Dolled-Filhart MP, Lordemann A, Dahl W, Haraksingh RH, Ou-Yang CW, Lin JC. Personalizing rare disease research: how genomics is revolutionizing the diagnosis and treatment of rare disease. Personalized Medicine, November 2012, Vol. 9, No. 8, Pages 805-819.
Lee, M, Lin JC. Overcoming the obstacles to returning genomic research results. Genetics Research. 2013 Apr 17:1-6.
Dolled-Filhart MP, Lee M Jr, Ou-Yang CW, Haraksingh RR, Lin JC. Computational and bioinformatics frameworks for next-generation whole exome and genome sequencing. Scientific World Journal. Epub 2013 Jan 13.
Lordemann A, Danielsson K, Lin JC. Innovative Funding Models for Rare Diseases. Orphan Diseases in the Age of Health 2.0. 2013. Springer.
Lin JC, Krissi Danielsson K, OuYang WC, Lordemann A, Mitra R. Target Enrichement Methods for Clinical Genomics. Chapter 3. Clinical Genomics. 2013.