| 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 | 2542 | 2014 |
| 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 | 2327 | 2012 |
| 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 | 1452 | 2015 |
| An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder DM Werling, H Brand, JY An, MR Stone, L Zhu, JT Glessner, RL Collins, ... Nature genetics 50 (5), 727-736, 2018 | 260 | 2018 |
| Modeling non-syndromic autism and the impact of TRPC6 disruption in human neurons K Griesi-Oliveira, A Acab, AR Gupta, DY Sunaga, T Chailangkarn, X Nicol, ... Molecular psychiatry 20 (11), 1350-1365, 2015 | 215 | 2015 |
| De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder S Dong, MF Walker, NJ Carriero, M DiCola, AJ Willsey, YY Adam, ... Cell reports 9 (1), 16-23, 2014 | 185 | 2014 |
| De novo coding variants are strongly associated with Tourette disorder AJ Willsey, TV Fernandez, D Yu, RA King, A Dietrich, J Xing, SJ Sanders, ... Neuron 94 (3), 486-499. e9, 2017 | 167 | 2017 |
| SynDB: a Synapse protein DataBase based on synapse ontology W Zhang, Y Zhang, H Zheng, C Zhang, W Xiong, JG Olyarchuk, M Walker, ... Nucleic Acids Research 35 (suppl_1), D737-D741, 2007 | 57 | 2007 |
| No Evidence for Association of Autism with Rare Heterozygous Point Mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin … JD Murdoch, AR Gupta, SJ Sanders, MF Walker, J Keaney, TV Fernandez, ... PLoS genetics 11 (1), e1004852, 2015 | 51 | 2015 |
| Neurogenetic analysis of childhood disintegrative disorder AR Gupta, A Westphal, DYJ Yang, CAW Sullivan, J Eilbott, S Zaidi, ... Molecular autism 8, 1-17, 2017 | 22 | 2017 |
| Limited contribution of rare, noncoding variation to autism spectrum disorder from sequencing of 2,076 genomes in quartet families DM Werling, H Brand, JY An, MR Stone, JT Glessner, L Zhu, RL Collins, ... BioRxiv, 127043, 2017 | 18 | 2017 |
| In Vitro Cultivation of Microphallus turgidus (Trematoda: Microphallidae) from Metacercaria to Ovigerous Adult with Continuation of the Life Cycle in the Laboratory OJ Pung, AR Burger, MF Walker, WL Barfield, MH Lancaster, CE Jarrous Journal of Parasitology 95 (4), 913-919, 2009 | 13 | 2009 |
| Synthesis and characterization of type II silicon clathrate films with low Na concentration Y Liu, WK Schenken, L Krishna, AAA Majid, TE Furtak, M Walker, CA Koh, ... Applied Physics Reviews 8 (4), 2021 | 7 | 2021 |
| Whole-exome sequencing in obsessive-compulsive disorder identifies rare mutations and immunological pathways C Cappi, H Brentani, L Lima, SJ Sanders, J Diniz, M Walker, VNS Reis, ... Biological Psychiatry, 2014 | 1 | 2014 |
| Formation of Type II Silicon Clathrate with Lithium Guests through Thermal Diffusion Y Liu, JP Briggs, AAA Majid, TE Furtak, M Walker, M Singh, CA Koh, ... Inorganic Chemistry 62 (18), 6882-6892, 2023 | | 2023 |
| Synaptic Proteins JD Murdoch, MF Walker Encyclopedia of Autism Spectrum Disorders, 4722-4724, 2021 | | 2021 |
| No Evidence for Association of Autism with Rare Heterozygous Point Mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or … S Sanders, JD Murdoch, AR Gupta, SJ Sanders, MF Walker, J Keaney, ... | | 2015 |
| The contribution of de novo coding mutations to autism spectrum disorder. M Ronemus, N Krumm, D Levy, H Stessman, K Witherspoon, L Vives, ... Nature 515 (7526), 2014 | | 2014 |
| Modeling non-syndromic autism and the impact of TRPC6 disruption in human neurons A Muotri, S Sanders, K Griesi-Oliveira, A Acab, AR Gupta, DY Sunaga, ... | | 2014 |
| Recessive Genes JD Murdoch, MF Walker Encyclopedia of Autism Spectrum Disorders, 2529-2530, 2013 | | 2013 |
