PubRank

Norma J Nowak

Author PubWeight™ 78.84‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 A gene expression atlas of the central nervous system based on bacterial artificial chromosomes. Nature 2003 16.48
2 Recurrent 16p11.2 microdeletions in autism. Hum Mol Genet 2007 6.75
3 Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder. Biol Psychiatry 2008 2.60
4 Molecular study of malignant gliomas treated with epidermal growth factor receptor inhibitors: tissue analysis from North American Brain Tumor Consortium Trials 01-03 and 00-01. Clin Cancer Res 2005 2.46
5 Mapping segmental and sequence variations among laboratory mice using BAC array CGH. Genome Res 2005 1.71
6 Genome-wide array CGH analysis of murine neuroblastoma reveals distinct genomic aberrations which parallel those in human tumors. Cancer Res 2003 1.67
7 20q11.1 amplification in giant-cell tumor of bone: Array CGH, FISH, and association with outcome. Genes Chromosomes Cancer 2006 1.56
8 Development and characterization of a novel human Waldenström macroglobulinemia cell line: RPCI-WM1, Roswell Park Cancer Institute - Waldenström Macroglobulinemia 1. Leuk Lymphoma 2012 1.50
9 A mouse model of Down syndrome trisomic for all human chromosome 21 syntenic regions. Hum Mol Genet 2010 1.42
10 Analytical and clinical validity of whole-genome oligonucleotide array comparative genomic hybridization for pediatric patients with mental retardation and developmental delay. Am J Med Genet A 2008 1.39
11 Application of bacterial artificial chromosome array-based comparative genomic hybridization and spectral karyotyping to the analysis of glioblastoma multiforme. Cancer Genet Cytogenet 2004 1.24
12 Gab2-mediated signaling promotes melanoma metastasis. Am J Pathol 2009 1.21
13 Molecular characterization of the t(3;9) associated with immortalization in the MCF10A cell line. Cancer Genet Cytogenet 2005 1.20
14 Novel amplicons on the short arm of chromosome 7 identified using high resolution array CGH contain over expressed genes in addition to EGFR in glioblastoma multiforme. Genes Chromosomes Cancer 2005 1.19
15 Epigenetic silencing of CYP24 in tumor-derived endothelial cells contributes to selective growth inhibition by calcitriol. J Biol Chem 2007 1.15
16 Two functional coding single nucleotide polymorphisms in STK15 (Aurora-A) coordinately increase esophageal cancer risk. Cancer Res 2005 1.15
17 Familial 4.3 Mb duplication of 21q22 sheds new light on the Down syndrome critical region. J Med Genet 2007 1.14
18 Role of alcohol metabolism in non-alcoholic steatohepatitis. PLoS One 2010 1.13
19 Genomic profiling of myeloid sarcoma by array comparative genomic hybridization. Genes Chromosomes Cancer 2005 1.10
20 Upregulation of hemoglobin expression by oxidative stress in hepatocytes and its implication in nonalcoholic steatohepatitis. PLoS One 2011 1.08
21 In vitro and in vivo irinotecan-induced changes in expression profiles of cell cycle and apoptosis-associated genes in acute myeloid leukemia cells. Mol Cancer Ther 2005 1.02
22 High-resolution analysis of genetic events in cancer cells using bacterial artificial chromosome arrays and comparative genome hybridization. Adv Cancer Res 2003 0.99
23 Gene-resolution analysis of DNA copy number variation using oligonucleotide expression microarrays. BMC Genomics 2007 0.98
24 Molecular karyotypes of Hodgkin and Reed-Sternberg cells at disease onset reveal distinct copy number alterations in chemosensitive versus refractory Hodgkin lymphoma. Clin Cancer Res 2011 0.97
25 Array CGH analysis of pediatric medulloblastomas. Genes Chromosomes Cancer 2006 0.97
26 Genetic analysis of Down syndrome-associated heart defects in mice. Hum Genet 2011 0.97
27 A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism. J Med Genet 2009 0.96
28 Long tandem repeats as a form of genomic copy number variation: structure and length polymorphism of a chromosome 5p repeat in control and schizophrenia populations. Psychiatr Genet 2009 0.96
