Jean Monlong

18.6k citations
16 papers · 949 · 1 hit paper · h-index 11

Impact in

  • Genetics top 5%
    • Glioma Diagnosis and Treatment
    • Genomics and Rare Diseases
    • Cancer Genomics and Diagnostics

Papers in

    • Genomics and Phylogenetic Studies 4
    • Single-cell and spatial transcriptomics 3
    • Bioinformatics and Genomic Networks 2
    • Genomics and Chromatin Dynamics 2
    • Genomic variations and chromosomal abnormalities 3
    • Genomics and Rare Diseases 2

Jean Monlong

15 papers receiving 940 citations

Jean Monlong's Hit Papers

Single-cell RNA-seq reveals that glioblastoma recapitulates a normal neurodevelopmental hierarchy 2020 · 325 citations
3250+2+4Years since publication100200300

Peers

Jean Monlong
Comparison fields: 5 of 88
  • Genetics 159
  • Cancer Research 168
  • Genetics 218
  • Molecular Biology 540
  • Oncology 114
Replace Olivier J. Bécherel with:
Olivier J. Bécherel Australia
Ozgur Oksuz United States
Michael P. Meers United States
Bruno Tesson France
Anthony P. Fejes Canada
Peyton Greenside United States
Cristina Pina United Kingdom
Ramya Raviram United States
Cricket A. Sloan United States
Xiongfong Chen United States
Jean Monlong relative to Olivier J. Bécherel Australia Olivier J. Bécherel's profile →
Citations per field
00.5×6.0×
Olivier J. Bécherel · 1×
Citations per year

Countries citing papers authored by Jean Monlong

Since Specialization
Citations

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

Fields of papers citing papers by Jean Monlong

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

16 of 16 papers shown
#Work
1
Single-cell RNA-seq reveals that glioblastoma recapitulates a normal neurodevelopmental hierarchy
Hit paper breakdown →
2020325
2 2021179
3 2020169
4 201477
5 201144
6 201836
7 201932
8 202224
9 201823
10 202313
11 202412
12 202410
13 20243
14 20181
15 20191
16 20210

About Jean Monlong

Jean Monlong is a scholar working on Molecular Biology, Genetics, Cancer Research, Oncology and Plant Science, having authored 16 papers that have together received 949 indexed citations. Recurring topics across this work include Genomics and Phylogenetic Studies (4 papers), Single-cell and spatial transcriptomics (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Genomics and Rare Diseases (2 papers), Cancer Genomics and Diagnostics (2 papers), Chromosomal and Genetic Variations (2 papers), Bioinformatics and Genomic Networks (2 papers) and Genomics and Chromatin Dynamics (2 papers). The work is most often cited by research in Genetics (159 citations), Cancer Research (168 citations), Genetics (218 citations), Molecular Biology (540 citations) and Oncology (114 citations). Jean Monlong has collaborated with scholars based in United States, Canada and France. Frequent co-authors include Benedict Paten, Jordan M. Eizenga, Glenn Hickey, Jouni Sirén, Adam M. Novak, Erik Garrison, Guillaume Bourque, Jonas A. Sibbesen, Miquel Calvo and Roderic Guigó. Their work appears in journals such as Nature Communications, Annual Review of Genomics and Human Genetics, Nature Methods, Veterinary Research and Cancer Research.

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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