Shan Dong

发表

Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex

Stephan J Sanders, Michael C. Gilson, K. Roeder, 2020, Cell reports.

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

Matthew W. Mosconi, Ryan L. Collins, Stephan J Sanders, 2019, Cell.

Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex

Stephan J Sanders, Michael C. Gilson, K. Roeder, 2019, bioRxiv.

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

Stephan J Sanders, Alicia R. Martin, K. Roeder, 2018, Cell.

Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk

Matthew W. Mosconi, Ryan L. Collins, Stephan J Sanders, 2018, bioRxiv.

De Novo Coding Variants Are Strongly Associated with Tourette Disorder

Jeffrey D. Mandell, Michael F. Walker, Stephan J Sanders, 2017, Neuron.

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

Christopher S. Poultney, Jeffrey D. Mandell, Michael F. Walker, 2015, Neuron.

Coexpression Networks Implicate Human Midfetal Deep Cortical Projection Neurons in the Pathogenesis of Autism

Wei Niu, Kathryn Roeder, Mingfeng Li, 2013, Cell.

H2A.Z Nucleosome Positioning Has No Impact on Genetic Variation in Drosophila Genome

Cizhong Jiang, Shan Dong, Yitao Tang, 2013, PloS one.

An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder

Ryan L. Collins, Ryan M. Layer, Jeffrey D. Mandell, 2018, Nature Genetics.

De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder.

Kathryn Roeder, Liping Wei, Jeanselle Dea, 2014, Cell reports.

Systematic evaluation of genome sequencing as a first-tier diagnostic test for prenatal and pediatric disorders

Ryan L. Collins, Stephan J Sanders, D. MacArthur, 2020 .

Whole genome sequencing in psychiatric disorders: the WGSPD consortium

Stephan J Sanders, M. Daly, G. Abecasis, 2017, bioRxiv.

Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder

Ryan L. Collins, Gabor T. Marth, Stephan J Sanders, 2018, Science.

Limited contribution of rare, noncoding variation to autism spectrum disorder from sequencing of 2,076 genomes in quartet families

Ryan L. Collins, Ryan M. Layer, Gabor T. Marth, 2017, bioRxiv.

Exome sequencing of fetuses with congenital diaphragmatic hernia supports a causal role for NR2F2, PTPN11, and WT1 variants.

Stephan J Sanders, Grace B. Schwartz, Shan Dong, 2021, American journal of surgery.

Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

Ryan L. Collins, Jack M. Fu, Stephan J Sanders, 2022, Nature Genetics.

Systematic evaluation of genome sequencing for the assessment of fetal structural anomalies

Ryan L. Collins, Jack M. Fu, Christopher W. Whelan, 2020, bioRxiv.

Intergenerational Conflicts and Transmission of Values in Raising 0–2-Year-Old Chinese Babies

Shan Dong, Yuejuan Pan, Lina Sun, 2017 .

The contribution of de novo coding mutations to autism spectrum disorder

Boris Yamrom, Kenny Q. Ye, Michael C. Schatz, 2014, Nature.

The female protective effect in autism spectrum disorder is not mediated by a single genetic locus

Stephan J Sanders, J. Constantino, J. Dougherty, 2015, Molecular Autism.

Prenatal exposure to paternal smoking and likelihood for autism spectrum disorder

Stephan J Sanders, B. Leventhal, M. Lim, 2021, Autism : the international journal of research and practice.

Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism

Ryan L. Collins, Jack M. Fu, Stephan J Sanders, 2021, medRxiv.

De Novo Insertions and Dele tions of Predominantly Paternal Origin Are Associated with Autism Spectrum Disorder Graphical

Jeffrey D. Mandell, Michael F. Walker, Michael J. DiCola, 2022 .

De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis

Jeffrey D. Mandell, Stephan J Sanders, N. Freimer, 2018, Cell reports.

University of Groningen De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis Tourette

Jeffrey D. Mandell, J. Buxbaum, P. Paschou, 2018 .

Whole genome sequencing in psychiatric disorders: the WGSPD consortium

Stephan J Sanders, M. Daly, G. Abecasis, 2017, bioRxiv.

A novel homozygous C-terminal deletion in BTG4 causes zygotic cleavage failure and female infertility

Y. Gong, Shan Dong, Molin Wang, 2022, Journal of Assisted Reproduction and Genetics.

Whole genome sequencing in psychiatric disorders: the WGSPD consortium

Hailiang Huang, Chiara Sabatti, Kevin Eggan, 2017, bioRxiv.

De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis.

Jeffrey D. Mandell, Stephan J Sanders, N. Freimer, 2018, Cell reports.

Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies.

Ryan L. Collins, Jack M. Fu, Christopher W. Whelan, 2023, American journal of human genetics.

Systematic evaluation of genome sequencing as a first-tier diagnostic test for prenatal and pediatric disorders

Ryan L. Collins, Stephan J Sanders, D. MacArthur, 2020 .

An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder

Ryan L. Collins, Ryan M. Layer, Gabor T. Marth, 2018, Nature Genetics.