List of works - Bing Yu

A comparison of the lengths of androgen receptor triplet repeats in brain and blood in motor neuron diseases

scientific article published on 13 November 2007

A gene-environment study of the paraoxonase 1 gene and pesticides in amyotrophic lateral sclerosis

article

A genome-wide analysis of brain DNA methylation identifies new candidate genes for sporadic amyotrophic lateral sclerosis.

scientific article published on October 2009

A method of oligochip for single nucleotide polymorphism genotyping in the promoter region of the interleukin-1 beta gene and its clinical application

article

A polymorphism in the poliovirus receptor gene differs in motor neuron disease

scientific article published in February 2004

Alterations of insulin-like growth factor-1 receptor gene copy number and protein expression are common in non-small cell lung cancer.

scientific article published on 12 August 2014

An analysis of the entire SOD1 gene in sporadic ALS

article

An approach to finding brain-situated mutations in sporadic Parkinson's disease

scientific article published on 13 September 2011

An online locus-specific mutation database for familial hypertrophic cardiomyopathy

scientific article published in January 1999

Analysis of clinically relevant somatic mutations in high-risk head and neck cutaneous squamous cell carcinoma.

scientific article published on 6 October 2017

Angiotensin-converting enzyme gene DD genotype is associated with increased systolic blood pressure in an Australian Rural Type 2 Diabetic Cohort

scientific article published on 13 December 2012

Are enteroviral receptors different in sporadic motor neuron disease?

scientific article published in February 2007

Are metallothionein genes silenced in ALS?

scientific article published on 15 November 2006

BRAF mutations in non-small cell lung cancer

scientific article

BRAF(V600E) and NRAS(Q61L/Q61R) mutation analysis in metastatic melanoma using immunohistochemistry: a study of 754 cases highlighting potential pitfalls and guidelines for interpretation and reporting.

scientific article

Capillary electrophoresis: new technology for DNA diagnostics

scientific article published on 01 August 1998

Challenges for clinical genetic DNA testing

scientific article published on March 2004

Combined effects of 19 common variations on type 2 diabetes in Chinese: results from two community-based studies

scientific article

Comprehensive analyses of somatic TP53 mutation in tumors with variable mutant allele frequency.

scientific article published on 5 September 2017

Computer-assisted reading of DNA sequences.

scientific article

Correlation of BRAF and NRAS mutation status with outcome, site of distant metastasis and response to chemotherapy in metastatic melanoma.

scientific article

DHPLC can be used to detect low-level mutations in amyotrophic lateral sclerosis

scientific article

DNA testing for haemochromatosis: diagnostic, predictive and screening implications

scientific article published on 01 November 2000

DNA testing in familial hypertrophic cardiomyopathy: clinical and laboratory implications

article

Development of an oligochip for genotyping human leukocyte antigen-B51 and its clinical application

scientific article published in January 2005

Dietary sialic acid supplementation improves learning and memory in piglets.

scientific article published in February 2007

Differential effects of calyculin A and okadaic acid on the glucose-induced regulation of glycogen synthase and phosphorylase activities in cultured hepatocytes

scientific article published on 01 November 1993

EGFR mutant-specific immunohistochemistry has high specificity and sensitivity for detecting targeted activating EGFR mutations in lung adenocarcinoma

scientific article published on 11 June 2013

EGFR-Co-Mutated Advanced NSCLC and Response to EGFR Tyrosine Kinase Inhibitors.

scientific article

Effects of metformin on glucose and glucagon regulated gluconeogenesis in cultured normal and diabetic hepatocytes.

scientific article published in August 1994

Environmental insults: critical triggers for amyotrophic lateral sclerosis

scientific article

Evidence for lymphatic pathogenesis of endosalpingiosis.

scientific article published on 22 December 2015

Exome sequencing of case-unaffected-parents trios reveals recessive and de novo genetic variants in sporadic ALS.

scientific article

Genetic susceptibility to environmental toxicants in ALS.

scientific article published in October 2007

Genetic variants in the promoter of TARDBP in sporadic amyotrophic lateral sclerosis

scientific article published on 19 August 2009

HER2 insertion YVMA mutant lung cancer: Long natural history and response to afatinib.

scientific article

In silico PCR analysis.

scientific article

In silico gene discovery.

scientific article published on January 2008

Looking for differences in copy number between blood and brain in sporadic amyotrophic lateral sclerosis

scientific article published on 8 August 2011

Low yield in screening patients with sporadic motor neuron disease for Kennedy disease

article

Mammary analogue secretory carcinoma: an evaluation of its clinicopathological and genetic characteristics.

scientific article published in December 2015

Molecular characterisation of neonatal cardiac hypertrophy and its regression

scientific article published in October 2004

Molecular characterization of pig ST8Sia IV--a critical gene for the formation of neural cell adhesion molecule and its response to sialic acid supplement in piglets

scientific article

Molecular pathology of familial hypertrophic cardiomyopathy caused by mutations in the cardiac myosin binding protein C gene.

