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Cyfip1 haploinsufficiency increases compulsive-like behavior and modulates palatable food intake: Implications for Prader-Willi Syndrome

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/eat.10140openalex-snapshot

Genetic and environmental contributions to obesity and binge eating

inferredcites →https://doi.org/10.1007/s00213-015-3967-1openalex-snapshot

Developmental emergence of an obsessive-compulsive phenotype and binge behavior in rats

inferredcites →https://doi.org/10.1007/s00213-015-4147-zopenalex-snapshot

Systems genetics of intravenous cocaine self-administration in the BXD recombinant inbred mouse panel

inferredcites →https://doi.org/10.1007/s40618-015-0312-9openalex-snapshot

Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings

inferredcites →https://doi.org/10.1016/j.appet.2012.05.022openalex-snapshot

Assessing binge eating. An analysis of data previously collected in bingeing rats

inferredcites →https://doi.org/10.1016/j.appet.2015.12.021openalex-snapshot

A review of chemosensory perceptions, food preferences and food-related behaviours in subjects with Prader–Willi Syndrome

inferredcites →https://doi.org/10.1016/j.bbr.2005.09.003openalex-snapshot

Individual differences in novelty-seeking behavior but not in anxiety response to a new environment can predict nicotine consumption in adolescent C57BL/6 mice

inferredcites →https://doi.org/10.1016/j.bbr.2006.01.018openalex-snapshot

Comparisons between anxiety tests for selection of anxious and non anxious mice

inferredcites →https://doi.org/10.1016/j.bbr.2007.10.029openalex-snapshot

Development of a mouse test for repetitive, restricted behaviors: Relevance to autism

inferredcites →https://doi.org/10.1016/j.biopsych.2006.03.040openalex-snapshot

The Prevalence and Correlates of Eating Disorders in the National Comorbidity Survey Replication

inferredcites →https://doi.org/10.1016/j.biopsych.2016.10.021openalex-snapshot

Cytoplasmic FMR1-Interacting Protein 2 Is a Major Genetic Factor Underlying Binge Eating

inferredcites →https://doi.org/10.1016/j.brainres.2015.10.015openalex-snapshot

Parental origin impairment of synaptic functions and behaviors in cytoplasmic FMRP interacting protein 1 (Cyfip1) deficient mice

inferredcites →https://doi.org/10.1016/j.neuron.2014.03.028openalex-snapshot

Fragile X Mental Retardation Protein Regulates Synaptic and Behavioral Plasticity to Repeated Cocaine Administration

inferredcites →https://doi.org/10.1016/j.physbeh.2016.05.013openalex-snapshot

Emotional profile of female rats showing binge eating behavior

inferredcites →https://doi.org/10.1016/j.ygeno.2005.02.004openalex-snapshot

A nonimprinted Prader–Willi Syndrome (PWS)-region gene regulates a different chromosomal domain in trans but the imprinted pws loci do not alter genome-wide mRNA levels

inferredcites →https://doi.org/10.1017/s0033291710000139openalex-snapshot

Binge eating disorder: a symptom-level investigation of genetic and environmental influences on liability

inferredcites →https://doi.org/10.1038/ijo.2011.204openalex-snapshot

Importance of reward and prefrontal circuitry in hunger and satiety: Prader–Willi syndrome vs simple obesity

inferredcites →https://doi.org/10.1038/mp.2014.124openalex-snapshot

Increased CYFIP1 dosage alters cellular and dendritic morphology and dysregulates mTOR

inferredcites →https://doi.org/10.1038/mp.2016.71openalex-snapshot

Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index

inferredcites →https://doi.org/10.1038/mp.2017.88openalex-snapshot

Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa

inferredcites →https://doi.org/10.1038/nature10163openalex-snapshot

A conditional knockout resource for the genome-wide study of mouse gene function

inferredcites →https://doi.org/10.1038/ncomms2336openalex-snapshot

Displays of paternal mouse pup retrieval following communicative interaction with maternal mates

inferredcites →https://doi.org/10.1038/ng.2776openalex-snapshot

Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism

inferredcites →https://doi.org/10.1038/nn.3202openalex-snapshot

The drive to eat: comparisons and distinctions between mechanisms of food reward and drug addiction

inferredcites →https://doi.org/10.1038/nprot.2008.73openalex-snapshot

Analyzing real-time PCR data by the comparative CT method

inferredcites →https://doi.org/10.1038/s41398-017-0085-3openalex-snapshot

Bipolar disorder with binge eating behavior: a genome-wide association study implicates PRR5-ARHGAP8

inferredcites →https://doi.org/10.1038/tp.2014.16openalex-snapshot

The autism and schizophrenia associated gene CYFIP1 is critical for the maintenance of dendritic complexity and the stabilization of mature spines

inferredcites →https://doi.org/10.1073/pnas.151231598openalex-snapshot

A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P

inferredcites →https://doi.org/10.1097/00004583-199903000-00021openalex-snapshot

Obsessive-Compulsive Symptoms in Prader-Willi and “Prader-Willi—Like” Patients

inferredcites →https://doi.org/10.1098/rstb.2016.0355openalex-snapshot

When the Lyon(ized chromosome) roars: ongoing expression from an inactive X chromosome

