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Page 1
Aberrant white matter microstructure in children with 16p11.2 deletions.
Owen JP, Chang YS, Pojman NJ, Bukshpun P, Wakahiro ML, Marco EJ, Berman JI, Spiro JE, Chung WK, Buckner RL, Roberts TP, Nagarajan SS, Sherr EH, Mukherjee P; Simons VIP Consortium. Owen JP, et al. Among authors: marco ej. J Neurosci. 2014 Apr 30;34(18):6214-23. doi: 10.1523/JNEUROSCI.4495-13.2014. J Neurosci. 2014. PMID: 24790192 Free PMC article.
The role of corpus callosum development in functional connectivity and cognitive processing.
Hinkley LB, Marco EJ, Findlay AM, Honma S, Jeremy RJ, Strominger Z, Bukshpun P, Wakahiro M, Brown WS, Paul LK, Barkovich AJ, Mukherjee P, Nagarajan SS, Sherr EH. Hinkley LB, et al. Among authors: marco ej. PLoS One. 2012;7(8):e39804. doi: 10.1371/journal.pone.0039804. Epub 2012 Aug 3. PLoS One. 2012. PMID: 22870191 Free PMC article. Clinical Trial.
Children with autism show reduced somatosensory response: an MEG study.
Marco EJ, Khatibi K, Hill SS, Siegel B, Arroyo MS, Dowling AF, Neuhaus JM, Sherr EH, Hinkley LN, Nagarajan SS. Marco EJ, et al. Autism Res. 2012 Oct;5(5):340-51. doi: 10.1002/aur.1247. Epub 2012 Aug 29. Autism Res. 2012. PMID: 22933354 Free PMC article.
Autism traits in individuals with agenesis of the corpus callosum.
Lau YC, Hinkley LB, Bukshpun P, Strominger ZA, Wakahiro ML, Baron-Cohen S, Allison C, Auyeung B, Jeremy RJ, Nagarajan SS, Sherr EH, Marco EJ. Lau YC, et al. Among authors: marco ej. J Autism Dev Disord. 2013 May;43(5):1106-18. doi: 10.1007/s10803-012-1653-2. J Autism Dev Disord. 2013. PMID: 23054201 Free PMC article.
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.
Zufferey F, Sherr EH, Beckmann ND, Hanson E, Maillard AM, Hippolyte L, Macé A, Ferrari C, Kutalik Z, Andrieux J, Aylward E, Barker M, Bernier R, Bouquillon S, Conus P, Delobel B, Faucett WA, Goin-Kochel RP, Grant E, Harewood L, Hunter JV, Lebon S, Ledbetter DH, Martin CL, Männik K, Martinet D, Mukherjee P, Ramocki MB, Spence SJ, Steinman KJ, Tjernagel J, Spiro JE, Reymond A, Beckmann JS, Chung WK, Jacquemont S; Simons VIP Consortium; 16p11.2 European Consortium. Zufferey F, et al. J Med Genet. 2012 Oct;49(10):660-8. doi: 10.1136/jmedgenet-2012-101203. J Med Genet. 2012. PMID: 23054248 Free PMC article.
129 results