Eric Yu, MD

Title(s)Clinical Assistant Professor of Medicine (Clinician Educator)
SchoolKeck School of Medicine of Usc
Address1200 N. State Street
University Park Campus
Los Angeles CA 90033
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    1. ASSOCIATIONS BETWEEN EPILEPSY-RELATED POLYGENIC RISK AND BRAIN MORPHOLOGY IN CHILDHOOD. bioRxiv. 2025 Jan 17. Ngo A, Liu L, Larivière S, Kebets V, Fett S, Weber CF, Royer J, Yu E, Rodríguez-Cruces R, Zhang Z, Ooi LQR, Thomas Yeo BT, Frauscher B, Paquola C, Caligiuri ME, Gambardella A, Concha L, Keller SS, Cendes F, Yasuda CL, Bonilha L, Gleichgerrcht E, Focke NK, Kotikalapudi R, O'Brien TJ, Sinclair B, Vivash L, Desmond PM, Lui E, Vaudano AE, Meletti S, Kälviäinen R, Soltanian-Zadeh H, Winston GP, Tiwari VK, Kreilkamp BAK, Lenge M, Guerrini R, Hamandi K, Rüber T, Bauer T, Devinsky O, Striano P, Kaestner E, Hatton SN, Caciagli L, Kirschner M, Duncan JS, Thompson PM, ENIGMA Consortium Epilepsy Working Group, McDonald CR, Sisodiya SM, Bernasconi N, Bernasconi A, Gan-Or Z, Bernhardt BC. PMID: 39868179; PMCID: PMC11760683.
      View in: PubMed   Mentions:
    2. Are rare heterozygous SYNJ1 variants associated with Parkinson's disease? NPJ Parkinsons Dis. 2024 Oct 25; 10(1):201. Senkevich K, Parlar SC, Chantereault C, Yu E, Ahmad J, Ruskey JA, Asayesh F, Spiegelman D, Waters C, Monchi O, Dauvilliers Y, Dupré N, Miliukhina I, Timofeeva A, Emelyanov A, Pchelina S, Greenbaum L, Hassin-Baer S, Alcalay RN, Gan-Or Z. PMID: 39455605; PMCID: PMC11512049.
      View in: PubMed   Mentions:
    3. Plasma glucosylceramide levels are regulated by ATP10D and are not involved in Parkinson's disease pathogenesis. medRxiv. 2024 Sep 16. Somerville EN, James A, Beetz C, Schwieger R, Barrel G, Kandaswamy KK, Iurascu MI, Bauer P, Ta M, Iwaki H, Senkevich K, Yu E, Alcalay RN, Gan-Or Z. PMID: 39371176; PMCID: PMC11451666.
      View in: PubMed   Mentions:
    4. Dopamine Pathway and Parkinson's Risk Variants Are Associated with Levodopa-Induced Dyskinesia. Mov Disord. 2024 Oct; 39(10):1773-1783. Sosero YL, Bandres-Ciga S, Ferwerda B, Tocino MTP, Belloso DR, Gómez-Garre P, Faouzi J, Taba P, Pavelka L, Marques TM, Gomes CPC, Kolodkin A, May P, Milanowski LM, Wszolek ZK, Uitti RJ, Heutink P, van Hilten JJ, Simon DK, Eberly S, Alvarez I, Krohn L, Yu E, Freeman K, Rudakou U, Ruskey JA, Asayesh F, Menéndez-Gonzàlez M, Pastor P, Ross OA, Krüger R, NCER-PD Consortium, Corvol JC, Koks S, Mir P, De Bie RMA, Iwaki H, Gan-Or Z, International Parkinson's Disease Genomic Consortium. PMID: 39132902; PMCID: PMC11490412.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    5. HLA-DQB1*05 subtypes and not DRB1*10:01 mediates risk in anti-IgLON5 disease. Brain. 2024 Jul 05; 147(7):2579-2592. Yogeshwar SM, Muñiz-Castrillo S, Sabater L, Peris-Sempere V, Mallajosyula V, Luo G, Yan H, Yu E, Zhang J, Lin L, Fagundes Bueno F, Ji X, Picard G, Rogemond V, Pinto AL, Heidbreder A, Höftberger R, Graus F, Dalmau J, Santamaria J, Iranzo A, Schreiner B, Giannoccaro MP, Liguori R, Shimohata T, Kimura A, Ono Y, Binks S, Mariotto S, Dinoto A, Bonello M, Hartmann CJ, Tambasco N, Nigro P, Prüss H, McKeon A, Davis MM, Irani SR, Honnorat J, Gaig C, Finke C, Mignot E. PMID: 38425314; PMCID: PMC11224611.