Author

LaDonna L. Immken

Dell Children's Medical Center of Central Texas

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

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 2 Genetics· 2

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 4 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1

Frequent Co-Authors

Brendan LeeiD· 2 shared Carlos A. BacinoiD· 2 shared Casie A. GenettiiD· 2 shared Jennifer Ellen PoseyiD· 2 shared Jill Anne RosenfeldiD· 2 shared John W. BelmontiD· 2 shared Mathilde NizoniD· 2 shared Rami Abou JamraiD· 2 shared

Activity by Year

2018-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 23 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenetics

Brendan LeeORCID

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Clinical, in vitro, and in vivo evidence of WAPL as a novel cohesinopathy gene and phenotypic driver of 10q22.3q23.2 genomic disorder

Philip M. Boone, Serkan Erdin, Abucar Mohamed, Sadegheh Haghshenas, Kamli N. W. Faour, Emeline M. Kao, Jack M. Fu, Chiara Auwerx, Ricardo Harripaul, Bimal Jana, Danielle Springer, Grey F. Hallström, Celine E. de Esch, Erica Rose Denhoff, Lauren Holmes, , Ilaria Parenti

The paper identifies WAPL as a novel cohesinopathy gene and driver of a genomic disorder, showing its role in developmental delay and other anomalies through clinical, in vitro, and in vivo analyses.

medRxiv · Feb 28, 2026 · PreprintGenetic & Genomic Medicine

Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior

Holly K. Harris, Tojo Nakayama, Jenny F. Lai, Boxun Zhao, Nikoleta Argyrou, Cynthia Sophia Gubbels, Aubrie Soucy, Casie A. Genetti, Victoria Suslovitch, Lance H. Rodan, George E. Tiller, Gaëtan Lesca, Karen Webster Gripp, Reza Asadollahi, Ada Hamosh, , Timothy W. Yu

The paper identifies RFX3, RFX4, and RFX7 mutations as causes of neurodevelopmental disorders including autism, ADHD, and intellectual disability, and links these genes to ASD risk genes through bioinformatic analysis.

Genetics in Medicine · Mar 3, 2021Peer-reviewedGenetic & Genomic Medicine

Microdeletions excluding YWHAE and PAFAH1B1 cause a unique leukoencephalopathy and hypermobility syndrome: Further delineation of the 17p13.3 microdeletion spectrum

Lisa Emrick, Jill Anne Rosenfeld, Seema R. Lalani, Mahim Jain, Nilesh K. Desai, Austin A Larson, Kimberly A. Kripps, Adeline L. Vanderver, Ryan J. Taft, Krista K. Bluske, Denise Perry, Honey Nagakura, LaDonna L. Immken, Lindsay Catherine Burrage, Carlos A. Bacino, , Brendan Lee

The paper investigates 17p13.3 deletions between YWHAE/CRK and PAFAH1B1, identifying white matter lesions and hypermobility, and narrows the critical region to 345 kb with RTN4RL1 as a candidate gene.

Genetics in Medicine · Dec 18, 2018Peer-reviewedGenetics

Phenotypic expansion in DDX3X -- a common cause of intellectual disability in females

Xia Wang, Jennifer Ellen Posey, Jill Anne Rosenfeld, Carlos A. Bacino, Fernando Scaglia, LaDonna L. Immken, Jill M. Harris, Scott E. Hickey, Theresa Mihalic Mosher, Anne Michele Slavotinek, Jing Zhang, Joke Beuten, Magalie S. Leduc, Weimin He, Francesco Vetrini, , Paolo M. Moretti

The paper identifies additional DDX3X variants in individuals with intellectual disability and expands the known phenotypic spectrum of DDX3X disorders.

Annals of Clinical and Translational Neurology · Sep 15, 2018Peer-reviewedGenetics