Not logged inEstablishing standardized transthoracic echocardiography reference ranges for mouse models: insights into the impact of anesthesia, sex, and age
Oestereicher, Manuela A.; Ward, Christopher S.; Schneltzer, Elida; Marschall, Susan; Fuchs, Helmut; Gailus-Durner, Valerie; Bou About, Ghina; Selloum, Mohammed; Meziane, Hamid; Stewart, Michelle; Teboul, Lydia; Norris, Clare; Pimm, Dale; Kan, Marina; Lopez Gomez, Federico; Wilson, Robert; Monroy, Mayra; Pasha, Sheraz; Zabrodska, Eva; Prochazka, Jan; Pajuelo Reguera, David; Nichtova, Zuzana; Herault, Yann; Wells, Sara; Parkinson, Helen; Heaney, Jason D.; Sedlacek, Radislav; Gao, Xiang; Hrabe de Angelis, Martin; Spielmann, Nadine .png)
Share.png)
SaveSystematic Ocular Phenotyping of Knockout Mouse Lines Identifies Genes Associated With Age-Related Corneal DystrophiesBriere, Andrew; Vo, Peter; Yang, Benjamin; Adams, David; Amano, Takanori; Amarie, Oana; Berberovic, Zorana; Bower, Lynette; Brown, Steve D. M.; Burrill, Samantha; Cho, Soo Young; Clementson-Mobbs, Sharon; D'souza, Abigail; Eskandarian, Mohammad; Flenniken, Ann M.; Fuchs, Helmut; Gailus-Durner, Valerie; Herault, Yann; de Angelis, Martin Hrabe; Jin, Shundan; Joynson, Russell; Kang, Yeon Kyung; Kim, Haerim; Masuya, Hiroshi; Meziane, Hamid; Nam, Ki-Hoan; Noh, Hyuna; Nutter, Lauryl M. J.; Palkova, Marcela; Prochazka, Jan; Raishbrook, Miles Joseph; Riet, Fabrice; Salazar, Jason; Sedlacek, Radislav; Selloum, Mohammed; Seo, Kyoung Yul; Seong, Je Kyung; Shin, Hae-Sol; Shiroishi, Toshihiko; Stewart, Michelle; Svenson, Karen; Tamura, Masaru; Tolentino, Heather; Wells, Sara; Wurst, Wolfgang; Yoshiki, Atsushi; Lanoue, Louise; Lloyd, K. C. Kent; Leonard, Brian C.; Roux, Michel J.; McKerlie, Colin; Moshiri, Ala Share Save Systematic ocular phenotyping of 8,707 knockout mouse lines identifies genes associated with abnormal corneal phenotypesVo, Peter; Imai-Leonard, Denise M.; Yang, Benjamin; Briere, Andrew; Shao, Andy; Casanova, M. Isabel; Adams, David; Amano, Takanori; Amarie, Oana; Berberovic, Zorana; Bower, Lynette; Braun, Robert; Brown, Steve; Burrill, Samantha; Cho, Soo Young; Clementson-Mobbs, Sharon; D'Souza, Abigail; Dickinson, Mary; Eskandarian, Mohammad; Flenniken, Ann M.; Fuchs, Helmut; Gailus-Durner, Valerie; Heaney, Jason; Herault, Yann; de Angelis, Martin Hrabe; Hsu, Chih-Wei; Jin, Shundan; Joynson, Russell; Kang, Yeon Kyung; Kim, Haerim; Masuya, Hiroshi; Meziane, Hamid; Murray, Steve; Nam, Ki-Hoan; Noh, Hyuna; Nutter, Lauryl M. J.; Palkova, Marcela; Prochazka, Jan; Raishbrook, Miles Joseph; Riet, Fabrice; Ryan, Jennifer; Salazar, Jason; Seavey, Zachery; Seavitt, John Richard; Sedlacek, Radislav; Selloum, Mohammed; Seo, Kyoung Yul; Seong, Je Kyung; Shin, Hae-Sol; Shiroishi, Toshihiko; Stewart, Michelle; Svenson, Karen; Tamura, Masaru; Tolentino, Heather; Udensi, Uchechukwu; Wells, Sara; White, Jacqueline; Willett, Amelia; Wotton, Janine; Wurst, Wolfgang; Yoshiki, Atsushi; Int Mouse Phenotyping