Author

Yuval Yaron

Tel Aviv Sourasky Medical Center - Cited by 8,948 - prenatal diagnosis genetics

Biography

Prof. Yuval Yaron has received his MD in the University of Tel Aviv in 1988. Currently, he is working as the Director of the Prenatal Genetic Diagnosis Unit at the Tel Aviv Medical Center and teaches at the Tel Aviv University. His research has included in vitro fertilization (IVF), biochemical and molecular screening, preimplantation genetic diagnosis  (PGD), chromosomal microarray (CMA), and non-invasive prenatal testing (NIPT). He is serving as an editorial member of Prenatal Diagnosis. He has authored > 200 research articles and chapters in books.
Title
Cited by
Year
An evidence-based scoring system for prioritizing mosaic aneuploid embryos following preimplantation genetic screening
FR Grati, G Gallazzi, L Branca, F Maggi, G Simoni, Y YaronReproductive biomedicine online 36 (4), 442-449, 2018201
115
2018
International Society for Prenatal Diagnosis Position Statement: cell free (cf) DNA screening for Down syndrome in multiple pregnancies
GE Palomaki, RWK Chiu, MD Pertile, EA Sistermans, Y Yaron, ...Prenatal diagnosis 41 (10), 1222-1232, 2020202
45
2020
Preimplantation genetic screening: results of a worldwide web-based survey
A Weissman, G Shoham, Z Shoham, S Fishel, M Leong, Y YaronReproductive biomedicine online (6), 693-700, 2017201
35
2017
Whole-exome sequencing in fetuses with central nervous system abnormalities
A Reches, L Hiersch, S Simchoni, D Barel, R Greenberg, L Ben Sira, ...Journal of Perinatology 38 (10), 1301-1308, 2018201
35
2018
Does the number of previous miscarriages influence the incidence of chromosomal aberrations in spontaneous pregnancy loss?
M Goldstein, R Svirsky, A Reches, Y YaronThe Journal of Maternal-Fetal & Neonatal Medicine 30 (24), 2956-2960, 2017201
32
2017
Understanding attitudes and behaviors towards cell-free DNA-based noninvasive prenatal testing (NIPT): a survey of European health-care providers
A Benachi, J Caffrey, P Calda, E Carreras, JC Jani, MD Kilby, HG Klein, ...European Journal of Medical Genetics 63 (1), 103616, 2020202
32
2020
Dilemmas in genetic counseling for low-penetrance neuro-susceptibility loci detected on prenatal chromosomal microarray analysis
D Brabbing-Goldstein, A Reches, R Svirsky, A Bar-Shira, Y YaronAmerican Journal of Obstetrics and Gynecology 218 (2), 247. e1-247. e12, 2018201
27
2018
Maternal plasma genome-wide cell-free DNA can detect fetal aneuploidy in early and recurrent pregnancy loss and can be used to direct further workup
Y Yaron, M Pauta, C Badenas, A Soler, V Borobio, C Illanes, F Paz-y-Miño, ...Human Reproduction 35 (5), 1222-1229, 2020202
21
2020
Oncofertility: insights from IVF specialists—a worldwide web-based survey analysis
G Shoham, R Levy-Toledano, M Leong, A Weissman, Y Yaron, Z ShohamJournal of assisted reproduction and genetics 36, 1013-1021, 2019201
16
2019
Exome sequencing as first‐tier test for fetuses with severe central nervous system structural anomalies
Y Yaron, V Ofen Glassner, A Mory, N Zunz Henig, A Kurolap, A Bar Shira, ...Ultrasound in Obstetrics & Gynecology 60 (1), 59-67, 2022202
15
2022
The genetic and clinical outcome of isolated fetal muscular ventricular septal defect (VSD)
R Svirsky, D Brabbing-Goldstein, U Rozovski, L Kapusta, A Reches, ...The Journal of Maternal-Fetal & Neonatal Medicine 32 (17), 2837-2841, 2019201
11
2019
Parental origin of the retained X chromosome in monosomy X miscarriages and ongoing pregnancies
M Grande, I Stergiotou, M Pauta, B Marquès, C Badenas, A Soler, ...Fetal Diagnosis and Therapy 45 (2), 118-124, 2019201
7
2019
Response: how PGS/PGT-A laboratories succeeded in losing all credibility
FR Grati, G Gallazzi, L Branca, F Maggi, G Simoni, Y YaronReproductive BioMedicine Online 7 (2), 246, 2018201
3
2018
Improving preimplantation genetic diagnosis (PGD) reliability by selection of sperm donor with the most informative haplotype
M Malcov, V Gold, S Peleg, T Frumkin, F Azem, A Amit, D Ben-Yosef, ...Reproductive Biology and Endocrinology 15 (1), 1-8, 2017201
3
2017
Paz-Y-Miño, F.; Martinez-Portilla, R.; Borrell, A. Maternal plasma genome-wide cell-free DNA can detect fetal aneuploidy in early and recurrent pregnancy loss and can be used …
Y Yaron, M Pauta, C Badenas, A Soler, V Borobio, C IllanesHum. Reprod 5, 1222-1229, 2020202
3
2020
Economic impact of using maternal plasma cell‐free DNA testing to guide further workup in recurrent pregnancy loss
S Peng, S Bhatt, A Borrell, Y YaronPrenatal Diagnosis 41 (10), 1215-1221, 2021202
3
2021
Improving renal phenotype and evolving extra-renal features of 17q12 deletion encompassing the HNF1B gene
R Cleper, A Reches, D Shapira, S Simchoni, L Reisman, L Ben-Sira, ...Translational Pediatrics 10 (12), 10, 2021202
3
2021
Can We Learn from the “Wisdom of the Crowd”? Finding the Sample-Size Sweet Spot–an Analysis of Internet-Based Crowdsourced Surveys of Fertility Professionals
G Shoham, M Leong, A Weissman, Y YaronJournal of Medical Statistics Informatics 30 (1), 3, 01901
2
2019
Familial Beckwith-Wiedemann syndrome: Prenatal manifestation and a possible expansion of the phenotype
D Brabbing-Goldstein, Y Yaron, A RechesEuropean Journal of Medical Genetics 64 (), 104137, 010
2
2021
Non‐immune hydrops fetalis caused by PIEZO1 compound heterozygous deletions detected only by exome sequencing
S Reytan, N Zunz Henig, Y Yinon, H Avnet, A Kurolap, Y Yaron, ...Prenatal Diagnosis 4 (7), 890-893, 0
2
2022

Referred From: https://scholar.google.com/citations?user=ZM0bKhAAAAAJ&hl=en

Cited by
Citations 8948
h-index 48
i10-index 157
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