Pharmacogenetics making cancer treatment safer and more effective /

door Newman, William G.
Gepubliceerd in 2010

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

door Banka, Siddharth, Newman, William G
Gepubliceerd in 2013

The Impact of CYP2D6 Genotyping on Tamoxifen Treatment

door Ferraldeschi, Roberta, Newman, William G.
Gepubliceerd in 2010

Delivery of a Clinical Genomics Service

door Newman, William G., Black, Graeme C.
Gepubliceerd in Genes (Basel) (2014)

Refusal of viral testing during the SARS-CoV-2 pandemic

door McDermott, John H, Newman, William G
Gepubliceerd in Clin Med (Lond) (2020)

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

door Wright, Stuart J., Newman, William G., Payne, Katherine
Gepubliceerd in Pharmacoeconomics (2019)

Epidermal Growth Factor Receptor in Pancreatic Cancer

door Oliveira-Cunha, Melissa, Newman, William G., Siriwardena, Ajith K.
Gepubliceerd in 2011

Effective cascade screening through identification of a mutation in RYR2 in a large family with a history of sudden death

door Bailey, Claire, Blair, Edward, Garratt, Clifford, Newman, William G.
Gepubliceerd in J Cardiol Cases (2015)

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

door McDermott, John H., Burn, John, Donnai, Dian, Newman, William G.
Gepubliceerd in Eur J Hum Genet (2021)

The Role of the U5 snRNP in Genetic Disorders and Cancer

door Wood, Katherine A., Eadsforth, Megan A., Newman, William G., O’Keefe, Raymond T.
Gepubliceerd in Front Genet (2021)

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

door Elliott, Graeme C., Gurtu, Rockesh, McCollum, Charles, Newman, William G., Wang, Tao
Gepubliceerd in 2014

Clinically diverse and perinatally lethal syndromes with urorectal septum malformation sequence

door Nayak, Shalini S., Harkness, Robert, Shukla, Anju, Banka, Siddharth, Newman, William G., Girisha, Katta M.
Gepubliceerd in Am J Med Genet A (2023)

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

door Cerra, Christian, Newman, William G., Tohlob, Dalia, Byers, Helen, Horne, Gregory, Roberts, Stephen A., Mohiyiddeen, Lamiya
Gepubliceerd in J Assist Reprod Genet (2016)

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

door Fagbemi, Andrew, Newman, William G, Tangye, Stuart G, Hughes, Stephen M, Cheesman, Edmund, Arkwright, Peter D
Gepubliceerd in World J Gastroenterol (2020)

Further delineation of the phenotype of severe congenital neutropenia type 4 due to mutations in G6PC3

door Banka, Siddharth, Chervinsky, Elena, Newman, William G, Crow, Yanick J, Yeganeh, Shay, Yacobovich, Joanne, Donnai, Dian, Shalev, Stavit
Gepubliceerd in 2011

Maternal mosaicism for IDUA deletion clarifies recurrence risk in MPS I

door Breen, Catherine, Mercer, Jean, Jones, Simon A, Jahic, Amir, Heptinstall, Lesley, Tylee, Karen, Newman, William G, Beetz, Christian
Gepubliceerd in Hum Genome Var (2016)

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

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

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

door Demain, Leigh A. M., Gerkes, Erica. H., Smith, Richard J. H., Molina-Ramirez, Leslie P., O’Keefe, Raymond T., Newman, William G.
Gepubliceerd in J Hum Genet (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

door Ibrahim, Sara T., Chinnadurai, Rajkumar, Ali, Ibrahim, Payne, Debbie, Rice, Gillian I., Newman, William G., Algohary, Eman, Adam, Ahmed G., Kalra, Philip A.
Gepubliceerd in PLoS One (2020)

Common variants modify the age of onset for basal cell carcinomas in Gorlin syndrome

door Yasar, Binnaz, Byers, Helen J, Smith, Miriam J, Lear, John, Oudit, Deemesh, Bholah, Zaynab, Roberts, Stephen A, Newman, William G, Evans, D Gareth
Gepubliceerd in Eur J Hum Genet (2015)