Anne‐Louise Leutenegger

5.0k total citations
46 papers, 1.5k citations indexed

About

Anne‐Louise Leutenegger is a scholar working on Genetics, Molecular Biology and Neurology. According to data from OpenAlex, Anne‐Louise Leutenegger has authored 46 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 21 papers in Molecular Biology and 7 papers in Neurology. Recurrent topics in Anne‐Louise Leutenegger's work include Genetic Associations and Epidemiology (15 papers), Genetic Mapping and Diversity in Plants and Animals (12 papers) and Genetic and phenotypic traits in livestock (9 papers). Anne‐Louise Leutenegger is often cited by papers focused on Genetic Associations and Epidemiology (15 papers), Genetic Mapping and Diversity in Plants and Animals (12 papers) and Genetic and phenotypic traits in livestock (9 papers). Anne‐Louise Leutenegger collaborates with scholars based in France, United States and Italy. Anne‐Louise Leutenegger's co-authors include Emmanuelle Génin, Marie‐Claude Babron, Françoise Clerget‐Darpoux, Mourad Sahbatou, Giancarlo Logroscino, Pierre‐Marie Preux, Philippe Couratier, Farid Boumédiène, Ettore Beghi and Benôıt Marin and has published in prestigious journals such as Science, Nucleic Acids Research and Bioinformatics.

In The Last Decade

Anne‐Louise Leutenegger

43 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anne‐Louise Leutenegger France 19 553 544 492 257 189 46 1.5k
Hussein Daoud Canada 24 971 1.8× 627 1.2× 1.1k 2.2× 631 2.5× 337 1.8× 58 2.4k
Erwin Petek Austria 21 77 0.1× 469 0.9× 669 1.4× 132 0.5× 111 0.6× 60 1.5k
Kiran K. Mantripragada United Kingdom 22 304 0.5× 853 1.6× 773 1.6× 51 0.2× 35 0.2× 41 1.8k
Hans‐Henrik M. Dahl Australia 17 242 0.4× 180 0.3× 1.2k 2.5× 58 0.2× 164 0.9× 20 1.9k
Mark Matsushita United States 23 152 0.3× 444 0.8× 675 1.4× 152 0.6× 147 0.8× 36 1.7k
Francisco Martı́nez Spain 24 219 0.4× 837 1.5× 1.1k 2.2× 135 0.5× 60 0.3× 118 1.8k
F. Lucy Raymond United Kingdom 25 74 0.1× 727 1.3× 1.0k 2.1× 138 0.5× 83 0.4× 51 1.8k
Kimberly M. Newberry United States 13 84 0.2× 236 0.4× 681 1.4× 58 0.2× 47 0.2× 20 1.1k
Florencia Pauli United States 14 94 0.2× 589 1.1× 1.8k 3.6× 75 0.3× 57 0.3× 14 2.3k
Robert‐Jan H. Galjaard Netherlands 22 277 0.5× 1.2k 2.1× 859 1.7× 23 0.1× 103 0.5× 65 2.2k

