Selected Publications
Tropea TF, Amari N, Han N, Rick J, Suh E, Akhtar RS, Dahodwala N, Deik A, Gonzalez-Alegre P, Hurtig H, Siderowf A, Spindler M, Stern M, Thenganatt MA, Weintraub D, Willis AW, Van Deerlin V, Chen-Plotkin A.: Whole Clinic Research Enrollment in Parkinson's Disease: The Molecular Integration in Neurological Diagnosis (MIND) Study J Parkinsons Dis 11 (2): 757-765,2021.
Melis C, Beauvais G, Muntean BS, Cirnaru MD, Otrimski G; Creus-Muncunill J, Martemyanov KA, Gonzalez-Alegre P, Ehrlich ME.: Striatal dopamine induced ERK phosphorylation is altered in mouse models of monogenic dystonia Mov Disord 36 (5): 1147-1157,2021.
Klapper J, Bardakjian T, Sigal I, Muralidharan K, Gonzalez-Alegre P.: Healthcare Delivery via Telehealth during the COVID-19 Pandemic: the Experience of a Huntington’s Disease Center Clin Parkinsonism Relat Disord 4 : 100093,2021.
Dratch L, Paul R, Baldwin A, Brzozowski M, Gonzalez-Alegre P, Tropea TF, Raper A, Bardakjian T: Transitioning to Telemedicine in the COVID-19 Era: Patient Satisfaction with Genetic Counseling via Telephone or Videoconferencing in Adult Neurology J Genet Couns : 2021.
Guo MH, Bardakjian TM, Brzozowski MR, Scherer SS, Quinn C, Elman L, Orthmann-Murphy J, Tropea TF, Ellis CA and Gonzalez-Alegre P.: Temporal trends and yield of clinical diagnostic genetic testing in adult neurology Am J Med Genet A : 2021.
Isonaka R, Goldstein DS, Zhu W, Yoon E, Ehrlich D, Schindler AB, Kokkinis AD, Sabir MS, Scholz SW, Bandres-Ciga S, Blauwendraat C, Gonzalez-Alegre P, Lopez G, Sidransky E, Narendra DP.: α-Synuclein deposition in sympathetic nerve fibers in genetic forms of Parkinson’s Disease Mov Disord : 2021.
Guo MH, Bardakjian TM, Brzozowski MR, Scherer SS, Quinn C, Elman L, Orthmann-Murphy J, Tropea TF, Ellis CA, Gonzalez-Alegre P.: Temporal trends and yield of clinical diagnostic genetic testing in adult neurology Am J Med Genet A. : 2021.
Cirnaru MD, Creus-Muncunill J, Nelson S, Lewis T, Watson J, Ellerby LM, Gonzalez-Alegre P*, Ehrlich ME*.: Striatal Dysfunction after Neonatal Decrease in X-linked Dystonia Parkinsonism Related TAF1 Isoforms Mov Disord : 2021.
Zech M, Jech R, Boesch S, Škorvánek M, Weber S, Wagner M, Zhao C, Jochim A, Necpál J, Dincer Y, Vill K, Distelmaier F, Stoklosa M, Krenn M, Grunwald S, Bock-Bierbaum T, Fečíková A, Havránková P, Roth J, Příhodová I, Adamovičová M, Ulmanová O, Bechyně K, Danhofer P, Veselý B, Haň V, Pavelekova P, Gdovinová Z, Mantel T, Meindl T, Sitzberger A, Schröder S, Blaschek A, Roser T, Bonfert MV, Haberlandt E, Plecko B, Leineweber B, Berweck S, Herberhold T, Langguth B, Švantnerová J, Minár M, Ramos-Rivera GA, Wojcik MH, Pajusalu S, Õunap K, Schatz UA, Pölsler L, Milenkovic I, Laccone F, Pilshofer V, Colombo R, Patzer S, Iuso A, Vera J, Troncoso M, Fang F, Prokisch H, Wilbert F, Eckenweiler M, Graf E, Westphal DS, Riedhammer KM, Brunet T, Alhaddad B, Berutti R, Strom TM, Hecht M, Baumann M, Wolf M, Telegrafi A, Person RE, Zamora FM, Henderson LB, Weise D, Musacchio T, Volkmann J, Szuto A, Becker J, Cremer K, Sycha T, Zimprich F, Kraus V, Makowski C, Gonzalez-Alegre P, Bardakjian TM, Ozelius LJ, Vetro A, Guerrini R, Maier E, Borggraefe I, Kuster A, Wortmann SB, Hackenberg A, Steinfeld R, Assmann B, Staufner C, Opladen T, Růžička E, Cohn RD, Dyment D, Chung WK, Engels H, Ceballos-Baumann A, Ploski R, Daumke O, Haslinger B, Mall V, Oexle K, Winkelmann J.: Monogenic variants in dystonia: an exome-wide sequencing study. Lancet Neurol 19 (11): 908-918,2020.
Robbins, N. M., Ozmore, J. R., Winder, T. L., Gonzalez-Alegre, P., Bardakjian, T. M.: A Novel SPAST/SPG4 Splice-Site Variant in a Family with Dominant Hereditary Spastic Paraplegia Case Rep Neurol Med 2020 : 7219514,2020.
Academic Contact Information
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