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Janine Senz
Author PubWeight™ 77.82
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Top papers
Rank
Title
Journal
Year
PubWeight™
‹?›
1
Mutational evolution in a lobular breast tumour profiled at single nucleotide resolution.
Nature
2009
18.08
2
ARID1A mutations in endometriosis-associated ovarian carcinomas.
N Engl J Med
2010
13.07
3
Mutation of FOXL2 in granulosa-cell tumors of the ovary.
N Engl J Med
2009
5.63
4
deFuse: an algorithm for gene fusion discovery in tumor RNA-Seq data.
PLoS Comput Biol
2011
4.66
5
SNVMix: predicting single nucleotide variants from next-generation sequencing of tumors.
Bioinformatics
2010
4.02
6
Founder and recurrent CDH1 mutations in families with hereditary diffuse gastric cancer.
JAMA
2007
3.62
7
Subtype-specific mutation of PPP2R1A in endometrial and ovarian carcinomas.
J Pathol
2011
2.64
8
Distinct evolutionary trajectories of primary high-grade serous ovarian cancers revealed through spatial mutational profiling.
J Pathol
2013
2.35
9
Recurrent somatic DICER1 mutations in nonepithelial ovarian cancers.
N Engl J Med
2011
2.25
10
Type-specific cell line models for type-specific ovarian cancer research.
PLoS One
2013
1.73
11
Molecular characterization of mucinous ovarian tumours supports a stratified treatment approach with HER2 targeting in 19% of carcinomas.
J Pathol
2013
1.47
12
Characterization of a recurrent germ line mutation of the E-cadherin gene: implications for genetic testing and clinical management.
Clin Cancer Res
2005
1.46
13
Hereditary diffuse gastric cancer: association with lobular breast cancer.
Fam Cancer
2008
1.45
14
Germline CDH1 deletions in hereditary diffuse gastric cancer families.
Hum Mol Genet
2009
1.39
15
Quantification of epigenetic and genetic 2nd hits in CDH1 during hereditary diffuse gastric cancer syndrome progression.
Gastroenterology
2009
1.21
16
MicroRNA profiling of BRCA1/2 mutation-carrying and non-mutation-carrying high-grade serous carcinomas of ovary.
PLoS One
2009
1.18
17
Allele-specific CDH1 downregulation and hereditary diffuse gastric cancer.
Hum Mol Genet
2009
1.13
18
BRCA1 and BRCA2 mutations correlate with TP53 abnormalities and presence of immune cell infiltrates in ovarian high-grade serous carcinoma.
Mod Pathol
2012
1.12
19
The specificity of the FOXL2 c.402C>G somatic mutation: a survey of solid tumors.
PLoS One
2009
1.07
20
Hereditary diffuse gastric cancer: diagnosis, genetic counseling, and prophylactic total gastrectomy.
Cancer
2008
1.06
21
FOXL2 is a sensitive and specific marker for sex cord-stromal tumors of the ovary.
Am J Surg Pathol
2011
1.01
22
Using next-generation sequencing for the diagnosis of rare disorders: a family with retinitis pigmentosa and skeletal abnormalities.
J Pathol
2011
0.94
23
FOXL2 molecular testing in ovarian neoplasms: diagnostic approach and procedural guidelines.
Mod Pathol
2013
0.90
24
beta-catenin (CTNNB1) gene amplification: a new mechanism of protein overexpression in cancer.
Genes Chromosomes Cancer
2005
0.89
25
Mutation discovery in regions of segmental cancer genome amplifications with CoNAn-SNV: a mixture model for next generation sequencing of tumors.
PLoS One
2012
0.79
26
[Hereditary diffuse gastric cancer (HDGC): presentation of a family with a new mutation of the CDH1 gene].
Acta Gastroenterol Latinoam
2007
0.78
27
Polymerase Epsilon Exonuclease Domain Mutations in Ovarian Endometrioid Carcinoma.
Int J Gynecol Cancer
2015
0.76
28
Correction: Type-Specific Cell Line Models for Type-Specific Ovarian Cancer Research.
PLoS One
2013
0.76
29
FOXL2 mutation is absent in uterine tumors resembling ovarian sex cord tumors.
Am J Surg Pathol
2015
0.75
30
Mechanisms of monozygotic (MZ) twinning: a possible role for the cell adhesion molecule, E-cadherin.
Am J Med Genet A
2003
0.75