학술논문


EBSCO Discovery Service
발행년
-
(예 : 2010-2015)
전자자료 공정이용 안내

우리 대학 도서관에서 구독·제공하는 모든 전자자료(데이터베이스, 전자저널, 전자책 등)는 국내외 저작권법과 출판사와의 라이선스 계약에 따라 엄격하게 보호를 받고 있습니다.
전자자료의 비정상적 이용은 출판사로부터의 경고, 서비스 차단, 손해배상 청구 등 학교 전체에 심각한 불이익을 초래할 수 있으므로, 아래의 공정이용 지침을 반드시 준수해 주시기 바랍니다.

공정이용 지침
  • 전자자료는 개인의 학습·교육·연구 목적의 비영리적 사용에 한하여 이용할 수 있습니다.
  • 합리적인 수준의 다운로드 및 출력만 허용됩니다. (일반적으로 동일 PC에서 동일 출판사의 논문을 1일 30건 이하 다운로드할 것을 권장하며, 출판사별 기준에 따라 다를 수 있습니다.)
  • 출판사에서 제공한 논문의 URL을 수업 관련 웹사이트에 게재할 수 있으나, 출판사 원문 파일 자체를 복제·배포해서는 안 됩니다.
  • 본인의 ID/PW를 타인에게 제공하지 말고, 도용되지 않도록 철저히 관리해 주시기 바랍니다.
불공정 이용 사례
  • 전자적·기계적 수단(다운로딩 프로그램, 웹 크롤러, 로봇, 매크로, RPA 등)을 이용한 대량 다운로드
  • 동일 컴퓨터 또는 동일 IP에서 단시간 내 다수의 원문을 집중적으로 다운로드하거나, 전권(whole issue) 다운로드
  • 저장·출력한 자료를 타인에게 배포하거나 개인 블로그·웹하드 등에 업로드
  • 상업적·영리적 목적으로 자료를 전송·복제·활용
  • ID/PW를 타인에게 양도하거나 타인 계정을 도용하여 이용
  • EndNote, Mendeley 등 서지관리 프로그램의 Find Full Text 기능을 이용한 대량 다운로드
  • 출판사 콘텐츠를 생성형 AI 시스템에서 활용하는 행위(업로드, 개발, 학습, 프로그래밍, 개선 또는 강화 등)
위반 시 제재
  • 출판사에 의한 해당 IP 또는 기관 전체 접속 차단
  • 출판사 배상 요구 시 위반자 개인이 배상 책임 부담
'학술논문' 에서 검색결과 57건 | 목록 1~20
Editorial & Opinion
Patel B; John van Geest Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.; Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.; Camacho M; John van Geest Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.; Evans JR; Nottingham University Hospital NHS Trust, Nottingham, UK.; Breen DP; Anne Rowling Regenerative Neurology Clinic, Institute for Neuroscience and Cardiovascular Research, University of Edinburgh, Edinburgh, UK.; Usher Institute of Population Health Sciences and Informatics, University of Edinburgh, Edinburgh, UK.; Foltynie T; Department of Movement and Clinical Neurosciences, UCL Institute of Neurology, Queen Square, London, UK.; Mason SL; John van Geest Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.; Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.; Cambridge and Peterborough NHS Foundation Trust, Cambridge, UK.; Cummins G; John van Geest Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.; Wijeyekoon R; John van Geest Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.; Barker RA; John van Geest Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.; Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.; Williams-Gray CH; John van Geest Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.; Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Publisher: Wiley-Liss Country of Publication: United States NLM ID: 8610688 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1531-8257 (Electronic) Linking ISSN: 08853185 NLM ISO Abbreviation: Mov Disord Subsets: MEDLINE
Academic Journal
Wijeyekoon, R S, Kronenberg-Versteeg, D, Scott, K M, Hayat, S, Kuan, W-L, Evans, J R, Breen, D P, Cummins, G, Jones, J L, Clatworthy, M R, Andres Floto, R, Barker, R A & Williams-Gray, C H 2020, ' Peripheral innate immune and bacterial signals relate to clinical heterogeneity in Parkinson's disease ', Brain, Behavior, and Immunity, vol. 87 . https://doi.org/10.1016/j.bbi.2020.01.018
Academic Journal
