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Search Results - de Foucauld, Helene
Search Results - de Foucauld, Helene
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Lipin1 deficiency causes sarcoplasmic reticulum stress and chaperone‐responsive myopathy
by
Rashid, Talha
,
Nemazanyy, Ivan
,
Paolini, Cecilia
,
Tatsuta, Takashi
,
Crespin, Paul
,
de Villeneuve, Delphine
,
Brodesser, Susanne
,
Benit, Paule
,
Rustin, Pierre
,
Baraibar, Martin A
,
Agbulut, Onnik
,
Olivier, Anne
,
Protasi, Feliciano
,
Langer, Thomas
,
Chrast, Roman
,
de Lonlay, Pascale
,
de Foucauld, Helene
,
Blaauw, Bert
,
Pende, Mario
Published in
The EMBO journal
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A systematic analysis of gene-gene interaction in multiple sclerosis
by
Slim, Lotfi
,
Chatelain, Clément
,
Foucauld, Hélène de
,
Azencott, Chloé-Agathe
Published in
BMC medical genomics
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ABHD11, a new diacylglycerol lipase involved in weight gain regulation
by
Escoubet, Johanna
,
Kenigsberg, Mireille
,
Derock, Murielle
,
Yaligara, Veeranagouda
,
Bock, Marie-Dominique
,
Roche, Sandrine
,
Massey, Florence
,
de Foucauld, Helene
,
Bettembourg, Charles
,
Olivier, Anne
,
Berthemy, Antoine
,
Capdevielle, Joel
,
Legoux, Richard
,
Perret, Eric
,
Buzy, Armelle
,
Chardenot, Pascale
,
Destelle, Valerie
,
Leroy, Aurelie
,
Cahours, Christophe
,
Teixeira, Sandrine
,
Juvet, Patrick
,
Gauthier, Pascal
,
Leguet, Michael
,
Rocheteau-Beaujouan, Laurence
,
Chatoux, Marie-Agnes
,
Deshayes, Willy
,
Clement, Margerie
,
Kabiri, Mostafa
,
Orsini, Cecile
,
Mikol, Vincent
,
Didier, Michel
,
Guillemot, Jean-Claude
Published in
PloS one
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Lipin1 deficiency causes sarcoplasmic reticulum stress and chaperone‐responsive myopathy
by
Rashid, Talha
,
Nemazanyy, Ivan
,
Paolini, Cecilia
,
Tatsuta, Takashi
,
Crespin, Paul
,
de Villeneuve, Delphine
,
Brodesser, Susanne
,
Benit, Paule
,
Rustin, Pierre
,
Baraibar, Martin A
,
Agbulut, Onnik
,
Olivier, Anne
,
Protasi, Feliciano
,
Langer, Thomas
,
Chrast, Roman
,
de Lonlay, Pascale
,
de Foucauld, Helene
,
Blaauw, Bert
,
Pende, Mario
Published in
The EMBO journal
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Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls
by
Bellenguez, Céline
,
Charbonnier, Camille
,
Grenier-Boley, Benjamin
,
Quenez, Olivier
,
Le Guennec, Kilan
,
Nicolas, Gaël
,
Chauhan, Ganesh
,
Wallon, David
,
Rousseau, Stéphane
,
Richard, Anne Claire
,
Boland, Anne
,
Bourque, Guillaume
,
Munter, Hans Markus
,
Olaso, Robert
,
Meyer, Vincent
,
Rollin-Sillaire, Adeline
,
Pasquier, Florence
,
Letenneur, Luc
,
Redon, Richard
,
Dartigues, Jean-François
,
Tzourio, Christophe
,
Frebourg, Thierry
,
Lathrop, Mark
,
Deleuze, Jean-François
,
Hannequin, Didier
,
Genin, Emmanuelle
,
Amouyel, Philippe
,
Debette, Stéphanie
,
Lambert, Jean-Charles
,
Campion, Dominique
,
Hannequin, Didier
,
Campion, Dominique
,
Wallon, David
,
Martinaud, Olivier
,
Zarea, Aline
,
Nicolas, Gaël
,
Rollin-Sillaire, Adeline
,
Bombois, Stéphanie
,
Mackowiak, Marie-Anne
,
Deramecourt, Vincent
,
Pasquier, Florence
,
Michon, Agnès
,
Le Ber, Isabelle
,
Dubois, Bruno
,
Godefroy, Olivier
,
Etcharry-Bouyx, Frédérique
,
Chauviré, Valérie
,
Chamard, Ludivine
,
Berger, Eric
,
Magnin, Eloi
,
Dartigues, Jean-Francois
,
Auriacombe, Sophie
,
Tison, François
,
Sayette, Vincent de la
,
Castan, Dominique
,
Dionet, Elsa
,
Sellal, Francois
,
Rouaud, Olivier
,
Thauvin, Christel
,
Moreaud, Olivier
,
Sauvée, Mathilde
,
Formaglio, Maïté
,
Mollion, Hélène
,
Roullet-Solignac, Isabelle
,
Vighetto, Alain
,
Croisile, Bernard
,
Didic, Mira
,
Félician, Olivier
,
Koric, Lejla
,
Ceccaldi, Mathieu
,
Gabelle, Audrey
,
Marelli, Cecilia
,
Labauge, Pierre
,
Jonveaux, Thérèse
,
Vercelletto, Martine
,
Boutoleau-Bretonnière, Claire
,
Castelnovo, Giovanni
,
Paquet, Claire
,
Dumurgier, Julien
,
Hugon, Jacques
,
De Boisgueheneuc, Foucauld
,
Belliard, Serge
,
Bakchine, Serge
,
Sarazin, Marie
,
Barrellon, Marie-Odile
,
Laurent, Bernard
,
Blanc, Frédéric
,
Pariente, Jérémie
,
Jurici, Snejana
Published in
Neurobiology of aging
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SORL1 rare variants: a major risk factor for familial early-onset Alzheimer’s disease
by
Nicolas, G
,
Charbonnier, C
,
Wallon, D
,
Quenez, O
,
Bellenguez, C
,
Grenier-Boley, B
,
Rousseau, S
,
Richard, A-C
,
Rovelet-Lecrux, A
,
Le Guennec, K
,
Bacq, D
,
Garnier, J-G
,
Olaso, R
,
Boland, A
,
Meyer, V
,
Deleuze, J-F
,
Amouyel, P
,
Munter, H M
,
Bourque, G
,
Lathrop, M
,
Frebourg, T
,
Redon, R
,
Letenneur, L
,
Dartigues, J-F
,
Génin, E
,
Lambert, J-C
,
Hannequin, D
,
Campion, D
Published in
Molecular psychiatry
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A genome-wide study reveals rare CNVs exclusive to extreme phenotypes of Alzheimer disease
by
ROVELET-LECRUX, Anne
,
LEGALLIC, Solenn
,
PUEL, Michele
,
PAQUET, Claire
,
CROISILE, Bernard
,
THOMAS-ANTERION, Catherine
,
VERCELLETTO, Martine
,
LEVY, Richard
,
FREBOURG, Thierry
,
HANNEQUIN, Didier
,
CAMPION, Dominique
,
WALLON, David
,
FLAMAN, Jean-Michel
,
MARTINAUD, Olivier
,
BOMBOIS, Stéphanie
,
ROLLIN-SILLAIRE, Adeline
,
MICHON, Agnes
,
LE BER, Isabelle
,
PARIENTE, Jérémie
Published in
European journal of human genetics : EJHG
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