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    6. Comorbid neurotrauma increases neurodegenerative-relevant cognitive, motor, and autonomic dysfunction in patients with rapid eye movement sleep behavior disorder: a substudy of the North American Prodromal Synucleinopathy Consortium. Sleep. 2024 Jun 13; 47(6). Elliott JE, Ligman BR, Bryant-Ekstrand MD, Keil AT, Powers K, Olivo C, Neilson LE, Postuma RB, Pelletier A, Gagnon JF, Gan-Or Z, Yu E, Liu L, St Louis EK, Forsberg LK, Fields JA, Ross OA, Huddleston DE, Bliwise DL, Avidan AY, Howell MJ, Schenck CH, McLeland J, Criswell SR, Videnovic A, During EH, Miglis MG, Shprecher DR, Lee-Iannotti JK, Boeve BF, Ju YS, Lim MM, North American Prodromal Synucleinopathy (NAPS) Consortium . PMID: 38181205; PMCID: PMC11519033.
      View in: PubMed   Mentions: 1     Fields:    
    7. Genome-wide association study of glucocerebrosidase activity modifiers. Res Sq. 2024 Jun 07. Somerville EN, Krohn L, Senkevich K, Yu E, Ahmad J, Asayesh F, Ruskey JA, Speigelman D, Fahn S, Waters C, Sardi SP, Alcalay RN, Gan-Or Z. PMID: 38883744; PMCID: PMC11177962.
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    8. Are rare heterozygous SYNJ1 variants associated with Parkinson's disease? medRxiv. 2024 Jun 01. Senkevich K, Parlar SC, Chantereault C, Yu E, Ahmad J, Ruskey JA, Asayesh F, Spiegelman D, Waters C, Monchi O, Dauvilliers Y, Dupré N, Miliukhina I, Timofeeva A, Emelyanov A, Pchelina S, Greenbaum L, Hassin-Baer S, Alcalay RN, Gan-Or Z. PMID: 38853950; PMCID: PMC11160829.
      View in: PubMed   Mentions:
    9. Autosomal Dominant Parkinson's Disease Caused by SNCA p.E46K Mutation in a Family with Russian Ancestry. Mov Disord. 2024 Aug; 39(8):1424-1425. Senkevich K, Miliukhina I, Zhuravlev A, Shumilova M, Beletskaia M, Skvortsova T, Yu E, Ahmad J, Asayesh F, Gan-Or Z, Emelyanov A, Pchelina S. PMID: 38661277.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    10. Genotype-phenotype correlation in PRKN-associated Parkinson's disease. NPJ Parkinsons Dis. 2024 Mar 29; 10(1):72. Menon PJ, Sambin S, Criniere-Boizet B, Courtin T, Tesson C, Casse F, Ferrien M, Mariani LL, Carvalho S, Lejeune FX, Rebbah S, Martet G, Houot M, Lanore A, Mangone G, Roze E, Vidailhet M, Aasly J, Gan Or Z, Yu E, Dauvilliers Y, Zimprich A, Tomantschger V, Pirker W, Álvarez I, Pastor P, Di Fonzo A, Bhatia KP, Magrinelli F, Houlden H, Real R, Quattrone A, Limousin P, Korlipara P, Foltynie T, Grosset D, Williams N, Narendra D, Lin HP, Jovanovic C, Svetel M, Lynch T, Gallagher A, Vandenberghe W, Gasser T, Brockmann K, Morris HR, Borsche M, Klein C, Corti O, Brice A, Lesage S, Corvol JC, French Parkinson disease Genetics Study Group (PDG). PMID: 38553467; PMCID: PMC10980707.
