List of works - Daniel J Park

Genome-wide association studies identify four ER negative-specific breast cancer risk loci

scientific article published in April 2013

Genome-wide association analysis identifies three new breast cancer susceptibility loci

scientific article published on 22 January 2012

A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11.

scientific article

A PALB2 mutation associated with high risk of breast cancer

scientific article

19p13.1 is a triple-negative-specific breast cancer susceptibility locus

scientific article published on 13 February 2012

A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age.

scientific article

Comparison of 6q25 breast cancer hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)

scientific article

The use of DNA from archival dried blood spots with the Infinium HumanMethylation450 array

scientific article

Rare mutations in RINT1 predispose carriers to breast and Lynch syndrome-spectrum cancers

scientific article

Prevalence of PALB2 mutations in Australasian multiple-case breast cancer families

scientific article published on 28 February 2013

Variant effect prediction tools assessed using independent, functional assay-based datasets: implications for discovery and diagnostics

scientific article published on 16 May 2017

Mutation screening of PALB2 in clinically ascertained families from the Breast Cancer Family Registry

scientific article

No evidence of MMTV-like env sequences in specimens from the Australian Breast Cancer Family Study

scientific article published on 30 May 2010

A high-plex PCR approach for massively parallel sequencing.

scientific article published on August 2013

COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration

scientific article published on 21 June 2013

Global measures of peripheral blood-derived DNA methylation as a risk factor in the development of mature B-cell neoplasms

scientific article published on 18 December 2015

Genome-wide measures of DNA methylation in peripheral blood and the risk of urothelial cell carcinoma: a prospective nested case-control study

scientific article published on 4 August 2016

Use of a phage-based assay for phenotypic detection of mycobacteria directly from sputum.

scientific article

FAN1 variants identified in multiple-case early-onset breast cancer families via exome sequencing: no evidence for association with risk for breast cancer

scientific article

Hi-Plex for high-throughput mutation screening: application to the breast cancer susceptibility gene PALB2

scientific article

Cross-platform compatibility of Hi-Plex, a streamlined approach for targeted massively parallel sequencing.

scientific article

ROVER variant caller: read-pair overlap considerate variant-calling software applied to PCR-based massively parallel sequencing datasets.

scientific article published on 24 January 2014

Comparative analysis of ATRX, a chromatin remodeling protein

scientific article

Evaluation of germline BRCA1 and BRCA2 mutations in a multi-ethnic Asian cohort of ovarian cancer patients

scientific article published on 2 November 2015

Abridged adapter primers increase the target scope of Hi-Plex

scientific article published in January 2015

FAVR (Filtering and Annotation of Variants that are Rare): methods to facilitate the analysis of rare germline genetic variants from massively parallel sequencing datasets

scientific article published on 25 February 2013

3' RACE walking along a large cDNA employing tiered suppression PCR.

scientific article

UNDR ROVER - a fast and accurate variant caller for targeted DNA sequencing

scientific article

Annokey: an annotation tool based on key term search of the NCBI Entrez Gene database.

scientific article published on 26 June 2014

Correction: Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)

scientific article published in PLoS ONE

Characterisation of the marsupial-specific ATRY gene: implications for the evolution of male-specific function.

scientific article published on 4 October 2005

Universal fast walking applied to cDNA.

scientific article published in May 2004

Mismatch repair gene pathogenic germline variants in a population-based cohort of breast cancer

scientific article published on 14 February 2020

Is RNASEL:p.Glu265* a modifier of early-onset breast cancer risk for carriers of high-risk mutations?

scientific article published on 8 February 2018

A new 5' terminal murine GAPDH exon identified using 5'RACE LaNe.

scientific article

Enhanced solid phase PCR for increased loading of amplicon onto solid support.

scientific article

Fine resolution mapping of double-strand break sites for human ribosomal DNA units

scientific article

Supplementary Table 6 from The Germline and Somatic Origins of Prostate Cancer Heterogeneity

Activities of Bacillus thuringiensis insecticidal crystal proteins Cyt1Aa and Cyt2Aa against three species of sheep blowfly

scientific article published on October 1998

Genetic testing in Poland and Ukraine: should comprehensive germline testing of BRCA1 and BRCA2 be recommended for women with breast and ovarian cancer?

scientific article published on 10 August 2020

Supplementary Table 3 from The Germline and Somatic Origins of Prostate Cancer Heterogeneity

Single nucleotide-level mapping of DNA double-strand breaks in human HEK293T cells

scientific article published on 11 November 2016

Use of a Novel Nonparametric Version of DEPTH to Identify Genomic Regions Associated with Prostate Cancer Risk

scientific article published on 18 August 2016

List of works by Daniel J Park

Genome-wide association studies identify four ER negative-specific breast cancer risk loci

Genome-wide association analysis identifies three new breast cancer susceptibility loci

A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11.

