Christine Bole

892 total citations
14 papers, 173 citations indexed

About

Christine Bole is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Christine Bole has authored 14 papers receiving a total of 173 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Christine Bole's work include Genomics and Rare Diseases (3 papers), Mitochondrial Function and Pathology (2 papers) and Renal and related cancers (2 papers). Christine Bole is often cited by papers focused on Genomics and Rare Diseases (3 papers), Mitochondrial Function and Pathology (2 papers) and Renal and related cancers (2 papers). Christine Bole collaborates with scholars based in France, United States and Netherlands. Christine Bole's co-authors include Claude–Agnès Reynaud, Matthieu Mahévas, Nicolas Cagnard, A. Robbins, Jean–Claude Weill, Zhicheng Zhou, Jérôme Megret, Simon Le Gallou, Étienne Crickx and Patrick Nitschké and has published in prestigious journals such as Blood, Journal of Allergy and Clinical Immunology and Journal of Investigative Dermatology.

In The Last Decade

Christine Bole

12 papers receiving 172 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Christine Bole France	7	63	43	31	25	24	14	173
Jessica Weaver United States	6	83 1.3×	108 2.5×	32 1.0×	47 1.9×	13 0.5×	7	245
Zhenmin Niu China	10	78 1.2×	25 0.6×	60 1.9×	25 1.0×	4 0.2×	24	171
Thomas Altmann United Kingdom	3	66 1.0×	79 1.8×	25 0.8×	6 0.2×	16 0.7×	4	152
Kazunori Yoshikiyo Japan	7	150 2.4×	79 1.8×	39 1.3×	16 0.6×	5 0.2×	8	252
Richard Herrscher United States	4	213 3.4×	74 1.7×	39 1.3×	11 0.4×	8 0.3×	8	322
Catherine Pitt Australia	9	70 1.1×	206 4.8×	23 0.7×	11 0.4×	21 0.9×	13	296
Matilde Immacolata Conte Italy	6	100 1.6×	80 1.9×	91 2.9×	25 1.0×	4 0.2×	9	202
Erica J. Brodie Australia	9	152 2.4×	167 3.9×	29 0.9×	31 1.2×	24 1.0×	9	352
Eduardo Caleiras Spain	11	157 2.5×	40 0.9×	17 0.5×	13 0.5×	5 0.2×	37	291
Michael Chiorazzi United States	7	132 2.1×	113 2.6×	14 0.5×	15 0.6×	33 1.4×	13	287

Countries citing papers authored by Christine Bole

Since Specialization

Citations

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

Fields of papers citing papers by Christine Bole

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christine Bole

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

Bole, Christine, et al.. (2025). Atypical Autoimmune Encephalitis: Diagnostic Challenges and Therapeutic Insights From a Case Series. Cureus. 17(4). e82384–e82384.

Assan, Florence, et al.. (2024). 280 ADAR1 mutations drive an interferon type I dependent psoriasis subtype. Journal of Investigative Dermatology. 144(12). S277–S277.

Mayeur, Anne, Nicolas Cagnard, Mohammed Zarhrate, et al.. (2023). A shared pattern of altered gene expression in human embryos affected by mitochondrial diseases. Human Reproduction. 38(5). 992–1002. 3 indexed citations

Tessier, Aude, Lucile Boutaud, Mélanie Parisot, et al.. (2023). Bi-allelic variations in CRB2, encoding the crumbs cell polarity complex component 2, lead to non-communicating hydrocephalus due to atresia of the aqueduct of sylvius and central canal of the medulla. Acta Neuropathologica Communications. 11(1). 29–29. 7 indexed citations

Chopra, Maya, Richard Caswell, Giulia Barcia, et al.. (2022). Mild MDPL in a patient with a novel de novo missense variant in the Cys-B region of POLD1. European Journal of Human Genetics. 30(8). 960–966. 1 indexed citations

Boutaud, Lucile, Bettina Bessières, Christine Bole, et al.. (2022). Biallelic THOC6 pathogenic variants: Prenatal phenotype and review of the literature. Birth Defects Research. 114(10). 499–504. 5 indexed citations

Picard, Jean‐Yves, G Morin, Mojgan Devouassoux‐Shisheboran, et al.. (2022). Persistent Müllerian duct syndrome associated with genetic defects in the regulatory subunit of myosin phosphatase. Human Reproduction. 37(12). 2952–2959. 5 indexed citations

Barbieux, Claire, Matthias Fahrner, Lam C. Tsoi, et al.. (2021). Netherton syndrome subtypes share IL-17/IL-36 signature with distinct IFN-α and allergic responses. Journal of Allergy and Clinical Immunology. 149(4). 1358–1372. 35 indexed citations

Marzin, Pauline, Geneviève Baujat, D. Gensburger, et al.. (2019). Heterozygous FGFR1 mutation may be responsible for an incomplete form of osteoglophonic dysplasia, characterized only by radiolucent bone lesions and teeth retentions. European Journal of Medical Genetics. 63(2). 103729–103729. 7 indexed citations

10.

Cavallin, Mara, Laurent Salomon, Christine Bole, et al.. (2018). Recurrent RTTN mutation leading to severe microcephaly, polymicrogyria and growth restriction. European Journal of Medical Genetics. 61(12). 755–758. 7 indexed citations

11.

Gallou, Simon Le, A. Robbins, Étienne Crickx, et al.. (2018). BAFF and CD4+ T cells are major survival factors for long-lived splenic plasma cells in a B-cell–depletion context. Blood. 131(14). 1545–1555. 57 indexed citations

12.

Steffann, Julie, Aurore Pouliet, Christine Bole, et al.. (2017). No correlation between mtDNA amount and methylation levels at the CpG island of POLG exon 2 in wild-type and mutant human differentiated cells. Journal of Medical Genetics. 54(5). 324–329. 4 indexed citations

13.

Zomer, Aldert, Thomas Nußbaumer, Christine Bole, et al.. (2016). Comprehensive Identification of Meningococcal Genes and Small Noncoding RNAs Required for Host Cell Colonization. mBio. 7(4). 20 indexed citations

14.

Thévenon, Julien, Caroline Michot, Christine Bole, et al.. (2015). RPL10 mutation segregating in a family with X‐linked syndromic Intellectual Disability. American Journal of Medical Genetics Part A. 167(8). 1908–1912. 22 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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