      View in: PubMed   Mentions: 10  
    11. Machine learning nominates the inositol pathway and novel genes in Parkinson's disease. Brain. 2024 03 01; 147(3):887-899. Yu E, Larivière R, Thomas RA, Liu L, Senkevich K, Rahayel S, Trempe JF, Fon EA, Gan-Or Z. PMID: 37804111; PMCID: PMC10907089.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    12. Dopamine pathway and Parkinson's risk variants are associated with levodopa-induced dyskinesia. medRxiv. 2023 Sep 20. Sosero YL, Bandres-Ciga S, Ferwerda B, Tocino MTP, Belloso DR, Gómez-Garre P, Faouzi J, Taba P, Pavelka L, Marques TM, Gomes CPC, Kolodkin A, May P, Milanowski LM, Wszolek ZK, Uitti RJ, Heutink P, van Hilten JJ, Simon DK, Eberly S, Alvarez I, Krohn L, Yu E, Freeman K, Rudakou U, Ruskey JA, Asayesh F, Menéndez-Gonzàlez M, Pastor P, Ross OA, Krüger R, Corvol JC, Koks S, Mir P, De Bie RMA, Iwaki H, Gan-Or Z. PMID: 37790572; PMCID: PMC10543218.
      View in: PubMed   Mentions:
    13. Multiancestry analysis of the HLA locus in Alzheimer's and Parkinson's diseases uncovers a shared adaptive immune response mediated by HLA-DRB1*04 subtypes. Proc Natl Acad Sci U S A. 2023 09 05; 120(36):e2302720120. Le Guen Y, Luo G, Ambati A, Damotte V, Jansen I, Yu E, Nicolas A, de Rojas I, Peixoto Leal T, Miyashita A, Bellenguez C, Lian MM, Parveen K, Morizono T, Park H, Grenier-Boley B, Naito T, Küçükali F, Talyansky SD, Yogeshwar SM, Sempere V, Satake W, Alvarez V, Arosio B, Belloy ME, Benussi L, Boland A, Borroni B, Bullido MJ, Caffarra P, Clarimon J, Daniele A, Darling D, Debette S, Deleuze JF, Dichgans M, Dufouil C, During E, Düzel E, Galimberti D, Garcia-Ribas G, García-Alberca JM, García-González P, Giedraitis V, Goldhardt O, Graff C, Grünblatt E, Hanon O, Hausner L, Heilmann-Heimbach S, Holstege H, Hort J, Jung YJ, Jürgen D, Kern S, Kuulasmaa T, Lee KH, Lin L, Masullo C, Mecocci P, Mehrabian S, de Mendonça A, Boada M, Mir P, Moebus S, Moreno F, Nacmias B, Nicolas G, Niida S, Nordestgaard BG, Papenberg G, Papma J, Parnetti L, Pasquier F, Pastor P, Peters O, Pijnenburg YAL, Piñol-Ripoll G, Popp J, Porcel LM, Puerta R, Pérez-Tur J, Rainero I, Ramakers I, Real LM, Riedel-Heller S, Rodriguez-Rodriguez E, Ross OA, Royo LJ, Rujescu D, Scarmeas N, Scheltens P, Scherbaum N, Schneider A, Seripa D, Skoog I, Solfrizzi V, Spalletta G, Squassina A, van Swieten J, Sánchez-Valle R, Tan EK, Tegos T, Teunissen C, Thomassen JQ, Tremolizzo L, Vyhnalek M, Verhey F, Waern M, Wiltfang J, Zhang J, EADB, GR@ACE study group, DEGESCO consortium, DemGene, EADI, GERAD, Asian Parkinson’s Disease Genetics consortium, Zetterberg H, Blennow K, He Z, Williams J, Amouyel P, Jessen F, Kehoe PG, Andreassen OA, Van Duin C, Tsolaki M, Sánchez-Juan P, Frikke-Schmidt R, Sleegers K, Toda T, Zettergren A, Ingelsson M, Okada Y, Rossi G, Hiltunen M, Gim J, Ozaki K, Sims R, Foo JN, van der Flier W, Ikeuchi T, Ramirez A, Mata I, Ruiz A, Gan-Or Z, Lambert JC, Greicius MD, Mignot E. PMID: 37643212; PMCID: PMC10483635.
