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

由 Garcelon, Nicolas, Neuraz, Antoine, Benoit, Vincent, Salomon, Rémi, Burgun, Anita
發表在 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

由 Barco, Tommaso Lo, Kuchenbuch, Mathieu, Garcelon, Nicolas, Neuraz, Antoine, Nabbout, Rima
發表在 Orphanet J Rare Dis (2021)

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

由 Looten, Vincent, Neuraz, Antoine, Garcelon, Nicolas, Burgun, Anita, Chatellier, Gilles, Rance, Bastien
發表在 J Med Internet Res (2021)

Osmoregulation Performance and Kidney Transplant Outcome

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

Diagnosis support systems for rare diseases: a scoping review

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

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

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

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

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

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

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

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

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

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

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

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

由 Hully, Marie, Lo Barco, Tommaso, Kaminska, Anna, Barcia, Giulia, Cances, Claude, Mignot, Cyril, Desguerre, Isabelle, Garcelon, Nicolas, Kabashi, Edor, Nabbout, Rima
發表在 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

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

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

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

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

由 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
出版 2011

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

由 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
發表在 Front Immunol (2021)

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

由 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
發表在 Haematologica (2020)

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

由 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
發表在 PLoS One (2018)