Shuoguo Wang

发表

De Novo Coding Variants Are Strongly Associated with Tourette Disorder

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

A comprehensive analysis of piRNAs from adult human testis and their relationship with genes and mobile elements

Cédric Feschotte, Jinchuan Xing, Jimin Song, 2014, BMC Genomics.

Germline Genetic Variation in ETV6 and Risk of Childhood Acute Lymphoblastic Leukemia: a Systematic Genetic Study

Pui, Michael N. Edmonson, R. Fulton, 2015, The Lancet. Oncology.

A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data

Gustavo Glusman, Paul Scheet, Mark Yandell, 2014, Nature Biotechnology.

A polygenic score for acute vaso-occlusive pain in pediatric sickle cell disease.

Heather L. Mulder, Jason R. Hodges, Celeste K. Kanne, 2021, Blood advances.

Hippocampal Formation Synchronization in Hybrid Neuronal Networks of the

Corey D. Acker, J. L. Hudson, J. White, 2015 .

phase-response curves and type 1 excitability Hippocampal CA1 pyramidal neurons exhibit type 1

C. Canavier, Shuoguo Wang, Maximilian M. Musharoff, 2015 .

A rare variant analysis framework using public genotype summary counts to prioritize disease-predisposition genes

D. Schaid, D. Ellison, Wenan Chen, 2022, Nature Communications.

Estimated number of adult survivors of childhood cancer in United States with cancer‐predisposing germline variants

Aman N. Patel, Heather L. Mulder, Carmen L. Wilson, 2019, Pediatric blood & cancer.

St. Jude Cloud—a Pediatric Cancer Genomic Data Sharing Ecosystem

Aman N. Patel, Carmen L. Wilson, Samuel W. Brady, 2020, bioRxiv.

Microsoft Word-30462222-file00.docx

E. Schuetz, Shuoguo Wang, K. Thummel, 2015 .

Insights into a divergent phenazine biosynthetic pathway governed by a plasmid-born esmeraldin gene cluster.

Shuoguo Wang, Wenjun Zhang, Z. Rui, 2012, Chemistry & biology.

Hippocampal CA1 pyramidal neurons exhibit type 1 phase-response curves and type 1 excitability.

Carmen C Canavier, Sonia Gasparini, Shuoguo Wang, 2013, Journal of neurophysiology.

Germline Mutations in Predisposition Genes in Pediatric Cancer.

Li Ding, Amar Gajjar, Xiaotu Ma, 2015, The New England journal of medicine.

Germline SAMD9 Mutation in Siblings with Monosomy 7 and Myelodysplastic Syndrome

S. Raimondi, J. Klco, T. Lamprecht, 2017, Leukemia.

Genetic alterations in uncommon low-grade neuroepithelial tumors: BRAF, FGFR1, and MYB mutations occur at high frequency and align with morphology

Heather L. Mulder, Michael C. Rusch, R. Wilson, 2016, Acta Neuropathologica.

A Primer for Disease Gene Prioritization Using Next-Generation Sequencing Data

Jinchuan Xing, Shuoguo Wang, Jinchuan Xing, 2013, Genomics & informatics.

Extremely low-coverage whole genome sequencing in South Asians captures population genomics information

Navin Rustagi, Jinchuan Xing, Naveen Ramesh, 2017, BMC Genomics.

St. Jude Cloud-a Pediatric Cancer Genomic Data Sharing Ecosystem.

Aman N. Patel, Carmen L. Wilson, Samuel W. Brady, 2021, Cancer discovery.

Structure and evolution of double minutes in diagnosis and relapse brain tumors

Heather L. Mulder, Michael C. Rusch, J. Downing, 2018, Acta Neuropathologica.

The genomic landscape of pediatric myelodysplastic syndromes

J. Klco, T. Lamprecht, Jing Ma, 2016, Nature Communications.

CoCoRV: a rare variant analysis framework using publicly available genotype summary counts to prioritize germline disease-predisposition genes

D. Ellison, Wenan Chen, Gang Wu, 2021, bioRxiv.

Clonal dynamics of donor-derived myelodysplastic syndrome after unrelated hematopoietic cell transplantation for high-risk pediatric B-lymphoblastic leukemia

Susana Raimondi, Jing Ma, Shuoguo Wang, 2018, Cold Spring Harbor molecular case studies.

Genetic Risk for Subsequent Neoplasms Among Long-Term Survivors of Childhood Cancer.

Yadav Sapkota, Celeste Rosencrance, Xiaotu Ma, 2018, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

The CYP2C19 Intron 2 Branch Point SNP is the Ancestral Polymorphism Contributing to the Poor Metabolizer Phenotype in Livers with CYP2C19*35 and CYP2C19*2 Alleles

D. Finkelstein, Gang Wu, E. Schuetz, 2015, Drug Metabolism and Disposition.

The CYP 2 C 19 Intron 2 Branch Point SNP is the Ancestral Polymorphism Contributing to the Poor Metabolizer Phenotype in Livers with CYP 2 C 19 * 35 and CYP 2 C 19 * 2 Alleles s

D. Finkelstein, Gang Wu, E. Schuetz, 2015 .

Single Cell Viewer (SCV): An interactive visualization data portal for single cell RNA sequence data

Isaac Neuhaus, M. Bolisetty, Shuoguo Wang, 2019, bioRxiv.

Chemotherapy induces dynamic immune responses in breast cancers that impact treatment outcome

J. Bienkowska, Shibing Deng, P. Rejto, 2020, Nature Communications.

Worldwide patterns of genomic variation and admixture in gray wolves

T. Marquès-Bonet, R. Wayne, Ilan Gronau, 2016, Genome research.

Apparent Variation in Neanderthal Admixture among African Populations is Consistent with Gene Flow from Non-African Populations

S. Tishkoff, Jinchuan Xing, J. Hey, 2013, Genome biology and evolution.

Evolution of the H9N2 influenza genotype that facilitated the genesis of the novel H7N9 virus

Baoli Zhu, Robert A. Carter, Guozhong Zhang, 2014, Proceedings of the National Academy of Sciences.

Antigenic evolution of H9N2 chicken influenza viruses isolated in China during 2009-2013 and selection of a candidate vaccine strain with broad cross-reactivity.

R. Webster, Gang Wu, G. Lemmon, 2016, Veterinary microbiology.

Genetic evolution of influenza H9N2 viruses isolated from various hosts in China from 1994 to 2013

R. Webster, Gang Wu, Shuoguo Wang, 2017, Emerging microbes & infections.

Longitudinal multi-omics study of palbociclib resistance in HR-positive/HER2-negative metastatic breast cancer

J. Bienkowska, Shibing Deng, P. Rejto, 2023, Genome Medicine.

Effect of phase response curve skew on synchronization with and without conduction delays

Carmen C. Canavier, Shuoguo Wang, Lakshmi Chandrasekaran, 2013, Front. Neural Circuits.

The genomic landscape of pediatric myelodysplastic syndromes

J. Klco, T. Lamprecht, Jing Ma, 2016, Nature Communications.

Short Conduction Delays Cause Inhibition Rather than Excitation to Favor Synchrony in Hybrid Neuronal Networks of the Entorhinal Cortex

John A. White, Carmen C. Canavier, Fernando R. Fernandez, 2012, PLoS Comput. Biol..