Lauren Grote

Lauren Grote

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Lauren Grote

Lauren Grote

Publications by authors named "Lauren Grote"

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Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia.

Am J Hum Genet 2018 05 12;102(5):744-759. Epub 2018 Apr 12.

Service de Génétique Médicale, CHU Nantes, 9 quai Moncousu, 44093 Nantes Cedex 1, France; l'institut du thorax, INSERM, CNRS, UNIV Nantes, 44007 Nantes, France. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2018.02.021DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5986661PMC
May 2018

Expanding the phenotype of feingold syndrome-2.

Am J Med Genet A 2015 Dec 11;167A(12):3219-25. Epub 2015 Sep 11.

Division of Clinical Genetics, Children's Mercy Hospital, University of Missouri-Kansas City School of Medicine, Kansas City, Missouri.

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http://dx.doi.org/10.1002/ajmg.a.37368DOI Listing
December 2015

A novel epileptic encephalopathy mutation in KCNB1 disrupts Kv2.1 ion selectivity, expression, and localization.

J Gen Physiol 2015 Nov;146(5):399-410

Department of Neurobiology, Physiology and Behavior, Department of Physiology and Membrane Biology, and Department of Anesthesiology and Pain Medicine, University of California, Davis, Davis, CA 95616 Department of Neurobiology, Physiology and Behavior, Department of Physiology and Membrane Biology, and Department of Anesthesiology and Pain Medicine, University of California, Davis, Davis, CA 95616

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http://dx.doi.org/10.1085/jgp.201511444DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4621747PMC
November 2015

Variable approaches to genetic counseling for microarray regions of homozygosity associated with parental relatedness.

Am J Med Genet A 2014 Jan 15;164A(1):87-98. Epub 2013 Nov 15.

Division of Human Genetics, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio; Division of Clinical Genetics, The Children's Mercy Hospital, Kansas City, Missouri.

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http://dx.doi.org/10.1002/ajmg.a.36206DOI Listing
January 2014

Regions of homozygosity identified by SNP microarray analysis aid in the diagnosis of autosomal recessive disease and incidentally detect parental blood relationships.

Genet Med 2013 Jan 2;15(1):70-8. Epub 2012 Aug 2.

Division of Human Genetics, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.

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http://www.nature.com/articles/gim201294
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http://dx.doi.org/10.1038/gim.2012.94DOI Listing
January 2013

Variability in laboratory reporting practices for regions of homozygosity indicating parental relatedness as identified by SNP microarray testing.

Genet Med 2012 Dec 12;14(12):971-6. Epub 2012 Jul 12.

Division of Human Genetics, Department of Pediatrics at Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.

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http://dx.doi.org/10.1038/gim.2012.83DOI Listing
December 2012