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- [21] Putative second hit rare genetic variants in families with seemingly GBA-associated Parkinson's diseaseNPJ GENOMIC MEDICINE, 2021, 6 (01)Aslam, Muhammad论文数: 0 引用数: 0 h-index: 0机构: Johannes Gutenberg Univ Mainz, Inst Pathophysiol, Univ Med Ctr, Mainz, Germany Johannes Gutenberg Univ Mainz, Inst Pathophysiol, Univ Med Ctr, Mainz, GermanyKandasamy, Nirosiya论文数: 0 引用数: 0 h-index: 0机构: Johannes Gutenberg Univ Mainz, Inst Pathophysiol, Univ Med Ctr, Mainz, Germany Johannes Gutenberg Univ Mainz, Inst Pathophysiol, Univ Med Ctr, Mainz, GermanyUllah, Anwar论文数: 0 引用数: 0 h-index: 0机构: Johannes Gutenberg Univ Mainz, Inst Pathophysiol, Univ Med Ctr, Mainz, Germany Inst Biomed & Genet Engn IBGE, Islamabad, Pakistan Quaid I Azam Univ, Dept Biochem, Islamabad, Pakistan Johannes Gutenberg Univ Mainz, Inst Pathophysiol, Univ Med Ctr, Mainz, GermanyParamasivam, Nagarajan论文数: 0 引用数: 0 h-index: 0机构: German Canc Res Ctr, Heidelberg Ctr Personalized Oncol DKFZ HIPO, Heidelberg, Germany Johannes Gutenberg Univ Mainz, Inst Pathophysiol, Univ Med Ctr, Mainz, GermanyOzturk, Mehmet Ali论文数: 0 引用数: 0 h-index: 0机构: Heidelberg Inst Theoret Studies HITS, Mol & Cellular Modeling Grp, Heidelberg, Germany Univ Freiburg, Signalling Res Ctr BIOSS, D-79104 Freiburg, Germany Univ Freiburg, Signalling Res Ctr CIBSS, D-79104 Freiburg, Germany Johannes Gutenberg Univ Mainz, Inst Pathophysiol, Univ Med Ctr, Mainz, GermanyNaureen, Saima论文数: 0 引用数: 0 h-index: 0机构: Johannes Gutenberg Univ Mainz, Inst Pathophysiol, Univ Med Ctr, Mainz, Germany PMAS Arid Agr Univ, Dept Zool, Rawalpindi, Pakistan Johannes Gutenberg Univ Mainz, Inst Pathophysiol, Univ Med Ctr, Mainz, GermanyArshad, Abida论文数: 0 引用数: 0 h-index: 0机构: PMAS Arid Agr Univ, Dept Zool, Rawalpindi, Pakistan Johannes Gutenberg Univ Mainz, Inst Pathophysiol, Univ Med Ctr, Mainz, GermanyBadshah, Mazhar论文数: 0 引用数: 0 h-index: 0机构: Shaheed Zulfigar Ali Bhutto Med Univ, Dept Neurol, Islamabad, Pakistan Johannes Gutenberg Univ Mainz, Inst Pathophysiol, Univ Med Ctr, Mainz, GermanyKhan, Kafaitullah论文数: 0 引用数: 0 h-index: 0机构: Univ Balochistan, Dept Microbiol, Quetta, Pakistan Johannes Gutenberg Univ Mainz, Inst Pathophysiol, Univ Med Ctr, Mainz, GermanyWajid, Muhammad论文数: 0 引用数: 0 h-index: 0机构: Univ Okara, Dept Biol Sci, Okara, Pakistan Johannes Gutenberg Univ Mainz, Inst Pathophysiol, Univ Med Ctr, Mainz, GermanyAbbasi, Rashda论文数: 0 引用数: 0 h-index: 0机构: Inst Biomed & Genet Engn IBGE, Islamabad, Pakistan Johannes Gutenberg Univ Mainz, Inst