Results
|
1.
|
|
|
2.
|
|
|
3.
|
|
|
4.
|
|
|
5.
|
|
|
6.
|
Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiology. [electronic resource] by
- Lahbib, Saida
- Leblond, Claire S
- Hamza, Mariem
- Regnault, Béatrice
- Lemée, Laure
- Mathieu, Alexandre
- Jaouadi, Hager
- Mkaouar, Rahma
- Youssef-Turki, Ilhem Ben
- Belhadj, Ahlem
- Kraoua, Ichraf
- Bourgeron, Thomas
- Abdelhak, Sonia
Producer: 20190516
In:
Journal of applied genetics vol. 60
Availability: No items available.
|
|
7.
|
11q24.2-25 micro-rearrangements in autism spectrum disorders: Relation to brain structures. [electronic resource] by
- Maruani, Anna
- Huguet, Guillaume
- Beggiato, Anita
- ElMaleh, Monique
- Toro, Roberto
- Leblond, Claire S
- Mathieu, Alexandre
- Amsellem, Frederique
- Lemière, Nathalie
- Verloes, Alain
- Leboyer, Marion
- Gillberg, Christopher
- Bourgeron, Thomas
- Delorme, Richard
Producer: 20161017
In:
American journal of medical genetics. Part A vol. 167A
Availability: No items available.
|
|
8.
|
Measuring and Estimating the Effect Sizes of Copy Number Variants on General Intelligence in Community-Based Samples. [electronic resource] by
- Huguet, Guillaume
- Schramm, Catherine
- Douard, Elise
- Jiang, Lai
- Labbe, Aurélie
- Tihy, Frédérique
- Mathonnet, Géraldine
- Nizard, Sonia
- Lemyre, Emmanuelle
- Mathieu, Alexandre
- Poline, Jean-Baptiste
- Loth, Eva
- Toro, Roberto
- Schumann, Gunter
- Conrod, Patricia
- Pausova, Zdenka
- Greenwood, Celia
- Paus, Tomas
- Bourgeron, Thomas
- Jacquemont, Sébastien
Producer: 20190923
In:
JAMA psychiatry vol. 75
Availability: No items available.
|
|
9.
|
Both rare and common genetic variants contribute to autism in the Faroe Islands. [electronic resource] by
- Leblond, Claire S
- Cliquet, Freddy
- Carton, Coralie
- Huguet, Guillaume
- Mathieu, Alexandre
- Kergrohen, Thomas
- Buratti, Julien
- Lemière, Nathalie
- Cuisset, Laurence
- Bienvenu, Thierry
- Boland, Anne
- Deleuze, Jean-François
- Stora, Tormodur
- Biskupstoe, Rannva
- Halling, Jónrit
- Andorsdóttir, Guðrið
- Billstedt, Eva
- Gillberg, Christopher
- Bourgeron, Thomas
Publication details: NPJ genomic medicine 2019
In:
NPJ genomic medicine vol. 4
Availability: No items available.
|
|
10.
|
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments. [electronic resource] by
- Leblond, Claire S
- Nava, Caroline
- Polge, Anne
- Gauthier, Julie
- Huguet, Guillaume
- Lumbroso, Serge
- Giuliano, Fabienne
- Stordeur, Coline
- Depienne, Christel
- Mouzat, Kevin
- Pinto, Dalila
- Howe, Jennifer
- Lemière, Nathalie
- Durand, Christelle M
- Guibert, Jessica
- Ey, Elodie
- Toro, Roberto
- Peyre, Hugo
- Mathieu, Alexandre
- Amsellem, Frédérique
- Rastam, Maria
- Gillberg, I Carina
- Rappold, Gudrun A
- Holt, Richard
- Monaco, Anthony P
- Maestrini, Elena
- Galan, Pilar
- Heron, Delphine
- Jacquette, Aurélia
- Afenjar, Alexandra
- Rastetter, Agnès
- Brice, Alexis
- Devillard, Françoise
- Assouline, Brigitte
- Laffargue, Fanny
- Lespinasse, James
- Chiesa, Jean
- Rivier, François
- Bonneau, Dominique
- Regnault, Beatrice
- Zelenika, Diana
- Delepine, Marc
- Lathrop, Mark
- Sanlaville, Damien
- Schluth-Bolard, Caroline
- Edery, Patrick
- Perrin, Laurence
- Tabet, Anne Claude
- Schmeisser, Michael J
- Boeckers, Tobias M
- Coleman, Mary
- Sato, Daisuke
- Szatmari, Peter
- Scherer, Stephen W
- Rouleau, Guy A
- Betancur, Catalina
- Leboyer, Marion
- Gillberg, Christopher
- Delorme, Richard
- Bourgeron, Thomas
Producer: 20151106
In:
PLoS genetics vol. 10
Availability: No items available.
