S. Shkedi-Rafid

发表

Is it time for prenatal chromosomal-microarray analysis to all women? A review of the diagnostic yield in structurally normal fetuses

H. Daum, S. Stern, S. Shkedi-Rafid, 2021, Current opinion in obstetrics & gynecology.

Information Women Choose to Receive About Prenatal Chromosomal Microarray Analysis.

H. Daum, A. Frumkin, S. Shkedi-Rafid, 2019, Obstetrics and gynecology.

Clinicians’ attitudes towards parental choice in the era of advanced genomic tests in pregnancy

V. Meiner, S. Shkedi-Rafid, H. Hochner, 2021, Prenatal diagnosis.

Psychiatric genetic counseling: A mapping exercise

K. McGhee, R. Moldovan, B. Meiser, 2019, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Egg freezing for age-related fertility decline: preventive medicine or a further medicalization of reproduction? Analyzing the new Israeli policy.

Yael Hashiloni-Dolev, S. Shkedi-Rafid, 2011, Fertility and sterility.

Mild Phenotype of Wolfram Syndrome Associated With a Common Pathogenic Variant Is Predicted by a Structural Model of Wolframin

R. Eliahou, Y. Goldberg, E. Pras, 2021, Neurology: Genetics.

Common founder BRCA2 pathogenic variants and breast cancer characteristics in Ethiopian Jews

S. Carmi, Y. Goldberg, I. Kedar, 2022, Breast Cancer Research and Treatment.

Fragmented responsibility: views of Israeli HCPs regarding patient recontact following variant reclassification

Aviad E. Raz, S. Timmermans, S. Shkedi-Rafid, 2021, Journal of Community Genetics.

Personalized prenatal genomic testing: Couples' experience with choice regarding uncertain and adult‐onset findings from chromosomal‐microarray‐analysis

S. Shkedi-Rafid, Liza Douiev, Talya Millo, 2020, Prenatal diagnosis.

Cancer patients’ understandings of genetic variants of uncertain significance in clinical care

Aviad E. Raz, S. Timmermans, S. Shkedi-Rafid, 2022, Journal of Community Genetics.

What results to disclose, when, and who decides? Healthcare professionals' views on prenatal chromosomal microarray analysis†

Sandi Dheensa, A. Lucassen, A. Fenwick, 2016, Prenatal diagnosis.

Postpartum women's attitudes to disclosure of adult‐onset conditions in pregnancy

S. Israel, Y. Friedlander, A. Frumkin, 2022, Prenatal diagnosis.

Genetic testing of children for adult-onset conditions: opinions of the British adult population and implications for clinical practice

Sandi Dheensa, A. Lucassen, A. Fenwick, 2014, European Journal of Human Genetics.

Management of Incidental Findings in Clinical Genomic Sequencing Studies

G. Bertier, Sandi Dheensa, A. Lucassen, 2016 .

The fertility myth: Israeli students' knowledge regarding age-related fertility decline and late pregnancies in an era of assisted reproduction technology.

Amit Kaplan, Yael Hashiloni-Dolev, S. Shkedi-Rafid, 2011, Human reproduction.

Egg freezing for non-medical uses: the lack of a relational approach to autonomy in the new Israeli policy and in academic discussion

Yael Hashiloni-Dolev, S. Shkedi-Rafid, 2011, Journal of Medical Ethics.

Universal chromosomal microarray analysis reveals high proportion of copy‐number variants in low‐risk pregnancies

D. Valsky, H. Daum, A. Frumkin, 2020, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

What is the meaning of a ‘genomic result’ in the context of pregnancy?

Rachel H Horton, A. Lucassen, S. Shkedi-Rafid, 2020, European Journal of Human Genetics.

Defining and managing incidental findings in genetic and genomic practice

Sandi Dheensa, A. Lucassen, A. Fenwick, 2014, Journal of Medical Genetics.

Health-care professionals' responsibility to patients' relatives in genetic medicine: a systematic review and synthesis of empirical research

Sandi Dheensa, A. Lucassen, A. Fenwick, 2015, Genetics in Medicine.

The Global State of the Genetic Counseling Profession

A. Obregon-Tito, K. Ormond, R. Moldovan, 2018, European Journal of Human Genetics.

Pregnant Genetic Counselors in an Era of Advanced Genomic Tests: What Do the Experts Test Prenatally?

Yael Hashiloni-Dolev, S. Shkedi-Rafid, 2018, Journal of Genetic Counseling.

Views of Israeli healthcare professionals regarding communication of genetic variants of uncertain significance to patients

Aviad E. Raz, S. Timmermans, S. Shkedi-Rafid, 2022, Journal of genetic counseling.

Detection of copy number variants associated with late-onset conditions in ~16 200 pregnancies: parameters for disclosure and pregnancy outcome

H. Daum, A. Frumkin, V. Meiner, 2022, Journal of Medical Genetics.

BRCA genetic testing of individuals from families with low prevalence of cancer: experiences of carriers and implications for population screening

E. Levy-Lahad, S. Shkedi-Rafid, E. Gabai-Kapara, 2012, Genetics in Medicine.

Receiving uncertain results from prenatal chromosomal microarray analysis: Women's decisions on continuation or termination of pregnancy

Y. Friedlander, S. Shkedi-Rafid, H. Hochner, 2023, Prenatal diagnosis.

Clinicians' Attitudes toward General Screening of the Ashkenazi-Jewish Population for Prevalent Founder BRCA1/2 and LRRK2 Mutations

V. Meiner, R. Calderon-Margalit, S. Shkedi-Rafid, 2013, Public Health Genomics.

Rescue Obligations and Collective Approaches: Complexities in Genomics

A. Lucassen, A. Fenwick, G. Crawford, 2015, The American journal of bioethics : AJOB.

Relative Risk and Relatives' Risks in Genomic Medicine

Anneke Lucassen, A. Lucassen, A. Fenwick, 2016, The American journal of bioethics : AJOB.

Fetal exome sequencing: yield and limitations in a tertiary referral center

D. Lev, T. Harel, H. Daum, 2019, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.