Author

Denae M. Golden

Observed names: Denae Golden, Denae M Golden

Institution: University of Nebraska Medical Center

Observed institutions: Nebraska Medical Center, University of Nebraska Medical Center

OpenAlex ID: A5110009622

An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities

2011 · Erin B Kaminsky, Vineith Kaul, et al. · Genetics in Medicine · 444

Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia

2010 · Daniel Moreno-De-Luca, Jennifer G. Mulle, et al. · The American Journal of Human Genetics · 325

Array-based comparative genomic hybridization analysis of 1176 consecutive clinical genetics investigations

2008 · Diane L. Pickering, James D. Eudy, et al. · Genetics in Medicine · 90

Copy number variant discrepancy resolution using the ClinGen dosage sensitivity map results in updated clinical interpretations in ClinVar

2018 · Erin R. Riggs, Tristan Nelson, et al. · Human Mutation · 38

Reprogramming of ovarian granulosa cells by YAP1 leads to development of high-grade cancer with mesenchymal lineage and serous features

2020 · Xiangmin Lv, Chunbo He, et al. · 中国科学通报：英文版 · 24

Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia

2011 · Daniel Moreno-De-Luca, Jennifer G. Mulle, et al. · The American Journal of Human Genetics · 11

Assessing the utility of confirmatory studies following identification of large-scale genomic imbalances by microarray

2015 · Jennifer N. Sanmann, Diane L. Pickering, et al. · Genetics in Medicine · 6

Works count: 7

Citation count: 938

H-index: 6

I10-index: 6