Association studies in outbred mice in a new era of full-genome sequencing

por Yalcin, Binnaz, Flint, Jonathan
Publicado em 2012

Next-generation sequencing of experimental mouse strains

por Yalcin, Binnaz, Adams, David J., Flint, Jonathan, Keane, Thomas M.
Publicado em 2012

Identification of structural variation in mouse genomes

por Keane, Thomas M., Wong, Kim, Adams, David J., Flint, Jonathan, Reymond, Alexandre, Yalcin, Binnaz
Publicado em 2014

Elusive Copy Number Variation in the Mouse Genome

por Agam, Avigail, Yalcin, Binnaz, Bhomra, Amarjit, Cubin, Matthew, Webber, Caleb, Holmes, Christopher, Flint, Jonathan, Mott, Richard
Publicado em 2010

The fine-scale architecture of structural variants in 17 mouse genomes

por Yalcin, Binnaz, Wong, Kim, Bhomra, Amarjit, Goodson, Martin, Keane, Thomas M, Adams, David J, Flint, Jonathan
Publicado em 2012

High resolution mapping of expression QTLs in heterogeneous stock mice in multiple tissues

por Huang, Guo-Jen, Shifman, Sagiv, Valdar, William, Johannesson, Martina, Yalcin, Binnaz, Taylor, Martin S., Taylor, Jennifer M., Mott, Richard, Flint, Jonathan
Publicado em 2009

Collaborative Cross mice and their power to map host susceptibility to Aspergillus fumigatus infection

por Durrant, Caroline, Tayem, Hanna, Yalcin, Binnaz, Cleak, James, Goodstadt, Leo, Pardo-Manuel de Villena, Fernando, Mott, Richard, Iraqi, Fuad A.
Publicado em 2011

The neuroanatomy of Eml1 knockout mice, a model of subcortical heterotopia

por Collins, Stephan C., Uzquiano, Ana, Selloum, Mohammed, Wendling, Olivia, Gaborit, Marion, Osipenko, Maria, Birling, Marie‐Christine, Yalcin, Binnaz, Francis, Fiona
Publicado no J Anat (2019)

Dissecting indirect genetic effects from peers in laboratory mice

por Baud, Amelie, Casale, Francesco Paolo, Barkley-Levenson, Amanda M., Farhadi, Nilgoun, Montillot, Charlotte, Yalcin, Binnaz, Nicod, Jerome, Palmer, Abraham A., Stegle, Oliver
Publicado no Genome Biol (2021)

The genomic landscape shaped by selection on transposable elements across 18 mouse strains

por Nellåker, Christoffer, Keane, Thomas M, Yalcin, Binnaz, Wong, Kim, Agam, Avigail, Belgard, T Grant, Flint, Jonathan, Adams, David J, Frankel, Wayne N, Ponting, Chris P
Publicado em 2012

The Immune Signaling Adaptor LAT Contributes to the Neuroanatomical Phenotype of 16p11.2 BP2-BP3 CNVs

por Loviglio, Maria Nicla, Arbogast, Thomas, Jønch, Aia Elise, Collins, Stephan C., Popadin, Konstantin, Bonnet, Camille S., Giannuzzi, Giuliana, Maillard, Anne M., Jacquemont, Sébastien, Yalcin, Binnaz, Katsanis, Nicholas, Golzio, Christelle, Reymond, Alexandre
Publicado no Am J Hum Genet (2017)

A knock‐in mouse model for KCNQ2‐related epileptic encephalopathy displays spontaneous generalized seizures and cognitive impairment

por Milh, Mathieu, Roubertoux, Pierre, Biba, Najoua, Chavany, Julie, Spiga Ghata, Adeline, Fulachier, Camille, Collins, Stephan Christopher, Wagner, Christel, Roux, Jean‐Christophe, Yalcin, Binnaz, Félix, Marie‐Solenne, Molinari, Florence, Lenck‐Santini, Pierre‐Pascal, Villard, Laurent
Publicado no Epilepsia (2020)

Commercially Available Outbred Mice for Genome-Wide Association Studies

por Yalcin, Binnaz, Nicod, Jérôme, Bhomra, Amarjit, Davidson, Stuart, Cleak, James, Farinelli, Laurent, Østerås, Magne, Whitley, Adam, Yuan, Wei, Gan, Xiangchao, Goodson, Martin, Klenerman, Paul, Satpathy, Ansu, Mathis, Diane, Benoist, Christophe, Adams, David J., Mott, Richard, Flint, Jonathan
Publicado em 2010

