Publications by authors named "Carolyn M Yrigollen"

22Publications

CRISPR to the Rescue: Advances in Gene Editing for the Gene.

Brain Sci 2019 Jan 21;9(1). Epub 2019 Jan 21.

The Raymond G. Perelman Center of Cellular and Molecular Therapeutics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

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http://dx.doi.org/10.3390/brainsci9010017DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6357057PMC
January 2019

Molecular biomarkers predictive of sertraline treatment response in young children with fragile X syndrome.

Brain Dev 2017 Jun 24;39(6):483-492. Epub 2017 Feb 24.

Department of Biochemistry and Molecular Medicine, University of California, Davis, School of Medicine, Davis, CA, USA; MIND Institute, University of California Davis Medical Center, Davis, CA, USA. Electronic address:

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http://dx.doi.org/10.1016/j.braindev.2017.01.012DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5420478PMC
June 2017

Clinical and Molecular Assessment in a Female with Fragile X Syndrome and Tuberous Sclerosis.

J Genet Disord Genet Rep 2016 15;5(3). Epub 2016 Jul 15.

MIND Institute, University of California, Davis, USA; Department of Biochemistry and Molecular Medicine, University of California, Davis, USA.

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http://dx.doi.org/10.4172/2327-5790.1000139DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5319728PMC
July 2016

Distribution of AGG interruption patterns within nine world populations.

Intractable Rare Dis Res 2014 Nov;3(4):153-61

Department of Biochemistry and Molecular Medicine, University of California Davis, School of Medicine, Davis, CA, USA; ; M.I.N.D. Institute, University of California Davis Medical Center, Davis, CA, USA.

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http://dx.doi.org/10.5582/irdr.2014.01028DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298645PMC
November 2014

Screening newborn blood spots for 22q11.2 deletion syndrome using multiplex droplet digital PCR.

Clin Chem 2015 Jan 11;61(1):182-90. Epub 2014 Nov 11.

Department of Biochemistry and Molecular Medicine, UC Davis Medical Center, Sacramento, CA; MIND Institute, UC Davis Medical Center, Sacramento, CA.

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http://dx.doi.org/10.1373/clinchem.2014.230086DOI Listing
January 2015

Differential increases of specific FMR1 mRNA isoforms in premutation carriers.

J Med Genet 2015 Jan 30;52(1):42-52. Epub 2014 Oct 30.

Department of Biochemistry and Molecular Medicine, University of California, School of Medicine, Davis, California, USA MIND Institute, University of California Davis Medical Center, Sacramento, California, USA.

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http://dx.doi.org/10.1136/jmedgenet-2014-102593DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4394606PMC
January 2015

Clinical and molecular implications of mosaicism in FMR1 full mutations.

Front Genet 2014 17;5:318. Epub 2014 Sep 17.

Department of Biochemistry and Molecular Medicine, School of Medicine, University of California at Davis Davis, CA, USA ; Department of Pediatrics, School of Medicine, University of California at Davis Davis, CA, USA.

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http://dx.doi.org/10.3389/fgene.2014.00318DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4166380PMC
October 2014

AGG interruptions and maternal age affect FMR1 CGG repeat allele stability during transmission.

J Neurodev Disord 2014 30;6(1):24. Epub 2014 Jul 30.

Department of Biochemistry and Molecular Medicine, University of California, Davis, School of Medicine, 2700 Stockton Blvd., Suite 2102, Sacramento, CA 95817, USA ; MIND Institute, University of California, Davis, School of Medicine, Davis, CA, USA.

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http://dx.doi.org/10.1186/1866-1955-6-24DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4126815PMC
August 2014

Schooling and variation in the COMT gene: the devil is in the details.

J Child Psychol Psychiatry 2013 Oct 19;54(10):1056-65. Epub 2013 Aug 19.

Yale University, New Haven, CT, USA.

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http://dx.doi.org/10.1111/jcpp.12120DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3786416PMC
October 2013

Gene variants associated with antisocial behaviour: a latent variable approach.

J Child Psychol Psychiatry 2013 Oct 3;54(10):1074-85. Epub 2013 Jul 3.

Yale Child Study Center, Yale University School of Medicine, New Haven, CT, USA.

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http://dx.doi.org/10.1111/jcpp.12109DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3766409PMC
October 2013

Transmission of an FMR1 premutation allele in a large family identified through newborn screening: the role of AGG interruptions.

J Hum Genet 2013 Aug 6;58(8):553-9. Epub 2013 Jun 6.

Department of Biochemistry and Molecular Medicine, University of California Davis, School of Medicine, Davis, CA, USA.

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http://dx.doi.org/10.1038/jhg.2013.50DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4003888PMC
August 2013

AGG interruptions within the maternal FMR1 gene reduce the risk of offspring with fragile X syndrome.

Genet Med 2012 Aug 12;14(8):729-36. Epub 2012 Apr 12.

Department of Biochemistry and Molecular Medicine, University of California-Davis School of Medicine, Davis, California, USA.

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http://dx.doi.org/10.1038/gim.2012.34DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3990283PMC
August 2012

The role of AGG interruptions in the transcription of FMR1 premutation alleles.

PLoS One 2011 19;6(7):e21728. Epub 2011 Jul 19.

Department of Biochemistry and Molecular Medicine, School of Medicine, University of California Davis, Davis, California, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0021728PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3139575PMC
December 2011

Genes controlling affiliative behavior as candidate genes for autism.

Biol Psychiatry 2008 May 22;63(10):911-6. Epub 2008 Jan 22.

Department of Statistics, Department of Epidemiology and PublicHealth, Yale University, NewHaven, CT 06519-1124, USA.

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http://dx.doi.org/10.1016/j.biopsych.2007.11.015DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2386897PMC
May 2008