Ingrid Burgelin

747 total citations
11 papers, 394 citations indexed

About

Ingrid Burgelin is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Ingrid Burgelin has authored 11 papers receiving a total of 394 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Neurology. Recurrent topics in Ingrid Burgelin's work include Genomic variations and chromosomal abnormalities (4 papers), Congenital limb and hand anomalies (2 papers) and Bacteriophages and microbial interactions (1 paper). Ingrid Burgelin is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Congenital limb and hand anomalies (2 papers) and Bacteriophages and microbial interactions (1 paper). Ingrid Burgelin collaborates with scholars based in France, Switzerland and Germany. Ingrid Burgelin's co-authors include Benoı̂t Arveiler, Didier Lacombe, Isabelle Coupry, Delphine Simon, Philippe Gorry, Hervé Perron, Aloïs B. Lang, François Curtin, Alexandra Madeira and Raphaël Faucard and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Annals of Neurology and Biochemical and Biophysical Research Communications.

In The Last Decade

Ingrid Burgelin

11 papers receiving 390 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ingrid Burgelin France	8	197	130	64	55	53	11	394
Tianxiang Huang China	13	182 0.9×	33 0.3×	42 0.7×	21 0.4×	49 0.9×	47	499
Pierangela Castorina Italy	19	494 2.5×	185 1.4×	29 0.5×	64 1.2×	21 0.4×	35	894
Ninette Cohen United States	15	352 1.8×	229 1.8×	11 0.2×	46 0.8×	62 1.2×	29	691
Suk-Won Jin United States	13	456 2.3×	90 0.7×	22 0.3×	20 0.4×	31 0.6×	18	733
Alexander Saveliev United Kingdom	13	611 3.1×	165 1.3×	18 0.3×	27 0.5×	49 0.9×	17	827
Caroline Thaung United Kingdom	13	319 1.6×	134 1.0×	19 0.3×	60 1.1×	8 0.2×	57	619
Uli Schmidt Germany	12	524 2.7×	93 0.7×	14 0.2×	21 0.4×	24 0.5×	38	716
Andrew J. Bendall Canada	12	454 2.3×	156 1.2×	15 0.2×	11 0.2×	14 0.3×	20	560
Nicole M. LeDouarin France	8	312 1.6×	95 0.7×	21 0.3×	21 0.4×	9 0.2×	11	476
Katarina Truvé Sweden	15	258 1.3×	167 1.3×	11 0.2×	48 0.9×	7 0.1×	17	542

Countries citing papers authored by Ingrid Burgelin

Since Specialization

Citations

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

Fields of papers citing papers by Ingrid Burgelin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ingrid Burgelin

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

All Works

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11 of 11 papers shown

Ullate‐Agote, Asier, Ingrid Burgelin, Jean Daraspe, et al.. (2020). Genome mapping of a LYST mutation in corn snakes indicates that vertebrate chromatophore vesicles are lysosome-related organelles. Proceedings of the National Academy of Sciences. 117(42). 26307–26317. 33 indexed citations

Faucard, Raphaël, Alexandra Madeira, François‐Jérôme Authier, et al.. (2016). Human Endogenous Retrovirus and Neuroinflammation in Chronic Inflammatory Demyelinating Polyradiculoneuropathy. EBioMedicine. 6. 190–198. 34 indexed citations

Madeira, Alexandra, Ingrid Burgelin, Hervé Perron, et al.. (2015). MSRV envelope protein is a potent, endogenous and pathogenic agonist of human toll-like receptor 4: Relevance of GNbAC1 in multiple sclerosis treatment. Journal of Neuroimmunology. 291. 29–38. 55 indexed citations

Rooryck, Caroline, Ingrid Burgelin, Robert Saura, et al.. (2010). Characterization of a de novo balanced translocation t(9;18)(p23;q12.2) in a patient with oculoauriculovertebral spectrum. European Journal of Medical Genetics. 53(2). 104–107. 6 indexed citations

Simon, Delphine, Thomas Barnetche, Caroline Rooryck, et al.. (2010). A mutation in the 3′-UTR of the HDAC6 gene abolishing the post-transcriptional regulation mediated by hsa-miR-433 is linked to a new form of dominant X-linked chondrodysplasia. Human Molecular Genetics. 19(10). 2015–2027. 77 indexed citations

Rooryck, Caroline, Marianne Stef, Ingrid Burgelin, et al.. (2009). 2.3 Mb terminal deletion in 12p13.33 associated with oculoauriculovertebral spectrum and evaluation of WNT5B as a candidate gene. European Journal of Medical Genetics. 52(6). 446–449. 30 indexed citations

Stef, Marianne, Delphine Simon, Marie‐Ange Delrue, et al.. (2007). Spectrum of CREBBP gene dosage anomalies in Rubinstein–Taybi Syndrome patients. European Journal of Human Genetics. 15(8). 843–847. 33 indexed citations

Jouary, Thomas, Cyril Goizet, Isabelle Coupry, et al.. (2007). Detection of an Intragenic Deletion Expands the Spectrum of CTSC Mutations in Papillon–Lefèvre Syndrome. Journal of Investigative Dermatology. 128(2). 322–325. 7 indexed citations

Sibon, Igor, Isabelle Coupry, Patrice Ménégon, et al.. (2007). COL4A1 mutation in Axenfeld–Rieger anomaly with leukoencephalopathy and stroke. Annals of Neurology. 62(2). 177–184. 109 indexed citations

10.

Stef, Marianne, Delphine Simon, Ingrid Burgelin, et al.. (2006). Testing and improving experimental parameters for the use of low molecular weight targets in array-CGH experiments. Human Mutation. 27(11). 1143–1150. 2 indexed citations

11.

Vaysse, Laurence, Christine Guillaume, Ingrid Burgelin, et al.. (2002). Proteolipidic Vectors for Gene Transfer to the Lung. Biochemical and Biophysical Research Communications. 290(5). 1489–1498. 8 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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