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Number of items: 5.


Rhodes, Christopher J, Batai, Ken, Bleda, Marta, Haimel, Matthias, Southgate, Laura, Germain, Marine, Pauciulo, Michael W, Hadinnapola, Charaka, Aman, Jurjan, Girerd, Barbara
et al (show 499 more authors) (2019) Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis. LANCET RESPIRATORY MEDICINE, 7 (3). pp. 227-238.


Hathazi, Denisa, Cox, Dan, D'Amico, Adele, Tasca, Giorgio, Charlton, Richard, Carlier, Robert-Yves, Baumann, Jennifer, Kollipara, Laxmikanth, Zahedi, René P, Feldmann, Ingo
et al (show 18 more authors) (2021) INPP5K and SIL1 associated pathologies with overlapping clinical phenotypes converge through dysregulation of PHGDH. Brain, 144 (8). pp. 2427-2442.


Themistocleous, Andreas C, Baskozos, Georgios, Blesneac, Iulia, Comini, Maddalena, Megy, Karyn, Chong, Sam, Deevi, Sri VV, Ginsberg, Lionel, Gosal, David, Hadden, Robert DM
et al (show 15 more authors) (2023) Investigating genotype-phenotype relationship of extreme neuropathic pain disorders in a UK national cohort. BRAIN COMMUNICATIONS, 5 (2). fcad037-.


Bansagi, Boglarka, Phan, Vietxuan, Baker, Mark R, O'Sullivan, J, Jennings, Matthew J, Whittaker, Roger G, Mueller, Juliane S, Duff, Jennifer, Griffin, Helen, Miller, James
et al (show 6 more authors) (2018) Multifocal demyelinating motor neuropathy and hamartoma syndrome associated with a de novo PTEN mutation. Neurology, 90 (21). e1842-e1848.


Farmery, James HR, Smith, Mike L, Lynch, Andy G, Huissoon, Aarnoud, Furnell, Abigail, Mead, Adam, Levine, Adam P, Manzur, Adnan, Thrasher, Adrian, Greenhalgh, Alan
et al (show 341 more authors) (2018) Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data (vol 8, 1300, 2018). SCIENTIFIC REPORTS, 8 (1). 13376-.

This list was generated on Sat Apr 13 16:53:33 2024 BST.