      View in: PubMed   Mentions: 12     Fields:    
    14. HLA in isolated REM sleep behavior disorder and Lewy body dementia. Ann Clin Transl Neurol. 2023 09; 10(9):1682-1687. Yu E, Krohn L, Ruskey JA, Asayesh F, Spiegelman D, Shah Z, Chia R, Arnulf I, Hu MTM, Montplaisir JY, Gagnon JF, Desautels A, Dauvilliers Y, Gigli GL, Valente M, Janes F, Bernardini A, Högl B, Stefani A, Ibrahim A, Heidbreder A, Sonka K, Dusek P, Kemlink D, Oertel W, Janzen A, Plazzi G, Antelmi E, Figorilli M, Puligheddu M, Mollenhauer B, Trenkwalder C, Sixel-Döring F, Cochen De Cock V, Ferini-Strambi L, Dijkstra F, Viaene M, Abril B, Boeve BF, Rouleau GA, Postuma RB, International LBD Genomics Consortium, Scholz SW, Gan-Or Z. PMID: 37401389; PMCID: PMC10502660.
      View in: PubMed   Mentions: 3     Fields:    
    15. Association of Rare Variants in ARSA with Parkinson's Disease. Mov Disord. 2023 10; 38(10):1806-1812. Senkevich K, Beletskaia M, Dworkind A, Yu E, Ahmad J, Ruskey JA, Asayesh F, Spiegelman D, Fahn S, Waters C, Monchi O, Dauvilliers Y, Dupré N, Greenbaum L, Hassin-Baer S, Nagornov I, Tyurin A, Miliukhina I, Timofeeva A, Emelyanov A, Trempe JF, Zakharova E, Alcalay RN, Pchelina S, Gan-Or Z. PMID: 37381728; PMCID: PMC10615669.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    16. Corrigendum: Clinical and genetic analysis of Costa Rican patients with Parkinson's disease. Front Neurol. 2023; 14:1227084. Torrealba-Acosta G, Yu E, Lobo-Prada T, Ruíz-Martínez J, Gorostidi-Pagola A, Gan-Or Z, Carazo-Céspedes K, Trempe JF, Mata IF, Fornaguera-Trías J. PMID: 37396761; PMCID: PMC10311411.
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    17. Potential Protective Link Between Type I Diabetes and Parkinson's Disease Risk and Progression. Mov Disord. 2023 07; 38(7):1350-1355. Senkevich K, Alipour P, Chernyavskaya E, Yu E, Noyce AJ, Gan-Or Z. PMID: 37148456.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    18. GALC variants affect galactosylceramidase enzymatic activity and risk of Parkinson's disease. Brain. 2023 05 02; 146(5):1859-1872. Senkevich K, Zorca CE, Dworkind A, Rudakou U, Somerville E, Yu E, Ermolaev A, Nikanorova D, Ahmad J, Ruskey JA, Asayesh F, Spiegelman D, Fahn S, Waters C, Monchi O, Dauvilliers Y, Dupré N, Greenbaum L, Hassin-Baer S, Grenn FP, Chiang MSR, Sardi SP, Vanderperre B, Blauwendraat C, Trempe JF, Fon EA, Durcan TM, Alcalay RN, Gan-Or Z. PMID: 36370000; PMCID: PMC10151180.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    19. Genome-wide association study stratified by MAPT haplotypes identifies potential novel loci in Parkinson's disease. medRxiv. 2023 Apr 15. Senkevich K, Bandres-Ciga S, Cisterna-García A, Yu E, Bustos BI, Krohn L, Lubbe SJ, Botía JA, International Parkinson’s Disease Genomics Consortium (IPDGC), Gan-Or Z. PMID: 37292720; PMCID: PMC10246147.
