Barak Markus

1.8k citations
26 papers · 1.3k · h-index 17

Impact in

  • Aging top 5%
  • Genetics top 5%
    • Genetic Associations and Epidemiology
    • Genomics and Rare Diseases
    • Genetics and Neurodevelopmental Disorders
    • Connective tissue disorders research
    • Genomic variations and chromosomal abnormalities
    • Forensic and Genetic Research

Papers in

    • Genomics and Rare Diseases 4
    • Genetic Associations and Epidemiology 4
    • Genetic Mapping and Diversity in Plants and Animals 2
    • Genetics and Neurodevelopmental Disorders 2
    • Bartonella species infections research 3

Barak Markus

26 papers receiving 1.3k citations

Peers

Barak Markus
Comparison fields: 5 of 108
  • Aging 47
  • Genetics 465
  • Clinical Biochemistry 32
  • Molecular Biology 409
  • Cell Biology 86
Replace Péter L. Nagy with:
Péter L. Nagy United States
Chong‐Feng Xu United States
János Kovács Hungary
Maria Angela C. Dani Brazil
James A. Letts United States
Richard Burke Australia
István Horváth Sweden
Bassam Abu‐Libdeh Israel
John S. Satterlee United States
David U. Mick Germany
Barak Markus relative to Péter L. Nagy United States Péter L. Nagy's profile →
Citations per field
00.5×2×4×5.9×
Péter L. Nagy · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Barak Markus, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Barak Markus Line = papers co-authored together Barak Markus links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 26 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2015262
2 2018163
3 2017126
4 201382
5 201074
6 201673
7 201468
8 201354
9 201853
10 201248
11 201146
12 201443
13 201342
14 201842
15 202031
16 201322
17 201418
18 201812
19 201912
20 201111

About Barak Markus

Barak Markus is a scholar working on Genetics, Parasitology, Clinical Biochemistry, Molecular Biology and Cellular and Molecular Neuroscience, having authored 26 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (4 papers), Genetic Associations and Epidemiology (4 papers), Hereditary Neurological Disorders (3 papers), Bartonella species infections research (3 papers), Retinal Development and Disorders (2 papers), Metabolism and Genetic Disorders (2 papers), Genetic Mapping and Diversity in Plants and Animals (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). The work is most often cited by research in Aging (47 citations), Genetics (465 citations), Clinical Biochemistry (32 citations), Molecular Biology (409 citations) and Cell Biology (86 citations). Barak Markus has collaborated with scholars based in Israel, United States and Costa Rica. Frequent co-authors include Ohad S. Birk, Melissa Gymrek, Yaniv Erlich, Idan Cohen, Alkes L. Price, Hagit Flusser, Haoyang Zeng, Stoyan Georgiev, Audrey Guilmatre and Jonathan K. Pritchard. Their work appears in journals such as European Journal of Human Genetics, Human Mutation, The American Journal of Human Genetics, PLoS ONE and Molecular Carcinogenesis.

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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