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Timothy W. Yu
Timothy W. Yu
Harvard Medical School and Boston Children's Hospital
Verified email at childrens.harvard.edu - Homepage
Title
Cited by
Cited by
Year
Synaptic, transcriptional and chromatin genes disrupted in autism
S De Rubeis, X He, AP Goldberg, CS Poultney, K Samocha, ...
Nature 515 (7526), 209-215, 2014
27092014
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
22541997
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
16582020
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
14632011
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
14442015
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ...
Nature genetics 45 (9), 984-994, 2013
7572013
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
5262009
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ...
Nature neuroscience 18 (2), 199-209, 2015
5232015
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
5082013
Patient-customized oligonucleotide therapy for a rare genetic disease
J Kim, C Hu, C Moufawad El Achkar, LE Black, J Douville, A Larson, ...
New England Journal of Medicine 381 (17), 1644-1652, 2019
4992019
Dynamic regulation of axon guidance
TW Yu, CI Bargmann
nature neuroscience 4, 1169-1176, 2001
4992001
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, 1-13, 2012
4622012
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
4552017
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
3562014
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
3462010
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24. 32 and a significant overlap with schizophrenia
Molecular autism 8, 1-17, 2017
3272017
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
2952001
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
2912003
Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical …
K Manickam, MR McClain, LA Demmer, S Biswas, HM Kearney, ...
Genetics in Medicine 23 (11), 2029-2037, 2021
2842021
Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism
MH Chahrour, TW Yu, ET Lim, B Ataman, ME Coulter, RS Hill, ...
PLoS genetics 8 (4), e1002635, 2012
2272012
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