Pierre Billuart

5.6k citations
63 papers · 4.0k · 2 hit papers · h-index 30

Impact in

Papers in

    • Genetics and Neurodevelopmental Disorders 36
    • Ubiquitin and proteasome pathways 8
    • Epigenetics and DNA Methylation 6
    • RNA Research and Splicing 5
    • Signaling Pathways in Disease 5

Pierre Billuart

63 papers receiving 3.9k citations

Pierre Billuart's Hit Papers

A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome 1998 · 634 citations
6340+9+18Years since publication250500750

Peers

Pierre Billuart
Comparison fields: 5 of 105
  • Developmental Neuroscience 479
  • Cellular and Molecular Neuroscience 917
  • Cell Biology 785
  • Genetics 1.1k
  • Molecular Biology 2.3k
Replace A. Paula Monaghan with:
A. Paula Monaghan United States
Hirotomo Saitsu Japan
Katrin Anlag Germany
Gil Levkowitz Israel
Chérif Beldjord France
Thomas Hiesberger United States
Angeliki Louvi United States
Fumitoshi Irie Japan
Markus Plomann Germany
Brian G. Condie United States
Pierre Billuart relative to A. Paula Monaghan United States A. Paula Monaghan's profile →
Citations per field
00.5×1.5×2.3×
A. Paula Monaghan · 1×
Citations per year

Countries citing papers authored by Pierre Billuart

Since Specialization
Citations

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

Fields of papers citing papers by Pierre Billuart

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 63 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Somatic mutations of the β-catenin gene are frequent in mouse and human hepatocellular carcinomas
Hit paper breakdown →
1998965
2
A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome
Hit paper breakdown →
1998634
3 1998414
4 2001184
5 2007115
6 2010103
7 200387
8 201980
9 202179
10 200976
11 200574
12 201156
13 200156
14 201154
15 201550
16 199749
17 200942
18 201738
19 201738
20 201936

About Pierre Billuart

Pierre Billuart is a scholar working on Genetics, Molecular Biology, Cellular and Molecular Neuroscience, Cell Biology and Cognitive Neuroscience, having authored 63 papers that have together received 4.0k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (36 papers), Ubiquitin and proteasome pathways (8 papers), Neuroscience and Neuropharmacology Research (8 papers), Neurogenesis and neuroplasticity mechanisms (7 papers), Cellular transport and secretion (7 papers), Epigenetics and DNA Methylation (6 papers), RNA Research and Splicing (5 papers) and Signaling Pathways in Disease (5 papers). The work is most often cited by research in Developmental Neuroscience (479 citations), Cellular and Molecular Neuroscience (917 citations), Cell Biology (785 citations), Genetics (1.1k citations) and Molecular Biology (2.3k citations). Pierre Billuart has collaborated with scholars based in France, Italy and United States. Frequent co-authors include Axel Kahn, Chérif Beldjord, Jamel Chelly, Claire-Angélique Renard, Monique Fabrè, Jamel Chelly, Christine Perret, Marie‐Annick Buendia, Olivier Soubrane and Béatrice Romagnolo. Their work appears in journals such as Human Molecular Genetics, Journal of Neuroscience, European Journal of Human Genetics, NeuroMolecular Medicine and Molecular Psychiatry.

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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