Huiying Yang

发表

Longitudinal study of the normal eyes in unilateral keratoconus patients.

Y. Rabinowitz, Xiaohui Li, K. Rasheed, 2004, Ophthalmology.

Keratoconus: Classification scheme based on videokeratography and clinical signs

Y. Rabinowitz, Xiaohui Li, Huiying Yang, 2009, Journal of cataract and refractive surgery.

Longitudinal study of keratoconus progression.

Xiaohui Li, Y. Rabinowitz, Xiaohui Li, 2007, Experimental eye research.

No VSX1 gene mutations associated with keratoconus.

Y. Rabinowitz, Huiying Yang, A. Aldave, 2006, Investigative ophthalmology & visual science.

Risk factors for gallstone formation during rapid loss of weight

Huiying Yang, M. Roth, L. Schoenfield, 1992, Digestive Diseases and Sciences.

[Study on candidate genes of benazepril related cough in Chinese hypertensives].

Huiying Yang, Li-ming Li, Xiao-hui Li, 2003, Zhonghua liu xing bing xue za zhi = Zhonghua liuxingbingxue zazhi.

Additional evidence of linkage between Crohn's disease and a putative locus on chromosome 12

S. Targan, J. Rotter, J. D. Ohmen, 1999, Genetics in Medicine.

Current Status of the Chinese National Twin Registry

Liming Li, Yonghua Hu, Huiying Yang, 2006, Twin Research and Human Genetics.

A functional SNP of interferon-gamma gene is important for interferon-alpha-induced and spontaneous recovery from hepatitis C virus infection.

C. Thio, C. Howell, X. Tong, 2007, Proceedings of the National Academy of Sciences of the United States of America.

Longitudinal Analysis of the Fellow Eyes in Unilateral Keratoconus

Y. Rabinowitz, Xiaohui Li, K. Rasheed, 2003 .

Higher order wavefront aberrations and topography in early and suspected keratoconus.

Y. Rabinowitz, Huiying Yang, B. Jafri, 2007, Journal of refractive surgery.

Genomewide linkage scan in a multigeneration Caucasian pedigree identifies a novel locus for keratoconus on chromosome 5q14.3-q21.1

K. Taylor, Y. Rabinowitz, Huiying Yang, 2005, Genetics in Medicine.

Two-stage genome-wide linkage scan in keratoconus sib pair families.

K. Taylor, Y. Rabinowitz, Xiaohui Li, 2006, Investigative ophthalmology & visual science.

Three VSX1 Gene Mutations, L159M, R166W, and H244R, Are Not Associated With Keratoconus

Y. Rabinowitz, Huiying Yang, Y. Picornell, 2008, Cornea.

Gene responsible for mitochondrial myopathy and sideroblastic anemia (MSA) maps to chromosome 12q24.33

K. Taylor, Y. Bykhovskaya, Huiying Yang, 2004, American journal of medical genetics. Part A.

Association of single nucleotide polymorphisms in interferon signaling pathway genes and interferon-stimulated genes with the response to interferon therapy for chronic hepatitis C.

Milton W. Taylor, T. Liang, C. Howell, 2008, Journal of hepatology.

Myxovirus‐1 and protein kinase haplotypes and fibrosis in chronic hepatitis C virus

R. Fontana, D. Kleiner, M. Ghany, 2007, Hepatology.

Two‐locus mitochondrial and nuclear gene models for mitochondrial disorders

J. Rotter, G. Vogler, Huiying Yang, 1992, Genetic epidemiology.

Lipoprotein lipase locus and progression of atherosclerosis in coronary-artery bypass grafts

K. Taylor, J. Rotter, P. Shah, 2004, Genetics in Medicine.

Human mitochondrial transcription factor B1 as a modifier gene for hearing loss associated with the mitochondrial A1555G mutation.

X. Estivill, Y. Bykhovskaya, Huiying Yang, 2004, Molecular genetics and metabolism.

Spinocerebellar ataxia type 2: polyQ repeat variation in the CACNA1A calcium channel modifies age of onset.

Luis Velazquez, S. Pulst, D. Huynh, 2005, Brain : a journal of neurology.

Polymorphism in the Human Major Histocompatibility Complex and Early Viral Decline during Treatment of Chronic Hepatitis C

T. Liang, H. Erlich, A. Wahed, 2008, Antimicrobial Agents and Chemotherapy.

A functional SNP of interferon-γ gene is important for interferon-α-induced and spontaneous recovery from hepatitis C virus infection

T. Liang, C. Thio, C. Howell, 2007, Proceedings of the National Academy of Sciences.

Selective decrease in hepatitis C virus–specific immunity among African Americans and outcome of antiviral therapy

H. Erlich, S. Belle, Huiying Yang, 2007, Hepatology.

Clinical Profiles of Chronic Hepatitis C in a Major County Medical Center Outpatient Setting in United States

Ying-Chao Lin, Huiying Yang, K. Lindsay, 2004, International journal of medical sciences.

Interleukin-6 (IL-6) haplotypes and the response to therapy of chronic hepatitis C virus infection

T. Liang, Huiying Yang, L. Yee, 2009, Genes and Immunity.

Modifier locus for mitochondrial DNA disease: Linkage and linkage disequilibrium mapping of a nuclear modifier gene for maternally inherited deafness

X. Estivill, K. Majamaa, Y. Bykhovskaya, 2001, Genetics in medicine : official journal of the American College of Medical Genetics.

Phenotype of non-syndromic deafness associated with the mitochondrial A1555G mutation is modulated by mitochondrial RNA modifying enzymes MTO1 and GTPBP3.

X. Estivill, Y. Bykhovskaya, Huiying Yang, 2004, Molecular genetics and metabolism.