Michael J Field (Mike Field, Michael Field)

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 11

Top Topics

Autism Spectrum Disorder

Clinical Evaluation

Top Venues

JCO precision oncology

Clinical genetics

European journal of human genetics : EJHG

Journal of medical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Cristina Fortuno, Bing-Jian Feng, Courtney Carroll, Giovanni Innella, Wendy K Kohlmann, Conxi Lazaro Garcia, Joan Brunet, Lidia Feliubadaló, Silvia Iglesias, Mireia Menéndez, Alex Teulé, Mandy L Ballinger, David M Thomas, Ainsley Campbell, Michael J Field, Marion Harris, Judy Kirk, Nicholas Pachter, Nicola K Poplawski, Rachel Susman, Katherine Tucker, Mathew J Wallis, Rachel Williams, Elisa Cops, David E Goldgar, null null, Paul A James, Amanda B Spurdle
Cancer Risks Associated With TP53 Pathogenic Variants: Maximum Likelihood Analysis of Extended Pedigrees for Diagnosis of First Cancers Beyond the Li-Fraumeni Syndrome Spectrum. JCO precision oncology 8 (2024)
Cristina Fortuno, Bing-Jian Feng, Courtney Carroll, Giovanni Innella, Wendy K Kohlmann, Conxi Lazaro Garcia, Joan Brunet, Lidia Feliubadaló, Silvia Iglesias, Mireia Menéndez, Alex Teulé, Mandy L Ballinger, David M Thomas, Ainsley Campbell, Michael J Field, Marion Harris, Judy Kirk, Nicholas Pachter, Nicola K Poplawski, Rachel Susman, Katherine Tucker, Mathew J Wallis, Rachel Williams, Elisa Cops, David E Goldgar, null null, Paul A James, Amanda B Spurdle
Cancer Risks Associated With TP53 Pathogenic Variants: Maximum Likelihood Analysis of Extended Pedigrees for Diagnosis of First Cancers Beyond the Li-Fraumeni Syndrome Spectrum. JCO precision oncology 8 (2024)
Cristina Fortuno, Bing-Jian Feng, Courtney Carroll, Giovanni Innella, Wendy K Kohlmann, Conxi Lazaro Garcia, Joan Brunet, Lidia Feliubadaló, Silvia Iglesias, Mireia Menéndez, Alex Teulé, Mandy L Ballinger, David M Thomas, Ainsley Campbell, Michael J Field, Marion Harris, Judy Kirk, Nicholas Pachter, Nicola K Poplawski, Rachel Susman, Katherine Tucker, Mathew J Wallis, Rachel Williams, Elisa Cops, David E Goldgar, null null, Paul A James, Amanda B Spurdle
Cancer Risks Associated With TP53 Pathogenic Variants: Maximum Likelihood Analysis of Extended Pedigrees for Diagnosis of First Cancers Beyond the Li-Fraumeni Syndrome Spectrum. JCO precision oncology 8 (2024)
Mathilda Wilding, Jane Fleming, Katrina Moore, Ashley Crook, Ranjani Reddy, Sarah Choi, Timothy E Schlub, Michael J Field, Lavvina Thiyagarajan, Jeff Thompson, Yemima D Berman
Clinical and imaging modality factors impacting radiological interpretation of breast screening in young women with neurofibromatosis type 1. Familial cancer (2023)
Melanie Leffler, Louise Christie, Anna Hackett, Bruce Bennetts, Himanshu Goel, David J Amor, Greg B Peters, Michael J Field, Tracy Dudding
Further delineation of dosage-sensitive K/L mediated Xq28 duplication syndrome includes incomplete penetrance. Clinical genetics (2023)
Melanie Leffler, Louise Christie, Anna Hackett, Bruce Bennetts, Himanshu Goel, David J Amor, Greg B Peters, Michael J Field, Tracy Dudding
Further delineation of dosage-sensitive K/L mediated Xq28 duplication syndrome includes incomplete penetrance. Clinical genetics (2023)