Consortium, Louise; Lanoue, Louise; Lloyd, K. C. Kent; Leonard, Brian C.; Roux, Michel J.; McKerlie, Colin; Moshiri, Ala Share Save Share Save Large-Scale Functional Assessment of Genes Involved in Rare Diseases with Intellectual Disabilities Unravels Unique Developmental and Behaviour Profiles in Mouse ModelsMeziane, Hamid; Birling, Marie-Christine; Wendling, Olivia; Leblanc, Sophie; Dubos, Aline; Selloum, Mohammed; Pavlovic, Guillaume; Sorg, Tania; Kalscheuer, Vera M.; Billuart, Pierre; Laumonnier, Frederic; Chelly, Jamel; van Bokhoven, Hans; Herault, Yann Share Save Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy (vol 1, pg 157, 2022)Spielmann, Nadine; Miller, Gregor; Oprea, Tudor I.; Hsu, Chih-Wei; Fobo, Gisela; Frishman, Goar; Montrone, Corinna; Haseli Mashhadi, Hamed; Mason, Jeremy; Munoz Fuentes, Violeta; Leuchtenberger, Stefanie; Ruepp, Andreas; Wagner, Matias; Westphal, Dominik S.; Wolf, Cordula; Goerlach, Agnes; Sanz-Moreno, Adrian; Cho, Yi-Li; Teperino, Raffaele; Brandmaier, Stefan; Sharma, Sapna; Galter, Isabella Rikarda; Ostereicher, Manuela A.; Zapf, Lilly; Mayer-Kuckuk, Philipp; Rozman, Jan; Teboul, Lydia; Bunton-Stasyshyn, Rosie K. A.; Cater, Heather; Stewart, Michelle; Christou, Skevoulla; Westerberg, Henrik; Willett, Amelia M.; Wotton, Janine M.; Roper, Willson B.; Christiansen, Audrey E.; Ward, Christopher S.; Heaney, Jason D.; Reynolds, Corey L.; Prochazka, Jan; Bower, Lynette; Clary, David; Selloum, Mohammed; Bou About, Ghina; Wendling, Olivia; Jacobs, Hugues; Leblanc, Sophie; Meziane, Hamid; Sorg, Tania; Audain, Enrique; Gilly, Arthur; Rayner, Nigel W.; Hitz, Marc-Phillip; Zeggini, Eleftheria; Wolf, Eckhard; Sedlacek, Radislav; Murray, Steven A.; Svenson, Karen L.; Braun, Robert E.; White, Jaqueline K.; Kelsey, Lois; Gao, Xiang; Shiroishi, Toshihiko; Xu, Ying; Seong, Je Kyung; Mammano, Fabio; Tocchini-Valentini, Glauco P.; Beaudet, Arthur L.; Meehan, Terrence F.; Parkinson, Helen; Smedley, Damian; Mallon, Ann-Marie; Wells, Sara E.; Grallert, Harald; Wurst, Wolfgang; Marschall, Susan; Fuchs, Helmut; Brown, Steve D. M.; Flenniken, Ann M.; Nutter, Lauryl M. J.; McKerlie, Colin; Herault, Yann; Lloyd, K. C. Kent; Dickinson, Mary E.; Gailus-Durner, Valerie; Hrabe de Angelis, Martin Share Save Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathySpielmann, Nadine; Miller, Gregor; Oprea, Tudor I.; Hsu, Chih-Wei; Fobo, Gisela; Frishman, Goar; Montrone, Corinna; Haseli Mashhadi, Hamed; Mason, Jeremy; Munoz Fuentes, Violeta; Leuchtenberger, Stefanie; Ruepp, Andreas; Wagner, Matias; Westphal, Dominik S.; Wolf, Cordula; Goerlach, Agnes; Sanz-Moreno, Adrian; Cho, Yi-Li; Teperino, Raffaele; Brandmaier, Stefan; Sharma, Sapna; Galter, Isabella Rikarda; Oestereicher, Manuela A.; Zapf, Lilly; Mayer-Kuckuk, Philipp; Rozman, Jan; Teboul, Lydia; Bunton-Stasyshyn, Rosie K. A.; Cater, Heather; Stewart, Michelle; Christou, Skevoulla; Westerberg, Henrik; Willett, Amelia M.; Wotton, Janine