Yuval Yaron

7.2k total citations
182 papers, 4.8k citations indexed

About

Yuval Yaron is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Yuval Yaron has authored 182 papers receiving a total of 4.8k indexed citations (citations by other indexed papers that have themselves been cited), including 108 papers in Pediatrics, Perinatology and Child Health, 61 papers in Genetics and 45 papers in Molecular Biology. Recurrent topics in Yuval Yaron's work include Prenatal Screening and Diagnostics (88 papers), Genomic variations and chromosomal abnormalities (25 papers) and Assisted Reproductive Technology and Twin Pregnancy (25 papers). Yuval Yaron is often cited by papers focused on Prenatal Screening and Diagnostics (88 papers), Genomic variations and chromosomal abnormalities (25 papers) and Assisted Reproductive Technology and Twin Pregnancy (25 papers). Yuval Yaron collaborates with scholars based in Israel, United States and United Kingdom. Yuval Yaron's co-authors include Avi Orr‐Urtreger, Joseph B. Lessing, Ami Amit, Yifat Ochshorn, Ralph L. Kramer, Mira Malcov, Israel Yovel, Ofer Lehavi, Dalit Ben‐Yosef and Foad Azem and has published in prestigious journals such as Cancer, Cell stem cell and The American Journal of Human Genetics.

In The Last Decade

Yuval Yaron

177 papers receiving 4.6k citations

Peers

Countries citing papers authored by Yuval Yaron

Since Specialization

Citations

This map shows the geographic impact of Yuval Yaron's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Yuval Yaron with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Yuval Yaron more than expected).

Fields of papers citing papers by Yuval Yaron

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yuval Yaron. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Yuval Yaron. The network helps show where Yuval Yaron may publish in the future.

