Experience of Asian males communicating cardiac genetic risk within the family

द्वारा Kam, Sylvia, Bylstra, Yasmin, Forrest, Laura, Macciocca, Ivan, Foo, Roger
में प्रकाशित J Community Genet (2018)

High school Tay–Sachs disease carrier screening: 5 to 11-year follow-up

द्वारा Curd, Helen, Lewis, Sharon, Macciocca, Ivan, Sahhar, Margaret, Petrou, Vicki, Bankier, Agnes, Lieberman, Sari, Levy-Lahad, Ephrat, Delatycki, Martin B.
प्रकाशित 2013

A clinically driven variant prioritization framework outperforms purely computational approaches for the diagnostic analysis of singleton WES data

द्वारा Stark, Zornitza, Dashnow, Harriet, Lunke, Sebastian, Tan, Tiong Y, Yeung, Alison, Sadedin, Simon, Thorne, Natalie, Macciocca, Ivan, Gaff, Clara, Oshlack, Alicia, White, Susan M, James, Paul A
में प्रकाशित Eur J Hum Genet (2017)

Prospective Evaluation of the Utility of Whole Exome Sequencing in Dilated Cardiomyopathy

द्वारा Ramchand, Jay, Wallis, Mathew, Macciocca, Ivan, Lynch, Elly, Farouque, Omar, Martyn, Melissa, Phelan, Dean, Chong, Belinda, Lockwood, Siobhan, Weintraub, Robert, Thompson, Tina, Trainer, Alison, Zentner, Dominica, Vohra, Jitendra, Chetrit, Michael, Hare, David L., James, Paul
में प्रकाशित J Am Heart Assoc (2020)

Cpipe: a shared variant detection pipeline designed for diagnostic settings

द्वारा Sadedin, Simon P., Dashnow, Harriet, James, Paul A., Bahlo, Melanie, Bauer, Denis C., Lonie, Andrew, Lunke, Sebastian, Macciocca, Ivan, Ross, Jason P., Siemering, Kirby R., Stark, Zornitza, White, Susan M., Taylor, Graham, Gaff, Clara, Oshlack, Alicia, Thorne, Natalie P.
में प्रकाशित Genome Med (2015)

ironXS: high-school screening for hereditary haemochromatosis is acceptable and feasible

द्वारा Delatycki, Martin B, Wolthuizen, Michelle, Collins, Veronica, Varley, Elizabeth, Craven, Joanna, Allen, Katrina J, Gurrin, Lyle C, Aitken, Maryanne, Trembath, M Kaye, Bond, Lyndal, Wilson, Gabrielle R, Stephenson, Sarah EM, Macciocca, Ivan, Hickerton, Chriselle, Lockhart, Paul J, Metcalfe, Sylvia A
प्रकाशित 2012

Diagnostic and cost utility of whole exome sequencing in peripheral neuropathy

द्वारा Walsh, Maie, Bell, Katrina M., Chong, Belinda, Creed, Emma, Brett, Gemma R., Pope, Kate, Thorne, Natalie P., Sadedin, Simon, Georgeson, Peter, Phelan, Dean G., Day, Timothy, Taylor, Jessica A., Sexton, Adrienne, Lockhart, Paul J., Kiers, Lynette, Fahey, Michael, Macciocca, Ivan, Gaff, Clara L., Oshlack, Alicia, Yiu, Eppie M., James, Paul A., Stark, Zornitza, Ryan, Monique M.
में प्रकाशित Ann Clin Transl Neurol (2017)

Diagnostic Impact and Cost-effectiveness of Whole-Exome Sequencing for Ambulant Children With Suspected Monogenic Conditions

द्वारा Tan, Tiong Yang, Dillon, Oliver James, Stark, Zornitza, Schofield, Deborah, Alam, Khurshid, Shrestha, Rupendra, Chong, Belinda, Phelan, Dean, Brett, Gemma R., Creed, Emma, Jarmolowicz, Anna, Yap, Patrick, Walsh, Maie, Downie, Lilian, Amor, David J., Savarirayan, Ravi, McGillivray, George, Yeung, Alison, Peters, Heidi, Robertson, Susan J., Robinson, Aaron J., Macciocca, Ivan, Sadedin, Simon, Bell, Katrina, Oshlack, Alicia, Georgeson, Peter, Thorne, Natalie, Gaff, Clara, White, Susan M.
में प्रकाशित JAMA Pediatr (2017)

The Global State of the Genetic Counseling Profession

द्वारा Abacan, MaryAnn, Alsubaie, Lamia, Barlow-Stewart, Kristine, Caanen, Beppy, Cordier, Christophe, Courtney, Eliza, Davoine, Emeline, Edwards, Janice, Elackatt, Niby J., Gardiner, Kate, Guan, Yue, Huang, Lian-Hua, Malmgren, Charlotta Ingvoldstad, Kejriwal, Sahil, Kim, Hyon J., Lambert, Deborah, Lantigua-Cruz, Paulina Araceli, Lee, Juliana M. H., Lodahl, Marianne, Lunde, Åshild, Macaulay, Shelley, Macciocca, Ivan, Margarit, Sonia, Middleton, Anna, Moldovan, Ramona, Ngeow, Joanne, Obregon-Tito, Alexandra J., Ormond, Kelly E., Paneque, Milena, Powell, Karen, Sanghavi, Kunal, Scotcher, Diana, Scott, Jenna, Juhé, Clara Serra, Shkedi-Rafid, Shiri, Wessels, Tina-Marié, Yoon, Sook-Yee, Wicklund, Catherine
में प्रकाशित Eur J Hum Genet (2018)