Samia Pichard

1.3k total citations
25 papers, 193 citations indexed

About

Samia Pichard is a scholar working on Physiology, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Samia Pichard has authored 25 papers receiving a total of 193 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Physiology, 8 papers in Molecular Biology and 8 papers in Clinical Biochemistry. Recurrent topics in Samia Pichard's work include Lysosomal Storage Disorders Research (12 papers), Metabolism and Genetic Disorders (8 papers) and Mitochondrial Function and Pathology (5 papers). Samia Pichard is often cited by papers focused on Lysosomal Storage Disorders Research (12 papers), Metabolism and Genetic Disorders (8 papers) and Mitochondrial Function and Pathology (5 papers). Samia Pichard collaborates with scholars based in France, United States and Belgium. Samia Pichard's co-authors include Manuel Schiff, Hélène Ogier de Baulny, Jean‐François Benoist, Stéphane Auvin, Catherine Caillaud, Juliette Bouchereau, Apolline Imbard, Monique Elmaleh, Odile Rigal and B. Chabrol and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and Clinical Chemistry.

In The Last Decade

Samia Pichard

25 papers receiving 190 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Samia Pichard France 9 103 64 64 40 37 25 193
Vincenza Gragnaniello Italy 9 126 1.2× 110 1.7× 34 0.5× 64 1.6× 56 1.5× 31 254
Fatma Tuba Eminoğlu Türkiye 8 63 0.6× 85 1.3× 58 0.9× 35 0.9× 18 0.5× 58 244
Ken Momosaki Japan 10 163 1.6× 102 1.6× 47 0.7× 77 1.9× 57 1.5× 22 286
Lénaïg Abily-Donval France 10 112 1.1× 157 2.5× 104 1.6× 32 0.8× 40 1.1× 22 311
Marian Girgis Egypt 10 79 0.8× 95 1.5× 84 1.3× 43 1.1× 13 0.4× 27 246
Ramona Salvarinova Canada 8 46 0.4× 109 1.7× 80 1.3× 24 0.6× 15 0.4× 18 202
Serap Sivri Türkiye 11 145 1.4× 120 1.9× 182 2.8× 62 1.6× 41 1.1× 53 342
Suresh Vijay United Kingdom 9 252 2.4× 68 1.1× 73 1.1× 79 2.0× 102 2.8× 31 337
Tanyel Zübarioğlu Türkiye 10 56 0.5× 108 1.7× 121 1.9× 41 1.0× 20 0.5× 52 281
Hsuan-Chieh Liao Taiwan 8 247 2.4× 86 1.3× 67 1.0× 97 2.4× 96 2.6× 8 315

Countries citing papers authored by Samia Pichard

Since Specialization
Citations

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

Fields of papers citing papers by Samia Pichard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Samia Pichard