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    20. HLA in isolated REM sleep behavior disorder and Lewy body dementia. medRxiv. 2023 Apr 03. Yu E, Krohn L, Ruskey JA, Asayesh F, Spiegelman D, Shah Z, Chia R, Arnulf I, Hu MTM, Montplaisir JY, Gagnon JF, Desautels A, Dauvilliers Y, Gigli GL, Valente M, Janes F, Bernardini A, Högl B, Stefani A, Ibrahim A, Heidbreder A, Sonka K, Dusek P, Kemlink D, Oertel W, Janzen A, Plazzi G, Antelmi E, Figorilli M, Puligheddu M, Mollenhauer B, Trenkwalder C, Sixel-Döring F, De Cock VC, Ferini-Strambi L, Dijkstra F, Viaene M, Abril B, Boeve BF, Rouleau GA, Postuma RB, Scholz SW, International LBD Genomics Consortium, Gan-Or Z. PMID: 36778313; PMCID: PMC9915822.
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    21. Association of rare variants in ARSA with Parkinson's disease. medRxiv. 2023 Mar 13. Senkevich K, Beletskaia M, Dworkind A, Yu E, Ahmad J, Ruskey JA, Asayesh F, Spiegelman D, Fahn S, Waters C, Monchi O, Dauvilliers Y, Dupré N, Greenbaum L, Hassin-Baer S, Nagornov I, Tyurin A, Miliukhina I, Timofeeva A, Emelyanov A, Zakharova E, Alcalay RN, Pchelina S, Gan-Or Z. PMID: 36993451; PMCID: PMC10055435.
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    22. NPC1 variants are not associated with Parkinson's disease, REM-sleep behavior disorder or dementia with Lewy bodies in European cohorts. Neurobiol Aging. 2023 07; 127:94-98. Somerville EN, Krohn L, Yu E, Rudakou U, Senkevich K, Ruskey JA, Asayesh F, Ahmad J, Spiegelman D, Dauvilliers Y, Arnulf I, Hu MTM, Montplaisir JY, Gagnon JF, Desautels A, Ibrahim A, Stefani A, Högl B, Gigli GL, Valente M, Janes F, Bernardini A, Dusek P, Sonka K, Kemlink D, Plazzi G, Antelmi E, Biscarini F, Mollenhauer B, Trenkwalder C, Sixel-Doring F, Figorilli M, Puligheddu M, De Cock VC, Oertel W, Janzen A, Ferini-Strambi L, Heibreder A, Monaca CC, Abril B, Dijkstra F, Viaene M, Boeve BF, Postuma RB, Rouleau GA, Gan-Or Z. PMID: 37032242.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    23. Neuroanatomical correlates of genetic risk for obesity in children. Transl Psychiatry. 2023 01 03; 13(1):1. Morys F, Yu E, Shishikura M, Paquola C, Vainik U, Nave G, Koellinger P, Gan-Or Z, Dagher A. PMID: 36596778; PMCID: PMC9810659.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    24. Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects. Nat Commun. 2022 12 05; 13(1):7496. Krohn L, Heilbron K, Blauwendraat C, Reynolds RH, Yu E, Senkevich K, Rudakou U, Estiar MA, Gustavsson EK, Brolin K, Ruskey JA, Freeman K, Asayesh F, Chia R, Arnulf I, Hu MTM, Montplaisir JY, Gagnon JF, Desautels A, Dauvilliers Y, Gigli GL, Valente M, Janes F, Bernardini A, Högl B, Stefani A, Ibrahim A, Šonka K, Kemlink D, Oertel W, Janzen A, Plazzi G, Biscarini F, Antelmi E, Figorilli M, Puligheddu M, Mollenhauer B, Trenkwalder C, Sixel-Döring F, Cochen De Cock V, Monaca CC, Heidbreder A, Ferini-Strambi L, Dijkstra F, Viaene M, Abril B, Boeve BF, 23andMe Research Team, Scholz SW, Ryten M, Bandres-Ciga S, Noyce A, Cannon P, Pihlstrøm L, Nalls MA, Singleton AB, Rouleau GA, Postuma RB, Gan-Or Z. PMID: 36470867; PMCID: PMC9722930.