Pathophysiol, Univ Med Ctr, Mainz, Germany论文数: 引用数: h-index:机构:Eils, Roland论文数: 0 引用数: 0 h-index: 0机构: Berlin Inst Hlth, Ctr Digital Hlth, Berlin, Germany Charite Univ Med Berlin, Berlin, Germany Heidelberg Univ, Med Fac, Hlth Data Sci Unit, Bioquant, Heidelberg, Germany Johannes Gutenberg Univ Mainz, Inst Pathophysiol, Univ Med Ctr, Mainz, GermanySchlesner, Matthias论文数: 0 引用数: 0 h-index: 0机构: German Canc Res Ctr, Bioinformat & Omics Data Analyt, Heidelberg, Germany Johannes Gutenberg Univ Mainz, Inst Pathophysiol, Univ Med Ctr, Mainz, GermanyWade, Rebecca C.论文数: 0 引用数: 0 h-index: 0机构: Heidelberg Inst Theoret Studies HITS, Mol & Cellular Modeling Grp, Heidelberg, Germany Univ Heidelberg ZMBH, DKFZ ZMBH Alliance, Ctr Mol Biol, Heidelberg, Germany Interdisciplinary Ctr Sci Comp IWR, Heidelberg, Germany Johannes Gutenberg Univ Mainz, Inst Pathophysiol, Univ Med Ctr, Mainz, GermanyAhmad, Nafees论文数: 0 引用数: 0 h-index: 0机构: Inst Biomed & Genet Engn IBGE, Islamabad, Pakistan Johannes Gutenberg Univ Mainz, Inst Pathophysiol, Univ Med Ctr, Mainz, Germanyvon Engelhardt, Jakob论文数: 0 引用数: 0 h-index: 0机构: Johannes Gutenberg Univ Mainz, Inst Pathophysiol, Univ Med Ctr, Mainz, Germany Johannes Gutenberg Univ Mainz, Inst Pathophysiol, Univ Med Ctr, Mainz, Germany
- [22] Genome-wide contribution of common short-tandem repeats to Parkinson's disease genetic riskBRAIN, 2023, 146 (01) : 65 - 74Bustos, Bernabe, I论文数: 0 引用数: 0 h-index: 0机构: Northwestern Univ, Ken & Ruth Davee Dept Neurol, Feinberg Sch Med, 320 East Super Ave,Morton 7-605, Chicago, IL 60611 USA Northwestern Univ, Simpson Querrey Ctr Neurogenet, Feinberg Sch Med, Chicago, IL 60611 USA Northwestern Univ, Ken & Ruth Davee Dept Neurol, Feinberg Sch Med, 320 East Super Ave,Morton 7-605, Chicago, IL 60611 USABillingsley, Kimberley论文数: 0 引用数: 0 h-index: 0机构: NIA, Mol Genet Sect, Lab Neurogenet, NIH, Bethesda, MD 20892 USA Northwestern Univ, Ken & Ruth Davee Dept Neurol, Feinberg Sch Med, 320 East Super Ave,Morton 7-605, Chicago, IL 60611 USABlauwendraat, Cornelis论文数: 0 引用数: 0 h-index: 0机构: NIA, Mol Genet Sect, Lab Neurogenet, NIH, Bethesda, MD 20892 USA Northwestern Univ, Ken & Ruth Davee Dept Neurol, Feinberg Sch Med, 320 East Super Ave,Morton 7-605, Chicago, IL 60611 USAGibbs, J. Raphael论文数: 0 引用数: 0 h-index: 0机构: NIA, Computat Biol Grp, Lab Neurogenet, NIH, Bethesda, MD 20892 USA Northwestern Univ, Ken & Ruth Davee Dept Neurol, Feinberg Sch Med, 320 East Super Ave,Morton 7-605, Chicago, IL 60611 USAGan-Or, Ziv论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Neuro