Author

Daniella Miller

Albert Einstein College of MedicineORCID 0000-0002-5889-9739Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Research Focus:differential expression· 1 Organism:human· 1 Organism:mouse· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Ann SwilleniD· 2 shared Anne S. BassettiD· 2 shared Bernice E. MorrowiD· 2 shared Beverly S. EmanueliD· 2 shared Carolina PutottoiD· 2 shared Daniel E. McGinniD· 2 shared Donna M. McDonald‐McGinniD· 2 shared Elaine H. ZackaiiD· 2 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Ann SwillenORCID

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2 papers

Recent·Most cited

Prevalence and spectrum of congenital heart disease in individuals with distal chromosome 22q11.22-23 deletions

Tanner J. Nelson, Daniel E. McGinn, Terrence Blaine Crowley, Lydia Rockart, Audrey Green, Victoria Giunta, Oanh Tran, Daniella Miller, Jeroen Breckpot, Ann Swillen, M. Cristina Digilio, Marta Unolt, Carolina Putotto, Federica Pulvirenti, Bruno Marino, , Donna M. McDonald‐McGinn

This study examines congenital heart disease in individuals with distal 22q11.22-23 deletions, finding lower prevalence compared to proximal deletions and identifying specific cardiac anomalies.

Clinical Genetics · Dec 8, 2025Peer-reviewedGenetic & Genomic Medicine

Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS and sporadic congenital heart disease

Yingjie Zhao, Yujue Wang, Lijie Shi, Donna M. McDonald‐McGinn, Terrence Blaine Crowley, Daniel E. McGinn, Oanh Tran, Daniella Miller, Elaine H. Zackai, H. Richard Johnston, Eva W.C. Chow, Jacob A. S. Vorstman, Claudia Vingerhoets, Thérèse van Amelsvoort, Doron Gothelf, , Bernice E. Morrow

The paper identifies chromatin regulatory genes as genetic modifiers of conotruncal heart defects in 22q11.2 deletion syndrome and links them to sporadic congenital heart disease.

bioRxiv · Sep 30, 2022 · PreprintGenetics