Flint, Jonathan.
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Jonathan Flint British behavior geneticist
Flint, J
VIAF ID: 74163883 (Personal)
Permalink: http://viaf.org/viaf/74163883
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Flint, Jonathan
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Flint, Jonathan
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Flint, Jonathan
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100 1 _ ‡a Flint, Jonathan
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100 1 _ ‡a Flint, Jonathan
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100 1 _ ‡a Flint, Jonathan
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Flint, Jonathan
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Flint, Jonathan
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100 1 _ ‡a Flint, Jonathan.
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Jonathan Flint
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British behavior geneticist
4xx's: Alternate Name Forms (3)
5xx's: Related Names (2)
Works
| Title | Sources |
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| Commentary: Response to commentary by Rutter on Munafo et al. (2014) |
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| How genes influence behavior |
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| Intragenic enhancers act as alternative promoters |
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| Is there an association between NPY and neuroticism? |
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| Is there an excess of significant findings in published studies of psychotherapy for depression? |
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| Is this mouse anxious? The difficulties of interpreting the effects of genetic action. Commentary on Belzung "The genetic basis of the pharmacological effects of anxiolytics" and Olivier et al. "The 5-HT(1A) receptor knockout mouse and anxiety". |
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| JEPEGMIX2-P: a novel transcriptomic pathway method that greatly enhances detection of the molecular underpinnings for complex traits |
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| Lack of association of the COMT |
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| Lack of consistent behavioural effects of Maudsley reactive and non-reactive rats in a number of animal tests of anxiety and activity |
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| Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A). |
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| Learned fear, emotional reactivity and fear of heights: a factor analytic map from a large F(2) intercross of Roman rat strains |
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| Leveraging eQTLs to identify individual-level tissue of interest for a complex trait |
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| Linkage analysis of extremely discordant and concordant sibling pairs identifies quantitative-trait loci that influence variation in the human personality trait neuroticism |
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| Little epistasis for anxiety-related measures in the DeFries strains of laboratory mice |
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| Management, presentation and interpretation of genome scans using GSCANDB. |
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| Mapping in structured populations by resample model averaging |
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| Mapping regulatory variants for the serotonin transporter gene based on allelic expression imbalance |
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| Meta-analyses of genome-wide linkage scans of anxiety-related phenotypes |
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| Minisatellite mutational processes reduce Fst estimates |
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| Molecular-cytogenetic detection of a deletion of 1p36.3. |
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| Molecular signatures of major depression |
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| Mouse genomic variation and its effect on phenotypes and gene regulation |
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| Multi-telomere FISH. |
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| Multiple laboratory mouse reference genomes define strain specific haplotypes and novel functional loci |
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| Mutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypes |
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| Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans |
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| Mutations in the beta-tubulin gene TUBB2B result in asymmetrical polymicrogyria |
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| Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans |
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| Natural polymorphisms in Tap2 influence negative selection and CD4∶CD8 lineage commitment in the rat |
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| The nature and identification of quantitative trait loci: a community's view |
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| Neuregulin 1 genotype and schizophrenia |
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| Neurogenomic evidence for a shared mechanism of the antidepressant effects of exercise and chronic fluoxetine in mice |
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| New semidominant mutations that affect mouse development |
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| Next-generation sequencing of experimental mouse strains |
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| No association between the BDNF Val66Met polymorphism and mood status in a non-clinical community sample of 7389 older adults |
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| Novel alpha haemoglobin haplotypes in horses |
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| An optimized set of human telomere clones for studying telomere integrity and architecture. |
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| Outside in |
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| Perfect endings: a review of subtelomeric probes and their use in clinical diagnosis |
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| Population bottlenecks in Polynesia revealed by minisatellites |
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| The population genetics of the haemoglobinopathies |
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| Power failure: why small sample size undermines the reliability of neuroscience |
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| Practice parameter: evaluation of the child with global developmental delay: report of the Quality Standards Subcommittee of the American Academy of Neurology and The Practice Committee of the Child Neurology Society |
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| Practitioner review: A critical perspective on gene-environment interaction models--what impact should they have on clinical perceptions and practice? |
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| Prioritization and association analysis of murine-derived candidate genes in anxiety-spectrum disorders |
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| Progress and prospects in rat genetics: a community view. |
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| Promise and pitfalls in the meta-analysis of genetic association studies: a response to Sen and Schinka |
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| Prospects for complex trait analysis in the mouse. |
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| Psychiatric diagnoses and disease |
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| QTL analysis of multiple behavioral measures of anxiety in mice |
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| QTL fine-mapping with recombinant-inbred heterogeneous stocks and in vitro heterogeneous stocks |
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| Quantitative trait locus mapping in laboratory mice derived from a replicated selection experiment for open-field activity |
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| Rapid genotype imputation from sequence without reference panels |
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| Rare genetic variants and schizophrenia |
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| Ha-ras hypervariable alleles in myelodysplasia |
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| Replication and heterogeneity in gene x environment interaction studies |
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| Resemblance of symptoms for major depression assessed at interview versus from hospital record review |
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| Response to Manly: Statistical stringency in tests of genetic association – implications for sample size and study design |
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| RETRACTED ARTICLE: 11,670 whole-genome sequences representative of the Han Chinese population from the CONVERGE project |
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| Reverse GWAS: Using genetics to identify and model phenotypic subtypes |
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| Screening chromosome ends for learning disability |
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| Sequence-based characterization of structural variation in the mouse genome |
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| Sequence comparison of human and yeast telomeres identifies structurally distinct subtelomeric domains |
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| Sequence, structure and pathology of the fully annotated terminal 2 Mb of the short arm of human chromosome 16 |
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| A simple genetic basis for a complex psychological trait in laboratory mice |
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| Simultaneous detection and fine mapping of quantitative trait loci in mice using heterogeneous stocks. |
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| So You Want Your Child to Be a Genius? |
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| Social adversity, the serotonin transporter (5-HTTLPR) polymorphism and major depressive disorder |
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| Spatial memory dissociations in mice lacking GluR1. |
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| Strategies for mapping and cloning quantitative trait genes in rodents |
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| Structure and evolution of the horse zeta globin locus |
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| Submicroscopic 8pter deletion, mild mental retardation, and behavioral problems caused by a familial t(8;20)(p23;p13). |
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| Submicroscopic subtelomeric 1qter deletions: a recognisable phenotype? |
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| Subtle chromosomal rearrangements in children with unexplained mental retardation |
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| Suicidal risk factors of recurrent major depression in Han Chinese women |
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| SW-ARRAY: a dynamic programming solution for the identification of copy-number changes in genomic DNA using array comparative genome hybridization data |
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| Swab-Seq: A high-throughput platform for massively scaled up SARS-CoV-2 testing |
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| Testing the genetics of behavior in mice. |
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| Transgenic and knockout models of neuropsychiatric disorders |
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| Unexpected complexity in the haplotypes of commonly used inbred strains of laboratory mice |
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| Unlearned anxiety predicts learned fear: a comparison among heterogeneous rats and the Roman rat strains. |
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| Using progenitor strain information to identify quantitative trait nucleotides in outbred mice |
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| Why are some genetic diseases common? Distinguishing selection from other processes by molecular analysis of globin gene variants |
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