29 Lipid in the livers of adolescents with nonalcoholic steatohepatitis: combined effects of pathways on steatosis. Metabolism 2010 0.94
30 Identification of metastasis-associated breast cancer genes using a high-resolution whole genome profiling approach. J Cancer Res Clin Oncol 2010 0.93
31 Differential copy number aberrations in novel candidate genes associated with progression from in situ to invasive ductal carcinoma of the breast. Genes Chromosomes Cancer 2012 0.90
32 FOXO1 regulates expression of a microRNA cluster on X chromosome. Aging (Albany NY) 2013 0.90
33 Characterization of the 1p/19q chromosomal loss in oligodendrogliomas using comparative genomic hybridization arrays (CGHa). J Neuropathol Exp Neurol 2004 0.89
34 aCGHViewer: a generic visualization tool for aCGH data. Cancer Inform 2006 0.89
35 Double minute chromosomes in acute myeloid leukemia and myelodysplastic syndrome: identification of new amplification regions by fluorescence in situ hybridization and spectral karyotyping. Genes Chromosomes Cancer 2002 0.88
36 Identification of consistent novel submegabase deletions in low-grade oligodendrogliomas using array-based comparative genomic hybridization. Genes Chromosomes Cancer 2005 0.87
37 Molecular characterization of a consistent 4.5-megabase deletion at 4q28 in prostate cancer cells. Cancer Genet Cytogenet 2005 0.86
38 aCGH local copy number aberrations associated with overall copy number genomic instability in colorectal cancer: coordinate involvement of the regions including BCR and ABL. Mutat Res 2007 0.85
39 Phase 1 study of arsenic trioxide, high-dose cytarabine, and idarubicin to down-regulate constitutive signal transducer and activator of transcription 3 activity in patients aged <60 years with acute myeloid leukemia. Cancer 2011 0.85
40 A GOG 210 aCGH study of gain at 1q23 in endometrioid endometrial cancer in the context of racial disparity and outcome. Genes Chromosomes Cancer 2010 0.84
41 Chromosome 11 genomic changes in parathyroid adenoma and hyperplasia: array CGH, FISH, and tissue microarrays. Genes Chromosomes Cancer 2008 0.84
42 Genomic profiles of colorectal cancers differ based on patient smoking status. Cancer Genet Cytogenet 2006 0.83
43 Estimating the arm-wise false discovery rate in array comparative genomic hybridization experiments. Stat Appl Genet Mol Biol 2007 0.82
44 Genomic instability of human aberrant crypt foci measured by inter-(simple sequence repeat) PCR and array-CGH. Mutat Res 2006 0.82
45 Targeted deletion of p73 in mice reveals its role in T cell development and lymphomagenesis. PLoS One 2009 0.81
46 Smith-Magenis syndrome and Moyamoya disease in a patient with del(17)(p11.2p13.1). Am J Med Genet A 2007 0.81
47 Genomic, immunophenotypic, and NPM1/FLT3 mutational studies on 17 patients with normal karyotype acute myeloid leukemia (AML) followed by aberrant karyotype AML at relapse. Cancer Genet Cytogenet 2010 0.80
48 The genomic relationship between primary breast carcinomas and their nodal metastases. Cancer Invest 2011 0.80
49 Uniparentalism in sporadic colorectal cancer is independent of imprint status, and coordinate for chromosomes 14 and 18. Cancer Genet Cytogenet 2009 0.79
50 Microcephaly, sensorineural deafness and Currarino triad with duplication-deletion of distal 7q. Eur J Pediatr 2009 0.78
51 Translocation (4;11)(p12;q23) with rearrangement of FRYL and MLL in therapy-related acute myeloid leukemia. Cancer Genet Cytogenet 2007 0.78
52 Common genetic variants are associated with accelerated bone mineral density loss after hematopoietic cell transplantation. PLoS One 2011 0.76
53 Rapid array-based genomic characterization of a subtle structural abnormality: a patient with psychosis and der(18)t(5;18)(p14.1;p11.23). Am J Med Genet A 2005 0.76
54 Familial 4.3 Mb duplication of 21q22 sheds new light on the Down syndrome critical region. BMJ Case Rep 2009 0.75
55 Cancer progression modeling using static sample data. Genome Biol 2014 0.75
56 Comparative genomic instabilities of thyroid and colon cancers. Arch Otolaryngol Head Neck Surg 2007 0.75