Manuel Schiff

5.9k total citations · 1 hit paper
115 papers, 2.3k citations indexed

About

Manuel Schiff is a scholar working on Clinical Biochemistry, Molecular Biology and Rheumatology. According to data from OpenAlex, Manuel Schiff has authored 115 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Clinical Biochemistry, 65 papers in Molecular Biology and 21 papers in Rheumatology. Recurrent topics in Manuel Schiff's work include Metabolism and Genetic Disorders (70 papers), Mitochondrial Function and Pathology (34 papers) and Folate and B Vitamins Research (18 papers). Manuel Schiff is often cited by papers focused on Metabolism and Genetic Disorders (70 papers), Mitochondrial Function and Pathology (34 papers) and Folate and B Vitamins Research (18 papers). Manuel Schiff collaborates with scholars based in France, United States and Germany. Manuel Schiff's co-authors include Hélène Ogier de Baulny, Pierre Rustin, Paule Bénit, Jean‐François Benoist, Carlo Dionisi‐Vici, Juliette Bouchereau, Riyad El‐Khoury, Henk J. Blom, Agnès Rötig and Arnold Münnich and has published in prestigious journals such as Nature, Nature Medicine and Nature Communications.

In The Last Decade

Manuel Schiff

110 papers receiving 2.3k citations

Hit Papers

Mitochondrial double-stra... 2018 2026 2020 2023 2018 100 200 300 400
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.

  1. Mitochondrial double-stranded RNA triggers antiviral signalling in humans
    2018 417 citations Agnès Rötig, Arnold Münnich et al. profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Manuel Schiff 1.3k 870 398 380 265 115 2.3k
Saskia B. Wortmann 1.9k 1.4× 1.0k 1.2× 233 0.6× 302 0.8× 148 0.6× 122 2.7k
J. Jaeken 2.0k 1.5× 606 0.7× 262 0.7× 649 1.7× 408 1.5× 90 2.8k
Si Houn Hahn 1.2k 0.9× 801 0.9× 203 0.5× 229 0.6× 101 0.4× 81 2.4k
David Cheillan 886 0.7× 414 0.5× 133 0.3× 489 1.3× 148 0.6× 79 1.9k
M. Estela Rubio‐Gozalbo 1.2k 0.9× 1.6k 1.9× 454 1.1× 806 2.1× 86 0.3× 114 2.8k
Antònia Ribes 2.5k 1.9× 2.1k 2.5× 558 1.4× 586 1.5× 113 0.4× 175 3.9k
C. Marsac 2.4k 1.8× 1.4k 1.7× 152 0.4× 445 1.2× 127 0.5× 102 3.4k
Lambert van den Heuvel 2.9k 2.1× 1.4k 1.6× 92 0.2× 239 0.6× 190 0.7× 62 3.6k
Giuseppe Fiermonte 3.0k 2.2× 1.5k 1.7× 194 0.5× 549 1.4× 93 0.4× 69 4.0k
J. G. M. Huijmans 867 0.6× 398 0.5× 190 0.5× 555 1.5× 85 0.3× 72 2.1k

Countries citing papers authored by Manuel Schiff

Since Specialization
Citations

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

Fields of papers citing papers by Manuel Schiff

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manuel Schiff

This figure shows the co-authorship network connecting the top 25 collaborators of Manuel Schiff. A scholar is included among the top collaborators of Manuel Schiff 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 Manuel Schiff. Manuel Schiff 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.
Maillot, F., Alain Fouilhoux, L. Astudillo, et al.. (2025). Bone mineral density in French adults with early-treated phenylketonuria. Molecular Genetics and Metabolism. 144(3). 109044–109044.
2.
Mansour‐Hendili, Lamisse, Cyril Gitiaux, Céline Latouche, et al.. (2024). Recurrent “outsider” intronic variation in the SLC5A6 gene causes severe mixed axonal and demyelinating neuropathy, cyclic vomiting and optic atrophy in 3 families from Maghreb. Frontiers in Genetics. 15. 1352006–1352006. 1 indexed citations
3.
Reinson, Karit, Marcello Bellusci, Julien H. Park, et al.. (2024). Current global vitamin and cofactor prescribing practices for primary mitochondrial diseases: Results of a European reference network survey. Journal of Inherited Metabolic Disease. 48(1). e12805–e12805. 2 indexed citations
4.
5.
Roux, Charles‐Joris, Marie Hully, Agnès Rötig, et al.. (2024). Polyradiculoneuritis on MRI. Neurology. 102(11). e209356–e209356.
6.
Geoerger, Birgit, Manuel Schiff, Virginie Penard‐Lacronique, et al.. (2023). Enasidenib treatment in two individuals with D-2-hydroxyglutaric aciduria carrying a germline IDH2 mutation. Nature Medicine. 29(6). 1358–1363. 5 indexed citations
7.
Pontoizeau, Clément, Marion Benoist, Pasqualina Colella, et al.. (2023). Successful treatment of severe MSUD in Bckdhb−/− mice with neonatal AAV gene therapy. Journal of Inherited Metabolic Disease. 47(1). 41–49. 4 indexed citations
8.
Imbard, Apolline, Juliette Bouchereau, Jean‐Baptiste Arnoux, et al.. (2023). Citrulline in the management of patients with urea cycle disorders. Orphanet Journal of Rare Diseases. 18(1). 207–207. 6 indexed citations
9.
Pontoizeau, Clément, Pasqualina Colella, M Girard, et al.. (2022). Neonatal gene therapy achieves sustained disease rescue of maple syrup urine disease in mice. Nature Communications. 13(1). 3278–3278. 14 indexed citations
10.
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
11.
12.
Martinelli, Diego, et al.. (2020). CUGC for lysinuric protein intolerance (LPI). European Journal of Human Genetics. 28(8). 1129–1134. 3 indexed citations
13.
Rötig, Agnès, Charles‐Joris Roux, R. Lévy, et al.. (2020). Heterogeneity of PNPT1 neuroimaging: mitochondriopathy, interferonopathy or both?. Journal of Medical Genetics. 59(2). 204–208. 5 indexed citations
14.
Bénit, Paule, Dominique Chrétien, Sylvie Bortoli, et al.. (2019). Evolutionarily conserved susceptibility of the mitochondrial respiratory chain to SDHI pesticides and its consequence on the impact of SDHIs on human cultured cells. PLoS ONE. 14(11). e0224132–e0224132. 48 indexed citations
15.
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
16.
Dewulf, Joseph P., Elsa Wiame, Imen Dorboz, et al.. (2019). SLC13A3 variants cause acute reversible leukoencephalopathy and α‐ketoglutarate accumulation. Annals of Neurology. 85(3). 385–395. 19 indexed citations
17.
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
18.
Fontaine, Monique, Anne‐Frédérique Dessein, Karine Mention-Mulliez, et al.. (2018). Fluxomic assay-assisted diagnosis orientation in a cohort of 11 patients with myopathic form of CPT2 deficiency. Molecular Genetics and Metabolism. 123(4). 441–448. 11 indexed citations
19.
Goetzman, Eric S., Zhenwei Gong, Manuel Schiff, Yan Wang, & Radhika Muzumdar. (2017). Metabolic pathways at the crossroads of diabetes and inborn errors. Journal of Inherited Metabolic Disease. 41(1). 5–17. 8 indexed citations
20.

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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