G. Nicolas
发表
R. Redon,
A. Vighetto,
G. Bourque,
2017,
Neurobiology of Aging.
Eden R Martin,
Seth Love,
Brian Lawlor,
2019,
Nature Genetics.
A. Toutain,
A. Wilkie,
J. Galbany,
2019,
Human mutation.
Olivier Rouaud,
Canan Ozsancak,
Valérie Chauviré,
2017,
PLoS medicine.
T. Lefèbvre,
L. Gouya,
H. Puy,
2019,
Molecular genetics and metabolism.
M. Sitbon,
D. Campion,
D. Hannequin,
2016,
Journal of Neurology.
C. Beaumont,
C. Oudin,
B. Grandchamp,
2012,
Human mutation.
C. López-Otín,
S. Vaulont,
A. Ramsay,
2011,
Blood.
C. López-Otín,
S. Vaulont,
A. Ramsay,
2011
.
S. Vaulont,
B. Durel,
G. Nicolas,
2010,
Haematologica.
C. López-Otín,
S. Vaulont,
A. Ramsay,
2010
.
S. Vaulont,
A. Kahn,
G. Nicolas,
2005,
Blood.
S. Vaulont,
G. Nicolas,
2005,
Medecine sciences : M/S.
Björn Rotter,
G. Nicolas,
M. Lecomte,
2006,
Biology of the cell.
C. Craescu,
G. Nicolas,
M. Lecomte,
1998,
The Biochemical journal.
D. Campion,
D. Wallon,
S. Epelbaum,
2022,
Stem cell research.
L. Malbert-Colas,
G. Nicolas,
M. Lecomte,
2003,
Comptes rendus biologies.
M. Fornage,
K. Lunetta,
S. Gabriel,
2018,
Molecular Psychiatry.
D. Campion,
O. Guillin,
V. Drouin‐Garraud,
2020,
Translational Psychiatry.
D. Hannequin,
P. Labauge,
X. Ayrignac,
2017,
JAMA neurology.
O. Martinaud,
D. Campion,
D. Hannequin,
2014,
Journal of Molecular Neuroscience.
E. Génin,
C. Tzourio,
D. Campion,
2018,
Translational Psychiatry.
Michaël E. Belloy,
W. M. van der Flier,
D. Rujescu,
2022,
JAMA neurology.
G. Fénelon,
A. Boland,
J. Deleuze,
2021,
Human molecular genetics.
L. Guyant‐Maréchal,
E. Gerardin,
P. Vivier,
2018,
Pediatric Radiology.
D. Campion,
A. Boland,
T. Frebourg,
2020,
Movement disorders : official journal of the Movement Disorder Society.
W. M. van der Flier,
D. Grozeva,
O. Martinaud,
2022,
Genome Medicine.
J. Hardy,
R. Guerreiro,
D. Campion,
2013,
JAMA neurology.
Björn Rotter,
G. Nicolas,
M. Lecomte,
2004,
The Biochemical journal.
J. Camonis,
L. Malbert-Colas,
B. Grandchamp,
2002,
Molecular and Cellular Biology.
Björn Rotter,
G. Nicolas,
M. Lecomte,
2005,
The Biochemical journal.
P. Cacoub,
G. Nicolas,
K. Peoc’h,
2020,
Scientific Reports.
C. Beaumont,
T. Lefèbvre,
L. Gouya,
2015,
Clinical chemistry and laboratory medicine.
C. Rondelli,
H. Puy,
J. Phillips,
2021,
The Journal of biological chemistry.
Ronan K. Carroll,
L. Shaw,
A. Weiss,
2016,
MicrobiologyOpen.
P. Petit,
G. Nicolas,
N. Rainey,
2019,
Cell Death Discovery.
N. Drouot,
O. Quenez,
K. Cassinari,
2022,
Human mutation.
Nick C Fox,
W. M. van der Flier,
A. Uitterlinden,
2022,
Genome Medicine.
S. Vaulont,
Z. Karim,
P. Langella,
2016,
FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
Nick C Fox,
Michelle K. Lupton,
Charles C. White,
2019,
Nature Genetics.
