Samuel Lessard

2.0k citations
19 papers · 911 · 1 hit paper · h-index 7

Impact in

  • Genetics top 5%
    • Hemoglobinopathies and Related Disorders
    • Virus-based gene therapy research
  • Hematology top 10%
    • Iron Metabolism and Disorders

Papers in

    • CRISPR and Genetic Engineering 5
    • Epigenetics and DNA Methylation 4
    • RNA modifications and cancer 4
    • RNA Research and Splicing 2
    • Hemoglobinopathies and Related Disorders 9

Samuel Lessard

17 papers receiving 899 citations

Samuel Lessard's Hit Papers

An Erythroid Enhancer of BCL11A Subject to Genetic Variation Determines Fetal Hemoglobin Level 2013 · 450 citations
4500+4+8Years since publication100200300400

Peers

Samuel Lessard
Comparison fields: 5 of 82
  • Genetics 292
  • Hematology 148
  • Business and International Management 24
  • Aging 17
  • Molecular Biology 651
Replace Zhenning He with:
Zhenning He United States
Victoria E. Brown United States
Deirdre McMenamin United States
Doris Kraemer Germany
Pascal Bailly France
Roman Ivanov Russia
Allison Dane Australia
Marios Phylactides Cyprus
Andrea C. Baines United States
Alexander Watson United Kingdom
Samuel Lessard relative to Zhenning He United States Zhenning He's profile →
Citations per field
00.5×4.1×
Zhenning He · 1×
Citations per year

Countries citing papers authored by Samuel Lessard

Since Specialization
Citations

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

Fields of papers citing papers by Samuel Lessard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

19 of 19 papers shown
#Work
1
An Erythroid Enhancer of BCL11A Subject to Genetic Variation Determines Fetal Hemoglobin Level
Hit paper breakdown →
2013450
2 2015183
3 201784
4 201771
5 201744
6 201832
7 201622
8 20205
9 20244
10 20184
11 20193
12 20232
13 20222
14 20162
15 20251
16 20191
17 20201
18 20240
19 20130

About Samuel Lessard

Samuel Lessard is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Hematology and Genetics, having authored 19 papers that have together received 911 indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (9 papers), CRISPR and Genetic Engineering (5 papers), Prenatal Screening and Diagnostics (4 papers), Epigenetics and DNA Methylation (4 papers), RNA modifications and cancer (4 papers), Iron Metabolism and Disorders (2 papers), RNA Research and Splicing (2 papers) and Erythrocyte Function and Pathophysiology (2 papers). The work is most often cited by research in Genetics (292 citations), Hematology (148 citations), Business and International Management (24 citations), Aging (17 citations) and Molecular Biology (651 citations). Samuel Lessard has collaborated with scholars based in United States, Canada and Japan. Frequent co-authors include Guillaume Lettre, Mélissa Beaudoin, Stuart H. Orkin, Daniel E. Bauer, Matthew C. Canver, Elenoe C. Smith, Yuko Fujiwara, Guo‐Cheng Yuan, Luca Pinello and Jeff Vierstra. Their work appears in journals such as Blood, PLoS ONE, Human Genetics and Genomics Advances, BMC Genomics and Science.

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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