Brandy Klotzle

Author PubWeight™ 38.24^‹?›

Top papers

Rank	Title	Journal	Year	PubWeight™‹?›
1	High density DNA methylation array with single CpG site resolution.	Genomics	2011	10.35
2	Epigenomic analysis detects widespread gene-body DNA hypomethylation in chronic lymphocytic leukemia.	Nat Genet	2012	3.08
3	Integrative molecular analysis of intrahepatic cholangiocarcinoma reveals 2 classes that have different outcomes.	Gastroenterology	2013	2.42
4	Whole-genome gene expression profiling of formalin-fixed, paraffin-embedded tissue samples.	PLoS One	2009	2.21
5	Succinate dehydrogenase mutation underlies global epigenomic divergence in gastrointestinal stromal tumor.	Cancer Discov	2013	2.11
6	Analysis of gene expression in stage I serous tumors identifies critical pathways altered in ovarian cancer.	Gynecol Oncol	2009	1.82
7	Whole-genome haplotyping by dilution, amplification, and sequencing.	Proc Natl Acad Sci U S A	2013	1.44
8	Differences in DNA methylation between human neuronal and glial cells are concentrated in enhancers and non-CpG sites.	Nucleic Acids Res	2013	1.15
9	Highly parallel genome-wide expression analysis of single mammalian cells.	PLoS One	2012	1.10
10	LTBP2 mutations cause Weill-Marchesani and Weill-Marchesani-like syndrome and affect disruptions in the extracellular matrix.	Hum Mutat	2012	1.09
11	PANK2 and C19orf12 mutations are common causes of neurodegeneration with brain iron accumulation.	Mov Disord	2012	1.08
12	Genetic and genomic analyses of RNA polymerase II-pausing factor in regulation of mammalian transcription and cell growth.	J Biol Chem	2011	0.97
13	Epigenome-wide ovarian cancer analysis identifies a methylation profile differentiating clear-cell histology with epigenetic silencing of the HERG K+ channel.	Hum Mol Genet	2013	0.97
14	The novel mutation p.Asp251Asn in the β-subunit of succinate-CoA ligase causes encephalomyopathy and elevated succinylcarnitine.	J Hum Genet	2013	0.90
15	Clinical investigational studies for validation of a next-generation sequencing in vitro diagnostic device for cystic fibrosis testing.	Expert Rev Mol Diagn	2014	0.87
16	Gene expression profiling of human whole blood samples with the Illumina WG-DASL assay.	BMC Genomics	2011	0.79
17	Manifestation of diffuse yellowish keratoderma on the palms and soles in autosomal recessive congenital ichthyosis patients may be indicative of mutations in NIPAL4.	J Dermatol	2011	0.78