PubRank

Svetlana D Pack

Author PubWeight™ 41.47‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. Neuron 2011 18.73
2 BORIS, a novel male germ-line-specific protein associated with epigenetic reprogramming events, shares the same 11-zinc-finger domain with CTCF, the insulator protein involved in reading imprinting marks in the soma. Proc Natl Acad Sci U S A 2002 2.62
3 Conditional expression of the CTCF-paralogous transcriptional factor BORIS in normal cells results in demethylation and derepression of MAGE-A1 and reactivation of other cancer-testis genes. Cancer Res 2005 2.08
4 Reciprocal binding of CTCF and BORIS to the NY-ESO-1 promoter coincides with derepression of this cancer-testis gene in lung cancer cells. Cancer Res 2005 1.74
5 Follicular lymphoma in situ: clinical implications and comparisons with partial involvement by follicular lymphoma. Blood 2011 1.58
6 Identification and characterization of a novel member of olfactomedin-related protein family, hGC-1, expressed during myeloid lineage development. Gene 2002 1.45
7 Clinical and molecular analysis of disseminated hemangioblastomatosis of the central nervous system in patients without von Hippel-Lindau disease. Report of four cases. J Neurosurg 2002 1.35
8 Human gamma-satellite DNA maintains open chromatin structure and protects a transgene from epigenetic silencing. Genome Res 2009 1.22
9 Identification of CARS-ALK fusion in primary and metastatic lesions of an inflammatory myofibroblastic tumor. Lab Invest 2003 1.07
10 Identification and characterization of SSTK, a serine/threonine protein kinase essential for male fertility. Mol Cell Biol 2005 1.02
11 The structural complexity of the human BORIS gene in gametogenesis and cancer. PLoS One 2010 1.02
12 ERG expression in epithelioid sarcoma: a diagnostic pitfall. Am J Surg Pathol 2013 0.97
13 Somatic mutations in VHL germline deletion kindred correlate with mild phenotype. Ann Neurol 2004 0.94
14 Elicitation of T cell responses to histologically unrelated tumors by immunization with the novel cancer-testis antigen, brother of the regulator of imprinted sites. J Immunol 2007 0.93
15 Localization of deletion to a 300 Kb interval of chromosome 11q13 in cervical cancer. Oncogene 2002 0.89
16 Somatic point mutation of the wild-type allele detected in tumors of patients with VHL germline deletion. Oncogene 2002 0.88
17 Tal1/SCL binding to pericentromeric DNA represses transcription. J Biol Chem 2005 0.85
18 Induction of glioblastoma multiforme in nonhuman primates after therapeutic doses of fractionated whole-brain radiation therapy. J Neurosurg 2002 0.84
19 Von hippel-lindau disease associated pulmonary carcinoid with cranial metastasis. J Clin Endocrinol Metab 2014 0.83
20 Characterization of fibroblast growth factor receptor 1 in small-cell lung cancer. J Thorac Oncol 2014 0.81
21 Amplification and overexpression of mutant RET in multiple endocrine neoplasia type 2-associated medullary thyroid carcinoma. J Clin Endocrinol Metab 2003 0.77
22 Interspecies comparative genomic hybridization (I-CGH): a new twist to study animal tumor models. Cell Cycle 2007 0.75
23 Tumor Young Investigator Award: induction of glioblastoma multiforme in primates after fractionated whole-brain irradiation in the therapeutic dose range. Clin Neurosurg 2003 0.75
24 Primary subcutaneous spindle cell Ewing sarcoma with strong S100 expression and EWSR1-FLI1 fusion: a case report. Pediatr Dev Pathol 2014 0.75
25 ER/PR positive epidermotropic primary cutaneous eccrine carcinoma as a cutaneous manifestation of MEN 2B. J Am Acad Dermatol 2013 0.75
26 Malignant round cell tumor of bone with EWSR1-NFATC2 gene fusion. Virchows Arch 2014 0.75