Shamir Zenvirt

1.7k total citations
22 papers, 1.2k citations indexed

About

Shamir Zenvirt is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Shamir Zenvirt has authored 22 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 12 papers in Genetics and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Shamir Zenvirt's work include Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Fetal and Pediatric Neurological Disorders (4 papers). Shamir Zenvirt is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Fetal and Pediatric Neurological Disorders (4 papers). Shamir Zenvirt collaborates with scholars based in Israel, United States and Germany. Shamir Zenvirt's co-authors include Avraham Shaag, Orly Elpeleg, Simon Edvardson, Asaf Ta‐Shma, Yuval Cinnamon, Albert Taraboulos, Klaus H. Kaestner, Gregory J. Hannon, Yaniv Erlich and Chaim Jalas and has published in prestigious journals such as Blood, PLoS ONE and Genetics.

In The Last Decade

Shamir Zenvirt

21 papers receiving 1.2k citations

Peers

Shamir Zenvirt

MB

GENET

CMN

NEURO

CB

Sharon Zeligson Israel

Chaim Jalas United States

Tommaso Pippucci Italy

Éléonore Eymard-Pierre France

Wojciech Wiszniewski United States

Thomas F. Wienker Germany

Francisco Martı́nez Spain

Christel Thauvin‐Robinet France

Mingyan Fang China

Mark E. Samuels Canada

Sharon Zeligson Israel

Shamir Zenvirt

731 ×1.2

MB

281 ×0.8

GENET

167 ×0.8

CMN

227 ×1.1

NEURO

77 ×0.4

CB

Citations per year, relative to Shamir Zenvirt Shamir Zenvirt (= 1×) peers Sharon Zeligson

Countries citing papers authored by Shamir Zenvirt

Since Specialization

Citations

This map shows the geographic impact of Shamir Zenvirt'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 Shamir Zenvirt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Shamir Zenvirt more than expected).

Fields of papers citing papers by Shamir Zenvirt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Shamir Zenvirt. 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 Shamir Zenvirt. The network helps show where Shamir Zenvirt may publish in the future.

Co-authorship network of co-authors of Shamir Zenvirt

This figure shows the co-authorship network connecting the top 25 collaborators of Shamir Zenvirt. A scholar is included among the top collaborators of Shamir Zenvirt 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 Shamir Zenvirt. Shamir Zenvirt is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

1.

Slovik, Maya, Shamir Zenvirt, Ilana Livyatan, et al.. (2025). High Concordance of Copy Number Variants Detected by Chromosomal Microarray and Exome Sequencing in Clinical Diagnostics. Clinical Genetics. 109(3). 529–538.

2.

Meiner, Vardiella, Simcha Yagel, Shamir Zenvirt, et al.. (2020). Universal chromosomal microarray analysis reveals high proportion of copy‐number variants in low‐risk pregnancies. Ultrasound in Obstetrics and Gynecology. 57(5). 813–820. 29 indexed citations

3.

Daum, Hagit, M. Nadjari, Shamir Zenvirt, et al.. (2018). Role of late amniocentesis in the era of modern genomic technologies. Ultrasound in Obstetrics and Gynecology. 53(5). 676–685. 23 indexed citations

4.

Cinnamon, Yuval, Yaacov Barak, Avraham Shaag, et al.. (2015). Deleterious mutation in SYCE1 is associated with non-obstructive azoospermia. Journal of Assisted Reproduction and Genetics. 32(6). 887–891. 88 indexed citations

5.

Edvardson, Simon, Shimrit Oz, Avraham Shaag, et al.. (2013). Early infantile epileptic encephalopathy associated with a high voltage gated calcium channelopathy. Journal of Medical Genetics. 50(2). 118–123. 55 indexed citations

6.

Ta‐Shma, Asaf, Ciro Leonardo Pierri, Polina Stepensky, et al.. (2013). Isolated truncus arteriosus associated with a mutation in the plexin‐D1 gene. American Journal of Medical Genetics Part A. 161(12). 3115–3120. 30 indexed citations

7.

