Neuroferritinopathy: iron in the brain

por Burn, John
Publicado 2014

Affordable diagnosis and prevention of genetic disease

por Burn, John
Publicado 2014

Clinical Genetics: A Review

por Burn, John
Publicado 1988

Colon cancer and Salicylates

por Dhanoya, Tanveer, Burn, John
Publicado 2016

Direct oral anticoagulants versus warfarin: is new always better than the old?

por Burn, John, Pirmohamed, Munir
Publicado 2018

EASI—enrichment of alternatively spliced isoforms

por Venables, Julian P., Burn, John
Publicado 2006

Survey of HNPCC Management Analysis of Responses from 18 International Cancer Centres

por Chow, Elizabeth, Macrae, Finlay, Burn, John
Publicado 2005

Three decades of the Human Genome Organization

por Lee, Charles, Antonarakis, Stylianos E., Hamosh, Ada, Burn, John
Publicado 2021

Association of stroke and bleed events in non-valvular atrial fibrillation patients with direct oral anticoagulant prescriptions in NHS England between 2013 and 2016

por Sheth, Harsh, McNally, Daniel, Santibanez-Koref, Mauro, Burn, John
Publicado 2019

Genetic testing and research in Lynch Syndrome - is it a choice or a responsibility?

por Cowley, Lorraine, McLaughlin, Janice, Finch, Tracy, Clavering, Emma, Burn, John
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

Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression

por Cunnington, Michael S., Santibanez Koref, Mauro, Mayosi, Bongani M., Burn, John, Keavney, Bernard
Publicado 2010

Clinical features and natural history of neuroferritinopathy caused by the 458dupA FTL mutation

por Devos, David, Tchofo, P. Jissendi, Vuillaume, Isabelle, Destée, Alain, Batey, Stephanie, Burn, John, Chinnery, Patrick F.
Publicado 2009

General practitioner attitudes towards prescribing aspirin to carriers of Lynch Syndrome: findings from a national survey

por Smith, Samuel G., Foy, Robbie, McGowan, Jennifer, Kobayashi, Lindsay C., Burn, John, Brown, Karen, Side, Lucy, Cuzick, Jack
Publicado 2017

How Should We Test for Lynch Syndrome? A Review of Current Guidelines and Future Strategies

por Gallon, Richard, Gawthorpe, Peter, Phelps, Rachel L., Hayes, Christine, Borthwick, Gillian M., Santibanez-Koref, Mauro, Jackson, Michael S., Burn, John
Publicado 2021

The influence of HLA genotype on the severity of COVID‐19 infection

por Langton, David J., Bourke, Stephen C., Lie, Benedicte A., Reiff, Gabrielle, Natu, Shonali, Darlay, Rebecca, Burn, John, Echevarria, Carlos
Publicado 2021

Tropomyosin Receptor Antagonism in Cylindromatosis (TRAC), an early phase trial of a topical tropomyosin kinase inhibitor as a treatment for inherited CYLD defective skin tumours:...

por Cranston, Amy, Stocken, Deborah D., Stamp, Elaine, Roblin, David, Hamlin, Julia, Langtry, James, Plummer, Ruth, Ashworth, Alan, Burn, John, Rajan, Neil
Publicado 2017

Dysregulated TRK Signalling is a Therapeutic Target in CYLD Defective Tumours

por Rajan, Neil, Elliott, Richard, Clewes, Oliver, Mackay, Alan, Reis-Filho, Jorge S., Burn, John, Langtry, James, Sieber-Blum, Maya, Lord, Christopher J., Ashworth, Alan
Publicado 2011

Diverse presentations of cutaneous mosaicism occur in CYLD cutaneous syndrome and may result in parent-to-child transmission

por Arefi, Majid, Wilson, Valerie, Muthiah, Siobhan, Zwolinski, Simon, Bajwa, Dalvir, Brennan, Paul, Blasdale, Katie, Bourn, David, Burn, John, Santibanez-Koref, Mauro, Rajan, Neil
Publicado 2019

Mismatch repair deficiency testing in Lynch syndrome-associated urothelial tumors

por Rasmussen, Maria, Sowter, Peter, Gallon, Richard, Durhuus, Jon Ambæk, Hayes, Christine, Andersen, Ove, Nilbert, Mef, Schejbel, Lone, Høgdall, Estrid, Santibanez-Koref, Mauro, Jackson, Michael S., Burn, John, Therkildsen, Christina
Publicado 2023