L
Lina Quteineh
Researcher at Pierre-and-Marie-Curie University
Publications - 7
Citations - 1827
Lina Quteineh is an academic researcher from Pierre-and-Marie-Curie University. The author has contributed to research in topics: Transplantation & Kidney transplantation. The author has an hindex of 4, co-authored 5 publications receiving 1776 citations.
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Journal ArticleDOI
Genetic Determinants of Response to Clopidogrel and Cardiovascular Events
Tabassome Simon,Céline Verstuyft,Murielle Mary-Krause,Lina Quteineh,Elodie Drouet,Nicolas Meneveau,P. Gabriel Steg,Jean Ferrières,Nicolas Danchin,Laurent Becquemont,Abstr Act +10 more
TL;DR: Among patients with an acute myocardial infarction who were receiving clopidogrel, those carrying CYP2C19 loss-of-function alleles had a higher rate of subsequent cardiovascular events than those who were not, particularly marked among the patients undergoing percutaneous coronary intervention.
Journal ArticleDOI
Influence of CYP3A5 genetic polymorphism on tacrolimus daily dose requirements and acute rejection in renal graft recipients.
Lina Quteineh,Céline Verstuyft,Valérie Furlan,Antoine Durrbach,Alexia Letierce,Sophie Ferlicot,Anne-Marie Taburet,Bernard Charpentier,Laurent Becquemont +8 more
TL;DR: CYP3A5 genetic polymorphism appeared in this study to affect tacrolimus daily dose requirements and transplantation outcome and Screening for this single nucleotide polymorphism before the transplantation might be helpful for the selection of adequate initial daily dose and to achieve the desired immunosuppression.
Journal ArticleDOI
SLCO1B1 genetic polymorphism influences mycophenolic acid tolerance in renal transplant recipients
Hugues Michelon,Jörg König,Antoine Durrbach,Lina Quteineh,Céline Verstuyft,Valérie Furlan,Sophie Ferlicot,Alexia Letierce,Bernard Charpentier,Martin F. Fromm,Laurent Becquemont +10 more
TL;DR: Results suggest for the first time that carriers of the SLCO1B1*5 allele seem to be protected from MPA-related ADRs.
Journal ArticleDOI
Vitamin K epoxide reductase (VKORC1) genetic polymorphism is associated to oral anticoagulant overdose.
Lina Quteineh,Céline Verstuyft,Christelle Descot,Liliane Dubert,Annie Robert,Patrice Jaillon,Laurent Becquemont +6 more
TL;DR: Vitamin K epoxide reductase (VKORC1) genetic polymorphism is associated to oral anticoagulant overdose and needs further investigation to establish a causative mechanism.
Journal ArticleDOI
An HNRNPK-specific DNA methylation signature makes sense of missense variants and expands the phenotypic spectrum of Au-Kline syndrome
Sanaa Choufani,Vanda T. K. McNiven,Cheryl Cytrynbaum,Maryam Jangjoo,Margaret P Adam,Hans T. Bjornsson,Jacqueline Harris,David A. Dyment,Gail E. Graham,Marjan M. Nezarati,Ritu B. Aul,Claudia Castiglioni,Jeroen Breckpot,Koenraad Devriendt,Helen Stewart,Benito Banos-Pinero,Sarju G. Mehta,Richard Sandford,C Dunn,Rémi Mathevet,Lionel Van Maldergem,Juliette Piard,Elise Brischoux-Boucher,Antonio Vitobello,Laurence Faivre,Marie Bournez,Frederic Tran-Mau,Isabelle Maystadt,Alberto Fernández-Jaén,Sara Alvarez,Irene Díez García-Prieto,Fowzan S. Alkuraya,Hessa S. Alsaif,Zuhair Rahbeeni,Karen El-Akouri,Mariam Almureikhi,Rebecca C. Spillmann,Vandana Shashi,Pedro A. Sanchez-Lara,John M. Graham,Amy Roberts,Odelia Chorin,Gilad D. Evrony,Minna Kraatari-Tiri,Tracy Dudding-Byth,Anamaria Richardson,David Hunt,Laura Hamilton,Sarah Dyack,Bryce A. Mendelsohn,Nicolás Rodríguez,Rosario Sánchez-Martínez,Jair Tenorio-Castaño,Julián Nevado,Pablo Lapunzina,Pilar Tirado,Maria-Teresa Carminho Amaro Rodrigues,Lina Quteineh,A. Micheil Innes,Antonie D. Kline,P.Y. Billie Au,Rosanna Weksberg +61 more
TL;DR: Au-Kline syndrome (AKS) is a neurodevelopmental disorder associated with multiple malformations and a characteristic facial gestalt as mentioned in this paper , and the first individuals ascertained carried de novo loss-of-function (LoF) variants in HNRNPK.