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All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year Sort by creator [A → Z]' creator [Z → A]' publishing year ↑ (asc)' publishing year ↓ (desc)' title [A → Z]' title [Z → A]' Simple Search Page: 1 2 Hits 1 – 20 of 23 1 Thalamo-cortical network hyperconnectivity in preclinical progranulin mutation carriers. Lee, Suzee E; Sias, Ana C; Kosik, Eena L. - : eScholarship, University of California, 2019 BASE Show details 2 Thalamo-cortical network hyperconnectivity in preclinical progranulin mutation carriers. Lee, Suzee E; Sias, Ana C; Kosik, Eena L... In: Lee, Suzee E; Sias, Ana C; Kosik, Eena L; Flagan, Taru M; Deng, Jersey; Chu, Stephanie A; et al.(2019). Thalamo-cortical network hyperconnectivity in preclinical progranulin mutation carriers. NeuroImage. Clinical, 22, 101751. doi:10.1016/j.nicl.2019.101751. UCLA: Retrieved from: http://www.escholarship.org/uc/item/6vv8g8qt (2019) BASE Show details 3 Thalamo-cortical network hyperconnectivity in preclinical progranulin mutation carriers. Lee, Suzee E; Sias, Ana C; Kosik, Eena L. - : eScholarship, University of California, 2019 BASE Show details 4 Thalamo-cortical network hyperconnectivity in preclinical progranulin mutation carriers Lee, Suzee E.; Sias, Ana C.; Kosik, Eena L.. - : Elsevier, 2019 BASE Show details 5 Increased prevalence of autoimmune disease within C9 and FTD/MND cohorts: Completing the picture. Miller, Zachary A; Sturm, Virginia E; Camsari, Gamze Balci... In: Neurology(R) neuroimmunology & neuroinflammation, vol 3, iss 6 (2016) BASE Show details 6 Increased prevalence of autoimmune disease within C9 and FTD/MND cohorts: Completing the picture. Miller, Zachary A; Sturm, Virginia E; Camsari, Gamze Balci... In: Neurology(R) neuroimmunology & neuroinflammation, vol 3, iss 6 (2016) BASE Show details 7 Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families. Leppa, Virpi M; Kravitz, Stephanie N; Martin, Christa Lese... In: American journal of human genetics, vol 99, iss 3 (2016) BASE Show details 8 VoICE: A semi-automated pipeline for standardizing vocal analysis across models. Burkett, Zachary D; Day, Nancy F; Peñagarikano, Olga... In: Scientific reports, vol 5, iss 1 (2015) BASE Show details 9 VoICE: A semi-automated pipeline for standardizing vocal analysis across models Burkett, Zachary D.; Day, Nancy F.; Peñagarikano, Olga. - : Nature Publishing Group, 2015 BASE Show details 10 CNTNAP2 and autism spectrum disorders Penagarikano, Olga; Geschwind, Daniel H. In: The autisms (Oxford, 2013), p. 274-285 MPI für Psycholinguistik Show details 11 Individual common variants exert weak effects on the risk for autism spectrum disorders Anney, Richard; Klei, Lambertus; Pinto, Dalila. - : Oxford University Press, 2012 BASE Show details 12 Individual common variants exert weak effects on risk for Autism Spectrum Disorders Anney, Richard; Klei, Lambertus; Pinto, Dalila. - : Oxford University Press, 2012 BASE Show details 13 Individual common variants exert weak effects on the risk for autism spectrum disorderspi Anney, Richard; Klei, Lambertus; Pinto, Dalila. - : Oxford University Press, 2012 BASE Show details 14 Individual common variants exert weak effects on the risk for autism spectrum disorderspi Anney, Richard; Klei, Lambertus; Pinto, Dalila. - : Oxford University Press, 2012 BASE Show details 15 Individual common variants exert weak effects on the risk for autism spectrum disorderspi Anney, Richard; Klei, Lambertus; Pinto, Dalila. - : Oxford University Press, 2012 BASE Show details 16 Autism spectrum disorders Amaral, David G.; Dawson, Geraldine; Geschwind, Daniel H.. - Oxford : Oxford University Press, 2011 MPI für Psycholinguistik Show details 17 Genetics of Autism Spectrum Disorders Geschwind, Daniel H.. - 2011 BASE Show details 18 Language-related Cntnap2 gene is differentially expressed in sexually dimorphic song nuclei essential for vocal learning in songbirds Panaitof, S. Carmen; Abrahams, Brett S.; Dong, Hongmei. - 2010 BASE Show details 19 Human-specific transcriptional regulation of CNS development genes by FOXP2 Konopka, Genevieve; Bomar, Jamee M.; Winden, Kellen... In: Nature. - London : Macmillan Publishers Limited, part of Springer Nature 462 (2009) 7270, 213-217 BLLDB Show details 20 Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene Alarcón, Maricela; Abrahams, Brett S.; Stone, Jennifer L.. - : American Society of Human Genetics, 2008 BASE Show details Page: 1 2

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