严重精神疾病代谢异质性的遗传聚类与单细胞功能基因组学研究博士研究员

PhD Studentship: Dissecting Metabolic Heterogeneity in Severe Mental Illness Through Genetic Clustering and Single-Cell Functional Genomics

University of Exeter · 英国 · Exeter

原帖优先:申请材料、截止时间与资格以原帖和学校官方说明为准。

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研究内容
本博士项目旨在通过遗传聚类和单细胞功能基因组学,剖析严重精神疾病(如精神分裂症和双相情感障碍)中代谢异质性的原因,探讨不同精神疾病遗传易感成分如何通过不同生物学途径影响代谢健康。
申请条件
原文未明确列出具体的学位等级、专业背景或成绩要求,但指出项目将提供统计遗传学、生物信息学、单细胞基因组学及分子细胞生物学等方面的多学科培训。
待遇
提供学费资助以及2026/7学年每年21,805英镑的生活津贴(stipend),由工程与物理科学研究委员会(EPSRC)资助。
申请方式
原文未提供具体的申请网址、截止日期操作细则或材料提交地址(提示截止日期为2026-12-08)。

由 gemini-2.5-flash-lite 生成,博士岗判定置信度 100%。

岗位信息

截止
(Europe/London) 剩 39 天
学科
生物化学、遗传与分子生物学
合同类型
雇佣合同
原文薪资
GBP 21,805 / 年(税前)
税后月薪(估)
¥13,700;房租后 ¥5,400
估算假设
单身、无子女、雇佣合同的粗略估算,以学校 offer 为准;扣除率 18%;汇率日期 2026-10-01
原帖发布
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内容更新
原帖导师候选(待核验)
Tyrrell
来源
jobs.ac.uk(英国博士项目及学术招聘) · 最近核对 2026-10-29
详情核验
判定依据(原文摘录)
  • 工作语言为英语(未提及本地语言要求),且提供奖学金资助
    The studentship will provide funding of fees and a stipend of £21,805 per annum for 2026/7.
原文

This PhD aims to understand why genetic liability to severe mental illness (SMI), particularly schizophrenia and bipolar disorder, is associated with different patterns of adiposity and metabolic health. Although obesity and type 2 diabetes (T2D) are more common in people with SMI, substantial heterogeneity exists, with many individuals remaining metabolically healthy despite a high burden of SMI risk.

We hypothesise distinct components of psychiatric genetic liability influence metabolic health through different biological pathways, with some increasing susceptibility to obesity and T2D while others have little metabolic consequence. The PhD builds on recent work led by supervisor Tyrrell demonstrating that genetic liability to major depressive disorder comprises biologically distinct clusters of variants with contrasting effects on T2D.

Building on this, the student will apply genetic clustering approaches to SMI traits to identify biologically distinct components of psychiatric risk that differentially influence obesity and T2D. By integrating statistical genetics, causal inference approaches and functional genomics, the PhD will move beyond psychiatric diagnoses as single entities to identify the biological mechanisms underlying metabolic heterogeneity.

First, the PhD will identify genetically distinct clusters of psychiatric risk variants using large-scale genome-wide association study data and characterise their associations with obesity and T2D. The biological and clinical consequences of these clusters will be explored across population biobanks. The PhD will then investigate the cellular mechanisms underlying these genetic pathways using unique single-cell multiomic datasets generated in Exeter. By integrating genetic association data with cell-type-specific gene expression and chromatin accessibility data, the student will determine whether metabolically distinct psychiatric risk pathways act through different neuronal and glial cell populations and identify the genes and regulatory networks involved.

Selected regulatory elements and candidate genes emerging from these analyses will be prioritised for functional investigation using experimental approaches (e.g. CRISPR-based perturbation, neuronal cell models). This will provide mechanistic insight into how distinct components of SMI genetic liability influence both brain function and metabolic health. The PhD will provide multidisciplinary training in statistical genetics, genetic epidemiology, bioinformatics, single-cell genomics and functional genomics.

The student will gain experience in large-scale genomic datasets, causal inference and clustering methods, integrating transcriptomic data, and undertaking lab-based functional studies. Training in R, Python and high-performance computing will be complemented by experimental skills in molecular and cellular biology. While the PhD has clearly defined objectives, there will be considerable scope for the student to shape the direction of the PhD according to their interests and emerging findings.

Opportunities may include focusing on a specific SMI, ancestry-specific mechanisms, method development, particular neuronal cell populations, or in-depth functional characterisation of candidate genes. This flexibility will support the development of an independent research profile. This PhD will address a key question in psychiatric and metabolic disease biology: why do some individuals with a high SMI genetic liability develop obesity and metabolic complications whilst others remain metabolically healthy?

By identifying biologically distinct components of SMI risk and characterising the molecular mechanisms, the PhD has the potential to reveal new pathways linking brain function and metabolic regulation, improve understanding of disease heterogeneity, and identify novel targets. It will equip the student with a broad, highly transferable skills relevant to careers in academia, biotechnology and precision medicine.

Funded by: EPSRC Engineering and Physical Sciences Research Council £21,805. The studentship will provide funding of fees and a stipend of £21,805 per annum for 2026/7.

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