Abderrahim Oussalah

ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 21

Top Venues

Allergy

Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology

Journal of medical genetics

Nature communications

University Hospital of Nancy, Faculty of Medicine of Nancy, University of Lorraine and INSERM 954

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University Hospital of Nancy, Faculty of Medicine of Nancy, University of Lorraine and INSERM 954

France

M.D., Ph.D. :: Department of Molecular Medicine and Personalized Therapeutics

Publications

Hortense Thomas, Tom Alix, Émeline Renard, Mathilde Renaud, Justine Wourms, Stéphane Zuily, Bruno Leheup, David Geneviève, Natacha Dreumont, Emmanuelle Schmitt, Myriam Bronner, Marc Muller, Marion Divoux, Marion Wandzel, Jean-Marie Ravel, Mylène Dexheimer, Aurélie Becker, Virginie Roth, Marjolaine Willems, Christine Coubes, Gaëlle Vieville, Françoise Devillard, Élise Schaefer, Sarah Baer, Amelie Piton, Bénédicte Gérard, Marie Vincent, Mathilde Nizon, Benjamin Cogné, Lyse Ruaud, Nathalie Couque, Audrey Putoux, Patrick Edery, Gaëtan Lesca, Nicolas Chatron, Marianne Till, Laurence Olivier-Faivre, Frédéric Tran-Mau-Them, Jean-Luc Alessandri, Marine Lebrun, Chloé Quélin, Sylvie Odent, Christèle Dubourg, Véronique David, Marie Faoucher, Cyril Mignot, Boris Keren, Élise Pisan, Alexandra Afenjar, Sophie Julia, Éric Bieth, Guillaume Banneau, Alice Goldenberg, Thomas Husson, Dominique Campion, Francois Lecoquierre, Gaël Nicolas, Camille Charbonnier, Anne De Saint Martin, Sophie Naudion, Manon Degoutin, Sophie Rondeau, Caroline Michot, Valérie Cormier-Daire, Abderrahim Oussalah, Carine Pourié, Laëtitia Lambert, Céline Bonnet
Expanding the genetic and clinical spectrum of Tatton-Brown-Rahman syndrome in a series of 24 French patients. Journal of medical genetics (2024)
Hortense Thomas, Tom Alix, Émeline Renard, Mathilde Renaud, Justine Wourms, Stéphane Zuily, Bruno Leheup, David Geneviève, Natacha Dreumont, Emmanuelle Schmitt, Myriam Bronner, Marc Muller, Marion Divoux, Marion Wandzel, Jean-Marie Ravel, Mylène Dexheimer, Aurélie Becker, Virginie Roth, Marjolaine Willems, Christine Coubes, Gaëlle Vieville, Françoise Devillard, Élise Schaefer, Sarah Baer, Amelie Piton, Bénédicte Gérard, Marie Vincent, Mathilde Nizon, Benjamin Cogné, Lyse Ruaud, Nathalie Couque, Audrey Putoux, Patrick Edery, Gaëtan Lesca, Nicolas Chatron, Marianne Till, Laurence Olivier-Faivre, Frédéric Tran-Mau-Them, Jean-Luc Alessandri, Marine Lebrun, Chloé Quélin, Sylvie Odent, Christèle Dubourg, Véronique David, Marie Faoucher, Cyril Mignot, Boris Keren, Élise Pisan, Alexandra Afenjar, Sophie Julia, Éric Bieth, Guillaume Banneau, Alice Goldenberg, Thomas Husson, Dominique Campion, Francois Lecoquierre, Gaël Nicolas, Camille Charbonnier, Anne De Saint Martin, Sophie Naudion, Manon Degoutin, Sophie Rondeau, Caroline Michot, Valérie Cormier-Daire, Abderrahim Oussalah, Carine Pourié, Laëtitia Lambert, Céline Bonnet
Expanding the genetic and clinical spectrum of Tatton-Brown-Rahman syndrome in a series of 24 French patients. Journal of medical genetics 61 (9) (2024)
Hortense Thomas, Tom Alix, Émeline Renard, Mathilde Renaud, Justine Wourms, Stéphane Zuily, Bruno Leheup, David Geneviève, Natacha Dreumont, Emmanuelle Schmitt, Myriam Bronner, Marc Muller, Marion Divoux, Marion Wandzel, Jean-Marie Ravel, Mylène Dexheimer, Aurélie Becker, Virginie Roth, Marjolaine Willems, Christine Coubes, Gaëlle Vieville, Françoise Devillard, Élise Schaefer, Sarah Baer, Amelie Piton, Bénédicte Gérard, Marie Vincent, Mathilde Nizon, Benjamin Cogné, Lyse Ruaud, Nathalie Couque, Audrey Putoux, Patrick Edery, Gaëtan Lesca, Nicolas Chatron, Marianne Till, Laurence Olivier-Faivre, Frédéric Tran-Mau-Them, Jean-Luc Alessandri, Marine Lebrun, Chloé Quélin, Sylvie Odent, Christèle Dubourg, Véronique David, Marie Faoucher, Cyril Mignot, Boris Keren, Élise Pisan, Alexandra Afenjar, Sophie Julia, Éric Bieth, Guillaume Banneau, Alice Goldenberg, Thomas Husson, Dominique Campion, Francois Lecoquierre, Gaël Nicolas, Camille Charbonnier, Anne De Saint Martin, Sophie Naudion, Manon Degoutin, Sophie Rondeau, Caroline Michot, Valérie Cormier-Daire, Abderrahim Oussalah, Carine Pourié, Laëtitia Lambert, Céline Bonnet
