Anne Guimier

967 total citations
14 papers, 84 citations indexed

About

Anne Guimier is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, Anne Guimier has authored 14 papers receiving a total of 84 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 5 papers in Neurology and 4 papers in Genetics. Recurrent topics in Anne Guimier's work include Neuroblastoma Research and Treatments (4 papers), Mitochondrial Function and Pathology (3 papers) and ATP Synthase and ATPases Research (2 papers). Anne Guimier is often cited by papers focused on Neuroblastoma Research and Treatments (4 papers), Mitochondrial Function and Pathology (3 papers) and ATP Synthase and ATPases Research (2 papers). Anne Guimier collaborates with scholars based in France, Austria and United Kingdom. Anne Guimier's co-authors include Jeanne Amiel, Gaëlle Pierron, Carole Coze, Olivier Delattre, Michel Peuchmaur, Gudrun Schleiermacher, Laurence Faivre, Véronique Mosseri, Serge Romana and Sandrine Ferrand and has published in prestigious journals such as PLoS ONE, European Journal of Human Genetics and International Journal of Oral and Maxillofacial Surgery.

In The Last Decade

Anne Guimier

14 papers receiving 84 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Anne Guimier France	6	42	23	21	16	16	14	84
Ares Solanes Spain	6	34 0.8×	23 1.0×	18 0.9×	22 1.4×	31 1.9×	9	97
Irene Hadjidemetriou United Kingdom	6	79 1.9×	11 0.5×	34 1.6×	51 3.2×	26 1.6×	9	179
Christina Tran United States	5	20 0.5×	11 0.5×	12 0.6×	8 0.5×	15 0.9×	11	70
Victoria McKay United Kingdom	5	41 1.0×	22 1.0×	36 1.7×	41 2.6×	10 0.6×	12	134
Ruth Armstrong United Kingdom	6	25 0.6×	8 0.3×	27 1.3×	14 0.9×	10 0.6×	16	108
Erika Leenders Netherlands	8	96 2.3×	11 0.5×	15 0.7×	20 1.3×	6 0.4×	19	131
Sami Al Shahwan Saudi Arabia	10	42 1.0×	14 0.6×	14 0.7×	5 0.3×	13 0.8×	18	325
Michelle L. Tas Netherlands	4	25 0.6×	68 3.0×	8 0.4×	10 0.6×	24 1.5×	4	78
Wallace Bourgeois United States	5	65 1.5×	8 0.3×	7 0.3×	4 0.3×	16 1.0×	15	137
Benjamin Kahn United States	5	46 1.1×	9 0.4×	10 0.5×	9 0.6×	21 1.3×	11	103

Countries citing papers authored by Anne Guimier

Since Specialization

Citations

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

Fields of papers citing papers by Anne Guimier

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anne Guimier

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

All Works

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14 of 14 papers shown

1.

Zanin, Sofia, Anne Guimier, Marie Hully, et al.. (2023). Novel ELAC2 Mutations in Individuals Presenting with Variably Severe Neurological Disease in the Presence or Absence of Cardiomyopathy. Life. 13(2). 445–445. 4 indexed citations

2.

Siquier-Pernet, Karine, Marlène Rio, Anne Guimier, et al.. (2022). 16p13.11p11.2 triplication syndrome: a new recognizable genomic disorder characterized by optical genome mapping and whole genome sequencing. European Journal of Human Genetics. 30(6). 712–720. 9 indexed citations

3.

Ranza, Emmanuelle, Anne Guimier, Sylvie Beaudoın, et al.. (2022). Retrospective evaluation of clinical and molecular data of 148 cases of esophageal atresia. American Journal of Medical Genetics Part A. 191(1). 77–83. 2 indexed citations

4.

Fabrè, Monique, V. Soupre, Anne Guimier, et al.. (2021). Cleft palate lateral synechia syndrome in two patients and literature review. International Journal of Oral and Maxillofacial Surgery. 51(3). 347–354. 1 indexed citations

5.

Ranza, Emmanuelle, Anne Guimier, Alain Verloès, et al.. (2020). Overlapping phenotypes between SHORT and Noonan syndromes in patients with PTPN11 pathogenic variants. Clinical Genetics. 98(1). 10–18. 10 indexed citations

6.

Guimier, Anne, Christopher T. Gordon, Marie Hully, et al.. (2019). A novel de novo PDGFRB variant in a child with severe cerebral malformations, intracerebral calcifications, and infantile myofibromatosis. American Journal of Medical Genetics Part A. 179(7). 1304–1309. 4 indexed citations

7.

Guimier, Anne, Fanny Bajolle, Christian Turner, et al.. (2018). PPA2 gene is involved in neonatal fatal acute dilated cardiomyopathy. Archives of Cardiovascular Diseases Supplements. 11(1). 134–134. 1 indexed citations

8.

Guimier, Anne, Fanny Bajolle, Christian Turner, et al.. (2018). PPA2 gene is involved in neonatal fatal acute dilated cardiomyopathy. Archives of Cardiovascular Diseases Supplements. 10(3-4). 282–282. 2 indexed citations

9.

Jackson, Carolyn C., Alain Lefèvre‐Utile, Anne Guimier, et al.. (2017). Kaposi sarcoma, oral malformations, mitral dysplasia, and scoliosis associated with 7q34‐q36.3 heterozygous terminal deletion. American Journal of Medical Genetics Part A. 173(7). 1858–1865. 4 indexed citations

10.

Bouvagnet, Patrice, Anne Guimier, Jeanne Amiel, & Christopher T. Gordon. (2016). Un gène codant une métalloprotéase impliqué dans l’hétérotaxie. médecine/sciences. 32(6-7). 551–553. 1 indexed citations

11.

Heide, Solveig, Julien Masliah‐Planchon, Bertrand Isidor, et al.. (2015). Oncologic Phenotype of Peripheral Neuroblastic Tumors Associated With PHOX2B Non‐Polyalanine Repeat Expansion Mutations. Pediatric Blood & Cancer. 63(1). 71–77. 15 indexed citations

12.

Guimier, Anne, Sandrine Ferrand, Gaëlle Pierron, et al.. (2014). Clinical Characteristics and Outcome of Patients with Neuroblastoma Presenting Genomic Amplification of Loci Other than MYCN. PLoS ONE. 9(7). e101990–e101990. 15 indexed citations

13.

Lehalle, Daphné, Damien Sanlaville, Anne Guimier, et al.. (2014). Multiple congenital anomalies‐intellectual disability (MCA‐ID) and neuroblastoma in a patient harboring a de novo 14q23.1q23.3 deletion. American Journal of Medical Genetics Part A. 164(5). 1310–1317. 7 indexed citations

14.

Guimier, Anne, Bruno Ragazzon, Guillaume Assié, et al.. (2013). AXIN genetic analysis in adrenocortical carcinomas updated.. PubMed. 36(11). 1000–3. 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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