7 Publications
2021
Rare and potentially pathogenic variants in hydroxycarboxylic acid receptor genes identified in breast cancer cases
Shepp, Kasey⋅Pugh, Jada⋅Bishop, Madison R and Merner, Nancy D
BMC Medical Genomics, vol. 14, pp. 1-13, 2021. | Journal Article
2020
Gene panel screening for insight towards breast cancer susceptibility in different ethnicities
Bishop, Madison R⋅Omeler-Fenaud, Sophonie M⋅Huskey, Anna L and Merner, Nancy D
PLoS One, vol. 15, (no. 8), Aug 2020. | Journal Article
2019
A research-based gene panel to investigate breast, ovarian and prostate cancer genetic risk
Bishop, Madison R⋅Huskey, Anna L⋅Hetzel, John and Merner, Nancy D
PLoS One, vol. 14, (no. 8), Aug 2019. | Journal Article
2017
Lower frequency of TLR9 variant associated with protection from breast cancer among African Americans
Chandler, Madison R⋅Keene, Kimberly S⋅Tuomela, Johanna M⋅Forero-Torres, Andres⋅Desmond, Renee⋅Vuopala, Katri S⋅Harris, Kevin W⋅Merner, Nancy D and Selander, Katri S
PLoS One, vol. 12, (no. 9), Sep 2017. | Journal Article
2015
Regulatory domain or CpG site variation in SLC12A5, encoding the chloride transporter KCC2, in human autism and schizophrenia
Merner, Nancy D⋅Merner, Nancy D⋅Chandler, Madison R⋅Chandler, Madison R⋅Bourassa, Cynthia⋅Bourassa, Cynthia⋅Liang, Bo⋅Liang, Bo⋅Khanna, Arjun R⋅Khanna, Arjun R⋅Dion, Patrick⋅Dion, Patrick⋅Rouleau, Guy A⋅Rouleau, Guy A⋅Kahle, Kristopher T and Kahle, Kristopher T
Frontiers in Cellular Neuroscience, Oct 12, 2015. | Journal Article
2009
Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15
Doucette, Lance⋅Doucette, Lance⋅Merner, Nancy D⋅Merner, Nancy D⋅Cooke, Sandra⋅Cooke, Sandra⋅Ives, Elizabeth⋅Ives, Elizabeth⋅Galutira, Dante⋅Galutira, Dante⋅Walsh, Vanessa⋅Walsh, Vanessa⋅Walsh, Tom⋅Walsh, Tom⋅MacLaren, Linda⋅Maclaren, Linda⋅Maclaren, Linda⋅Cater, Tracey⋅Cater, Tracey⋅Fernandez, Bridget⋅Fernandez, Bridget⋅Green, Jane S⋅Green, Jane S⋅Wilcox, Edward R⋅Wilcox, Edward R⋅Shotland, Lawrence I⋅Shotland, Larry⋅Shotland, Larry⋅Li, Xiaoyan C⋅Li, X C⋅Lee, Ming⋅Li, Xiaoyan Cindy⋅Lee, Ming⋅Li, X C⋅King, Mary Claire⋅King, Mary-claire⋅Young, Terry Lynn⋅Young, Terry-lynn⋅Lee, Ming⋅King, Mary-Claire and Young, Terry-Lynn
European Journal of Human Genetics : EJHG, vol. 17, (no. 5), pp. 554-64, May 2009. | Journal Article
 
Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15
Doucette, Lance⋅Doucette, Lance⋅Merner, Nancy D⋅Merner, Nancy D⋅Cooke, Sandra⋅Cooke, Sandra⋅Ives, Elizabeth⋅Ives, Elizabeth⋅Galutira, Dante⋅Galutira, Dante⋅Walsh, Vanessa⋅Walsh, Vanessa⋅Walsh, Tom⋅Walsh, Tom⋅MacLaren, Linda⋅Maclaren, Linda⋅Maclaren, Linda⋅Cater, Tracey⋅Cater, Tracey⋅Fernandez, Bridget⋅Fernandez, Bridget⋅Green*, Jane S⋅Green, Jane S⋅Green, Jane⋅Wilcox, Edward R⋅Wilcox, Edward R⋅Shotland, Larry⋅Shotland*, Larry⋅Shotland, Larry⋅Li, X C⋅Li*, X. C⋅Li, X⋅Lee*, Ming⋅Lee, Ming⋅Lee, Ming⋅King, Mary Claire⋅King, Mary-claire⋅Young, Terry-lynn and Young, Terry Lynn
European Journal of Human Genetics : EJHG, vol. 17, (no. 10), pp. 1363, Oct 2009. | Journal Article