Pediatric Evans syndrome is associated with a high frequency of potentially damaging variants in immune genes J Hadjadj, N Aladjidi, H Fernandes, G Leverger, A Magérus-Chatinet, ... Blood, The Journal of the American Society of Hematology 134 (1), 9-21, 2019 | 123 | 2019 |
A clinician friendly data warehouse oriented toward narrative reports: Dr. Warehouse N Garcelon, A Neuraz, R Salomon, H Faour, V Benoit, A Delapalme, ... Journal of biomedical informatics 80, 52-63, 2018 | 123 | 2018 |
New findings for phenotype–genotype correlations in a large European series of holoprosencephaly cases S Mercier, C Dubourg, N Garcelon, B Campillo-Gimenez, I Gicquel, ... Journal of medical genetics 48 (11), 752-760, 2011 | 118 | 2011 |
NPHS2 Mutations in Steroid‐Resistant Nephrotic Syndrome: A Mutation Update and the Associated Phenotypic Spectrum K Bouchireb, O Boyer, O Gribouval, F Nevo, E Huynh‐Cong, V Morinière, ... Human mutation 35 (2), 178-186, 2014 | 102 | 2014 |
Natural language processing for rapid response to emergent diseases: case study of calcium channel blockers and hypertension in the COVID-19 pandemic A Neuraz, I Lerner, W Digan, N Paris, R Tsopra, A Rogier, D Baudoin, ... Journal of medical Internet research 22 (8), e20773, 2020 | 71 | 2020 |
Association between FIASMAs and Reduced Risk of Intubation or Death in Individuals Hospitalized for Severe COVID‐19: an observational multicenter study N Hoertel, M Sánchez‐Rico, E Gulbins, J Kornhuber, A Carpinteiro, ... Clinical Pharmacology & Therapeutics 110 (6), 1498-1511, 2021 | 67 | 2021 |
Obesity doubles mortality in patients hospitalized for severe acute respiratory syndrome coronavirus 2 in Paris hospitals, France: a cohort study on 5,795 patients S Czernichow, N Beeker, C Rives‐Lange, E Guerot, JL Diehl, S Katsahian, ... Obesity 28 (12), 2282-2289, 2020 | 63 | 2020 |
Diagnosis support systems for rare diseases: a scoping review C Faviez, X Chen, N Garcelon, A Neuraz, B Knebelmann, R Salomon, ... Orphanet Journal of Rare Diseases 15, 1-16, 2020 | 63 | 2020 |
Electronic health records for the diagnosis of rare diseases N Garcelon, A Burgun, R Salomon, A Neuraz Kidney international 97 (4), 676-686, 2020 | 55 | 2020 |
Hepatobiliary complications in children with sickle cell disease: a retrospective review of medical records from 616 patients S Allali, M de Montalembert, V Brousse, C Heilbronner, M Taylor, J Brice, ... Journal of clinical medicine 8 (9), 1481, 2019 | 54 | 2019 |
Improving a full-text search engine: the importance of negation detection and family history context to identify cases in a biomedical data warehouse N Garcelon, A Neuraz, V Benoit, R Salomon, A Burgun Journal of the American Medical Informatics Association 24 (3), 607-613, 2017 | 50 | 2017 |
Roogle: an information retrieval engine for clinical data warehouse M Cuggia, N Garcelon, B Campillo-Gimenez, T Bernicot, JF Laurent, ... User Centred Networked Health Care, 584-588, 2011 | 47 | 2011 |
RAVEL: retrieval and visualization in ELectronic health records. F Thiessard, F Mougin, G Diallo, V Jouhet, S Cossin, N Garcelon, ... MIE, 194-198, 2012 | 46 | 2012 |
Finding patients using similarity measures in a rare diseases-oriented clinical data warehouse: Dr. Warehouse and the needle in the needle stack N Garcelon, A Neuraz, V Benoit, R Salomon, S Kracker, F Suarez, ... Journal of biomedical informatics 73, 51-61, 2017 | 44 | 2017 |
Full-text automated detection of surgical site infections secondary to neurosurgery in Rennes, France. B Campillo-Gimenez, N Garcelon, P Jarno, JM Chapplain, M Cuggia Studies in health technology and informatics 192, 572-5, 2012 | 41 | 2012 |
Hydroxychloroquine with or without azithromycin and in-hospital mortality or discharge in patients hospitalized for COVID-19 infection: a cohort study of 4,642 in-patients in … E Sbidian, J Josse, G Lemaitre, I Meyer, M Bernaux, A Gramfort, ... MedRxiv, 2020.06. 16.20132597, 2020 | 40 | 2020 |
Next generation phenotyping using narrative reports in a rare disease clinical data warehouse N Garcelon, A Neuraz, R Salomon, N Bahi-Buisson, J Amiel, C Picard, ... Orphanet journal of rare diseases 13, 1-11, 2018 | 32 | 2018 |
Early magnetic resonance imaging to detect presymptomatic leptomeningeal angioma in children with suspected Sturge–Weber syndrome C Bar, JM Pedespan, O Boccara, N Garcelon, R Levy, D Grévent, ... Developmental Medicine & Child Neurology 62 (2), 227-233, 2020 | 29 | 2020 |
Evidence for a MAIT-17–high phenotype in children with severe asthma G Lezmi, R Abou-Taam, N Garcelon, C Dietrich, F Machavoine, ... Journal of Allergy and Clinical Immunology 144 (6), 1714-1716. e6, 2019 | 28 | 2019 |
Association of antihypertensive agents with the risk of in-hospital death in patients with Covid-19 L Chouchana, N Beeker, N Garcelon, B Rance, N Paris, E Salamanca, ... Cardiovascular Drugs and Therapy, 1-6, 2022 | 23 | 2022 |