Barak Markus

1.8k total citations
25 papers, 1.1k citations indexed

About

Barak Markus is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Barak Markus has authored 25 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 10 papers in Genetics and 4 papers in Cell Biology. Recurrent topics in Barak Markus's work include Genetic Mapping and Diversity in Plants and Animals (4 papers), Genetic Associations and Epidemiology (3 papers) and Epigenetics and DNA Methylation (3 papers). Barak Markus is often cited by papers focused on Genetic Mapping and Diversity in Plants and Animals (4 papers), Genetic Associations and Epidemiology (3 papers) and Epigenetics and DNA Methylation (3 papers). Barak Markus collaborates with scholars based in Israel, United States and United Kingdom. Barak Markus's co-authors include Ohad S. Birk, Yaniv Erlich, Melissa Gymrek, Idan Cohen, Alkes L. Price, Hagit Flusser, Haoyang Zeng, Stoyan Georgiev, Mark J. Daly and Andrew J. Sharp and has published in prestigious journals such as Science, Nature Genetics and The Journal of Cell Biology.

In The Last Decade

Barak Markus

25 papers receiving 1.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Barak Markus Israel 16 672 339 147 81 81 25 1.1k
Shiwani Sharma Australia 23 872 1.3× 238 0.7× 88 0.6× 47 0.6× 52 0.6× 56 1.4k
Ulrich Elling Austria 17 1.1k 1.7× 231 0.7× 76 0.5× 54 0.7× 76 0.9× 37 1.4k
Lisa Warner United States 21 693 1.0× 180 0.5× 103 0.7× 107 1.3× 74 0.9× 42 1.2k
Rebecca Rimini Italy 12 694 1.0× 263 0.8× 75 0.5× 69 0.9× 70 0.9× 13 1.1k
Jyoti Srivastava India 14 598 0.9× 152 0.4× 162 1.1× 65 0.8× 70 0.9× 39 963
Christopher M. Adams United States 18 1.1k 1.6× 380 1.1× 196 1.3× 125 1.5× 35 0.4× 29 1.7k
Michael W. Hofmann Germany 19 771 1.1× 145 0.4× 180 1.2× 70 0.9× 56 0.7× 39 1.3k
Hannah M. Brown Australia 25 610 0.9× 329 1.0× 70 0.5× 39 0.5× 124 1.5× 45 1.7k
Yixiao Zhang China 22 1.3k 1.9× 178 0.5× 195 1.3× 70 0.9× 78 1.0× 56 1.7k
Lisa Henry United States 15 1.4k 2.1× 373 1.1× 273 1.9× 140 1.7× 69 0.9× 17 1.9k

