David Cheillan

4.2k citations

79 papers · 2.0k · h-index 25

Impact in

Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
Cell Biology top 5%
- Muscle metabolism and nutrition
- Cellular transport and secretion

Papers in

Molecular Biology 28
- Sphingolipid Metabolism and Signaling 8
- Peroxisome Proliferator-Activated Receptors 6
- Glycosylation and Glycoproteins Research 5
Clinical Biochemistry 23
- Metabolism and Genetic Disorders 23

Co-authors: Christine Vianey‐Saban (11 shared papers)Monique Piraud (6 shared papers)Marie‐Caroline Michalski (12 shared papers)Nathalie Guffon (5 shared papers)Michel Roussey (4 shared papers)Anne‐Frédérique Dessein (2 shared papers)Dries Dobbelaere (1 shared paper)Jòseph Vamecq (2 shared papers)
Journals: International Journal of Neonatal Screening (7 papers)Journal of Inherited Metabolic Disease (6 papers)Molecular Genetics and Metabolism (6 papers)Biochimie (3 papers)Journal of Cystic Fibrosis (3 papers)
Partner nations: France United States Netherlands

In The Last Decade

David Cheillan

76 papers receiving 1.9k citations

Peers

Countries citing papers authored by David Cheillan

Since Specialization

Citations

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

Fields of papers citing papers by David Cheillan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside David Cheillan, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with David Cheillan Line = papers co-authored together David Cheillan links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 79 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Creatine biosynthesis and transport in health and disease Biochimie ·Marie Joncquel-Chevalier Curt, Pia‐Manuela Voicu, Monique Fontaine, Anne‐Frédérique Dessein, Nicole Porchet, Karine Mention-Mulliez, Dries Dobbelaere, Gustavo Soto‐Ares, David Cheillan, Jòseph Vamecq	2015	169
2	TMEM165 Deficiency Causes a Congenital Disorder of Glycosylation The American Journal of Human Genetics ·François Foulquier, Mustapha Amyere, Jaak Jaeken, Renate Zeevaert, Els Schollen, Valérie Race, Riet Bammens, Willy Morelle, Claire Rosnoblet, Dominique Legrand, Didier Demaegd, Neil R.M. Buist, David Cheillan, Nathalie Guffon, Pierre Morsomme, Willem Annaert, Hudson H. Freeze, Emile Van Schaftingen, Miikka Vikkula, Gert Matthijs	2012	166
3	Steroid Profiling by Tandem Mass Spectrometry Improves the Positive Predictive Value of Newborn Screening for Congenital Adrenal Hyperplasia The Journal of Clinical Endocrinology & Metabolism ·Carla Minutti, Jean M. Lacey, Mark J Magera, Si Houn Hahn, Mark McCann, Andreas Schulze, David Cheillan, C. Dorche, Donald H. Chace, James Lymp, Donald Zimmerman, Piero Rinaldo, Dietrich Matern	2004	124
4	Early Neurodegeneration Progresses Independently of Microglial Activation by Heparan Sulfate in the Brain of Mucopolysaccharidosis IIIB Mice PLoS ONE ·Jérôme Ausseil, Nathalie Desmaris, Stéphanie Bigou, Ruben Attali, Sébastien Corbineau, Sandrine Vitry, Mathieu Parent, David Cheillan, Maria Fuller, Irène Maire, Marie‐Thérèse Vanier, Jean‐Michel Heard	2008	112
5	TNF-α- and tumor-induced skeletal muscle atrophy involves sphingolipid metabolism Skeletal Muscle ·Joffrey De Larichaudy, Alessandra Zufferli, Filippo Serra, Andrea M. Isidori, Fabio Naro, Kévin Dessalle, Marine Desgeorges, Monique Piraud, David Cheillan, Hubert Vidal, Étienne Lefai, Georges Némoz	2012	104
6	High frequency of creatine deficiency syndromes in patients with unexplained mental retardation Neurology ·Laurence Lion‐François, David Cheillan, G. Pitelet, Cécile Acquaviva, G. Bussy, François Cotton, Laurent Guibaud, Daniel Gérard, Clotilde Rivier, Christine Vianey‐Saban, C. Jakobs, Gajja S. Salomons, V. des Portes	2006	74
7	Increased incidence of congenital hypothyroidism in France from 1982 to 2012: a nationwide multicenter analysis Annals of Epidemiology ·Yaya Barry, Christophe Bonaldi, V. Goulet, R. Coutant, Juliane Léger, A.-C. Paty, Dominique Delmas, David Cheillan, Michel Roussey	2015	69
8	Polar lipid composition of bioactive dairy co-products buttermilk and butterserum: Emphasis on sphingolipid and ceramide isoforms Food Chemistry ·(unknown), David Cheillan, Marielle Blot, Patricia Daira, Michèle Trauchessec, Séverine Ruet, Jean-Yves Gassi, Eric Beaucher, Benoît Robert, Nadine Leconte, Saı̈d Bouhallab, Frédéric Gaucheron, Geneviève Gésan-Guiziou, Marie‐Caroline Michalski	2017	69