Lisa Jean Ewans, Andre E Minoche, Deborah Schofield, Rupendra Shrestha, Clare Puttick, Ying Zhu, Alexander P Drew, Velimir Gayevskiy, George Elakis, Corrina Walsh, Lesley C Adès, Alison Colley, Carolyn Ellaway, Carey-Anne Evans, Mary-Louise Freckmann, Linda Goodwin, Anna Hackett, Benjamin Kamien, Edwin P Kirk, Michelle Lipke, David Mowat, Emma Elizabeth Palmer, Sulekha Rajagopalan, Anne Ronan, Rani Sachdev, William Stevenson, Anne Turner, Meredith Wilson, Lisa Worgan, Marie-Christine Morel-Kopp, Michael J Field, Michael F Buckley, Mark J Cowley, Marcel E Dinger, Tony Roscioli
Whole exome and genome sequencing in mendelian disorders: a diagnostic and health economic analysis. European journal of human genetics : EJHG 30 (10) (2022)
Emma Elizabeth Palmer, Michael Pusch, Alessandra Picollo, Caitlin Forwood, Matthew H Nguyen, Vanessa Suckow, Jessica Gibbons, Alva Hoff, Lisa Sigfrid, Andre Megarbane, Mathilde Nizon, Benjamin Cogné, Claire Beneteau, Fowzan Sami Alkuraya, Aziza Chedrawi, Mais O Hashem, Hannah Stamberger, Sarah Weckhuysen, Arnaud Vanlander, Berten Ceulemans, Sulekha Rajagopalan, Kenneth Nunn, Stéphanie Arpin, Martine Raynaud, Constance S Motter, Catherine Ward-Melver, Katrien Janssens, Marije Meuwissen, Diane Beysen, Nicola Dikow, Mona Grimmel, Tobias B Haack, Emma Clement, Amy McTague, David Hunt, Sharron Townshend, Michelle Ward, Linda J Richards, Cas Simons, Gregory Costain, Lucie Dupuis, Roberto Mendoza-Londono, Tracy Dudding-Byth, Jackie Boyle, Carol Saunders, Emily Fleming, Salima El Chehadeh, Marie-Aude Spitz, Amelie Piton, Bénédicte Gerard, Marie-Thérèse Abi Warde, Gillian Rea, Caoimhe McKenna, Sofia Douzgou, Siddharth Banka, Cigdem Akman, Jennifer M Bain, Tristan T Sands, Golder N Wilson, Erin J Silvertooth, Lauren Miller, Damien Lederer, Rani Sachdev, Rebecca Macintosh, Olivier Monestier, Deniz Karadurmus, Felicity Collins, Melissa Carter, Luis Rohena, Marjolein H Willemsen, Charlotte W Ockeloen, Rolph Pfundt, Sanne D Kroft, Michael J Field, Francisco E R Laranjeira, Ana M Fortuna, Ana Rita Soares, Vincent Michaud, Sophie Naudion, Sailaja Golla, David D Weaver, Lynne M Bird, Jennifer Friedman, Virginia Clowes, Shelagh Joss, Laura Pölsler, Philippe M Campeau, Maria Blazo, Emilia K Bijlsma, Jill A Rosenfeld, Christian Beetz, Zöe Powis, Kirsty McWalter, Tracy Brandt, Erin Torti, Mikaël Mathot, Shekeeb S Mohammad, Ruth Armstrong, Vera M Kalscheuer
Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition. Molecular psychiatry (2022)
Emma K Baker, Merlin G Butler, Samantha N Hartin, Ling Ling, Minh Bui, David Francis, Carolyn Rogers, Michael J Field, Jennie Slee, Dinusha Gamage, David J Amor, David E Godler
Relationships between UBE3A and SNORD116 expression and features of autism in chromosome 15 imprinting disorders. Translational psychiatry 10 (1) (2020)
Emma Tudini, Aimee L Davidson, Uwe Dressel, Lesley Andrews, Yoland Antill, Ashley Crook, Michael J Field, Michael Gattas, Rebecca Harris, Bettina Meiser, Nicholas Pachter, Lucinda Salmon, Rachel Susman, Sharron Townshend, Alison H Trainer, Katherine M Tucker, Gillian Mitchell, Paul A James, Robyn L Ward, Helen Mar Fan, Nicola K Poplawski, Amanda B Spurdle
Implementing gene curation for hereditary cancer susceptibility in Australia: achieving consensus on genes with clinical utility. Journal of medical genetics 58 (12) (2020)
Tiffany Wotton, Veronica Wiley, Bruce Bennetts, Louise Christie, Bridget Wilcken, Gemma Jenkins, Carolyn Rogers, Jackie Boyle, Michael J Field
Are We Ready for Fragile X Newborn Screening Testing?-Lessons Learnt from a Feasibility Study. International journal of neonatal screening 4 (1) (2018)