Countries citing papers authored by Anne‐Louise Leutenegger

Since Specialization
Citations

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

Fields of papers citing papers by Anne‐Louise Leutenegger

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anne‐Louise Leutenegger

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

All Works

20 of 20 papers shown
1.
Leutenegger, Anne‐Louise, et al.. (2025). Improving patient clustering by incorporating structured variable label relationships in similarity measures. BMC Medical Research Methodology. 25(1). 72–72.
2.
Bocher, Ozvan, Chaker Aloui, Anne‐Louise Leutenegger, et al.. (2024). PSAP‐Genomic‐Regions: A Method Leveraging Population Data to Prioritize Coding and Non‐Coding Variants in Whole Genome Sequencing for Rare Disease Diagnosis. Genetic Epidemiology. 49(1). e22593–e22593. 1 indexed citations
3.
Leutenegger, Anne‐Louise, et al.. (2023). Tracking clusters of patients over time enables extracting information from medico-administrative databases. Journal of Biomedical Informatics. 139. 104309–104309. 2 indexed citations
4.
Delous, Marion, Audrey Putoux, Anne‐Louise Leutenegger, et al.. (2022). Mutations in the non-codingRNU4ATACgene affect the homeostasis and function of the Integrator complex. Nucleic Acids Research. 51(2). 712–727. 3 indexed citations
5.
Arnould, Minh, Cécile Otten, Salim Abdelilah‐Seyfried, et al.. (2020). Novel Chronic Mouse Model of Cerebral Cavernous Malformations. Stroke. 51(4). 1272–1278. 18 indexed citations
6.
Benoit‐Pilven, Clara, Audrey Putoux, Claire Benetollo, et al.. (2020). Clinical interpretation of variants identified in RNU4ATAC, a non-coding spliceosomal gene. PLoS ONE. 15(7). e0235655–e0235655. 10 indexed citations
7.
Benoit‐Pilven, Clara, Audrey Putoux, Amandine Campan-Fournier, et al.. (2019). New insights into minor splicing—a transcriptomic analysis of cells derived from TALS patients. RNA. 25(9). 1130–1149. 26 indexed citations
8.
Nutile, Teresa, Daniela Ruggiero, Alfonsina Tirozzi, et al.. (2019). Whole-Exome Sequencing in the Isolated Populations of Cilento from South Italy. Scientific Reports. 9(1). 4059–4059. 6 indexed citations
9.
Marin, Benôıt, Farid Boumédiène, Giancarlo Logroscino, et al.. (2016). Variation in worldwide incidence of amyotrophic lateral sclerosis: a meta-analysis. International Journal of Epidemiology. 46(1). dyw061–dyw061. 234 indexed citations
10.
Gazal, Steven, Mourad Sahbatou, Marie‐Claude Babron, Emmanuelle Génin, & Anne‐Louise Leutenegger. (2015). High level of inbreeding in final phase of 1000 Genomes Project. Scientific Reports. 5(1). 17453–17453. 47 indexed citations
11.
Gazal, Steven, Emmanuelle Génin, & Anne‐Louise Leutenegger. (2015). Relationship inference from the genetic data on parents or offspring: A comparative study. Theoretical Population Biology. 107. 31–38. 1 indexed citations
12.
Marin, Benôıt, Giancarlo Logroscino, Farid Boumédiène, et al.. (2015). Clinical and demographic factors and outcome of amyotrophic lateral sclerosis in relation to population ancestral origin. European Journal of Epidemiology. 31(3). 229–245. 82 indexed citations
13.
Sorice, Rossella, Daniela Ruggiero, Teresa Nutile, et al.. (2012). Genetic and Environmental Factors Influencing the Placental Growth Factor (PGF) Variation in Two Populations. PLoS ONE. 7(8). e42537–e42537. 12 indexed citations
14.
Génin, Emmanuelle, Mourad Sahbatou, Steven Gazal, et al.. (2012). Could Inbred Cases Identified in GWAS Data Succeed in Detecting Rare Recessive Variants Where Affected Sib-Pairs Have Failed?. Human Heredity. 74(3-4). 142–152. 5 indexed citations
15.
Edery, Patrick, Charles Marcaillou, Mourad Sahbatou, et al.. (2011). Association of TALS Developmental Disorder with Defect in Minor Splicing Component U4atac snRNA. Science. 332(6026). 240–243. 159 indexed citations
16.
Leutenegger, Anne‐Louise, Mourad Sahbatou, Steven Gazal, Howard M. Cann, & Emmanuelle Génin. (2011). Consanguinity around the world: what do the genomic data of the HGDP-CEPH diversity panel tell us?. European Journal of Human Genetics. 19(5). 583–587. 45 indexed citations
17.
Leutenegger, Anne‐Louise, Audrey Labalme, Emmanuelle Génin, et al.. (2006). Using Genomic Inbreeding Coefficient Estimates for Homozygosity Mapping of Rare Recessive Traits: Application to Taybi-Linder Syndrome. The American Journal of Human Genetics. 79(1). 62–66. 35 indexed citations
18.
Babron, Marie‐Claude, Catherine Bourgain, Anne‐Louise Leutenegger, & Françoise Clerget‐Darpoux. (2005). Detection of susceptibility loci by genome-wide linkage analysis. BMC Genetics. 6(S1). S18–S18. 5 indexed citations
19.
Bourgey, Mathieu, Anne‐Louise Leutenegger, Emmanuelle Cousin, et al.. (2005). Modeling the effect of a genetic factor for a complex trait in a simulated population. BMC Genetics. 6(S1). S87–S87. 1 indexed citations
20.
Leutenegger, Anne‐Louise, Bernard Prum, Emmanuelle Génin, et al.. (2003). Estimation of the Inbreeding Coefficient through Use of Genomic Data. The American Journal of Human Genetics. 73(3). 516–523. 187 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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