Author

Emily Fleming

Children's Mercy HospitalORCID 0000-0003-0641-3271Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Emily Fleming1 paper

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 1

Frequent Co-Authors

Alexandra DürriD· 1 shared Birsen KaramaniD· 1 shared Bonnie R. SullivaniD· 1 shared Carol SaundersiD· 1 shared Carolyn LeiD· 1 shared Delphine HéroniD· 1 shared Elizabeth George· 1 shared Elliott H. SherriD· 1 shared

Activity by Year

2024-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alexandra DürrORCID

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1 paper

Recent·Most cited

Basic helix-loop-helix transcription factor BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, tone and movement abnormalities

Carolyn Le, Emanuela Argilli, Elizabeth George, Tuğba Kalaycı, Zehra Oya Uyguner, Birsen Karaman, Tanju Demirören, Stephanie P. DiTroia, Delphine Héron, Isabelle Sabatier, Lance H. Rodan, Katta M. Girisha, Periyasamy Radhakrishnan, Carol Saunders, Bonnie R. Sullivan, , Elliott H. Sherr

medRxiv · Oct 11, 2024 · PreprintGenetic & Genomic Medicine