| Regulatory domain or CpG site variation in SLC12A5, encoding the chloride transporter KCC2, in human autism and schizophrenia ND Merner, MR Chandler, C Bourassa, B Liang, AR Khanna, P Dion, ... Frontiers in cellular neuroscience 9, 386, 2015 | 108 | 2015 |
| A review of whole‐exome sequencing efforts toward hereditary breast cancer susceptibility gene discovery MR Chandler, EP Bilgili, ND Merner Human mutation 37 (9), 835-846, 2016 | 60 | 2016 |
| Genome-wide enrichment of de novo coding mutations in orofacial cleft trios MR Bishop, KKD Perez, M Sun, S Ho, P Chopra, N Mukhopadhyay, ... The American Journal of Human Genetics 107 (1), 124-136, 2020 | 58 | 2020 |
| Whole genome sequencing of orofacial cleft trios from the Gabriella Miller Kids First Pediatric Research Consortium identifies a new locus on chromosome 21 N Mukhopadhyay, M Bishop, M Mortillo, P Chopra, JB Hetmanski, ... Human genetics 139, 215-226, 2020 | 25 | 2020 |
| Establishment of the Alabama Hereditary Cancer Cohort‐strategies for the inclusion of underrepresented populations in cancer genetics research MR Bishop, A Shah, M Shively, ALW Huskey, SM Omeler, EP Bilgili, ... Molecular Genetics & Genomic Medicine 6 (5), 766-778, 2018 | 12 | 2018 |
| Lower frequency of TLR9 variant associated with protection from breast cancer among African Americans MR Chandler, KS Keene, JM Tuomela, A Forero-Torres, R Desmond, ... PLoS One 12 (9), e0183832, 2017 | 12 | 2017 |
| A research-based gene panel to investigate breast, ovarian and prostate cancer genetic risk MR Bishop, ALW Huskey, J Hetzel, ND Merner PLoS One 14 (8), e0220929, 2019 | 9 | 2019 |
| Gene panel screening for insight towards breast cancer susceptibility in different ethnicities MR Bishop, SM Omeler-Fenaud, ALW Huskey, ND Merner PLoS One 15 (8), e0238295, 2020 | 8 | 2020 |
| Rare and potentially pathogenic variants in hydroxycarboxylic acid receptor genes identified in breast cancer cases C McGuire Sams, K Shepp, J Pugh, MR Bishop, ND Merner BMC Medical Genomics 14, 1-13, 2021 | 5 | 2021 |
| Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting KK Diaz Perez, SW Curtis, A Sanchis-Juan, X Zhao, ST Head, S Ho, ... medRxiv, 2022.08. 15.22278795, 2022 | 4 | 2022 |
| Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting KKD Perez, SW Curtis, A Sanchis-Juan, X Zhao, T Head, S Ho, B Carter, ... Genetics in Medicine 25 (10), 100918, 2023 | 3 | 2023 |
| Abstract A29: investigation of RECQL variants in European and African American breast cancer cohorts MR Chandler, S Bergstresser, ALW Huskey, E Stallworth, A Davis, ... Molecular Cancer Research 16 (8_Supplement), A29-A29, 2018 | 2 | 2018 |
| Abstract C041: FAN1 splice variant as a possible risk variant for African American hereditary breast cancer and understanding its role in tumorigenesis SR Glover, CMG Sams, M Bishop, T LoBue, I Mcneely, ND Merner Cancer Epidemiology, Biomarkers & Prevention 32 (1_Supplement), C041-C041, 2023 | | 2023 |
| HCAR breast cancer mutations N Merner, C McGuire Sams, K Shepp, J Pugh, M Bishop Auburn University, 2021 | | 2021 |
| Abstract B043: Getting proximate: Facing the truth about African American hereditary breast cancer research–insight from Alabama N Merner, E Stallworth, M Bishop, S Omeler-Fenaud, I McNeely, A Huskey Cancer Epidemiology, Biomarkers & Prevention 29 (6_Supplement_2), B043-B043, 2020 | | 2020 |
| Abstract C041: Complexities of hereditary breast cancer: Investigating a large African American family S Omeler-Fenaud, M Bishop, E Stallworth, I McNeely, N Merner Cancer Epidemiology, Biomarkers & Prevention 29 (6_Supplement_2), C041-C041, 2020 | | 2020 |
| Coding de novo mutations identified by WGS reveal novel orofacial cleft genes MR Bishop, KD Perez, M Sun, S Ho, P Chopra, N Mukhopadhyay, ... bioRxiv, 2020.04. 01.019927, 2020 | | 2020 |
| This information was published in Molecular Genetics and Genomic Medicine in 2018 MR Bishop, A Shah, M Shively, ALW Huskey, SM Omeler, EP Bilgili, ... The establishment of the Alabama Hereditary Cancer Cohort and genetic …, 2018 | | 2018 |
| Investigation of RECQL variants in European and African American breast cancer cohorts. MR Chandler, S Bergstresser, ALW Huskey, E Stallworth, A Davis, ... MOLECULAR CANCER RESEARCH 16 (8), 40-40, 2018 | | 2018 |
| The establishment of the Alabama Hereditary Cancer Cohort and genetic analysis MR Bishop Auburn University, 2018 | | 2018 |
