Lesch-Nyhan Syndrome: Models, Theories, and Therapies.. Mol Syndromol. 7(6):302-311.
M
Chen GG, Gross JA, Lutz P-E, Vaillancourt K, Maussion G, Bramoulle A, Théroux J-F, Gardini ES, Ehlert U, Bourret G et al..  2017.  Medium throughput bisulfite sequencing for accurate detection of 5-methylcytosine and 5-hydroxymethylcytosine.. BMC Genomics. 18(1):96.
Chen ES, Gigek CO, Rosenfeld JA, Diallo AB, Maussion G, Chen GG, Vaillancourt K, Lopez JP, Crapper L, Poujol R et al..  2014.  Molecular convergence of neurodevelopmental disorders.. Am J Hum Genet. 95(5):490-508.
Gigek CO, Chen ES, Ota VK, Maussion G, Peng H, Vaillancourt K, Diallo AB, Lopez JP, Crapper L, Vasuta C et al..  2015.  A molecular model for neurodevelopmental disorders.. Transl Psychiatry. 5:e565.
N
W Farmer T, Abrahamsson T, Chierzi S, Lui C, Zaelzer C, Jones EV, Bally BPonroy, Chen GG, Théroux J-F, Peng J et al..  2016.  Neurons diversify astrocytes in the adult brain through sonic hedgehog signaling.. Science. 351(6275):849-54.
P
Jacobsen JC, Erdin S, Chiang C, Hanscom C, Handley RR, Barker DD, Stortchevoi A, Blumenthal I, Reid SJ, Snell RG et al..  2017.  Potential molecular consequences of transgene integration: The R6/2 mouse example.. Sci Rep. 7:41120.
Ernst C.  2016.  Proliferation and Differentiation Deficits are a Major Convergence Point for Neurodevelopmental Disorders.. Trends Neurosci. 39(5):290-9.
R
Bell S, Peng H, Crapper L, Kolobova I, Maussion G, Vasuta C, Yerko V, Wong TPan, Ernst C.  2017.  A Rapid Pipeline to Model Rare Neurodevelopmental Disorders with Simultaneous CRISPR/Cas9 Gene Editing.. Stem Cells Transl Med. 6(3):886-896.
S
Hettige NC, Manzano-Vargas K, Jefri M, Ernst C.  2017.  Strategies to advance drug discovery in rare monogenic intellectual disability syndromes.. Int J Neuropsychopharmacol.
T
Blumenthal I, Ragavendran A, Erdin S, Klei L, Sugathan A, Guide JR, Manavalan P, Zhou JQ, Wheeler VC, Levin JZ et al..  2014.  Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism families.. Am J Hum Genet. 94(6):870-83.