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Alexis Brice

CNRS

153H-index
1.2KPaper Count
11.6WCitation Count
Published Papers 518
Publication Date
Genome-wide association study of copy number variations in Parkinson’s disease
err2026-04-20
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errOAAI
errZied Landoulsi; Ashwin Ashok Kumar Sreelatha; Nicole Kuznetsov; Claudia Schulte; Dheeraj Reddy Bobbili; Ludovica Montanucci; Costin Leu; Lisa-Marie Niestroj; Emadeldin Hassanin; Cloé Domenighetti; Pierre-Emmanuel Sugier; Milena Radivojkov-Blagojevic; Peter Lichtner; Berta Portugal; Connor Edsall; Jens Krüger; Dena G. Hernandez; Cornelis Blauwendraat; George D. Mellick; Alexander Zimprich; Walter Pirker; Manuela Tan; Ekaterina Rogaeva; Anthony Lang; Sulev Koks; Pille Taba; Suzanne Lesage; Alexis Brice; Jean-Christophe Corvol; Marie-Christine Chartier-Harlin; Eugenie Mutez; Kathrin Brockmann; Angela B. Deutschländer; Georges M. Hadjigeorgiou; Efthimos Dardiotis; Leonidas Stefanis; Athina Maria Simitsi; Enza Maria Valente; Simona Petrucci; Letizia Straniero; Anna Zecchinelli; Gianni Pezzoli; Laura Brighina; Carlo Ferrarese; Grazia Annesi; Andrea Quattrone; Monica Gagliardi; Lena F. Burbulla; Hirotaka Matsuo; Akiyoshi Nakayama; Nobutaka Hattori; Kenya Nishioka; Sun Ju Chung; Yun Joong Kim; Lukas Pavelka; Pierre Kolber; Bart PC van de Warrenburg; Bastiaan R. Bloem; Andrew B. Singleton; Dan Vitale; Mathias Toft; Lasse Pihlstrom; Leonor Correia Guedes; Joaquim J. Ferreira; Soraya Bardien; Jonathan Carr; Eduardo Tolosa; Mario Ezquerra; Pau Pastor; Karin Wirdefeldt; Nancy L. Pedersen; Caroline Ran; Andrea C. Belin; Andreas Puschmann; Carl E. Clarke; Karen E. Morrison; Dimitri Krainc; Matt J. Farrer; Dennis Lal; Alexis Elbaz; Thomas Gasser; Rejko Krüger; Manu Sharma; Patrick May
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Variants in the proteasome regulator PSMF1 cause a phenotypic spectrum from parkinsonism to perinatal lethality
err2026-04-15
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errOAAI
errFrancesca Magrinelli; Christelle Tesson; Plamena R. Angelova; Jose A. Rodriguez; Annarita Scardamaglia; Benjamin O’Callaghan; Simon A. Lowe; Ainara Salazar-Villacorta; Brian Hon-Yin Chung; Matthew Jaconelli; Barbara Vona; Noemi Esteras; Angela Mammana; Junko Shimazu; Anna Ka-Yee Kwong; Thomas Courtin; Shahryar Alavi; Reza Maroofian; Raja Nirujogi; Mariasavina Severino; Edoardo Monfrini; Clarissa Rocca; Patrick A. Lewis; Stephanie Efthymiou; Rebecca Buchert; Linda Sofan; Pawel Lis; Chloé Pinon; Guido J. Breedveld; Martin Man-Chun Chui; David Murphy; Vanessa Pitz; Mary B. Makarious; Simone Baiardi; Marina Volin; Marlene Cassar; Bassem A. Hassan; Sana Iftikhar; Peter Bauer; Michele Tinazzi; Marina Svetel; Bedia Samanci; Haşmet A. Hanağası; Basar Bilgiç; Francesco Cavallieri; Mario Santangelo; José A. Obeso; Monica M. Kurtis; Guillaume Cogan; Güneş Kiziltan; Tuğçe Gül-Demirkale; Hülya Tireli; Gülbün A. Yüksel; Gül Yalçın-Cakmakli; Bülent Elibol; Nina Barišić; Earny Wei-Sen Ng; Sze-Shing Fan; Tova Hershkovitz; Karin Weiss; Javeria Raza Alvi; Tipu Sultan; Issam Azmi Alkhawaja; Tawfiq Froukh; Hadeel Abdollah E. Alrukban; Muhammad Nadeem Anjum; Anjum Saeed; Huma Arshad Cheema; Christine Fauth; Ulrich A. Schatz; Thomas Zöggeler; Michael Zech; Karen Stals; Vinod Varghese; Sonia Gandhi; Cornelis Blauwendraat; John A. Hardy; Alessio Di Fonzo; Vincenzo Bonifati; Tobias B. Haack; Aida M. Bertoli-Avella; Suzanne Lesage; Ayşe Nazlı Başak; Robert Steinfeld; Piero Parchi; James E. C. Jepson; Dario R. Alessi; Alexis Brice; Hermann Steller; Andrey Y. Abramov; Kailash P. Bhatia; Henry Houlden
