J. Moran

M. Owen, M. O’Donovan, P. Sullivan, 2017, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes 1 2 Primary

John P. Rice, Melissa J. Green, Robert C. Thompson, 2018 .

Genome‐wide significant locus for Research Diagnostic Criteria Schizoaffective Disorder Bipolar type

G. Kirov, D. Grozeva, N. Craddock, 2017, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Exome arrays capture polygenic rare variant contributions to schizophrenia

M. Owen, M. O’Donovan, S. Mccarroll, 2016, Human molecular genetics.

De Novo Exon Duplication in a New Allele of Mouse Glra1 (Spasmodic)

J. Moran, D. Beier, M. Meisler, 2006, Genetics.

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

John P. Rice, Melissa J. Green, Robert C. Thompson, 2017, Cell.

Rescue of the Mouse DDK Syndrome by Parent-of-Origin-Dependent Modifiers1

F. P. Villena, D. Pomp, J. Moran, 2007, Biology of reproduction.

Lethal skeletal dysplasia in mice and humans lacking the golgin GMAP-210.

Andrew D Bolton, Danielle K. Manning, S. Nelson, 2010, The New England journal of medicine.

Manic fringe is not required for embryonic development, and fringe family members do not exhibit redundant functions in the axial skeleton, limb, or hindbrain

J. Moran, T. Vogt, S. Cole, 2009, Developmental dynamics : an official publication of the American Association of Anatomists.

Latent TGF-β-binding protein 4 modifies muscular dystrophy in mice (The Journal of Clinical Investigation (2010) 120, 2, (645) DOI

A. Palmer, J. Moran, D. Beier, 2010 .

A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis

Jianning Tao, J. Moran, D. Beier, 2012, PloS one.

A high incidence of Shigella-induced arthritis in a primate species: major histocompatibility complex class I molecules associated with resistance and susceptiblity, and their relationship to HLA-B27

Todd M. Allen, T. Allen, D. Watkins, 2000, Immunogenetics.

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

Stephan J Sanders, Alicia R. Martin, K. Roeder, 2018, Cell.

Cholesterol Metabolism Is Required for Intracellular Hedgehog Signal Transduction In Vivo

J. Moran, D. Beier, R. Kelley, 2011, PLoS genetics.

The IFT-A complex regulates Shh signaling through cilia structure and membrane protein trafficking

K. Anderson, K. Liem, J. Moran, 2012, The Journal of cell biology.

Concurrent Lpin1 and Nrcam Mouse Mutations Result in Severe Peripheral Neuropathy with Transitory Hindlimb Paralysis

J. Moran, D. Beier, Xiang-jun Chen, 2009, The Journal of Neuroscience.

An N-ethyl-N-nitrosourea mutagenesis recessive screen identifies two candidate regions for murine cardiomyopathy that map to chromosomes 1 and 15

J. Moran, D. Beier, D. Marchuk, 2009, Mammalian Genome.

Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia

M. Daly, H. Stefánsson, D. Rujescu, 2016, Molecular Psychiatry.

A Family With Multiple Cases of Schizophrenia and Mild Intellectual Impairment Also Associated With Retinitis Pigmentosa and / or Progressive Hearing Loss

P. Visscher, N. Wray, A. McRae, 2013 .

Polymorphisms in TLR4 Underlie Susceptibility

J. Moran, D. Beier, J. Kagan, 2012 .

Bile duct proliferation in Jag1/fringe heterozygous mice identifies candidate modifiers of the alagille syndrome hepatic phenotype

N. Spinner, J. Moran, S. Cole, 2008, Hepatology.

Genomic structure, mapping, and expression analysis of the mammalian Lunatic, Manic, and Radical fringe genes

A. Bowcock, J. Moran, T. Vogt, 1999, Mammalian Genome.

A mouse mutation in the 12R-lipoxygenase, Alox12b, disrupts formation of the epidermal permeability barrier.

J. Moran, D. Beier, A. Brash, 2007, The Journal of investigative dermatology.

A mouse model of Waardenburg syndrome type IV resulting from an ENU-induced mutation in endothelin 3.

