Dudding TE - Search Results

Year	Number of Results
1998	1
2004	2
2006	1
2008	1
2010	2
2012	2
2022	1
2024	1
2025	0

1

RNA variant assessment using transactivation and transdifferentiation.

Nicolas-Martinez EC, Robinson O, Pflueger C, Gardner A, Corbett MA, Ritchie T, Kroes T, van Eyk CL, Scheffer IE, Hildebrand MS, Barnier JV, Rousseau V, Genevieve D, Haushalter V, Piton A, Denommé-Pichon AS, Bruel AL, Nambot S, Isidor B, Grigg J, Gonzalez T, Ghedia S, Marchant RG, Bournazos A, Wong WK, Webster RI, Evesson FJ, Jones KJ; PERSYST Investigator Team; Cooper ST, Lister R, Gecz J, Jolly LA. Nicolas-Martinez EC, et al. Am J Hum Genet. 2024 Aug 8;111(8):1673-1699. doi: 10.1016/j.ajhg.2024.06.018. Epub 2024 Jul 30. Am J Hum Genet. 2024. PMID: 39084224 Free PMC article.

2

Lessons from the skin--cutaneous features of familial cancer.

Winship IM, Dudding TE. Winship IM, et al. Among authors: dudding te. Lancet Oncol. 2008 May;9(5):462-72. doi: 10.1016/S1470-2045(08)70126-8. Lancet Oncol. 2008. PMID: 18452857 Review.

3

Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia.

Huang L, Warman-Chardon J, Carter MT, Friend KL, Dudding TE, Schwartzentruber J, Zou R, Schofield PW, Douglas S, Bulman DE, Boycott KM. Huang L, et al. Among authors: dudding te. Orphanet J Rare Dis. 2022 Mar 29;17(1):143. doi: 10.1186/s13023-022-02297-7. Orphanet J Rare Dis. 2022. PMID: 35351177 Free PMC article. No abstract available.

4

Maternal factor V Leiden and adverse pregnancy outcome: deciding whether or not to test.

Dudding TE, Attia J. Dudding TE, et al. J Matern Fetal Neonatal Med. 2012 Jul;25(7):889-94. doi: 10.3109/14767058.2011.608815. Epub 2012 Apr 25. J Matern Fetal Neonatal Med. 2012. PMID: 21854123 Review.

5

Nevoid hypertrichosis with multiple patches of hair that underwent almost complete spontaneous resolution.

Dudding TE, Rogers M, Roddick LG, Relic J, Edwards MJ. Dudding TE, et al. Am J Med Genet. 1998 Sep 23;79(3):195-6. doi: 10.1002/(sici)1096-8628(19980923)79:3<195::aid-ajmg8>3.0.co;2-m. Am J Med Genet. 1998. PMID: 9788560 Review.

6

Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia.

Huang L, Chardon JW, Carter MT, Friend KL, Dudding TE, Schwartzentruber J, Zou R, Schofield PW, Douglas S, Bulman DE, Boycott KM. Huang L, et al. Among authors: dudding te. Orphanet J Rare Dis. 2012 Sep 17;7:67. doi: 10.1186/1750-1172-7-67. Orphanet J Rare Dis. 2012. PMID: 22986007 Free PMC article.

7

The virtual consultation: practitioners' experiences of genetic counseling by videoconferencing in Australia.

Zilliacus E, Meiser B, Lobb E, Dudding TE, Barlow-Stewart K, Tucker K. Zilliacus E, et al. Among authors: dudding te. Telemed J E Health. 2010 Apr;16(3):350-7. doi: 10.1089/tmj.2009.0108. Telemed J E Health. 2010. PMID: 20406122

8

Screening behavior in women at increased familial risk for breast cancer.

Antill YC, Reynolds J, Young MA, Kirk JA, Tucker KM, Bogtstra TL, Wong SS, Dudding TE, Di Iulio JL, Phillips KA. Antill YC, et al. Among authors: dudding te. Fam Cancer. 2006;5(4):359-68. doi: 10.1007/s10689-006-0006-8. Epub 2006 Jul 7. Fam Cancer. 2006. PMID: 16817030

9

The association between adverse pregnancy outcomes and maternal factor V Leiden genotype: a meta-analysis.

Dudding TE, Attia J. Dudding TE, et al. Thromb Haemost. 2004 Apr;91(4):700-11. doi: 10.1160/TH03-10-0637. Thromb Haemost. 2004. PMID: 15045131

10

Array comparative genomic hybridization for the detection of submicroscopic copy number variations of the X chromosome in women with premature ovarian failure.

Dudding TE, Lawrence O, Winship I, Froyen G, Vandewalle J, Scott R, Shelling AN. Dudding TE, et al. Hum Reprod. 2010 Dec;25(12):3159-60; author reply 3160-1. doi: 10.1093/humrep/deq284. Epub 2010 Oct 16. Hum Reprod. 2010. PMID: 20952765 No abstract available.

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