Andrew Pocklington

University of Chicago — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

38h-index23.1kcitations106works4.82yr avg
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Research Topics

Genetic Associations and Epidemiology(42), Genetics and Neurodevelopmental Disorders(24), Genomic variations and chromosomal abnormalities(22), Genomics and Rare Diseases(21), Neuroscience and Neuropharmacology Research(10)

Publications86 total

Efficient Simulation of Nontrivial Dissipative Spin Chains via Stochastic Unraveling
PRX Quantum·2025Open Access
Accelerating Dissipative State Preparation with Adaptive Open Quantum Dynamics
Physical Review Letters·2025· 3 citedOpen Access
Impaired oxysterol-liver X receptor signaling underlies aberrant cortical neurogenesis in a stem cell model of neurodevelopmental disorder
Cell Reports·2024· 10 citedOpen Access
Stability via symmetry breaking in interacting driven systems
arXiv (Cornell University)·2023Open Access
Exact Results for a Boundary-Driven Double Spin Chain and Resource-Efficient Remote Entanglement Stabilization
arXiv (Cornell University)·2023· 1 citedOpen Access
Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions
Cell Genomics·2023· 37 citedOpen Access
Oxysterol-liver X receptor signaling mediates CYFIP1 regulation of cortical neurogenesis
2023Open Access
Two hits in one – the neurobiology of schizophrenia
TheScienceBreaker·2023Open Access
Dissipative Pairing Interactions: Quantum Instabilities, Topological Light, and Volume-Law Entanglement
arXiv (Cornell University)·2022Open Access
Genetic risk for schizophrenia is associated with increased proportion of indirect connections in brain networks revealed by a semi-metric analysis: evidence from population sample stratified for polygenic risk
Cerebral Cortex·2022· 4 citedOpen Access
Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants
Nature Communications·2022· 27 citedOpen Access
Rare Copy Number Variants Are Associated With Poorer Cognition in Schizophrenia
Biological Psychiatry·2020· 34 citedOpen Access
Genetic association of FMRP targets with psychiatric disorders
Molecular Psychiatry·2020· 29 citedOpen Access
Polygenic risk for schizophrenia and subcortical brain anatomy in the UK Biobank cohort
Translational Psychiatry·2020· 34 citedOpen Access
Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia
UNC Libraries·2020Open Access
Genetic association of FMRP targets with psychiatric disorders
2020· 6 citedOpen Access
De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia
Nature Neuroscience·2020· 137 citedOpen Access
Synaptic protein DLG2 controls neurogenic transcriptional programs disrupted in schizophrenia and related disorders
White Rose Research Online (University of Leeds, The University of Sheffield, University of York)·2020
<i>DLG2</i> knockout reveals neurogenic transcriptional programs underlying neuropsychiatric disorders and cognition
2020· 2 citedOpen Access
A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia
Human Molecular Genetics·2019· 73 citedOpen Access
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Frequent Co-authors

Michael O’Donovan(32), Peter Holmans(30), Michael J. Owen(30), James Walters(22), Elliott Rees(20), George Kirov(17), Antonio F. Pardiñas(16), Valentina Escott‐Price(13), Sophie E. Legge(11), Noa Carrera(9), Steven A. McCarroll(9), Seth G. N. Grant(8), Marian L. Hamshere(7), Jun Han(7), Jennifer L. Moran(7), Alexander Richards(7), Douglas M. Ruderfer(6), Nicholas E. Clifton(6), Lynsey S. Hall(6), Jérémy Hall(6)