Selected Publications

Favilla, C.G., Ford, A.F., Khazaal, O., Cristancho, D., Grodinsky, E., Dawod, J., Kasner, S.E.: Reliability of past medical history in a single hospital participating in Get With the Guidelines- Stroke registry. J Am Heart Assoc. 5 (11): 2022.

Kim, H.J., Mohassel, P., Donkervoort, S., Guo, L., O’Donovan, K., Coughlin, M., Lornage, X., Foulds, N., Hammans, S.R., Foley, A.R., Fare, C.M., Ford, A.F., Ogasawara, M., Sato, A., Iida, A., Munot, P., Ambegaonkar, G., Phadke, R., O’Donovan, D.G., Buchert, R., Grimmel, M., Topf, A., Zaharieva, I.T., Brady, L., Hu, Y., Lloyd, T.E., Klein, A., Steinlin, M., Kuster, A., Mercier, S., Marcorelles, P., Pereon, Y., Fleurence, E., Manzur, A., Ennis, S., Upstill-Goddard, R., Bello, L., Bertolin, C., Pegoraro, E., Salviati, L., French, C.E., Shatillo, A., Raymond, F.L., Haack, T., Quijano-Roy, S., Bohm, J., Nelson, I., Stojkovic, T., Evangelista, T., Straub, V., Romero, N.B., Laporte, J., Muntoni, F., Nishino, I., Tarnopolsky, M.A., Shorter, J., Bonnemann, C.G., Taylor, J.P.: Heterozygous frameshift variants in hnRNPA2B1 cause early-onset oculopharyngeal muscular dystrophy. Nature Communications 13 (1): 2022.

Beijer, D., Kim, H.J., Guo, L., O’Donovan, K., Mademan, I., Deconinck, T., Van Schil, K., Fare, C.M., Drake, L.E., Ford, A.F., Kochanski, A., Kabzinska, D., Dubuisson, N., Van den Bergh, P., Voermans, N.C., Lemmers, R.J.L.F., van der Maarel, S.M., Bonner, D., Sampson, J.B., Wheeler, M.T., Mehrabyan, A., Palmer, S., De Jonghe, P., Shorter, J., Taylor, J.P., Baets, J.: Characterization of HNRNPA1 mutations defines diversity in pathogenic mechanisms and clinical presentation. JCI Insight 6 (14): 2021 .

Ford, A.F., George, D.K.: A 34-year-old woman with numbness, weakness, and vision loss. Healio, Ace the Case https://cme.healio.com/neurology/ace-the-case/20210610/a-34-year-old-woman-withnumbness-weakness-and-vision-loss/overview : 2021.

Harrison, A.F., Shorter, J.: RNA-binding proteins with prion-like domains in health and disease. Biochemical Journal 474 (8): 1417-1438,2017.

Ford, A.F., Shorter, J.: Fleeting amyloid-like forms of Rim4 ensure meiotic fidelity. Cell 163 (2): 275-276,2015.

Kim, H.J., Kim, N.C., Wang, Y.D., Scarborough, E.A., Moore, J., Diaz, Z., MacLea, K.S., Freibaum, B., Li, S., Molliex, A., Kanagaraj, A.P., Carter, R., Boylan, K.B., Wojtas, A.M., Rademakers, R., Pinkus, J.L., Greenberg, S.A., Trojanowski, J.Q., Traynor, B.J., Smith, B.N., Topp, S., Gkazi, A.S., Miller, J., Shaw, C.E., Kottlors, M., Kirschner, J., Pestronk, A., Li, Y.R., Ford, A.F., Gitler, A.D., Benatar, M., King, O.D., Kimonis, V.E., Ross, E.D., Weihl, C.C., Shorter, J., Taylor, J.P.: Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS. Nature. : 2013.

Ford, A.F., Schall, J.J.: Relative clonal proportions over time in mixed-genotype infections of the lizard malaria parasite Plasmodium mexicanum International Journal for Parasitology : 2011.

Ford, A.F., Vardo-Zalik, A.M., Schall, J.J.: Relative clonal density of malaria parasites in mixed-genotype infections: validation of a technique using microsatellite markers for Plasmodium falciparum and P. mexicanum. Journal of Parasitology 96 : 2010.

Vardo-Zalik, A.M., Ford, A.F., Schall, J.J.: Detecting number of clones, and their relative abundance, of a malaria parasite (Plasmodium mexicanum) infecting its vertebrate host Parasitology Research : 2009.

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