A citation-based method for searching scientific literature

Aude Magerus-Chatinet, Bénédicte Neven, Marie-Claude Stolzenberg, Cécile Daussy, Peter D Arkwright, Nina Lanzarotti, Catherine Schaffner, Sophie Cluet-Dennetiere, Filomeen Haerynck, Gérard Michel, Christine Bole-Feysot, Mohammed Zarhrate, Isabelle Radford-Weiss, Serge P Romana, Capucine Picard, Alain Fischer, Frédéric Rieux-Laucat. J Clin Invest 2011
Times Cited: 78



F Le Deist, J F Emile, F Rieux-Laucat, M Benkerrou, I Roberts, N Brousse, A Fischer. Lancet 1996
Times Cited: 152




List of shared articles



Times cited


Impact of human CD95 mutations on cell death and autoimmunity: a model.
Kamil Seyrek, Nikita V Ivanisenko, Fabian Wohlfromm, Johannes Espe, Inna N Lavrik. Trends Immunol 2022
1


A missense mutation in the extracellular domain of Fas: the most common change in Argentinean patients with autoimmune lymphoproliferative syndrome represents a founder effect.
María Gabriela Simesen de Bielke, Judith Yancoski, Carlos Rocco, Laura E Pérez, Claudio Cantisano, Néstor Pérez, Matías Oleastro, Silvia Danielian. J Clin Immunol 2012
8

The Autoimmune Lymphoproliferative Syndrome with Defective FAS or FAS-Ligand Functions.
Frédéric Rieux-Laucat, Aude Magérus-Chatinet, Bénédicte Neven. J Clin Immunol 2018
34

What's up in the ALPS.
Frédéric Rieux-Laucat. Curr Opin Immunol 2017
17

Clinical, immunological, and genetic features in 780 patients with autoimmune lymphoproliferative syndrome (ALPS) and ALPS-like diseases: A systematic review.
Nasim Hafezi, Majid Zaki-Dizaji, Matineh Nirouei, Gelayol Asadi, Niusha Sharifinejad, Mahnaz Jamee, Seyed Erfan Rasouli, Haleh Hamedifar, Araz Sabzevari, Zahra Chavoshzadeh,[...]. Pediatr Allergy Immunol 2021
7


A survey of 90 patients with autoimmune lymphoproliferative syndrome related to TNFRSF6 mutation.
Bénédicte Neven, Aude Magerus-Chatinet, Benoit Florkin, Delphine Gobert, Olivier Lambotte, Lien De Somer, Nina Lanzarotti, Marie-Claude Stolzenberg, Brigitte Bader-Meunier, Nathalie Aladjidi,[...]. Blood 2011
89

Optimal Management of Autoimmune Lymphoproliferative Syndrome in Children.
Lindsey A George, David T Teachey. Paediatr Drugs 2016
11

FAS haploinsufficiency is a common disease mechanism in the human autoimmune lymphoproliferative syndrome.
Hye Sun Kuehn, Iusta Caminha, Julie E Niemela, V Koneti Rao, Joie Davis, Thomas A Fleisher, João B Oliveira. J Immunol 2011
38

Somatic loss of heterozygosity, but not haploinsufficiency alone, leads to full-blown autoimmune lymphoproliferative syndrome in 1 of 12 family members with FAS start codon mutation.
Fabian Hauck, Aude Magerus-Chatinet, Stephanie Vicca, Anne Rensing-Ehl, Angela Roesen-Wolff, Joachim Roesler, Frédéric Rieux-Laucat. Clin Immunol 2013
12

Diagnosis of autoimmune lymphoproliferative syndrome caused by FAS deficiency in adults.
Olivier Lambotte, Bénédicte Neven, Lionel Galicier, Aude Magerus-Chatinet, Nicolas Schleinitz, Olivier Hermine, Isabelle Meyts, Capucine Picard, Bertrand Godeau, Alain Fischer,[...]. Haematologica 2013
14

In utero and early postnatal presentation of autoimmune lymphoproliferative syndrome in a family with a novel FAS mutation.
Jordan R Hansford, Manika Pal, Nicola Poplawski, Eric Haan, Bernadette Boog, Antonio Ferrante, Joie Davis, Julie E Niemela, V Koneti Rao, Ram Suppiah. Haematologica 2013
3

FAS and RAS related Apoptosis defects: From autoimmunity to leukemia.
Sonia Meynier, Frédéric Rieux-Laucat. Immunol Rev 2019
22

Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes.
Barthelemy Caron, Etienne Patin, Maxime Rotival, Bruno Charbit, Matthew L Albert, Lluis Quintana-Murci, Darragh Duffy, Antonio Rausell. Genome Med 2022
0

ALPS, FAS, and beyond: from inborn errors of immunity to acquired immunodeficiencies.
Filippo Consonni, Eleonora Gambineri, Claudio Favre. Ann Hematol 2022
1