9	Milk Polar Lipids Affect In Vitro Digestive Lipolysis and Postprandial Lipid Metabolism in Mice Journal of Nutrition ·Manon Lecomte, Claire Bourlieu‐Lacanal, Emmanuelle Meugnier, Armelle Penhoat, David Cheillan, Gaëlle Pineau, Emmanuelle Loizon, Michèle Trauchessec, Mathilde Claude, Olivia Ménard, Alain Géloën, Fabienne Laugerette, Marie‐Caroline Michalski	2015	59
10	Whole‐exome sequencing improves the diagnosis yield in sporadic infantile spasm syndrome Clinical Genetics ·S. Dimassi, (unknown), Dorothée Ville, Alain Calender, Cyril Mignot, Nadia Boutry‐Kryza, Julitta de Bellescize, Clotilde Rivier-Ringenbach, Emilie Bourel‐Ponchel, David Cheillan, Thomas Simonet, Kim Maincent, Massimiliano Rossi, Marianne Till, Soumaya Mougou-Zerelli, Patrick Edery, A. Saad, Delphine Héron, V. des Portes, Damien Sanlaville, Gaëtan Lesca	2015	58
11	Sphingolipid-mediated inflammatory signaling leading to autophagy inhibition converts erythropoiesis to myelopoiesis in human hematopoietic stem/progenitor cells Cell Death and Differentiation ·Marion Orsini, Sébastien Chateauvieux, Jiyun Rhim, Anthoula Gaigneaux, David Cheillan, Christo Christov, Mario Dicato, Franck Morceau, Marc Diederich	2018	55
12	LC-MS/MS multiplex analysis of lysosphingolipids in plasma and amniotic fluid: A novel tool for the screening of sphingolipidoses and Niemann-Pick type C disease PLoS ONE ·Magali Pettazzoni, Roseline Froissart, Cécile Pagan, Marie T. Vanier, Séverine Ruet, Philippe Latour, Nathalie Guffon, Alain Fouilhoux, Dominique P. Germain, Thierry Levade, Christine Vianey‐Saban, Monique Piraud, David Cheillan	2017	51
13	Treatment by oral creatine, L‐arginine and L‐glycine in six severely affected patients with creatine transporter defect Journal of Inherited Metabolic Disease ·Vassili Valayannopoulos, Nathalie Boddaert, A. Chabli, Valérie Barbier, Isabelle Desguerre, Anne Philippe, Alexandra Afenjar, Michel Mazzuca, David Cheillan, Arnold Münnich, Yves de Keyzer, Cornelis Jakobs, Gajja S. Salomons, Pascale de Lonlay	2011	48
14	Milk Polar Lipids in a High‐Fat Diet Can Prevent Body Weight Gain: Modulated Abundance of Gut Bacteria in Relation with Fecal Loss of Specific Fatty Acids Molecular Nutrition & Food Research ·Marine Milard, Fabienne Laugerette, Annie Durand, Charline Buisson, Emmanuelle Meugnier, Emmanuelle Loizon, Corinne Louche‐Pélissier, Valérie Sauvinet, Lorna Garnier, Sébastien Viel, Karène Bertrand, Florent Joffre, David Cheillan, Lydie Humbert, Dominique Rainteau, Pascale Plaisancié, Laure B. Bindels, Audrey M. Neyrinck, Nathalie M. Delzenne, Marie‐Caroline Michalski	2019	47
15	Determination of Guanidinoacetate and Creatine in Urine and Plasma by Liquid Chromatography–Tandem Mass Spectrometry Clinical Chemistry ·S. Cognat, David Cheillan, Monique Piraud, Birthe Roos, Cornelis Jakobs, Christine Vianey‐Saban	2004	38
16	Thirteen New Patients with Guanidinoacetate Methyltransferase Deficiency and Functional Characterization of Nineteen Novel Missense Variants in theGAMTGene Human Mutation ·Saadet Mercimek‐Mahmutoglu, Joseph Ndika, Warsha A. Kanhai, Thierry Billette de Villemeur, David Cheillan, Ernst Christensen, Nathalie Dorison, Vickie Hannig, Yvonne Hendriks, Floris C. Hofstede, Laurence Lion‐François, Allan M. Lund, Helen Mundy, Gaele Pitelet, Miquel Raspall‐Chaure, Jessica A. Scott-Schwoerer, Katalin Szakszon, Vassili Valayannopoulos, Monique Williams, Gajja S. Salomons	2014	38
17	Neonatal screening for cystic fibrosis: Comparing the performances of IRT/DNA and IRT/PAP Journal of Cystic Fibrosis ·Jacques Sarles, Roch Giorgi, Patrice Berthézène, Anne Munck, David Cheillan, Jean–Charles Dagorn, Michel Roussey	2014	34
18	A new mutation in COG7 extends the spectrum of COG subunit deficiencies European Journal of Medical Genetics ·Renate Zeevaert, François Foulquier, David Cheillan, Isabelle Cloix, Nathalie Guffon, Luisella Sturiale, Domenico Garozzo, Gert Matthijs, Jaak Jaeken	2009	32
19	Acute effects of milk polar lipids on intestinal tight junction expression: towards an impact of sphingomyelin through the regulation of IL-8 secretion? The Journal of Nutritional Biochemistry ·Marine Milard, Armelle Penhoat, Annie Durand, Charline Buisson, Emmanuelle Loizon, Emmanuelle Meugnier, Karène Bertrand, Florent Joffre, David Cheillan, Lorna Garnier, Sébastien Viel, Fabienne Laugerette, Marie‐Caroline Michalski	2018	31
20	Clinical and economic aspects of newborn screening for severe combined immunodeficiency: DEPISTREC study results Clinical Immunology ·Caroline Thomas, Isabelle Durand‐Zaleski, J. Frenkiel, S. Mirallié, Alexandra Léger, David Cheillan, Capucine Pïcard, Nizar Mahlaoui, Valéry-Pierre Riche, Michel Roussey, Véronique Sebille, Hasina Rabetrano, Cécile Dert, Alain Fischer, Marie Audrain	2019	31

