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, Agnès Rötig, Henk J. Blom 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

align trajectories

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.

Mitochondrial double-stranded RNA triggers antiviral signalling in humans

2018 417 citations Agnès Rötig, Arnold Münnich et al. profile →

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Bone mineral density in French adults with early-treated phenylketonuria 2025 ·Molecular Genetics and Metabolism ·(unknown), F. Maillot, (unknown), Alain Fouilhoux, L. Astudillo, Christian Lavigne, (unknown), Sylvie Odent, Claire Gay, Manuel Schiff, K. Mazodier, Alice Kuster, (unknown), (unknown), V. Leguy‐Seguin, Claire Douillard, Sybil Charrière	0
2	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 2024 ·Frontiers in Genetics ·Lamisse Mansour‐Hendili, Cyril Gitiaux, (unknown), Céline Latouche, Bénédicte Héron, Tanya Stojkovic, (unknown), Thomas Smol, (unknown), Karine Mention, Yann Nadjar, Manuel Schiff, Julie Lemale, Jamal Ghoumid, Frédèric Gottrand, Cécile Talbotec, Agnès Rötig, Benoît Funalot, Isabelle Desguerre	1
3	Current global vitamin and cofactor prescribing practices for primary mitochondrial diseases: Results of a European reference network survey 2024 ·Journal of Inherited Metabolic Disease ·(unknown), Karit Reinson, Marcello Bellusci, Julien H. Park, Omar Hikmat, Enrico Bertini, Manuel Schiff, Shamima Rahman	2
4	Polyradiculoneuritis on MRI 2024 ·Neurology ·Charles‐Joris Roux, (unknown), Marie Hully, Agnès Rötig, Manuel Schiff, Pascale de Lonlay, Mélodie Aubart, Marianne Alison, (unknown), R. Lévy, Volodia Dangouloff‐Ros, Giulia Barcia, Isabelle Desguerre, Arnold Münnich, Cyril Gitiaux, Nathalie Boddaert	0
5	Late‐onset refractory hemolytic anemia in siblings treated for methionine synthase reductase deficiency: A rare complication possibly prevented by hydroxocobalamin dose escalation? 2024 ·JIMD Reports ·(unknown), Samuel Deshayes, (unknown), Apolline Imbard, Lamisse Mansour‐Hendili, (unknown), Jean François Benoist, Manuel Schiff	1
6	Successful treatment of severe MSUD in Bckdhb^−/− mice with neonatal AAV gene therapy 2023 ·Journal of Inherited Metabolic Disease ·Clément Pontoizeau, (unknown), (unknown), (unknown), (unknown), Marion Benoist, Pasqualina Colella, Antonin Lamazière, Anaïs Brassier, Jean‐Baptiste Arnoux, Agnès Rötig, Chris Ottolenghi, Pascale de Lonlay, Federico Mingozzi, Marina Cavazzana, Manuel Schiff	4
7	Citrulline in the management of patients with urea cycle disorders 2023 ·Orphanet Journal of Rare Diseases ·Apolline Imbard, Juliette Bouchereau, Jean‐Baptiste Arnoux, Anaïs Brassier, Manuel Schiff, (unknown), Clément Pontoizeau, Jean‐François Benoist, Constant Josse, François Montestruc, Pascale de Lonlay	6
8	Enasidenib treatment in two individuals with D-2-hydroxyglutaric aciduria carrying a germline IDH2 mutation 2023 ·Nature Medicine ·Birgit Geoerger, Manuel Schiff, Virginie Penard‐Lacronique, Niklas Darín, (unknown), (unknown), Antonin Lamazière, (unknown), Clément Pontoizeau, Pablo Berlanga, Stéphane Ducassou, Katharine Yen, Michael Su, David P. Schenkein, Chris Ottolenghi, Stéphane de Botton	5
9	Neonatal gene therapy achieves sustained disease rescue of maple syrup urine disease in mice 2022 ·Nature Communications ·Clément Pontoizeau, (unknown), (unknown), (unknown), (unknown), (unknown), Pasqualina Colella, M Girard, Maria Grazia Biferi, Jean‐Baptiste Arnoux, Agnès Rötig, Chris Ottolenghi, Pascale de Lonlay, Federico Mingozzi, Marina Cavazzana, Manuel Schiff	14