C. Bole-Feysot,
P. Nitschké,
P. Mayeux,
2019,
Blood.
D. Campion,
D. Wallon,
A. Boland,
2022,
Genome medicine.
C. López-Otín,
S. Vaulont,
A. Ramsay,
2014,
Blood.
C. Beaumont,
B. Grandchamp,
S. Vaulont,
2002,
Proceedings of the National Academy of Sciences of the United States of America.
S. Vaulont,
G. Nicolas,
D. Lou,
2010
.
N. Andrews,
S. Vaulont,
A. Kahn,
2004
.
D. Hannequin,
A. Brice,
D. Wallon,
2014,
Neurobiology of Aging.
D. Geschwind,
G. Coppola,
D. Campion,
2015,
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
C. Lelliott,
P. Croucher,
Y. Maugars,
2019,
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.
N. Andrews,
C. Beaumont,
S. Vaulont,
2003,
Nature Genetics.
C. V. van Ravenswaaij-Arts,
T. Frebourg,
S. Coutant,
2020,
Human mutation.
P. Petit,
G. Nicolas,
N. Rainey,
2019,
bioRxiv.
G. Velasco,
C. Beaumont,
B. Grandchamp,
2011,
British journal of haematology.
Mutation in the 3’untranslated region of APP as a genetic determinant of cerebral amyloid angiopathy
J. Dartigues,
S. Hébert,
J. Lambert,
2015,
European Journal of Human Genetics.
C. Beaumont,
S. Vaulont,
G. Nicolas,
2003
.
S. Coutant,
F. Lecoquierre,
B. Sadikovic,
2022,
European journal of medical genetics.
O. Martinaud,
G. Nicolas,
2017,
Alzheimer disease and associated disorders.
D. Hannequin,
A. Laquérriere,
G. Nicolas,
2017,
Neurology: Genetics.
B. Grandchamp,
P. Gallagher,
G. Nicolas,
1997,
Blood.
D. Wallon,
L. Grangeon,
G. Nicolas,
2020,
Brain : a journal of neurology.
A. Laquérriere,
T. Frebourg,
O. Quenez,
2016,
American journal of medical genetics. Part A.
A. Afenjar,
N. Philip,
V. Cormier-Daire,
2019,
Genetics in Medicine.
Y. Crow,
G. Coppola,
D. Campion,
2015,
Human mutation.
S. Coutant,
F. Lecoquierre,
M. Vezain,
2022,
Human Genetics.
T. Lefèbvre,
J. Deybach,
L. Gouya,
2019,
American journal of human genetics.
D. Hannequin,
T. Frebourg,
K. Cassinari,
2021,
American journal of medical genetics. Part A.
B. Viollet,
M. Birnbaum,
D. Carling,
2003,
The Journal of clinical investigation.
M. Magnani,
M. Paiardini,
G. Nicolas,
2000
.
N. Vitale,
M. Bader,
S. Gasman,
2019,
IUBMB life.
C. Duyckaerts,
H. Chabriat,
D. Hervé,
2018,
Acta Neuropathologica.
A. Saiardi,
M. Sitbon,
X. Ayrignac,
2020,
The Journal of Biological Chemistry.
N. Drouot,
A. Boland,
D. Lacombe,
2022,
Human mutation.
Nick C Fox,
W. M. van der Flier,
A. Uitterlinden,
2022,
Nature Genetics.
K. Baye,
G. Nicolas,
C. Humblot,
2019,
Scientific Reports.
J. Pariente,
F. Pasquier,
O. Martinaud,
2016,
Neurology.
L. Defebvre,
M. Vidailhet,
J. Pariente,
2019,
Brain : a journal of neurology.
W. M. van der Flier,
D. Rujescu,
I. Giegling,
2022,
Acta Neuropathologica.
D. Campion,
D. Wallon,
B. Croisile,
2021,
Neurology: Genetics.
