Author

Ya‐Gang Xie

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy

1998 · Bernard Brais, Jean-Pierre Bouchard, et al. · Nature Genetics · 805

Comparison of multifrequency bioelectrical impedance analysis with dual-energy X-ray absorptiometry for assessment of percentage body fat in a large, healthy population

2005 · Guang Sun, Curtis R French, et al. · American Journal of Clinical Nutrition · 377

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The oculopharyngeal muscular dystrophy locus maps to the region of the cardiac α and β myosin heavy chain genes on chromosome 14q11.2−q13

1995 · Bernard Brais, Ya-Gang Xie, et al. · Human Molecular Genetics · 153

Deletions on chromosome 22 in sporadic meningioma

1994 · Martin H. Ruttledge, Ya‐Gang Xie, et al. · Genes Chromosomes and Cancer · 127

The human LARGE gene from 22q12.3-q13.1 is a new, distinct member of the glycosyltransferase gene family

1999 · Myriam Peyrard, Eyal Seroussi, et al. · Proceedings of the National Academy of Sciences · 120

Serum visfatin concentrations are positively correlated with serum triacylglycerols and down-regulated by overfeeding in healthy young men

2007 · Guang Sun, Jessica Bishop, et al. · American Journal of Clinical Nutrition · 117

Characterization of a new member of the human /-adaptin gene family from chromosome 22q12, a candidate meningioma gene

1994 · Myriam Peyrard, Ingegerd Fransson, et al. · Human Molecular Genetics · 99

Combined carrier status of prothrombin 20210A and factor XIII-A Leu34 alleles as a strong risk factor for myocardial infarction: evidence of a gene-gene interaction

2003 · Christopher Butt, Hong Zheng, et al. · Blood · 76

Iron Overload Is Rare in Patients Homozygous for the H63D Mutation

2014 · Melissa Kelley, Nikhil Joshi, et al. · Canadian Journal of Gastroenterology and Hepatology · 46

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Concordance of BAI and BMI with DXA in the Newfoundland Population

2013 · Guang Sun, Farrell Cahill, et al. · Obesity · 37

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Using the full power of linkage analysis in 11 French Canadian families to fine map the oculopharyngeal muscular dystrophy gene

1997 · Bernard Brais, Jean-Pierre Bouchard, et al. · Neuromuscular Disorders · 27

Gender Dependent Association of Thrombospondin-4 A387P Polymorphism With Myocardial Infarction

2004 · Jianxun Cui, Edward Randell, et al. · Arteriosclerosis Thrombosis and Vascular Biology · 26

Thrombospondin-4 1186G>C (A387P) is a sex-dependent risk factor for myocardial infarction: A large replication study with increased sample size from the same population

2006 · Jianxun Cui, Edward Randell, et al. · American Heart Journal · 24

Individuals Homozygous for the H63D Mutation Have Significantly Elevated Iron Indexes

2006 · Jason Samarasena, Wendy Winsor, et al. · Digestive Diseases and Sciences · 23

An Association Between the Common Hereditary Hemochromatosis Mutation and the Factor V Leiden Allele in a Population With Thrombosis

1998 · Ya-Gang Xie, David P. Lillicrap, et al. · Blood · 17

An Extremely Low Prevalence of Factor V Leiden, FIIG20210A and FXIIIV34L in Taiwan Chinese Population

2002 · Hong Zheng, Tzeng Ching-Chemg, et al. · Thrombosis and Haemostasis · 15

Physical Mapping of the NF2/Meningioma Region on Human Chromosome 22q12

1994 · Martin H. Ruttledge, Ya-Gang Xie, et al. · Genomics · 12

Direct and inverted reciprocal chromosome insertions between chromosomes 7 and 14 in a woman with recurrent miscarriages

1994 · Ying‐Tai Wang, Svetlana Bajalica, et al. · American Journal of Medical Genetics · 10

Restriction Map of a YAC and Cosmid Contig Encompassing the Oculopharyngeal Muscular Dystrophy Candidate Region on Chromosome 14q11.2–q13

1998 · Ya-Gang Xie, Daniel Rochefort, et al. · Genomics · 9

Identification, characterisation and clinical applications of cosmids from the telomeric and centromeric regions of the long arm of chromosome 22

1994 · Ya-Gang Xie, Fei-Yu Han, et al. · Human Genetics · 6

A pharmacogenetic analysis of the Canadian Cancer Trials Group MY.10 clinical trial of maintenance therapy for multiple myeloma

2016 · Ming Han, Alli Murugesan, et al. · Blood · 4

Clinical Medicine: Endocrinology and Diabetes: Abnormality of Serum Lipids are Independently Associated with Increased Serum Calcium Level in the Adult Newfoundland Population

2009 · Aaron Kennedy, Sudesh Vasdev, et al. · Clinical Medicine Insights Endocrinology and Diabetes · 4

MTHFR677T and 1298C Play Independent but Opposite Effects in Stroke - Additive Co-Effect of two Intragenic Alleles

2019 · Ya-Gang Xie · Biomedical Journal of Scientific & Technical Research · 3

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#17 Serum metabolic profiling analysis of Gitelman syndrome by untargeted metabolomics

2025 · Jian Han, Lanxin MA, et al. · Nephrology Dialysis Transplantation · 1

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Puzzle of the role for the MTHFR C. 677C>T variant and C. 1298A>C in cardiovascular diseases

2017 · Yagang Xie, Jianxun Cui, et al. · Atherosclerosis

Works count: 27

Citation count: 2,138

H-index: 15

I10-index: 18