Author

Lauren E. Blizzard

Cincinnati Children's Hospital Medical Center

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Developmental Biology· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:mouse· 2 Research Focus:cell type annotation· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Rolf W. StottmanniD· 2 shared Andrew DiStasio· 1 shared Cynthia A. ProwsiD· 1 shared Erin Finnerty· 1 shared Howard M. SaaliD· 1 shared Kristen Lipscomb SundiD· 1 shared Marshall Lukacs· 1 shared Robert B. HufnageliD· 1 shared

Activity by Year

2018-2020 · peak 1/yr

Co-Author Collaboration Network

9 top collaborators · 29 mutual co-author links

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2 shared papersDevelopmental Biology

Rolf W. StottmannORCID

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2 papers

Recent·Most cited

CNS Glycosylphosphatidylinositol Deficiency Results in Delayed White Matter Development, Ataxia, and Premature Death in a Novel Mouse Model

Marshall Lukacs, Lauren E. Blizzard, Rolf W. Stottmann

This study generates a novel mouse model of inherited GPI deficiency, showing delayed white matter development, ataxia, and premature death due to CNS-specific GPI biosynthesis disruption.

Human Molecular Genetics · Mar 11, 2020Peer-reviewedDevelopmental Biology

Using human sequencing to guide craniofacial research.

Ryan P. Liegel, Erin Finnerty, Lauren E. Blizzard, Andrew DiStasio, Robert B. Hufnagel, Howard M. Saal, Kristen Lipscomb Sund, Cynthia A. Prows, Rolf W. Stottmann

The paper discusses using human sequencing and CRISPR-Cas9 to study a novel craniofacial syndrome, finding that a variant in AMOTL1 causes lethality in mice but its pathogenicity in humans remains unclear.

genesis · Oct 30, 2018Peer-reviewedGenetics