W. Pavan, J. Moran, D. Beier, 2007, Pigment cell research.

The Mouse Spam1 maps to proximal Chromosome 6 and is a candidate for the sperm dysfunction in Rb(6.16)24Lub and Rb(6.15)lAld heterozygotes

N. Copeland, D. Gilbert, N. Jenkins, 1997, Mammalian Genome.

A polygenic burden of rare disruptive mutations in schizophrenia

Eric S. Lander, Patrick F. Sullivan, Jyoti S. Choudhary, 2014, Nature.

ERG Measurements of the Spectral Sensitivity of Common Chimpanzee (Pan troglodytes)

G. H. Jacobs, J. Moran, J. F. Deegan, 1996, Vision Research.

Focusing Forward Genetics: A Tripartite ENU Screen for Neurodevelopmental Mutations in the Mouse

J. Moran, D. Beier, E. Driver, 2011, Genetics.

Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology

Dan J Stein, Melissa J. Green, Janice M. Fullerton, 2021, Nature Genetics.

Genome wide meta-analysis identifies genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders

Hunna J. Watson, Ryan L. Collins, Dan J Stein, 2019, bioRxiv.

Discovery of the first genome-wide significant risk loci for ADHD

Jakob Grove, Esben Agerbo, Anders D. Børglum, 2017, bioRxiv.

Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

Laura J. Scott, Naomi R. Wray, Margaret A. Pericak-Vance, 2015, Nature Neuroscience.

Schizophrenia risk conferred by protein-coding de novo mutations

M. Daly, S. Mccarroll, N. Laird, 2018 .

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

Wei Cheng, Jianxin Shi, Elvira Bramon, 2016, Nature Genetics.

Exome sequencing and the genetic basis of complex traits

Adam Kiezun, Patrik Magnusson, Shamil R Sunyaev, 2012, Nature Genetics.

Limbs move beyond the Radical fringe

J. Moran, T. Vogt, J. Levorse, 1999, Nature.

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

Michael F. Green, Max W. Y. Lam, Catherine A. Sugar, 2022, Nature.

Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations

M. Daly, S. Mccarroll, N. Laird, 2019, Nature Neuroscience.

A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder

Alicia R. Martin, N. Eriksson, N. Wray, 2017, Biological Psychiatry.

Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia

Giulio Genovese, Patrick F Sullivan, Menachem Fromer, 2016, Nature Neuroscience.

Identification of common genetic risk variants for autism spectrum disorder

Alicia R. Martin, K. Roeder, M. Daly, 2019, Nature Genetics.

Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia

G. Kirov, M. Owen, M. O’Donovan, 2015, Neuron.

A polygenic resilience score moderates the genetic risk for schizophrenia

M. Pirinen, P. Donnelly, C. Spencer, 2019, Molecular Psychiatry.

Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

Benjamin A. Logsdon, Hae Kyung Im, Solveig K Sieberts, 2019, Nature Genetics.

The Penetrance of Copy Number Variations for Schizophrenia and Developmental Delay

G. Kirov, M. Owen, M. O’Donovan, 2014, Biological Psychiatry.

A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts

John P. Rice, Robert M. Maier, C. Spencer, 2020, Biological Psychiatry.

Implication of a rare deletion at distal 16p11.2 in schizophrenia.

J. Sebat, D. Malhotra, Annette Lee, 2013, JAMA psychiatry.

A rare deletion at distal 16 p 11 . 2 is implicated in schizophrenia

Degenhardt, Dheeraj, Franziska, 2013 .

zCall: a rare variant caller for array-based genotyping: Genetics and population analysis

Patrick F. Sullivan, Menachem Fromer, Benjamin M. Neale, 2012, Bioinform..

Gene expression changes during mouse skeletal myoblast differentiation revealed by transcriptional profiling.

Yizheng Li, J. Moran, A. Hill, 2002, Physiological genomics.

Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder

Hoang T. Nguyen, G. Abecasis, H. Kang, 2021, Molecular Psychiatry.

De novo CNVs in bipolar affective disorder and schizophrenia

Peter Holmans, Steven McCarroll, Michael J. Owen, 2014, Human molecular genetics.

Complement genes contribute sex-biased vulnerability in diverse illnesses

Simon C. Potter, Christopher W. Whelan, M. Pirinen, 2020, Nature.

Exome Aggregation Consortium

Adam Kiezun, Sergio Islas-Andrade, Pierre Fontanillas, 2016 .