D. Wallon,
D. Maltête,
L. Guyant‐Maréchal,
2012,
Journal of the American Geriatrics Society.
R. Redon,
N. Drouot,
J. Dartigues,
2020,
European Journal of Human Genetics.
Gaël Nicolas,
Isabelle Devaux,
C. Beaumont,
2002,
The Journal of clinical investigation.
D. Campion,
D. Hannequin,
D. Wallon,
2015,
Molecular Psychiatry.
W. Chung,
A. Munnich,
B. Menten,
2021,
Human Genetics.
Nick C Fox,
Catherine A. Macleod,
W. M. van der Flier,
2022,
Nature Genetics.
D. Campion,
A. Rovelet-Lecrux,
K. L. Guennec,
2016,
Molecular Psychiatry.
W. M. van der Flier,
M. Fornage,
D. Rujescu,
2021,
Nature Communications.
K. Blennow,
C. van Broeckhoven,
S. Engelborghs,
2020,
PLoS medicine.
Nick C Fox,
Michelle K. Lupton,
Charles C. White,
2019,
Nature Genetics.
D. Geschwind,
P. Svenningsson,
A. Aguzzi,
2013,
Nature Genetics.
D. Geschwind,
M. Vidailhet,
D. Galasko,
2018,
European Journal of Human Genetics.
D. Geschwind,
M. Vidailhet,
D. Galasko,
2018,
European Journal of Human Genetics.
D. Geschwind,
P. Svenningsson,
J. Pariente,
2015,
Nature Genetics.
O. Martinaud,
D. Campion,
D. Hannequin,
2014,
Journal of Molecular Neuroscience.
Y. Béjot,
M. Giroud,
D. Campion,
2014,
European Journal of Human Genetics.
L. Defebvre,
J. Pariente,
M. Vérin,
2013,
Brain : a journal of neurology.
L. Defebvre,
J. Pariente,
O. Martinaud,
2013,
Neurology.
S. Julia,
E. Pasmant,
A. Sabbagh,
2021,
Cancers.
C. Duyckaerts,
D. Campion,
V. Deramecourt,
2022,
Acta neuropathologica communications.
J. Pariente,
F. Pasquier,
O. Martinaud,
2019,
Journal of Alzheimer's disease : JAD.
J. Veltman,
G. Nicolas,
2018,
Acta Neuropathologica.
D. Campion,
C. Charbonnier,
G. Nicolas,
2016,
Human Heredity.
A. Montpetit,
G. Bourque,
J. Pariente,
2015,
European Journal of Human Genetics.
C. Beaumont,
B. Grandchamp,
S. Vaulont,
2001,
Proceedings of the National Academy of Sciences of the United States of America.
B. Paw,
T. Baker,
S. Ducamp,
2017,
Proceedings of the National Academy of Sciences.
N. Andrews,
H. Bujard,
K. Schönig,
2006,
Blood.
L. Rénia,
S. Vaulont,
A. Kahn,
2005,
Hepatology.
C. Beaumont,
S. Vaulont,
A. Kahn,
2002,
Blood cells, molecules & diseases.
R Redon,
R. Redon,
M. Bihoreau,
2017,
Molecular Psychiatry.
M. Shaw,
N. de Leeuw,
J. Gécz,
2020,
American journal of human genetics.
S. Coutant,
F. Lecoquierre,
S. Marret,
2021,
Life.
V. Drouin‐Garraud,
A. Boland,
T. Frebourg,
2021,
European journal of medical genetics.
H. Galehdari,
T. Frebourg,
R. Maroofian,
2020,
European journal of medical genetics.
Jean-François Deleuze,
Gaël Nicolas,
Anne Boland,
2019,
Clinical chemistry.
R. Redon,
G. Bourque,
E. Génin,
2016,
Neurology.
M. Vérin,
D. Campion,
D. Hannequin,
2016,
European Journal of Human Genetics.
R. Redon,
G. Bourque,
E. Génin,
2016,
Molecular Psychiatry.
R. Redon,
N. Drouot,
J. Dartigues,
2020,
European Journal of Human Genetics.
