Cécile Grohs

3.2k total citations
55 papers, 1.3k citations indexed

About

Cécile Grohs is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Cécile Grohs has authored 55 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Genetics, 16 papers in Molecular Biology and 10 papers in Plant Science. Recurrent topics in Cécile Grohs's work include Genetic and phenotypic traits in livestock (33 papers), Genetic Mapping and Diversity in Plants and Animals (20 papers) and Animal Genetics and Reproduction (16 papers). Cécile Grohs is often cited by papers focused on Genetic and phenotypic traits in livestock (33 papers), Genetic Mapping and Diversity in Plants and Animals (20 papers) and Animal Genetics and Reproduction (16 papers). Cécile Grohs collaborates with scholars based in France, Morocco and United Kingdom. Cécile Grohs's co-authors include Didier Boichard, Hubert H. Levéziel, Aurélien Capitan, Sébastien Fritz, Andre A. Eggen, Mekki Boussaha, André Neau, Yves Amigues, Daniel Vaiman and Florence T. Bourgeois and has published in prestigious journals such as Nature Genetics, PLoS ONE and Genetics.

In The Last Decade

Cécile Grohs

47 papers receiving 1.2k citations

Peers

Cécile Grohs

GENET

ACS

A. Eggen France

Juan-José Arranz Spain

Finnian Hanrahan Ireland

Paola Crepaldi Italy

Katayoun Moazami‐Goudarzi France

B. M. Burns Australia

Salvatore Mastrangelo Italy

Christa Kühn Germany

Matthew McClure United States

Hélène Hayes France

A. Eggen France

Cécile Grohs

1.4k ×1.3

GENET

386 ×1.5

231 ×1.0

ACS

153 ×0.7

459 ×2.1

Citations per year, relative to Cécile Grohs Cécile Grohs (= 1×) peers A. Eggen

Countries citing papers authored by Cécile Grohs

Since Specialization

Citations

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

Fields of papers citing papers by Cécile Grohs

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cécile Grohs

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

Grohs, Cécile, et al.. (2025). A recessive deleterious missense variant in PEX7 causes a lethal form of chondrodysplasia in Bazadaise cattle. Animal Genetics. 56(4).

Grohs, Cécile, Sébastien Fritz, Cécile Donnadieu, et al.. (2025). Application of a French cattle pangenome, from structural variant discovery to association studies on key phenotypes. Genetics Selection Evolution. 57(1). 61–61.

Boulling, Arnaud, Cécile Grohs, Anne Barbat, et al.. (2025). A bovine model of rhizomelic chondrodysplasia punctata caused by a deep intronic splicing variant in the GNPAT gene. Genetics Selection Evolution. 57(1). 23–23. 1 indexed citations

Grohs, Cécile, Mekki Boussaha, F. Besnard, et al.. (2024). A recurrent de novo missense mutation in COL1A1 causes osteogenesis imperfecta type II and preterm delivery in Normande cattle. Genetics Selection Evolution. 56(1). 39–39. 2 indexed citations

Faraut, Thomas, Nathalie Bonnet, Anne Barbat, et al.. (2023). Large-scale detection and characterization of interchromosomal rearrangements in normozoospermic bulls using massive genotype and phenotype data sets. Genome Research. 33(6). 957–971. 7 indexed citations

Iampietro, Carole, Claire Kuchly, Arnaud Di Franco, et al.. (2023). A Bos taurus sequencing methods benchmark for assembly, haplotyping, and variant calling. Scientific Data. 10(1). 369–369. 5 indexed citations

Besnard, F., Hélène Leclerc, Mekki Boussaha, et al.. (2022). Detailed analysis of mortality rates in the female progeny of 1,001 Holstein bulls allows the discovery of new dominant genetic defects. Journal of Dairy Science. 106(1). 439–451. 6 indexed citations

Vaiman, Anne, Sébastien Fritz, Christian Beauvallet, et al.. (2022). Mutation of the MYH3 gene causes recessive cleft palate in Limousine cattle. Genetics Selection Evolution. 54(1). 71–71. 5 indexed citations

Martin, Pauline, Cécile V. Denis, Cécile Grohs, et al.. (2021). Determination of immunoglobulin concentrations and genetic parameters for colostrum and calf serum in Charolais animals. Journal of Dairy Science. 104(3). 3240–3249. 23 indexed citations

10.

Sanchez, Marie-Pierre, Raphaël R. Guatteo, Cécile Grohs, et al.. (2020). Identification of the ABCC4, IER3, and CBFA2T2 candidate genes for resistance to paratuberculosis from sequence-based GWAS in Holstein and Normande dairy cattle. Genetics Selection Evolution. 52(1). 14–14. 28 indexed citations

11.

Boichard, Didier, Mekki Boussaha, Aurélien Capitan, et al.. (2018). Experience from large scale use of the EuroGenomics custom SNP chip in cattle. Prodinra (INRA Bordeaux-Aquitaine). 23 indexed citations

12.

Fritz, Sébastien, Chris Hozé, Emmanuelle Rebours, et al.. (2018). An initiator codon mutation in SDE2 causes recessive embryonic lethality in Holstein cattle. Journal of Dairy Science. 101(7). 6220–6231. 34 indexed citations

13.

Fritz, Sébastien, Anne Barbat, Mekki Boussaha, et al.. (2017). A missense mutation in PFAS (phosphoribosylformylglycinamidine synthase) is likely causal for embryonic lethality associated with the MH1 haplotype in Montbéliarde dairy cattle. Journal of Dairy Science. 100(10). 8176–8187. 22 indexed citations

14.

Gautier, Mathieu, Katayoun Moazami‐Goudarzi, Hubert H. Levéziel, et al.. (2016). Deciphering the Wisent Demographic and Adaptive Histories from Individual Whole-Genome Sequences. Molecular Biology and Evolution. 33(11). 2801–2814. 32 indexed citations

15.

Fritz, Sébastien, Aurélien Capitan, Anis Djari, et al.. (2013). Detection of Haplotypes Associated with Prenatal Death in Dairy Cattle and Identification of Deleterious Mutations in GART, SHBG and SLC37A2. PLoS ONE. 8(6). e65550–e65550. 143 indexed citations

16.

Duchesne, Amandine, Mathieu Gautier, Sead Chadi, et al.. (2006). Identification of a doublet missense substitution in the bovine LRP4 gene as a candidate causal mutation for syndactyly in Holstein cattle. Genomics. 88(5). 610–621. 43 indexed citations

17.

Druet, Tom, Sébastien Fritz, Alain Malafosse, et al.. (2004). Preliminary work for the use of linkage disequilibrium in French MAS program. Open Repository and Bibliography (University of Liège). 1 indexed citations

18.

Vaiman, Daniel, A. Eggen, Dominique Mercier, et al.. (1995). A genetic and physical map of bovine chromosome 3. Animal Genetics. 26(1). 21–25. 8 indexed citations

19.

Vaiman, Daniel, et al.. (1994). Conservation of a syntenic group of microsatellite loci between cattle and sheep. Mammalian Genome. 5(5). 310–314. 21 indexed citations

20.

Levéziel, Hubert H., C. Rodellar, Christine Leroux, et al.. (1994). A microsatellite within the bovine K‐casein gene reveals a polymorphism correlating strongly with polymorphisms previously described at the protein as well as the DNA level. Animal Genetics. 25(4). 223–228. 7 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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