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1.

Rare germline variants in PALB2 and BRCA2 in familial and sporadic chordoma.

Xia, Bing; Biswas, Kajal; Foo, Tzeh K; Gomes, Thiago T; Riedel-Topper, Maximilian; Southon, Eileen; Kang, Zhihua; Huo, Yanying; Reid, Susan; Stauffer, Stacey; Zhou, Weiyin; Zhu, Bin; Koka, Hela; Yepes, Sally; Brodie, Seth A; Jones, Kristine; Vogt, Aurelie; Zhu, Bin; Carter, Brian; Freedman, Neal D; Hicks, Belynda; Yeager, Meredith; Chanock, Stephen J; Couch, Fergus; Parry, Dilys M; Monteiro, Alvaro N; Goldstein, Alisa M; Carvalho, Marcelo A; Sharan, Shyam K; Yang, Xiaohong R.

Hum Mutat ; 43(10): 1396-1407, 2022 10.

Artículo en Inglés | MEDLINE | ID: mdl-35762214

2.

Characterization of T gene sequence variants and germline duplications in familial and sporadic chordoma.

Kelley, Michael J; Shi, Jianxin; Ballew, Bari; Hyland, Paula L; Li, Wen-Qing; Rotunno, Melissa; Alcorta, David A; Liebsch, Norbert J; Mitchell, Jason; Bass, Sara; Roberson, David; Boland, Joseph; Cullen, Michael; He, Ji; Burdette, Laurie; Yeager, Meredith; Chanock, Stephen J; Parry, Dilys M; Goldstein, Alisa M; Yang, Xiaohong R.

Hum Genet ; 133(10): 1289-97, 2014 Oct.

Artículo en Inglés | MEDLINE | ID: mdl-24990759

3.

Gene Expression Profiling Identifies Two Chordoma Subtypes Associated with Distinct Molecular Mechanisms and Clinical Outcomes.

Bai, Jiwei; Shi, Jianxin; Zhang, Yazhuo; Li, Chuzhong; Xiong, Yujia; Koka, Hela; Wang, Difei; Zhang, Tongwu; Song, Lei; Luo, Wen; Zhu, Bin; Hicks, Belynda; Hutchinson, Amy; Kirk, Erin; Troester, Melissa A; Li, Mingxuan; Shen, Yutao; Ma, Tianshun; Wang, Junmei; Liu, Xing; Wang, Shuai; Gui, Songbai; McMaster, Mary L; Chanock, Stephen J; Parry, Dilys M; Goldstein, Alisa M; Yang, Xiaohong R.

Clin Cancer Res ; 29(1): 261-270, 2023 01 04.

Artículo en Inglés | MEDLINE | ID: mdl-36260525

4.

Clinical features distinguish childhood chordoma associated with tuberous sclerosis complex (TSC) from chordoma in the general paediatric population.

McMaster, Mary L; Goldstein, Alisa M; Parry, Dilys M.

J Med Genet ; 48(7): 444-9, 2011 Jul.

Artículo en Inglés | MEDLINE | ID: mdl-21266383

5.

Rare Germline Variants in Chordoma-Related Genes and Chordoma Susceptibility.

Yepes, Sally; Shah, Nirav N; Bai, Jiwei; Koka, Hela; Li, Chuzhong; Gui, Songbai; McMaster, Mary Lou; Xiao, Yanzi; Jones, Kristine; Wang, Mingyi; Vogt, Aurelie; Zhu, Bin; Zhu, Bin; Hutchinson, Amy; Yeager, Meredith; Hicks, Belynda; Carter, Brian; Freedman, Neal D; Beane-Freeman, Laura; Chanock, Stephen J; Zhang, Yazhuo; Parry, Dilys M; Yang, Xiaohong R; Goldstein, Alisa M.

Cancers (Basel) ; 13(11)2021 May 30.

Artículo en Inglés | MEDLINE | ID: mdl-34070849

6.

Whole genome sequencing of skull-base chordoma reveals genomic alterations associated with recurrence and chordoma-specific survival.

