NaEshia Ancalade

发表

Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia

P. Sullivan, A. Ameur, C. Hultman, 2020, Nature Communications.

Schizophrenia and a high-resolution map of the three-dimensional chromatin interactome of adult and fetal cortex

Yun Li, Yan Li, Danielle Posthuma, 2018, bioRxiv.

Characterization of Single Gene Copy Number Variants in Schizophrenia

G. Kirov, M. Owen, P. Sullivan, 2019, Biological Psychiatry.

Characterization of Single Gene Copy Number Variants in Schizophrenia

G. Kirov, M. Owen, P. Sullivan, 2019, Biological Psychiatry.

Gene expression changes following chronic antipsychotic exposure in single cells from mouse striatum

P. Sullivan, G. Stuber, Rainbo Hultman, 2022, Molecular Psychiatry.

Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia

R. Yuen, Yun Li, P. Magnusson, 2022, Molecular Psychiatry.

Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia

A. Ameur, Yun Li, P. Magnusson, 2020, Nature Communications.

Disruption of the MicroRNA 137 Primary Transcript Results in Early Embryonic Lethality in Mice

Viktoriya D. Nikolova, P. Sullivan, Kara L. Agster, 2015, Biological Psychiatry.

Latin American Trans-ancestry INitiative for OCD genomics (LATINO): Study Protocol

Darpan I. Patel, Leonardo Franklin Fontenelle, Elizabeth G. Atkinson, 2023, medRxiv.

Exploration of large, rare copy number variants associated with psychiatric and neurodevelopmental disorders in individuals with anorexia nervosa

E. Zeggini, P. Sullivan, J. González, 2017, Psychiatric genetics.

Common-variant associations with fragile X syndrome

P. Sullivan, J. Piven, G. Crawford, 2017, bioRxiv.

Exploration of Large, Rare CNVs Associated with Psychiatric and Neurodevelopmental Disorders in Individuals with Anorexia Nervosa

E. Zeggini, M. Gratacós, G. Escaramís, 2017 .