Sophie Farrow

University of Auckland — New Zealand

Medicine · Health Sciences

8h-index204citations18works5.52yr avg
OpenAlex↗ORCID↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Parkinson's Disease Mechanisms and Treatments(7), RNA regulation and disease(5), Genomics and Chromatin Dynamics(4), Genetic Associations and Epidemiology(4), Genomics and Rare Diseases(4)

Publications18 total

Replication-first reciprocal genome editing resolves ANKRD1 as a convergent regulatory target at the 17q21.31 locus
2026Open Access
From blood vessels to brain cells: Connecting the circulatory system and Parkinson's disease
Journal of Parkinson s Disease·2025· 2 citedOpen Access
Benchmarking nanopore sequencing and rapid genomics feasibility: validation at a quaternary hospital in New Zealand
npj Genomic Medicine·2024· 13 citedOpen Access
Benchmarking and quality control for nanopore sequencing and feasibility of rapid genomics in New Zealand: validation phase at a single quaternary hospital
2024Open Access
Identification of 27 allele-specific regulatory variants in Parkinson’s disease using a massively parallel reporter assay
npj Parkinson s Disease·2024· 10 citedOpen Access
Discovering genetic mechanisms underlying the co-occurrence of Parkinson’s disease and non-motor traits
npj Parkinson s Disease·2024· 8 citedOpen Access
Fine-mapping identifies 27 allele-specific MPRA regulatory variants in Parkinson’s disease related loci
Research Square (Research Square)·2023Open Access
Identifying the genetic links between Parkinson’s disease and non-motor symptoms: novel insights into disease mechanisms
Research Square (Research Square)·2023· 1 citedOpen Access
Redefining the hypotheses driving Parkinson’s diseases research
npj Parkinson s Disease·2022· 26 citedOpen Access
Establishing gene regulatory networks from Parkinson’s disease risk loci
Brain·2022· 20 citedOpen Access
Machine Learning Identifies Six Genetic Variants and Alterations in the Heart Atrial Appendage as Key Contributors to PD Risk Predictivity
Frontiers in Genetics·2022· 10 citedOpen Access
Integrating Multimorbidity into a Whole-Body Understanding of Disease Using Spatial Genomics
Results and problems in cell differentiation·2022· 1 cited
Assigning function to SNPs: Considerations when interpreting genetic variation
Seminars in Cell and Developmental Biology·2021· 45 cited
Machine learning identifies six genetic variants and alterations in the Heart Atrial Appendage as key contributors to PD risk predictivity
2021· 3 citedOpen Access
Establishing gene regulatory networks from Parkinson’s disease risk loci
2021· 8 citedOpen Access
Genetic variants associated with alcohol dependence co-ordinate regulation of ADH genes in gastrointestinal and adipose tissues
Scientific Reports·2020· 8 citedOpen Access
Common Variants Coregulate Expression of <scp><i>GBA</i></scp> and Modifier Genes to Delay Parkinson's Disease Onset
Movement Disorders·2020· 31 citedOpen Access
A transcription regulatory network within the ACE2 locus may promote a pro-viral environment for SARS-CoV-2 by modulating expression of host factors
2020· 18 citedOpen Access

Frequent Co-authors

Justin M. O’Sullivan(17), Antony A. Cooper(13), William Schierding(10), Sreemol Gokuladhas(9), Tayaza Fadason(8), Denis M. Nyaga(6), Evgeniia Golovina(5), Jo K. Perry(3), Daniel Ho(3), Peter Tsai(2), Clare Gebbie(2), Hui Hui Phua(2), Patrick Yap(2), Polona Le Quesne Stabej(2), Jing Rong(2), Gergely Toldi(2), Eric B. Thorstensen(2), Zornitza Stark(2), Sebastian Lunke(2), Kimberley Gamet(2)