      View in: PubMed   Mentions: 19     Fields:    
    25. Alzheimer's Disease Polygenic Risk Score Is Not Associated With Cognitive Decline Among Older Adults With Type 2 Diabetes. Front Aging Neurosci. 2022; 14:853695. Manzali SB, Yu E, Ravona-Springer R, Livny A, Golan S, Ouyang Y, Lesman-Segev O, Liu L, Ganmore I, Alkelai A, Gan-Or Z, Lin HM, Heymann A, Schnaider Beeri M, Greenbaum L. PMID: 36110429; PMCID: PMC9468264.
      View in: PubMed   Mentions: 2  
    26. Gene-based burden analysis of damaging private variants in PRKN, PARK7 and PINK1 in Parkinson's disease cohorts of European descent. Neurobiol Aging. 2022 11; 119:136-138. Hu J, Waters CH, Spiegelman D, Fon EA, Yu E, Asayesh F, Krohn L, Saini P, Alcalay RN, Hassin-Baer S, Gan-Or Z, Krainc D, Zhang B, Bustos BI, Lubbe SJ, International Parkinson's Disease Genomics Consortium (IPDGC). PMID: 36305379.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    27. Genetic, structural and clinical analysis of spastic paraplegia 4. Parkinsonism Relat Disord. 2022 05; 98:62-69. Varghaei P, Estiar MA, Ashtiani S, Veyron S, Mufti K, Leveille E, Yu E, Spiegelman D, Rioux MF, Yoon G, Tarnopolsky M, Boycott KM, Dupre N, Suchowersky O, Trempe JF, Rouleau GA, Gan-Or Z. PMID: 35487127.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    28. Axial Impairment Following Deep Brain Stimulation in Parkinson's Disease: A Surgicogenomic Approach. J Parkinsons Dis. 2022; 12(1):117-128. Visanji NP, Ghani M, Yu E, Kakhki EG, Sato C, Moreno D, Naranian T, Poon YY, Abdollahi M, Naghibzadeh M, Rajalingam R, Lozano AM, Kalia SK, Hodaie M, Cohn M, Statucka M, Boutet A, Elias GJB, Germann J, Munhoz R, Lang AE, Gan-Or Z, Rogaeva E, Fasano A. PMID: 34602499; PMCID: PMC8842751.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    29. Rare PSAP Variants and Possible Interaction with GBA in REM Sleep Behavior Disorder. J Parkinsons Dis. 2022; 12(1):333-340. Sosero YL, Yu E, Estiar MA, Krohn L, Mufti K, Rudakou U, Ruskey JA, Asayesh F, Laurent SB, Spiegelman D, Trempe JF, Quinnell TG, Oscroft N, Arnulf I, Montplaisir JY, Gagnon JF, Desautels A, Dauvilliers Y, Gigli GL, Valente M, Janes F, Bernardini A, Sonka K, Kemlink D, Oertel W, Janzen A, Plazzi G, Antelmi E, Biscarini F, Figorilli M, Puligheddu M, Mollenhauer B, Trenkwalder C, Sixel-Döring F, Cochen De Cock V, Monaca CC, Heidbreder A, Ferini-Strambi L, Dijkstra F, Viaene M, Abril B, Boeve BF, Postuma RB, Rouleau GA, Ibrahim A, Stefani A, Högl B, Hu MTM, Gan-Or Z. PMID: 34690151.
      View in: PubMed   Mentions: 3     Fields:    
    30. Fine mapping of the HLA locus in Parkinson's disease in Europeans. NPJ Parkinsons Dis. 2021 Sep 21; 7(1):84. Yu E, Ambati A, Andersen MS, Krohn L, Estiar MA, Saini P, Senkevich K, Sosero YL, Sreelatha AAK, Ruskey JA, Asayesh F, Spiegelman D, Toft M, Viken MK, Sharma M, Blauwendraat C, Pihlstrøm L, Mignot E, Gan-Or Z. PMID: 34548497; PMCID: PMC8455634.