M.; Roper, Willson B.; Christiansen, Audrey E.; Ward, Christopher S.; Heaney, Jason D.; Reynolds, Corey L.; Prochazka, Jan; Bower, Lynette; Clary, David; Selloum, Mohammed; Bou About, Ghina; Wendling, Olivia; Jacobs, Hugues; Leblanc, Sophie; Meziane, Hamid; Sorg, Tania; Audain, Enrique; Gilly, Arthur; Rayner, Nigel W.; Aguilar-Pimentel, Juan A.; Becker, Lore; Garrett, Lillian; Hoelter, Sabine M.; Amarie, Oana V.; Calzada-Wack, Julia; Klein-Rodewald, Tanja; da Silva-Buttkus, Patricia; Lengger, Christoph; Stoeger, Claudia; Gerlini, Raffaele; Rathkolb, Birgit; Mayr, Daniela; Seavitt, John; Gaspero, Angelina; Green, Jennie R.; Garza, Arturo; Bohat, Ritu; Wong, Leeyean; Mcelwee, Melissa L.; Kalaga, Sowmya; Rasmussen, Tara L.; Lorenzo, Isabel; Lanza, Denise G.; Samaco, Rodney C.; Veeraragaven, Surabi; Gallegos, Juan J.; Kasparek, Petr; Petrezselyova, Silvia; King, Ruairidh; Johnson, Sara; Cleak, James; Szkoe-Kovacs, Zsombor; Codner, Gemma; Mackenzie, Matthew; Caulder, Adam; Kenyon, Janet; Gardiner, Wendy; Phelps, Hayley; Hancock, Rhys; Norris, Claire; Moore, Michayla A.; Seluke, Audrie M.; Urban, Rachel; Kane, Coleen; Goodwin, Leslie O.; Peterson, Kevin A.; Mckay, Matthew; Cook, Jenn J.; Lowy, Jacob P.; Mcfarland, Michael; Wood, Joshua A.; Willis, Brandon J.; Tolentino, Heather; Tolentino, Todd; Schuchbauer, Michael; Salazar, Jason; Johnson, Jennifer; Munson, Rebecca; Ayadi, Abdel; Pavlovic, Guillaume; Birling, Marie-Christine; Jacquot, Sylvie; Ali-Hadji, Dalila; Charles, Philippe; Andre, Philippe; Champy, Marie-France; Riet, Fabrice; Vukobradovic, Igor; Berberovic, Zorana; Qu, Dawei; Guo, Ruolin; D'Souza, Abigail; Huang, Ziyue; Camilleri, Susan; Ganguly, Milan; Adissu, Hibret; Eskandarian, Mohammed; Shang, Xueyuan; Duffin, Kyle; Xu, Catherine; Roberton, Kyle; Laurin, Valerie; Lan, Qing; Sleep, Gillian; Creighton, Amie; Lintott, Lauri; Gertsenstein, Marina; Pereira, Monica; Tondat, Sandra; Patel, Amit; Cruz, Maribelle; Bezginov, Alex; Miller, David; Hy, Wang; Yoshiki, Atsushi; Tanaka, Nobuhiko; Tamura, Masaru; Liu, Zhiwei; Ermakova, Olga; Ferrara, Anna; Fruscoloni, Paolo; Seisenberger, Claudia; Buerger, Antje; Giesert, Florian; Ambrose, J. C.; Gam, Arumu P.; Bevers, R.; Bleda, M.; Boardman-Pretty, F.; Boustred, C. R.; Brittain, H.; Caulfield, M. J.; Chan, G. C.; Fowler, T.; Giess, A.; Hamblin, A.; Henderson, S.; Hubbard, T. J. P.; Jackson, R.; Jones, L. J.; Kasperaviciute, D.; Kayikci, M.; Kousathanas, A.; Lahnstein, L.; Leigh, S. E. A.; Leong, I. U. S.; Lopez, F. J.; Maleady-Crowe, F.; Mcentagart, M.; Minneci, F.; Moutsianas, L.; Mueller, M.; Murugaesu, N.; Need, A. C.; O'Donovan, P.; Odhams, C. A.; Patch, C.; Perez-Gil, D.; Pereira, M. B.; Pullinger, J.; Rahim, T.; Rendon, A.; Rogers, T.; Savage, K.; Sawant, K.; Scott, R. H.; Siddiq, A.; Sieghart, A.; Smith, S. C.; Sosinsky, A.; Stuckey, A.; Tanguy, M.; Taylor-Tavares, A. L.; Thomas, E. R. A.; Thompson, S. R.; Tucci, A.; Welland, M. J.; Williams, E.; Witkowska, K.; Wood, S. M.; Hitz, Marc-Phillip; Zeggini, Eleftheria; Wolf, Eckhard; Sedlacek, Radislav; Murray, Steven