Raymond T O'Keefe (Raymond O'Keefe)

ORCID

Publication Activity (10 Years)

Years Active: 2016-2023
Publications (10 Years): 14

Top Venues

University of Manchester

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of Manchester

United Kingdom

Senior Lecturer :: Faculty of Biology Medicine and Health

Publications

Thomas B Smith, Alessandro Rea, Huw B Thomas, Kyle Thompson, Monika Oláhová, Reza Maroofian, Mina Zamani, Langping He, Saeid Sadeghian, Hamid Galehdari, Nava Shaul Lotan, Tal Gilboa, Kristin C Herman, Thomas J McCorvie, Wyatt W Yue, Henry Houlden, Robert W Taylor, William G Newman, Raymond T O'Keefe
Novel homozygous variants in PRORP expand the genotypic spectrum of combined oxidative phosphorylation deficiency 54. European journal of human genetics : EJHG (2023)
Matthew Wenjie Feng, Daniela Delneri, Catherine B Millar, Raymond T O'Keefe
Eisosome disruption by noncoding RNA deletion increases protein secretion in yeast. PNAS nexus 1 (5) (2022)
Matthew Wenjie Feng, Daniela Delneri, Catherine B Millar, Raymond T O'Keefe
Eisosome disruption by noncoding RNA deletion increases protein secretion in yeast. PNAS nexus 1 (5) (2022)
Ranjay Jayadev, Mychel Raony P T Morais, Jamie M Ellingford, Sandhya Srinivasan, Richard W Naylor, Craig Lawless, Anna S Li, Jack F Ingham, Eric Hastie, Qiuyi Chi, Maryline Fresquet, Nikki-Maria Koudis, Huw B Thomas, Raymond T O'Keefe, Emily Williams, Antony D Adamson, Helen M Stuart, Siddharth Banka, Damian Smedley, null null, David R Sherwood, Rachel Lennon
A basement membrane discovery pipeline uncovers network complexity, regulators, and human disease associations. Science advances 8 (20) (2022)
Laura Natalia Balarezo-Cisneros, Steven Parker, Marcin G Fraczek, Soukaina Timouma, Ping Wang, Raymond T O'Keefe, Catherine B Millar, Daniela Delneri
Functional and transcriptional profiling of non-coding RNAs in yeast reveal context-dependent phenotypes and in trans effects on the protein regulatory network. PLoS genetics 17 (1) (2021)
Rabia Faridi, Alessandro Rea, Cristina Fenollar-Ferrer, Raymond T O'Keefe, Shoujun Gu, Zunaira Munir, Asma Ali Khan, Sheikh Riazuddin, Michael Hoa, Sadaf Naz, William G Newman, Thomas B Friedman
New insights into Perrault syndrome, a clinically and genetically heterogeneous disorder. Human genetics (2021)
Lei Shi, Peter Magee, Angelo Paolo Dei Tos, Sudhakar Sahoo, Hui Sun Leong, Dave Lee, Robert Sellers, Laura Brulle-Soumare, Stefano Cairo, Tiziana Monteverde, Stefano Volinia, Duncan D Smith, Gianpiero Di Leva, Francesca Galuppini, Athanasios R Paliouras, Kang Zeng, Raymond T O'Keefe, Michela Garofalo
A KRAS-responsive long non-coding RNA controls microRNA processing. Nature communications 12 (1) (2021)
Katherine A Wood, Jamie M Ellingford, Huw B Thomas, null null, Sofia Douzgou Houge, Glenda M Beaman, Emma Hobson, Katrina Prescott, Raymond T O'Keefe, William G Newman
Expanding the genotypic spectrum of TXNL4A variants in Burn-McKeown syndrome. Clinical genetics (2021)
