| 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 | 376 | 2019 |
| The fertility myth: Israeli students' knowledge regarding age-related fertility decline and late pregnancies in an era of assisted reproduction technology Y Hashiloni-Dolev, A Kaplan, S Shkedi-Rafid Human reproduction 26 (11), 3045-3053, 2011 | 141 | 2011 |
| Egg freezing for age-related fertility decline: preventive medicine or a further medicalization of reproduction? Analyzing the new Israeli policy S Shkedi-Rafid, Y Hashiloni-Dolev Fertility and sterility 96 (2), 291-294, 2011 | 108 | 2011 |
| Health-care professionals’ responsibility to patients’ relatives in genetic medicine: a systematic review and synthesis of empirical research S Dheensa, A Fenwick, S Shkedi-Rafid, G Crawford, A Lucassen Genetics in Medicine 18 (4), 290-301, 2016 | 103 | 2016 |
| Defining and managing incidental findings in genetic and genomic practice S Shkedi-Rafid, S Dheensa, G Crawford, A Fenwick, A Lucassen Journal of medical genetics 51 (11), 715-723, 2014 | 79 | 2014 |
| On new reproductive technologies and family ethics: Pre-implantation genetic diagnosis for sibling donor in Israel and Germany Y Hashiloni-Dolev, S Shkedi Social Science & Medicine 65 (10), 2081-2092, 2007 | 75 | 2007 |
| Fetal exome sequencing: yield and limitations in a tertiary referral center H Daum, V Meiner, O Elpeleg, T Harel, Collaborating Authors, L Bar‐Or, ... Ultrasound in Obstetrics & Gynecology 53 (1), 80-86, 2019 | 60 | 2019 |
| Egg freezing for non-medical uses: the lack of a relational approach to autonomy in the new Israeli policy and in academic discussion S Shkedi-Rafid, Y Hashiloni-Dolev Journal of Medical Ethics 38 (3), 154-157, 2012 | 53 | 2012 |
| Role of late amniocentesis in the era of modern genomic technologies H Daum, A Ben David, M Nadjari, S Zenvirt, S Helman, N Yanai, V Meiner, ... Ultrasound in obstetrics & Gynecology 53 (5), 676-685, 2019 | 38 | 2019 |
| Psychiatric genetic counseling: A mapping exercise R Moldovan, KA McGhee, D Coviello, A Hamang, A Inglis, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 180 …, 2019 | 34 | 2019 |
| BRCA genetic testing of individuals from families with low prevalence of cancer: experiences of carriers and implications for population screening S Shkedi-Rafid, E Gabai-Kapara, J Grinshpun-Cohen, E Levy-Lahad Genetics in medicine 14 (7), 688-694, 2012 | 33 | 2012 |
| Genetic testing of children for adult-onset conditions: opinions of the British adult population and implications for clinical practice S Shkedi-Rafid, A Fenwick, S Dheensa, AM Lucassen European Journal of Human Genetics 23 (10), 1281-1285, 2015 | 31 | 2015 |
| Universal chromosomal microarray analysis reveals high proportion of copy‐number variants in low‐risk pregnancies S Stern, N Hacohen, V Meiner, S Yagel, S Zenvirt, S Shkedi‐Rafid, ... Ultrasound in Obstetrics & Gynecology 57 (5), 813-820, 2021 | 28 | 2021 |
| What results to disclose, when, and who decides? Healthcare professionals' views on prenatal chromosomal microarray analysis S Shkedi‐Rafid, A Fenwick, S Dheensa, D Wellesley, AM Lucassen Prenatal diagnosis 36 (3), 252-259, 2016 | 27 | 2016 |
| Mild phenotype of wolfram syndrome associated with a common pathogenic variant is predicted by a structural model of wolframin A Wilf-Yarkoni, O Shor, A Fellner, MA Hellmann, E Pras, H Yonath, ... Neurology: Genetics 7 (2), e578, 2021 | 18 | 2021 |
| What is the meaning of a ‘genomic result’in the context of pregnancy? S Shkedi-Rafid, R Horton, A Lucassen European Journal of Human Genetics 29 (2), 225-230, 2021 | 13 | 2021 |
| Information women choose to receive about prenatal chromosomal microarray analysis H Hochner, H Daum, L Douiev, N Zvi, A Frumkin, M Macarov, ... Obstetrics & Gynecology 135 (1), 149-157, 2020 | 13 | 2020 |
| Clinicians' attitudes toward general screening of the Ashkenazi-Jewish population for prevalent founder BRCA1/2 and LRRK2 mutations S Shkedi-Rafid, G Ofer-Bialer, V Meiner, R Calderon-Margalit Public Health Genomics 16 (4), 174-183, 2013 | 10 | 2013 |
| Cancer patients’ understandings of genetic variants of uncertain significance in clinical care Y Amano, A Raz, S Timmermans, S Shkedi-Rafid Journal of community genetics 13 (4), 381-388, 2022 | 9 | 2022 |
| Personalized prenatal genomic testing: Couples' experience with choice regarding uncertain and adult‐onset findings from chromosomal‐microarray‐analysis T Millo, L Douiev, D Popper, S Shkedi‐Rafid Prenatal Diagnosis 41 (3), 376-383, 2021 | 9 | 2021 |