A.; Svenson, Karen L.; Braun, Robert E.; White, Jaqueline K.; Kelsey, Lois; Gao, Xiang; Shiroishi, Toshihiko; Xu, Ying; Seong, Je Kyung; Mammano, Fabio; Tocchini-Valentini, Glauco P.; Beaudet, Arthur L.; Meehan, Terrence F.; Parkinson, Helen; Smedley, Damian; Mallon, Ann-Marie; Wells, Sara E.; Grallert, Harald; Wurst, Wolfgang; Marschall, Susan; Fuchs, Helmut; Brown, Steve D. M.; Flenniken, Ann M.; Nutter, Lauryl M. J.; Mckerlie, Colin; Herault, Yann; Lloyd, K. C. Kent; Dickinson, Mary E.; Gailus-Durner, Valerie; Hrabe de Angelis, Martin Share Save Dyrk1a gene dosage in glutamatergic neurons has key effects in cognitive deficits observed in mouse models of MRD7 and Down syndromeBrault, Veronique; Nguyen, Thu Lan; Flores-Gutierrez, Javier; Iacono, Giovanni; Birling, Marie-Christine; Lalanne, Valerie; Meziane, Hamid; Manousopoulou, Antigoni; Pavlovic, Guillaume; Lindner, Loic; Selloum, Mohammed; Sorg, Tania; Yu, Eugene; Garbis, Spiros D.; Herault, Yann Share Save Multi-influential genetic interactions alter behaviour and cognition through six main biological cascades in Down syndrome mouse modelsDuchon, Arnaud; Moreno, Maria Del Mar Muniz; Lorenzo, Sandra Martin; de Souza, Marcia Priscilla Silva; Chevalier, Claire; Nalesso, Valerie; Meziane, Hamid; de Sousa, Paulo Loureiro; Noblet, Vincent; Armspach, Jean-Paul; Brault, Veronique; Herault, Yann Share Save Conditional switching of KIF2A mutation provides new insights into cortical malformation pathogenyGilet, Johan G.; Ivanova, Ekaterina L.; Trofimova, Daria; Rudolf, Gabrielle; Meziane, Hamid; Broix, Loic; Drouot, Nathalie; Courraud, Jeremie; Skory, Valerie; Voulleminot, Paul; Osipenko, Maria; Bahi-Buisson, Nadia; Yalcin, Binnaz; Birling, Marie-Christine; Hinckelmann, Maria-Victoria; Kwok, Benjamin H.; Allingham, John S.; Chelly, Jamel Share Save Identification of genes required for eye development by high-throughput screening of mouse knockouts (vol 1, 236, 2018)Moore, Bret A.; Leonard, Brian C.; Sebbag, Lionel; Edwards, Sydney G.; Cooper, Ann; Imai, Denise M.; Straiton, Ewan; Santos, Luis; Reilly, Christopher; Griffey, Stephen M.; Bower, Lynette; Clary, David; Mason, Jeremy; Roux, Michel J.; Meziane, Hamid; Herault, Yann; McKerlie, Colin; Flenniken, Ann M.; Nutter, Lauryl M. J.; Berberovic, Zorana; Owen, Celeste; Newbigging, Susan; Adissu, Hibret; Eskandarian, Mohammed; Hsu, Chih-Wei; Kalaga, Sowmya; Udensi, Uchechukwu; Asomugha, Chinwe; Bohat, Ritu; Gallegos, Juan J.; Seavitt, John R.; Heaney, Jason D.; Beaudet, Arthur L.; Dickinson, Mary E.; Justice, Monica J.; Philip, Vivek; Kumar, Vivek; Svenson, Karen L.; Braun, Robert E.; Wells, Sara; Cater, Heather; Stewart, Michelle; Clementson-Mobbs, Sharon; Joynson, Russell; Gao, Xiang; Suzuki, Tomohiro; Wakana, Shigeharu; Smedley, Damian; Seong, J. K.; Tocchini-Valentini, Glauco; Moore, Mark; Fletcher, Colin; Karp, Natasha; Ramirez-Solis, Ramiro; White, Jacqueline