Author

Deborah Krakow

University of California, Los AngelesORCID 0000-0001-9906-4968Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:cell type annotation· 1 Research Focus:clustering· 1 Research Focus:differential expression· 1 Assay:imaging· 1 Research Focus:spatial domain detection· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Mahim JainiD· 2 shared Anita E Beck· 1 shared Brendan H Lee· 1 shared Brendan LeeiD· 1 shared Carlos A Bacino· 1 shared Cathleen RaggioiD· 1 shared Colby T Marvin· 1 shared Danielle Gomez· 1 shared

Activity by Year

2015-2018 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersGenetics

Mahim JainORCID

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2 papers

Recent·Most cited

GeneticsEuropean Journal of Medical GeneticsPeer-reviewedDec 26, 2018

Dental and facial characteristics of osteogenesis imperfecta type V

Jean‐Marc Retrouvey, Doaa Taqi, Faleh Tamimi…·Frank Rauch

This study describes the dental and craniofacial characteristics of OI type V, finding missing permanent teeth but not dentinogenesis imperfecta, and a distinct craniofacial phenotype compared to other OI types.

21 citations

humanimaging

𝕏 PostBluesky

GeneticsThe American Journal of Human GeneticsPeer-reviewedMay 1, 2015

Autosomal dominant multiple pterygium syndrome is caused by mutations in MYH3

Jessica X Chong, Lindsay C Burrage, Anita E Beck…·Michael J Bamshad

This study identifies mutations in MYH3 as the cause of autosomal dominant multiple pterygium syndrome, with mutations in the tail domain of the protein.

DOI 10.1016/j.ajhg.2015.04.004

humanwhole-exome sequencing

𝕏 PostBluesky