| Targeted prostate cancer screening in BRCA1 and BRCA2 mutation carriers: results from the initial screening round of the IMPACT study EK Bancroft, EC Page, E Castro, H Lilja, A Vickers, D Sjoberg, M Assel, ... European urology 66 (3), 489-499, 2014 | 311 | 2014 |
| Interim results from the IMPACT study: evidence for prostate-specific antigen screening in BRCA2 mutation carriers EC Page, EK Bancroft, MN Brook, M Assel, MH Al Battat, S Thomas, ... European urology 76 (6), 831-842, 2019 | 250 | 2019 |
| Opportunistic genomic screening. Recommendations of the European society of human genetics G de Wert, W Dondorp, A Clarke, EMC Dequeker, C Cordier, Z Deans, ... European Journal of Human Genetics 29 (3), 365-377, 2021 | 138 | 2021 |
| Global public perceptions of genomic data sharing: what shapes the willingness to donate DNA and health data? A Middleton, R Milne, MA Almarri, S Anwer, J Atutornu, EE Baranova, ... The American Journal of Human Genetics 107 (4), 743-752, 2020 | 132 | 2020 |
| Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics D Carrieri, HC Howard, C Benjamin, AJ Clarke, S Dheensa, S Doheny, ... European Journal of Human Genetics 27 (2), 169-182, 2019 | 94 | 2019 |
| Preferences for prenatal tests for Down syndrome: an international comparison of the views of pregnant women and health professionals M Hill, JA Johnson, S Langlois, H Lee, S Winsor, B Dineley, M Horniachek, ... European Journal of Human Genetics 24 (7), 968-975, 2016 | 91 | 2016 |
| The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice F Forzano, O Antonova, A Clarke, G de Wert, S Hentze, Y Jamshidi, ... European Journal of Human Genetics 30 (5), 493-495, 2022 | 76 | 2022 |
| Demonstrating trustworthiness when collecting and sharing genomic data: public views across 22 countries R Milne, KI Morley, MA Almarri, S Anwer, J Atutornu, EE Baranova, ... Genome medicine 13 (1), 92, 2021 | 50 | 2021 |
| Oestrogen receptor status, treatment and breast cancer prognosis in Icelandic BRCA2 mutation carriers JG Jonasson, OA Stefansson, OT Johannsson, H Sigurdsson, ... British journal of cancer 115 (7), 776-783, 2016 | 49 | 2016 |
| Effects of knowledge, education, and experience on acceptance of first trimester screening for chromosomal anomalies V Stefansdottir, H Skirton, K Jonasson, H Hardardottir, JJ Jonsson Acta obstetricia et gynecologica Scandinavica 89 (7), 931-938, 2010 | 44 | 2010 |
| The Gen-Equip Project: evaluation and impact of genetics e-learning resources for primary care in six European languages L Jackson, A O’Connor, M Paneque, V Curtisova, PW Lunt, RK Pourova, ... Genetics in Medicine 21 (3), 718-726, 2019 | 32 | 2019 |
| Implementing genetic education in primary care: the Gen-Equip programme M Paneque, MC Cornel, V Curtisova, E Houwink, L Jackson, A Kent, ... Journal of Community Genetics 8 (2), 147-150, 2017 | 29 | 2017 |
| Web-based return of BRCA2 research results: one-year genetic counselling experience in Iceland V Stefansdottir, E Thorolfsdottir, HB Hognason, C Patch, C van El, ... European Journal of Human Genetics 28 (12), 1656-1661, 2020 | 23 | 2020 |
| Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition C Mikropoulos, CGH Selkirk, S Saya, E Bancroft, E Vertosick, T Dadaev, ... British Journal of Cancer 118 (2), 266-276, 2018 | 19 | 2018 |
| The use of genealogy databases for risk assessment in genetic health service: a systematic review V Stefansdottir, OT Johannsson, H Skirton, L Tryggvadottir, H Tulinius, ... Journal of community genetics 4, 1-7, 2013 | 18 | 2013 |
| Experience of social media support group for BRCA carriers V Stefansdottir Journal of genetic counseling 25 (6), 1342-1344, 2016 | 12 | 2016 |
| Iceland—Genetic Counseling Services V Stefansdottir, R Arngrimsson, JJ Jonsson Journal of genetic counseling 22, 907-910, 2013 | 11 | 2013 |
| Return of genomic results does not motivate intent to participate in research for all: Perspectives across 22 countries R Milne, KI Morley, MA Almarri, J Atutornu, EE Baranova, P Bevan, ... Genetics in Medicine 24 (5), 1120-1129, 2022 | 10 | 2022 |
| Molecular genetics of inherited retinal degenerations in Icelandic patients DA Thorsteinsson, V Stefansdottir, T Eysteinsson, S Thorisdottir, ... Clinical genetics 100 (2), 156-167, 2021 | 9 | 2021 |
| A population-based survey of FBN1 variants in Iceland reveals underdiagnosis of Marfan syndrome EO Klemenzdottir, GA Arnadottir, BO Jensson, A Jonasdottir, ... European Journal of Human Genetics 32 (1), 44-51, 2024 | 8 | 2024 |
Heather SkirtonProfessor of Applied Health Genetics, Plymouth UniversityEmail verificata su plymouth.ac.uk