K.; de Angelis, Martin Hrabe; Wurst, Wolfgang; Thomasy, Sara M.; Flicek, Paul; Parkinson, Helen; Brown, Steve D. M.; Meehan, Terrence F.; Nishina, Patsy M.; Murray, Stephen A.; Krebs, Mark P.; Mallon, Ann-Marie; Lloyd, K. C. Kent; Murphy, Christopher J.; Moshiri, Ala; Swan, Anna; King, Ruairidh; Keskivali-Bond, Piia; Kelsey, Lois; Vukobradovic, Igor; Qu, Dawei; Guo, Ruolin; Tran, Elisa; Morikawa, Lily; Ganguly, Milan; Law, Napoleon; Shang, Xueyuan; Feugas, Patricia; Wang, Yanchun; Zhu, Yingchun; Duffin, Kyle; Ramirez, Ayexa; Penton, Patricia; Laurin, Valerie; Clarke, Shannon; Lan, Qing; Sleep, Gillian; Creighton, Amie; Jacob, Elsa; Danisment, Ozge; Joeng, Joanna; Gertsenstein, Marina; Pereira, Monica; MacMaster, Sue; Tondat, Sandra; Carroll, Tracy; Cabezas, Jorge; Patel, Amit; Hunter, Jane; Clark, Gregory; Bubshait, Mohammed; Miller, David; Sohel, Khondoker; Bezginov, Alexandr; Mckay, Matthew; Peterson, Kevin; Goodwin, Leslie; Urban, Rachel; Kales, Susan; Hallett, Rob; Nguyen-Bresinsky, Dong; Leach, Timothy; Seluke, Audrie; Perkins, Sara; Slater, Amanda; Bedigian, Rick; Donahue, Leah Rae; Taft, Robert; Denegre, James; Seavey, Zachery; Willett, Amelia; Bates, Lindsay; Haynes, Leslie; Creed, Julie; Witmeyer, Catherine; Roper, Willson; Clark, James; Stanley, Pamela; Burrill, Samantha; Ryan, Jennifer; Obata, Yuichi; Tamura, Masaru; Kaneda, Hideki; Furuse, Tamio; Kobayashi, Kimio; Miura, Ikuo; Yamada, Ikuko; Masuya, Hiroshi; Tanaka, Nobuhiko; Ayabe, Shinya; Yoshiki, Atsushi; Vancollie, Valerie; Chiani, Francesco; Di Pietro, Chiara; Di Segni, Gianfranco; Ermakova, Olga; Ferrara, Filomena; Fruscoloni, Paolo; Gambadoro, Alessia; Gastaldi, Serena; Golini, Elisabetta; La Sala, Gina; Mandillo, Silvia; Marazziti, Daniela; Massimi, Marzia; Matteoni, Rafaele; Orsini, Tiziana; Pasquini, Miriam; Raspa, Marcello; Rauch, Aline; Rossi, Gianfranco; Rossi, Nicoletta; Putti, Sabrina; Scavizzi, Ferdinando; Tocchini-Valentini, Giuseppe D. Share Save Identification of genes required for eye development by high-throughput screening of mouse knockoutsMoore, Bret A.; Leonard, Brian C.; Sebbag, Lionel; Edwards, Sydney G.; Cooper, Ann; Imai, Denise M.; Straiton, Ewan; Santos, Luis; Reilly, Christopher; Griffey, Stephen M.; Bower, Lynette; Clary, David; Mason, Jeremy; Roux, Michel J.; Meziane, Hamid; Herault, Yann; McKerlie, Colin; Flenniken, Ann M.; Nutter, Lauryl M. J.; Berberovic, Zorana; Owen, Celeste; Newbigging, Susan; Adissu, Hibret; Eskandarian, Mohammed; Hsu, Chih-Wei; Kalaga, Sowmya; Udensi, Uchechukwu; Asomugha, Chinwe; Bohat, Ritu; Gallegos, Juan J.; Seavitt, John R.; Heaney, Jason D.; Beaudet, Arthur L.; Dickinson, Mary E.; Justice, Monica J.; Philip, Vivek; Kumar, Vivek; Svenson, Karen L.; Braun, Robert E.; Wells, Sara; Cater, Heather; Stewart, Michelle; Clementson-Mobbs, Sharon; Joynson, Russell; Gao, Xiang; Suzuki, Tomohiro; Wakana, Shigeharu; Smedley, Damian; Seong, J. K.; Tocchini-Valentini, Glauco; Moore, Mark; Fletcher, Colin; Karp, Natasha; Ramirez-Solis, Ramiro; White, Jacqueline