G. Barcia
发表
A. Munnich,
N. Boddaert,
A. Rötig,
2021,
Molecular genetics and metabolism.
A. Munnich,
A. Rötig,
J. Steffann,
2020,
Expert review of molecular diagnostics.
Peter Donnelly,
Gil McVean,
Jean-Baptiste Cazier,
2014,
Human molecular genetics.
N. Chémaly,
A. Macaya,
G. Barcia,
2020
.
N. Boddaert,
S. Auvin,
R. Nabbout,
2019,
Neurology: Genetics.
Ethan M. Goldberg,
A. Munnich,
E. Goldberg,
2018,
Genetics in Medicine.
I. Scheffer,
H. Mefford,
A. Munnich,
2019,
Human mutation.
N. Boddaert,
O. Dulac,
R. Nabbout,
2014,
European journal of medical genetics.
A. Munnich,
N. Franck,
N. Boddaert,
2019,
Psychiatric genetics.
A. Munnich,
M. Till,
G. Barcia,
2018,
Journal of autism and developmental disorders.
I. Jambaqué,
G. Dellatolas,
O. Dulac,
2013,
Orphanet Journal of Rare Diseases.
A. Munnich,
N. Boddaert,
A. Rötig,
2018,
Journal of Medical Genetics.
R. Nabbout,
G. Barcia,
M. Kuchenbuch,
2020,
Epilepsia open.
J. Thevenon,
R. Nabbout,
D. Ville,
2022,
European journal of medical genetics.
A. Munnich,
N. Boddaert,
S. Hanein,
2018,
Brain : a journal of neurology.
F. Denoyelle,
S. Lyonnet,
R. Caswell,
2022,
European journal of human genetics : EJHG.
B. Cogné,
A. Piton,
L. Villard,
2021,
Journal of Medical Genetics.
S. Auvin,
R. Nabbout,
A. Kaminska,
2019,
Brain : a journal of neurology.
H. Prokisch,
S. Hanein,
A. Rötig,
2018,
American journal of human genetics.
R. Nabbout,
D. Ville,
B. Desnous,
2022,
Epilepsia.
A. Munnich,
N. Boddaert,
A. Rötig,
2021,
Molecular genetics and metabolism.
Ethan M. Goldberg,
A. Munnich,
C. Davidson,
2018,
Genetics in Medicine.
A. Munnich,
N. Boddaert,
C. Bole-Feysot,
2016,
Orphanet Journal of Rare Diseases.
R. Ganetzky,
H. Prokisch,
E. Eklund,
2022,
Genetics in medicine : official journal of the American College of Medical Genetics.
M. Tartaglia,
R. Maroofian,
H. Houlden,
2022,
American journal of human genetics.
A. Munnich,
N. Boddaert,
A. Rötig,
2020,
Journal of medical genetics.
Robert W. Taylor,
A. Rötig,
N. Hauser,
2019,
Genetics in Medicine.
C. Garel,
N. Boddaert,
A. Laquérriere,
2022
.
D. Mei,
S. Zuberi,
G. Barcia,
2022,
European journal of medical genetics.
R. Nabbout,
I. Desguerre,
L. Colleaux,
2019,
Clinical genetics.
L. Kaczmarek,
A. Munnich,
J. Casanova,
2012,
Nature Genetics.
A. Munnich,
N. Boddaert,
A. Rötig,
2020,
Neuromuscular Disorders.
N. Boddaert,
Y. Péréon,
A. Kaminska,
2018,
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
W. Chung,
A. Munnich,
B. Menten,
2021,
Human Genetics.
Y. Ville,
V. Tsatsaris,
F. Encha-Razavi,
2019,
Prenatal diagnosis.
A. Munnich,
Philippe P Roux,
N. Boddaert,
2014,
American journal of human genetics.
Human slack potassium channel mutations increase positive cooperativity between individual channels.
L. Kaczmarek,
Jenny C. Taylor,
E. Blair,
2014,
Cell reports.
R. Nabbout,
L. Ouss,
I. Desguerre,
2018,
Epilepsia open.
A. Munnich,
A. Saiardi,
N. Boddaert,
2020,
Nature Communications.
R. Nabbout,
A. Kaminska,
B. Bernardina,
2021,
Clinical Neurophysiology.
C. Walsh,
L. Zon,
A. Munnich,
2014,
American journal of human genetics.
Rebecca C. Spillmann,
Q. K. Tan,
J. Lupski,
2023,
medRxiv.
R. Pfundt,
D. Baralle,
I. Thiffault,
2022,
American journal of human genetics.
I. Scheffer,
H. Mefford,
A. Munnich,
2020,
Epilepsia.
A. Munnich,
N. Boddaert,
A. Rötig,
2018,
Human mutation.
J. Arenas,
A. Delmiro,
F. Martínez-Azorín,
2017,
Clinical genetics.
Ethan M. Goldberg,
A. Munnich,
C. Davidson,
2018,
Genetics in Medicine.
V. Fellman,
Matteo P. Ferla,
Jenny C. Taylor,
2021,
Annals of clinical and translational neurology.
A. Munnich,
N. Boddaert,
S. Hanein,
2019,
Molecular Autism.
A. Munnich,
M. Till,
G. Barcia,
2018,
Journal of Autism and Developmental Disorders.
C. Garel,
N. Boddaert,
J. Baptista,
2022,
American journal of human genetics.
F. Wendling,
R. Nabbout,
A. Kaminska,
2018,
Epilepsia.
Anne de Saint Martin,
A. Afenjar,
P. Berquin,
2021,
Epilepsy & Behavior.
A. Munnich,
Y. Ville,
A. Rötig,
2020,
Genetics in Medicine.
A. Munnich,
N. Boddaert,
A. Rötig,
2020,
Haematologica.
Manuela Pendziwiat,
I. Helbig,
G. Kuhlenbäumer,
2020,
Annals of clinical and translational neurology.
Ulrich Brandt,
Sergio Guerrero-Castillo,
Benoît Funalot,
2016,
American journal of human genetics.
A. Munnich,
R. Nabbout,
C. Barnérias,
2013,
European journal of medical genetics.
A. Munnich,
N. Boddaert,
A. Rötig,
2019,
Molecular genetics and metabolism reports.
A. Munnich,
N. Boddaert,
A. Rötig,
2020,
Human mutation.
N. Boddaert,
F. Brunelle,
O. Dulac,
2013,
Developmental medicine and child neurology.
Meghan C Towne,
E. Eichler,
H. Hakonarson,
2023,
Science Translational Medicine.
S. Lyonnet,
T. Kinoshita,
M. Hully,
2021,
Blood.
A. Munnich,
N. Boddaert,
R. Nabbout,
2023,
European journal of neurology.
A. Afenjar,
V. Cormier-Daire,
J. Amiel,
2022,
Orphanet Journal of Rare Diseases.
A. Munnich,
N. Boddaert,
A. Rötig,
2019,
Molecular genetics and metabolism reports.
A. Munnich,
J. Steffann,
M. Raynaud,
2019,
Prenatal diagnosis.
Anne de Saint Martin,
I. Scheffer,
H. Mefford,
2019
.
N. Garcelon,
R. Nabbout,
A. Kaminska,
2021,
Genetics in Medicine.
R. Rodenburg,
A. Rötig,
B. Funalot,
2016,
American journal of human genetics.