Montreal Neurol Inst Hosp, Montreal, PQ, Canada McGill Univ, Dept Human Genet, Montreal, PQ, Canada McGill Univ, Dept Neurol & Neurosurg, Montreal, PQ, Canada Northwestern Univ, Ken & Ruth Davee Dept Neurol, Feinberg Sch Med, 320 East Super Ave,Morton 7-605, Chicago, IL 60611 USAKrainc, Dimitri论文数: 0 引用数: 0 h-index: 0机构: Northwestern Univ, Ken & Ruth Davee Dept Neurol, Feinberg Sch Med, 320 East Super Ave,Morton 7-605, Chicago, IL 60611 USA Northwestern Univ, Simpson Querrey Ctr Neurogenet, Feinberg Sch Med, Chicago, IL 60611 USA Northwestern Univ, Ken & Ruth Davee Dept Neurol, Feinberg Sch Med, 320 East Super Ave,Morton 7-605, Chicago, IL 60611 USASingleton, Andrew B.论文数: 0 引用数: 0 h-index: 0机构: NIA, Mol Genet Sect, Lab Neurogenet, NIH, Bethesda, MD 20892 USA Northwestern Univ, Ken & Ruth Davee Dept Neurol, Feinberg Sch Med, 320 East Super Ave,Morton 7-605, Chicago, IL 60611 USALubbe, Steven J.论文数: 0 引用数: 0 h-index: 0机构: Northwestern Univ, Ken & Ruth Davee Dept Neurol, Feinberg Sch Med, 320 East Super Ave,Morton 7-605, Chicago, IL 60611 USA Northwestern Univ, Simpson Querrey Ctr Neurogenet, Feinberg Sch Med, Chicago, IL 60611 USA Northwestern Univ, Ken & Ruth Davee Dept Neurol, Feinberg Sch Med, 320 East Super Ave,Morton 7-605, Chicago, IL 60611 USA
- [23] A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease riskHUMAN MOLECULAR GENETICS, 2013, 22 (04) : 816 - 824Chapman, Jade论文数: 0 引用数: 0 h-index: 0机构: Cardiff Univ, Sch Med, Med Res Council Ctr Neuropsychiat Genet & Genom, Inst Psychol Med & Clin Neurosci, Cardiff CF14 4XN, S Glam, Wales Cardiff Univ, Sch Med, Med Res Council Ctr Neuropsychiat Genet & Genom, Inst Psychol Med & Clin Neurosci, Cardiff CF14 4XN, S Glam, WalesRees, Elliott论文数: 0 引用数: 0 h-index: 0机构: Cardiff Univ, Sch Med, Med Res Council Ctr Neuropsychiat Genet & Genom, Inst Psychol Med & Clin Neurosci, Cardiff CF14 4XN, S Glam, Wales Cardiff Univ, Sch Med, Med Res Council Ctr Neuropsychiat Genet & Genom, Inst Psychol Med & Clin Neurosci, Cardiff CF14 4XN, S Glam, Wales论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Gerrish, Amy论文数: 0 引用数: 0 h-index: 0机构: Cardiff Univ, Sch Med, Med Res Council Ctr Neuropsychiat Genet & Genom, Inst Psychol Med & Clin Neurosci, Cardiff CF14 4XN, S Glam, Wales Cardiff Univ, Sch Med, Med Res Council Ctr Neuropsychiat Genet & Genom, Inst Psychol Med & Clin Neurosci, Cardiff CF14 4XN, S Glam, WalesSims, Rebecca论文数: 0 引用数: 0 h-index: 0机构: Cardiff Univ, Sch Med, Med Res Council Ctr Neuropsychiat Genet & Genom, Inst Psychol Med & Clin