Lisong Shi

Author PubWeight™ 14.42^‹?›

Top papers

Rank	Title	Journal	Year	PubWeight™‹?›
1	A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9.	Nat Genet	2012	2.12
2	CADgene: a comprehensive database for coronary artery disease genes.	Nucleic Acids Res	2010	1.23
3	Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID population.	Hum Genet	2010	1.09
4	Identification of NPPA variants associated with atrial fibrillation in a Chinese GeneID population.	Clin Chim Acta	2010	1.09
5	A novel heterozygous deletion in the EVC2 gene causes Weyers acrofacial dysostosis.	Hum Genet	2006	1.07
6	Functional dominant-negative mutation of sodium channel subunit gene SCN3B associated with atrial fibrillation in a Chinese GeneID population.	Biochem Biophys Res Commun	2010	1.03
7	Minor allele C of chromosome 1p32 single nucleotide polymorphism rs11206510 confers risk of ischemic stroke in the Chinese Han population.	Stroke	2010	1.03
8	The same chromosome 9p21.3 locus is associated with type 2 diabetes and coronary artery disease in a Chinese Han population.	Diabetes	2011	1.02
9	A new congenital nuclear cataract caused by a missense mutation in the gammaD-crystallin gene (CRYGD) in a Chinese family.	Mol Vis	2005	0.88
10	An integrative pipeline for multi-modal discovery of disease relationships.	Pac Symp Biocomput	2015	0.86
11	Mutations in the EDA gene are responsible for X-linked hypohidrotic ectodermal dysplasia and hypodontia in Chinese kindreds.	Eur J Oral Sci	2008	0.83
12	A PTPN11 allele encoding a catalytically impaired SHP2 protein in a patient with a Noonan syndrome phenotype.	Am J Med Genet A	2014	0.82
13	Slow cardiac myosin regulatory light chain 2 (MYL2) was down-expressed in chronic heart failure patients.	Clin Cardiol	2010	0.81
14	Further evidence of genetic heterogeneity segregating with hereditary gingival fibromatosis.	J Clin Periodontol	2009	0.80