| The global state of the genetic counseling profession MA Abacan, L Alsubaie, K Barlow-Stewart, B Caanen, C Cordier, ... European Journal of Human Genetics 27 (2), 183-197, 2019 | 312 | 2019 |
| Transcriptome profiling in neurodegenerative disease E Courtney, S Kornfeld, K Janitz, M Janitz Journal of neuroscience methods 193 (2), 189-202, 2010 | 79 | 2010 |
| The influence of Malay cultural beliefs on breast cancer screening and genetic testing: A focus group study T Shaw, D Ishak, D Lie, S Menon, E Courtney, ST Li, J Ngeow Psycho‐Oncology 27 (12), 2855-2861, 2018 | 43 | 2018 |
| Evaluating empowerment in genetic counseling using patient‐reported outcomes J Yuen, SY Lee, E Courtney, J Lim, H Soh, ST Li, Y Chen, M McAllister, ... Clinical genetics 97 (2), 246-256, 2020 | 33 | 2020 |
| Impact of free cancer predisposition cascade genetic testing on uptake in Singapore E Courtney, AKL Chok, ZL Ting Ang, T Shaw, ST Li, J Yuen, J Ngeow NPJ Genomic Medicine 4 (1), 22, 2019 | 32 | 2019 |
| Impact of appointment waiting time on attendance rates at a clinical cancer genetics service T Shaw, J Metras, ZAL Ting, E Courtney, ST Li, J Ngeow Journal of genetic counseling 27, 1473-1481, 2018 | 27 | 2018 |
| Factors influencing the decision to share cancer genetic results among family members: An in‐depth interview study of women in an Asian setting ST Li, S Sun, D Lie, M Met‐Domestici, E Courtney, S Menon, GH Lim, ... Psycho‐Oncology 27 (3), 998-1004, 2018 | 27 | 2018 |
| Germline pathogenic variants in homologous recombination and DNA repair genes in an Asian cohort of young-onset colorectal cancer MR Toh, JB Chiang, ST Chong, SH Chan, NDB Ishak, E Courtney, ... JNCI cancer spectrum 2 (4), pky054, 2018 | 24 | 2018 |
| Predictors of next-generation sequencing panel selection using a shared decision-making approach E Courtney, ST Li, T Shaw, Y Chen, JC Allen Jr, J Ngeow NPJ genomic medicine 3 (1), 11, 2018 | 14 | 2018 |
| Understanding patients' views and willingness toward the use of telehealth in a cancer genetics service in Asia J Sim, T Shaw, ST Li, E Courtney, J Yuen, J Chiang, M Nazir, R Tan, ... Journal of genetic counseling 30 (6), 1658-1670, 2021 | 13 | 2021 |
| Clinical management of pheochromocytoma and paraganglioma in Singapore: missed opportunities for genetic testing WHW Chew, E Courtney, KH Lim, ST Li, Y Chen, MH Tan, A Chung, ... Molecular Genetics & Genomic Medicine 5 (5), 602-607, 2017 | 11 | 2017 |
| An in-depth exploration of the post-test informational needs of BRCA1 and BRCA2 pathogenic variant carriers in Asia J Yuen, SM Fung, CL Sia, M Venkatramani, T Shaw, E Courtney, ST Li, ... Hereditary Cancer in Clinical Practice 18, 1-10, 2020 | 10 | 2020 |
| The impact of coding germline variants on contralateral breast cancer risk and survival A Morra, N Mavaddat, TA Muranen, TU Ahearn, J Allen, IL Andrulis, ... The American Journal of Human Genetics 110 (3), 475-486, 2023 | 9 | 2023 |
| Functional analysis of clinical BARD1 germline variants MR Toh, ST Chong, SH Chan, CE Low, NDB Ishak, JQ Lim, E Courtney, ... Molecular Case Studies 5 (4), a004093, 2019 | 8 | 2019 |
| Risk management adherence following genetic testing for hereditary cancer syndromes: a Singaporean experience E Courtney, XW Chin, J Yuen, ST Li, Y Chen, JC Allen, V Tan, GH Lim, ... Familial Cancer 17, 621-626, 2018 | 8 | 2018 |
| Identifying ataxia‐telangiectasia in cancer patients: Novel insights from an interesting case and review of literature J Cao, RYC Tan, ST Li, E Courtney, RCH Goh, BE Fan, K Sommat, ... Clinical Case Reports 9 (2), 995-1009, 2021 | 7 | 2021 |
| Investigation into the origins of an ancient BRCA1 founder mutation identified among Chinese families in Singapore T Shaw, SH Chan, JX Teo, ST Chong, ST Li, E Courtney, D Ishak, ... International Journal of Cancer 148 (3), 637-645, 2021 | 6 | 2021 |
| Evaluation of the relative effectiveness of the 2017 updated Manchester scoring system for predicting BRCA1/2 mutations in a Southeast Asian country W Chew, RB Moorakonda, E Courtney, H Soh, ST Li, Y Chen, T Shaw, ... Journal of Medical Genetics 55 (5), 344-350, 2018 | 6 | 2018 |
| FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women G Figlioli, A Billaud, TU Ahearn, NN Antonenkova, H Becher, ... European Journal of Human Genetics 31 (5), 578-587, 2023 | 5 | 2023 |
| A delayed diagnosis of Pallister-Hall syndrome in an adult male following the incidental detection of a hypothalamic hamartoma E Courtney, DS Swee, D Ishak, J Ngeow Human Genome Variation 5 (1), 31, 2018 | 5 | 2018 |