Régine Marlin,
C. Houdayer,
T. Frebourg,
2020,
European journal of medical genetics.
Nick C Fox,
Catherine A. Macleod,
W. M. van der Flier,
2020
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Pavel P. Kuksa,
D. Rujescu,
S. Djurovic,
2020,
medRxiv.
M. Shaw,
N. de Leeuw,
J. Gécz,
2021,
American journal of human genetics.
C. Beaumont,
B. Grandchamp,
S. Vaulont,
2004,
FEBS letters.
N. Andrews,
S. Vaulont,
A. Kahn,
2004,
Blood.
N. Karboul,
J. Deybach,
L. Gouya,
2018,
Human molecular genetics.
D. Bertrand,
S. Coutant,
F. Lecoquierre,
2022,
Genetics in medicine : official journal of the American College of Medical Genetics.
D. Campion,
D. Hannequin,
D. Wallon,
2018,
Journal of Alzheimer's disease : JAD.
Ronald C. Petersen,
Guojun Bu,
Cyril Pottier,
2016,
Neurobiology of Aging.
M. Fornage,
K. Lunetta,
J. Haines,
2019,
JAMA neurology.
Laurent Gouya,
Hervé Puy,
J. Deybach,
2015,
Clinics and research in hepatology and gastroenterology.
C. Ged,
J. Blouin,
E. Richard,
2020,
Haematologica.
D. Campion,
T. Frebourg,
G. Riou,
2021,
Acta Neuropathologica Communications.
D. Campion,
C. Charbonnier,
G. Nicolas,
2019,
Acta Neuropathologica.
A. Hoischen,
J. Attems,
J. Veltman,
2018,
Alzheimer's & Dementia.
G. Grimber,
S. Vaulont,
A. Kahn,
2004,
Blood.
W. Gratzer,
G. Nicolas,
J. Pinder,
1999,
European Biophysics Journal.
F. Pasquier,
O. Martinaud,
J. Laplanche,
2016,
Journal of Alzheimer's disease : JAD.
O. Martinaud,
D. Campion,
D. Hannequin,
2014,
Journal of Alzheimer's disease : JAD.
D. Hannequin,
D. Maltête,
L. Guyant‐Maréchal,
2011,
American journal of medical genetics. Part A.
D. Hannequin,
O. Guillin,
R. Lefaucheur,
2013,
General hospital psychiatry.
W. M. van der Flier,
A. Uitterlinden,
R. Redon,
2021,
Alzheimer's & dementia : the journal of the Alzheimer's Association.
J. Veltman,
D. Campion,
C. Charbonnier,
2018,
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
R. Desnick,
L. Gouya,
H. Puy,
2021
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D. Campion,
T. Frebourg,
O. Quenez,
2021,
Acta Neuropathologica Communications.
S. Ducamp,
L. Gouya,
H. Puy,
2021,
Haematologica.
Variants in CLDN5 cause a syndrome characterized by seizures, microcephaly and brain calcifications.
S. Scherer,
C. Cytrynbaum,
R. Weksberg,
2022,
Brain : a journal of neurology.
K. Lohmann,
C. Klein,
M. Kasten,
2021,
Movement disorders : official journal of the Movement Disorder Society.
Melissa J. Green,
Emma M. Rath,
R. Redon,
2023,
Science.
S. Coutant,
F. Lecoquierre,
J. Thevenon,
2021,
medRxiv.
C. Rondelli,
H. Puy,
J. Phillips,
2020,
bioRxiv.
Nick C Fox,
Davide,
A. Uitterlinden,
2020
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Y. Colin,
D. Eladari,
G. Nicolas,
2007,
Journal of Biological Chemistry.
D. Geschwind,
D. Dickson,
G. Coppola,
2017,
Neurology: Genetics.
D. Wallon,
L. Grangeon,
G. Nicolas,
2019,
Brain : a journal of neurology.
D. Campion,
D. Wallon,
A. Boland,
2021,
bioRxiv.
S. Hébert,
M. Lathrop,
O. Martinaud,
2019,
Journal of Alzheimer's disease : JAD.
