The contribution of imprinted genes to neurodevelopmental and neuropsychiatric disorders
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Title
The contribution of imprinted genes to neurodevelopmental and neuropsychiatric disorders
Authors
Keywords
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Journal
Translational Psychiatry
Volume 12, Issue 1, Pages -
Publisher
Springer Science and Business Media LLC
Online
2022-05-21
DOI
10.1038/s41398-022-01972-4
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Note: Only part of the references are listed.- Dlk1 dosage regulates hippocampal neurogenesis and cognition
- (2021) Raquel Montalbán-Loro et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Growth Restriction and Genomic Imprinting-Overlapping Phenotypes Support the Concept of an Imprinting Network
- (2021) Thomas Eggermann et al. Genes
- Maternal Metabolic Programming of the Developing Central Nervous System: Unified Pathways to Metabolic and Psychiatric Disorders
- (2021) Rachel N. Lippert et al. BIOLOGICAL PSYCHIATRY
- Features and mechanisms of canonical and noncanonical genomic imprinting
- (2021) Courtney W. Hanna et al. GENES & DEVELOPMENT
- Placental endocrine insufficiency programs anxiety, deficits in cognition and atypical social behaviour in offspring
- (2021) David J Harrison et al. HUMAN MOLECULAR GENETICS
- Comparison of mouse models reveals a molecular distinction between psychotic illness in PWS and schizophrenia
- (2021) Simona K. Zahova et al. Translational Psychiatry
- Deficiency of the paternally inherited gene Magel2 alters the development of separation‐induced vocalization and maternal behavior in mice
- (2021) Gabriela M. Bosque Ortiz et al. GENES BRAIN AND BEHAVIOR
- Loss of Snord116 alters cortical neuronal activity in mice: a pre-clinical investigation of Prader-Willi syndrome
- (2020) Marta Pace et al. HUMAN MOLECULAR GENETICS
- The placental programming hypothesis: Placental endocrine insufficiency and the co-occurrence of low birth weight and maternal mood disorders
- (2020) H.D.J. Creeth et al. PLACENTA
- Does SNORD116 mediate aspects of psychosis in Prader-Willi syndrome? Evidence from a non-clinical population
- (2020) Iiro Salminen et al. PSYCHIATRY RESEARCH
- Temple syndrome and Kagami-Ogata syndrome: clinical presentations, genotypes, models and mechanisms
- (2020) Rexxi Prasasya et al. HUMAN MOLECULAR GENETICS
- Do assisted reproductive technologies and in vitro embryo culture influence the epigenetic control of imprinted genes and transposable elements in children?
- (2020) J Barberet et al. HUMAN REPRODUCTION
- Genomic Imprinting and Physiological Processes in Mammals
- (2019) Valter Tucci et al. CELL
- Genetic variation of UBE3A is associated with schizotypy in a population of typical individuals
- (2019) Iiro Salminen et al. PSYCHIATRY RESEARCH
- Potential of Epigenetic Therapy for Prader-Willi Syndrome
- (2019) Sung Eun Wang et al. TRENDS IN PHARMACOLOGICAL SCIENCES
- Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes
- (2018) Douglas M. Ruderfer et al. CELL
- Hypothalamic loss of Snord116 recapitulates the hyperphagia of Prader-Willi syndrome
- (2018) Joseph Polex-Wolf et al. JOURNAL OF CLINICAL INVESTIGATION
- Convergence of placenta biology and genetic risk for schizophrenia
- (2018) Gianluca Ursini et al. NATURE MEDICINE
- Maternal care boosted by paternal imprinting in mammals
- (2018) H. D. J. Creeth et al. PLOS BIOLOGY
- Schaaf-Yang syndrome overview: Report of 78 individuals
- (2018) John McCarthy et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Intragenomic conflict over bet-hedging
- (2018) Jon F. Wilkins et al. PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES
- New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome
- (2017) Jasmin Beygo et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Temple syndrome: comprehensive molecular and clinical findings in 32 Japanese patients
- (2017) Masayo Kagami et al. GENETICS IN MEDICINE
- Loss of offspring Peg3 reduces neonatal ultrasonic vocalizations and increases maternal anxiety in wild-type mothers
- (2017) G I McNamara et al. HUMAN MOLECULAR GENETICS
- Imprinted genes and the regulation of placental endocrine function: Pregnancy and beyond
- (2017) Rosalind M. John PLACENTA
- The imprinted Phlda2 gene modulates a major endocrine compartment of the placenta to regulate placental demands for maternal resources
- (2016) S.J. Tunster et al. DEVELOPMENTAL BIOLOGY
- Deletion of the miR-379/miR-410 gene cluster at the imprintedDlk1-Dio3locus enhances anxiety-related behaviour
- (2016) Virginie Marty et al. HUMAN MOLECULAR GENETICS
- Paradoxical leanness in the imprinting-centre deletion mouse model for Prader–Willi syndrome
- (2016) David M Golding et al. JOURNAL OF ENDOCRINOLOGY
- Targeting the histone methyltransferase G9a activates imprinted genes and improves survival of a mouse model of Prader–Willi syndrome
- (2016) Yuna Kim et al. NATURE MEDICINE
- Maternal prenatal depression is associated with decreased placental expression of the imprinted gene PEG3
- (2016) A. B. Janssen et al. PSYCHOLOGICAL MEDICINE
- Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders
- (2016) Anthony R. Isles et al. PLoS Genetics
