Frank Li, PhD

Markowitz, Sanford D, et al. “A Germline Variant on Chromosome 4q31.1 Associates With Susceptibility to Developing Colon Cancer Metastasis.”. PLoS One, vol. 11, no. 1, 2016, p. e0146435, https://doi.org/10.1371/journal.pone.0146435.

Li, Frank, et al. “Nebulin Deficiency in Adult Muscle Causes Sarcomere Defects and Muscle-Type-Dependent Changes in Trophicity: Novel Insights in Nemaline Myopathy.”. Hum Mol Genet, vol. 24, no. 18, Sept. 2015, pp. 5219-33, https://doi.org/10.1093/hmg/ddv243.

Granzier, Henk L, et al. “Deleting Titin’s I-Band A-Band Junction Reveals Critical Roles for Titin in Biomechanical Sensing and Cardiac Function.”. Proc Natl Acad Sci U S A, vol. 111, no. 40, Oct. 2014, pp. 14589-94, https://doi.org/10.1073/pnas.1411493111.

Ganguly, Sourik S, et al. “The Host Microenvironment Influences Prostate Cancer Invasion, Systemic Spread, Bone Colonization, and Osteoblastic Metastasis.”. Front Oncol, vol. 4, Jan. 2014, p. 364, https://doi.org/10.3389/fonc.2014.00364.

Schaibley, Valerie M, et al. “The Influence of Genomic Context on Mutation Patterns in the Human Genome Inferred from Rare Variants.”. Genome Res, vol. 23, no. 12, Dec. 2013, pp. 1974-84, https://doi.org/10.1101/gr.154971.113.

Maubaret, Cécilia G, et al. “Association of TERC and OBFC1 Haplotypes With Mean Leukocyte Telomere Length and Risk for Coronary Heart Disease.”. PLoS One, vol. 8, no. 12, 2013, p. e83122, https://doi.org/10.1371/journal.pone.0083122.

Bedoyan, Jirair Krikor, et al. “Disruption of RAB40AL Function Leads to Martin--Probst Syndrome, a Rare X-Linked Multisystem Neurodevelopmental Human Disorder.”. J Med Genet, vol. 49, no. 5, May 2012, pp. 332-40, https://doi.org/10.1136/jmedgenet-2011-100575.

Kolb, Justin, et al. “Thin Filament Length in the Cardiac Sarcomere Varies With Sarcomere Length But Is Independent of Titin and Nebulin.”. J Mol Cell Cardiol, vol. 97, pp. 286-94, https://doi.org/10.1016/j.yjmcc.2016.04.013.