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ProMetIS, deep phenotyping of mouse models by combined proteomics and metabolomics analysis.
Published in:
Scientific Data, 2021, v. 8, n. 1, p. 1, doi. 10.1038/s41597-021-01095-3
By:
- Imbert, Alyssa;
- Rompais, Magali;
- Selloum, Mohammed;
- Castelli, Florence;
- Mouton-Barbosa, Emmanuelle;
- Brandolini-Bunlon, Marion;
- Chu-Van, Emeline;
- Joly, Charlotte;
- Hirschler, Aurélie;
- Roger, Pierrick;
- Burger, Thomas;
- Leblanc, Sophie;
- Sorg, Tania;
- Ouzia, Sadia;
- Vandenbrouck, Yves;
- Médigue, Claudine;
- Junot, Christophe;
- Ferro, Myriam;
- Pujos-Guillot, Estelle;
- de Peredo, Anne Gonzalez
Publication type:
Article
Increased H3K9 methylation and impaired expression of Protocadherins are associated with the cognitive dysfunctions of the Kleefstra syndrome.
Published in:
Nucleic Acids Research, 2018, v. 46, n. 10, p. 4950, doi. 10.1093/nar/gky196
By:
- Iacono, Giovanni;
- Dubos, Aline;
- Méziane, Hamid;
- Benevento, Marco;
- Habibi, Ehsan;
- Mandoli, Amit;
- Riet, Fabrice;
- Selloum, Mohammed;
- Feil, Robert;
- Zhou, Huiqing
Publication type:
Article
Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition.
Published in:
PLoS Genetics, 2017, v. 13, n. 7, p. 1, doi. 10.1371/journal.pgen.1006886
By:
- Arbogast, 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;
- Nadif Kasri, Nael;
- Koolen, David A.;
- Stunnenberg, Henk G.;
- Henkelman, R. Mark;
- Kopanitsa, Maksym;
- Humeau, Yann;
- De Vries, Bert B. A.;
- Herault, Yann
Publication type:
Article
Identification of Genes and Networks Driving Cardiovascular and Metabolic Phenotypes in a Mouse F2 Intercross.
Published in:
PLoS ONE, 2010, v. 5, n. 12, p. 1, doi. 10.1371/journal.pone.0014319
By:
- Derry, Jonathan M. J.;
- Hua Zhong;
- Molony, Cliona;
- MacNeil, Doug;
- Guhathakurta, Debraj;
- Bin Zhang;
- Mudgett, John;
- Small, Kersten;
- Fertak, Lahcen El;
- Guimond, Alain;
- Selloum, Mohammed;
- Wenqing Zhao;
- Champy, Marie France;
- Monassier, Laurent;
- Vogt, Tom;
- Cully, Doris;
- Kasarskis, Andrew;
- Schadt, Eric E.
Publication type:
Article
BAHD1 haploinsufficiency results in anxiety-like phenotypes in male mice.
Published in:
PLoS ONE, 2020, v. 15, n. 5, p. 1, doi. 10.1371/journal.pone.0232789
By:
- Pourpre, Renaud;
- Naudon, Laurent;
- Meziane, Hamid;
- Lakisic, Goran;
- Jouneau, Luc;
- Varet, Hugo;
- Legendre, Rachel;
- Wendling, Olivia;
- Selloum, Mohammed;
- Proux, Caroline;
- Coppée, Jean-Yves;
- Herault, Yann;
- Bierne, Hélène
Publication type:
Article
Dissecting the autism-associated 16p11.2 locus identifies multiple drivers in neuroanatomical phenotypes and unveils a male-specific role for the major vault protein.
Published in:
Genome Biology, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s13059-023-03092-8
By:
- Kretz, Perrine F.;
- Wagner, Christel;
- Mikhaleva, Anna;
- Montillot, Charlotte;
- Hugel, Sylvain;
- Morella, Ilaria;
- Kannan, Meghna;
- Fischer, Marie-Christine;
- Milhau, Maxence;
- Yalcin, Ipek;
- Brambilla, Riccardo;
- Selloum, Mohammed;
- Herault, Yann;
- Reymond, Alexandre;
- Collins, Stephan C.;
- Yalcin, Binnaz
Publication type:
Article
A new mouse model of ARX dup24 recapitulates the patients behavioral and fine motor alterations.
Published in:
Human Molecular Genetics, 2018, v. 27, n. 12, p. 2138, doi. 10.1093/hmg/ddy122
By:
- Dubos, Aline;
- Meziane, Hamid;
- Iacono, Giovanni;
- Curie, Aurore;
- Riet, Fabrice;
- Martin, Christelle;
- Loaëc, Nade'ge;
- Birling, Marie-Christine;
- Selloum, Mohammed;
- Normand, Elisabeth;
- Pavlovic, Guillaume;
- Sorg, Tania;
- Stunnenberg, Henk G.;
- Chelly, Jamel;
- Humeau, Yann;
- Friocourt, Gaë lle;
- Hérault, Yann
Publication type:
Article
Fasudil treatment in adult reverses behavioural changes and brain ventricular enlargement in Oligophrenin-1 mouse model of intellectual disability.
Published in:
Human Molecular Genetics, 2016, v. 25, n. 11, p. 2314, doi. 10.1093/hmg/ddw102
By:
- Meziane, 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
Publication type:
Article
Conditional depletion of intellectual disability and Parkinsonism candidate gene ATP6AP2 in fly and mouse induces cognitive impairment and neurodegeneration.
