Nicole L. Hoppman
WinnMed(US)
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Acute Myeloid Leukemia Research, Acute Lymphoblastic Leukemia research, Prenatal Screening and Diagnostics, Chronic Myeloid Leukemia Treatments
Most-Cited Works
- → Chromosomal microarray impacts clinical management(2013)90 cited
- → SVAtools for junction detection of genome-wide chromosomal rearrangements by mate-pair sequencing (MPseq)(2017)74 cited
- → Polymorphisms in Both Promoters of Hepatocyte Nuclear Factor 4-α Are Associated With Type 2 Diabetes in the Amish(2004)67 cited
- → False-negative rates for MYC fluorescence in situ hybridization probes in B-cell neoplasms(2018)64 cited
- → Patterns of homozygosity in patients with uniparental disomy: detection rate and suggested reporting thresholds for SNP microarrays(2018)61 cited
- → Copy number variant analysis using genome‐wide mate‐pair sequencing(2018)52 cited
- → Genetic testing for hearing loss in the United States should include deletion/duplication analysis for the deafness/infertility locus at 15q15.3(2013)44 cited
- → A functional haplotype in EIF2AK3, an ER stress sensor, is associated with lower bone mineral density(2011)42 cited
- → Combining copy number, methylation markers, and mutations as a panel for endometrial cancer detection via intravaginal tampon collection(2019)40 cited
- → Mate pair sequencing improves detection of genomic abnormalities in acute myeloid leukemia(2018)40 cited