scientific article

Molecular patterns in salivary duct carcinoma identify prognostic subgroups

scientific article published on 26 May 2020

Mutation surveyor: an in silico tool for sequencing analysis

scientific article

PD-L1 expression is a favorable prognostic factor in early stage non-small cell carcinoma.

scientific article

Patterns of DNA mutations and ALK rearrangement in resected node negative lung adenocarcinoma.

scientific article published on April 2013

Phaeochromocytoma, neurofibromatosis and gastrointestinal stromal tumour: just a random event?

scientific article published on 01 February 2011

Pharmacogenetic polymorphisms of the AR and metabolism and susceptibility to hormone-induced azoospermia

scientific article

Placental deficiency of interleukin-10 (IL-10) in preeclampsia and its relationship to an IL10 promoter polymorphism

Plasma total bilirubin levels predict amputation events in type 2 diabetes mellitus: the Fenofibrate Intervention and Event Lowering in Diabetes (FIELD) study

scientific article published on 17 January 2013

Polymorphisms of SP110 are associated with both pulmonary and extra-pulmonary tuberculosis among the Vietnamese

scientific article

SRp54 (SFRS11), a regulator for tau exon 10 alternative splicing identified by an expression cloning strategy

scientific article

Salivary duct carcinoma: Clinicopathologic features, morphologic spectrum, and somatic mutations.

scientific article

Screening for ROS1 gene rearrangements in non-small-cell lung cancers using immunohistochemistry with FISH confirmation is an effective method to identify this rare target.

scientific article published on 6 September 2016

Screening the metallothionein III gene in sporadic amyotrophic lateral sclerosis

scientific article published in June 2005

Setting up next-generation sequencing in the medical laboratory

scientific article

Sudden cardiac death in familial hypertrophic cardiomyopathy: are “benign” mutations really benign? ⬇️

article by C. Semsarian et al published August 1997 in Pathology

The EPAS1 gene influences the aerobic-anaerobic contribution in elite endurance athletes

scientific article

The future of genetic research in exercise science and sports medicine

scientific article

The molecular profile of metastatic melanoma in Australia

scientific article

The severity of hereditary porphyria is modulated by the porphyrin exporter and Lan antigen ABCB6.

scientific article published on 10 August 2016

The suitability of small biopsy and cytology specimens for EGFR and other mutation testing in non-small cell lung cancer

scientific article

The unique expression profile of the androgen receptor gene in a rat model of neonatal cardiac hypertrophy

article

Transmission of C9orf72 hexanucleotide repeat expansions in sporadic amyotrophic lateral sclerosis: an Australian trio study

article

UBE3A "mutations" in two unrelated and phenotypically different Angelman syndrome patients

scientific article published on April 1998

Using case-parent trios to look for rare de novo genetic variants in adult-onset neurodegenerative diseases.

scientific article published on 15 March 2011

Whole genome analyses reveal no pathogenetic single nucleotide or structural differences between monozygotic twins discordant for amyotrophic lateral sclerosis.

scientific article

Zinc transporter-8 gene (SLC30A8) is associated with type 2 diabetes in Chinese

scientific article published on 15 July 2008

List of works by Bing Yu

A comparison of the lengths of androgen receptor triplet repeats in brain and blood in motor neuron diseases

A gene-environment study of the paraoxonase 1 gene and pesticides in amyotrophic lateral sclerosis

A genome-wide analysis of brain DNA methylation identifies new candidate genes for sporadic amyotrophic lateral sclerosis.

A method of oligochip for single nucleotide polymorphism genotyping in the promoter region of the interleukin-1 beta gene and its clinical application

A polymorphism in the poliovirus receptor gene differs in motor neuron disease

Alterations of insulin-like growth factor-1 receptor gene copy number and protein expression are common in non-small cell lung cancer.

An analysis of the entire SOD1 gene in sporadic ALS

An approach to finding brain-situated mutations in sporadic Parkinson's disease

An online locus-specific mutation database for familial hypertrophic cardiomyopathy

Analysis of clinically relevant somatic mutations in high-risk head and neck cutaneous squamous cell carcinoma.

Angiotensin-converting enzyme gene DD genotype is associated with increased systolic blood pressure in an Australian Rural Type 2 Diabetic Cohort

Are enteroviral receptors different in sporadic motor neuron disease?

Are metallothionein genes silenced in ALS?

BRAF mutations in non-small cell lung cancer

BRAF(V600E) and NRAS(Q61L/Q61R) mutation analysis in metastatic melanoma using immunohistochemistry: a study of 754 cases highlighting potential pitfalls and guidelines for interpretation and reporting.

Capillary electrophoresis: new technology for DNA diagnostics

Challenges for clinical genetic DNA testing

Combined effects of 19 common variations on type 2 diabetes in Chinese: results from two community-based studies

Comprehensive analyses of somatic TP53 mutation in tumors with variable mutant allele frequency.

