GWAS: heritability missing in action?

nork Clarke, Angus J, Cooper, David N
Argitaratua 2010

Ethics in genetic counselling

nork Clarke, Angus J., Wallgren-Pettersson, Carina
Argitaratua izan da J Community Genet (2018)

Recontact in clinical practice: a survey of clinical genetics services in the United Kingdom

nork Carrieri, Daniele, Lucassen, Anneke M., Clarke, Angus J., Dheensa, Sandi, Doheny, Shane, Turnpenny, Peter D., Kelly, Susan E.
Argitaratua izan da Genet Med (2016)

Recontacting in clinical practice: an investigation of the views of healthcare professionals and clinical scientists in the United Kingdom

nork Carrieri, Daniele, Dheensa, Sandi, Doheny, Shane, Clarke, Angus J, Turnpenny, Peter D, Lucassen, Anneke M, Kelly, Susan E
Argitaratua izan da Eur J Hum Genet (2017)

Recontacting in clinical genetics and genomic medicine? We need to talk about it

nork Carrieri, Daniele, Dheensa, Sandi, Doheny, Shane, Clarke, Angus J, Turnpenny, Peter D, Lucassen, Anneke M, Kelly, Susan E
Argitaratua izan da Eur J Hum Genet (2017)

Recontacting in clinical practice: the views and expectations of patients in the United Kingdom

nork Carrieri, Daniele, Dheensa, Sandi, Doheny, Shane, Clarke, Angus J, Turnpenny, Peter D, Lucassen, Anneke M, Kelly, Susan E
Argitaratua izan da Eur J Hum Genet (2017)

Reply to Bombard and Mighton

nork Carrieri, Daniele, Howard, Heidi C., Clarke, Angus J., Stefansdottir, Vigdis, Cornel, Martina C., van El, Carla G., Forzano, Francesca
Argitaratua izan da Eur J Hum Genet (2019)

A case-note review of continued pregnancies found to be at a high risk of Huntington’s disease: considerations for clinical practice

nork Wadrup, Felicity, Holden, Simon, MacLeod, Rhona, Miedzybrodzka, Zosia, Németh, Andrea H., Owens, Shan, Pasalodos, Sara, Quarrell, Oliver, Clarke, Angus J.
Argitaratua izan da Eur J Hum Genet (2019)

A Nonsense Mutation in the IKBKG Gene in Mares with Incontinentia Pigmenti

nork Towers, Rachel E., Murgiano, Leonardo, Millar, David S., Glen, Elise, Topf, Ana, Jagannathan, Vidhya, Drögemüller, Cord, Goodship, Judith A., Clarke, Angus J., Leeb, Tosso
Argitaratua 2013

‘Sifting the significance from the data’ - the impact of high-throughput genomic technologies on human genetics and health care

nork Clarke Angus J, Cooper David N, Krawczak Michael, Tyler-Smith Chris, Wallace Helen M, Wilkie Andrew O M, Raymond Frances, Chadwick Ruth, Craddock Nick, John Ros, Gallacher John, Chiano Mathias
Argitaratua 2012-08-01

‘Sifting the significance from the data’ - the impact of high-throughput genomic technologies on human genetics and health care

nork Clarke, Angus J, Cooper, David N, Krawczak, Michael, Tyler-Smith, Chris, Wallace, Helen M, Wilkie, Andrew O M, Raymond, Frances Lucy, Chadwick, Ruth, Craddock, Nick, John, Ros, Gallacher, John, Chiano, Mathias
Argitaratua 2012

Rett Syndrome: Revised Diagnostic Criteria and Nomenclature

nork Neul, Jeffrey L., Kaufmann, Walter E., Glaze, Daniel G., Christodoulou, John, Clarke, Angus J., Bahi-Buisson, Nadia, Leonard, Helen, Bailey, Mark E. S., Schanen, N. Carolyn, Zappella, Michele, Renieri, Alessandra, Huppke, Peter, Percy, Alan K.
Argitaratua 2010

NTNG1 Mutations are a Rare Cause of Rett Syndrome

nork Archer, Hayler L., Evans, Julie C., Millar, David S., Thompson, Peter W., Kerr, Alison M., Leonard, Helen, Christodoulou, John, Ravine, David, Lazarou, Lazarus, Grove, Lucy, Verity, Christopher, Whatley, Sharon D., Pilz, Daniela T., Sampson, Julian R., Clarke, Angus J.
Argitaratua 2006

Ectodermal Dysplasias: Classification and Organization by Phenotype, Genotype and Molecular Pathway

nork Timothy, Wright, Fete, Mary, Schneider, Holm, Zinser, Madeline, Koster, Maranke I., Clarke, Angus J., Rabia, Smail Hadj, Tadini, Gianluca, Pagnan, Nina, Visinoni, Atila Fernando, Bergendal, Birgitta, Abbott, Becky, Fete, Timothy, Stanford, Clark, Butcher, Clayton, Souza, Rena D’, Sybert, Virginia
Argitaratua izan da Am J Med Genet A (2019)

Somatic mutations in salivary duct carcinoma and potential therapeutic targets

nork Khoo, Timothy K., Yu, Bing, Smith, Joel A., Clarke, Angus J., Luk, Peter P., Selinger, Christina I., Mahon, Kate L., Kraitsek, Spiridoula, Palme, Carsten, Boyer, Michael J., Dinger, Marcel E., Cowley, Mark J., O’Toole, Sandra A., Clark, Jonathan R., Gupta, Ruta
Argitaratua izan da Oncotarget (2017)

Recontacting or not recontacting? A survey of current practices in clinical genetics centres in Europe

nork Sirchia, Fabio, Carrieri, Daniele, Dheensa, Sandi, Benjamin, Caroline, Kayserili, Hülya, Cordier, Christophe, van El, Carla G., Turnpenny, Peter D., Melegh, Bela, Mendes, Álvaro, Halbersma-Konings, Tanya F., van Langen, Irene M., Lucassen, Anneke M., Clarke, Angus J., Forzano, Francesca, Kelly, Susan E.
Argitaratua izan da Eur J Hum Genet (2018)

Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics

nork Carrieri, Daniele, Howard, Heidi C., Benjamin, Caroline, Clarke, Angus J., Dheensa, Sandi, Doheny, Shane, Hawkins, Naomi, Halbersma-Konings, Tanya F., Jackson, Leigh, Kayserili, Hülya, Kelly, Susan E., Lucassen, Anneke M., Mendes, Álvaro, Rial-Sebbag, Emmanuelle, Stefánsdóttir, Vigdís, Turnpenny, Peter D., van El, Carla G., van Langen, Irene M., Cornel, Martina C., Forzano, Francesca
Argitaratua izan da Eur J Hum Genet (2018)

European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death

nork Fellmann, Florence, van El, Carla G., Charron, Philippe, Michaud, Katarzyna, Howard, Heidi C., Boers, Sarah N., Clarke, Angus J., Duguet, Anne-Marie, Forzano, Francesca, Kauferstein, Silke, Kayserili, Hülya, Lucassen, Anneke, Mendes, Álvaro, Patch, Christine, Radojkovic, Dragica, Rial-Sebbag, Emmanuelle, Sheppard, Mary N., Tassé, Anne-Marie, Temel, Sehime G., Sajantila, Antti, Basso, Cristina, Wilde, Arthur A. M., Cornel, Martina C.
Argitaratua izan da Eur J Hum Genet (2019)