James M Eales, Xiao Jiang, Xiaoguang Xu, Sushant Saluja, Artur Akbarov, Eddie Cano-Gamez, Michelle T McNulty, Christopher Finan, Hui Guo, Wojciech Wystrychowski, Monika Szulińska, Huw B Thomas, Sanjeev Pramanik, Sandesh Chopade, Priscilla R Prestes, Ingrid Wise, Evangelos Evangelou, Mahan Salehi, Yusif Shakanti, Mikael Ekholm, Matthew Denniff, Alicja Nazgiewicz, Felix Eichinger, Bradley Godfrey, Andrzej Antczak, Maciej Glyda, Robert Król, Stephen Eyre, Jason Brown, Carlo Berzuini, John David Bowes, Mark J Caulfield, Ewa Zukowska-Szczechowska, Joanna Zywiec, Pawel Bogdanski, Matthias Kretzler, Adrian S Woolf, David Talavera, Bernard D Keavney, Pasquale Maffia, Tomasz J Guzik, Raymond T O'Keefe, Gosia Trynka, Nilesh J Samani, Aroon D Hingorani, Matthew Gordon Sampson, Andrew P Morris, Fadi J Charchar, Maciej Tomaszewski
Uncovering genetic mechanisms of hypertension through multi-omic analysis of the kidney. Nature genetics 53 (5) (2021)
Katherine A Wood, Charlie F Rowlands, Huw B Thomas, Steven Woods, Julieta O'Flaherty, Sofia Douzgou, Susan J Kimber, William G Newman, Raymond T O'Keefe
Modelling the developmental spliceosomal craniofacial disorder Burn-McKeown syndrome using induced pluripotent stem cells. PloS one 15 (7) (2020)
Huw B Thomas, Katherine A Wood, Weronika A Buczek, Christopher T Gordon, Véronique Pingault, Tania Attie-Bitach, Kathryn E Hentges, Vinod C Varghese, Jeanne Amiel, William G Newman, Raymond T O'Keefe
EFTUD2 missense variants disrupt protein function and splicing in mandibulofacial dysostosis Guion-Almeida type. Human mutation 41 (8) (2020)
Steven Parker, Marcin G Fraczek, Jian Wu, Sara Shamsah, Alkisti Manousaki, Kobchai Dungrattanalert, Rogerio Alves de Almeida, Edith Invernizzi, Tim Burgis, Walid Omara, Sam Griffiths-Jones, Daniela Delneri, Raymond T O'Keefe
Large-scale profiling of noncoding RNA function in yeast. PLoS genetics 14 (3) (2018)
Steven Parker, Marcin G Fraczek, Jian Wu, Sara Shamsah, Alkisti Manousaki, Kobchai Dungrattanalert, Rogerio Alves de Almeida, Diego Estrada-Rivadeneyra, Walid Omara, Daniela Delneri, Raymond T O'Keefe
A resource for functional profiling of noncoding RNA in the yeast Saccharomyces cerevisiae. RNA (New York, N.Y.) 23 (8) (2017)
Emma M Jenkinson, Mathieu P Rodero, Paul R Kasher, Carolina Uggenti, Anthony Oojageer, Laurence C Goosey, Yoann Rose, Christopher J Kershaw, Jill E Urquhart, Simon G Williams, Sanjeev S Bhaskar, James O'Sullivan, Gabriela M Baerlocher, Monika Haubitz, Geraldine Aubert, Kristin W Barañano, Angela J Barnicoat, Roberta Battini, Andrea Berger, Edward M Blair, Janice E Brunstrom-Hernandez, Johannes A Buckard, David M Cassiman, Rosaline Caumes, Duccio Maria Cordelli, Liesbeth M De Waele, Alexander J Fay, Patrick Ferreira, Nicholas A Fletcher, Alan E Fryer, Himanshu Goel, Cheryl A Hemingway, Marco Henneke, Imelda Hughes, Rosalind J Jefferson, Ram Kumar, Lieven Lagae, Pierre G Landrieu, Charles Marques Lourenço, Timothy J Malpas, Sarju G Mehta, Imke Metz, Sakkubai Naidu, Katrin Õunap, Axel Panzer, Prab Prabhakar, Gerardine Quaghebeur, Raphael Schiffmann, Elliott H Sherr, Kanaga R Sinnathuray, Calvin Soh, Helen S Stewart, John Stone, Hilde Van Esch, Christine E G Van Mol, Adeline Vanderver, Emma L Wakeling, Andrea Whitney, Graham D Pavitt, Sam Griffiths-Jones, Gillian I Rice, Patrick Revy, Marjo S van der Knaap, John H Livingston, Raymond T O'Keefe, Yanick J Crow
Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts. Nature genetics 48 (10) (2016)

Raymond T O'Keefe.css-eqlu8i{font-size:small;padding-left:4px;} (Raymond O'Keefe)

Publication Activity (10 Years)

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Raymond T O'Keefe (Raymond O'Keefe)