Countries citing papers authored by Barak Markus

Since Specialization
Citations

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

Fields of papers citing papers by Barak Markus

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Barak Markus

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

All Works

20 of 20 papers shown
1.
Sousa, Keyla Carstens Marques de, Ricardo Gutiérrez, Tali Shalit, et al.. (2022). Genomic structural plasticity of rodent‐associated Bartonella in nature. Molecular Ecology. 31(14). 3784–3797. 3 indexed citations
2.
Gutiérrez, Ricardo, Tali Shalit, Barak Markus, et al.. (2020). Bartonella kosoyi sp. nov. and Bartonella krasnovii sp. nov., two novel species closely related to the zoonotic Bartonella elizabethae, isolated from black rats and wild desert rodent-fleas. INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY. 70(3). 1656–1665. 24 indexed citations
3.
Paz-Elizur, Tamar, Yael Leitner‐Dagan, Kerstin B. Meyer, et al.. (2019). DNA Repair Biomarker for Lung Cancer Risk and its Correlation With Airway Cells Gene Expression. JNCI Cancer Spectrum. 4(1). pkz067–pkz067. 11 indexed citations
4.
Kaplanis, Joanna, Assaf Gordon, Tal Shor, et al.. (2018). Quantitative analysis of population-scale family trees with millions of relatives. Science. 360(6385). 171–175. 131 indexed citations
5.
Ben‐Moshe, Noa Bossel, Shlomit Gilad, Gili Perry, et al.. (2018). mRNA-seq whole transcriptome profiling of fresh frozen versus archived fixed tissues. BMC Genomics. 19(1). 419–419. 33 indexed citations
6.
Wormser, Ohad, Libe Gradstein, Yuval Yogev, et al.. (2018). Combined CNV, haplotyping and whole exome sequencing enable identification of two distinct novel EYS mutations causing RP in a single inbred tribe. American Journal of Medical Genetics Part A. 176(12). 2695–2703. 2 indexed citations
7.
Georgeson, Joseph M., Tal Ilani, Vladimir Kiss, et al.. (2017). Protein recognition by a pattern-generating fluorescent molecular probe. Nature Nanotechnology. 12(12). 1161–1168. 110 indexed citations
8.
Yagil, Yoram, et al.. (2016). Three Interacting Genomic Loci Incorporating Two Novel Mutations Underlie the Evolution of Diet-induced Diabetes. Molecular Medicine. 22(1). 560–569. 3 indexed citations
9.
Kadir, Rotem, Tamar Harel, Barak Markus, et al.. (2016). ALFY-Controlled DVL3 Autophagy Regulates Wnt Signaling, Determining Human Brain Size. PLoS Genetics. 12(3). e1005919–e1005919. 62 indexed citations
10.
Gymrek, Melissa, Thomas Willems, Audrey Guilmatre, et al.. (2015). Abundant contribution of short tandem repeats to gene expression variation in humans. Nature Genetics. 48(1). 22–29. 245 indexed citations
11.
Flusser, Hagit, Barak Markus, Zamir Shorer, et al.. (2014). A syndrome of congenital microcephaly, intellectual disability and dysmorphism with a homozygous mutation in FRMD4A. European Journal of Human Genetics. 23(12). 1729–1734. 13 indexed citations
12.
Zielinski, Dina, Barak Markus, Mona A. Sheikh, et al.. (2014). OTX2 Duplication Is Implicated in Hemifacial Microsomia. PLoS ONE. 9(5). e96788–e96788. 35 indexed citations
13.
Markus, Barak, et al.. (2013). Deciphering the fine-structure of tribal admixture in the Bedouin population using genomic data. Heredity. 112(2). 182–189. 18 indexed citations
14.
Perez, Yonatan, Libe Gradstein, Hagit Flusser, et al.. (2013). Isolated foveal hypoplasia with secondary nystagmus and low vision is associated with a homozygous SLC38A8 mutation. European Journal of Human Genetics. 22(5). 703–706. 38 indexed citations
15.
Tee, Meng Kian, Neta Loewenthal, Mark Harris, et al.. (2013). Varied Clinical Presentations of Seven Patients With Mutations inCYP11A1Encoding the Cholesterol Side-Chain Cleavage Enzyme, P450scc. The Journal of Clinical Endocrinology & Metabolism. 98(2). 713–720. 37 indexed citations
16.
Volodarsky, Michael, Barak Markus, Idan Cohen, et al.. (2013). A Deletion Mutation in TMEM38B Associated with Autosomal Recessive Osteogenesis Imperfecta. Human Mutation. 34(4). n/a–n/a. 69 indexed citations
17.
Markus, Barak, Ginat Narkis, Daniella Landau, et al.. (2012). Autosomal recessive lethal congenital contractural syndrome type 4 (LCCS4) caused by a mutation in MYBPC1. Human Mutation. 33(10). 1435–1438. 45 indexed citations
18.
Flusser, Hagit, Barak Markus, Ilan Shelef, et al.. (2011). The desmosterolosis phenotype: spasticity, microcephaly and micrognathia with agenesis of corpus callosum and loss of white matter. European Journal of Human Genetics. 19(9). 942–946. 37 indexed citations
19.
Markus, Barak, Iris Noyman, Hagit Flusser, et al.. (2011). Response to Biancheri et al. and Boepsflug-Tanguy et al.: AIMP1/p43 Connatal PMLD. The American Journal of Human Genetics. 88(3). 393–395. 1 indexed citations
20.
Markus, Barak, Iris Noyman, Hagit Flusser, et al.. (2010). Pelizaeus-Merzbacher-like Disease Caused by AIMP1/p43 Homozygous Mutation. The American Journal of Human Genetics. 87(6). 820–828. 62 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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