Clémence Vanlerberghe

619 total citations
12 papers, 108 citations indexed

About

Clémence Vanlerberghe is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Clémence Vanlerberghe has authored 12 papers receiving a total of 108 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Clémence Vanlerberghe's work include Congenital heart defects research (3 papers), Hedgehog Signaling Pathway Studies (2 papers) and Congenital Heart Disease Studies (2 papers). Clémence Vanlerberghe is often cited by papers focused on Congenital heart defects research (3 papers), Hedgehog Signaling Pathway Studies (2 papers) and Congenital Heart Disease Studies (2 papers). Clémence Vanlerberghe collaborates with scholars based in France, Netherlands and United States. Clémence Vanlerberghe's co-authors include Florence Petit, Sylvie Manouvrier‐Hanu, Jamal Ghoumid, Fabienne Escande, Frédéric Frénois, Anne‐Sophie Jourdain, Thomas Smol, Guy Vaksmann, Matthieu Jung and Nathalie Boutry and has published in prestigious journals such as Frontiers in Psychology, Genetics in Medicine and European Journal of Human Genetics.

In The Last Decade

Clémence Vanlerberghe

9 papers receiving 108 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Clémence Vanlerberghe France	6	67	34	15	13	13	12	108
Billur Moghaddam United States	4	22 0.3×	53 1.6×	10 0.7×	6 0.5×	12 0.9×	4	78
Shahida Moosa South Africa	10	96 1.4×	91 2.7×	8 0.5×	4 0.3×	16 1.2×	29	169
María de la Luz Arenas‐Sordo Mexico	7	42 0.6×	44 1.3×	6 0.4×	2 0.2×	13 1.0×	21	109
Hatice Mutlu Albayrak Türkiye	7	67 1.0×	41 1.2×	17 1.1×	2 0.2×	14 1.1×	26	147
Fiorenza Soli Italy	6	41 0.6×	33 1.0×	9 0.6×	4 0.3×	5 0.4×	10	72
Ina Amarillo United States	9	100 1.5×	127 3.7×	7 0.5×	5 0.4×	10 0.8×	22	188
Madhura Bakshi Australia	5	58 0.9×	69 2.0×	16 1.1×	2 0.2×	10 0.8×	8	160
Laura Konczal United States	6	77 1.1×	119 3.5×	6 0.4×	3 0.2×	19 1.5×	13	185
Kévin Cassinari France	9	56 0.8×	34 1.0×	8 0.5×		9 0.7×	18	150
Charlene Schramm United States	4	64 1.0×	21 0.6×	9 0.6×	9 0.7×	14 1.1×	5	95

Countries citing papers authored by Clémence Vanlerberghe

Since Specialization

Citations

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

Fields of papers citing papers by Clémence Vanlerberghe

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Clémence Vanlerberghe

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

Vanlerberghe, Clémence, Frédéric Frénois, Thomas Smol, et al.. (2024). RPL26 variants: A rare cause of Diamond-Blackfan anemia syndrome with multiple congenital anomalies at the forefront. Genetics in Medicine. 26(12). 101266–101266.

Brunelle, Perrine, C. Thuillier, Clémence Vanlerberghe, et al.. (2024). Expanded phenotypic spectrum of UDP‐glucose‐6‐dehydrogenase recessive neurodevelopmental disorder: Two novel descriptions with or without epileptic encephalopathy. American Journal of Medical Genetics Part A. 194(12). e63820–e63820. 1 indexed citations

Vanlerberghe, Clémence, Frédéric Frénois, Emilie Ait‐Yahya, et al.. (2024). Functional characterization vs in silico prediction for TBX5 missense and splice variants in Holt-Oram syndrome. Genetics in Medicine. 26(12). 101267–101267.

Colson, Cindy, et al.. (2024). Primary Failure of Dental Eruption Due to Variants Parathyroid Hormone Receptor 1: Retrospective Study and Proposal of Guidelines Treatment. Journal of Craniofacial Surgery. 35(2). e209–e213.

Vanlerberghe, Clémence, et al.. (2023). Parenting stress and needs for social support in mothers and fathers of deaf or hard of hearing children. Frontiers in Psychology. 14. 1229420–1229420. 9 indexed citations

Delsart, Pascal, Clémence Vanlerberghe, Françis Juthier, et al.. (2021). The natural history of a family with aortic dissection associated with a novel ACTA2 variant. Annals of Vascular Surgery. 77. 348.e7–348.e11. 5 indexed citations

Lyonnet, Stanislas, B. van der Zwaag, Maartje J. Vogel, et al.. (2020). Fraser syndrome without cryptophthalmos: Two cases. European Journal of Medical Genetics. 63(4). 103839–103839. 3 indexed citations

Vanlerberghe, Clémence, Anne‐Sophie Jourdain, Jamal Ghoumid, et al.. (2018). Holt-Oram syndrome: clinical and molecular description of 78 patients with TBX5 variants. European Journal of Human Genetics. 27(3). 360–368. 29 indexed citations

Vanlerberghe, Clémence, Nathalie Boutry, & Florence Petit. (2018). Genetics of patella hypoplasia/agenesis. Clinical Genetics. 94(1). 43–53. 7 indexed citations

10.

Ghoumid, Jamal, Florence Petit, Odile Boute‐Bénéjean, et al.. (2017). Cerebellar hypoplasia with endosteal sclerosis is a POLR3-related disorder. European Journal of Human Genetics. 25(8). 1011–1014. 10 indexed citations

11.

Ghoumid, Jamal, Anne‐Sophie Jourdain, Frédéric Frénois, et al.. (2017). Blepharocheilodontic syndrome is a CDH1 pathway–related disorder due to mutations in CDH1 and CTNND1. Genetics in Medicine. 19(9). 1013–1021. 35 indexed citations

12.

Vanlerberghe, Clémence, Laurence Faivre, Florence Petit, et al.. (2014). Intrafamilial variability of ZRS‐associated syndrome: characterization of a mosaic ZRS mutation by pyrosequencing. Clinical Genetics. 88(5). 479–483. 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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