J. Biroschak

Familial haemophagocytic lymphohistiocytosis in patients who are heterozygous for the A91V perforin variation is often associated with other genetic defects

R. Wenstrup, A. Filipovich, J. Villanueva, 2007, International journal of immunogenetics.

Detection of a novel RET gene fusion in a non-small cell lung cancer patient using AMP chemistry

P. Fang, Zhenyu Yan, Weihua Liu, 2016 .

Macrophage activation syndrome in patients with systemic juvenile idiopathic arthritis is associated with MUNC13-4 polymorphisms.

D. Glass, Kejian Zhang, S. Thompson, 2008, Arthritis and rheumatism.

STX11 mutations and clinical phenotypes of familial hemophagocytic lymphohistiocytosis in North America

N. Satake, Kejian Zhang, A. Filipovich, 2010, Pediatric blood & cancer.

Abstract 4261: Oncomine® Cancer Panel: simultaneous detection of clinically relevant hotspot mutations, CNVs, and gene fusions in solid tumors

P. Fang, Zhenyu Yan, Weihua Liu, 2015 .