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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
29532014
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
24262013
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
22961997
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
20052020
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
15722015
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
15232011
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
6052019
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
5482009
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
5452015
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
5362013
Dynamic regulation of axon guidance
TW Yu, CI Bargmann
nature neuroscience 4, 1169-1176, 2001
5082001
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
5002017
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
4812012
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
4262021
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
3882014
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
3612010
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
3602017
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
2982001
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
2952003
Interpretation of genomic sequencing results in healthy and ill newborns: results from the BabySeq Project
O Ceyhan-Birsoy, JB Murry, K Machini, MS Lebo, WY Timothy, S Fayer, ...
The American Journal of Human Genetics 104 (1), 76-93, 2019
2552019
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