Lista de obras -

A Genome-Wide Scan Identifies Variants in NFIB Associated with Metastasis in Patients with Osteosarcoma

artículo científico publicado en 2015

A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer

artículo científico publicado en 2018

Age-related DNA methylation in paired normal and tumour breast tissue in Chinese breast cancer patients

scientific article published on 24 September 2020

Association analysis identifies 65 new breast cancer risk loci.

artículo científico publicado en 2017

Association between GWAS-identified lung adenocarcinoma susceptibility loci and EGFR mutations in never-smoking Asian women, and comparison with findings from Western populations

artículo científico publicado en 2016

Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis

article by Xiang Shu et al published 1 October 2018 in International Journal of Epidemiology

Effect of Recipient Age and Stem Cell Source on the Association between Donor Telomere Length and Survival after Allogeneic Unrelated Hematopoietic Cell Transplantation for Severe Aplastic Anemia

artículo científico publicado en 2016

Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome

artículo científico publicado en 2016

Genetic and epigenetic intratumor heterogeneity impacts prognosis of lung adenocarcinoma

artículo científico publicado en 2020

Genome-Wide Association Study in Irradiated Childhood Cancer Survivors Identifies HTR2A for Subsequent Basal Cell Carcinoma

scientific article published on 22 March 2019

Genome-Wide Association Study to Identify Susceptibility Loci That Modify Radiation-Related Risk for Breast Cancer After Childhood Cancer

artículo científico publicado en 2017

Genome-wide Association Study Identifies HLA-DPB1 as a Significant Risk Factor for Severe Aplastic Anemia

scientific article published on 30 January 2020

Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility

artículo científico publicado en 2020

High-throughput single nucleotide polymorphism genotyping using nanofluidic Dynamic Arrays

artículo científico publicado en 2009

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

artículo científico publicado en 2017

Loci associated with skin pigmentation identified in African populations.

artículo científico publicado en 2017

No association between donor telomere length and outcomes after allogeneic unrelated hematopoietic cell transplant in patients with acute leukemia.

artículo científico publicado en 2017

Population Frequency of Fanconi Pathway Gene Variants and Their Association with Survival After Hematopoietic Cell Transplantation for Severe Aplastic Anemia

scientific article published on 23 January 2020

Pre-transplant short telomeres are associated with high mortality risk after unrelated donor haematopoietic cell transplant for severe aplastic anaemia

scientific article published on 19 August 2019

Rare Germline Copy Number Variations and Disease Susceptibility in Familial Melanoma

artículo científico publicado en 2016

Rare germline variants in known melanoma susceptibility genes in familial melanoma

artículo científico publicado en 2017

Relative Telomere Length before Hematopoietic Cell Transplantation and Outcome after Unrelated Donor Hematopoietic Cell Transplantation for Acute Leukemia.

artículo científico publicado en 2017

Somatic Genomics and Clinical Features of Lung Adenocarcinoma: A Retrospective Study.

artículo científico publicado en 2016

Successful use of whole genome amplified DNA from multiple source types for high-density Illumina SNP microarrays.

artículo científico publicado en 2018

Telomere Length Calibration from qPCR Measurement: Limitations of Current Method

artículo científico publicado en 2018

The genomic and epigenomic evolutionary history of papillary renal cell carcinomas

scientific article published on 18 June 2020

Tuberculosis infection and lung adenocarcinoma: Mendelian randomization and pathway analysis of genome-wide association study data from never-smoking Asian women

artículo científico publicado en 2019

Two high-risk susceptibility loci at 6p25.3 and 14q32.13 for Waldenström macroglobulinemia

artículo científico publicado en 2018

Whole exome sequencing in 75 high-risk families with validation and replication in independent case-control studies identifies TANGO2, OR5H14, and CHAD as new prostate cancer susceptibility genes

artículo científico publicado en 2016

Whole exome sequencing in families at high risk for Hodgkin lymphoma: identification of a predisposing mutation in the KDR gene

artículo científico publicado en 2016

Whole exome sequencing in families with CLL detects a variant in Integrin β 2 associated with disease susceptibility

artículo científico publicado en 2016

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

artículo científico publicado en 2021

Lista de obras de

A Genome-Wide Scan Identifies Variants in NFIB Associated with Metastasis in Patients with Osteosarcoma

A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer

Age-related DNA methylation in paired normal and tumour breast tissue in Chinese breast cancer patients

Association analysis identifies 65 new breast cancer risk loci.

Association between GWAS-identified lung adenocarcinoma susceptibility loci and EGFR mutations in never-smoking Asian women, and comparison with findings from Western populations

Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis

Effect of Recipient Age and Stem Cell Source on the Association between Donor Telomere Length and Survival after Allogeneic Unrelated Hematopoietic Cell Transplantation for Severe Aplastic Anemia

Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome

Genetic and epigenetic intratumor heterogeneity impacts prognosis of lung adenocarcinoma

Genome-Wide Association Study in Irradiated Childhood Cancer Survivors Identifies HTR2A for Subsequent Basal Cell Carcinoma

Genome-Wide Association Study to Identify Susceptibility Loci That Modify Radiation-Related Risk for Breast Cancer After Childhood Cancer

Genome-wide Association Study Identifies HLA-DPB1 as a Significant Risk Factor for Severe Aplastic Anemia

Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility

High-throughput single nucleotide polymorphism genotyping using nanofluidic Dynamic Arrays

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

Loci associated with skin pigmentation identified in African populations.

No association between donor telomere length and outcomes after allogeneic unrelated hematopoietic cell transplant in patients with acute leukemia.

Population Frequency of Fanconi Pathway Gene Variants and Their Association with Survival After Hematopoietic Cell Transplantation for Severe Aplastic Anemia

Pre-transplant short telomeres are associated with high mortality risk after unrelated donor haematopoietic cell transplant for severe aplastic anaemia

Rare Germline Copy Number Variations and Disease Susceptibility in Familial Melanoma

Rare germline variants in known melanoma susceptibility genes in familial melanoma

Relative Telomere Length before Hematopoietic Cell Transplantation and Outcome after Unrelated Donor Hematopoietic Cell Transplantation for Acute Leukemia.

Somatic Genomics and Clinical Features of Lung Adenocarcinoma: A Retrospective Study.

Successful use of whole genome amplified DNA from multiple source types for high-density Illumina SNP microarrays.

Telomere Length Calibration from qPCR Measurement: Limitations of Current Method

The genomic and epigenomic evolutionary history of papillary renal cell carcinomas

Tuberculosis infection and lung adenocarcinoma: Mendelian randomization and pathway analysis of genome-wide association study data from never-smoking Asian women

Two high-risk susceptibility loci at 6p25.3 and 14q32.13 for Waldenström macroglobulinemia

Whole exome sequencing in 75 high-risk families with validation and replication in independent case-control studies identifies TANGO2, OR5H14, and CHAD as new prostate cancer susceptibility genes

Whole exome sequencing in families at high risk for Hodgkin lymphoma: identification of a predisposing mutation in the KDR gene

Whole exome sequencing in families with CLL detects a variant in Integrin β 2 associated with disease susceptibility

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