Neurosci, Cardiff CF14 4XN, S Glam, Wales Cardiff Univ, Sch Med, Med Res Council Ctr Neuropsychiat Genet & Genom, Inst Psychol Med & Clin Neurosci, Cardiff CF14 4XN, S Glam, WalesHollingworth, Paul论文数: 0 引用数: 0 h-index: 0机构: Cardiff Univ, Sch Med, Med Res Council Ctr Neuropsychiat Genet & Genom, Inst Psychol Med & Clin Neurosci, Cardiff CF14 4XN, S Glam, Wales Cardiff Univ, Sch Med, Med Res Council Ctr Neuropsychiat Genet & Genom, Inst Psychol Med & Clin Neurosci, Cardiff CF14 4XN, S Glam, WalesStretton, Alexandra论文数: 0 引用数: 0 h-index: 0机构: Cardiff Univ, Sch Med, Med Res Council Ctr Neuropsychiat Genet & Genom, Inst Psychol Med & Clin Neurosci, Cardiff CF14 4XN, S Glam, Wales Cardiff Univ, Sch Med, Med Res Council Ctr Neuropsychiat Genet & Genom, Inst Psychol Med & Clin Neurosci, Cardiff CF14 4XN, S Glam, WalesHolmans, Peter论文数: 0 引用数: 0 h-index: 0机构: Cardiff Univ, Sch Med, Med Res Council Ctr Neuropsychiat Genet & Genom, Inst Psychol Med & Clin Neurosci, Cardiff CF14 4XN, S Glam, Wales Cardiff Univ, Sch Med, Med Res Council Ctr Neuropsychiat Genet & Genom, Inst Psychol Med & Clin Neurosci, Cardiff CF14 4XN, S Glam, WalesOwen, Michael J.论文数: 0 引用数: 0 h-index: 0机构: Cardiff Univ, Sch Med, Med Res Council Ctr Neuropsychiat Genet & Genom, Inst Psychol Med & Clin Neurosci, Cardiff CF14 4XN, S Glam, Wales Cardiff Univ, Sch Med, Med Res Council Ctr Neuropsychiat Genet & Genom, Inst Psychol Med & Clin Neurosci, Cardiff CF14 4XN, S Glam, WalesODonovan, Michael C.论文数: 0 引用数: 0 h-index: 0机构: Cardiff Univ, Sch Med, Med Res Council Ctr Neuropsychiat Genet & Genom, Inst Psychol Med & Clin Neurosci, Cardiff CF14 4XN, S Glam, Wales Cardiff Univ, Sch Med, Med Res Council Ctr Neuropsychiat Genet & Genom, Inst Psychol Med & Clin Neurosci, Cardiff CF14 4XN, S Glam, Wales论文数: 引用数: h-index:机构:Kirov, George论文数: 0 引用数: 0 h-index: 0机构: Cardiff Univ, Sch Med, Med Res Council Ctr Neuropsychiat Genet & Genom, Inst Psychol Med & Clin Neurosci, Cardiff CF14 4XN, S Glam, Wales Cardiff Univ, Sch Med, Med Res Council Ctr Neuropsychiat Genet & Genom, Inst Psychol Med & Clin Neurosci, Cardiff CF14 4XN, S Glam, Wales
- [24] A genome wide pleiotropic approach to identify the genetic architecture of multiple system atrophy and its interaction with Parkinson's diseaseMOVEMENT DISORDERS, 2019, 34 : S312 - S314Sreelatha, A. AshokKumar论文数: 0 引用数: 0 h-index: 0Shadrin, A.论文数: 0 引用数: 0 h-index: 0Blauwendraat, C.论文数: 0 引用数: 0 h-index: 0Frei, O.论文数: 0 引用数: 0 h-index: 0Gasser, T.论文数: 0 引用数: 0 h-index: 0Wenning, G.论文数: 0 引用数: 0 h-index: 0Singleton, A.论文数: 0 引用数: 0 h-index: 0Houlden, H.论文数: 0 引用数: 0 h-index: 0Scholz, S.论文数: 0 引用数: 0 h-index: 0Andreassen, O.论文数: 0 引用数: 0 h-index: 0Sharma, M.论文数: 0 引用数: 0 h-index: 0
