Delphine Bacq

1.9k total citations
12 papers, 888 citations indexed

About

Delphine Bacq is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Delphine Bacq has authored 12 papers receiving a total of 888 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Genetics. Recurrent topics in Delphine Bacq's work include Coagulation, Bradykinin, Polyphosphates, and Angioedema (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Blood Coagulation and Thrombosis Mechanisms (2 papers). Delphine Bacq is often cited by papers focused on Coagulation, Bradykinin, Polyphosphates, and Angioedema (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Blood Coagulation and Thrombosis Mechanisms (2 papers). Delphine Bacq collaborates with scholars based in France, United Kingdom and Spain. Delphine Bacq's co-authors include Arnold Münnich, Dimitri Schlemmer, Gustav Dallner, Agnès Rötig, Agnés Delahodde, Irina Giurgea, Dominique Chrétien, Pascale de Lonlay, David V. Milford and Olivier Gribouval and has published in prestigious journals such as Science, Journal of Clinical Investigation and Nature Communications.

In The Last Decade

Delphine Bacq

12 papers receiving 874 citations

Peers

Delphine Bacq

GENET

HEMAT

EEE

David R. Bachinsky United States

Sutip Navankasattusas United States

Dorota Piekutowska‐Abramczuk Poland

Marta Albajar Spain

Alessandra Drusco United States

Simone Clamens France

Silvia Di Giandomenico Italy

Jason Ho Canada

V. Poulaki United States

Xinchun Pi United States

David R. Bachinsky United States

Delphine Bacq

1.2k ×2.4

380 ×1.3

GENET

81 ×0.5

29 ×0.3

HEMAT

30 ×0.4

EEE

Citations per year, relative to Delphine Bacq Delphine Bacq (= 1×) peers David R. Bachinsky

Countries citing papers authored by Delphine Bacq

Since Specialization

Citations

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

Fields of papers citing papers by Delphine Bacq

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Delphine Bacq

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

All Works

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12 of 12 papers shown

Vallée, Maxime, Tiffany M. Delhomme, E. Maubec, et al.. (2021). The PI3K/mTOR Pathway Is Targeted by Rare Germline Variants in Patients with Both Melanoma and Renal Cell Carcinoma. Cancers. 13(9). 2243–2243. 5 indexed citations

Wendeu‐Foyet, Gaëlle, Yves Akoli Koudou, Sylvie Cénée, et al.. (2019). Circadian genes and risk of prostate cancer: Findings from the EPICAP study. International Journal of Cancer. 145(7). 1745–1753. 22 indexed citations

Letouzé, Éric, Jayendra Shinde, Victor Renault, et al.. (2017). Mutational signatures reveal the dynamic interplay of risk factors and cellular processes during liver tumorigenesis. Nature Communications. 8(1). 1315–1315. 176 indexed citations

Santos, Reinaldo S. Dos, Anne Philippi, Lorella Marselli, et al.. (2017). dUTPase (DUT) Is Mutated in a Novel Monogenic Syndrome With Diabetes and Bone Marrow Failure. Diabetes. 66(4). 1086–1096. 19 indexed citations

Zinovieva, Elena, Catherine Bourgain, Amir Kadi, et al.. (2009). Comprehensive Linkage and Association Analyses Identify Haplotype, Near to the TNFSF15 Gene, Significantly Associated with Spondyloarthritis. PLoS Genetics. 5(6). e1000528–e1000528. 46 indexed citations

Giurgea, Irina, Dimitri Schlemmer, Gustav Dallner, et al.. (2007). Prenyldiphosphate synthase, subunit 1 (PDSS1) and OH-benzoate polyprenyltransferase (COQ2) mutations in ubiquinone deficiency and oxidative phosphorylation disorders. Journal of Clinical Investigation. 117(3). 765–772. 193 indexed citations

Borck, Guntram, Marlène Rio, Damien Sanlaville, et al.. (2004). Genome‐wide screening using automated fluorescent genotyping to detect cryptic cytogenetic abnormalities in children with idiopathic syndromic mental retardation. Clinical Genetics. 66(2). 122–127. 6 indexed citations

Almasy, Laura, José Manuel Soria, Juan Carlos Souto, et al.. (2003). A Quantitative Trait Locus Influencing Free Plasma Protein S Levels on Human Chromosome 1q. Arteriosclerosis Thrombosis and Vascular Biology. 23(3). 508–511. 25 indexed citations

Soria, José Manuel, Laura Almasy, Juan Carlos Souto, et al.. (2002). A Quantitative-Trait Locus in the Human Factor XII Gene Influences Both Plasma Factor XII Levels and Susceptibility to Thrombotic Disease. The American Journal of Human Genetics. 70(3). 567–574. 72 indexed citations

10.

Mollet, Géraldine, Rémi Salomon, Olivier Gribouval, et al.. (2002). The gene mutated in juvenile nephronophthisis type 4 encodes a novel protein that interacts with nephrocystin. Nature Genetics. 32(2). 300–305. 158 indexed citations

11.

Faivre, Laurence, André Mégarbané, Abdulrahman Alswaid, et al.. (2002). Homozygosity mapping of a Weill-Marchesani syndrome locus to chromosome 19p13.3-p13.2. Human Genetics. 110(4). 366–370. 28 indexed citations

12.

Molinari, Florence, Marlène Rio, Virginia Meskenaïte, et al.. (2002). Truncating Neurotrypsin Mutation in Autosomal Recessive Nonsyndromic Mental Retardation. Science. 298(5599). 1779–1781. 138 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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