| Molecular genetics of tetrahydrobiopterin‐responsive phenylalanine hydroxylase deficiency MR Zurflüh, J Zschocke, M Lindner, F Feillet, C Chery, A Burlina, ... Human mutation 29 (1), 167-175, 2008 | 245 | 2008 |
| The 18 kDa peanut oleosin is a candidate allergen for IgE‐mediated reactions to peanuts L Pons, C Chery, A Romano, F Namour, MC Artesani, JL Guéant Allergy 57, 88-93, 2002 | 138 | 2002 |
| HLA-DRA variants predict penicillin allergy in genome-wide fine-mapping genotyping JL Guéant, A Romano, JA Cornejo-Garcia, A Oussalah, C Chery, ... Journal of Allergy and Clinical Immunology 135 (1), 253-259. e10, 2015 | 94 | 2015 |
| A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients JL Guéant, C Chéry, A Oussalah, J Nadaf, D Coelho, T Josse, J Flayac, ... Nature Communications 9 (1), 67, 2018 | 83 | 2018 |
| Elastase and exacerbation of neutrophil innate immunity are involved in multi‐visceral manifestations of COVID‐19 JL Guéant, RM Guéant‐Rodriguez, J Fromonot, A Oussalah, H Louis, ... Allergy 76 (6), 1846-1858, 2021 | 78 | 2021 |
| A splicing variant leads to complete loss of function of betaine–homocysteine methyltransferase (BHMT) gene in hepatocellular carcinoma H Pellanda, F Namour, A Bressenot, JM Alberto, C Chéry, A Ayav, ... The international journal of biochemistry & cell biology 44 (2), 385-392, 2012 | 50 | 2012 |
| Vitamin B12-impaired metabolism produces apoptosis and Parkinson phenotype in rats expressing the transcobalamin-oleosin chimera in substantia nigra CE Orozco-Barrios, SF Battaglia-Hsu, ML Arango-Rodriguez, ... PloS one 4 (12), 2009 | 42 | 2009 |
| Interaction between methionine synthase isoforms and MMACHC: characterization in cblG-variant, cblG and cblC inherited causes of megaloblastic anaemia MB Fofou-Caillierez, NT Mrabet, C Chéry, N Dreumont, J Flayac, ... Human molecular genetics 22 (22), 4591-4601, 2013 | 39 | 2013 |
| Interaction between methionine synthase isoforms and MMACHC: characterization in cblG-variant, cblG and cblC inherited causes of megaloblastic anaemia MB Fofou-Caillierez, NT Mrabet, C Chéry, N Dreumont, J Flayac, ... Human molecular genetics 22 (22), 4591-4601, 2013 | 39 | 2013 |
| Purification and cloning of two high molecular mass isoforms of peanut seed oleosin encoded by cDNAs of equal sizes L Pons, C Chéry, N Mrabet, H Schohn, F Lapicque, JL Guéant Plant Physiology and Biochemistry 43 (7), 659-668, 2005 | 34 | 2005 |
| Hyperhomocysteinemia is related to a decreased blood level of vitamin B12 in the second and third trimester of normal pregnancy C Chéry, F Barbé, C Lequere, I Abdelmouttaleb, P Gérard, P Barbarino, ... Clinical chemistry and laboratory medicine 40 (11), 1105-1108, 2002 | 34 | 2002 |
| Luminal expression of cubilin is impaired in Imerslund-Gräsbeck syndrome with compound AMN mutations in intron 3 and exon 7 F Namour, G Dobrovoljski, C Chery, S Audonnet, F Feillet, W Sperl, ... haematologica 96 (11), 1715, 2011 | 32 | 2011 |
| Folate can promote the methionine-dependent reprogramming of glioblastoma cells towards pluripotency R Zgheib, SF Battaglia-Hsu, S Hergalant, M Quéré, JM Alberto, C Chéry, ... Cell Death & Disease 10 (8), 596, 2019 | 30 | 2019 |
| Genotype-phenotype associations in French patients with phenylketonuria and importance of genotype for full assessment of tetrahydrobiopterin responsiveness E Jeannesson-Thivisol, F Feillet, C Chéry, P Perrin, SF Battaglia-Hsu, ... Orphanet journal of rare diseases 10, 1-22, 2015 | 29 | 2015 |
| Gastric intrinsic factor deficiency with combined GIF heterozygous mutations and FUT2 secretor variant C Chery, A Hehn, N Mrabet, A Oussalah, E Jeannesson, C Besseau, ... Biochimie 95 (5), 995-1001, 2013 | 29 | 2013 |
| Life-threatening methylenetetrahydrofolate reductase (MTHFR) deficiency with extremely early onset: characterization of two novel mutations in compound heterozygous patients T Forges, C Chery, S Audonnet, F Feillet, JL Gueant Molecular genetics and metabolism 100 (2), 143-148, 2010 | 29 | 2010 |
| Allergy to betalactams and nucleotide‐binding oligomerization domain (NOD) gene polymorphisms AC Bursztejn, A Romano, RM Guéant‐Rodriguez, JA Cornejo, ... Allergy 68 (8), 1076-1080, 2013 | 28 | 2013 |
| Evaluation of neonatal BH4 loading test in neonates screened for hyperphenylalaninemia F Feillet, C Chery, F Namour, A Kimmoun, E Favre, E Lorentz, ... Early human development 84 (9), 561-567, 2008 | 27 | 2008 |
| Helicobacter pylori serologic status has no influence on the association between fucosyltransferase 2 polymorphism (FUT2 461 G→ A) and vitamin B-12 in Europe and West Africa A Oussalah, C Besseau, C Chery, E Jeannesson, RM Gueant-Rodriguez, ... The American journal of clinical nutrition 95 (2), 514-521, 2012 | 24 | 2012 |
| Exome-wide association study identifies new low-frequency and rare UGT1A1 coding variants and UGT1A6 coding variants influencing serum bilirubin in elderly subjects: a strobe … A Oussalah, P Bosco, G Anello, R Spada, RM Gueant-Rodriguez, ... Medicine 94 (22), e925, 2015 | 21 | 2015 |
