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da Rocha, Lummertz, C. Kubaczka, W. W. Sugden, M. A. Najia, R. Jing, A. Markel, Z. C. LeBlanc, et al. 2022. “CellComm Infers Cellular Crosstalk That Drives Haematopoietic Stem and Progenitor Cell Development”. Nat Cell Biol 24: 579-89.

Shepherd, Amy, Laurence Feinstein, Svetlana Sabel, Daniella Rastelli, Esther Mezhibovsky, Lynley Matthews, Anoohya Muppirala, et al. 2024. “RET Signaling Persists in the Adult Intestine and Stimulates Motility by Limiting PYY Release From Enteroendocrine Cells.”. Gastroenterology 166 (3): 437-49.

Singh, Bandana, Kui Cui, Shahram Eisa-Beygi, Bo Zhu, Douglas B. Cowan, Jinjun Shi, Chris A. Bashur, et al. 2024. “Elucidating the Crosstalk Between Endothelial-to-Mesenchymal Transition (EndoMT) and Endothelial Autophagy in the Pathogenesis of Atherosclerosis”. Vascular Pharmacology 155: 107368.

Sanoudou, Despina, Mark Corbett, Mei Han, Majid Ghoddusi, Mai-Anh Nguyen, Nicole Vlahovich, Edna Hardeman, and Alan Beggs. 2006. “Skeletal Muscle Repair in a Mouse Model of Nemaline Myopathy.”. Hum Mol Genet 15 (17): 2603-12.

Cerletti, Massimiliano, Michael Molloy, Kinga Tomczak, Soonsang Yoon, Marco Ramoni, Alvin Kho, Alan Beggs, and Emanuela Gussoni. 2006. “Melanoma Cell Adhesion Molecule Is a Novel Marker for Human Fetal Myogenic Cells and Affects Myoblast Fusion.”. J Cell Sci 119 (Pt 15): 3117-27.

Bitoun, Marc, Svetlana Maugenre, Pierre-Yves Jeannet, Emmanuelle Lacène, Xavier Ferrer, Pascal Laforêt, Jean-Jacques Martin, et al. 2005. “Mutations in Dynamin 2 Cause Dominant Centronuclear Myopathy.”. Nat Genet 37 (11): 1207-9.

Kang, Peter, Alvin Kho, Despina Sanoudou, Judith Haslett, Chad Dow, Mei Han, Jessica Blasko, Hart Lidov, Alan Beggs, and Louis Kunkel. 2005. “Variations in Gene Expression Among Different Types of Human Skeletal Muscle.”. Muscle Nerve 32 (4): 483-91.

Gazda, Hanna, Rong Zhong, Lilia Long, Edyta Niewiadomska, Jeffrey Lipton, Anna Ploszynska, Jan Zaucha, et al. 2004. “RNA and Protein Evidence for Haplo-Insufficiency in Diamond-Blackfan Anaemia Patients With RPS19 Mutations.”. Br J Haematol 127 (1): 105-13.

Wallgren-Pettersson, Carina, Katarina Pelin, Kristen Nowak, Francesco Muntoni, Norma Romero, Hans Goebel, Kathryn North, Alan Beggs, Nigel Laing, and ENMC International Consortium On Nemaline Myopathy. 2004. “Genotype-Phenotype Correlations in Nemaline Myopathy Caused by Mutations in the Genes for Nebulin and Skeletal Muscle Alpha-Actin.”. Neuromuscul Disord 14 (8-9): 461-70.

Haslett, Judith, Despina Sanoudou, Alvin Kho, Richard Bennett, Steven Greenberg, Isaac Kohane, Alan Beggs, and Louis Kunkel. 2002. “Gene Expression Comparison of Biopsies from Duchenne Muscular Dystrophy (DMD) and Normal Skeletal Muscle.”. Proc Natl Acad Sci U S A 99 (23): 15000-5.