Stepensky, Polina, Ann Saada, Marianne Cowan, et al.. (2013). The Thr224Asn mutation in the VPS45 gene is associated with the congenital neutropenia and primary myelofibrosis of infancy. Blood. 121(25). 5078–5087. 44 indexed citations

8.

Nevo, Yoram, Bruria Ben‐Zeev, Adi Tabib, et al.. (2012). CD59 deficiency is associated with chronic hemolysis and childhood relapsing immune-mediated polyneuropathy. Blood. 121(1). 129–135. 111 indexed citations

9.

Spiegel, Ronen, Ophry Pines, Asaf Ta‐Shma, et al.. (2012). Infantile Cerebellar-Retinal Degeneration Associated with a Mutation in Mitochondrial Aconitase, ACO2. The American Journal of Human Genetics. 90(3). 518–523. 76 indexed citations

10.

Edvardson, Simon, Martina Mühlenhoff, Oliver Stephan, et al.. (2012). West syndrome caused by ST3Gal‐III deficiency. Epilepsia. 54(2). e24–7. 58 indexed citations

11.

Aker, Memet, Alex Rouvinski, Asaf Ta‐Shma, et al.. (2012). An SNX10 mutation causes malignant osteopetrosis of infancy. Journal of Medical Genetics. 49(4). 221–226. 78 indexed citations

12.

Edvardson, Simon, Yuval Cinnamon, Asaf Ta‐Shma, et al.. (2012). A Deleterious Mutation in DNAJC6 Encoding the Neuronal-Specific Clathrin-Uncoating Co-Chaperone Auxilin, Is Associated with Juvenile Parkinsonism. PLoS ONE. 7(5). e36458–e36458. 217 indexed citations

13.

Edvardson, Simon, Chaim Jalas, Avraham Shaag, et al.. (2011). A deleterious mutation in the LOXHD1 gene causes autosomal recessive hearing loss in Ashkenazi Jews. American Journal of Medical Genetics Part A. 155(5). 1170–1172. 29 indexed citations

14.

Erlich, Yaniv, Simon Edvardson, Emily Hodges, et al.. (2011). Exome sequencing and disease-network analysis of a single family implicate a mutation in KIF1A in hereditary spastic paraparesis. Genome Research. 21(5). 658–664. 134 indexed citations

15.

Ben‐Neriah, Ziva, Rachel Michaelson‐Cohen, Michal Inbar‐Feigenberg, et al.. (2011). A deleterious founder mutation in the BMPER gene causes diaphanospondylodysostosis (DSD). American Journal of Medical Genetics Part A. 155(11). 2801–2806. 10 indexed citations

16.

Berger, Itai, Ziva Ben‐Neriah, Avraham Shaag, et al.. (2011). Early prenatal ventriculomegaly due to an AIFM1 mutation identified by linkage analysis and whole exome sequencing. Molecular Genetics and Metabolism. 104(4). 517–520. 75 indexed citations

17.

Straussberg, Rachel, Hanna Mandel, Aviva Fattal‐Valevski, et al.. (2010). Infantile Cerebral and Cerebellar Atrophy Is Associated with a Mutation in the MED17 Subunit of the Transcription Preinitiation Mediator Complex. The American Journal of Human Genetics. 87(5). 667–670. 58 indexed citations

18.

Edvardson, Simon, Avraham Shaag, Shamir Zenvirt, et al.. (2010). Joubert Syndrome 2 (JBTS2) in Ashkenazi Jews Is Associated with a TMEM216 Mutation. The American Journal of Human Genetics. 86(2). 294–294. 4 indexed citations

19.

Edvardson, Simon, Avraham Shaag, Shamir Zenvirt, et al.. (2010). Joubert Syndrome 2 (JBTS2) in Ashkenazi Jews Is Associated with a TMEM216 Mutation. The American Journal of Human Genetics. 86(1). 93–97. 73 indexed citations

20.

Zenvirt, Shamir, Yael Nevo‐Caspi, Sigal Rencus‐Lazar, & Daniel Segal. (2008). Drosophila LIM-Only Is a Positive Regulator of Transcription During Thoracic Bristle Development. Genetics. 179(4). 1989–1999. 7 indexed citations

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.

Explore authors with similar magnitude of impact