|
|
11.
|
A framework to identify contributing genes in patients with Phelan-McDermid syndrome. [electronic resource] by
- Tabet, Anne-Claude
- Rolland, Thomas
- Ducloy, Marie
- Lévy, Jonathan
- Buratti, Julien
- Mathieu, Alexandre
- Haye, Damien
- Perrin, Laurence
- Dupont, Céline
- Passemard, Sandrine
- Capri, Yline
- Verloes, Alain
- Drunat, Séverine
- Keren, Boris
- Mignot, Cyril
- Marey, Isabelle
- Jacquette, Aurélia
- Whalen, Sandra
- Pipiras, Eva
- Benzacken, Brigitte
- Chantot-Bastaraud, Sandra
- Afenjar, Alexandra
- Héron, Delphine
- Le Caignec, Cédric
- Beneteau, Claire
- Pichon, Olivier
- Isidor, Bertrand
- David, Albert
- El Khattabi, Laila
- Kemeny, Stephan
- Gouas, Laetitia
- Vago, Philippe
- Mosca-Boidron, Anne-Laure
- Faivre, Laurence
- Missirian, Chantal
- Philip, Nicole
- Sanlaville, Damien
- Edery, Patrick
- Satre, Véronique
- Coutton, Charles
- Devillard, Françoise
- Dieterich, Klaus
- Vuillaume, Marie-Laure
- Rooryck, Caroline
- Lacombe, Didier
- Pinson, Lucile
- Gatinois, Vincent
- Puechberty, Jacques
- Chiesa, Jean
- Lespinasse, James
- Dubourg, Christèle
- Quelin, Chloé
- Fradin, Mélanie
- Journel, Hubert
- Toutain, Annick
- Martin, Dominique
- Benmansour, Abdelamdjid
- Leblond, Claire S
- Toro, Roberto
- Amsellem, Frédérique
- Delorme, Richard
- Bourgeron, Thomas
Publication details: NPJ genomic medicine 2017
In:
NPJ genomic medicine vol. 2
Availability: No items available.
|
|
12.
|
Erratum: Author Correction: A framework to identify contributing genes in patients with Phelan-McDermid syndrome. [electronic resource] by
- Tabet, Anne-Claude
- Rolland, Thomas
- Ducloy, Marie
- Lévy, Jonathan
- Buratti, Julien
- Mathieu, Alexandre
- Haye, Damien
- Perrin, Laurence
- Dupont, Céline
- Passemard, Sandrine
- Capri, Yline
- Verloes, Alain
- Drunat, Séverine
- Keren, Boris
- Mignot, Cyril
- Marey, Isabelle
- Jacquette, Aurélia
- Whalen, Sandra
- Pipiras, Eva
- Benzacken, Brigitte
- Chantot-Bastaraud, Sandra
- Afenjar, Alexandra
- Héron, Delphine
- Le Caignec, Cédric
- Beneteau, Claire
- Pichon, Olivier
- Isidor, Bertrand
- David, Albert
- El Khattabi, Laila
- Kemeny, Stephan
- Gouas, Laetitia
- Vago, Philippe
- Mosca-Boidron, Anne-Laure
- Faivre, Laurence
- Missirian, Chantal
- Philip, Nicole
- Sanlaville, Damien
- Edery, Patrick
- Satre, Véronique
- Coutton, Charles
- Devillard, Françoise
- Dieterich, Klaus
- Vuillaume, Marie-Laure
- Rooryck, Caroline
- Lacombe, Didier
- Pinson, Lucile
- Gatinois, Vincent
- Puechberty, Jacques
- Chiesa, Jean
- Lespinasse, James
- Dubourg, Christèle
- Quelin, Chloé
- Fradin, Mélanie
- Journel, Hubert
- Toutain, Annick
- Martin, Dominique
- Benmansour, Abdelamdjid
- Leblond, Claire S
- Toro, Roberto
- Amsellem, Frédérique
- Delorme, Richard
- Bourgeron, Thomas
Publication details: NPJ genomic medicine 2019
In:
NPJ genomic medicine vol. 4
Availability: No items available.
|