Genome-wide human brain eQTLs: In-depth analysis and insights using the UKBEC dataset

por Sng, Letitia M. F., Thomson, Peter C., Trabzuni, Daniah
Publicado 2019

Author Correction: Genome-wide human brain eQTLs: In-depth analysis and insights using the UKBEC dataset

por Sng, Letitia M. F., Thomson, Peter C., Trabzuni, Daniah
Publicado 2020

Comparison Between Expression Microarrays and RNA-Sequencing Using UKBEC Dataset Identified a trans-eQTL Associated with MPZ Gene in Substantia Nigra

por Sng, Letitia M.F., Thomson, Peter C., Trabzuni, Daniah
Publicado 2020

Increased brain expression of GPNMB is associated with genome wide significant risk for Parkinson’s disease on chromosome 7p15.3

por Murthy, Megha N., Blauwendraat, Cornelis, Guelfi, Sebastian, Hardy, John, Lewis, Patrick A., Trabzuni, Daniah
Publicado 2017

Insights into the Influence of Specific Splicing Events on the Structural Organization of LRRK2

por Vlachakis, Dimitrios, Labrou, Nikolaos E., Iliopoulos, Costas, Hardy, John, Lewis, Patrick A., Rideout, Hardy, Trabzuni, Daniah
Publicado 2018

Quality control parameters on a large dataset of regionally dissected human control brains for whole genome expression studies

por Trabzuni, Daniah, Ryten, Mina, Walker, Robert, Smith, Colin, Imran, Sabaena, Ramasamy, Adaikalavan, Weale, Michael E, Hardy, John
Publicado 2011

Widespread sex differences in gene expression and splicing in the adult human brain

por Trabzuni, Daniah, Ramasamy, Adaikalavan, Imran, Sabaena, Walker, Robert, Smith, Colin, Weale, Michael E., Hardy, John, Ryten, Mina
Publicado 2013

Genetic evidence for a pathogenic role for the vitamin D3 metabolizing enzyme CYP24A1 in multiple sclerosis()

por Ramasamy, Adaikalavan, Trabzuni, Daniah, Forabosco, Paola, Smith, Colin, Walker, Robert, Dillman, Allissa, Sveinbjornsdottir, Sigurlaug, Hardy, John, Weale, Michael E., Ryten, Mina
Publicado 2014

Major Shifts in Glial Regional Identity Are a Transcriptional Hallmark of Human Brain Aging

por Soreq, Lilach, Rose, Jamie, Soreq, Eyal, Hardy, John, Trabzuni, Daniah, Cookson, Mark R., Smith, Colin, Ryten, Mina, Patani, Rickie, Ule, Jernej
Publicado 2017

Mutations in HPCA Cause Autosomal-Recessive Primary Isolated Dystonia

por Charlesworth, Gavin, Angelova, Plamena R., Bartolomé-Robledo, Fernando, Ryten, Mina, Trabzuni, Daniah, Stamelou, Maria, Abramov, Andrey Y., Bhatia, Kailash P., Wood, Nicholas W.
Publicado 2015

Genomewide association study in cervical dystonia demonstrates possible association with sodium leak channel

por Mok, Kin Y, Schneider, Susanne A, Trabzuni, Daniah, Stamelou, Maria, Edwards, Mark, Kasperaviciute, Dalia, Pickering-Brown, Stuart, Silverdale, Monty, Hardy, John, Bhatia, Kailash P
Publicado 2014

Insights into TREM2 biology by network analysis of human brain gene expression data

por Forabosco, Paola, Ramasamy, Adaikalavan, Trabzuni, Daniah, Walker, Robert, Smith, Colin, Bras, Jose, Levine, Adam P., Hardy, John, Pocock, Jennifer M., Guerreiro, Rita, Weale, Michael E., Ryten, Mina
Publicado 2013