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The genetics of autosomal recessive early-onset Parkinson's disease
err2025-11-17
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PREAI
errGuillaume Cogan; Suzanne Lesage; Alexis Brice
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Should ITSN1 be considered as a Mendelian Parkinson’s disease gene? Description of three novel families
err2025-10-17
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errOAAI
errGuillaume Cogan; Christelle Tesson; Lisa Welment; Fabienne Clot; Eric LeGuern; Aymeric Lanore; Alexandra Dürr; Florence Cormier-Dequaire; Bérengère Debilly; Marc Planes; Graziella Mangone; Suzanne Lesage; Alexis Brice
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Classification of GBA1 variants and their impact on Parkinson’s disease: an in silico score analysis
err2025-08-02
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errOAAI
errAymeric Lanore; Christelle Tesson; Aymeric Basset; François-Xavier Lejeune; Guillaume Cogan; Graziella Mangone; Sara Sambin; Nathalie Bertille; Mathieu Anheim; Isabelle Arnulf; Solène Ansquer; Jean-Philippe Brandel; Christine Brefel-Courbon; Luc Defebvre; Sophie Drapier; Alexandre Eusebsio; Margherita Fabbri; Caroline Giordana; Elodie Hainque; Stephane Lehericy; Ana Marques; Caroline Moreau; Elena Moro; Fabienne Ory; Anne-Sophie Rolland; Stéphane Thobois; Marie Vidailhet; David Devos; Louise-Laure Mariani; Suzanne Lesage; Alexis Brice; Jean-Christophe Corvol
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Expanding the clinical spectrum of RAB3A: from cerebellar ataxia to spastic paraplegia
errBRAIN
IF11.7
err2025-08-01
err1
PREAI
errMouraux, Charlotte; Mereaux, Jean-Loup; Davoine, Claire-Sophie; Guillot-Noel, Lena; Brice, Alexis; Durr, Alexandra; Coarelli, Giulia
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Late-onset cerebellar ataxia in three European patients with repeat expansions in RFC1 and FGF14: a case series
err2025-07-10
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PREAI
errArmand Hocquel; David Pellerin; Jean loup Méreaux; Vincent Huin; Marios Hadjivassiliou; Guillemette Clément; Felipe Villa; Salomé Puisieux; Solène Frismand; Marion Wandzel; Virginie Roth; Anna Wissocq; Thomas Wirth; Matt C. Danzi; Isabelle Quadrio; Stephan Zuchner; Laetitia Lambert; Fanny Mochel; Matthis Synofzik; Mathieu Anheim; Henry Houlden; Alexis Brice; Carine Pourié; Bernard Brais; Céline Bonnet; Alexandra Durr; Mathilde Renaud
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Impact of Y chromosome loss on the risk of Parkinson's disease and progression
err2025-05-29
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PREAI
errJunhao Wang; Xinyi Chen; Wenxuan Du; Cha Lin; Yu Liao; Jean-Christophe Corvol; Jodi Maple-Grødem; Meghan C. Campbell; Alexis Elbaz; Suzanne Lesage; Alexis Brice; Michael A. Schwarzschild; Pille Taba; Sulev Kõks; Guido Alves; Ole-Bjørn Tysnes; Joel S. Perlmutter; Baijayanta Maiti; Jacobus J. van Hilten; Roger A. Barker; Caroline H. Williams-Gray; Clemens R. Scherzer; Ganqiang Liu