      View in: PubMed   Mentions: 20  
    31. Clinical and Genetic Analysis of Costa Rican Patients With Parkinson's Disease. Front Neurol. 2021; 12:656342. Torrealba-Acosta G, Yu E, Lobo-Prada T, Ruíz-Martínez J, Gorostidi-Pagola A, Gan-Or Z, Carazo-Céspedes K, Trempe JF, Mata IF, Fornaguera-Trías J. PMID: 34421783; PMCID: PMC8371686.
      View in: PubMed   Mentions: 4  
    32. Lack of Causal Effects or Genetic Correlation between Restless Legs Syndrome and Parkinson's Disease. Mov Disord. 2021 08; 36(8):1967-1972. Estiar MA, Senkevich K, Yu E, Varghaei P, Krohn L, Bandres-Ciga S, Noyce AJ, Rouleau GA, Gan-Or Z. PMID: 33974305; PMCID: PMC9017317.
      View in: PubMed   Mentions: 4     Fields:    
    33. Common X-Chromosome Variants Are Associated with Parkinson Disease Risk. Ann Neurol. 2021 07; 90(1):22-34. Le Guen Y, Napolioni V, Belloy ME, Yu E, Krohn L, Ruskey JA, Gan-Or Z, Kennedy G, Eger SJ, Greicius MD. PMID: 33583074; PMCID: PMC8601399.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansCells
    34. Targeted sequencing of Parkinson's disease loci genes highlights SYT11, FGF20 and other associations. Brain. 2021 03 03; 144(2):462-472. Rudakou U, Yu E, Krohn L, Ruskey JA, Asayesh F, Dauvilliers Y, Spiegelman D, Greenbaum L, Fahn S, Waters CH, Dupré N, Rouleau GA, Hassin-Baer S, Fon EA, Alcalay RN, Gan-Or Z. PMID: 33349842; PMCID: PMC7940168.
      View in: PubMed   Mentions: 26     Fields:    Translation:Humans
    35. LRRK2 p.M1646T is associated with glucocerebrosidase activity and with Parkinson's disease. Neurobiol Aging. 2021 07; 103:142.e1-142.e5. Sosero YL, Yu E, Krohn L, Rudakou U, Mufti K, Ruskey JA, Asayesh F, Laurent SB, Spiegelman D, Fahn S, Waters C, Sardi SP, Bandres-Ciga S, Alcalay RN, Gan-Or Z, Senkevich K. PMID: 33781610; PMCID: PMC8178224.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    36. Evidence for Non-Mendelian Inheritance in Spastic Paraplegia 7. Mov Disord. 2021 07; 36(7):1664-1675. Estiar MA, Yu E, Haj Salem I, Ross JP, Mufti K, Akçimen F, Leveille E, Spiegelman D, Ruskey JA, Asayesh F, Dagher A, Yoon G, Tarnopolsky M, Boycott KM, Dupre N, Dion PA, Suchowersky O, Trempe JF, Rouleau GA, Gan-Or Z. PMID: 33598982.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    37. Novel Associations of BST1 and LAMP3 With REM Sleep Behavior Disorder. Neurology. 2021 03 09; 96(10):e1402-e1412. Mufti K, Yu E, Rudakou U, Krohn L, Ruskey JA, Asayesh F, Laurent SB, Spiegelman D, Arnulf I, Hu MTM, Montplaisir JY, Gagnon JF, Desautels A, Dauvilliers Y, Gigli GL, Valente M, Janes F, Bernardini A, Högl B, Stefani A, Holzknecht E, Sonka K, Kemlink D, Oertel W, Janzen A, Plazzi G, Antelmi E, Figorilli M, Puligheddu M, Mollenhauer B, Trenkwalder C, Sixel-Döring F, Cochen De Cock V, Monaca CC, Heidbreder A, Ferini-Strambi L, Dijkstra F, Viaene M, Abril B, Boeve BF, Trempe JF, Rouleau GA, Postuma RB, Gan-Or Z. PMID: 33397775; PMCID: PMC8055320.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    38. No Evidence for a Causal Relationship Between Cancers and Parkinson's Disease. J Parkinsons Dis. 2021; 11(2):801-809. Senkevich K, Bandres-Ciga S, Yu E, Liyanage UE, International Parkinson Disease Genomics Consortium (IPDGC), Noyce AJ, Gan-Or Z. PMID: 33646179; PMCID: PMC9719261.
