PubRank

Shibo Li

Author PubWeight™ 48.84‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Double trisomy. Am J Med Genet A 2004 1.99
2 Klinefelter's syndrome (47,XXY) in male systemic lupus erythematosus patients: support for the notion of a gene-dose effect from the X chromosome. Arthritis Rheum 2008 1.64
3 RBPJ mutations identified in two families affected by Adams-Oliver syndrome. Am J Hum Genet 2012 1.34
4 Intravascular large B-cell lymphoma with hemophagocytic syndrome (Asian variant) in a Caucasian patient. Int J Clin Exp Pathol 2012 1.04
5 Chromosome 2q terminal deletion: report of 6 new patients and review of phenotype-breakpoint correlations in 66 individuals. Am J Med Genet A 2004 1.00
6 Automated classification of metaphase chromosomes: optimization of an adaptive computerized scheme. J Biomed Inform 2008 1.00
7 Trisomy 8: a common finding in mouse embryonic stem (ES) cell lines. Mol Cytogenet 2013 0.97
8 Automated identification of analyzable metaphase chromosomes depicted on microscopic digital images. J Biomed Inform 2007 0.97
9 A rule-based computer scheme for centromere identification and polarity assignment of metaphase chromosomes. Comput Methods Programs Biomed 2008 0.94
10 Uterine tumor resembling ovarian sex cord tumor: report of a case with t(X;6)(p22.3;q23.1) and t(4;18)(q21.1;q21.3). Diagn Mol Pathol 2003 0.94
11 Sex chromosome aneuploidies among men with systemic lupus erythematosus. J Autoimmun 2011 0.94
12 Loss of SDHB and NF1 genes in a malignant phyllodes tumor of the breast as detected by oligo-array comparative genomic hybridization. Cancer Genet Cytogenet 2010 0.93
13 Relevance of JAK2V617F positivity to hematological diseases--survey of samples from a clinical genetics laboratory. J Hematol Oncol 2011 0.92
14 Re-assigned diagnosis of D4ST1-deficient Ehlers-Danlos syndrome (adducted thumb-clubfoot syndrome) after initial diagnosis of Marden-Walker syndrome. Am J Med Genet A 2012 0.90
15 Heterogeneity of primary glioblastoma cells in the expression of caspase-8 and the response to TRAIL-induced apoptosis. Apoptosis 2011 0.89
16 Automated detection and analysis of fluorescent in situ hybridization spots depicted in digital microscopic images of Pap-smear specimens. J Biomed Opt 2009 0.88
17 Klinefelter's syndrome (47,XXY) among men with systemic lupus erythematosus. Acta Paediatr 2011 0.87
18 Male-only systemic lupus. J Rheumatol 2010 0.86
19 Leiomyosarcoma of the breast: a pathologic and comparative genomic hybridization study of two cases. Cancer Genet Cytogenet 2004 0.85
20 Ring chromosome 9 [r(9)(p24q34)]: a report of two cases. Am J Med Genet A 2005 0.85
21 Impact of the optical depth of field on cytogenetic image quality. J Biomed Opt 2012 0.84
22 Characterization of novel RS1 exonic deletions in juvenile X-linked retinoschisis. Mol Vis 2013 0.84
23 Automated analysis of fluorescent in situ hybridization (FISH) labeled genetic biomarkers in assisting cervical cancer diagnosis. Technol Cancer Res Treat 2010 0.83
24 Molecular characterization of a ring chromosome 16 from a patient with bilateral cataracts. Am J Med Genet 2002 0.83
25 Automated identification of abnormal metaphase chromosome cells for the detection of chronic myeloid leukemia using microscopic images. J Biomed Opt 2010 0.83
26 High-resolution analysis of copy number variants in adults with simple-to-moderate congenital heart disease. Am J Med Genet A 2013 0.82
27 Cytogenetic and molecular cytogenetic studies of a variant of t(21;22), ins(22;21)(q12;q21q22), with a deletion of the 3' EWSR1 gene in a patient with Ewing sarcoma. Cancer Genet Cytogenet 2005 0.81
28 Ring chromosome 4 in a patient with early onset type 2 diabetes, deafness, and developmental delay. Am J Med Genet A 2005 0.81
29 A computer-aided method to expedite the evaluation of prognosis for childhood acute lymphoblastic leukemia. Technol Cancer Res Treat 2006 0.81
30 Down syndrome with pure partial trisomy 21q22 due to a paternal insertion (4;21) uncovered by uncultured amniotic fluid interphase FISH. Am J Med Genet A 2005 0.81
31 Molecular cytogenetic characterization of undifferentiated embryonal sarcoma of the liver: a case report and literature review. Mol Cytogenet 2012 0.80
32 A possible 5'-NRIP1/UHRF1-3' fusion gene detected by array CGH analysis in a Ph+ ALL patient. Cancer Genet 2011 0.80
33 Lipoprotein abnormalities in compound heterozygous lipoprotein lipase deficiency after treatment with a low-fat diet and orlistat. J Clin Lipidol 2012 0.79