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Linking polygenic risk scores to dopaminergic neuron loss using neuromelanin-sensitive imaging
errBrain
IF11.7
err2025-05-16
err0
PREAI
errAymeric Lanore; Rahul Gaurav; François-Xavier Lejeune; Aymeric Basset; Christelle Tesson; Gatepe Cedoine Kodjovi; Sara Sambin; Graziella Mangone; Isabelle Arnulf; Marie Vidailhet; Louise-Laure Mariani; Alexis Brice; Suzanne Lesage; Stephane Lehericy; Jean-Christophe Corvol; Marie Vidailhet; Jean-Christophe Corvol; Isabelle Arnulf; Stephane Lehericy; Graziella Mangone; Sara Sambin; Poornima Menon; Jonas Ihle; Caroline Weill; David Grabli; Florence Cormier-Dequaire; Louise Laure Mariani; Bertrand Degos; Richard Levy; Fanny Pineau; Julie Socha; Eve Benchetrit; Virginie Czernecki; Marie-Alexandrine; Sophie Rivaud-Pechoux; Elodie Hainque; Smaranda Leu Semenescu; Pauline Dodet; Samir Bekadar; Alexis Brice; Suzanne Lesage; Fanny Mochel; Farid Ichou; Vincent Perlbarg; Benoit Colsch; Arthur Tenenhaus; Rahul Gaurav; Nadya Pyatigorskaya; Lydia Yahia-Cherif; Romain Valabregue; Cécile Galléa; Marie-Odile Habert; Dijana Petrovska; Laetitia Jeancolas; Alizé Chalançon; Carole Dongmo-Kenfack; Christelle Laganot; Valentine Maheo; Manon Gomes; Mickaël Lé
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Exploration of Neurodegenerative Diseases Using Long-Read Sequencing and Optical Genome Mapping Technologies
err2025-03-03
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errOAAI
errGuillaume Cogan MD; Kensuke Daida MD, PhD; Cornelis Blauwendraat PhD; Kimberley Billingsley PhD; Alexis Brice MD
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Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy (vol 19, 61, 2024)
err2024-10-14
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errOAAI
errWang, Hui; Chang, Timothy S.; Dombroski, Beth A.; Cheng, Po-Liang; Patil, Vishakha; Valiente-Banuet, Leopoldo; Farrell, Kurt; Mclean, Catriona; Molina-Porcel, Laura; Rajput, Alex; De Deyn, Peter Paul; Le Bastard, Nathalie; Gearing, Marla; Kaat, Laura Donker; Van Swieten, John C.; Dopper, Elise; Ghetti, Bernardino F.; Newell, Kathy L.; Troakes, Claire; de Yebenes, Justo G.; Rabano-Gutierrez, Alberto; Meller, Tina; Oertel, Wolfgang H.; Respondek, Gesine; Stamelou, Maria; Arzberger, Thomas; Roeber, Sigrun; Mueller, Ulrich; Hopfner, Franziska; Pastor, Pau; Brice, Alexis; Durr, Alexandra; Le Ber, Isabelle; Beach, Thomas G.; Serrano, Geidy E.; Hazrati, Lili-Naz; Litvan, Irene; Rademakers, Rosa; Ross, Owen A.; Galasko, Douglas; Boxer, Adam L.; Miller, Bruce L.; Seeley, Willian W.; Van Deerlin, Vivanna M.; Lee, Edward B.; White III, Charles L.; Morris, Huw; de Silva, Rohan; Crary, John F.; Goate, Alison M.; Friedman, Jeffrey S.; Leung, Yuk Yee; Coppola, Giovanni; Naj, Adam C.; Wang, Li-San; Dalgard, Clifton; Dickson, Dennis W.; Hoeglinger, Guenter U.; Schellenberg, Gerard D.; Geschwind, Daniel H.; Lee, Wan-Ping
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Confirmation of RAB32 Ser71Arg Involvement in Parkinson's Disease
err2024-09-23
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errOAAI
errCogan, Guillaume; Tesson, Christelle; Brefel-Courbon, Christine; Lanore, Aymeric; Kodjovi, Gatepe Cedoine; Welment, Lisa; Clot, Fabienne; Lesage, Suzanne; Brice, Alexis
