Emmanuelle Génin

13.2k total citations · 1 hit paper
169 papers, 5.8k citations indexed

About

Emmanuelle Génin is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Emmanuelle Génin has authored 169 papers receiving a total of 5.8k indexed citations (citations by other indexed papers that have themselves been cited), including 95 papers in Genetics, 61 papers in Molecular Biology and 14 papers in Surgery. Recurrent topics in Emmanuelle Génin's work include Genetic Associations and Epidemiology (59 papers), Genetic Mapping and Diversity in Plants and Animals (29 papers) and Genomic variations and chromosomal abnormalities (25 papers). Emmanuelle Génin is often cited by papers focused on Genetic Associations and Epidemiology (59 papers), Genetic Mapping and Diversity in Plants and Animals (29 papers) and Genomic variations and chromosomal abnormalities (25 papers). Emmanuelle Génin collaborates with scholars based in France, United States and United Kingdom. Emmanuelle Génin's co-authors include Nicolás de Roux, Jean‐Claude Carel, Fumihiko Matsuda, Edwin Milgröm, Jean-Louis Chaussain, Françoise Clerget‐Darpoux, Anne‐Louise Leutenegger, Catherine Bourgain, Roger Jeannot and E. Sauvard and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Journal of Clinical Investigation.

In The Last Decade

Emmanuelle Génin

166 papers receiving 5.7k 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.

Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54

2003 1.8k citations Nicolás de Roux, Emmanuelle Génin et al. Proceedings of the National Academy of Sciences profile →

Peers

Emmanuelle Génin

GENET

EAS

RHEUM

Claude Labrie Canada

Michaela Luconi Italy

Takahiro Μatsumoto Japan

C. Wayne Bardin United States

William Rosner United States

C. Wayne Bardin United States

Van Luu‐The Canada

Bruce D. Weintraub United States

Jacques Simard Canada

Matti Poutanen Finland

Claude Labrie Canada

Emmanuelle Génin

2.3k ×1.1

3.6k ×1.8

GENET

1.3k ×0.8

171 ×0.4

EAS

228 ×0.6

RHEUM

Citations per year, relative to Emmanuelle Génin Emmanuelle Génin (= 1×) peers Claude Labrie

Countries citing papers authored by Emmanuelle Génin

Since Specialization

Citations

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

Fields of papers citing papers by Emmanuelle Génin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emmanuelle Génin

This figure shows the co-authorship network connecting the top 25 collaborators of Emmanuelle Génin. A scholar is included among the top collaborators of Emmanuelle Génin 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 Emmanuelle Génin. Emmanuelle Génin 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

Wu, Hao, Jin‐Huan Lin, Xin‐Ying Tang, et al.. (2024). Combining full-length gene assay and SpliceAI to interpret the splicing impact of all possible SPINK1 coding variants. Human Genomics. 18(1). 21–21. 4 indexed citations

Uguen, Kévin, Jacques L. Michaud, & Emmanuelle Génin. (2024). Short Tandem Repeats in the era of next-generation sequencing: from historical loci to population databases. European Journal of Human Genetics. 32(9). 1037–1044. 3 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

Bocher, Ozvan, Thomas Ludwig, Gaëlle Marenne, et al.. (2022). Testing for association with rare variants in the coding and non-coding genome: RAVA-FIRST, a new approach based on CADD deleteriousness score. PLoS Genetics. 18(9). e1009923–e1009923. 6 indexed citations

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

Génin, Emmanuelle, et al.. (2020). Role of the Common PRSS1-PRSS2 Haplotype in Alcoholic and Non-Alcoholic Chronic Pancreatitis: Meta- and Re-Analyses. Genes. 11(11). 1349–1349. 7 indexed citations

Lerat, Justine, Crystel Bonnet, François Cartault, et al.. (2018). High prevalence of congenital deafness on Reunion Island is due to a founder variant of LHFPL5. Clinical Genetics. 95(1). 177–181. 3 indexed citations

Guey, Stéphanie, Markus Kraemer, Dominique Hervé, et al.. (2017). Rare RNF213 variants in the C-terminal region encompassing the RING-finger domain are associated with moyamoya angiopathy in Caucasians. European Journal of Human Genetics. 25(8). 995–1003. 84 indexed citations

Génin, Emmanuelle & Françoise Clerget‐Darpoux. (2015). Revisiting the Polygenic Additive Liability Model through the Example of Diabetes Mellitus. Human Heredity. 80(4). 171–177. 11 indexed citations

10.

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

11.

Ratbi, Ilham, Emmanuelle Génin, Marie Legendre, et al.. (2008). Cystic fibrosis carrier frequency and estimated prevalence of the disease in Morocco. Journal of Cystic Fibrosis. 7(5). 440–443. 15 indexed citations

12.

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

13.

Khlat, Myriam, Marie-Hélène Cazes, Emmanuelle Génin, & Marguerite Guiguet. (2004). Robustness of Case-Control Studies of Genetic Factors to Population Stratification: Magnitude of Bias and Type I Error. Cancer Epidemiology Biomarkers & Prevention. 13(10). 1660–1664. 31 indexed citations

14.

Roux, Nicolás de, Emmanuelle Génin, Jean‐Claude Carel, et al.. (2003). Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54. Proceedings of the National Academy of Sciences. 100(19). 10972–10976. 1813 indexed citations breakdown →

15.

Cousin, Emmanuelle, Didier Hannequin, Sylvain Ricard, et al.. (2003). A risk for early-onset Alzheimer's disease associated with the APBB1 gene (FE65) intron 13 polymorphism. Neuroscience Letters. 342(1-2). 5–8. 12 indexed citations

16.

Jeannot, Roger, Hassan Sabik, E. Sauvard, & Emmanuelle Génin. (2000). Application of liquid chromatography with mass spectrometry combined with photodiode array detection and tandem mass spectrometry for monitoring pesticides in surface waters. Journal of Chromatography A. 879(1). 51–71. 136 indexed citations

17.

Raas‐Rothschild, Annick, Valérie Cormier‐Daire, Ming Bao, et al.. (2000). Molecular basis of variant pseudo-Hurler polydystrophy (mucolipidosis IIIC). Journal of Clinical Investigation. 105(5). 673–681. 136 indexed citations

18.

Génin, Emmanuelle & Françoise Clerget‐Darpoux. (1998). Reply to Weeks and Sinsheimer. The American Journal of Human Genetics. 62(3). 731–736. 5 indexed citations

19.

Génin, Emmanuelle & Françoise Clerget‐Darpoux. (1996). Association studies in consanguineous populations.. PubMed Central. 58(4). 861–6. 18 indexed citations

20.

Génin, Emmanuelle, María Martínez, & Françoise Clerget‐Darpoux. (1995). Posterior probability of linkage and maximal lod score. Annals of Human Genetics. 59(1). 123–132. 9 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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