Sandra Mercier

3.8k total citations
41 papers, 662 citations indexed

About

Sandra Mercier is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Sandra Mercier has authored 41 papers receiving a total of 662 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 13 papers in Genetics and 9 papers in Genetics. Recurrent topics in Sandra Mercier's work include Hedgehog Signaling Pathway Studies (9 papers), Muscle Physiology and Disorders (7 papers) and Neurogenetic and Muscular Disorders Research (7 papers). Sandra Mercier is often cited by papers focused on Hedgehog Signaling Pathway Studies (9 papers), Muscle Physiology and Disorders (7 papers) and Neurogenetic and Muscular Disorders Research (7 papers). Sandra Mercier collaborates with scholars based in France, United States and United Kingdom. Sandra Mercier's co-authors include Sylvie Odent, Christèle Dubourg, Véronique David, Yann Péréon, Daniel Pineda‐Alvarez, Maximilian Muenke, Claude Bendavid, Benjamin D. Solomon, Valérie Dupé and Erich Roessler and has published in prestigious journals such as Development, Neurology and Scientific Reports.

In The Last Decade

Sandra Mercier

35 papers receiving 652 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sandra Mercier France 13 486 331 108 104 69 41 662
Shila Mekhoubad United States 5 1.2k 2.5× 356 1.1× 147 1.4× 99 1.0× 36 0.5× 5 1.3k
Katherine Holman Australia 15 529 1.1× 522 1.6× 31 0.3× 28 0.3× 53 0.8× 31 911
Pamela Magini Italy 16 347 0.7× 349 1.1× 53 0.5× 52 0.5× 39 0.6× 38 717
Lorraine Lawrence United Kingdom 10 394 0.8× 195 0.6× 47 0.4× 47 0.5× 17 0.2× 11 602
Mahdi Sarmady United States 13 577 1.2× 297 0.9× 14 0.1× 32 0.3× 27 0.4× 23 933
Oz Pomp United States 15 441 0.9× 106 0.3× 30 0.3× 29 0.3× 53 0.8× 18 638
Anne Destrèe Belgium 11 219 0.5× 253 0.8× 31 0.3× 68 0.7× 21 0.3× 13 458
Pierpaolo Peruzzi United States 14 470 1.0× 90 0.3× 26 0.2× 173 1.7× 108 1.6× 29 785
Pamela Brock United States 15 277 0.6× 286 0.9× 45 0.4× 55 0.5× 68 1.0× 39 712
Adam B. Kanis United States 11 477 1.0× 255 0.8× 40 0.4× 43 0.4× 33 0.5× 13 745