This figure shows the co-authorship network connecting the top 25 collaborators of Samia Pichard. A scholar is included among the top collaborators of Samia Pichard 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 Samia Pichard. Samia Pichard 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.
Brassier, Anaïs, Pierre Broué, Claude Cancés, et al.. (2023). Effects of miglustat therapy on neurological disorder and survival in early-infantile Niemann-Pick disease type C: a national French retrospective study. Orphanet Journal of Rare Diseases. 18(1). 204–204. 7 indexed citations
2.
Brassier, Anaïs, Samia Pichard, Manuel Schiff, et al.. (2023). Motor outcomes in patients with infantile and juvenile Pompe disease: Lessons from neurophysiological findings. Molecular Genetics and Metabolism. 139(4). 107650–107650. 1 indexed citations
3.
Pichard, Samia, Soumeya Bekri, Catherine Caillaud, et al.. (2023). Natural history of GM1 gangliosidosis—Retrospective cohort study of 61 French patients from 1998 to 2019. Journal of Inherited Metabolic Disease. 46(5). 972–981. 5 indexed citations
4.
Arnoux, Armelle, Anaïs Brassier, Samia Pichard, et al.. (2022). Transition from child to adult health care for patients with lysosomal storage diseases in France: current status and priorities—the TENALYS study, a patient perspective survey. Orphanet Journal of Rare Diseases. 17(1). 68–68. 8 indexed citations
5.
Imbard, Apolline, Anne Spraul, Valérie Barbier, et al.. (2022). Initial presentation, management and follow-up data of 33 treated patients with hereditary tyrosinemia type 1 in the absence of newborn screening. Molecular Genetics and Metabolism Reports. 33. 100933–100933. 4 indexed citations
6.
Schlemmer, Dimitri, Juliette Bouchereau, Samia Pichard, et al.. (2021). LC-MS/MS Identification of Prolidase Deficiency: A Rare Cause of Infantile Hepatosplenomegaly. Clinical Chemistry. 68(3). 478–480. 2 indexed citations
7.
Davison, James, Anaïs Brassier, Alexander Broomfield, et al.. (2021). Mini-COMET study: Effects of repeat avalglucosidase alfa dosing on ptosis in participants with infantile-onset Pompe disease (IOPD) who were previously treated with alglucosidase alfa. Molecular Genetics and Metabolism. 132(2). S31–S32. 1 indexed citations
8.
Cano, Aline, Samia Pichard, Didier Scavarda, et al.. (2020). Cerliponase alfa changes the natural history of children with neuronal ceroid lipofuscinosis type 2: The first French cohort. European Journal of Paediatric Neurology. 30. 17–21. 13 indexed citations
9.
Imbard, Apolline, Bérengère Koehl, Mathie Lorrot, et al.. (2020). Nitrous oxide and vitamin B12 in sickle cell disease: Not a laughing situation. Molecular Genetics and Metabolism Reports. 23. 100579–100579. 4 indexed citations
10.
Dubourg, Christèle, Samia Pichard, Virginie Gandemer, et al.. (2020). Incidental diagnosis of mucopolysaccharidosis type I in an infant with chronic intestinal pseudoobstruction by exome sequencing. Molecular Genetics and Metabolism Reports. 24. 100621–100621. 3 indexed citations
11.
Imbard, Apolline, Jean‐François Benoist, Samia Pichard, et al.. (2019). Diagnostic contribution of metabolic workup for neonatal inherited metabolic disorders in the absence of expanded newborn screening. Scientific Reports. 9(1). 14098–14098. 18 indexed citations
12.
Herenger, Yvan, et al.. (2019). Determining factors of the cognitive outcome in early treated PKU: A study of 39 pediatric patients. Molecular Genetics and Metabolism Reports. 20. 100498–100498. 9 indexed citations
13.
Imbard, Apolline, Nuria García Segarra, M. Tardieu, et al.. (2018). Long-term liver disease in methylmalonic and propionic acidemias. Molecular Genetics and Metabolism. 123(4). 433–440. 15 indexed citations
14.
Bouchereau, Juliette, Edward L. Huttlin, Virgínia Guarani, et al.. (2018). DNAJC12: A molecular chaperone involved in proteostasis, PKU, biogenic amines metabolism and beyond?. Molecular Genetics and Metabolism. 123(3). 285–286. 6 indexed citations
15.
Brassier, Anaïs, Pierre Broué, Claude Cancés, et al.. (2018). Effects of miglustat therapy on neurological disorder and survival in early-infantile Niemann-Pick disease type C: A national French retrospective study. Molecular Genetics and Metabolism. 123(2). S48–S48. 1 indexed citations
16.
Bourillon, Agnès, Samia Pichard, Jean‐François Benoist, et al.. (2017). Mitochondrial acetoacetyl‐CoA thiolase deficiency: basal ganglia impairment may occur independently of ketoacidosis. Journal of Inherited Metabolic Disease. 40(3). 415–422. 11 indexed citations
17.
Dorboz, Imen, Samia Pichard, Agnès Bourillon, et al.. (2016). Transient neonatal renal failure and massive polyuria in MEGDEL syndrome. Molecular Genetics and Metabolism Reports. 7. 8–10. 4 indexed citations
18.
Lucia, Silvana De, et al.. (2016). An unfortunate challenge: Ketogenic diet for the treatment of Lennox–Gastaut syndrome in tyrosinemia type 1. European Journal of Paediatric Neurology. 20(4). 674–677. 6 indexed citations
19.
Pichard, Samia, Hélène Maurey, Nuria García Segarra, et al.. (2015). Angelman syndrome and isovaleric acidemia: What is the link?. SHILAP Revista de lepidopterología. 3. 36–38. 2 indexed citations
20.
Sabourdy, Frédérique, Lionel Mourey, Nathalie Bednarek, et al.. (2015). Natural disease history and characterisation of SUMF1 molecular defects in ten unrelated patients with multiple sulfatase deficiency. Orphanet Journal of Rare Diseases. 10(1). 31–31. 28 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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