Mark Samuels

5.4k citations
48 papers · 3.2k indexed · 2 hit papers · h-index 27
    • RNA Research and Splicing 11
    • RNA and protein synthesis mechanisms 10
    • Extracellular vesicles in disease 7
    • RNA Interference and Gene Delivery 4
    • Genomics and Chromatin Dynamics 4
  • Genetics top 2%
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
    • MicroRNA in disease regulation 4
  • Neurology top 10%
    • Lipoproteins and Cardiovascular Health 3

Mark Samuels

46 papers receiving 3.1k citations

Hit Papers

[35] In Vitro transcription: Whole-cell extract286198220261996201150100150200250

Peers

Mark Samuels
Comparison fields: 5 of 100
  • Molecular Biology 2.4k
  • Genetics 779
  • Cancer Research 246
  • Clinical Biochemistry 89
  • Neurology 89
Replace R. E. K. Fournier with:
R. E. K. Fournier United States
Periannan Senapathy United States
Dengwen Li China
P.A. Lalley United States
N A Jenkins United States
Carlo Rivolta Switzerland
Christian Delphin France
Vasily Ramensky Russia
Ritva Tikkanen Germany
Keiko Ozato United States
Mark Samuels relative to R. E. K. Fournier United States R. E. K. Fournier's profile →
Citations per field
00.5×10.6×
R. E. K. Fournier · 1×
Citations per year

Countries citing papers authored by Mark Samuels

Since Specialization
Citations

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

Fields of papers citing papers by Mark Samuels

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

20 of 20 papers shown
#Work
1 20252
2 20250
3 20250
4 20246
5 20248
6 202315
7 20235
8 202322
9 202221
10
Goliath, a Variant of DAVID Syndrome?
20141
11 201425
12
Mutations in a novel serine protease PRSS56 in families with nanophthalmos.
201143
13 200948
14 2009181
15 200668
16 2004259
17 200232
18 199839
19 198826
20 1984230

About Mark Samuels

Mark Samuels is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry, having authored 48 papers that have together received 3.2k indexed citations. Recurring topics across this work include RNA Research and Splicing (11 papers), RNA and protein synthesis mechanisms (10 papers), Extracellular vesicles in disease (7 papers), RNA Interference and Gene Delivery (4 papers), MicroRNA in disease regulation (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers), Genomics and Chromatin Dynamics (4 papers) and Lipoproteins and Cardiovascular Health (3 papers). The work is most often cited by research in Molecular Biology (2.4k citations), Genetics (779 citations) and Cancer Research (246 citations). Mark Samuels has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Phillip A. Sharp, Andrew Fire, Paul Schedl, James L. Manley, Lewis A. Chodosh, Thomas W. Cline, Paul N. Hopkins, Duane L. Guernsey, Mark H. Skolnick and Marie‐Pierre Dubé. Their work appears in journals such as Journal of Biological Chemistry, Molecular and Cellular Biology, Nature Genetics, International Journal of Molecular Sciences and The Journal of Pediatrics.

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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2026