- Genomic imprinting in the human placenta
- (2015) David Monk AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY
- Comprehensive clinical studies in 34 patients with molecularly defined UPD(14)pat and related conditions (Kagami–Ogata syndrome)
- (2015) Masayo Kagami et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Calorie seeking, but not hedonic response, contributes to hyperphagia in a mouse model for Prader-Willi syndrome
- (2015) Jennifer R. Davies et al. EUROPEAN JOURNAL OF NEUROSCIENCE
- No Evidence for Enrichment in Schizophrenia for Common Allelic Associations at Imprinted Loci
- (2015) Valentina Escott-Price et al. PLoS One
- Towards a therapy for Angelman syndrome by targeting a long non-coding RNA
- (2014) Linyan Meng et al. NATURE
- Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
- (2014) John R. B. Perry et al. NATURE
- Cross-talk between imprinted loci in Prader-Willi syndrome
- (2014) Adele Murrell NATURE GENETICS
- The noncoding RNA IPW regulates the imprinted DLK1-DIO3 locus in an induced pluripotent stem cell model of Prader-Willi syndrome
- (2014) Yonatan Stelzer et al. NATURE GENETICS
- The role of genomic imprinting in biology and disease: an expanding view
- (2014) Jo Peters NATURE REVIEWS GENETICS
- Dosage-sensitivity of imprinted genes expressed in the brain: 15q11–q13 and neuropsychiatric illness: Figure 1
- (2013) Gráinne I. McNamara et al. BIOCHEMICAL SOCIETY TRANSACTIONS
- Analysis of copy number variations at 15 schizophrenia-associated loci
- (2013) Elliott Rees et al. BRITISH JOURNAL OF PSYCHIATRY
- Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism
- (2013) Christian P Schaaf et al. NATURE GENETICS
- Placental hormones and the control of maternal metabolism and fetal growth
- (2013) Dorothee Newbern et al. Current Opinion in Endocrinology Diabetes and Obesity
- Placental programming of anxiety in adulthood revealed by Igf2-null models
- (2013) Mikael Allan Mikaelsson et al. Nature Communications
- Prader-Willi syndrome
- (2012) Suzanne B. Cassidy et al. GENETICS IN MEDICINE
- Maternal-fetal resource allocation: Co-operation and conflict
- (2012) A.L. Fowden et al. PLACENTA
- Maternally Derived Microduplications at 15q11-q13: Implication of Imprinted Genes in Psychotic Illness
- (2011) Andrés Ingason et al. AMERICAN JOURNAL OF PSYCHIATRY
- Genomic Imprinting: A Mammalian Epigenetic Discovery Model
- (2011) Denise P. Barlow Annual Review of Genetics
- Genomic imprinting; the cost of mother's care
- (2011) Anthony R. Isles BIOESSAYS
- Developmental regulation of somatic imprints
- (2011) Rosalind M. John et al. DIFFERENTIATION
- Topoisomerase inhibitors unsilence the dormant allele of Ube3a in neurons
- (2011) Hsien-Sung Huang et al. NATURE
- Postnatal loss of Dlk1 imprinting in stem cells and niche astrocytes regulates neurogenesis
- (2011) Sacri R. Ferrón et al. NATURE
- Genomic imprinting: the emergence of an epigenetic paradigm
- (2011) Anne C. Ferguson-Smith NATURE REVIEWS GENETICS
- Increased Gene Dosage of Ube3a Results in Autism Traits and Decreased Glutamate Synaptic Transmission in Mice
- (2011) S. E. P. Smith et al. Science Translational Medicine
- Early Life Programming and Neurodevelopmental Disorders
- (2010) Tracy L. Bale et al. BIOLOGICAL PSYCHIATRY
- The Angelman Syndrome Protein Ube3A Regulates Synapse Development by Ubiquitinating Arc
- (2010) Paul L. Greer et al. CELL
- Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader–Willi syndrome
- (2010) Angela L Duker et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- A Single-Tube Quantitative High-Resolution Melting Curve Method for Parent-of-Origin Determination of 15q Duplications
- (2010) Nora Urraca et al. Genetic Testing and Molecular Biomarkers
- Altered Ultrasonic Vocalization and Impaired Learning and Memory in Angelman Syndrome Mouse Model with a Large Maternal Deletion from Ube3a to Gabrb3
- (2010) Yong-hui Jiang et al. PLoS One
- Behavioural and cognitive abnormalities in an imprinting centre deletion mouse model for PraderâWilli syndrome
- (2009) Dinko Relkovic et al. EUROPEAN JOURNAL OF NEUROSCIENCE
- Parental origin of sequence variants associated with complex diseases
- (2009) Augustine Kong et al. NATURE
- Prenatal Malnutrition and Adult Schizophrenia: Further Evidence From the 1959-1961 Chinese Famine
- (2009) Ming-Qing Xu et al. SCHIZOPHRENIA BULLETIN
- Genomic imprinting and disorders of the social brain; shades of grey rather than black and white
- (2008) William Davies et al. BEHAVIORAL AND BRAIN SCIENCES
- Psychosis and autism as diametrical disorders of the social brain
- (2008) Bernard Crespi et al. BEHAVIORAL AND BRAIN SCIENCES
- Battle of the sexes may set the brain
- (2008) Christopher Badcock et al. NATURE
- Prader-Willi and snoRNAs
- (2008) Jo Peters NATURE GENETICS
- Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster
- (2008) Trilochan Sahoo et al. NATURE GENETICS
- SnoRNA Snord116 (Pwcr1/MBII-85) Deletion Causes Growth Deficiency and Hyperphagia in Mice
- (2008) Feng Ding et al. PLoS One
- Persistent epigenetic differences associated with prenatal exposure to famine in humans
- (2008) B. T. Heijmans et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
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