Expanding the genetic and clinical spectrum of Tatton-Brown-Rahman syndrome in a series of 24 French patients. Journal of medical genetics 61 (9) (2024)
Richard Belmonte, Maël Silva Rodriguez, Françoise Barbé, Mouni Bensenane, Vincent Haghenejad, Isabelle Vrillon, Asma Alla, Adrien Flahault, Raphael Kormann, Alice Corbel, Zakia Aitdjafer, Didier Quilliot, Laurence Derain-Dubourg, Farès Namour, Jean-Louis Guéant, Jean-Pierre Bronowicki, Abderrahim Oussalah
Multiparametric renal function assessment in cirrhotic patients shows high prevalence of medically actionable changes in multiple modules. Hepatology research : the official journal of the Japan Society of Hepatology (2024)
Chloé Grosyeux, Asma Alla, Françoise Barbé, Laurence Derain Dubourg, Laurence Chardon, Jean-Louis Guéant, Luc Frimat, Abderrahim Oussalah, Isabelle Vrillon
The EKFC equation outperforms the CKD-EPI and CKiD equations for GFR estimation in adolescent and young adult kidney transplant patients. Nephrology (Carlton, Vic.) (2024)
Ramia Safar, Abderrahim Oussalah, Lina Mayorga, Stefan Vieths, Domingo Barber, Maria Jose Torres, Jean-Louis Guéant
Epigenome alterations in food allergy: A systematic review of candidate gene and epigenome-wide association studies. Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 53 (3) (2023)
Ramia Safar, Abderrahim Oussalah, Lina Mayorga, Stefan Vieths, Domingo Barber, Maria Jose Torres, Jean-Louis Guéant
Epigenome alterations in food allergy: A systematic review of candidate gene and epigenome-wide association studies. Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 53 (3) (2023)
Ramia Safar, Abderrahim Oussalah, Lina Mayorga, Stefan Vieths, Domingo Barber, Maria Jose Torres, Jean-Louis Guéant
Epigenome alterations in food allergy: A systematic review of candidate gene and epigenome-wide association studies. Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology (2023)
Youssef Siblini, Farès Namour, Abderrahim Oussalah, Jean-Louis Guéant, Céline Chéry
Stemness of Normal and Cancer Cells: The Influence of Methionine Needs and SIRT1/PGC-1α/PPAR-α Players. Cells 11 (22) (2022)
Jean-Louis Guéant, Rosa-Maria Guéant-Rodriguez, Julien Fromonot, Abderrahim Oussalah, Huguette Louis, Celine Chery, Mickael Gette, Stanislas Gleye, Jonas Callet, Jeremie Raso, François Blanchecotte, Patrick Lacolley, Régis Guieu, Véronique Regnault
Elastase and exacerbation of neutrophil innate immunity are involved in multi-visceral manifestations of COVID-19. Allergy 76 (6) (2021)
Clémence Berthezène, Nejla Aissa, Anne Elisabeth Manteaux, Jean-Louis Guéant, Abderrahim Oussalah, Alain Lozniewski
Accuracy of procalcitonin for diagnosing peripheral blood culture contamination among patients with positive blood culture for potential contaminants. Infection 49 (6) (2021)
Jean-Philippe Mergnac, Arnaud Wiedemann, Céline Chery, Jean-Marie Ravel, Farès Namour, Jean-Louis Guéant, François Feillet, Abderrahim Oussalah
Diagnostic yield of clinical exome sequencing as a first-tier genetic test for the diagnosis of genetic disorders in pediatric patients: results from a referral center study. Human genetics (2021)
Antonino Romano, Abderrahim Oussalah, Celine Chery, Rosa-Maria Guéant-Rodriguez, Francesco Gaeta, José Antonio Cornejo-Garcia, Pierre Rouyer, Thomas Josse, Cristobalina Mayorga, Torres María José, Jean-Louis Guéant
Next-generation sequencing and genotype association studies reveal the association of HLA-DRB3*02:02 with delayed hypersensitivity to penicillins. Allergy (2021)
