1. A monograph proposing the use of canine mammary tumours as a model for the study of hereditary breast cancer susceptibility genes in humans. Issue 2 (21st March 2017) Authors: Goebel, Katie; Merner, Nancy D. Journal: Veterinary medicine and science Issue: Volume 3:Issue 2(2017) Page Start: 51 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A Review of Whole‐Exome Sequencing Efforts Toward Hereditary Breast Cancer Susceptibility Gene Discovery. Issue 9 (27th June 2016) Authors: Chandler, Madison R.; Bilgili, Erin P.; Merner, Nancy D. Journal: Human mutation Issue: Volume 37:Issue 9(2016) Page Start: 835 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Cover. Issue 5 (27th September 2018) Authors: Bishop, Madison R.; Shah, Amit; Shively, Melissa; Huskey, Anna L. W.; Omeler, Sophonie M.; Bilgili, Erin P.; Jackson, Ebony; Daniell, Kathleen; Stallworth, Elizabeth; Spina, Stephanie; Shepp, Kasey; Bergstresser, Sydney; Davis, Amber; Dean, Holly; Gibson, Jantunn; Johnson, Brandon; Merner, Nancy D. Journal: Molecular genetics & genomic medicine Issue: Volume 6:Issue 5(2018) Page Start: i Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Establishment of the Alabama Hereditary Cancer Cohort ‐ strategies for the inclusion of underrepresented populations in cancer genetics research. Issue 5 (1st July 2018) Authors: Bishop, Madison R.; Shah, Amit; Shively, Melissa; Huskey, Anna L. W.; Omeler, Sophonie M.; Bilgili, Erin P.; Jackson, Ebony; Daniell, Kathleen; Stallworth, Elizabeth; Spina, Stephanie; Shepp, Kasey; Bergstresser, Sydney; Davis, Amber; Dean, Holly; Gibson, Jantunn; Johnson, Brandon; Merner, Nancy D. Journal: Molecular genetics & genomic medicine Issue: Volume 6:Issue 5(2018) Page Start: 766 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Gain-of-function missense variant in SLC12A2, encoding the bumetanide-sensitive NKCC1 cotransporter, identified in human schizophrenia. (June 2016) Authors: Merner, Nancy D.; Mercado, Adriana; Khanna, Arjun R.; Hodgkinson, Alan; Bruat, Vanessa; Awadalla, Philip; Gamba, Gerardo; Rouleau, Guy A.; Kahle, Kristopher T. Journal: Journal of psychiatric research Issue: Volume 77(2016:Jun.) Page Start: 22 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