- [25] Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's diseaseNEUROSCIENCE RESEARCH, 2010, 68 : E71 - E71Satake, Wataru论文数: 0 引用数: 0 h-index: 0机构: Kobe Univ, Grad Sch Med, Div Neurol Mol Brain Sci, Kobe, Hyogo 657, Japan Osaka Univ, Grad Sch Med, Dept Neurol, Suita, Osaka, Japan Kobe Univ, Grad Sch Med, Div Neurol Mol Brain Sci, Kobe, Hyogo 657, JapanMizuta, Ikuko论文数: 0 引用数: 0 h-index: 0机构: Kobe Univ, Grad Sch Med, Div Neurol Mol Brain Sci, Kobe, Hyogo 657, Japan Kobe Univ, Grad Sch Med, Div Neurol Mol Brain Sci, Kobe, Hyogo 657, JapanKubo, Michiaki论文数: 0 引用数: 0 h-index: 0机构: RIKEN, Ctr Genom Med, Yokohama, Kanagawa, Japan Kobe Univ, Grad Sch Med, Div Neurol Mol Brain Sci, Kobe, Hyogo 657, JapanKawaguchi, Takahisa论文数: 0 引用数: 0 h-index: 0机构: RIKEN, Ctr Genom Med, Yokohama, Kanagawa, Japan Kobe Univ, Grad Sch Med, Div Neurol Mol Brain Sci, Kobe, Hyogo 657, JapanTsunoda, Tatsuhiko论文数: 0 引用数: 0 h-index: 0机构: RIKEN, Ctr Genom Med, Yokohama, Kanagawa, Japan Kobe Univ, Grad Sch Med, Div Neurol Mol Brain Sci, Kobe, Hyogo 657, JapanYoshikawa, Takeo论文数: 0 引用数: 0 h-index: 0机构: RIKEN, Brain Sci Inst, Saitama, Japan Kobe Univ, Grad Sch Med, Div Neurol Mol Brain Sci, Kobe, Hyogo 657, JapanSakoda, Saburo论文数: 0 引用数: 0 h-index: 0机构: Osaka Univ, Grad Sch Med, Dept Neurol, Suita, Osaka, Japan Kobe Univ, Grad Sch Med, Div Neurol Mol Brain Sci, Kobe, Hyogo 657, JapanYamamoto, Mitsutoshi论文数: 0 引用数: 0 h-index: 0机构: Kagawa Prefectural Cent Hosp, Dept Neurol, Takamatsu, Kagawa, Japan Kobe Univ, Grad Sch Med, Div Neurol Mol Brain Sci, Kobe, Hyogo 657, JapanHattori, Nobutaka论文数: 0 引用数: 0 h-index: 0机构: Juntendo Univ, Sch Med, Dept Neurol, Tokyo 113, Japan Kobe Univ, Grad Sch Med, Div Neurol Mol Brain Sci, Kobe, Hyogo 657, JapanMurata, Miho论文数: 0 引用数: 0 h-index: 0机构: Natl Ctr Hosp Neurol & Psychiat, Dept Neurol, Kodaira, Tokyo, Japan Kobe Univ, Grad Sch Med, Div Neurol Mol Brain Sci, Kobe, Hyogo 657, JapanNakamura, Yusuke论文数: 0 引用数: 0 h-index: 0机构: RIKEN, Ctr Genom Med, Yokohama, Kanagawa, Japan Univ Tokyo, Inst Med Sci, Ctr Human Genome, Tokyo, Japan Kobe Univ, Grad Sch Med, Div Neurol Mol Brain Sci, Kobe, Hyogo 657, JapanToda, Tatsushi论文数: 0 引用数: 0 h-index: 0机构: Kobe Univ, Grad Sch Med, Div Neurol Mol Brain Sci, Kobe, Hyogo 657, Japan Kobe Univ, Grad Sch Med, Div Neurol Mol Brain Sci, Kobe, Hyogo 657, Japan
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