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Ali, Naeem A, Alice A Gaughan, Charles G Orosz, Chris P Baran, Sara McMaken, Yijie Wang, Timothy D Eubank, et al. 2008. “Latency Associated Peptide Has in Vitro and in Vivo Immune Effects Independent of TGF-Beta1.”. PloS One 3 (4): e1914.

Tan, Kemin, Mark Duquette, Jin-huan Liu, Kumaran Shanmugasundaram, Andrzej Joachimiak, John T Gallagher, Alan C Rigby, Jia-huai Wang, and Jack Lawler. 2008. “Heparin-Induced Cis- and Trans-Dimerization Modes of the Thrombospondin-1 N-Terminal Domain.”. The Journal of Biological Chemistry 283 (7): 3932-41.

Zhang, Xuefeng, and Jack Lawler. 2007. “Thrombospondin-Based Antiangiogenic Therapy.”. Microvascular Research 74 (2-3): 90-9.

Zwicker, Jeffrey I, Flora Peyvandi, Roberta Palla, Rossana Lombardi, Maria Teresa Canciani, Andrea Cairo, Diego Ardissino, et al. 2006. “The Thrombospondin-1 N700S Polymorphism Is Associated With Early Myocardial Infarction Without Altering Von Willebrand Factor Multimer Size.”. Blood 108 (4): 1280-3.

Ren, Bin, Karen O Yee, Jack Lawler, and Roya Khosravi-Far. 2006. “Regulation of Tumor Angiogenesis by Thrombospondin-1.”. Biochimica et Biophysica Acta 1765 (2): 178-88.

Ortega-Rojas, Jenny, Carlos E Arboleda-Bustos, Luis Morales, Bruno A Benitez, Diana Beltrán, Álvaro Izquierdo, Humberto Arboleda, and Rafael Vásquez. 2017. “[Study of Genetic Variants in the BDNF, COMT, DAT1 and SERT Genes in Colombian Children With Attention Deficit Disorder].”. Revista Colombiana de Psiquiatria 46 (4): 222-28.

Jin, Sheng Chih, Bruno A Benitez, Yuetiva Deming, and Carlos Cruchaga. 2016. “Pooled-DNA Sequencing for Elucidating New Genomic Risk Factors, Rare Variants Underlying Alzheimer’s Disease.”. Methods in Molecular Biology (Clifton, N.J.) 1303: 299-314.

Anasagasti, Ander, Olatz Barandika, Cristina Irigoyen, Bruno A Benitez, Breanna Cooper, Carlos Cruchaga, Adolfo Lopez de Munain, and Javier Ruiz-Ederra. 2013. “Genetic High Throughput Screening in Retinitis Pigmentosa Based on High Resolution Melting (HRM) Analysis.”. Experimental Eye Research 116: 386-94.

Harms, Matthew, Bruno A Benitez, Nigel Cairns, Breanna Cooper, Paul Cooper, Kevin Mayo, David Carrell, et al. 2013. “C9orf72 Hexanucleotide Repeat Expansions in Clinical Alzheimer Disease.”. JAMA Neurology 70 (6): 736-41.

Benitez, Bruno A, Diego A Forero, Gonzalo H Arboleda, Luis A Granados, Juan J Yunis, William Fernandez, and Humberto Arboleda. 2010. “Exploration of Genetic Susceptibility Factors for Parkinson’s Disease in a South American Sample.”. Journal of Genetics 89 (2): 229-32.