A clinical and molecular review of ubiquitous glucose-6-phosphatase deficiency caused by G6PC3 mutations

por Banka, Siddharth, Newman, William G
Publicado 2013

The Impact of CYP2D6 Genotyping on Tamoxifen Treatment

por Ferraldeschi, Roberta, Newman, William G.
Publicado 2010

Delivery of a Clinical Genomics Service

por Newman, William G., Black, Graeme C.
Publicado 2014

Accounting for Capacity Constraints in Economic Evaluations of Precision Medicine: A Systematic Review

por Wright, Stuart J., Newman, William G., Payne, Katherine
Publicado 2019

Quantifying the Impact of Capacity Constraints in Economic Evaluations: An Application in Precision Medicine

por Wright, Stuart J., Newman, William G., Payne, Katherine
Publicado 2021

Epidermal Growth Factor Receptor in Pancreatic Cancer

por Oliveira-Cunha, Melissa, Newman, William G., Siriwardena, Ajith K.
Publicado 2011

The rise of point-of-care genetics: how the SARS-CoV-2 pandemic will accelerate adoption of genetic testing in the acute setting

por McDermott, John H., Burn, John, Donnai, Dian, Newman, William G.
Publicado 2021

The Role of the U5 snRNP in Genetic Disorders and Cancer

por Wood, Katherine A., Eadsforth, Megan A., Newman, William G., O’Keefe, Raymond T.
Publicado 2021

Foramen Ovale Closure Is a Process of Endothelial-to-Mesenchymal Transition Leading to Fibrosis

por Elliott, Graeme C., Gurtu, Rockesh, McCollum, Charles, Newman, William G., Wang, Tao
Publicado 2014

The Genomic Architecture of Bladder Exstrophy Epispadias Complex

por Beaman, Glenda M., Cervellione, Raimondo M., Keene, David, Reutter, Heiko, Newman, William G.
Publicado 2021

Characterizing pharmacogenetic programs using the consolidated framework for implementation research: A structured scoping review

por McDermott, John H., Wright, Stuart, Sharma, Videha, Newman, William G., Payne, Katherine, Wilson, Paul
Publicado 2022

AMH type II receptor and AMH gene polymorphisms are not associated with ovarian reserve, response, or outcomes in ovarian stimulation

por Cerra, Christian, Newman, William G., Tohlob, Dalia, Byers, Helen, Horne, Gregory, Roberts, Stephen A., Mohiyiddeen, Lamiya
Publicado 2016

Refractory very early-onset inflammatory bowel disease associated with cytosolic isoleucyl-tRNA synthetase deficiency: A case report

por Fagbemi, Andrew, Newman, William G, Tangye, Stuart G, Hughes, Stephen M, Cheesman, Edmund, Arkwright, Peter D
Publicado 2020

The role of CYP2C19 genotyping to guide antiplatelet therapy following ischemic stroke or transient ischemic attack

por McDermott, John H, Leach, Marc, Sen, Dwaipayan, Smith, Craig J., Newman, William G., Bath, Philip M.
Publicado 2022

Maternal mosaicism for IDUA deletion clarifies recurrence risk in MPS I

por Breen, Catherine, Mercer, Jean, Jones, Simon A, Jahic, Amir, Heptinstall, Lesley, Tylee, Karen, Newman, William G, Beetz, Christian
Publicado 2016

Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in Xenopus

por Roberts, Neil A., Woolf, Adrian S., Stuart, Helen M., Thuret, Raphaël, McKenzie, Edward A., Newman, William G., Hilton, Emma N.
Publicado 2014

A recurrent missense variant in HARS2 results in variable sensorineural hearing loss in three unrelated families

por Demain, Leigh A. M., Gerkes, Erica. H., Smith, Richard J. H., Molina-Ramirez, Leslie P., O’Keefe, Raymond T., Newman, William G.
Publicado 2019

Genetic polymorphism in C3 is associated with progression in chronic kidney disease (CKD) patients with IgA nephropathy but not in other causes of CKD

por Ibrahim, Sara T., Chinnadurai, Rajkumar, Ali, Ibrahim, Payne, Debbie, Rice, Gillian I., Newman, William G., Algohary, Eman, Adam, Ahmed G., Kalra, Philip A.
Publicado 2020

A prospective, randomized, placebo-controlled, double-blind, multicenter study of the effects of irbesartan on aortic dilatation in Marfan syndrome (AIMS trial): study protocol

por Mullen, Michael J, Flather, Marcus D, Jin, Xu Yu, Newman, William G, Erdem, Guliz, Gaze, David, Valencia, Oswaldo, Banya, Winston, Foley, Claire E, Child, Anne
Publicado 2013

Modelling the developmental spliceosomal craniofacial disorder Burn-McKeown syndrome using induced pluripotent stem cells

por Wood, Katherine A., Rowlands, Charlie F., Thomas, Huw B., Woods, Steven, O’Flaherty, Julieta, Douzgou, Sofia, Kimber, Susan J., Newman, William G., O’Keefe, Raymond T.
Publicado 2020