Tracy Dudding (Tracy Dudding-Byth)

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 7

Top Topics

Autism Spectrum Disorder

Intellectual Disability

Top Venues

Clinical genetics

The Australian & New Zealand journal of obstetrics & gynaecology

BMC biotechnology

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

Publications

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)
Paige Cornell, Taylah Armstrong, Rina Fyfe, Carly A Mallise, Tracy Dudding, Linda E Campbell
Experiences of non-invasive prenatal screening: A survey study. The Australian & New Zealand journal of obstetrics & gynaecology (2021)
Cheryl A Shoubridge, Robert J Harvey, Tracy Dudding
IQSEC2 mutation update and review of the female-specific phenotype spectrum including intellectual disability and epilepsy. Human mutation 40 (1) (2018)
Raman Kumar, Alison Gardner, Claire C Homan, Evelyn Douglas, Heather Mefford, Dagmar Wieczorek, Hermann-Josef Lüdecke, Zornitza Stark, Simon Sadedin, null null, Catherine Bearce Nowak, Jessica Douglas, Gretchen Parsons, Paul Mark, Lourdes Loidi, Gail E Herman, Theresa Mihalic Mosher, Meredith K Gillespie, Lauren Brady, Mark Tarnopolsky, Irene Madrigal, Jesús Eiris, Laura Domènech Salgado, Raquel Rabionet, Tim M Strom, Naoko Ishihara, Hidehito Inagaki, Hiroki Kurahashi, Tracy Dudding, Emma Elizabeth Palmer, Michael Field, Jozef Gecz
Severe neurocognitive and growth disorders due to variation in THOC2, an essential component of nuclear mRNA export machinery. Human mutation 39 (8) (2018)
Zandra A Jenkins, Alison Macharg, Cheng-Yee Chang, Margriet van Kogelenberg, Tim Morgan, Sophia Frentz, Wenhua Wei, Jacek Pilch, Mark Hannibal, Nicola Foulds, George McGillivray, Richard J Leventer, Sixto García-Miñaúr, Stuart Sugito, Scott Nightingale, David M Markie, Tracy Dudding, Raj P Kapur, Stephen P Robertson
Differential regulation of two FLNA transcripts explains some of the phenotypic heterogeneity in the loss-of-function filaminopathies. Human mutation 39 (1) (2017)
Tracy Dudding, Anne Baxter, Elizabeth G Holliday, Anna Hackett, Sheridan O'Donnell, Susan M White, John Attia, Han Brunner, Bert de Vries, David Koolen, Tjitske Kleefstra, Seshika Ratwatte, Carlos Riveros, Steve Brain, Brian C Lovell
Computer face-matching technology using two-dimensional photographs accurately matches the facial gestalt of unrelated individuals with the same syndromic form of intellectual disability. BMC biotechnology 17 (1) (2017)