Anne Boland

24.8k total citations · 1 hit paper
119 papers, 5.0k citations indexed

About

Anne Boland is a scholar working on Genetics, Molecular Biology and Immunology. According to data from OpenAlex, Anne Boland has authored 119 papers receiving a total of 5.0k indexed citations (citations by other indexed papers that have themselves been cited), including 58 papers in Genetics, 43 papers in Molecular Biology and 17 papers in Immunology. Recurrent topics in Anne Boland's work include Genomics and Rare Diseases (12 papers), Yersinia bacterium, plague, ectoparasites research (10 papers) and Genomic variations and chromosomal abnormalities (9 papers). Anne Boland is often cited by papers focused on Genomics and Rare Diseases (12 papers), Yersinia bacterium, plague, ectoparasites research (10 papers) and Genomic variations and chromosomal abnormalities (9 papers). Anne Boland collaborates with scholars based in France, Belgium and United States. Anne Boland's co-authors include Guy R. Cornelis, Marie‐Paule Sory, Maite Iriarte, Isabelle Lambermont, Aoife Boyd, Cécile Neyt, Isabelle Stainier, Scott D. Mills, Jean‐François Deleuze and Patrick Van Deŕ Smissen and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Anne Boland

114 papers receiving 4.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The Virulence Plasmid ofYersinia, an Antihost Genome

1998 644 citations Guy R. Cornelis, Anne Boland et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Anne Boland France	34	2.4k	1.8k	939	555	393	119	5.0k
Emmanuel Lemichez France	39	774 0.3×	3.5k 1.9×	536 0.6×	1.0k 1.8×	669 1.7×	121	6.0k
Donna M. Muzny United States	49	2.7k 1.1×	5.1k 2.8×	55 0.1×	650 1.2×	518 1.3×	163	8.9k
Kenneth S. K. Tung United States	57	1.1k 0.5×	2.9k 1.6×	204 0.2×	4.7k 8.4×	461 1.2×	224	10.9k
Gilles Thomas United States	38	4.7k 1.9×	3.7k 2.1×	276 0.3×	4.3k 7.7×	848 2.2×	72	11.5k
Roberto Bonasio United States	41	1.8k 0.8×	5.7k 3.2×	322 0.3×	2.1k 3.8×	348 0.9×	70	9.6k
Merete Fredholm Denmark	40	3.4k 1.4×	2.3k 1.3×	138 0.1×	287 0.5×	223 0.6×	204	6.6k
Edward K. Wakeland United States	64	2.1k 0.9×	3.1k 1.8×	114 0.1×	8.3k 14.9×	623 1.6×	209	13.5k
David S. Schneider United States	37	771 0.3×	1.6k 0.9×	197 0.2×	3.4k 6.0×	802 2.0×	72	7.0k
Carla Fiorentini Italy	40	1.0k 0.4×	2.2k 1.2×	934 1.0×	944 1.7×	854 2.2×	127	4.8k
Brian D. Robertson United Kingdom	51	777 0.3×	3.1k 1.8×	227 0.2×	732 1.3×	2.4k 6.1×	151	7.1k

Countries citing papers authored by Anne Boland

Since Specialization

Citations

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

Fields of papers citing papers by Anne Boland

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anne Boland

This figure shows the co-authorship network connecting the top 25 collaborators of Anne Boland. A scholar is included among the top collaborators of Anne Boland 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 Anne Boland. Anne Boland is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Brucato, Nicolas, Danat Yermakovich, Francesco Montinaro, et al.. (2024). Positive selection in the genomes of two Papua New Guinean populations at distinct altitude levels. Nature Communications. 15(1). 3352–3352. 14 indexed citations

Loe-Mie, Yann, Caroline Dubertret, Takeo Yoshikawa, et al.. (2024). De Novo Variants Found in Three Distinct Schizophrenia Populations Hit a Common Core Gene Network Related to Microtubule and Actin Cytoskeleton Gene Ontology Classes. Life. 14(2). 244–244. 2 indexed citations

Féraudy, Yvan de, Norma B. Romero, Raphaël Schneider, et al.. (2024). Exome sequencing in undiagnosed congenital myopathy reveals new genes and refines genes–phenotypes correlations. Genome Medicine. 16(1). 87–87. 4 indexed citations

Chalabi, Smahane, Laëtitia Michou, François Cornélis, et al.. (2024). MYLK*FLNB and DOCK1*LAMA2 gene–gene interactions associated with rheumatoid arthritis in the focal adhesion pathway. Frontiers in Genetics. 15. 1375036–1375036.