Sequence based characterization of structural variation in the mouse genome

por Yalcin, Binnaz, Wong, Kim, Agam, Avigail, Goodson, Martin, Keane, Thomas M., Gan, Xiangchao, Nellåker, Christoffer, Goodstadt, Leo, Nicod, Jérôme, Bhomra, Amarjit, Hernandez-Pliego, Polinka, Whitley, Helen, Cleak, James, Dutton, Rebekah, Janowitz, Deborah, Mott, Richard, Adams, David J., Flint, Jonathan
Publicado em 2011

Trappc9 deficiency causes parent-of-origin dependent microcephaly and obesity

por Liang, Zhengzheng S., Cimino, Irene, Yalcin, Binnaz, Raghupathy, Narayanan, Vancollie, Valerie E., Ibarra-Soria, Ximena, Firth, Helen V., Rimmington, Debra, Farooqi, I. Sadaf, Lelliott, Christopher J., Munger, Steven C., O’Rahilly, Stephen, Ferguson-Smith, Anne C., Coll, Anthony P., Logan, Darren W.
Publicado no PLoS Genet (2020)

Large-scale neuroanatomical study uncovers 198 gene associations in mouse brain morphogenesis

por Collins, Stephan C., Mikhaleva, Anna, Vrcelj, Katarina, Vancollie, Valerie E., Wagner, Christel, Demeure, Nestor, Whitley, Helen, Kannan, Meghna, Balz, Rebecca, Anthony, Lauren F. E., Edwards, Andrew, Moine, Hervé, White, Jacqueline K., Adams, David J., Reymond, Alexandre, Lelliott, Christopher J., Webber, Caleb, Yalcin, Binnaz
Publicado no Nat Commun (2019)

Conditional switching of KIF2A mutation provides new insights into cortical malformation pathogeny

por Gilet, 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
Publicado no Hum Mol Genet (2020)

SCA7 Mouse Cerebellar Pathology Reveals Preferential Downregulation of Key Purkinje Cell-Identity Genes and Shared Disease Signature with SCA1 and SCA2

por Niewiadomska-Cimicka, Anna, Doussau, Frédéric, Perot, Jean-Baptiste, Roux, Michel J., Keime, Celine, Hache, Antoine, Piguet, Françoise, Novati, Ariana, Weber, Chantal, Yalcin, Binnaz, Meziane, Hamid, Champy, Marie-France, Grandgirard, Erwan, Karam, Alice, Messaddeq, Nadia, Eisenmann, Aurélie, Brouillet, Emmanuel, Nguyen, Hoa Huu Phuc, Flament, Julien, Isope, Philippe, Trottier, Yvon
Publicado no J Neurosci (2021)

TUBG1 missense variants underlying cortical malformations disrupt neuronal locomotion and microtubule dynamics but not neurogenesis

por Ivanova, Ekaterina L., Gilet, Johan G., Sulimenko, Vadym, Duchon, Arnaud, Rudolf, Gabrielle, Runge, Karen, Collins, Stephan C., Asselin, Laure, Broix, Loic, Drouot, Nathalie, Tilly, Peggy, Nusbaum, Patrick, Vincent, Alexandre, Magnant, William, Skory, Valerie, Birling, Marie-Christine, Pavlovic, Guillaume, Godin, Juliette D., Yalcin, Binnaz, Hérault, Yann, Dráber, Pavel, Chelly, Jamel, Hinckelmann, Maria-Victoria
Publicado no Nat Commun (2019)

WD40-repeat 47, a microtubule-associated protein, is essential for brain development and autophagy

por Kannan, Meghna, Bayam, Efil, Wagner, Christel, Rinaldi, Bruno, Kretz, Perrine F., Tilly, Peggy, Roos, Marna, McGillewie, Lara, Bär, Séverine, Minocha, Shilpi, Chevalier, Claire, Po, Chrystelle, Chelly, Jamel, Mandel, Jean-Louis, Borgatti, Renato, Piton, Amélie, Kinnear, Craig, Loos, Ben, Adams, David J., Hérault, Yann, Collins, Stephan C., Friant, Sylvie, Godin, Juliette D., Yalcin, Binnaz
Publicado no Proc Natl Acad Sci U S A (2017)