About David Cheillan

David Cheillan is a scholar working on Molecular Biology, Clinical Biochemistry, Cell Biology, Physiology and Pulmonary and Respiratory Medicine, having authored 79 papers that have together received 2.0k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (23 papers), Cystic Fibrosis Research Advances (9 papers), Muscle metabolism and nutrition (8 papers), Sphingolipid Metabolism and Signaling (8 papers), Peroxisome Proliferator-Activated Receptors (6 papers), Glycosylation and Glycoproteins Research (5 papers), Lysosomal Storage Disorders Research (5 papers) and Tracheal and airway disorders (5 papers). The work is most often cited by research in Clinical Biochemistry (360 citations), Cell Biology (374 citations), Physiology (441 citations), Biochemistry (94 citations) and Nutrition and Dietetics (178 citations). David Cheillan has collaborated with scholars based in France, United States and Netherlands. Frequent co-authors include Christine Vianey‐Saban, Monique Piraud, Marie‐Caroline Michalski, Nathalie Guffon, Michel Roussey, Anne‐Frédérique Dessein, Dries Dobbelaere, Jòseph Vamecq, Gustavo Soto‐Ares and Nicole Porchet. Their work appears in journals such as International Journal of Neonatal Screening, Journal of Inherited Metabolic Disease, Molecular Genetics and Metabolism, Biochimie and Journal of Cystic Fibrosis.

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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David Cheillan

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