K.; de Angelis, Martin Hrabe; Wurst, Wolfgang; Thomasy, Sara M.; Flicek, Paul; Parkinson, Helen; Brown, Steve D. M.; Meehan, Terrence F.; Nishina, Patsy M.; Murray, Stephen A.; Krebs, Mark P.; Mallon, Ann-Marie; Lloyd, K. C. Kent; Murphy, Christopher J.; Moshiri, Ala; Swan, Anna; King, Ruairidh; Keskivali-Bond, Piia; Kelsey, Lois; Vukobradovic, Igor; Qu, Dawei; Guo, Ruolin; Tran, Elisa; Morikawa, Lily; Ganguly, Milan; Law, Napoleon; Shang, Xueyuan; Feugas, Patricia; Wang, Yanchun; Zhu, Yingchun; Duffin, Kyle; Ramirez, Ayexa; Penton, Patricia; Laurin, Valerie; Clarke, Shannon; Lan, Qing; Sleep, Gillian; Creighton, Amie; Jacob, Elsa; Danisment, Ozge; Joeng, Joanna; Gertsenstein, Marina; Pereira, Monica; Macmaster, Sue; Tondat, Sandra; Carroll, Tracy; Cabezas, Jorge; Patel, Amit; Hunter, Jane; Clark, Gregory; Bubshait, Mohammed; Miller, David; Sohel, Khondoker; Bezginov, Alexandr; McKay, Matthew; Peterson, Kevin; Goodwin, Leslie; Urban, Rachel; Kales, Susan; Hallett, Rob; Nguyen-Bresinsky, Dong; Leach, Timothy; Seluke, Audrie; Perkins, Sara; Slater, Amanda; Bedigian, Rick; Donahue, Leah Rae; Taft, Robert; Denegre, James; Seavey, Zachery; Willett, Amelia; Bates, Lindsay; Haynes, Leslie; Creed, Julie; Witmeyer, Catherine; Roper, Willson; Clark, James; Stanley, Pamela; Burrill, Samantha; Ryan, Jennifer; Obata, Yuichi; Tamura, Masaru; Kaneda, Hideki; Furuse, Tamio; Kobayashi, Kimio; Miura, Ikuo; Yamada, Ikuko; Masuya, Hiroshi; Tanaka, Nobuhiko; Ayabe, Shinya; Yoshiki, Atsushi; Vancollie, Valerie; Chiani, Francesco; Di Pietro, Chiara; Di Segni, Gianfranco; Ermakova, Olga; Ferrara, Filomena; Fruscoloni, Paolo; Gambadoro, Alessia; Gastaldi, Serena; Golini, Elisabetta; La Sala, Gina; Mandillo, Silvia; Marazziti, Daniela; Massimi, Marzia; Matteoni, Rafaele; Orsini, Tiziana; Pasquini, Miriam; Raspa, Marcello; Rauch, Aline; Rossi, Gianfranco; Rossi, Nicoletta; Putti, Sabrina; Scavizzi, Ferdinando; Tocchini-Valentini, Giuseppe D. Share Save Share Save A new mouse model of ARX dup24 recapitulates the patients' behavioral and fine motor alterationsDubos, Aline; Meziane, Hamid; Iacono, Giovanni; Curie, Aurore; Riet, Fabrice; Martin, Christelle; Loaec, Nadege; Birling, Marie-Christine; Selloum, Mohammed; Normand, Elisabeth; Pavlovic, Guillaume; Sorg, Tania; Stunnenberg, Henk G.; Chelly, Jamel; Humeau, Yann; Friocourt, Gaelle; Herault, Yann Share Save Increased H3K9 methylation and impaired expression of Protocadherins are associated with the cognitive dysfunctions of the Kleefstra syndromeIacono, Giovanni; Dubos, Aline; Meziane, Hamid; Benevento, Marco; Habibi, Ehsan; Mandoli, Amit; Riet, Fabrice; Selloum, Mohammed; Feil, Robert; Zhou, Huiqing; Kleefstra, Tjitske; Kasri, Nael Nadif; van Bokhoven, Hans; Herault, Yann; Stunnenberg, Hendrik G. Share Save A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunctionBowl, Michael