B. Strooper,
D. Campion,
D. Wallon,
2017,
Neurobiology of Disease.
F. Durif,
D. Campion,
D. Hannequin,
2014,
neurogenetics.
M. Frosch,
D. Campion,
D. Hannequin,
2017,
Journal of Alzheimer's disease : JAD.
O. Martinaud,
H. Chabriat,
D. Wallon,
2022,
Journal of Alzheimer's disease : JAD.
C. Duyckaerts,
M. Sarazin,
D. Campion,
2021,
Acta Neuropathologica.
N. Drouot,
A. Boland,
O. Quenez,
2023,
Human Genetics.
S. Lyonnet,
T. Kinoshita,
M. Hully,
2021,
Blood.
M. Iordanov,
D. Tshala-Katumbay,
D. Kretzschmar,
2012,
Journal of Molecular Neuroscience.
G. Labesse,
M. Sitbon,
D. Maltête,
2019,
Scientific Reports.
D. Rujescu,
O. Andreassen,
G. Spalletta,
2023,
JAMA network open.
J. Pariente,
C. Duyckaerts,
D. Campion,
2023,
Alzheimer's Research & Therapy.
Saskia M. J. Hopman,
L. Vissers,
R. Pfundt,
2023,
American journal of human genetics.
J. Lecerf,
B. Coulombe,
J. Ferrières,
2022,
Metabolites.
M. Fornage,
K. Lunetta,
S. Gabriel,
2019,
Molecular Psychiatry.
A. Afenjar,
N. Philip,
V. Cormier-Daire,
2019,
Genetics in Medicine.
A. Boland,
T. Frebourg,
O. Quenez,
2019,
American journal of medical genetics. Part A.
Nick C Fox,
R. Redon,
D. Grozeva,
2020,
medRxiv.
Michaël E. Belloy,
W. M. van der Flier,
D. Rujescu,
2021,
medRxiv.
G. Nicolas,
M. Lecourtois,
Laetitia Miguel,
2023,
Journal of Alzheimer's disease : JAD.
O. Martinaud,
D. Campion,
D. Hannequin,
2013,
Journal of the American Geriatrics Society.
G. Nicolas,
H. Gautero,
S. Pedroni,
1997,
BioTechniques.
Genetic,
Nick C Fox,
Michelle K. Lupton,
2019,
Nature Genetics.
O. Martinaud,
M. Chastan,
G. Nicolas,
2019,
Neuropsychology.
Gael R Nicolas,
Pamela V. Chang,
G. Nicolas,
2019,
Trends in pharmacological sciences.
M. Pericak-Vance,
G. Schellenberg,
M. Greicius,
2023,
medRxiv.
P. Petit,
G. Nicolas,
N. Rainey,
2019,
Cell Death Discovery.
C. Depienne,
O. Guillin,
A. Afenjar,
2023,
European journal of human genetics : EJHG.
B. Paw,
T. Baker,
S. Ducamp,
2017,
Proceedings of the National Academy of Sciences.
W. M. van der Flier,
D. Grozeva,
R. Sims,
2020
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Nick C Fox,
Pavel P. Kuksa,
W. M. van der Flier,
2022,
Nature Genetics.
G. Nicolas,
2024,
Revue neurologique.
G. Nicolas,
2024,
Current opinion in neurology.
A. Bruneau,
T. Lefèbvre,
K. Baye,
2024,
Gut microbes.
O. Martinaud,
K. Bennys,
V. de la Sayette,
2024,
Genetics in medicine : official journal of the American College of Medical Genetics.
R. Sims,
C. Mulle,
M. Hulsman,
2024,
bioRxiv.
S. Julia,
A. Afenjar,
F. Lecoquierre,
2024,
Journal of medical genetics.
F. Lecoquierre,
B. Cogné,
W. Deb,
2024,
European journal of medical genetics.
J. R. Oliveira,
C. Charbonnier,
G. Nicolas,
2015,
Journal of Molecular Neuroscience.