10	Real‐world management of maple syrup urine disease (MSUD) metabolic decompensations with branched chain amino acid‐free formulas in France and Germany: A retrospective observational study 2021 ·JIMD Reports ·Pascale de Lonlay, Roland Posset, Ulrike Mütze, Karine Mention, Delphine Lamireau, Manuel Schiff, Aude Servais, (unknown), Anaïs Brassier, (unknown), Claire Douillard, Chris Ottolenghi, Clément Pontoizeau, (unknown), (unknown)	6
11	LC-MS/MS Identification of Prolidase Deficiency: A Rare Cause of Infantile Hepatosplenomegaly 2021 ·Clinical Chemistry ·(unknown), Dimitri Schlemmer, Juliette Bouchereau, (unknown), Samia Pichard, E. Bourrat, Isabelle Melki, Manuel Schiff, Jean‐François Benoist, Apolline Imbard	2
12	Heterogeneity of PNPT1 neuroimaging: mitochondriopathy, interferonopathy or both? 2020 ·Journal of Medical Genetics ·(unknown), Agnès Rötig, Charles‐Joris Roux, R. Lévy, Marco Henneke, Jutta Gärtner, (unknown), (unknown), Uluç Yiş, Laura Konczal, (unknown), (unknown), Pauline Gaignard, Claude Besmond, Laurence Hubert, Marlène Rio, Giulia Barcia, Arnold Münnich, Nathalie Boddaert, Manuel Schiff	5
13	CUGC for lysinuric protein intolerance (LPI) 2020 ·European Journal of Human Genetics ·Diego Martinelli, Manuel Schiff, (unknown), Emanuele Agolini, Antonio Novelli, Carlo Dionisi‐Vici	3
14	Evolutionarily conserved susceptibility of the mitochondrial respiratory chain to SDHI pesticides and its consequence on the impact of SDHIs on human cultured cells 2019 ·PLoS ONE ·Paule Bénit, (unknown), Dominique Chrétien, Sylvie Bortoli, Laurence Huc, Manuel Schiff, Anne‐Paule Gimenez‐Roqueplo, Judith Favier, Pierre Gressèns, Malgorzata Rak, Pierre Rustin	48
15	SLC13A3 variants cause acute reversible leukoencephalopathy and α‐ketoglutarate accumulation 2019 ·Annals of Neurology ·Joseph P. Dewulf, Elsa Wiame, Imen Dorboz, Monique Elmaleh, Apolline Imbard, Dana Dumitriu, Malgorzata Rak, Agnès Bourillon, Raphaël Helaers, (unknown), Florence Renaldo, Odile Boespflug‐Tanguy, Marie‐Françoise Vincent, Jean‐François Benoist, Ron A. Wevers, Avner Schlessinger, Emile Van Schaftingen, Marie‐Cécile Nassogne, Manuel Schiff	19
16	Diagnostic contribution of metabolic workup for neonatal inherited metabolic disorders in the absence of expanded newborn screening 2019 ·Scientific Reports ·(unknown), Apolline Imbard, Jean‐François Benoist, Samia Pichard, Odile Rigal, Olivier Baud, Manuel Schiff	18
17	Long-term liver disease in methylmalonic and propionic acidemias 2018 ·Molecular Genetics and Metabolism ·Apolline Imbard, Nuria García Segarra, M. Tardieu, Pierre Broué, Juliette Bouchereau, Samia Pichard, Hélène Ogier de Baulny, Abdelhamid Slama, Charlotte Mussini, Guy Touati, Marie Danjoux, Pauline Gaignard, Hannes Vogel, F. Labarthe, Manuel Schiff, Jean‐François Benoist	15
18	Fluxomic assay-assisted diagnosis orientation in a cohort of 11 patients with myopathic form of CPT2 deficiency 2018 ·Molecular Genetics and Metabolism ·Monique Fontaine, (unknown), Anne‐Frédérique Dessein, Karine Mention-Mulliez, Dries Dobbelaere, Claire Douillard, Guilhem Solé, Manuel Schiff, R. Jaussaud, Caroline Espil‐Taris, Audrey Boutron, Wim Wuyts, Cécile Acquaviva, Christine Vianey‐Saban, Dominique Roland, Marie Joncquel-Chevalier Curt, Jòseph Vamecq	11
19	Metabolic pathways at the crossroads of diabetes and inborn errors 2017 ·Journal of Inherited Metabolic Disease ·Eric S. Goetzman, Zhenwei Gong, Manuel Schiff, Yan Wang, Radhika Muzumdar	8
20	Correction: Should Metabolic Diseases Be Systematically Screened in Nonsyndromic Autism Spectrum Disorders? 2011 ·PLoS ONE ·Manuel Schiff, (unknown), (unknown), Odile Boespflug‐Tanguy, Marie–Christine Mouren, (unknown), Richard Delorme	9

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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