Computer-assisted reading of DNA sequences.

Correlation of BRAF and NRAS mutation status with outcome, site of distant metastasis and response to chemotherapy in metastatic melanoma.

DHPLC can be used to detect low-level mutations in amyotrophic lateral sclerosis

DNA testing for haemochromatosis: diagnostic, predictive and screening implications

DNA testing in familial hypertrophic cardiomyopathy: clinical and laboratory implications

Development of an oligochip for genotyping human leukocyte antigen-B51 and its clinical application

Dietary sialic acid supplementation improves learning and memory in piglets.

Differential effects of calyculin A and okadaic acid on the glucose-induced regulation of glycogen synthase and phosphorylase activities in cultured hepatocytes

EGFR mutant-specific immunohistochemistry has high specificity and sensitivity for detecting targeted activating EGFR mutations in lung adenocarcinoma

EGFR-Co-Mutated Advanced NSCLC and Response to EGFR Tyrosine Kinase Inhibitors.

Effects of metformin on glucose and glucagon regulated gluconeogenesis in cultured normal and diabetic hepatocytes.

Environmental insults: critical triggers for amyotrophic lateral sclerosis

Evidence for lymphatic pathogenesis of endosalpingiosis.

Exome sequencing of case-unaffected-parents trios reveals recessive and de novo genetic variants in sporadic ALS.

Genetic susceptibility to environmental toxicants in ALS.

Genetic variants in the promoter of TARDBP in sporadic amyotrophic lateral sclerosis

HER2 insertion YVMA mutant lung cancer: Long natural history and response to afatinib.

In silico PCR analysis.

In silico gene discovery.

Looking for differences in copy number between blood and brain in sporadic amyotrophic lateral sclerosis

Low yield in screening patients with sporadic motor neuron disease for Kennedy disease

Mammary analogue secretory carcinoma: an evaluation of its clinicopathological and genetic characteristics.

Molecular characterisation of neonatal cardiac hypertrophy and its regression

Molecular characterization of pig ST8Sia IV--a critical gene for the formation of neural cell adhesion molecule and its response to sialic acid supplement in piglets

Molecular pathology of familial hypertrophic cardiomyopathy caused by mutations in the cardiac myosin binding protein C gene.

Molecular patterns in salivary duct carcinoma identify prognostic subgroups

Mutation surveyor: an in silico tool for sequencing analysis

PD-L1 expression is a favorable prognostic factor in early stage non-small cell carcinoma.

Patterns of DNA mutations and ALK rearrangement in resected node negative lung adenocarcinoma.

Phaeochromocytoma, neurofibromatosis and gastrointestinal stromal tumour: just a random event?

Pharmacogenetic polymorphisms of the AR and metabolism and susceptibility to hormone-induced azoospermia

Placental deficiency of interleukin-10 (IL-10) in preeclampsia and its relationship to an IL10 promoter polymorphism

Plasma total bilirubin levels predict amputation events in type 2 diabetes mellitus: the Fenofibrate Intervention and Event Lowering in Diabetes (FIELD) study

Polymorphisms of SP110 are associated with both pulmonary and extra-pulmonary tuberculosis among the Vietnamese

SRp54 (SFRS11), a regulator for tau exon 10 alternative splicing identified by an expression cloning strategy

Salivary duct carcinoma: Clinicopathologic features, morphologic spectrum, and somatic mutations.

Screening for ROS1 gene rearrangements in non-small-cell lung cancers using immunohistochemistry with FISH confirmation is an effective method to identify this rare target.

Screening the metallothionein III gene in sporadic amyotrophic lateral sclerosis

Setting up next-generation sequencing in the medical laboratory

Sudden cardiac death in familial hypertrophic cardiomyopathy: are “benign” mutations really benign? ⬇️

The EPAS1 gene influences the aerobic-anaerobic contribution in elite endurance athletes

The future of genetic research in exercise science and sports medicine

The molecular profile of metastatic melanoma in Australia

The severity of hereditary porphyria is modulated by the porphyrin exporter and Lan antigen ABCB6.

The suitability of small biopsy and cytology specimens for EGFR and other mutation testing in non-small cell lung cancer

The unique expression profile of the androgen receptor gene in a rat model of neonatal cardiac hypertrophy

Transmission of C9orf72 hexanucleotide repeat expansions in sporadic amyotrophic lateral sclerosis: an Australian trio study

UBE3A "mutations" in two unrelated and phenotypically different Angelman syndrome patients

Using case-parent trios to look for rare de novo genetic variants in adult-onset neurodegenerative diseases.

Whole genome analyses reveal no pathogenetic single nucleotide or structural differences between monozygotic twins discordant for amyotrophic lateral sclerosis.

Zinc transporter-8 gene (SLC30A8) is associated with type 2 diabetes in Chinese