Michael Wangler

24PUBLICATIONS
69CO-AUTHORS
Developmental genetics (incl. sex determination)Aircraft performance and flight control systemsInfant and child healthNeurology and neuromuscular diseasesMedical biochemistry - proteins and peptides (incl. medical proteomics)
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Publications (24)

|May 07, 2026
Genetic analysis of the X-linked adrenoleukodystrophy gene ABCD1 in Drosophila uncovers a conserved phenotype.

|Apr 03, 2026
NLGN3 autism variants have distinct functional impact on synapses and sleep behavior in Drosophila.

Rebekah Townsley, Jonathan Andrews, Saurabh Srivastav

|Jan 28, 2026
Metabolomic Profiling Reveals Brain Lipid Alterations in PEX7-Deficient Models of Rhizomelic Chondrodysplasia Punctata.

Riya Sankhe, Meredith I Williams, Wedad Fallatah

|Sep 04, 2025
Altered Gating of Two CaV2.1 Variants Linked to Neurodevelopmental Disorders With Epilepsy and Migraine.

Ulises Meza, Catalina Romero-Méndez, Danira A Ramírez-De León

|Jul 07, 2025
Distinguishing PEX2 and PEX16 gene variant severity for mild, severe and atypical peroxisome biogenesis disorders.

Vanessa A Gomez, Oguz Kanca, Sharayu V Jangam

|Jun 11, 2025
Drosophila models uncover substrate channeling effects on phospholipids and sphingolipids in peroxisomal biogenesis disorders.

Michael F Wangler, Yu-Hsin Chao, Mary Roth

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Frequent Collaborators

7 joint publications

Shinya Yamamoto

5 joint publications

Sharayu V Jangam

4 joint publications

Hugo J Bellen

4 joint publications

Jonathan C Andrews