Lecoquierre, François, Olivier Quenez, Sophie Coutant, et al.. (2023). High diagnostic potential of short and long read genome sequencing with transcriptome analysis in exome-negative developmental disorders. Human Genetics. 142(6). 773–783. 4 indexed citations

Lokmer, Ana, Delphine Bacq‐Daian, Anne Boland, et al.. (2023). Risperidone Response in Patients with Schizophrenia Drives DNA Methylation Changes in Immune and Neuronal Systems. Epigenomics. 15(1). 21–38. 5 indexed citations

Estrada‐Cuzcano, Alejandro, Véronique Geoffroy, Julien Tarabeux, et al.. (2023). WGS Revealed Novel BBS5 Pathogenic Variants, Missed by WES, Causing Ciliary Structure and Function Defects. International Journal of Molecular Sciences. 24(10). 8729–8729. 5 indexed citations

Poirier, Karine, Richard Belvindrah, Imane Moutkine, et al.. (2022). Novel role of the synaptic scaffold protein Dlgap4 in ventricular surface integrity and neuronal migration during cortical development. Nature Communications. 13(1). 2746–2746. 4 indexed citations

Drogou, Catherine, Danielle Gomez-Mérino, Arnaud Rabat, et al.. (2021). Genetics and Cognitive Vulnerability to Sleep Deprivation in Healthy Subjects: Interaction of ADORA2A, TNF-α and COMT Polymorphisms. Life. 11(10). 1110–1110. 3 indexed citations

10.

Velo‐Suárez, Lourdes, Anne Boland, Hélène Blanché, et al.. (2021). Evaluation of saliva as a source of accurate whole‐genome and microbiome sequencing data. Genetic Epidemiology. 45(5). 537–548. 4 indexed citations

11.

Orlova, Marianna, Nguyen Van Thuc, Vu Hong Thai, et al.. (2020). Family-based genome-wide association study of leprosy in Vietnam. PLoS Pathogens. 16(5). e1008565–e1008565. 6 indexed citations

12.

Jamain, Stéphane, Dick Schijven, Bochao Lin, et al.. (2020). A new genetic locus for antipsychotic-induced weight gain: A genome-wide study of first-episode psychosis patients using amisulpride (from the OPTiMiSE cohort). Journal of Psychopharmacology. 34(5). 524–531. 9 indexed citations

13.

Wendeu‐Foyet, Gaëlle, Sylvie Cénée, Yves Akoli Koudou, et al.. (2020). Circadian genes polymorphisms, night work and prostate cancer risk: Findings from the EPICAP study. International Journal of Cancer. 147(11). 3119–3129. 19 indexed citations

14.

Drogou, Catherine, Danielle Gomez-Mérino, Arnaud Metlaine, et al.. (2019). The Impact of Genetic Variations in ADORA2A in the Association between Caffeine Consumption and Sleep. Genes. 10(12). 1021–1021. 34 indexed citations

15.

Uzquiano, Ana, Carmen Cifuentes-Díaz, Ammar Jabali, et al.. (2019). Mutations in the Heterotopia Gene Eml1/EML1 Severely Disrupt the Formation of Primary Cilia. Cell Reports. 28(6). 1596–1611.e10. 33 indexed citations

16.

Díez‐Fuertes, Francisco, Erick De La Torre Tarazona, Esther Calonge, et al.. (2019). Association of a single nucleotide polymorphism in the ubxn6 gene with long-term non-progression phenotype in HIV-positive individuals. Clinical Microbiology and Infection. 26(1). 107–114. 3 indexed citations

17.

Deveau, Paul, Léo Colmet‐Daage, Derek A. Oldridge, et al.. (2018). QuantumClone: clonal assessment of functional mutations in cancer based on a genotype-aware method for clonal reconstruction. Bioinformatics. 34(11). 1808–1816. 18 indexed citations

18.

Ramus, Claire, Jonathan Perot, Marie Arlotto, et al.. (2017). Bdf1 Bromodomains Are Essential for Meiosis and the Expression of Meiotic-Specific Genes. PLoS Genetics. 13(1). e1006541–e1006541. 10 indexed citations

19.

Boland, Anne, Marcel Ricard, Paule Opolon, et al.. (2000). Adenovirus-mediated transfer of the thyroid sodium/iodide symporter gene into tumors for a targeted radiotherapy.. PubMed. 60(13). 3484–92. 188 indexed citations

20.

Boland, Anne & Guy R. Cornelis. (2000). Interaction of Yersinia with Host Cells. Sub-cellular biochemistry. 33. 343–382. 3 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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