Publications by authors named "Tracy Dudding"

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Further phenotypical delineation of DLG3-related neurodevelopmental disorders.
Marlène Malbos, Thierry Gautier, Amelle Shillington, Estelle Colin, Xavier Le Guillou, Tracy Dudding

Eur J Hum Genet· December 2025

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The spectrum of heart defects in the -related multiple congenital anomalies-intellectual disability syndrome.
Elise Pisan, Chiara De Luca, Francesco Brancati, Rossana Sanchez Russo, Dong Li, Tracy Dudding

Proc Natl Acad Sci U S A· March 2024

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Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia.
Lijia Huang, Jodi Warman-Chardon, Melissa T Carter, Kathie L Friend, Tracy E Dudding

Orphanet J Rare Dis· March 2022

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Differential regulation of two FLNA transcripts explains some of the phenotypic heterogeneity in the loss-of-function filaminopathies.
Zandra A Jenkins, Alison Macharg, Cheng-Yee Chang, Margriet van Kogelenberg, Tim Morgan, Tracy Dudding

Hum Mutat· January 2018

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Erratum: Hwang Y.T. et al. Molecular Inconsistencies in a Fragile X Male with Early Onset Ataxia. Genes 2016, 7, 68.
Yun Tae Hwang, Tracy Dudding, Solange Mabel Aliaga, Marta Arpone, David Francis

Genes (Basel)· January 2017

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Somatic-gonadal mosaicism causing Sotos syndrome.
Benjamin Kamien, Tessa Dadd, Melissa Buckman, Anne Ronan, Tracy Dudding

Am J Med Genet A· December 2016

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Molecular Inconsistencies in a Fragile X Male with Early Onset Ataxia.
Yun Tae Hwang, Tracy Dudding, Solange Mabel Aliaga, Marta Arpone, David Francis

Genes (Basel)· September 2016

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Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genes.
Renske Oegema, Thomas D Cushion, Ian G Phelps, Seo-Kyung Chung, Jennifer C Dempsey, Tracy Dudding

Hum Mol Genet· September 2015

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Diverse phenotypic consequences of mutations affecting the C-terminus of FLNA.
Margriet van Kogelenberg, Alice R Clark, Zandra Jenkins, Tim Morgan, Ananda Anandan, Tracy Dudding

J Mol Med (Berl)· July 2015

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Carbimazole/methimazole embryopathy in siblings: a possible genetic susceptibility.
Himanshu Goel, Tracy Dudding

Birth Defects Res A Clin Mol Teratol· November 2013

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Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia.
Lijia Huang, Jodi Warman Chardon, Melissa T Carter, Kathie L Friend, Tracy E Dudding

Orphanet J Rare Dis· September 2012

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Maternal factor V Leiden and adverse pregnancy outcome: deciding whether or not to test.
Tracy E Dudding, John Attia

J Matern Fetal Neonatal Med· July 2012

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Frameshift mutation hotspot identified in Smith-Magenis syndrome: case report and review of literature.
Hoa T Truong, Tracy Dudding, Christopher L Blanchard, Sarah H Elsea

BMC Med Genet· October 2010

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Lessons from the skin--cutaneous features of familial cancer.
Ingrid M Winship, Tracy E Dudding

Lancet Oncol· May 2008

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A randomized controlled trial of a decision aid for women considering genetic testing for breast and ovarian cancer risk.
Claire E Wakefield, Bettina Meiser, Judi Homewood, Michelle Peate, Alan Taylor, Tracy Dudding

Breast Cancer Res Treat· January 2008

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Atypical Angelman syndrome with macrocephaly due to a familial imprinting center deletion.
Anne Ronan, Karin Buiting, Tracy Dudding

Am J Med Genet A· January 2008

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Screening behavior in women at increased familial risk for breast cancer.
Yoland C Antill, John Reynolds, Mary Anne Young, Judy A Kirk, Katherine M Tucker, Tracy E Dudding

Fam Cancer· September 2007

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Risk-reducing surgery in women with familial susceptibility for breast and/or ovarian cancer.
Yoland Antill, John Reynolds, Mary-Anne Young, Judy Kirk, Katherine Tucker, Tracy Dudding

Eur J Cancer· March 2006

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Addendum to: The association between adverse pregnancy outcomes and maternal factor V Leiden genotype. A meta-analysis.
John Attia, Tracy Dudding, Claire Infante-Rivard

Thromb Haemost· August 2004

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The association between adverse pregnancy outcomes and maternal factor V Leiden genotype: a meta-analysis.
Tracy E Dudding, John Attia

Thromb Haemost· April 2004

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