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Longitudinal Changes of Clinical, Imaging, and Fluid Biomarkers in Preataxic and Early Ataxic Spinocerebellar Ataxia Type 2 and 7 Carriers
err2024-09-10
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errOAAI
errCoarelli, Giulia; Dubec-Fleury, Charlotte; Petit, Emilien; Sayah, Sabrina; Fischer, Clara; Nassisi, Marco; Gatignol, Peggy; Dorgham, Karim; Daghsen, Lina; Daye, Pierre; Cunha, Paulina; Kacher, Radhia; Hilab, Rania; Hurmic, Hortense; Lamaziere, Antonin; Lamy, Jean-Charles; Welter, Marie-Laure; Chupin, Marie; Mangin, Jean-Francois; Lane, Roger; Gaymard, Bertrand; Pouget, Pierre; Audo, Isabelle; Brice, Alexis; Tezenas du Montcel, Sophie; Durr, Alexandra
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Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy
err2024-08-16
err2
errOAAI
errWang, Hui; Chang, Timothy S.; Dombroski, Beth A.; Cheng, Po-Liang; Patil, Vishakha; Valiente-Banuet, Leopoldo; Farrell, Kurt; Mclean, Catriona; Molina-Porcel, Laura; Rajput, Alex; De Deyn, Peter Paul; Le Bastard, Nathalie; Gearing, Marla; Kaat, Laura Donker; Van Swieten, John C.; Dopper, Elise; Ghetti, Bernardino F.; Newell, Kathy L.; Troakes, Claire; de Yebenes, Justo G.; Rabano-Gutierrez, Alberto; Meller, Tina; Oertel, Wolfgang H.; Respondek, Gesine; Stamelou, Maria; Arzberger, Thomas; Roeber, Sigrun; Mueller, Ulrich; Hopfner, Franziska; Pastor, Pau; Brice, Alexis; Durr, Alexandra; Le Ber, Isabelle; Beach, Thomas G.; Serrano, Geidy E.; Hazrati, Lili-Naz; Litvan, Irene; Rademakers, Rosa; Ross, Owen A.; Galasko, Douglas; Boxer, Adam L.; Miller, Bruce L.; Seeley, Willian W.; Van Deerlin, Vivanna M.; Lee, Edward B.; White III, Charles L.; Morris, Huw; de Silva, Rohan; Crary, John F.; Goate, Alison M.; Friedman, Jeffrey S.; Leung, Yuk Yee; Coppola, Giovanni; Naj, Adam C.; Wang, Li-San; Dalgard, Clifton; Dickson, Dennis W.; Hoeglinger, Guenter U.; Schellenberg, Gerard D.; Geschwind, Daniel H.; Lee, Wan-Ping
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Association of Body Mass Index and Parkinson Disease A Bidirectional Mendelian Randomization Study
err2024-08-13
err1
PREAI
errDomenighetti, Cloe; Sugier, Pierre-Emmanuel; Ashok Kumar Sreelatha, Ashwin; Schulte, Claudia; Grover, Sandeep; Portugal, Berta; Lee, Pei-Chen; May, Patrick; Bobbili, Dheeraj; Radivojkov Blagojevic, Milena; Lichtner, Peter; Singleton, Andrew B.; Hernandez, Dena; Edsall, Connor; Mellick, George D.; Zimprich, Alexander A.; Pirker, Walter; Rogaeva, Ekaterina A.; Lang, Anthony E.; Koks, Sulev; Taba, Pille; Lesage, Suzanne; Brice, Alexis; Corvol, Jean-Christophe; Chartier-Harlin, Marie-Christine; Mutez, Eugenie; Brockmann, Kathrin; Deutschlander, Angela B.; Hadjigeorgiou, Georgios M.; Dardiotis, Efthimios; Stefanis, Leonidas; Simitsi, Athina Maria; Valente, Enza Maria; Petrucci, Simona; Straniero, Letizia; Zecchinelli, Anna L.; Pezzoli, Gianni; Brighina, Laura; Ferrarese, Carlo; Annesi, Grazia; Quattrone, Andrea; Gagliardi, Monica; Matsuo, Hirotaka; Nakayama, Akiyoshi; Hattori, Nobutaka; Nishioka, Kenya; Chung, Sun Ju; Kim, Yun Joong; Kolber, Pierre; Van De Warrenburg, Bart P. C.; Bloem, Bastiaan R.; Toft, Mathias; Pihlstrm, Lasse; Correia Guedes, Leonor; Ferreira, Joaquim J.; Bardien, Soraya; Carr, Jonathan; Tolosa, Eduardo; Ezquerra, Mario; Pastor, Pau; Diez-Fairen, Monica; Wirdefeldt, Karin; Pedersen, Nancy L.; Ran, Caroline; Belin, Andrea C.; Puschmann, Andreas; Hellberg, Clara; Clarke, Carl E.; Morrison, Karen E.; Tan, Manuela M.; Krainc, Dimitri; Burbulla, Lena F.; Farrer, Matthew; Kruger, Rejko; Gasser, Thomas; Sharma, Manu; Elbaz, Alexis