Countries citing papers authored by Sandra Mercier

Since Specialization
Citations

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

Fields of papers citing papers by Sandra Mercier

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sandra Mercier

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

All Works

20 of 20 papers shown
1.
Grand, Katheryn, Pedro A. Sanchez‐Lara, Thierry Levade, et al.. (2025). Acid Ceramidase Deficiency. Neurology Genetics. 11(2). e200243–e200243.
2.
Li, Dong, Armelle Magot, Yann Péréon, et al.. (2024). Expanding the Spectrum of Congenital Myopathy Linked to Variants in the MYBPC1 Gene. Neurology Clinical Practice. 14(3). e200228–e200228. 1 indexed citations
3.
Fernández‐Eulate, Gorka, Girolamo Alfieri, Marco Spinazzi, et al.. (2024). Phenotype variability and natural history of X-linked myopathy with excessive autophagy. Journal of Neurology. 271(7). 4008–4018. 1 indexed citations
4.
Bezieau, Stéphane, Wallid Deb, Sandra Mercier, et al.. (2023). Understanding neurodevelopmental proteasomopathies as new rare disease entities: A review of current concepts, molecular biomarkers, and perspectives. Genes & Diseases. 11(6). 101130–101130. 2 indexed citations
5.
6.
Pacault, Mathilde, Marie Vincent, Thomas Besnard, et al.. (2018). New splicing pathogenic variant in EBP causing extreme familial variability of Conradi–Hünermann–Happle Syndrome. European Journal of Human Genetics. 26(12). 1784–1790. 5 indexed citations
7.
Pastré, Jean, et al.. (2018). Fibrose pulmonaire au cours de la poïkilodermie héréditaire sclérosante associée à la mutation du gène FAM111B : à propos d’un cas. Revue des Maladies Respiratoires. 35(9). 968–973. 6 indexed citations
8.
Nizon, Mathilde, Jean‐Michel Vallat, Madeleine Joubert, et al.. (2016). Two novel variants in CNTNAP1 in two siblings presenting with congenital hypotonia and hypomyelinating neuropathy. European Journal of Human Genetics. 25(1). 150–152. 17 indexed citations
9.
Péréon, Yann, Sandra Mercier, & Armelle Magot. (2015). Physiopathologie de la dystrophie musculaire de Duchenne. Archives de Pédiatrie. 22(12). 12S18–12S23. 3 indexed citations
10.
Küry, Sébastien, Sandra Mercier, Gasnat Shaboodien, et al.. (2015). CUGC for hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis (POIKTMP). European Journal of Human Genetics. 24(5). 779–779. 8 indexed citations
11.
Magot, Armelle, Sandra Mercier, & Yann Péréon. (2015). Particularités de la dystrophie musculaire de Becker et des femmes conductrices. Archives de Pédiatrie. 22(12). 12S31–12S36. 1 indexed citations
12.
Magot, Armelle, Philippe Latour, Julie Perrier, et al.. (2014). Clinical and electrophysiological features in a French family presenting with seipinopathy. Neuromuscular Disorders. 25(2). 161–164. 3 indexed citations
13.
Isidor, Bertrand, Tiphaine Lefebvre, S. Barbarot, et al.. (2013). Palmo‐Plantar hyperkeratosis, intellectual disability, and spastic paraplegia in two maternal half brothers: Further evidence for an X‐linked inheritance. American Journal of Medical Genetics Part A. 161(6). 1390–1393. 1 indexed citations
14.
Mercier, Sandra, Christèle Dubourg, Nicolas Garcelon, et al.. (2011). New findings for phenotype–genotype correlations in a large European series of holoprosencephaly cases. Journal of Medical Genetics. 48(11). 752–760. 73 indexed citations
15.
Dubourg, Christèle, Véronique David, Andrea Gropman, et al.. (2010). Clinical utility gene card for: Holoprosencephaly. European Journal of Human Genetics. 19(1). 3–3. 11 indexed citations
16.
Solomon, Benjamin D., Daniel Pineda‐Alvarez, Sandra Mercier, et al.. (2010). Holoprosencephaly flashcards: A summary for the clinician. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 154C(1). 3–7. 13 indexed citations
17.
Dupé, Valérie, Lucie Rochard, Sandra Mercier, et al.. (2010). NOTCH, a new signaling pathway implicated in holoprosencephaly. Human Molecular Genetics. 20(6). 1122–1131. 37 indexed citations
18.
Mercier, Sandra, Christèle Dubourg, Laurent Pasquier, et al.. (2010). Genetic counseling and “molecular” prenatal diagnosis of holoprosencephaly (HPE). American Journal of Medical Genetics Part C Seminars in Medical Genetics. 154C(1). 191–196. 31 indexed citations
19.
Sigal, R., A Margulis, Sandra Mercier, et al.. (2000). [Cerebral magnetic resonance imaging (MRI) in the diagnosis of leptomeningeal carcinomatosis in melanoma patients].. PubMed. 127(1). 29–32. 5 indexed citations
20.
Lassau, Nathalie, Sandra Mercier, Serge Koscielny, et al.. (1999). Prognostic value of high-frequency sonography and color Doppler sonography for the preoperative assessment of melanomas.. American Journal of Roentgenology. 172(2). 457–461. 54 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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