Stephan J. Sanders
Stephan J. Sanders
Assistant Professor, UCSF
Email verificata su ucsf.edu
TitoloCitata daAnno
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, 2012
15582012
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, 2014
12232014
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, 2014
11112014
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
10372011
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
9902013
Most genetic risk for autism resides with common variation
T Gaugler, L Klei, SJ Sanders, CA Bodea, AP Goldberg, AB Lee, ...
Nature genetics 46 (8), 881, 2014
6012014
A framework for the interpretation of de novo mutation in human disease
KE Samocha, EB Robinson, SJ Sanders, C Stevens, A Sabo, LM McGrath, ...
Nature genetics 46 (9), 944, 2014
5612014
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
5582015
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, 2013
5462013
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
4942013
Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations
K Bilgvar, AK ztrk, A Louvi, KY Kwan, M Choi, B Tatlı, D Yalnızoğlu, ...
Nature 467 (7312), 207, 2010
4702010
Using whole-exome sequencing to identify inherited causes of autism
WY Timothy, MH Chahrour, ME Coulter, S Jiralerspong, K Okamura-Ikeda, ...
Neuron 77 (2), 259-273, 2013
3472013
Search for new physics in the multijet and missing transverse momentum final state in proton-proton collisions at = 8 TeV
S Chatrchyan, V Khachatryan, AM Sirunyan, A Tumasyan, W Adam, ...
Journal of High Energy Physics 2014 (6), 55, 2014
3112014
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), 9, 2012
3042012
De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies
J Homsy, S Zaidi, Y Shen, JS Ware, KE Samocha, KJ Karczewski, ...
Science 350 (6265), 1262-1266, 2015
2642015
L-histidine decarboxylase and Tourette's syndrome
AG Ercan-Sencicek, AA Stillman, AK Ghosh, K Bilguvar, BJ O'Roak, ...
New England Journal of Medicine 362 (20), 1901-1908, 2010
2602010
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia
D Moreno-De-Luca, JG Mulle, EB Kaminsky, SJ Sanders, SM Myers, ...
The American Journal of Human Genetics 87 (5), 618-630, 2010
2522010
Sex and gender differences in autism spectrum disorder: summarizing evidence gaps and identifying emerging areas of priority
AK Halladay, S Bishop, JN Constantino, AM Daniels, K Koenig, K Palmer, ...
Molecular autism 6 (1), 36, 2015
2322015
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population
EB Robinson, B St Pourcain, V Anttila, JA Kosmicki, B Bulik-Sullivan, ...
Nature genetics 48 (5), 552, 2016
2082016
Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders
ET Lim, S Raychaudhuri, SJ Sanders, C Stevens, A Sabo, DG MacArthur, ...
Neuron 77 (2), 235-242, 2013
2082013
Il sistema al momento non pu eseguire l'operazione. Riprova pi tardi.
Articoli 1–20