Marc Gastou

605 total citations
10 papers, 238 citations indexed

About

Marc Gastou is a scholar working on Molecular Biology, Epidemiology and Genetics. According to data from OpenAlex, Marc Gastou has authored 10 papers receiving a total of 238 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 2 papers in Epidemiology and 1 paper in Genetics. Recurrent topics in Marc Gastou's work include RNA modifications and cancer (5 papers), Autophagy in Disease and Therapy (2 papers) and Cancer-related gene regulation (2 papers). Marc Gastou is often cited by papers focused on RNA modifications and cancer (5 papers), Autophagy in Disease and Therapy (2 papers) and Cancer-related gene regulation (2 papers). Marc Gastou collaborates with scholars based in United States, France and Netherlands. Marc Gastou's co-authors include Lydie Da Costa, Jérôme Larghero, Narla Mohandas, Thierry Leblanc, William Vainchenker, Narjesse Karboul, Olivier Hermine, Alyson W. MacInnes, Liwen Xu and Freja K. Ekman and has published in prestigious journals such as Cell, Blood and Nature Biotechnology.

In The Last Decade

Marc Gastou

9 papers receiving 238 citations

Peers

Marc Gastou

MB

ONCOL

GENET

EPIDE

PHYSI

Elisa Pavesi Italy

Te Ling China

Mami Kishima Japan

Phong Tran Sweden

Dianne Lumaquin United States

G. Rowley United Kingdom

Kai Ling Liang United Kingdom

Qianli Zhuang Canada

Tharshana Stephen France

Kaitavjeet Chowdhary United States

Elisa Pavesi Italy

Marc Gastou

202 ×1.1

MB

26 ×0.7

ONCOL

30 ×0.9

GENET

19 ×0.6

EPIDE

40 ×1.5

PHYSI

Citations per year, relative to Marc Gastou Marc Gastou (= 1×) peers Elisa Pavesi

Countries citing papers authored by Marc Gastou

Since Specialization

Citations

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

Fields of papers citing papers by Marc Gastou

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marc Gastou

This figure shows the co-authorship network connecting the top 25 collaborators of Marc Gastou. A scholar is included among the top collaborators of Marc Gastou based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Marc Gastou. Marc Gastou is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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10 of 10 papers shown

1.

Ghoochani, Ali, Eshaan S. Rawat, Domenico Di Fraia, et al.. (2026). Cell-type resolved protein atlas of brain lysosomes identifies SLC45A1-associated disease as a lysosomal disorder. Cell. 189(3). 765–782.e31.

2.

Gastou, Marc, et al.. (2025). Generation of SLC45A1 Knockout iPSC Line (WTC11-Ngn2 Line) v1. 1 indexed citations

3.

Selvaraj, Sridhar, Sébastien Viel, Sriram Vaidyanathan, et al.. (2023). High-efficiency transgene integration by homology-directed repair in human primary cells using DNA-PKcs inhibition. Nature Biotechnology. 42(5). 731–744. 40 indexed citations

4.

Borrelli, Mimi R., Julia T. Garcia, Michelle Griffin, et al.. (2020). Abstract 186: CD36 Antagonism Minimizes Skin Scarring By Inhibiting JUN-dependent Fibrotic Pathways Within Fibrogenic Fibroblast Subpopulations. Plastic & Reconstructive Surgery Global Open. 8(4S). 126–127. 2 indexed citations

5.

Gastou, Marc, Narjesse Karboul, Hana Manceau, et al.. (2019). Regulation of globin-heme balance in Diamond-Blackfan anemia by HSP70/GATA1. Blood. 133(12). 1358–1370. 41 indexed citations

6.

Włodarski, Marcin W., Lydie Da Costa, Marie-Françoise O’Donohue, et al.. (2018). Recurring mutations in RPL15 are linked to hydrops fetalis and treatment independence in Diamond-Blackfan anemia. Haematologica. 103(6). 949–958. 17 indexed citations

7.

Włodarski, Marcin W., Lydie Da Costa, Marie-Françoise O’Donohue, et al.. (2017). Mutations in Ribosomal Protein Genes L9 and L15 Link to DBA with Specific Clinical Phenotypes. Blood. 130. 1172–1172. 1 indexed citations

8.

Gastou, Marc, Michaël Dussiot, Narjesse Karboul, et al.. (2017). The severe phenotype of Diamond-Blackfan anemia is modulated by heat shock protein 70. Blood Advances. 1(22). 1959–1976. 29 indexed citations

9.

Heijnen, Harry F.G., Richard van Wijk, Tamara C. Pereboom, et al.. (2014). Ribosomal Protein Mutations Induce Autophagy through S6 Kinase Inhibition of the Insulin Pathway. PLoS Genetics. 10(5). e1004371–e1004371. 49 indexed citations

10.

Gastou, Marc, Thierry Leblanc, Corinne Hurtaud, et al.. (2012). Primary hematopoietic cells from DBA patients with mutations in RPL11 and RPS19 genes exhibit distinct erythroid phenotype in vitro. Cell Death and Disease. 3(7). e356–e356. 58 indexed citations

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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