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Nicolas Garcelon
Nicolas Garcelon
UMR 1163, institut Imagine, université Paris-Descartes, Sorbonne Paris-Cité, 75015 Paris, France
Dirección de correo verificada de institutimagine.org
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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
1212019
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
1212018
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
1162011
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
1022014
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
702020
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
672021
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
632020
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
622020
Electronic health records for the diagnosis of rare diseases
N Garcelon, A Burgun, R Salomon, A Neuraz
Kidney international 97 (4), 676-686, 2020
552020
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
532019
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
502017
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
472011
RAVEL: retrieval and visualization in ELectronic health records.
F Thiessard, F Mougin, G Diallo, V Jouhet, S Cossin, N Garcelon, ...
MIE, 194-198, 2012
462012
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
442017
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
412012
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
402020
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
322018
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
292020
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
272019
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
232022
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