Investigating the utility of human embryonic stem cell-derived neurons to model ageing and neurodegenerative disease using whole-genome gene expression and splicing analysis

por Patani, Rickie, Lewis, Patrick A, Trabzuni, Daniah, Puddifoot, Clare A, Wyllie, David J A, Walker, Robert, Smith, Colin, Hardingham, Giles E, Weale, Michael, Hardy, John, Chandran, Siddharthan, Ryten, Mina
Publicado 2012

Assessment of common variability and expression quantitative trait loci for genome-wide associations for progressive supranuclear palsy

por Ferrari, Raffaele, Ryten, Mina, Simone, Roberto, Trabzuni, Daniah, Nicolaou, Naiya, Hondhamuni, Geshanthi, Ramasamy, Adaikalavan, Vandrovcova, Jana, Weale, Michael E., Lees, Andrew J., Momeni, Parastoo, Hardy, John, de Silva, Rohan
Publicado 2014

Corrigendum to “Assessment of common variability and expression quantitative trait loci for genome-wide associations for progressive supranuclear palsy.” [Neurobiol. Aging 35 (2014...

por Ferrari, Raffaele, Ryten, Mina, Simone, Roberto, Trabzuni, Daniah, Nicolaou, Nayia, Hondhamuni, Geshanthi, Ramasamy, Adaikalavan, Vandrovcova, Jana, Weale, Michael E., Lees, Andrew J., Momeni, Parastoo, Hardy, John, de Silva, Rohan
Publicado 2015

Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets

por Kia, Demis A., Zhang, David, Guelfi, Sebastian, Manzoni, Claudia, Hubbard, Leon, Reynolds, Regina H., Botía, Juan, Ryten, Mina, Ferrari, Raffaele, Lewis, Patrick A., Williams, Nigel, Trabzuni, Daniah, Hardy, John, Wood, Nicholas W.
Publicado 2021

Recursive splicing in long vertebrate genes

por Sibley, Christopher R, Emmett, Warren, Blazquez, Lorea, Faro, Ana, Haberman, Nejc, Briese, Michael, Trabzuni, Daniah, Ryten, Mina, Weale, Michael E, Hardy, John, Modic, Miha, Curk, Tomaž, Wilson, Stephen W, Plagnol, Vincent, Ule, Jernej
Publicado 2015

A comprehensive introduction to the genetic basis of non-syndromic hearing loss in the Saudi Arabian population

por Imtiaz, Faiqa, Taibah, Khalid, Ramzan, Khushnooda, Bin-Khamis, Ghada, Kennedy, Shelley, Al-Mubarak, Bashayer, Trabzuni, Daniah, Allam, Rabab, Al-Mostafa, Abeer, Sogaty, Sameera, Al-Shaikh, Abdulmoneem H, Bamukhayyar, Saeed S, Meyer, Brian F, Al-Owain, Mohammed
Publicado 2011

Resolving the polymorphism-in-probe problem is critical for correct interpretation of expression QTL studies

por Ramasamy, Adaikalavan, Trabzuni, Daniah, Gibbs, J. Raphael, Dillman, Allissa, Hernandez, Dena G., Arepalli, Sampath, Walker, Robert, Smith, Colin, Ilori, Gigaloluwa Peter, Shabalin, Andrey A., Li, Yun, Singleton, Andrew B., Cookson, Mark R., Hardy, John, Ryten, Mina, Weale, Michael E.
Publicado 2013

Novel C12orf65 mutations in patients with axonal neuropathy and optic atrophy

por Tucci, Arianna, Liu, Yo-Tsen, Preza, Elisabeth, Pitceathly, Robert D S, Chalasani, Annapurna, Plagnol, Vincent, Land, John M, Trabzuni, Daniah, Ryten, Mina, Jaunmuktane, Zane, Reilly, Mary M, Brandner, Sebastian, Hargreaves, Iain, Hardy, John, Singleton, Andrew B, Abramov, Andrey Y, Houlden, Henry
Publicado 2014