Published in:
Human Molecular Genetics, 2015, v. 24, n. 23, p. 6736, doi. 10.1093/hmg/ddv380
By:
- Dubos, Aline;
- Castells-Nobau, Anna;
- Meziane, Hamid;
- Oortveld, Merel A. W.;
- Houbaert, Xander;
- Iacono, Giovanni;
- Martin, Christelle;
- Mittelhaeuser, Christophe;
- Lalanne, Valérie;
- Kramer, Jamie M.;
- Bhukel, Anuradha;
- Quentin, Christine;
- Slabbert, Jan;
- Verstreken, Patrik;
- Sigrist, Stefan J.;
- Messaddeq, Nadia;
- Birling, Marie-Christine;
- Selloum, Mohammed;
- Stunnenberg, Henk G.;
- Humeau, Yann
Publication type:
Article
INFRAFRONTIER quality principles in systemic phenotyping.
Published in:
Mammalian Genome, 2022, v. 33, n. 1, p. 120, doi. 10.1007/s00335-021-09892-2
By:
- Ehlich, Hilke;
- Cater, Heather L.;
- Flenniken, Ann M.;
- Goncalves Da Cruz, Isabelle;
- Mura, Anne-Marie;
- Ntafis, Vasileios;
- Raess, Michael;
- Selloum, Mohammed;
- Stoeger, Claudia;
- Suchanova, Sarka;
- Vuolteenaho, Reetta;
- Brown, Steve D. M.;
- Hérault, Yann;
- Hinttala, Reetta;
- Hrabě de Angelis, Martin;
- Kollias, George;
- Kontoyiannis, Dimitris L.;
- Malissen, Bernard;
- McKerlie, Colin;
- Sedláček, Radislav
Publication type:
Article
Genetic background determines metabolic phenotypes in the mouse.
Published in:
Mammalian Genome, 2008, v. 19, n. 5, p. 318, doi. 10.1007/s00335-008-9107-z
By:
- Champy, Marie-France;
- Selloum, Mohammed;
- Zeitler, Valérie;
- Caradec, Claudia;
- Jung, Barbara;
- Rousseau, Stéphane;
- Pouilly, Laurent;
- Sorg, Tania;
- Auwerx, Johan
Publication type:
Article
Mouse functional genomics requires standardization of mouse handling and housing conditions.
Published in:
Mammalian Genome, 2004, v. 15, n. 10, p. 768, doi. 10.1007/s00335-004-2393-1
By:
- Champy, Marie-France;
- Selloum, Mohammed;
- Piard, Laetitia;
- Zeitler, Valerie;
- Caradec, Claudia;
- Chambon, Pierre;
- Auwerx, Johan
Publication type:
Article
Large-Scale Functional Assessment of Genes Involved in Rare Diseases with Intellectual Disabilities Unravels Unique Developmental and Behaviour Profiles in Mouse Models.
Published in:
Biomedicines, 2022, v. 10, n. 12, p. 3148, doi. 10.3390/biomedicines10123148
By:
- Meziane, Hamid;
- Birling, Marie-Christine;
- Wendling, Olivia;
- Leblanc, Sophie;
- Dubos, Aline;
- Selloum, Mohammed;
- Pavlovic, Guillaume;
- Sorg, Tania;
- Kalscheuer, Vera M.;
- Billuart, Pierre;
- Laumonnier, Frédéric;
- Chelly, Jamel;
- van Bokhoven, Hans;
- Herault, Yann
Publication type:
Article
The neuroanatomy of Eml1 knockout mice, a model of subcortical heterotopia.
Published in:
Journal of Anatomy, 2019, v. 235, n. 3, p. 637, doi. 10.1111/joa.13013
By:
- Collins, Stephan C.;
- Uzquiano, Ana;
- Selloum, Mohammed;
- Wendling, Olivia;
- Gaborit, Marion;
- Osipenko, Maria;
- Birling, Marie‐Christine;
- Yalcin, Binnaz;
- Francis, Fiona
Publication type:
Article
Behavioral Testing Design for Evaluation of Cognitive Disabilities.
Published in:
Current Protocols, 2022, v. 2, n. 2, p. 1, doi. 10.1002/cpz1.382
By:
- Riet, Fabrice;
- Mittelhaeuser, Christophe;
- Lux, Aline;
- Bour, Raphael;
- Selloum, Mohammed;
- Sorg, Tania;
- Herault, Yann;
- Meziane, Hamid
Publication type:
Article
Dyrk1a gene dosage in glutamatergic neurons has key effects in cognitive deficits observed in mouse models of MRD7 and Down syndrome.
Published in:
PLoS Genetics, 2021, v. 17, n. 9, p. 1, doi. 10.1371/journal.pgen.1009777
By:
- Brault, Véronique;
- Nguyen, Thu Lan;
- Flores-Gutiérrez, Javier;
- Iacono, Giovanni;
- Birling, Marie-Christine;
- Lalanne, Valérie;
- Meziane, Hamid;
- Manousopoulou, Antigoni;
- Pavlovic, Guillaume;
- Lindner, Loïc;
- Selloum, Mohammed;
- Sorg, Tania;
- Yu, Eugene;
- Garbis, Spiros D.;
- Hérault, Yann
Publication type:
Article
The Rogdi knockout mouse is a model for Kohlschütter–Tönz syndrome.
Published in:
Scientific Reports, 2024, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-50870-2
By:
- Jimenez-Armijo, Alexandra;
- Morkmued, Supawich;
- Ahumada, José Tomás;
- Kharouf, Naji;
- de Feraudy, Yvan;
- Gogl, Gergo;
- Riet, Fabrice;
- Niederreither, Karen;
- Laporte, Jocelyn;
- Birling, Marie Christine;
- Selloum, Mohammed;
- Herault, Yann;
- Hernandez, Magali;
- Bloch-Zupan, Agnès
Publication type:
Article

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