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The parkin V380L variant is a genetic modifier of Machado-Joseph disease with impact on mitophagy
err2024-08-01
err0
errOAAI
errWeber, Jonasz J.; Czisch, Leah; Sena, Priscila Pereira; Fath, Florian; Huridou, Chrisovalantou; Schwarz, Natasa; Eltemur, Rana D. Incebacak; Wuerth, Anna; Weishaeupl, Daniel; Doecker, Miriam; Blumenstock, Gunnar; Martins, Sandra; Sequeiros, Jorge; Rouleau, Guy A.; Jardim, Laura Bannach; Saraiva-Pereira, Maria-Luiza; Franca Jr, Marcondes C.; Gordon, Carlos R.; Zaltzman, Roy; Cornejo-Olivas, Mario R.; van de Warrenburg, Bart P. C.; Durr, Alexandra; Brice, Alexis; Bauer, Peter; Klockgether, Thomas; Schoels, Ludger; Riess, Olaf; Schmidt, Thorsten
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Long-Read Sequencing Unravels the Complexity of Structural Variants in PRKN in Two Individuals with Early-Onset Parkinson's Disease
err2024-06-28
err0
errOAAI
errCogan, Guillaume; Daida, Kensuke; Billingsley, Kimberley J.; Tesson, Christelle; Forlani, Sylvie; Jornea, Ludmila; Arnaud, Lionel; Tissier, Laurene; LeGuern, Eric; Singleton, Andrew B.; Ferrien, Melanie; Bernard, Helene Gervais; Lesage, Suzanne; Blauwendraat, Cornelis; Brice, Alexis
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Genome-wide determinants of mortality and motor progression in Parkinson's disease
err2024-06-07
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errOAAI
errTan, Manuela M. X.; Lawton, Michael A.; Pollard, Miriam I.; Brown, Emmeline; Real, Raquel; Carrasco, Alejandro Martinez; Bekadar, Samir; Jabbari, Edwin; Reynolds, Regina H.; Iwaki, Hirotaka; Blauwendraat, Cornelis; Kanavou, Sofia; Hubbard, Leon; Malek, Naveed; Grosset, Katherine A.; Bajaj, Nin; Barker, Roger A.; Burn, David J.; Bresner, Catherine; Foltynie, Thomas; Wood, Nicholas W.; Williams-Gray, Caroline H.; Andreassen, Ole A.; Toft, Mathias; Elbaz, Alexis; Artaud, Fanny; Brice, Alexis; Corvol, Jean-Christophe; Aasly, Jan; Farrer, Matthew J.; Nalls, Michael A.; Singleton, Andrew B.; Williams, Nigel M.; Ben-Shlomo, Yoav; Hardy, John; Hu, Michele T. M.; Grosset, Donald G.; Shoai, Maryam; Pihlstrom, Lasse; Morris, Huw R.
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Genetic variation and pesticide exposure influence blood DNA methylation signatures in females with early-stage Parkinson's disease
err2024-05-07
err1
errOAAI
errSchaffner, S. L.; Casazza, W.; Artaud, F.; Konwar, C.; Merrill, S. M.; Domenighetti, C.; Schulze-Hentrich, J. M.; Lesage, S.; Brice, A.; Corvol, J. C.; Mostafavi, S.; Dennis, J. K.; Elbaz, A.; Kobor, M. S.
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CAG repeat mosaicism is gene specific in spinocerebellar ataxias
err2024-05-01
err7
errOAAI
errKacher, Radhia; Lejeune, Francois-Xavier; David, Isabelle; Boluda, Susana; Coarelli, Giulia; Leclere-Turbant, Sabrina; Heinzmann, Anna; Marelli, Cecilia; Charles, Perrine; Goizet, Cyril; Kabir, Nisha; Hilab, Rania; Jornea, Ludmila; Six, Julie; Dommergues, Marc; Fauret, Anne-Laure; Brice, Alexis; Humbert, Sandrine; Durr, Alexandra
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