inferredcites →https://doi.org/10.1111/cen.12766openalex-snapshot

Metabolic profiling in Prader–Willi syndrome and nonsyndromic obesity: sex differences and the role of growth hormone

inferredcites →https://doi.org/10.1111/gbb.12143openalex-snapshot

Sex chromosome complement influences operant responding for a palatable food in mice

inferredcites →https://doi.org/10.1111/gbb.12397openalex-snapshot

Casein kinase 1‐epsilon deletion increases mu opioid receptor‐dependent behaviors and binge eating1

inferredcites →https://doi.org/10.1111/j.1365-2788.1985.tb00313.xopenalex-snapshot

TYPE AND STRENGTH OF FOOD PREFERENCES OF INDIVIDUALS WITH PRADER‐WILLI SYNDROME*

inferredcites →https://doi.org/10.1111/j.1365-2788.2006.00812.xopenalex-snapshot

An investigation into food preferences and the neural basis of food‐related incentive motivation in Prader–Willi syndrome

inferredcites →https://doi.org/10.1111/j.1365-2788.2006.00916.xopenalex-snapshot

The relationship between compulsive behaviour and academic achievement across the three genetic subtypes of Prader–Willi syndrome

inferredcites →https://doi.org/10.1111/j.1469-7610.1996.tb01496.xopenalex-snapshot

Obsessions and Compulsions in Prader‐Willi Syndrome

inferredcites →https://doi.org/10.1111/j.1469-7610.2005.01520.xopenalex-snapshot

Prader‐Willi syndrome: intellectual abilities and behavioural features by genetic subtype

inferredcites →https://doi.org/10.1136/jmg.32.12.925openalex-snapshot

X inactivation of the FMR1 fragile X mental retardation gene.

inferredcites →https://doi.org/10.1155/2015/294127openalex-snapshot

Gender Differences in the Behavioral Symptom Severity of Prader-Willi Syndrome

inferredcites →https://doi.org/10.1371/journal.pgen.1003207openalex-snapshot

Magel2 Is Required for Leptin-Mediated Depolarization of POMC Neurons in the Hypothalamic Arcuate Nucleus in Mice

inferredcites →https://doi.org/10.1371/journal.pgen.1005713openalex-snapshot

Hnrnph1 Is A Quantitative Trait Gene for Methamphetamine Sensitivity

inferredcites →https://doi.org/10.1371/journal.pgen.1006498openalex-snapshot

Genetic Variation in the Social Environment Contributes to Health and Disease

inferredcites →https://doi.org/10.1371/journal.pone.0042422openalex-snapshot

Haploinsufficiency of Cyfip1 Produces Fragile X-Like Phenotypes in Mice

inferredcites →https://doi.org/10.1371/journal.pone.0077896openalex-snapshot

Changes in Sensitivity of Reward and Motor Behavior to Dopaminergic, Glutamatergic, and Cholinergic Drugs in a Mouse Model of Fragile X Syndrome

inferredcites →https://doi.org/10.1523/jneurosci.0511-15.2016openalex-snapshot

Cyfip1 Regulates Presynaptic Activity during Development

inferredcites →https://doi.org/10.1542/peds.2006-0424openalex-snapshot

Expression of 4 Genes Between Chromosome 15 Breakpoints 1 and 2 and Behavioral Outcomes in Prader-Willi Syndrome

inferredcites →https://doi.org/10.17615/rdkb-n146openalex-snapshot

C57BL/6N Mutation in Cytoplasmic FMRP interacting protein 2 Regulates Cocaine Response

inferredcites →https://doi.org/10.3389/fnbeh.2014.00450openalex-snapshot

Behavioral architecture of opioid reward and aversion in C57BL/6 substrains

inferredcites →https://doi.org/10.3390/diseases4010002openalex-snapshot

Prader-Willi Syndrome and Schaaf-Yang Syndrome: Neurodevelopmental Diseases Intersecting at the MAGEL2 Gene

inferredcites →https://doi.org/10.3791/50978openalex-snapshot

Marble Burying and Nestlet Shredding as Tests of Repetitive, Compulsive-like Behaviors in Mice

inferredcites →https://doi.org/10.3945/jn.108.097618openalex-snapshot

Homeostatic and Hedonic Signals Interact in the Regulation of Food Intake

inferredcites →https://doi.org/10.5582/irdr.2016.01082openalex-snapshot

The neurobiology of the Prader-Willi phenotype of fragile X syndrome

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1001/jamapsychiatry.2019.3779openalex-snapshot

Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition

inferred← citeshttps://doi.org/10.1016/j.physbeh.2018.09.013openalex-snapshot

Genetic differences in the behavioral organization of binge eating, conditioned food reward, and compulsive-like eating in C57BL/6J and DBA/2J strains

inferred← citeshttps://doi.org/10.3390/ijms20061459openalex-snapshot

Parent-of-Origin Effects in 15q11.2 BP1-BP2 Microdeletion (Burnside-Butler) Syndrome

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