Author
UCL Queen Square Institute of NeurologyORCID 0009-0009-5289-0010Unclaimed ORCID profile · follow to get notified of new preprints
6 papers
Recent·Most cited
Katherine Fodder, Megha N. Murthy, Joshua Harvey, Ehsan Pishva, Katie Lunnon, Towfique Raj, Kurt W. Farrell, Rohan de Silva, Jack Humphrey, Conceição Bettencourt
The paper identifies shared genetic and epigenetic mechanisms at the MOBP locus linking ALS and PSP, with distinct patterns from MSA.
bioRxiv · Sep 1, 2026 · PreprintNeuroscience
Katherine Fodder, Hannah M. G. Smith, Ümran Yaman, Ignazio Stefano Piras, Megha N. Murthy, John Hardy, Tammaryn Lashley, Rohan de Silva, Dervis A. M. Salih, Conceição Bettencourt
The paper identifies an oligodendrocyte DNA methylation signature in Alzheimer's disease that is preserved across brain regions and disease stages, and is associated with altered gene expression in OLGs.
Molecular Psychiatry · Jun 18, 2026Peer-reviewedNeuroscience
Ariana P. Gatt, Yazead Buhidma, Katherine Fodder, Jack Humphrey, Sandrine C. Foti, Barbara Frias, Bridget C. Benson, Priya Gami‐Patel, Lauren M. Gittings, Christina E. Toomey, Tammaryn Lashley
This study investigates the hnRNP network's role in FTLD-TDP subtypes using single-nuclei RNA-sequencing and immunohistochemistry, finding glial-specific RNA processing changes associated with different pathological subtypes.
bioRxiv · Jul 14, 2025 · PreprintNeuroscience
Naiomi Rambarack, Katherine Fodder, Megha N. Murthy, Christina E. Toomey, Rohan de Silva, Peter Heutink, Jack Humphrey, Towfique Raj, Tammaryn Lashley, Conceição Bettencourt
The paper investigates DNA methylation changes in FTLD risk genes across different subtypes and finds shared hypomethylation in STX6 and other loci, with significant effects in PSP cases.
Acta Neuropathologica Communications · Jul 5, 2025Peer-reviewedNeuroscience
Megha N. Murthy, Katherine Fodder, Yasuo Miki, Naiomi Rambarack, Eduardo De Pablo‐Fernández, Lasse Pihlstrøm, Jonathan S. Mill, Thomas T. Warner, Tammaryn Lashley, Conceição Bettencourt
The paper compares DNA methylation patterns in white matter of MSA, PD, and PSP to identify shared and disease-specific alterations.
Acta Neuropathologica · Jul 12, 2024Peer-reviewedNeuroscience
Katherine Fodder, Megha N. Murthy, Patrizia Rizzu, Christina E. Toomey, Rahat Hasan, Jack Humphrey, Towfique Raj, Katie Lunnon, Jonathan S. Mill, Peter Heutink, Tammaryn Lashley, Conceição Bettencourt
This study identifies DNA methylation changes in FTLD subtypes, finding OTUD4 as a key gene with consistent expression dysregulation across subtypes.
Acta Neuropathologica · May 7, 2023Peer-reviewedNeuroscience