A systematic review on machine learning approaches in the diagnosis and prognosis of rare genetic diseases by Roman-Naranjo, P., Parra-Perez, A.M., Lopez-Escamez, J.A.

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Rare coding variants involving MYO7A and other genes encoding stereocilia link proteins in familial meniere disease by Roman-Naranjo, P., Moleon, M.D.C., Aran, I., Escalera-Balsera, A., Soto-Varela, A., Bächinger, D., Gomez-Fiñana, M., Eckhard, A.H., Lopez-Escamez, J.A.

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Using coding and non-coding rare variants to target candidate genes in patients with severe tinnitus by Gallego-Martinez, Alvaro, Escalera-Balsera, Alba, Trpchevska, Natalia, Robles-Bolivar, Paula, Roman-Naranjo, Pablo, Frejo, Lidia, Perez-Carpena, Patricia, Bulla, Jan, Gallus, Silvano, Canlon, Barbara, Cederroth, Christopher R., Lopez-Escamez, Jose A.

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Rare Coding Variants in Patients with Non-Syndromic Vestibular Dysfunction by Sumalde, Angelo Augusto M, Scholes, Melissa A, Kalmanson, Olivia A, Terhune, Elizabeth A, Frejo, Lidia, Wethey, Cambria I, Roman-Naranjo, Pablo, Carry, Patrick M, Gubbels, Samuel P, Lopez-Escamez, Jose A, Hadley-Miller, Nancy, Santos-Cortez, Regie Lyn P

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