Publications by authors named "Nancy D Merner"

Claim this Profile
E
Extra-Virgin Olive Oil Enhances the Blood-Brain Barrier Function in Mild Cognitive Impairment: A Randomized Controlled Trial.
Amal Kaddoumi, Thomas S Denney, Gopikrishna Deshpande, Jennifer L Robinson, Ronald J Beyers, Nancy D Merner

Nutrients· December 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
An investigation into the role of inherited CEACAM gene family variants and colorectal cancer risk.
Anna L W Huskey, Nancy D Merner

BMC Res Notes· February 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Rare and potentially pathogenic variants in hydroxycarboxylic acid receptor genes identified in breast cancer cases.
Cierla McGuire Sams, Kasey Shepp, Jada Pugh, Madison R Bishop, Nancy D Merner

BMC Med Genomics· December 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
Gene Family Mutations Associated With Inherited Breast Cancer Risk - A Comparative Oncology Approach to Discovery.
Anna L W Huskey, Isaac McNeely, Nancy D Merner

Front Genet· August 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Gene panel screening for insight towards breast cancer susceptibility in different ethnicities.
Madison R Bishop, Sophonie M Omeler-Fenaud, Anna L W Huskey, Nancy D Merner

PLoS One· October 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A research-based gene panel to investigate breast, ovarian and prostate cancer genetic risk.
Madison R Bishop, Anna L W Huskey, John Hetzel, Nancy D Merner

PLoS One· March 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Establishment of the Alabama Hereditary Cancer Cohort - strategies for the inclusion of underrepresented populations in cancer genetics research.
Madison R Bishop, Amit Shah, Melissa Shively, Anna L W Huskey, Sophonie M Omeler, Nancy D Merner

Mol Genet Genomic Med· September 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Lower frequency of TLR9 variant associated with protection from breast cancer among African Americans.
Madison R Chandler, Kimberly S Keene, Johanna M Tuomela, Andres Forero-Torres, Renee Desmond, Nancy D Merner

PLoS One· October 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A monograph proposing the use of canine mammary tumours as a model for the study of hereditary breast cancer susceptibility genes in humans.
Katie Goebel, Nancy D Merner

Vet Med Sci· May 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genome-wide association study in essential tremor identifies three new loci.
Stefanie H Müller, Simon L Girard, Franziska Hopfner, Nancy D Merner, Cynthia V Bourassa

Brain· December 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A Review of Whole-Exome Sequencing Efforts Toward Hereditary Breast Cancer Susceptibility Gene Discovery.
Madison R Chandler, Erin P Bilgili, Nancy D Merner

Hum Mutat· September 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Gain-of-function missense variant in SLC12A2, encoding the bumetanide-sensitive NKCC1 cotransporter, identified in human schizophrenia.
Nancy D Merner, Adriana Mercado, Arjun R Khanna, Alan Hodgkinson, Vanessa Bruat

J Psychiatr Res· June 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Regulatory domain or CpG site variation in SLC12A5, encoding the chloride transporter KCC2, in human autism and schizophrenia.
Nancy D Merner, Madison R Chandler, Cynthia Bourassa, Bo Liang, Arjun R Khanna

Front Cell Neurosci· November 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genetically encoded impairment of neuronal KCC2 cotransporter function in human idiopathic generalized epilepsy.
Kristopher T Kahle, Nancy D Merner, Perrine Friedel, Liliya Silayeva, Bo Liang

EMBO Rep· July 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Recurrent missense mutations in TMEM43 (ARVD5) due to founder effects cause arrhythmogenic cardiomyopathies in the UK and Canada.
Annika F M Haywood, Nancy D Merner, Kathy A Hodgkinson, Jim Houston, Petros Syrris

Eur Heart J· April 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
V
VAMP1 mutation causes dominant hereditary spastic ataxia in Newfoundland families.
Cynthia V Bourassa, Inge A Meijer, Nancy D Merner, Kanwal K Grewal, Mark G Stefanelli

Am J Hum Genet· September 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Exome sequencing identifies FUS mutations as a cause of essential tremor.
Nancy D Merner, Simon L Girard, Hélène Catoire, Cynthia V Bourassa, Véronique V Belzil

Am J Hum Genet· August 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15.
Lance Doucette, Nancy D Merner, Sandra Cooke, Elizabeth Ives, Dante Galutira

Eur J Hum Genet· May 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene.
Nancy D Merner, Kathy A Hodgkinson, Annika F M Haywood, Sean Connors, Vanessa M French

Am J Hum Genet· April 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis