Annick Francis

1.3k total citations
16 papers, 800 citations indexed

About

Annick Francis is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Annick Francis has authored 16 papers receiving a total of 800 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 7 papers in Genetics and 2 papers in Surgery. Recurrent topics in Annick Francis's work include Pluripotent Stem Cells Research (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Congenital heart defects research (4 papers). Annick Francis is often cited by papers focused on Pluripotent Stem Cells Research (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Congenital heart defects research (4 papers). Annick Francis collaborates with scholars based in Belgium, Netherlands and United Kingdom. Annick Francis's co-authors include Danny Huylebroeck, Tom Van de Putte, L Nelles, An Zwijsen, Mitsuji Maruhashi, Yujiro Higashi, Lieve Umans, Elke Maas, Iván M. Moya and Karen Beets and has published in prestigious journals such as Nature Communications, PLoS ONE and Development.

In The Last Decade

Annick Francis

15 papers receiving 795 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Annick Francis Belgium	11	496	153	125	109	106	16	800
Laura Kerosuo United States	15	411 0.8×	91 0.6×	90 0.7×	87 0.8×	70 0.7×	27	643
Zhiyv Niu United States	14	562 1.1×	122 0.8×	118 0.9×	58 0.5×	71 0.7×	41	768
Tamara Grigoryan Germany	7	699 1.4×	82 0.5×	93 0.7×	95 0.9×	104 1.0×	8	887
Byambajav Buyandelger United States	13	475 1.0×	93 0.6×	65 0.5×	100 0.9×	104 1.0×	16	862
Kathryn C. Davidson Australia	11	899 1.8×	179 1.2×	95 0.8×	74 0.7×	56 0.5×	20	1.1k
Tara Davidson Australia	6	509 1.0×	133 0.9×	187 1.5×	309 2.8×	121 1.1×	6	862
Daihachiro Tomotsune Japan	15	689 1.4×	138 0.9×	114 0.9×	62 0.6×	70 0.7×	29	823
Claude Van Campenhout Belgium	16	360 0.7×	91 0.6×	136 1.1×	170 1.6×	68 0.6×	26	711
Angelique Schnerch Canada	7	848 1.7×	152 1.0×	78 0.6×	76 0.7×	111 1.0×	11	986
Priscilla S. Chang United States	6	899 1.8×	123 0.8×	122 1.0×	67 0.6×	95 0.9×	7	1.1k

Countries citing papers authored by Annick Francis

Since Specialization

Citations

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

Fields of papers citing papers by Annick Francis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Annick Francis

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

All Works

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16 of 16 papers shown

Francis, Annick, Elise Pepermans, Geert Baggerman, et al.. (2024). Altered socio-affective communication and amygdala development in mice with protocadherin10-deficient interneurons. Open Biology. 14(6). 240113–240113. 2 indexed citations

Boel, Annekatrien, Adrian Janiszewski, Annick Francis, et al.. (2023). The Wnt/TCF7L1 transcriptional repressor axis drives primitive endoderm formation by antagonizing naive and formative pluripotency. Nature Communications. 14(1). 1210–1210. 17 indexed citations

Stappers, Elke, Ruben Dries, Elise Peyre, et al.. (2020). Multifaceted actions of Zeb2 in postnatal neurogenesis from the ventricular-subventricular zone to the olfactory bulb. Development. 147(10). 6 indexed citations

Radaelli, Enrico, et al.. (2017). Truncal Skin Tumour Development in Mice with Inducible and Conditional Oncogenic BRAF expression and PTEN Deletion Under the Tyrosinase Promoter. Journal of Comparative Pathology. 156(1). 67–67.

Stryjewska, Agata, Ruben Dries, Tim Pieters, et al.. (2016). Zeb2 Regulates Cell Fate at the Exit from Epiblast State in Mouse Embryonic Stem Cells. Stem Cells. 35(3). 611–625. 42 indexed citations

Radaelli, Enrico, Els Hermans, Annick Francis, et al.. (2015). Spontaneous Post-Transplant Disorders in NOD.Cg- Prkdcscid Il2rgtm1Sug/JicTac (NOG) Mice Engrafted with Patient-Derived Metastatic Melanomas. PLoS ONE. 10(5). e0124974–e0124974. 21 indexed citations

Moya, Iván M., Lieve Umans, Elke Maas, et al.. (2012). Stalk Cell Phenotype Depends on Integration of Notch and Smad1/5 Signaling Cascades. Developmental Cell. 22(3). 501–514. 178 indexed citations

Vermeire, Liesbeth, Abdelilah Ibrahimi, Thierry Voet, et al.. (2009). Essential validation of gene trap mouse ES cell lines: a test case with the gene Ttrap. The International Journal of Developmental Biology. 53(7). 1045–1051. 4 indexed citations

Maas, Nicole, Tom Van de Putte, Cindy Melotte, et al.. (2009). TheC20orf133gene is disrupted in a patient with Kabuki syndrome. BMJ Case Reports. 2009. bcr0620091994–bcr0620091994. 3 indexed citations

10.

Putte, Tom Van de, Annick Francis, L Nelles, Leo A. van Grunsven, & Danny Huylebroeck. (2007). Neural crest-specific removal of Zfhx1b in mouse leads to a wide range of neurocristopathies reminiscent of Mowat–Wilson syndrome. Human Molecular Genetics. 16(12). 1423–1436. 65 indexed citations

11.

Maas, Nicole, Tom Van de Putte, Cindy Melotte, et al.. (2007). The C20orf133 gene is disrupted in a patient with Kabuki syndrome. Journal of Medical Genetics. 44(9). 562–569. 46 indexed citations

12.

Bosman, Erika A., Kirstie A. Lawson, Joke Debruyn, et al.. (2006). Smad5 determines murine amnion fate through the control of bone morphogenetic protein expression and signalling levels. Development. 133(17). 3399–3409. 22 indexed citations

13.

Putte, Tom Van de, Mitsuji Maruhashi, Annick Francis, et al.. (2003). Mice Lacking Zfhx1b, the Gene That Codes for Smad-Interacting Protein-1, Reveal a Role for Multiple Neural Crest Cell Defects in the Etiology of Hirschsprung Disease–Mental Retardation Syndrome. The American Journal of Human Genetics. 72(2). 465–470. 228 indexed citations

14.

Verhoeven, Kristien, Peter De Jonghe, Tom Van de Putte, et al.. (2003). Slowed Conduction and Thin Myelination of Peripheral Nerves Associated with Mutant Rho Guanine-Nucleotide Exchange Factor 10. The American Journal of Human Genetics. 73(4). 926–932. 90 indexed citations

15.

Umans, Lieve, Liesbeth Vermeire, Annick Francis, et al.. (2003). Generation of a floxed allele of Smad5 for cre‐mediated conditional knockout in the mouse. genesis. 37(1). 5–11. 39 indexed citations

16.

Putte, Tom Van de, An Zwijsen, Vladimir Rybin, et al.. (2001). Mice with a homozygous gene trap vector insertion in mgcRacGAP die during pre-implantation development. Mechanisms of Development. 102(1-2). 33–44. 37 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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