1.

2.
A novel indel variant in LDLR responsible for familial hypercholesterolemia in a Chinese family
by Hongyan Shu
PLoS ONE, 01 January 2017, Vol.12(12), p.e0189316

3.
Retinal Diseases Caused by Mutations in Genes Not Specifically Associated with the Clinical Diagnosis.
by Wang, Xia
PloS one, 2016, Vol.11(10), p.e0165405

4.
Inhibition of ADP-induced platelet aggregation by clopidogrel is related to CYP2C19 genetic polymorphisms.
by Chen, Bi-Lian
Clinical and experimental pharmacology & physiology, August 2008, Vol.35(8), pp.904-908

5.

6.
H19 overexpression promotes leukemogenesis and predicts unfavorable prognosis in acute myeloid leukemia
by Ting-Juan Zhang
Clinical Epigenetics, 01 April 2018, Vol.10(1), pp.1-12

7.
Methylation‐associated DOK1 and DOK2 down‐regulation: Potential biomarkers for predicting adverse prognosis in acute myeloid leukemia
by He, Pin‐Fang
Journal of Cellular Physiology, September 2018, Vol.233(9), pp.6604-6614

8.
Efficient screening method of the thiopurine methyltransferase polymorphisms for patients considering taking thiopurine drugs in a Chinese Han population in Henan Province (central...
by Zhang, Li-Rong
Clinica Chimica Acta, 01 February 2007, Vol.376(1-2), pp.45-51

9.
Sparse whole-genome sequencing identifies two loci for major depressive disorder.
by Cai, Na
Nature, July 30, 2015, Vol.523(7562), pp.588-591

10.
Organic anion transporting polypeptide-1B1 haplotypes in Chinese patients
by Lin-Yong Xu
Acta Pharmacologica Sinica, 2007, Vol.28(10), p.1693