Co-authorship network of co-authors of Yuval Yaron

This figure shows the co-authorship network connecting the top 25 collaborators of Yuval Yaron. A scholar is included among the top collaborators of Yuval Yaron based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Yuval Yaron. Yuval Yaron is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	A multicenter study reveals a novel pathogenic splice-site founder variant in OTOF 2025 ·Human Genomics ·Zippora Brownstein, (unknown), (unknown), (unknown), (unknown), Yoel Hirsch, (unknown), (unknown), Hagar Mor‐Shaked, Bella Davidov, Yuval Yaron, Karen B. Avraham	0
2	Exploring the factors affecting classification and reporting of uncertain prenatal microarray findings, using a “virtual fetus” model‐a pilot study 2024 ·Prenatal Diagnosis ·Rachel Michaelson‐Cohen, (unknown), (unknown), Yuval Yaron, Adi Reches, Hagith Yonath, (unknown), Hagit Shani, Gheona Altarescu, Reeval Segel, Rivka Sukenik‐Halevy, Hagit Daum, Tamar Harel, Vardiella Meiner, Lina Basel‐Salmon, Lena Sagi‐Dain, Idit Maya	1
3	Predictive Factors and Risk Assessment for Hospitalization in Chest Pain Patients Admitted to the Emergency Department 2024 ·Diagnostics ·Nadya Kagansky, (unknown), (unknown), Yuval Yaron, (unknown), Tomer Ziv‐Baran, (unknown), (unknown), Yochai Levy, (unknown)	1
4	Prenatal Diagnosis of a KIDINS220 De Novo Heterozygous Variant in a Fetus With a Complex CNS Anomaly 2024 ·Prenatal Diagnosis ·Hadas Miremberg, R. Birnbaum, (unknown), (unknown), Yuval Yaron, Adi Mory, G. Malinger, Karina Krajden Haratz	0
5	800 Variation in genetic workup of polyhydramnios: An international and inter-specialty survey 2024 ·American Journal of Obstetrics and Gynecology ·Lena Sagi‐Dain, Yuval Yaron, (unknown)	1
6	SMARCC1 is a susceptibility gene for congenital hydrocephalus with an autosomal dominant inheritance mode and incomplete penetrance 2023 ·Prenatal Diagnosis ·(unknown), Alina Kurolap, Adi Mory, Karina Krajden Haratz, Dvora Kidron, G. Malinger, Hagit Baris Feldman, Yuval Yaron	3
7	Upgrading an intronic TMEM67 variant of unknown significance to likely pathogenic through RNA studies and community data sharing 2022 ·Prenatal Diagnosis ·Alina Kurolap, Adi Mory, (unknown), Karina Krajden Haratz, G. Malinger, R. Birnbaum, Hagit Baris Feldman, Yuval Yaron	3
8	Non‐immune hydrops fetalis caused by PIEZO1 compound heterozygous deletions detected only by exome sequencing 2022 ·Prenatal Diagnosis ·(unknown), (unknown), Yoav Yinon, (unknown), Alina Kurolap, Yuval Yaron, Hagit Baris Feldman	1
9	Exome sequencing as first‐tier test for fetuses with severe central nervous system structural anomalies 2022 ·Ultrasound in Obstetrics and Gynecology ·Yuval Yaron, (unknown), Adi Mory, (unknown), Alina Kurolap, Anat Bar Shira, (unknown), Daphna Marom, (unknown), Hagit Baris Feldman, G. Malinger, Karina Krajden Haratz, Adi Reches	48
10	International Society for Prenatal Diagnosis Position Statement: cell free (cf)DNA screening for Down syndrome in multiple pregnancies 2020 ·Prenatal Diagnosis ·Glenn E. Palomaki, Rossa W. K. Chiu, Mark D. Pertile, Erik A. Sistermans, Yuval Yaron, Joris Vermeesch, Neeta L. Vora, Robert G. Best, Louise Wilkins‐Haug	41
11	Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restriction 2012 ·Journal of Medical Genetics ·Agostina De Crescenzo, Angela Sparago, Flavia Cerrato, Orazio Palumbo, Massimo Carella, Marco Miceli, Moshe Bronshtein, Andrea Riccio, Yuval Yaron	33
12	Preimplantation genetic diagnosis for fragile X syndrome: is there increased transmission of abnormal FMR1 alleles among female heterozygotes? 2008 ·Prenatal Diagnosis ·Adi Reches, Mira Malcov, Dalit Ben‐Yosef, Foad Azem, Ami Amit, Yuval Yaron	12
13	Genome-wide expression analysis of cultured trophoblast with trisomy 21 karyotype 2007 ·Human Reproduction ·Uri Rozovski, (unknown), Anat Bar‐Shira, Yifat Ochshorn, Myriam Goldstein, Yuval Yaron	33
14	Detection of Spinal Muscular Atrophy Carriers by Nested Polymerase Chain Reaction of Single Sperm Cells 2006 ·Genetic Testing ·Yuval Yaron, (unknown), (unknown), Tamar Schwartz, Ami Amit, Mira Malcov	4
15	Evidence for blood chimerism in dizygotic spontaneous twin pregnancy discordant for Down syndrome 2006 ·Prenatal Diagnosis ·Stavit Shalev, Eliezer Shalev, Elon Pras, (unknown), Ephraim Gazit, Yuval Yaron, Ron Loewenthal	26
16	Screening for Familial Dysautonomia in Israel: Evidence for Higher Carrier Rate among Polish Ashkenazi Jews 2003 ·Genetic Testing ·Ofer Lehavi, Orna Aizenstein, Dani Bercovich, (unknown), Ruth Shomrat, Avi Orr‐Urtreger, Yuval Yaron	35
17	Spontaneous Abortions in Couples Declining Multifetal Pregnancy Reduction 2002 ·Fetal Diagnosis and Therapy ·Mark I. Evans, Ronald J. Wapner, Melissa A. Ayoub, (unknown), Baruch Feldman, Yuval Yaron	9
18	High Frequency of a Common Bloom Syndrome Ashkenazi Mutation Among Jews of Polish Origin 1998 ·Genetic Testing ·(unknown), Ruth Shomrat, Yuval Yaron, Avi Orr‐Urtreger, Joanna Groden, Cyril Legum	41
19	Selective termination and elective reduction in twin pregnancies: 10 years experience at a single centre 1998 ·Human Reproduction ·Yuval Yaron, (unknown), Peter Bryant-Greenwood, Ralph L. Kramer, Mark P. Johnson, Mark I. Evans	30
20	Genetic Testing for Male Infertility: A Postulated Role for Mutations in Sperm Nuclear Matrix Attachment Regions 1997 ·Genetic Testing ·Jeffrey A. Kramer, Sizhong Zhang, Yuval Yaron, Yali Zhao, Stephen A. Krawetz	24

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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