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- [1] Rare variants in dementia genes and Parkinson's diseaseEUROPEAN JOURNAL OF HUMAN GENETICS, 2016, 24 (12) : 1661 - 1662Iqbal, ZafarPihlstrom, LasseRengmark, AinaHenriksen, Sandra PilarLinder, JanForsgren, LarsToft, Mathias
- [2] Rare variants in Alzheimer's disease and frontotemporal dementia genes in Parkinson's diseaseMOVEMENT DISORDERS, 2013, 28 : S403 - S403Schulte, E. C.Fukumori, A.Mollenhauer, B.Hor, H.Perneczky, R.Kurz, A.Huell, M.Arzberger, T.Lichtner, P.Eckstein, G.Zimprich, A.Haubenberger, D.Pirker, W.Bruecke, T.Bereznai, B.Molnar, M. J.Lorenzo-Betancor, O.Pastor, P.Peters, A.Gieger, C.Estivill, X.Kretzschmar, H. A.Meitinger, T.Trenkwalder, C.Haass, C.Winkelmann, J.
- [3] Rare Variants in Specific Lysosomal Genes Are Associated With Parkinson's DiseaseMOVEMENT DISORDERS, 2020, 35 (07) : 1245 - 1248Hopfner, FranziskaMueller, Stefanie H.Szymczak, SilkeJunge, OlafTittmann, LukasMay, SandraLohmann, KatjaGrallert, HaraldLieb, WolfgangStrauch, KonstantinMueller-Nurasyid, MartinaBerger, KlausSchormair, BarbaraWinkelmann, JulianeMollenhauer, BritTrenkwalder, ClaudiaMaetzler, WalterBerg, DanielaKasten, MeikeKlein, ChristineHoeglinger, Guenter U.Gasser, ThomasDeuschl, GuentherFranke, AndreKrawczak, MichaelDempfle, AstridKuhlenbaeumer, Gregor
- [4] Pleiotropic Effects of Variants in Dementia Genes in Parkinson DiseaseFRONTIERS IN NEUROSCIENCE, 2018, 12Ibanez, LauraDube, UmberDavis, Albert A.Fernandez, Maria V.Budde, JohnCooper, BreannaDiez-Fairen, MonicaOrtega-Cubero, SaraPastor, PauPerlmutter, Joel S.Cruchaga, CarlosBenitez, Bruno A.
- [5] Rare variants analysis of cutaneous malignant melanoma genes in Parkinson's diseaseNEUROBIOLOGY OF AGING, 2016, 48 : 222.e1 - 222.e7Lubbe, S. J.Escott-Price, V.Brice, A.Gasser, T.Pittman, A. M.Bras, J.Hardy, J.Heutink, P.Wood, N. M.Singleton, A. B.Grosset, D. G.Carroll, C. B.Law, M. H.Demenais, F.Iles, M. M.Bishop, D. T.Newton-Bishop, J.Williams, N. M.Morris, H. R.
- [6] Evaluation of common and rare variants of Alzheimer's disease-causal genes in Parkinson's diseasePARKINSONISM & RELATED DISORDERS, 2022, 97 : 8 - 14Zeng, QianPan, HongxuZhao, YuwenWang, YigeXu, QianTan, JieqiongYan, XinxiangLi, JinchenTang, BeishaGuo, Jifeng
- [7] Enriched burden of rare coding variants in hereditary parkinsonism genes in Parkinson's diseaseMOVEMENT DISORDERS, 2020, 35 : S203 - S203Kim, Y.Lee, J.Kim, N.Hong, S.Cho, Y.Yoon, J.
- [8] Association of Rare Variants in ARSA with Parkinson's DiseaseMOVEMENT DISORDERS, 2023, 38 (10) : 1806 - 1812Senkevich, KonstantinBeletskaia, MariiaDworkind, AlizaYu, EricAhmad, JamilRuskey, Jennifer A.Asayesh, FarnazSpiegelman, DanFahn, StanleyWaters, CherylMonchi, OuryDauvilliers, YvesDupre, NicolasGreenbaum, LiorHassin-Baer, SharonNagornov, IlyaTyurin, AlexandrMiliukhina, IrinaTimofeeva, AllaEmelyanov, AntonTrempe, Jean-FrancoisZakharova, EkaterinaAlcalay, Roy N.Pchelina, SofyaGan-Or, Ziv
- [9] Dementia with Lewy Bodies: A Role for Dementia and Parkinson's Disease Genes?MOVEMENT DISORDERS, 2010, 25 : S614 - S614Meeus, B.Verstraeten, A.Nuytemans, K.Crosiers, D.Engelborghs, S.Van den Broeck, M.Brys, J.Mattheijssens, M.Peeters, K.Corsmit, E.Elinck, E.Pickut, B.Cras, P.Vandenberghe, R.De Deyn, P. P.Van Broeckhoven, C.Theuns, J.
- [10] Enrichment of rare variants of BIN1 but not APOE genes in Chinese patients with Parkinson's diseaseJOURNAL OF INTERNAL MEDICINE, 2022, 291 (05) : 698 - 701Li, Chun YuOu, Ru WeiChen, Yong PingGu, Xiao JingWei, Qian QianHou, Yan BingCao, BeiZhang, Ling YuLin, Jun YuLiu, Kun ChengSong, WeiZhao, BiWu, YingShang, Hui Fang