Harrison Brand

Expectations and blind spots for structural variation detection from short-read alignment and long-read assembly

Tobias Marschall, Jan O. Korbel, Mark Walker, 2020, bioRxiv.

Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome

Ryan L. Collins, Joon-Yong An, Stephan J. Sanders, 2017, Genome Biology.

Cryptic and complex chromosomal aberrations in early-onset neuropsychiatric disorders.

Ryan L. Collins, Ryan E. Mills, Ryan L Collins, 2014, American journal of human genetics.

Efficient ablation of genes in human hematopoietic stem and effector cells using CRISPR/Cas9.

David Bryder, Christian L. Boutwell, Todd M. Allen, 2014, Cell stem cell.

An open resource of structural variation for medical and population genetics

Grace Tiao, Daniel G. MacArthur, Ryan L. Collins, 2019 .

Multi-platform discovery of haplotype-resolved structural variation in human genomes

Li Ding, Amina Noor, Ali Bashir, 2018, Nature Communications.

Paired-Duplication Signatures Mark Cryptic Inversions and Other Complex Structural Variation.

Ryan L. Collins, Ryan L Collins, Michael E Talkowski, 2015, American journal of human genetics.

The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies

Edwin Cuppen, Claire Redin, Ryan L. Collins, 2016, Nature Genetics.

Efficient Ablation of Genes in Human Hematopoietic Stem and Effector Cells using CRISPR / Cas 9 Graphical

David Bryder, Ryan L. Collins, Christian L. Boutwell, 2014 .