Bai, Jiwei; Shi, Jianxin; Li, Chuzhong; Wang, Shuai; Zhang, Tongwu; Hua, Xing; Zhu, Bin; Koka, Hela; Wu, Ho-Hsiang; Song, Lei; Wang, Difei; Wang, Mingyi; Zhou, Weiyin; Ballew, Bari J; Zhu, Bin; Hicks, Belynda; Mirabello, Lisa; Parry, Dilys M; Zhai, Yixuan; Li, Mingxuan; Du, Jiang; Wang, Junmei; Zhang, Shuheng; Liu, Qian; Zhao, Peng; Gui, Songbai; Goldstein, Alisa M; Zhang, Yazhuo; Yang, Xiaohong R.

Nat Commun ; 12(1): 757, 2021 02 03.

Artículo en Inglés | MEDLINE | ID: mdl-33536423

7.

Neurofibromatosis type 2.

Asthagiri, Ashok R; Parry, Dilys M; Butman, John A; Kim, H Jeffrey; Tsilou, Ekaterini T; Zhuang, Zhengping; Lonser, Russell R.

Lancet ; 373(9679): 1974-86, 2009 Jun 06.

Artículo en Inglés | MEDLINE | ID: mdl-19476995

8.

Monozygotic twins discordant for neurofibromatosis 1.

Kaplan, Lee; Foster, Rosemary; Shen, Yiping; Parry, Dilys M; McMaster, Mary L; O'Leary, Melanie Collins; Gusella, James F.

Am J Med Genet A ; 152A(3): 601-6, 2010 Mar.

Artículo en Inglés | MEDLINE | ID: mdl-20186797

9.

Clinical findings in families with chordoma with and without T gene duplications and in patients with sporadic chordoma reported to the Surveillance, Epidemiology, and End Results program.

Parry, Dilys M; McMaster, Mary L; Liebsch, Norbert J; Patronas, Nicholas J; Quezado, Martha M; Zametkin, Deborah; Yang, Xiaohong R; Goldstein, Alisa M.

J Neurosurg ; 134(5): 1399-1408, 2020 Jun 19.

Artículo en Inglés | MEDLINE | ID: mdl-32559743

10.

Predictors of vestibular schwannoma growth in patients with neurofibromatosis Type 2.

Baser, Michael E; Makariou, Erini V; Parry, Dilys M.

J Neurosurg ; 96(2): 217-22, 2002 Feb.

Artículo en Inglés | MEDLINE | ID: mdl-11838793

11.

NF2 and spinal tumors.

Parry, Dilys M.

J Neurosurg Spine ; 5(2): 179; author reply 179, 2006 Aug.

Artículo en Inglés | MEDLINE | ID: mdl-16925089

12.

T (brachyury) gene duplication confers major susceptibility to familial chordoma.

Yang, Xiaohong R; Ng, David; Alcorta, David A; Liebsch, Norbert J; Sheridan, Eamonn; Li, Sufeng; Goldstein, Alisa M; Parry, Dilys M; Kelley, Michael J.

Nat Genet ; 41(11): 1176-8, 2009 Nov.

Artículo en Inglés | MEDLINE | ID: mdl-19801981

13.

Laminar organization of spinal dorsal horn neurones activated by C- vs. A-heat nociceptors and their descending control from the periaqueductal grey in the rat.

Koutsikou, Stella; Parry, Dilys M; MacMillan, Frankie M; Lumb, Bridget M.

Eur J Neurosci ; 26(4): 943-52, 2007 Aug.

Artículo en Inglés | MEDLINE | ID: mdl-17714188

14.

Corroboration of a familial chordoma locus on chromosome 7q and evidence of genetic heterogeneity using single nucleotide polymorphisms (SNPs).

Yang, Xiaohong ' Rose '; Beerman, Michael; Bergen, Andrew W; Parry, Dilys M; Sheridan, Eamonn; Liebsch, Norbert J; Kelley, Michael J; Chanock, Stephen; Goldstein, Alisa M.

Int J Cancer ; 116(3): 487-91, 2005 Sep 01.

Artículo en Inglés | MEDLINE | ID: mdl-15818627

15.

Loss of heterozygosity for the NF2 gene in retinal and optic nerve lesions of patients with neurofibromatosis 2.

Chan, Chi-Chao; Koch, Christian A; Kaiser-Kupfer, Muriel I; Parry, Dilys M; Gutmann, David H; Zhuang, Zhengping; Vortmeyer, Alexander O.

J Pathol ; 198(1): 14-20, 2002 Sep.

Artículo en Inglés | MEDLINE | ID: mdl-12210058

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