Mark Z. Kos

471 citations
14 papers · 273 · h-index 8

Impact in

    • Genetic Associations and Epidemiology
    • Genetic Syndromes and Imprinting
    • Epigenetics and DNA Methylation
    • Cancer-related gene regulation

Papers in

    • Genetic Associations and Epidemiology 7
    • Genetics and Neurodevelopmental Disorders 3
    • Genomics and Rare Diseases 2
    • Genetic Syndromes and Imprinting 2
    • Epigenetics and DNA Methylation 3
    • Peroxisome Proliferator-Activated Receptors 2

Mark Z. Kos

13 papers receiving 268 citations

Peers

Mark Z. Kos
Comparison fields: 5 of 66
  • Genetics 107
  • Molecular Biology 168
  • Pediatrics, Perinatology and Child Health 44
  • Obstetrics and Gynecology 11
  • Cellular and Molecular Neuroscience 24
Replace Brian J. Shayota with:
Brian J. Shayota United States
Jiangtao Zhang China
M. Danielle Fallin United States
Amna Khamis United Kingdom
Anne Rochtus Belgium
Ana Carolina Proença da Fonseca Brazil
Radha Rama Devi Akella India
Smeeta Shrestha Singapore
Yu Qian China
Audrey Guérardel Switzerland
Mark Z. Kos relative to Brian J. Shayota United States Brian J. Shayota's profile →
Citations per field
00.5×10×15×17.5×
Brian J. Shayota · 1×
Citations per year

Countries citing papers authored by Mark Z. Kos

Since Specialization
Citations

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

Fields of papers citing papers by Mark Z. Kos

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mark Z. Kos. 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 Mark Z. Kos. The network helps show where Mark Z. Kos may publish in the future.

Co-authors

The 25 scholars most cited alongside Mark Z. Kos, 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 Mark Z. Kos Line = papers co-authored together Mark Z. Kos links everyone, so they are left out of the graph.

All Works

14 of 14 papers shown
#Work
1 2015108
2 201339
3 201339
4 201319
5 201518
6 202217
7 201710
8 20179
9 20215
10 20203
11 20143
12 20232
13 20211
14 20180

About Mark Z. Kos

Mark Z. Kos is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Cellular and Molecular Neuroscience and Pediatrics, Perinatology and Child Health, having authored 14 papers that have together received 273 indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (7 papers), Alcohol Consumption and Health Effects (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Epigenetics and DNA Methylation (3 papers), Peroxisome Proliferator-Activated Receptors (2 papers), Genomics and Rare Diseases (2 papers), Genetic Syndromes and Imprinting (2 papers) and Atherosclerosis and Cardiovascular Diseases (1 paper). The work is most often cited by research in Genetics (107 citations), Molecular Biology (168 citations), Pediatrics, Perinatology and Child Health (44 citations), Obstetrics and Gynecology (11 citations) and Cellular and Molecular Neuroscience (24 citations). Mark Z. Kos has collaborated with scholars based in United States, Australia and China. Frequent co-authors include Laura Almasy, Melanie A. Carless, Joanne E. Curran, John Blangero, Harald H.H. Göring, Hemant Kulkarni, Anthony G. Comuzzie, Michael C. Mahaney, Thomas D. Dyer and Jennifer Neary. Their work appears in journals such as American Journal of Medical Genetics Part B Neuropsychiatric Genetics, Schizophrenia Bulletin, Frontiers in Psychiatry, Genes Brain & Behavior and European Journal of Human Genetics.

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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