Timothy W. Yu
Timothy W. Yu
Harvard Medical School and Boston Children's Hospital
childrens.harvard.edu üzerinde doğrulanmış e-posta adresine sahip - Ana Sayfa
Başlık
Alıntı yapanlar
Alıntı yapanlar
Yıl
Dentate granule cell neurogenesis is increased by seizures and contributes to aberrant network reorganization in the adult rat hippocampus
JM Parent, TW Yu, RT Leibowitz, DH Geschwind, RS Sloviter, ...
The Journal of Neuroscience 17 (10), 3727-3738, 1997
20751997
Synaptic, transcriptional and chromatin genes disrupted in autism
S De Rubeis, X He, AP Goldberg, CS Poultney, K Samocha, AE Cicek, ...
Nature 515 (7526), 209-215, 2014
17972014
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
SH Lee, S Ripke, BM Neale, SV Faraone, SM Purcell, RH Perlis, ...
Nature genetics 45 (9), 984, 2013
17852013
Multiple recurrent de novo CNVs, including duplications of the 7q11. 23 Williams syndrome region, are strongly associated with autism
SJ Sanders, AG Ercan-Sencicek, V Hus, R Luo, MT Murtha, ...
Neuron 70 (5), 863-885, 2011
12072011
Insights into autism spectrum disorder genomic architecture and biology from 71 risk loci
SJ Sanders, X He, AJ Willsey, AG Ercan-Sencicek, KE Samocha, ...
Neuron 87 (6), 1215-1233, 2015
8932015
Dynamic regulation of axon guidance
TW Yu, CI Bargmann
nature neuroscience 4, 1169-1176, 2001
449*2001
A proprotein convertase subtilisin/kexin type 9 neutralizing antibody reduces serum cholesterol in mice and nonhuman primates
JCY Chan, DE Piper, Q Cao, D Liu, C King, W Wang, J Tang, Q Liu, ...
Proceedings of the National Academy of Sciences 106 (24), 9820-9825, 2009
4252009
Using whole-exome sequencing to identify inherited causes of autism
TW Yu, MH Chahrour, ME Coulter, S Jiralerspong, K Okamura-Ikeda, ...
Neuron 77 (2), 259-273, 2013
3952013
Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism
FK Satterstrom, JA Kosmicki, J Wang, MS Breen, S De Rubeis, JY An, ...
Cell 180 (3), 568-584. e23, 2020
3782020
Common genetic variants, acting additively, are a major source of risk for autism
L Klei, SJ Sanders, MT Murtha, V Hus, JK Lowe, AJ Willsey, ...
Molecular autism 3 (1), 1-13, 2012
3672012
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
T Network, C O'Dushlaine, L Rossin, PH Lee, L Duncan, NN Parikshak, ...
Nature neuroscience 18 (2), 199, 2015
2952015
Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture
TW Yu, GH Mochida, DJ Tischfield, SK Sgaier, L Flores-Sarnat, CM Sergi, ...
Nature genetics 42 (11), 1015-1020, 2010
2772010
Somatic mutations in cerebral cortical malformations
SS Jamuar, ATN Lam, M Kircher, AM D’Gama, J Wang, BJ Barry, X Zhang, ...
New England Journal of Medicine 371 (8), 733-743, 2014
2672014
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders
DJ Weiner, EM Wigdor, S Ripke, RK Walters, JA Kosmicki, J Grove, ...
Nature genetics 49 (7), 978-985, 2017
2632017
C. elegans slit acts in midline, dorsal-ventral, and anterior-posterior guidance via the SAX-3/Robo receptor
JC Hao, TW Yu, K Fujisawa, JG Culotti, K Gengyo-Ando, S Mitani, ...
Neuron 32 (1), 25-38, 2001
2632001
The netrin receptor UNC-40/DCC stimulates axon attraction and outgrowth through enabled and, in parallel, Rac and UNC-115/AbLIM
Z Gitai, WY Timothy, EA Lundquist, M Tessier-Lavigne, CI Bargmann
Neuron 37 (1), 53-65, 2003
2562003
Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism
MH Chahrour, WY Timothy, ET Lim, B Ataman, ME Coulter, RS Hill, ...
PLoS Genet 8 (4), e1002635, 2012
1962012
Shared receptors in axon guidance: SAX-3/Robo signals via UNC-34/Enabled and a Netrin-independent UNC-40/DCC function
TW Yu, JC Hao, W Lim, M Tessier-Lavigne, CI Bargmann
Nature neuroscience 5 (11), 1147-1154, 2002
1772002
Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome
MC Manzini, DE Tambunan, RS Hill, TW Yu, TM Maynard, EL Heinzen, ...
The American Journal of Human Genetics 91 (3), 541-547, 2012
1702012
Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder
R Maier, G Moser, GB Chen, S Ripke, D Absher, I Agartz, H Akil, F Amin, ...
The American Journal of Human Genetics 96 (2), 283-294, 2015
1522015
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Makaleler 1–20