Danielle C. Kimble

Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia

Settara C. Chandrasekharappa, Francis P. Lach, Danielle C. Kimble et al. · Blood · 2013 · 89 citations · Full text

Multiplexed CRISPR/Cas9-mediated knockout of 19 Fanconi anemia pathway genes in zebrafish revealed their roles in growth, sexual development and fertility

Ramanagouda Ramanagoudr‐Bhojappa, Blake Carrington, Mukundhan Ramaswami et al. · PLoS Genetics · 2018 · 74 citations · Full text

Genetics, Genomic Mechanism, Molecular Genetics +19

A comprehensive approach to identification of pathogenic FANCA variants in Fanconi anemia patients and their families

Danielle C. Kimble, Francis P. Lach, Siobhán Q. Gregg et al. · Human Mutation · 2017 · 62 citations · Full text

Comprehensive Analysis of Pathogenic Deletion Variants in Fanconi Anemia Genes

Elizabeth K. Flynn, Aparna A. Kamat, Francis P. Lach et al. · Human Mutation · 2014 · 45 citations · Full text

Association of clinical severity with FANCB variant type in Fanconi anemia

Moonjung Jung, Ramanagouda Ramanagoudr‐Bhojappa, Sylvie van Twest et al. · Blood · 2020 · 34 citations · Full text