R.; Simon, Michelle M.; Ingham, Neil J.; Greenaway, Simon; Santos, Luis; Cater, Heather; Taylor, Sarah; Mason, Jeremy; Kurbatova, Natalja; Pearson, Selina; Bower, Lynette R.; Clary, Dave A.; Meziane, Hamid; Reilly, Patrick; Minowa, Osamu; Kelsey, Lois; Tocchini-Valentini, Glauco P.; Gao, Xiang; Bradley, Allan; Skarnes, William C.; Moore, Mark; Beaudet, Arthur L.; Justice, Monica J.; Seavitt, John; Dickinson, Mary E.; Wurst, Wolfgang; de Angelis, Martin Hrabe; Herault, Yann; Wakana, Shigeharu; Nutter, Lauryl M. J.; Flenniken, Ann M.; McKerlie, Colin; Murray, Stephen A.; Svenson, Karen L.; Braun, Robert E.; West, David B.; Lloyd, K. C. Kent; Adams, David J.; White, Jacqui; Karp, Natasha; Flicek, Paul; Smedley, Damian; Meehan, Terrence F.; Parkinson, Helen E.; Teboul, Lydia M.; Wells, Sara; Steel, Karen P.; Mallon, Ann-Marie; Brown, Steve D. M. Share Save Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognitionArbogast, Thomas; Iacono, Giovanni; Chevalier, Claire; Afinowi, Nurudeen O.; Houbaert, Xander; van Eede, Matthijs C.; Laliberte, Christine; Birling, Marie-Christine; Linda, Katrin; Meziane, Hamid; Selloum, Mohammed; Sorg, Tania; Kasri, Nael Nadif; Koolen, David A.; Stunnenberg, Henk G.; Henkelman, R. Mark; Kopanitsa, Maksym; Humeau, Yann; De Vries, Bert B. A.; Herault, Yann Share Save Ptchd1 deficiency induces excitatory synaptic and cognitive dysfunctions in mouseUng, D. C.; Iacono, G.; Meziane, H.; Blanchard, E.; Papon, M-A; Selten, M.; van Rhijn, J-R; Montjean, R.; Rucci, J.; Martin, S.; Fleet, A.; Birling, M-C; Marouillat, S.; Roepman, R.; Selloum, M.; Lux, A.; Thepault, R-A; Hamel, P.; Mittal, K.; Vincent, J. B.; Dorseuil, O.; Stunnenberg, H. G.; Billuart, P.; Kasri, N. Nadif; Herault, Y.; Laumonnier, F. Share Save Translation of Expanded CGG Repeats into FMRpolyG Is Pathogenic and May Contribute to Fragile X Tremor Ataxia SyndromeSellier, Chantal; Buijsen, Ronald A. M.; He, Fang; Natla, Sam; Jung, Laura; Tropel, Philippe; Gaucherot, Angeline; Jacobs, Hugues; Meziane, Hamid; Vincent, Alexandre; Champy, Marie-France; Sorg, Tania; Pavlovic, Guillaume; Wattenhofer-Donze, Marie; Birling, Marie-Christine; Oulad-Abdelghani, Mustapha; Eberling, Pascal; Ruffenach, Frank; Joint, Mathilde; Anheim, Mathieu; Martinez-Cerdeno, Veronica; Tassone, Flora; Willemsen, Rob; Hukema, Renate K.; Viville, Stephane; Martinat, Cecile; Todd, Peter K.; Charlet-Berguerand, Nicolas Share Save Fasudil treatment in adult reverses behavioural changes and brain ventricular enlargement in Oligophrenin-1 mouse model of intellectual disabilityMeziane, Hamid; Khelfaoui, Malik; Morello, Noemi; Hiba, Bassem; Calcagno, Eleonora; Reibel-Foisset, Sophie; Selloum, Mohammed; Chelly, Jamel; Humeau, Yann; Riet, Fabrice; Zanni, Ginevra; Herault, Yann; Bienvenu, Thierry; Giustetto, Maurizio; Billuart, Pierre Share Save 
.png){kind=icon}
.png){kind=icon}
.png){kind=icon}
.png){kind=icon}
.png){kind=icon}