34 Development and Assessment of an Integrated Computer-Aided Detection Scheme for Digital Microscopic Images of Metaphase Chromosomes. J Electron Imaging 2008 0.79
35 Generation and characterization of a highly effective protein substrate for analysis of FLT3 activity. J Hematol Oncol 2012 0.79
36 A novel subtelomeric translocation t(5;9) and a deletion of the RB1 gene in a patient with acute myeloid leukemia (AML-M0). Cancer Genet Cytogenet 2008 0.79
37 De novo three-way chromosome translocation 46,XY,t(4;6;21)(p16;p21.1;q21) in a male with cleidocranial dysplasia. Am J Med Genet A 2008 0.79
38 Fluorescence in situ hybridization (FISH) signal analysis using automated generated projection images. Anal Cell Pathol (Amst) 2012 0.79
39 Reversed clinical phenotype due to a microduplication of Sotos syndrome region detected by array CGH: microcephaly, developmental delay and delayed bone age. Am J Med Genet A 2011 0.79
40 Expression of HPV16 E5 produces enlarged nuclei and polyploidy through endoreplication. Virology 2010 0.79
41 Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia. Chin Med J (Engl) 2003 0.78
42 Acquired genomic copy number changes in CML patients with the Philadelphia chromosome (Ph+). Cancer Genet 2012 0.78
43 Generation and analysis of partially haploid cells with Cre-mediated chromosome deletion in the lymphoid system. J Biol Chem 2010 0.78
44 A novel t(8;13)(q21;q22) translocation in a pediatric lipoma. Cancer Genet 2011 0.78
45 Loss of fragile histidine triad and amplification of 1p36.22 and 11p15.5 in primary gastric adenocarcinomas. World J Gastroenterol 2012 0.77
46 Chan-Yu-Bao-Yuan-Tang and 5-fluorouracil synergistically induce apoptosis by means of the caspase-3 signaling pathway in lung and cervical cancer cells. Mol Med Rep 2010 0.77
47 Trisomy 1q in a patient with severe aplastic anemia. Cancer Genet Cytogenet 2006 0.77
48 Cryptic and complex chromosomal rearrangements and the deletion of TP53 gene in a patient with leukemic mantle cell lymphoma. Cancer Genet Cytogenet 2006 0.77
49 Potential clinical impact of three-dimensional visualization for fluorescent in situ hybridization image analysis. J Biomed Opt 2012 0.77
50 Continuous in vitro exposure to low-dose genistein induces genomic instability in breast epithelial cells. Cancer Genet Cytogenet 2008 0.77
51 Prenatal identification of a novel R937P L1CAM missense mutation. Genet Test Mol Biomarkers 2009 0.77
52 An Association Study Identifies Two Single Nucleotide Polymorphisms on Chromosome 11q23.3 as a Risk Locus for Acute Myocardial Infarction in the Chinese Han Population. Clin Lab 2015 0.76
53 Hypogonadotropic hypogonadism presenting with arhinia: a case report. J Med Case Rep 2013 0.75
54 Evaluations of auto-focusing methods under a microscopic imaging modality for metaphase chromosome image analysis. Anal Cell Pathol (Amst) 2013 0.75
55 The impact of the condenser on cytogenetic image quality in digital microscope system. Anal Cell Pathol (Amst) 2013 0.75
56 Trisomy chromosome 5 is a recurrent cytogenetic lesion in mammary tumors from parous MMTV-erbB-2 transgenic mice. Oncol Lett 2011 0.75
57 Deletion of 14q24.1 approximately q24.3 in a patient with acute lymphoblastic leukemia: a hidden chromosomal anomaly detected by array-based comparative genomic hybridization. Cancer Genet Cytogenet 2008 0.75
58 Characterization of a novel t(2;5;11) in a patient with concurrent AML and CLL: a case report and literature review. Cancer Genet 2011 0.75
59 [Effect of the cytoplasmic DNA sensor DAI on replication of hepatitis B virus]. Zhonghua Gan Zang Bing Za Zhi 2015 0.75
60 "Understanding Adam" multiple reciprocal translocations: complex case presentation. J Perinat Neonatal Nurs 2009 0.75
61 Chromosomal abnormalities in patients with recurrent spontaneous abortions in northeast China. J Reprod Med 2011 0.75
62 Duplication 15q as the sole anomaly in an acute promyelocytic leukemia patient without t(15;17). Cancer Genet Cytogenet 2002 0.75
63 Duplication 15q in a patient with t(8;21) acute myeloblastic leukemia (M2). Cancer Genet Cytogenet 2002 0.75
64 A variant t(8;10;21) in a patient with pathological features mimicking atypical chronic myeloid leukemia. Cancer Genet Cytogenet 2005 0.75
65 Cytogenetic and comparative genomic hybridization studies of an esophageal giant fibrovascular polyp: a case report. Hum Pathol 2011 0.75