A PALB2 mutation associated with high risk of breast cancer

19p13.1 is a triple-negative-specific breast cancer susceptibility locus

A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age.

Comparison of 6q25 breast cancer hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)

The use of DNA from archival dried blood spots with the Infinium HumanMethylation450 array

Rare mutations in RINT1 predispose carriers to breast and Lynch syndrome-spectrum cancers

Prevalence of PALB2 mutations in Australasian multiple-case breast cancer families

Variant effect prediction tools assessed using independent, functional assay-based datasets: implications for discovery and diagnostics

Mutation screening of PALB2 in clinically ascertained families from the Breast Cancer Family Registry

No evidence of MMTV-like env sequences in specimens from the Australian Breast Cancer Family Study

A high-plex PCR approach for massively parallel sequencing.

COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration

Global measures of peripheral blood-derived DNA methylation as a risk factor in the development of mature B-cell neoplasms

Genome-wide measures of DNA methylation in peripheral blood and the risk of urothelial cell carcinoma: a prospective nested case-control study

Use of a phage-based assay for phenotypic detection of mycobacteria directly from sputum.

FAN1 variants identified in multiple-case early-onset breast cancer families via exome sequencing: no evidence for association with risk for breast cancer

Hi-Plex for high-throughput mutation screening: application to the breast cancer susceptibility gene PALB2

Cross-platform compatibility of Hi-Plex, a streamlined approach for targeted massively parallel sequencing.

ROVER variant caller: read-pair overlap considerate variant-calling software applied to PCR-based massively parallel sequencing datasets.

Comparative analysis of ATRX, a chromatin remodeling protein

Evaluation of germline BRCA1 and BRCA2 mutations in a multi-ethnic Asian cohort of ovarian cancer patients

Abridged adapter primers increase the target scope of Hi-Plex

FAVR (Filtering and Annotation of Variants that are Rare): methods to facilitate the analysis of rare germline genetic variants from massively parallel sequencing datasets

3' RACE walking along a large cDNA employing tiered suppression PCR.

UNDR ROVER - a fast and accurate variant caller for targeted DNA sequencing

Annokey: an annotation tool based on key term search of the NCBI Entrez Gene database.

Correction: Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)

Characterisation of the marsupial-specific ATRY gene: implications for the evolution of male-specific function.

Universal fast walking applied to cDNA.

Mismatch repair gene pathogenic germline variants in a population-based cohort of breast cancer

Is RNASEL:p.Glu265* a modifier of early-onset breast cancer risk for carriers of high-risk mutations?

A new 5' terminal murine GAPDH exon identified using 5'RACE LaNe.

Enhanced solid phase PCR for increased loading of amplicon onto solid support.

Fine resolution mapping of double-strand break sites for human ribosomal DNA units

Supplementary Table 6 from The Germline and Somatic Origins of Prostate Cancer Heterogeneity

Activities of Bacillus thuringiensis insecticidal crystal proteins Cyt1Aa and Cyt2Aa against three species of sheep blowfly

Genetic testing in Poland and Ukraine: should comprehensive germline testing of BRCA1 and BRCA2 be recommended for women with breast and ovarian cancer?

Supplementary Table 3 from The Germline and Somatic Origins of Prostate Cancer Heterogeneity

Single nucleotide-level mapping of DNA double-strand breaks in human HEK293T cells

Use of a Novel Nonparametric Version of DEPTH to Identify Genomic Regions Associated with Prostate Cancer Risk

Figure 7 from The Germline and Somatic Origins of Prostate Cancer Heterogeneity

Supplementary Table 4 from The Germline and Somatic Origins of Prostate Cancer Heterogeneity