Andy Drackley

15PUBLICATIONS
34CO-AUTHORS
Medical devicesSystems physiologyMedical molecular engineering of nucleic acids and proteinsEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)
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Publications (15)

|May 04, 2026
A Case of Aymé-Gripp Syndromic Congenital Cataracts and Pigmentary Retinopathy Caused by a Novel MAF Variant in the N-Terminal Transactivation Domain-A Case Report and Literature Review.

|Mar 11, 2026
Recognition of a Critical Functional Domain and Improved PHOX2B Missense Variant Interpretation by Utilization of In Silico Prediction Tools.

Andy Drackley, Andrew D Skol, Casey M Rand

|Feb 20, 2026
Infantile Cataracts Associated with a Homozygous Missense MSMO1 Variant-Case Report and Literature Review.

Nick Hassas, Andy Drackley, Jelena Ivanisevic

|Dec 04, 2025
Long-Read Genome Sequencing Establishes Biallelic Pathogenic Variants in DNM1 With Distinct Functional Effects as the Cause of Early Infantile Developmental and Epileptic Encephalopathy.

Andy Drackley, Merlene Peter, Heba H Akbari

|Oct 08, 2025
Measuring historical variant reclassification in inherited retinal disease and its impact on clinical genetic testing.

Karly Kern, Adam Gordon, Andy Drackley

|Aug 28, 2025
GPR143-Associated Ocular Albinism in a Hispanic Family and Review of the Literature.

Anushree Aneja, Brenda L Bohnsack, Valerie Allegretti

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Frequent Collaborators

11 joint publications

Alexander Ing

4 joint publications

Kai Lee Yap

3 joint publications

Patrick McMullen

3 joint publications

Brenda L Bohnsack