Youssef Siblini, Céline Chéry, Pierre Rouyer, Jérémie Raso, Amélia Julien, Sébastien Hergalant, Aurélie François, Lina Bezdetnaya, Guillaume Vogin, Jean-Louis Guéant, Abderrahim Oussalah
Ionizing radiations induce shared epigenomic signatures unraveling adaptive mechanisms of cancerous cell lines with or without methionine dependency. Clinical epigenetics 13 (1) (2021)
Abderrahim Oussalah, Vincent Yip, Cristobalina Mayorga, Miguel Blanca, Annick Barbaud, Alla Nakonechna, Josefina Cernadas, Maia Gotua, Knut Brockow, Jean-Christoph Caubet, Andreas Bircher, Marina Atanaskovic-Markovic, Pascal Demoly, Luciana Kase Tanno, Ingrid Terreehorst, José Julio Laguna, Antonino Romano, Jean-Louis Guéant, Munir Pirmohamed, null null
Genetic variants associated with T cell-mediated cutaneous adverse drug reactions: A PRISMA-compliant systematic review-An EAACI position paper. Allergy 75 (5) (2021)
Arnaud Wiedemann, Céline Chery, David Coelho, Justine Flayac, Naïg Gueguen, Valérie Desquiret-Dumas, François Feillet, Christian Lavigne, Jean-Philippe Neau, Brian Fowler, Matthias R Baumgartner, Pascal Reynier, Jean-Louis Guéant, Abderrahim Oussalah
Mutations in MTHFR and POLG impaired activity of the mitochondrial respiratory chain in 46-year-old twins with spastic paraparesis. Journal of human genetics 65 (2) (2019)
Abderrahim Oussalah, Mélissa Julien, Julien Levy, Olivia Hajjar, Claire Franczak, Charlotte Stephan, Elodie Laugel, Marion Wandzel, Pierre Filhine-Tresarrieu, Ralph Green, Jean-Louis Guéant
Global Burden Related to Nitrous Oxide Exposure in Medical and Recreational Settings: A Systematic Review and Individual Patient Data Meta-Analysis. Journal of clinical medicine 8 (4) (2019)
Miguel Blanca, Abderrahim Oussalah, José Antonio Cornejo-Garcia, Natalia Blanca-López, Rosa-Maria Guéant-Rodriguez, Immaculada Doña, Cristobalina Mayorga, Celine Chery, Pierre Rouyer, Francisco David Carmona, Lara Bossini Castillo, Gabriela Canto, Javier Martin, Torres María José, Jean-Louis Guéant
GNAI2 variants predict nonsteroidal anti-inflammatory drug hypersensitivity in a genome-wide study. Allergy 75 (5) (2019)
Jean-Louis Guéant, Céline Chéry, Abderrahim Oussalah, Javad Nadaf, David Coelho, Thomas Josse, Justine Flayac, Aurélie Robert, Isabelle Koscinski, Isabelle Gastin, Pierre Filhine-Tresarrieu, Mihaela Pupavac, Alison Brebner, David Watkins, Tomi Pastinen, Alexandre Montpetit, Fadi Hariri, David Tregouët, Benjamin A Raby, Wendy K Chung, Pierre-Emmanuel Morange, D Sean Froese, Matthias R Baumgartner, Jean-François Benoist, Can Ficicioglu, Virginie Marchand, Yuri Motorin, Chrystèle Bonnemains, François Feillet, Jacek Majewski, David S Rosenblatt
Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients. Nature communications 9 (1) (2018)
Jean-Louis Guéant, Céline Chéry, Abderrahim Oussalah, Javad Nadaf, David Coelho, Thomas Josse, Justine Flayac, Aurélie Robert, Isabelle Koscinski, Isabelle Gastin, Pierre Filhine-Tresarrieu, Mihaela Pupavac, Alison Brebner, David Watkins, Tomi Pastinen, Alexandre Montpetit, Fadi Hariri, David Tregouët, Benjamin A Raby, Wendy K Chung, Pierre-Emmanuel Morange, D Sean Froese, Matthias R Baumgartner, Jean-François Benoist, Can Ficicioglu, Virginie Marchand, Yuri Motorin, Chrystèle Bonnemains, François Feillet, Jacek Majewski, David S Rosenblatt
APRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients. Nature communications 9 (1) (2018)
Abderrahim Oussalah, Julien Levy, Pierre Filhine-Trésarrieu, Fares Namour, Jean-Louis Guéant
Association of TCN2 rs1801198 c.776G>C polymorphism with markers of one-carbon metabolism and related diseases: a systematic review and meta-analysis of genetic association studies. The American journal of clinical nutrition 106 (4) (2017)

Abderrahim Oussalah.css-eqlu8i{font-size:small;padding-left:4px;}

Publication Activity (10 Years)

Top Topics

Top Venues

Abderrahim Oussalah