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

Tekijä Garcelon, Nicolas, Neuraz, Antoine, Benoit, Vincent, Salomon, Rémi, Burgun, Anita
Julkaisussa 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

Tekijä Barco, Tommaso Lo, Kuchenbuch, Mathieu, Garcelon, Nicolas, Neuraz, Antoine, Nabbout, Rima
Julkaisussa Orphanet J Rare Dis (2021)

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

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

Osmoregulation Performance and Kidney Transplant Outcome

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

Diagnosis support systems for rare diseases: a scoping review

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Tekijä 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
Julkaistu 2011

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

Tekijä 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
Julkaisussa Front Immunol (2021)

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

Tekijä 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
Julkaisussa Haematologica (2020)

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

Tekijä 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
Julkaisussa PLoS One (2018)