E. Ghiban

发表

De Novo Gene Disruptions in Children on the Autistic Spectrum

Kenny Q. Ye, M. Schatz, J. Troge, 2012, Neuron.

De novo Mutations in Schizophrenia Implicate Chromatin Remodeling and Support a Genetic Overlap with Autism and Intellectual Disability

Seungtai Yoon, S. McCarthy, M. Gill, 2014, Molecular Psychiatry.

DNA sequence-level analyses reveal potential phenotypic modifiers in a large family with psychiatric disorders

Niamh M. Ryan, I. Deary, S. McCarthy, 2018, Molecular Psychiatry.

New whole genome de novo assemblies of three divergent strains of rice (O. sativa) documents novel gene space of aus and indica

Mark H. Wright, M. Schatz, W. McCombie, 2014, bioRxiv.

Ordered and deterministic cancer genome evolution after p53 loss

A. Krasnitz, J. Kendall, N. Socci, 2022, Nature.

Whole genome de novo assemblies of three divergent strains of rice, Oryza sativa, document novel gene space of aus and indica

Doreen Ware, Michael C Schatz, Eric Antoniou, 2014, Genome Biology.

708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits

J. D. Watson, P. Visscher, A. McRae, 2013, Molecular Psychiatry.

Exome Sequencing of Familial Bipolar Disorder.

V. Willour, J. Potash, P. Zandi, 2016, JAMA psychiatry.

Explorer 708 Common and 2010 rare DISC 1 locus variants identified in 1542 subjects

S. McCarthy, W. Hennah, I. Deary, 2013 .

SU7 BEYOND THE TRANSLOCATION: WHOLE GENOME SEQUENCING ANALYSIS OF THE SCOTTISH T(1;11) FAMILY

Niamh M. Ryan, S. McCarthy, S. Lawrie, 2019, European Neuropsychopharmacology.

Using deep long-read RNAseq in Alzheimer’s disease brain to assess clinical relevance of RNA isoform diversity

Mark E. Wadsworth, N. Seyfried, Sara Goodwin, 2023, bioRxiv.

Mapping medically relevant RNA isoform diversity in the aged human frontal cortex with deep long-read RNA-seq.

Mark T. W. Ebbert, Mark E. Wadsworth, M. Ryten, 2024, Nature biotechnology.