Howard R. Slater - Publications

Significantly Elevated FMR1 mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X Testing.

Journal: International journal of molecular sciences

Published: July 02, 2019

Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features.

Journal: Molecular autism

Published: January 30, 2019

Diagnostic application of kidney allograft-derived absolute cell-free DNA levels during transplant dysfunction.

Journal: American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons

Published: May 27, 2018

ADGRV1 is implicated in myoclonic epilepsy.

Journal: Epilepsia

Published: November 20, 2017

β-glucuronidase use as a single internal control gene may confound analysis in FMR1 mRNA toxicity studies.

Journal: PloS one

Published: July 25, 2017

Reliability of the English version of the painDETECT questionnaire.

Journal: Current medical research and opinion

Published: February 07, 2017

Erratum: Hwang Y.T. et al. Molecular Inconsistencies in a Fragile X Male with Early Onset Ataxia. Genes 2016, 7, 68.

Journal: Genes

Published: January 20, 2017

Brain structure and intragenic DNA methylation are correlated, and predict executive dysfunction in fragile X premutation females.

Journal: Translational psychiatry

Published: September 15, 2016

Use of ubiquitous, highly heterozygous copy number variants and digital droplet polymerase chain reaction to monitor chimerism after allogeneic haematopoietic stem cell transplantation.

Journal: Experimental hematology

Published: July 27, 2016

Molecular Inconsistencies in a Fragile X Male with Early Onset Ataxia.

Journal: Genes

Published: May 12, 2016

β-glucuronidase mRNA levels are correlated with gait and working memory in premutation females: understanding the role of FMR1 premutation alleles.

Journal: Scientific reports

Published: March 21, 2016

Detection of skewed X-chromosome inactivation in Fragile X syndrome and X chromosome aneuploidy using quantitative melt analysis.

Journal: Expert reviews in molecular medicine

Published: July 02, 2015