Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments
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
Published in PLoS genetics (01.09.2014)
Published in PLoS genetics (01.09.2014)
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Common variants in left/right asymmetry genes and pathways are associated with relative hand skill
Brandler, William M, Morris, Andrew P, Evans, David M, Scerri, Thomas S, Kemp, John P, Timpson, Nicholas J, St Pourcain, Beate, Smith, George Davey, Ring, Susan M, Stein, John, Monaco, Anthony P, Talcott, Joel B, Fisher, Simon E, Webber, Caleb, Paracchini, Silvia
Published in PLoS genetics (01.09.2013)
Published in PLoS genetics (01.09.2013)
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Human VPS13A is associated with multiple organelles and influences mitochondrial morphology and lipid droplet motility
Yeshaw, Wondwossen M, van der Zwaag, Marianne, Pinto, Francesco, Lahaye, Liza L, Faber, Anita Ie, Gómez-Sánchez, Rubén, Dolga, Amalia M, Poland, Conor, Monaco, Anthony P, van IJzendoorn, Sven Cd, Grzeschik, Nicola A, Velayos-Baeza, Antonio, Sibon, Ody Cm
Published in eLife (11.02.2019)
Published in eLife (11.02.2019)
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A Functional Genetic Link between Distinct Developmental Language Disorders
Vernes, Sonja C, Newbury, Dianne F, Abrahams, Brett S, Winchester, Laura, Nicod, Jérôme, Groszer, Matthias, Alarcón, Maricela, Oliver, Peter L, Davies, Kay E, Geschwind, Daniel H, Monaco, Anthony P, Fisher, Simon E
Published in The New England journal of medicine (27.11.2008)
Published in The New England journal of medicine (27.11.2008)
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Impact of Fine Particulate Matter (PM2.5) Exposure During Wildfires on Cardiovascular Health Outcomes
Haikerwal, Anjali, Akram, Muhammad, Del Monaco, Anthony, Smith, Karen, Sim, Malcolm R, Meyer, Mick, Tonkin, Andrew M, Abramson, Michael J, Dennekamp, Martine
Published in Journal of the American Heart Association (15.07.2015)
Published in Journal of the American Heart Association (15.07.2015)
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Infection and Malignancy Outweigh Cardiovascular Mortality in Kidney Transplant Recipients: Post Hoc Analysis of the FAVORIT Trial
Weinrauch, Larry A., D'Elia, John A., Weir, Matthew R., Bunnapradist, Suphamai, Finn, Peter V., Liu, Jiankang, Claggett, Brian, Monaco, Anthony P.
Published in The American journal of medicine (01.02.2018)
Published in The American journal of medicine (01.02.2018)
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The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years on
Guidi, Luiz G., Velayos‐Baeza, Antonio, Martinez‐Garay, Isabel, Monaco, Anthony P., Paracchini, Silvia, Bishop, Dorothy V. M., Molnár, Zoltán
Published in The European journal of neuroscience (01.11.2018)
Published in The European journal of neuroscience (01.11.2018)
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A Whole-Genome Scan and Fine-Mapping Linkage Study of Auditory-Visual Synesthesia Reveals Evidence of Linkage to Chromosomes 2q24, 5q33, 6p12, and 12p12
Asher, Julian E., Lamb, Janine A., Brocklebank, Denise, Cazier, Jean-Baptiste, Maestrini, Elena, Addis, Laura, Sen, Mallika, Baron-Cohen, Simon, Monaco, Anthony P.
Published in American journal of human genetics (13.02.2009)
Published in American journal of human genetics (13.02.2009)
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The genetic lexicon of dyslexia
Paracchini, Silvia, Scerri, Thomas, Monaco, Anthony P
Published in Annual review of genomics and human genetics (01.01.2007)
Published in Annual review of genomics and human genetics (01.01.2007)
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DCDC2, KIAA0319 and CMIP Are Associated with Reading-Related Traits
Scerri, Tom S, Morris, Andrew P, Buckingham, Lyn-Louise, Newbury, Dianne F, Miller, Laura L, Monaco, Anthony P, Bishop, Dorothy V.M, Paracchini, Silvia
Published in Biological psychiatry (1969) (01.08.2011)
Published in Biological psychiatry (1969) (01.08.2011)
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Molecular evolution of FOXP2 , a gene involved in speech and language
Pääbo, Svante, Enard, Wolfgang, Przeworski, Molly, Fisher, Simon E, Lai, Cecilia S. L, Wiebe, Victor, Kitano, Takashi, Monaco, Anthony P
Published in Nature (London) (22.08.2002)
Published in Nature (London) (22.08.2002)
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AU040320 deficiency leads to disruption of acrosome biogenesis and infertility in homozygous mutant mice
Guidi, Luiz G., Holloway, Zoe G., Arnoult, Christophe, Ray, Pierre F., Monaco, Anthony P., Molnár, Zoltán, Velayos-Baeza, Antonio
Published in Scientific reports (10.07.2018)
Published in Scientific reports (10.07.2018)
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