Au CH - Search Results

1

Mutation Spectrum Comparison between Benign Breast Lesion Cohort, Unselected Cancer Cohort and High-Risk Breast Cancer Cohort.

Kwong A, Ho CYS, Leung HCM, Leung AWS, Au CH, Ma ESK. Kwong A, et al. Among authors: au ch. Cancers (Basel). 2024 Sep 3;16(17):3066. doi: 10.3390/cancers16173066. Cancers (Basel). 2024. PMID: 39272924 Free PMC article.

2

Mutation screening of germline TP53 mutations in high-risk Chinese breast cancer patients.

Kwong A, Shin VY, Ho CYS, Au CH, Slavin TP, Weitzel JN, Chan TL, Ma ESK. Kwong A, et al. Among authors: au ch. BMC Cancer. 2020 Nov 2;20(1):1053. doi: 10.1186/s12885-020-07476-y. BMC Cancer. 2020. PMID: 33138793 Free PMC article.

3

Germline PALB2 Mutation in High-Risk Chinese Breast and/or Ovarian Cancer Patients.

Kwong A, Shin VY, Ho CYS, Khalid A, Au CH, Chan KKL, Ngan HYS, Chan TL, Ma ESK. Kwong A, et al. Among authors: au ch. Cancers (Basel). 2021 Aug 20;13(16):4195. doi: 10.3390/cancers13164195. Cancers (Basel). 2021. PMID: 34439348 Free PMC article.

4

Effect on Germline Mutation Rate in a High-Risk Chinese Breast Cancer Cohort after Compliance with The National Comprehensive Cancer Network (NCCN) 2023 v.1 Testing Criteria.

Kwong A, Ho CYS, Luk WP, Fung LH, Au CH, Ma ESK. Kwong A, et al. Among authors: au ch. Cancers (Basel). 2023 May 6;15(9):2635. doi: 10.3390/cancers15092635. Cancers (Basel). 2023. PMID: 37174101 Free PMC article.

5

Double Heterozygosity for Germline Mutations in Chinese Breast Cancer Patients.

Kwong A, Ho CYS, Au CH, Ma ESK. Kwong A, et al. Among authors: au ch. Cancers (Basel). 2024 Jul 15;16(14):2547. doi: 10.3390/cancers16142547. Cancers (Basel). 2024. PMID: 39061189 Free PMC article.

6

The importance of analysis of long-range rearrangement of BRCA1 and BRCA2 in genetic diagnosis of familial breast cancer.

Kwong A, Chen J, Shin VY, Ho JC, Law FB, Au CH, Chan TL, Ma ES, Ford JM. Kwong A, et al. Among authors: au ch. Cancer Genet. 2015 Sep;208(9):448-54. doi: 10.1016/j.cancergen.2015.05.031. Epub 2015 Jun 9. Cancer Genet. 2015. PMID: 26271414

7

INDELseek: detection of complex insertions and deletions from next-generation sequencing data.

Au CH, Leung AY, Kwong A, Chan TL, Ma ES. Au CH, et al. BMC Genomics. 2017 Jan 5;18(1):16. doi: 10.1186/s12864-016-3449-9. BMC Genomics. 2017. PMID: 28056804 Free PMC article.

8

BAMClipper: removing primers from alignments to minimize false-negative mutations in amplicon next-generation sequencing.

Au CH, Ho DN, Kwong A, Chan TL, Ma ESK. Au CH, et al. Sci Rep. 2017 May 8;7(1):1567. doi: 10.1038/s41598-017-01703-6. Sci Rep. 2017. PMID: 28484262 Free PMC article.

9

Somatic mutation profiling in BRCA-negative breast and ovarian cancer patients by multigene panel sequencing.

Kwong A, Cheuk IW, Shin VY, Ho CY, Au CH, Ho DN, Wong EY, Yu SW, Chen J, Chan KK, Ngan HY, Chan TL, Ma ES. Kwong A, et al. Among authors: au ch. Am J Cancer Res. 2020 Sep 1;10(9):2919-2932. eCollection 2020. Am J Cancer Res. 2020. PMID: 33042626 Free PMC article.

10

A Case Report of Germline Compound Heterozygous Mutations in the BRCA1 Gene of an Ovarian and Breast Cancer Patient.

Kwong A, Ho CYS, Shin VY, Au CH, Chan TL, Ma ESK. Kwong A, et al. Among authors: au ch. Int J Mol Sci. 2021 Jan 17;22(2):889. doi: 10.3390/ijms22020889. Int J Mol Sci. 2021. PMID: 33477375 Free PMC article.

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