Bernard Aral

3.6k total citations · 1 hit paper
31 papers, 1.9k citations indexed

About

Bernard Aral is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Bernard Aral has authored 31 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 10 papers in Genetics and 6 papers in Clinical Biochemistry. Recurrent topics in Bernard Aral's work include Metabolism and Genetic Disorders (6 papers), Biochemical and Molecular Research (4 papers) and Blood disorders and treatments (4 papers). Bernard Aral is often cited by papers focused on Metabolism and Genetic Disorders (6 papers), Biochemical and Molecular Research (4 papers) and Blood disorders and treatments (4 papers). Bernard Aral collaborates with scholars based in France, United States and Lebanon. Bernard Aral's co-authors include M. Mitze, Karlheinz Schlenger, Uwe Schäffer, Peter Vaupel, Michael Höckel, P. Kamoun, Laurence Faivre, Chantal Benelli, Nadège Gigot and Guangxu Liu and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and Annals of Neurology.

In The Last Decade

Bernard Aral

31 papers receiving 1.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Association between tumor hypoxia and malignant progression in advanced cancer of the uterine cervix.

1996 1.5k citations Bernard Aral et al. PubMed profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Bernard Aral France	12	925	713	391	286	245	31	1.9k
Uwe Schäffer Germany	9	1.1k 1.2×	680 1.0×	511 1.3×	370 1.3×	332 1.4×	18	2.1k
Paul F.J.W. Rijken Netherlands	24	667 0.7×	502 0.7×	530 1.4×	206 0.7×	212 0.9×	40	1.5k
Kolbein Sundfør Norway	23	1.2k 1.3×	978 1.4×	644 1.6×	406 1.4×	300 1.2×	42	2.5k
J. Loncaster United Kingdom	14	814 0.9×	481 0.7×	450 1.2×	234 0.8×	274 1.1×	24	1.6k
H. Charles Manning United States	18	623 0.7×	769 1.1×	336 0.9×	544 1.9×	240 1.0×	35	1.7k
Davina J. Honess United Kingdom	21	506 0.5×	521 0.7×	357 0.9×	232 0.8×	212 0.9×	49	1.3k
Mary J. Dorie United States	23	846 0.9×	978 1.4×	197 0.5×	611 2.1×	218 0.9×	34	1.9k
Kanthi Galappathi Norway	19	802 0.9×	824 1.2×	377 1.0×	437 1.5×	123 0.5×	28	1.8k
Berit Mathiesen Norway	22	853 0.9×	831 1.2×	474 1.2×	406 1.4×	148 0.6×	30	1.9k
Michael Hoeckel Germany	13	608 0.7×	349 0.5×	288 0.7×	220 0.8×	225 0.9×	17	1.2k

Countries citing papers authored by Bernard Aral

Since Specialization

Citations

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

Fields of papers citing papers by Bernard Aral

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bernard Aral

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

Garrec, Céline, Fabrice Airaud, Nathalie Contentin, et al.. (2023). Germline JAK2 E846D Substitution as the Cause of Erythrocytosis?. Genes. 14(5). 1066–1066. 2 indexed citations

Sonzogni, Laurène, Adeline Granzotto, Mira Maalouf, et al.. (2023). Molecular and Cellular Responses to Ionization Radiation in Untransformed Fibroblasts from the Rothmund–Thomson Syndrome: Influence of the Nucleo-Shuttling of the ATM Protein Kinase. SHILAP Revista de lepidopterología. 3(1). 21–38. 4 indexed citations

Giansily‐Blaizot, Muriel, Guillaume Bouyer, Laurent Pérès, et al.. (2020). Increased incidence of germline PIEZO1 mutations in individuals with idiopathic erythrocytosis. Blood. 137(13). 1828–1832. 23 indexed citations

Aral, Bernard, et al.. (2018). Germline JAK2 L611S mutation in a child with thrombocytosis. Haematologica. 103(8). e372–e373. 8 indexed citations

Marle, Nathalie, Anne‐Laure Mosca‐Boidron, Laurence Faivre, et al.. (2015). 6q16.3q23.3 duplication associated with Prader-Willi-like syndrome. Molecular Cytogenetics. 8(1). 42–42. 8 indexed citations

