PubRank

Xiang-Min Xu

Author PubWeight™ 16.94‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Validation of VKORC1 and CYP2C9 genotypes on interindividual warfarin maintenance dose: a prospective study in Chinese patients. Pharmacogenet Genomics 2009 1.41
2 Phylogeographic analysis of mitochondrial DNA haplogroup F2 in China reveals T12338C in the initiation codon of the ND5 gene not to be pathogenic. J Hum Genet 2004 0.97
3 Carrier screening for alpha- and beta-thalassemia in pregnancy: the results of an 11-year prospective program in Guangzhou Maternal and Neonatal hospital. Prenat Diagn 2005 0.96
4 Molecular characterization of SMN copy number derived from carrier screening and from core families with SMA in a Chinese population. Eur J Hum Genet 2010 0.91
5 SYBR Green-based real-time PCR assay for detection of VKORC1 and CYP2C9 polymorphisms that modulate warfarin dose requirement. Clin Chem Lab Med 2009 0.89
6 A novel mutation of -73(A-->T) in the CCAAT box of the beta-globin gene identified in a patient with the mild beta-thalassemia intermedia. Ann Hematol 2007 0.86
7 Development and evaluation of a reverse dot blot assay for the simultaneous detection of six common Chinese G6PD mutations and one polymorphism. Blood Cells Mol Dis 2008 0.85
8 Mutation analysis of 73 southern Chinese Wilson's disease patients: identification of 10 novel mutations and its clinical correlation. J Hum Genet 2011 0.84
9 Homogeneous label-free genotyping of single nucleotide polymorphism using ligation-mediated strand displacement amplification with DNAzyme-based chemiluminescence detection. Anal Chem 2011 0.80
10 Reliable detection of paternal SNPs within deletion breakpoints for non-invasive prenatal exclusion of homozygous α-thalassemia in maternal plasma. PLoS One 2011 0.80
11 Evidence of recent natural selection on the Southeast Asian deletion (--(SEA)) causing α-thalassemia in South China. BMC Evol Biol 2013 0.80
12 Evidence of gene conversion in the evolutionary process of the codon 41/42 (-CTTT) mutation causing beta-thalassemia in southern China. J Mol Evol 2008 0.79
13 Rapid determination of human globin chains using reversed-phase high-performance liquid chromatography. J Chromatogr B Analyt Technol Biomed Life Sci 2012 0.79
14 Rapid, accurate genotyping of alcohol dehydrogenase-1B and aldehyde dehydrogenase-2 based on the use of denaturing HPLC. Clin Chem Lab Med 2005 0.79
15 Rapid genotyping of known mutations and polymorphisms in beta-globin gene based on the DHPLC profile patterns of homoduplexes and heteroduplexes. Clin Biochem 2008 0.79
16 Rapid, accurate genotyping of beta-thalassaemia mutations using a novel multiplex primer extension/denaturing high-performance liquid chromatography assay. Br J Haematol 2003 0.78
17 A quantitative assay to detect α-thalassemia deletions and triplications using multiplex nested real-time quantitative polymerase chain reaction. Anal Biochem 2012 0.78
18 A rapid and accurate DHPLC assay for determination of apolipoprotein E genotypes. J Alzheimers Dis 2007 0.77
19 Rapid, accurate detection of TMPRSS6 gene causative mutations with a high-resolution melting assay. Blood Cells Mol Dis 2011 0.76
20 Rapid simultaneous genotyping of polymorphisms in ADH1B and ALDH2 using high resolution melting assay. Clin Chem Lab Med 2013 0.76
21 A novel COL7A1 gene mutation causing pretibial epidermolysis bullosa: report of a Chinese family with intra-familial phenotypical diversity. Gene 2013 0.75
22 Evaluation and comparison of three assays for molecular detection of spinal muscular atrophy. Clin Chem Lab Med 2016 0.75
23 A novel fusion gene and a common α(0)-thalassemia deletion cause hemoglobin H disease in a Chinese family. Blood Cells Mol Dis 2013 0.75
24 Simultaneous identification of point mutations via DNA ligase-mediated gold nanoparticle assembly. Analyst 2008 0.75
25 An electrochemical sensor for detection of laccase activities from Penicillium simplicissimum in compost based on carbon nanotubes modified glassy carbon electrode. Bioresour Technol 2008 0.75
26 Multimodal Estimation of Distribution Algorithms. IEEE Trans Cybern 2016 0.75
27 Evaluation of clinical application of gap-PCR as a routine method for alpha-thalassemia carrier detection. Di Yi Jun Yi Da Xue Xue Bao 2002 0.75
28 Reliable and high-throughput mutation screening for beta-thalassemia by a single-base extension/fluorescence polarization assay. Genet Test 2004 0.75
29 Molecular characterization of a novel 27.6-kb deletion causing α(+) thalassemia in a Chinese family. Ann Hematol 2010 0.75