دنبال کردن
Matthew State
Matthew State
ایمیل تأیید شده در ucsf.edu - صفحهٔ اصلی
عنوان
نقل شده توسط
نقل شده توسط
سال
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
The contribution of de novo coding mutations to autism spectrum disorder
I Iossifov, BJ O’roak, SJ Sanders, M Ronemus, N Krumm, D Levy, ...
Nature 515 (7526), 216-221, 2014
27702014
De novo mutations revealed by whole-exome sequencing are strongly associated with autism
SJ Sanders, MT Murtha, AR Gupta, JD Murdoch, MJ Raubeson, ...
Nature 485 (7397), 237-241, 2012
24512012
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
24242013
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
20372020
Autism spectrum disorder
C Lord, TS Brugha, T Charman, J Cusack, G Dumas, T Frazier, EJH Jones, ...
Nature reviews Disease primers 6 (1), 5, 2020
17182020
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Nature genetics 39 (3), 319-328, 2007
16442007
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
15832015
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
15382011
Sequence Variants in SLITRK1 Are Associated with Tourette's Syndrome
JF Abelson, KY Kwan, BJ O'Roak, DY Baek, AA Stillman, TM Morgan, ...
Science 310 (5746), 317-320, 2005
12612005
Common genetic variants on 5p14. 1 associate with autism spectrum disorders
K Wang, H Zhang, D Ma, M Bucan, JT Glessner, BS Abrahams, ...
Nature 459 (7246), 528-533, 2009
11422009
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism
AJ Willsey, SJ Sanders, M Li, S Dong, AT Tebbenkamp, RA Muhle, ...
Cell 155 (5), 997-1007, 2013
10232013
De novo mutations in histone-modifying genes in congenital heart disease
S Zaidi, M Choi, H Wakimoto, L Ma, J Jiang, JD Overton, ...
Nature 498 (7453), 220-223, 2013
10082013
Rare independent mutations in renal salt handling genes contribute to blood pressure variation
W Ji, JN Foo, BJ O'Roak, H Zhao, MG Larson, DB Simon, C Newton-Cheh, ...
Nature genetics 40 (5), 592-599, 2008
9712008
Genomic Analysis of Non-NF2 Meningiomas Reveals Mutations in TRAF7, KLF4, AKT1, and SMO
VE Clark, EZ Erson-Omay, A Serin, J Yin, J Cotney, K Özduman, T Avşar, ...
Science 339 (6123), 1077-1080, 2013
9102013
Practice parameter for the assessment and treatment of children and adolescents with autism spectrum disorder
F Volkmar, M Siegel, M Woodbury-Smith, B King, J McCracken, M State, ...
Journal of the American Academy of Child & Adolescent Psychiatry 53 (2), 237-257, 2014
8072014
Integrative functional genomic analysis of human brain development and neuropsychiatric risks
M Li, G Santpere, Y Imamura Kawasawa, OV Evgrafov, FO Gulden, ...
Science 362 (6420), eaat7615, 2018
7292018
Functional and evolutionary insights into human brain development through global transcriptome analysis
MB Johnson, YI Kawasawa, CE Mason, Ž Krsnik, G Coppola, ...
Neuron 62 (4), 494-509, 2009
6792009
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
6262015
Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders
B Bakkaloglu, BJ O'Roak, A Louvi, AR Gupta, JF Abelson, TM Morgan, ...
The American Journal of Human Genetics 82 (1), 165-173, 2008
6242008
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مقاله‌ها 1–20