John Hicks

MYCN-driven fatty acid uptake is a metabolic vulnerability in neuroblastoma

Pavel Sumazin, C. Coarfa, Zihua Zeng, 2022, Nature Communications.

COPB2 loss of function causes a coatopathy with osteoporosis and developmental delay.

David R. Murdock, Lisa T. Emrick, Alyssa A. Tran, 2021, American journal of human genetics.

Connective tissue alterations in Fkbp10 2 / 2 mice

Brendan H. Lee, D. Eyre, Yuqing Chen, 2014 .

The RNA-binding protein Rbfox1 regulates splicing required for skeletal muscle structure and function.

Qianxing Mo, Amy D. Hanna, Mark Knoblauch, 2015, Human molecular genetics.

skeletal muscle structure and function

Amy D. Hanna, T. Cooper, Q. Mo, 2015 .

Genetic diagnosis and renal biopsy findings in the setting of a renal genetics clinic

M. Bekheirnia, M. Braun, N. Bekheirnia, 2022, American journal of medical genetics. Part C, Seminars in medical genetics.