Improving a full-text search engine: the importance of negation detection and family history context to identify cases in a biomedical data warehouse

par Garcelon, Nicolas, Neuraz, Antoine, Benoit, Vincent, Salomon, Rémi, Burgun, Anita
Publié dans J Am Med Inform Assoc (2017)

Improving early diagnosis of rare diseases using Natural Language Processing in unstructured medical records: an illustration from Dravet syndrome

par Barco, Tommaso Lo, Kuchenbuch, Mathieu, Garcelon, Nicolas, Neuraz, Antoine, Nabbout, Rima
Publié dans Orphanet J Rare Dis (2021)

The Epidemiology of Patients' Email Addresses in a French University Hospital: Case-Control Study

par Looten, Vincent, Neuraz, Antoine, Garcelon, Nicolas, Burgun, Anita, Chatellier, Gilles, Rance, Bastien
Publié dans J Med Internet Res (2021)

Osmoregulation Performance and Kidney Transplant Outcome

par Mazloum, Manal, Jouffroy, Jordan, Brazier, François, Legendre, Christophe, Neuraz, Antoine, Garcelon, Nicolas, Prié, Dominique, Anglicheau, Dany, Bienaimé, Frank
Publié dans J Am Soc Nephrol (2019)

Diagnosis support systems for rare diseases: a scoping review

par Faviez, Carole, Chen, Xiaoyi, Garcelon, Nicolas, Neuraz, Antoine, Knebelmann, Bertrand, Salomon, Rémi, Lyonnet, Stanislas, Saunier, Sophie, Burgun, Anita
Publié dans Orphanet J Rare Dis (2020)

Hepatobiliary Complications in Children with Sickle Cell Disease: A Retrospective Review of Medical Records from 616 Patients

par Allali, Slimane, de Montalembert, Mariane, Brousse, Valentine, Heilbronner, Claire, Taylor, Melissa, Brice, Josephine, Manzali, Elisabetta, Garcelon, Nicolas, Lacaille, Florence
Publié dans J Clin Med (2019)

Evaluation of Hydroxychloroquine Blood Concentrations and Effects in Childhood-Onset Systemic Lupus Erythematosus

par Zahr, Noël, Urien, Saik, Funck-Brentano, Christian, Vantomme, Hélène, Garcelon, Nicolas, Melki, Isabelle, Boistault, Margaux, Boyer, Olivia, Bader-Meunier, Brigitte
Publié dans Pharmaceuticals (Basel) (2021)

Next generation phenotyping using narrative reports in a rare disease clinical data warehouse

par Garcelon, Nicolas, Neuraz, Antoine, Salomon, Rémi, Bahi-Buisson, Nadia, Amiel, Jeanne, Picard, Capucine, Mahlaoui, Nizar, Benoit, Vincent, Burgun, Anita, Rance, Bastien
Publié dans Orphanet J Rare Dis (2018)

Association of Antihypertensive Agents with the Risk of In-Hospital Death in Patients with Covid-19

par Chouchana, Laurent, Beeker, Nathanaël, Garcelon, Nicolas, Rance, Bastien, Paris, Nicolas, Salamanca, Elisa, Polard, Elisabeth, Burgun, Anita, Treluyer, Jean-Marc, Neuraz, Antoine
Publié dans Cardiovasc Drugs Ther (2021)

Correction to: Association of Antihypertensive Agents with the Risk of In-Hospital Death in Patients with Covid-19

par Chouchana, Laurent, Beeker, Nathanaël, Garcelon, Nicolas, Rance, Bastien, Paris, Nicolas, Salamanca, Elisa, Polard, Elisabeth, Burgun, Anita, Treluyer, Jean-Marc, Neuraz, Antoine
Publié dans Cardiovasc Drugs Ther (2021)

Deep phenotyping unstructured data mining in an extensive pediatric database to unravel a common KCNA2 variant in neurodevelopmental syndromes

par Hully, Marie, Lo Barco, Tommaso, Kaminska, Anna, Barcia, Giulia, Cances, Claude, Mignot, Cyril, Desguerre, Isabelle, Garcelon, Nicolas, Kabashi, Edor, Nabbout, Rima
Publié dans Genet Med (2021)

Natural Language Processing for Rapid Response to Emergent Diseases: Case Study of Calcium Channel Blockers and Hypertension in the COVID-19 Pandemic

par Neuraz, Antoine, Lerner, Ivan, Digan, William, Paris, Nicolas, Tsopra, Rosy, Rogier, Alice, Baudoin, David, Cohen, Kevin Bretonnel, Burgun, Anita, Garcelon, Nicolas, Rance, Bastien
Publié dans J Med Internet Res (2020)

Healthcare trajectory of children with rare bone disease attending pediatric emergency departments

par Yang, David Dawei, Baujat, Geneviève, Neuraz, Antoine, Garcelon, Nicolas, Messiaen, Claude, Sandrin, Arnaud, Cheron, Gérard, Burgun, Anita, Pejin, Zagorka, Cormier-Daire, Valérie, Angoulvant, François
Publié dans Orphanet J Rare Dis (2020)

New findings for phenotype-genotype correlations in a large European series of holoprosencephaly cases

par Mercier, Sandra, Dubourg, Christèle, Garcelon, Nicolas, Campillo-Gimenez, Boris, Gicquel, Isabelle, Belleguic, Marion, Ratié, Leslie, Pasquier, Laurent, Loget, Philippe, Bendavid, Claude, Jaillard, Sylvie, Rochard, Lucie, Quélin, Chloé, Dupé, Valérie, David, Véronique, Odent, Sylvie
Publié 2011

A Comprehensive Analysis of Immune Constituents in Blood and Bronchoalveolar Lavage Allows Identification of an Immune Signature of Severe Asthma in Children

par Adel-Patient, Karine, Grauso, Marta, Abou-Taam, Rola, Guillon, Blanche, Dietrich, Céline, Machavoine, François, Briard, Mélanie, Garcelon, Nicolas, Faour, Hassan, Neuraz, Antoine, Delacourt, Christophe, Molina, Thierry Jo, Leite-de-Moraes, Maria, Lezmi, Guillaume
Publié dans Front Immunol (2021)

Safety and efficacy of brentuximab vedotin as a treatment for lymphoproliferative disorders in primary immunodeficiencies

par Pincez, Thomas, Bruneau, Julie, Berteloot, Laureline, Piekarski, Eve, Thomas, Caroline, Marçais, Ambroise, Trinquand, Amélie, Castelle, Martin, Garcelon, Nicolas, Plantaz, Dominique, Cheminant, Morgane, Moshous, Despina, Molina, Thierry Jo, Hermine, Olivier, Macintyre, Elizabeth, Fischer, Alain, Blanche, Stéphane, Suarez, Felipe, Neven, Bénédicte
Publié dans Haematologica (2020)

Copy number variations and founder effect underlying complete IL-10Rβ deficiency in Portuguese kindreds

par Charbit-Henrion, Fabienne, Bègue, Bernadette, Sierra, Anaïs, Hanein, Sylvain, Stolzenberg, Marie-Claude, Li, Zhi, Pellegrini, Sandra, Garcelon, Nicolas, Jeanpierre, Marc, Neven, Bénédicte, Loge, Isabelle, Picard, Capucine, Rosain, Jérémie, Bustamante, Jacinta, Le Lorc’h, Marc, Pigneur, Bénédicte, Fernandes, Alicia, Rieux-Laucat, Frédéric, Amil Dias, Jorge, Ruemmele, Frank M., Cerf-Bensussan, Nadine
Publié dans PLoS One (2018)