Elalaoui, Siham Chafai, Laurence Duplomb, Jean‐Baptiste Rivière, et al.. (2014). Autosomal-recessive SASH1 variants associated with a new genodermatosis with pigmentation defects, palmoplantar keratoderma and skin carcinoma. European Journal of Human Genetics. 23(7). 957–962. 37 indexed citations

Gueneau, Lucie, Laurence Duplomb, Pierre Sarda, et al.. (2013). Congenital neutropenia with retinopathy, a new phenotype without intellectual deficiency or obesity secondary to VPS13B mutations. American Journal of Medical Genetics Part A. 164(2). 522–527. 11 indexed citations

Fradin, Mélanie, Bernard Aral, Jean Muller, et al.. (2013). Long-Term Follow-Up and Molecular Characterization of a Patient with a RECQL4 Mutation Spectrum Disorder. Dermatology. 226(4). 353–357. 8 indexed citations

Ceballos-Picot, Irène, Franck Augé, Rong Fu, et al.. (2013). Phenotypic variation among seven members of one family with deficiency of hypoxanthine–guanine phosphoribosyltransferase. Molecular Genetics and Metabolism. 110(3). 268–274. 11 indexed citations

10.

Chehadeh-Djebbar, Salima El, Edward Blair, Muriel Holder‐Espinasse, et al.. (2012). Changing facial phenotype in Cohen syndrome: towards clues for an earlier diagnosis. European Journal of Human Genetics. 21(7). 736–742. 22 indexed citations

11.

Lopez, Estelle, Patrick Callier, Valérie Cormier‐Daire, et al.. (2012). Search for a gene responsible for Floating‐Harbor syndrome on chromosome 12q15q21.1. American Journal of Medical Genetics Part A. 158A(2). 333–339. 6 indexed citations

12.

Piard, Juliette, Muriel Holder‐Espinasse, Bernard Aral, et al.. (2011). Systematic search for neutropenia should be part of the first screening in patients with poikiloderma. European Journal of Medical Genetics. 55(1). 8–11. 18 indexed citations

13.

Ea, Hang‐Korng, et al.. (2009). Severe gouty arthritis and mild neurologic symptoms due to F199C, a newly identified variant of the hypoxanthine guanine phosphoribosyltransferase. Arthritis & Rheumatism. 60(7). 2201–2204. 22 indexed citations

14.

Thauvin‐Robinet, Christel, Brunella Franco, Orsetta Zuffardi, et al.. (2009). Search for genomic imbalances in a cohort of 20 patients with oral–facial–digital syndromes negative for mutations and large rearrangements in the OFD1 gene. American Journal of Medical Genetics Part A. 149A(8). 1846–1849. 4 indexed citations

15.

Malan, Valérie, Jelena Martinović, Férechté Encha‐Razavi, et al.. (2008). Prenatal diagnosis of a ring chromosome 14 in a fetus with a severe skeletal dysplasia. Prenatal Diagnosis. 28(1). 69–71. 2 indexed citations

16.

Lonlay, Pascale de, Chantal Benelli, Françoise Fouque, et al.. (2001). Hyperinsulinism and Hyperammonemia Syndrome: Report of Twelve Unrelated Patients. Pediatric Research. 50(3). 353–357. 55 indexed citations

17.

Rouillac, Christelle, Bernard Aral, Dominique Marchant, et al.. (1999). First prenatal diagnosis of defects in theHsPDX1 gene encoding protein X, an additional lipoyl-containing subunit of the human pyruvate dehydrogenase complex. Prenatal Diagnosis. 19(12). 1160–1164. 7 indexed citations

18.

Kamoun, P., et al.. (1998). [A new inherited metabolic disease: delta1-pyrroline 5-carboxylate synthetase deficiency].. PubMed. 182(1). 131–7; discussion 138. 20 indexed citations

19.

Aral, Bernard & P. Kamoun. (1997). The proline biosynthesis in living organisms. Amino Acids. 13(3-4). 189–217. 25 indexed citations

20.

Liu, Guang, et al.. (1996). Assignment of the Human Gene Encoding the Δ1-Pyrroline-5-carboxylate Synthetase (P5CS) to 10q24.3 byin SituHybridization. Genomics. 37(1). 145–146. 5 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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