Intersection of diverse neuronal genomes and neuropsychiatric disease: The Brain Somatic Mosaicism Network
MJ McConnell, John Moran, A Abyzov, S Akbarian, T Bae, I Cortes-Ciriano, JA Erwin, L Fasching, DA Flasch, D Freed, J Ganz, AE Jaffe, Kenneth Kwan, M Kwon, MA Lodato, Ryan Mills, ACM Paquola, RE Rodin, C Rosenbluh, N Sestan, MA Sherman, JH Shin, S Song, RE Straub, J Thorpe, . Weinberger, AE Urban, B Zhou, FH Gage, T Lehner, G Senthil, CA Walsh, A Chess, E Courchesne, JG Gleeson, Jeffrey Kidd, PJ Park, J Pevsner, FM Vaccarino
TSHZ3 deletion causes an autism syndrome and defects in cortical projection neurons
X Caubit, P Gubellini, J Andrieux, PL Roubertoux, M Metwaly, B Jacq, A Fatmi, L Had-Aissouni, Kenneth Kwan, P Salin, M Carlier, A Liedén, E Rudd, M Shinawi, C Vincent-Delorme, JM Cuisset, MP Lemaitre, F Abderrehamane, B Duban, JF Lemaitre, AS Woolf, D Bockenhauer, D Severac, E Dubois, Y Zhu, N Sestan, AN Garratt, L Kerkerian-Le Goff, L Fasano
Recessive LAMC3 mutations cause malformations of occipital cortical development
T Barak, Kenneth Kwan, A Louvi, V Demirbilek, S Saygi, B Tüysüz, M Choi, H Boyaci, K Doerschner, Y Zhu, H Kaymakçalan, S Yilmaz, M Bakircǧlu, AO Çaǧlayan, AK Öztürk, K Yasuno, WJ Brunken, E Atalar, C Yalçnkaya, A Dinçer, RA Bronen, S Mane, T Özçelik, RP Lifton, N Šestan, K Bilgüvar, M Günel
Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations
K Bilgüvar, AK Öztürk, A Louvi, Kenneth Kwan, M Choi, B Tatli, D Yalnizoǧlu, B Tüysüz, AO Çaǧlayan, S Gökben, H Kaymakçalan, T Barak, M Bakircioǧlu, K Yasuno, W Ho, S Sanders, Y Zhu, S Yilmaz, A Dinçer, MH Johnson, RA Bronen, N Koçer, H Per, S Mane, MN Pamir, C Yalçinkaya, S Kumandaş, M Topçu, M Özmen, N Šestan, RP Lifton, MW State, M Günel
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