Manuela Vecsler

708 total citations
11 papers, 524 citations indexed

About

Manuela Vecsler is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Manuela Vecsler has authored 11 papers receiving a total of 524 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Cognitive Neuroscience. Recurrent topics in Manuela Vecsler's work include Genetics and Neurodevelopmental Disorders (4 papers), Pharmacogenetics and Drug Metabolism (3 papers) and Autism Spectrum Disorder Research (3 papers). Manuela Vecsler is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Pharmacogenetics and Drug Metabolism (3 papers) and Autism Spectrum Disorder Research (3 papers). Manuela Vecsler collaborates with scholars based in Israel, United States and Belgium. Manuela Vecsler's co-authors include Eva Gak, Hillel Halkin, Shlomo Almog, Ronen Loebstein, Daniel Kurnik, Ninette Amariglio, Gideon Rechavi, Boleslav Goldman, Bruria Ben Zeev and Andreea Nissenkorn and has published in prestigious journals such as Blood, PLoS ONE and Epilepsia.

In The Last Decade

Manuela Vecsler

10 papers receiving 509 citations

Peers

Manuela Vecsler

PHARM

EDM

GENET

BIOCH

Zhuoshan Huang China

Barton Cobert United States

Michael P. Endsley United States

Vladimir O. Pustylnyak Russia

Fjodor H. van der Sluijs Netherlands

T Matsunaga Japan

Adolfo Cruz Spain

Yathindar S. Rao United States

Şükrü Aynacıoğlu Türkiye

Shaojun Mei United States

Zhuoshan Huang China

Manuela Vecsler

109 ×0.4

PHARM

113 ×0.7

46 ×0.3

EDM

46 ×0.4

GENET

24 ×0.3

BIOCH

Citations per year, relative to Manuela Vecsler Manuela Vecsler (= 1×) peers Zhuoshan Huang

Countries citing papers authored by Manuela Vecsler

Since Specialization

Citations

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

Fields of papers citing papers by Manuela Vecsler

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manuela Vecsler

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

All Works

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11 of 11 papers shown

Cyrta, Joanna, Vincent Cockenpot, Rita Canas‐Marques, et al.. (2024). 65P Multi-site European study of a fully automated artificial intelligence solution for HER2 IHC scoring in breast cancer. ESMO Open. 9. 103071–103071.

Cohen, Meital, et al.. (2013). Unbiased transcriptome signature of in vivo cell proliferation reveals pro- and antiproliferative gene networks. Cell Cycle. 12(18). 2992–3000. 20 indexed citations

Vecsler, Manuela, et al.. (2013). Using Standard Optical Flow Cytometry for Synchronizing Proliferating Cells in the G1 Phase. PLoS ONE. 8(12). e83935–e83935. 16 indexed citations

Vecsler, Manuela, et al.. (2013). Gas2l3, a Novel Constriction Site-Associated Protein Whose Regulation Is Mediated by the APC/CCdh1 Complex. PLoS ONE. 8(2). e57532–e57532. 20 indexed citations

Vecsler, Manuela, Bruria Ben Zeev, Igor Nudelman, et al.. (2011). Ex Vivo Treatment with a Novel Synthetic Aminoglycoside NB54 in Primary Fibroblasts from Rett Syndrome Patients Suppresses MECP2 Nonsense Mutations. PLoS ONE. 6(6). e20733–e20733. 42 indexed citations

Vecsler, Manuela, Anthony Simon, Ninette Amariglio, Gideon Rechavi, & Eva Gak. (2010). MeCP2 deficiency down-regulates specific nuclear proteins that could be partially recovered by valproic acid in vitro. Epigenetics. 5(1). 61–67. 23 indexed citations

Nissenkorn, Andreea, et al.. (2010). Epilepsy in Rett syndrome—The experience of a National Rett Center. Epilepsia. 51(7). 1252–1258. 68 indexed citations

Vecsler, Manuela, Ronen Loebstein, Shlomo Almog, et al.. (2006). Combined genetic profiles of components and regulators of the vitamin K-dependent γ-carboxylation system affect individual sensitivity to warfarin. Thrombosis and Haemostasis. 95(2). 205–211. 128 indexed citations

Loebstein, Ronen, Hillel Halkin, Manuela Vecsler, et al.. (2006). A coding VKORC1 Asp36Tyr polymorphism predisposes to warfarin resistance. Blood. 109(6). 2477–2480. 125 indexed citations

10.

Greenbaum, Ira F., Manuela Vecsler, Boleslaw Goldman, et al.. (2006). Comprehensive diagnosis of Rett’s syndrome relying on genetic, epigenetic and expression evidence of deficiency of the methyl-CpG-binding protein 2 gene: study of a cohort of Israeli patients. Journal of Medical Genetics. 43(12). e56–e56. 14 indexed citations

11.

Loebstein, Ronen, Manuela Vecsler, Daniel Kurnik, et al.. (2005). Common genetic variants of microsomal epoxide hydrolase affect warfarin dose requirements beyond the effect of cytochrome P450 2C9. Clinical Pharmacology & Therapeutics. 77(5). 365–372. 68 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.

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