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    39. Association of the CD2AP locus with cognitive functioning among middle-aged individuals with a family history of Alzheimer's disease. Neurobiol Aging. 2021 05; 101:50-56. Manzali SB, Ravona-Springer R, Alkelai A, Yu E, Gan-Or Z, Ganmore I, Heymann A, Beeri MS, Greenbaum L. PMID: 33578194.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    40. Association study of DNAJC13, UCHL1, HTRA2, GIGYF2, and EIF4G1 with Parkinson's disease. Neurobiol Aging. 2021 04; 100:119.e7-119.e13. Saini P, Rudakou U, Yu E, Ruskey JA, Asayesh F, Laurent SB, Spiegelman D, Fahn S, Waters C, Monchi O, Dauvilliers Y, Dupré N, Greenbaum L, Hassin-Baer S, Espay AJ, Rouleau GA, Alcalay RN, Fon EA, Postuma RB, Gan-Or Z. PMID: 33239198; PMCID: PMC7940813.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    41. Comprehensive Analysis of Familial Parkinsonism Genes in Rapid-Eye-Movement Sleep Behavior Disorder. Mov Disord. 2021 01; 36(1):235-240. Mufti K, Rudakou U, Yu E, Krohn L, Ruskey JA, Asayesh F, Laurent SB, Spiegelman D, Arnulf I, Hu MTM, Montplaisir JY, Gagnon JF, Desautels A, Dauvilliers Y, Gigli GL, Valente M, Janes F, Högl B, Stefani A, Holzknecht E, Šonka K, Kemlink D, Oertel W, Janzen A, Plazzi G, Antelmi E, Figorilli M, Puligheddu M, Mollenhauer B, Trenkwalder C, Sixel-Döring F, Cochen De Cock V, Monaca CC, Heidbreder A, Ferini-Strambi L, Dijkstra F, Viaene M, Abril B, Boeve BF, Postuma RB, Rouleau GA, Gan-Or Z. PMID: 33001463.
      View in: PubMed   Mentions: 8     Fields:    
    42. Analysis of Heterozygous PRKN Variants and Copy-Number Variations in Parkinson's Disease. Mov Disord. 2021 01; 36(1):178-187. Yu E, Rudakou U, Krohn L, Mufti K, Ruskey JA, Asayesh F, Estiar MA, Spiegelman D, Surface M, Fahn S, Waters CH, Greenbaum L, Espay AJ, Dauvilliers Y, Dupré N, Rouleau GA, Hassin-Baer S, Fon EA, Alcalay RN, Gan-Or Z. PMID: 32970363.
      View in: PubMed   Mentions: 21     Fields:    Translation:Humans
    43. Variants in the Niemann-Pick type C gene NPC1 are not associated with Parkinson's disease. Neurobiol Aging. 2020 09; 93:143.e1-143.e4. Ouled Amar Bencheikh B, Senkevich K, Rudakou U, Yu E, Mufti K, Ruskey JA, Asayesh F, Laurent SB, Spiegelman D, Fahn S, Waters C, Monchi O, Dauvilliers Y, Espay AJ, Dupré N, Greenbaum L, Hassin-Baer S, Rouleau GA, Alcalay RN, Fon EA, Gan-Or Z. PMID: 32371106; PMCID: PMC7302975.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansCells
    44. Contrast echocardiography: putting things into perspective - a Canadian Cardiovascular Society/Canadian Society of Echocardiography joint commentary. Can J Cardiol. 2008 Nov; 24(11):835-7. Amyot R, Yu E, Honos G, Choy J, Schnell G, Leong-Poi H. PMID: 18987756; PMCID: PMC2644535.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
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