Contribution of Rare Copy Number Variants to Bipolar Disorder Risk Is Limited to Schizoaffective Cases

N. Craddock, S. Mccarroll, H. Nicolini, 2018, Biological Psychiatry.

CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1

Patrick F. Sullivan, Brien Riley, Giulio Genovese, 2013, Human molecular genetics.

Disentangling polygenic associations between attention-deficit/hyperactivity disorder, educational attainment, literacy and language

Chin Yang Shapland, Alicia R. Martin, M. Daly, 2019, Translational Psychiatry.

Genetic correlation between amyotrophic lateral sclerosis and schizophrenia

Denis C. Bauer, Annelot M. Dekker, Ashley R. Jones, 2017, Nature Communications.

ENU mutagenesis in mice identifies candidate genes for hypogonadism

J. Moran, D. Beier, J. Jameson, 2012, Mammalian Genome.

High resolution mapping and positional cloning of ENU-induced mutations in the Rw region of mouse chromosome 5

T. Fennell, E. Mauceli, K. Lindblad-Toh, 2010, BMC Genetics.

Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse.

Andrew D Bolton, Danielle K. Manning, R. Kucherlapati, 2006, Genome research.

schizophrenia-associated loci Analysis of copy number variations at 15

M. Owen, M. O’Donovan, K. Chambert, 2014 .

CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1

G. Kirov, M. Gill, M. Owen, 2013, Human molecular genetics.

Mosaic copy number variation in schizophrenia

D. Clair, G. Kirov, M. Owen, 2013, European Journal of Human Genetics.

Exome Sequencing of Familial Bipolar Disorder.

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

Analysis of genetic deletions and duplications in the University College London bipolar disorder case control sample

S. Purcell, P. Sklar, H. Gurling, 2011, European Journal of Human Genetics.

The genomic psychiatry cohort: Partners in discovery

S. Mccarroll, H. Nicolini, S. Purcell, 2013, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

No evidence for rare recessive and compound heterozygous disruptive variants in schizophrenia

P. Sullivan, S. Mccarroll, P. Holmans, 2014, European Journal of Human Genetics.

Latent TGF-beta-binding protein 4 modifies muscular dystrophy in mice.

A. Palmer, J. Moran, D. Beier, 2009, The Journal of clinical investigation.

Evidence of Common Genetic Overlap Between Schizophrenia and Cognition

M. Owen, M. O’Donovan, K. Tansey, 2015, Schizophrenia bulletin.

Genome-wide SNP analysis of Tg.AC transgenic mice reveals an oncogenic collaboration between v-Ha-ras and Ink4a, which is absent in p53 deficiency

P. Leder, J. Moran, D. Beier, 2008, Oncogene.

Elevated polygenic burden for autism is associated with differential DNA methylation at birth

Shan V Andrews, Alicia R. Martin, T. Werge, 2018, Genome Medicine.

Structural basis of clade‐specific HIV‐1 neutralization by humanized anti‐V3 monoclonal antibody KD‐247

S. Sarafianos, S. Matsushita, J. Moran, 2015, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

Kristen K. Dang, D. A. Lewis, C. Spencer, 2019, Nature Genetics.

Polygenic overlap between schizophrenia risk and antipsychotic response: a genomic medicine approach.

Michael J. Keiser, P. Sullivan, J. Dudley, 2016, The lancet. Psychiatry.

A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability

P. Visscher, N. Wray, A. McRae, 2013, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genome-wide association study identi ﬁ es SESTD1 as a novel risk gene for lithium-responsive bipolar disorder

N. Craddock, S. Mccarroll, K. Gordon-Smith, 2023 .

Complement genes contribute sex-biased vulnerability in diverse disorders

Christopher W. Whelan, M. Pirinen, C. Spencer, 2020, Nature.

Erratum: Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia

M. Daly, H. Stefánsson, D. Rujescu, 2016, Molecular Psychiatry.

Polymorphisms in Toll-Like Receptor 4 Underlie Susceptibility to Tumor Induction by the Mouse Polyomavirus

J. Moran, D. Beier, T. Benjamin, 2012, Journal of Virology.

A forward genetic screen with a thalamocortical axon reporter mouse yields novel neurodevelopment mutants and a distinct emx2 mutant phenotype

Danielle K. Manning, C. Walsh, D. O'Leary, 2011, Neural Development.

Three loci on mouse chromosome 5 and 10 modulate sex determination in XX Ods/+ mice

C. Bishop, J. Moran, D. Beier, 2007, Genesis.