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Number of items: 20.


Billingsley, Kimberley, Quinn, John ORCID: 0000-0003-3551-7803 and Bubb, Vivien ORCID: 0000-0003-2763-7004
(2019) Analysis of repetitive element expression in the blood and skin of patients with Parkinson’s disease identifies differential expression of satellite elements. Scientific Reports, 9 (1). 4369-.


Khursheed, Kejhal ORCID: 0000-0002-3778-1643, Wilm, Thomas, Cashman, Christine, Quinn, John ORCID: 0000-0003-3551-7803, Bubb, Vivien ORCID: 0000-0003-2763-7004 and Moss, Diana
(2015) Characterisation of multiple regulatory domains spanning the major transcriptional start site of the FUS gene, a candidate gene for motor neurone disease. Brain Research, 1595. pp. 1-9.


Warburton, Alix, Breen, Gerome, Rujescu, D, Bubb, Vivien ORCID: 0000-0003-2763-7004 and Quinn, John ORCID: 0000-0003-3551-7803
(2015) Characterization of a REST-Regulated Internal Promoter in the Schizophrenia Genome-Wide Associated Gene MIR137. Schizophrenia Bulletin, 41 (3). pp. 698-707.


Koron, R
(2018) DNA signatures as a predictor of breast cancer risk. Doctor of Medicine thesis, University of Liverpool.


Savage, Abigail ORCID: 0000-0002-2231-9800, Wilm, Thomas, Khursheed, Kejhal ORCID: 0000-0002-3778-1643, Shatunov, Alexsey ORCID: 0000-0002-2671-8040, Morrison, Karen, Shaw, Pamela, Shaw, Christopher, Smith, Bradley, Breen, Gerome, Al-Chalabi, Ammar
et al (show 3 more authors) (2014) An Evaluation of a SVA Retrotransposon in the FUS Promoter as a Transcriptional Regulator and Its Association to ALS. PLoS ONE, 9 (6). e90833-.


Warburton, Alix, Breen, Gerome, Bubb, Vivien ORCID: 0000-0003-2763-7004 and Quinn, John ORCID: 0000-0003-3551-7803
(2016) A GWAS SNP for Schizophrenia Is Linked to the Internal MIR137 Promoter and Supports Differential Allele-Specific Expression. Schizophrenia Bulletin, 42 (4). pp. 1003-1008.


Billingsley, Kimberley, Barbosa, Ines, Bandrés-Ciga, Sara, Quinn, John ORCID: 0000-0003-3551-7803, Bubb, Vivien, Deshpande, Charu, Botia, Juan, Reynolds, Regina, Zhang, David, Simpson, Michael ORCID: 0000-0002-8539-8753
et al (show 8 more authors) (2018) Genetic variation within genes associated with mitochondrial function is significantly associated with later age at onset of Parkinson disease and contributes to disease risk. BioRxiv.


Billingsley, Kimberley J, Ding, Jinhui, Jerez, Pilar Alvarez, Illarionova, Anastasia, Levine, Kristin, Grenn, Francis P, Makarious, Mary B, Moore, Anni, Vitale, Daniel, Reed, Xylena
et al (show 31 more authors) (2023) Genome-Wide Analysis of Structural Variants in Parkinson Disease. ANNALS OF NEUROLOGY, 93 (5). pp. 1012-1022.


Illera, Ana
(2019) Healthy cognitive ageing: focussing on the role of repetitive DNA elements. PhD thesis, University of Liverpool.


Savage, Abigail
Hominid retrotransposons as a modulator of genomic function. Doctor of Philosophy thesis, University of Liverpool.


Nalls, Mike A, Blauwendraat, Cornelis, Vallerga, Costanza L, Heilbron, Karl, Bandres-Ciga, Sara, Chang, Diana, Tan, Manuela, Kia, Demis A, Noyce, Alastair J, Xue, Angli
et al (show 260 more authors) (2019) Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies. The Lancet Neurology, 18 (12). pp. 1091-1102.


Kõks, Sulev, Pfaff, Abigail, Bubb, Vivien ORCID: 0000-0003-2763-7004 and Quinn, John ORCID: 0000-0003-3551-7803
(2021) Longitudinal intronic RNA-Seq analysis of Parkinson’s Disease patients reveals disease-specific nascent transcription.


Gillies, Stuart
The NRSF and USF transcription factor families regulate pro-convulsant neuropeptides and are targets for anti-convulsant drug treatment: implications for epilepsy. Doctor of Philosophy thesis, University of Liverpool.


Pfaff, Abigail, Bubb, Vivien ORCID: 0000-0003-2763-7004, Quinn, John and Koks, Sulev ORCID: 0000-0001-6087-6643
(2020) Reference SVA insertion polymorphisms are associated with dopaminergic degeneration in Parkinson’s Disease and differential gene expression in the PPMI cohort. Unknown.


Price, Emma ORCID: 0000-0002-7538-7831
(2020) Retrotransposons in chronic pain: focusing on roles in gene regulation and neuroinflammation. PhD thesis, University of Liverpool.


Savage, AL ORCID: 0000-0002-2231-9800, Schumann, Gerald, Breen, Gerome, Bubb, Vivien ORCID: 0000-0003-2763-7004, Al-Chalabi, Ammar and Quinn, John ORCID: 0000-0003-3551-7803
(2019) Retrotransposons in the development and progression of amyotrophic lateral sclerosis. Journal of Neurology Neurosurgery and Psychiatry, 90 (3). pp. 284-293.


Koks, Sulev ORCID: 0000-0001-6087-6643, Pfaff, Abigail, Bubb, Vivien and Quinn, John ORCID: 0000-0003-3551-7803
(2021) Transcript Variants of Genes Involved in Neurodegeneration Are Differentially Regulated by the Apoe and Mapt Haplotypes. Genes.


Hall, Ashley ORCID: 0000-0003-2962-6384
(2022) Transposable elements and SVA insertion polymorphisms in gene regulation and Parkinson’s Disease. PhD thesis, University of Liverpool.


Middlehurst, Ben
(2021) The role of endogenous retrotransposable elements in Parkinson’s disease. PhD thesis, University of Liverpool.


Marshall, Jack
(2021) The role of non-coding tandem repeat DNA and non-LTR retrotransposons in Amyotrophic Lateral Sclerosis risk loci. PhD thesis, University of Liverpool.

This list was generated on Fri Jan 26 01:57:26 2024 GMT.