Stephan Sanders

Professor of Paediatric Neurogenetics

University of Oxford

United Kingdom

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Articles (20)

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2024

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2022

Collaborators (18)

Rikke S. Møller

the faculty of health sciences university of southern denmark odense denmark

DENMARK

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Caroline Tanner

Professor

University of California, San Francisco

UNITED STATES

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Nadav Ahituv

Professor

University of California, San Francisco

UNITED STATES

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Donna Werling

Assistant Professor

University of Wisconsin-Madison

UNITED STATES

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Caroline Cusick

Broad Institute

UNITED STATES

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Joon-Yong An

Assistant Professor

Korea University

SOUTH KOREA

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Anne Goriely

University of Oxford

UNITED KINGDOM

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Jenny Lord

University of Southampton

UNITED KINGDOM

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Bradford Powell

University of North Carolina

UNITED STATES

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Fumitaka Inoue

Associate Professor

Kyoto University

JAPAN

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Silvia De Rubeis

Associate Professor

Icahn School of Medicine at Mount Sinai

UNITED STATES

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Ruebena Dawes

University of Oxford

UNITED KINGDOM

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Ronald Yurko

Assistant Teaching Professor

Carnegie Mellon University

UNITED STATES

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STEPHANIE HAO

Boston University

UNITED STATES

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Guido Rubboli

Københavns Universitet

DENMARK

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Charles Nemeroff

Matthew P. Nemeroff Chair, Director Institute for Early Life Adversity Research, Professor

The University of Texas at Austin Dell Medical School

UNITED STATES

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Naomichi Matsumoto

Professor and Chair

Yokohama City University Graduate School of Medicine

JAPAN

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William Rowles

Swedish Neuroscience Institute

UNITED STATES

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Stephan Sanders

Research Interests

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Articles (20)

De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome

Sex-Differential Gene Expression in Developing Human Cortex and Its Intersection With Autism Risk Pathways

The Conundrum of Mechanics Versus Genetics in Congenital Hydrocephalus and Its Implications for Fetal Therapy Approaches: A Scoping Review.

Examining Sex Differences in Autism Heritability.

Five autism-associated transcriptional regulators target shared loci proximal to brain-expressed genes.

Haploinsufficiency underlies the neurodevelopmental consequences of SLC6A1 variants.

A comprehensive AI model development framework for consistent Gleason grading

CWAS-Plus: estimating category-wide association of rare noncoding variation from whole-genome sequencing data with cell-type-specific functional data.

Physical and functional convergence of the autism risk genes Scn2a and Ank2 in neocortical pyramidal cell dendrites.

Prenatal delivery of a therapeutic antisense oligonucleotide achieves broad biodistribution in the brain and ameliorates Angelman syndrome phenotype in mice.

In Search of Biomarkers to Guide Interventions in Autism Spectrum Disorder: A Systematic Review

Characterization of De Novo Promoter Variants in Autism Spectrum Disorder with Massively Parallel Reporter Assays

Neuropsychiatric biomarker discovery: go big or go home

KCNT2-Related Disorders: Phenotypes, Functional, and Pharmacological Properties.

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

Enhancing Clinical Information Display to Improve Patient Encounters: Human-Centered Design and Evaluation of the Parkinson Disease-BRIDGE Platform

Spatiotemporal and genetic regulation of A-to-I editing throughout human brain development.

Diverse mutations in autism-related genes and their expression in the developing brain.

Prenatal Somatic Cell Gene Therapies: Charting a Path Toward Clinical Applications (Proceedings of the CERSI-FDA Meeting).

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

Collaborators (18)

Rikke S. Møller

Caroline Tanner

Nadav Ahituv

Donna Werling

Caroline Cusick

Joon-Yong An

Anne Goriely

Jenny Lord

Bradford Powell

Fumitaka Inoue

Silvia De Rubeis

Ruebena Dawes

Ronald Yurko

STEPHANIE HAO

Guido Rubboli

Charles Nemeroff

Naomichi Matsumoto

William Rowles

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