Robak, Laurie AJansen, Iris Evan Rooij, JeroenUitterlinden, André GKraaij, RobertJankovic, JosephHeutink, PeterShulman, Joshua MNalls, Mike APlagnol, VincentHernandez, Dena GSharma, ManuSheerin, Una-MarieSaad, MohamadSimón-Sánchez, JavierSchulte, ClaudiaLesage, SuzanneSveinbjörnsdóttir, SigurlaugArepalli, SampathBarker, RogerBen-, YoavBerendse, Henk WBerg, DanielaBhatia, Kailashde Bie, Rob M ABiffi, AlessandroBloem, BasBochdanovits, ZoltanBonin, MichaelBras, Jose MBrockmann, KathrinBrooks, JanetBurn, David JMajounie, ElisaCharlesworth, GavinLungu, CodrinChen, HongleiChinnery, Patrick FChong, SeanClarke, Carl ECookson, Mark RMark Cooper, JCorvol, Jean ChristopheCounsell, CarlDamier, PhilippeDartigues, Jean-FrançoisDeloukas, PanosDeuschl, GüntherDexter, David Tvan Dijk, Karin DDillman, AllissaDurif, FrankDürr, AlexandraEdkins, SarahEvans, Jonathan RFoltynie, ThomasDong, JingGardner, MichelleRaphael Gibbs, JGoate, AlisonGray, EmmaGuerreiro, RitaHarris, Clarevan Hilten, Jacobus JHofman, AlbertHollenbeck, AlbertHolton, JaniceHu, MicheleHuang, XuemeiWurster, IsabelMätzler, WalterHudson, GavinHunt, Sarah EHuttenlocher, JohannaIllig, ThomasJónsson, Pálmi VLambert, Jean-CharlesLangford, CordeliaLees, AndrewLichtner, PeterLimousin, PatriciaLopez, GriselLorenz, DeliaLungu, CodrinMcNeill, AlisdairMoorby, CatrionaMoore, MatthewMorris, Huw RMorrison, Karen EEscott-Price, ValentinaMudanohwo, EseO’Sullivan, Sean SPearson, JustinPerlmutter, Joel SPétursson, HjörvarPollak, PierrePost, BartPotter, SimonRavina, BernardRevesz, TamasRiess, OlafRivadeneira, FernandoRizzu, PatriziaRyten, MinaSawcer, StephenSchapira, AnthonyScheffer, HansShaw, KarenShoulson, IraShulman, JoshuaSidransky, EllenSmith, ColinSpencer, Chris C AStefánsson, HreinnBettella, FrancescoStockton, Joanna DStrange, AmyTalbot, KevinTanner, Carlie MTashakkori-Ghanbaria, AvazehTison, FrançoisTrabzuni, DaniahTraynor, Bryan JUitterlinden, André GVelseboer, DaanVidailhet, MarieWalker, Robertvan de Warrenburg, BartWickremaratchi, MirdhuWilliams, NigelWilliams-Gray, Caroline HWinder-Rhodes, SophieStefánsson, KáriMartinez, MariaWood, Nicholas WHardy, JohnHeutink, PeterBrice, AlexisGasser, ThomasSingleton, Andrew B
Brain. Dec 01, 2017 140(12):3191-3203
Academic Journal
Geissler, Julia MRomanos, MarcelSheerin, Una-MarieScheffer, HansShaw, KarenShoulson, IraSidransky, EllenSmith, ColinSpencer, Chris C AStefánsson, HreinnSteinberg, StacyStockton, Joanna DStrange, AmySaad, MohamadTalbot, KevinTanner, Carlie MTashakkori-Ghanbaria, AvazehTison, FrançoisTrabzuni, DaniahTraynor, Bryan JUitterlinden, André GVelseboer, DaanVidailhet, MarieWalker, RobertSimón-Sánchez, Javiervan de Warrenburg, BartWickremaratchi, MirdhuWilliams, NigelWilliams-Gray, Caroline HWinder-Rhodes, SophieStefánsson, KáriMartinez, MariaHardy, JohnHeutink, PeterBrice, AlexisSchulte, ClaudiaGasser, ThomasSingleton, Andrew BWood, Nicholas WLesage, SuzanneSveinbjörnsdóttir, SigurlaugArepalli, SampathBarker, RogerBen-Shlomo, YoavBerendse, Henk WGerlach, ManfredBerg, DanielaBhatia, Kailashde Bie, Rob M ABiffi, AlessandroBloem, BasBochdanovits, ZoltanBonin, MichaelBras, Jose MBrockmann, KathrinBrooks, JanetBurn, David JCharlesworth, GavinChen, HongleiChinnery, Patrick FChong, SeanClarke, Carl ECookson, Mark RCooper, J MarkCorvol, Jean ChristopheCounsell, CarlDamier, PhilippeDartigues, Jean-FrançoisDeloukas, PanosDeuschl, GüntherDexter, David Tvan Dijk, Karin DDillman, AllissaDurif, FrankDürr, AlexandraEdkins, Sarahmembers, International Parkinson Disease Genomics ConsortiumEvans, Jonathan RFoltynie, ThomasGao, JianjunGardner, MichelleGibbs, J RaphaelGoate, AlisonGray, EmmaGuerreiro, RitaGústafsson, ÓmarHarris, ClareNalls, Mikevan Hilten, Jacobus JHofman, AlbertHollenbeck, AlbertHolton, JaniceHu, MicheleHuang, XuemeiHuber, HeikoHudson, GavinHunt, Sarah EHuttenlocher, JohannaPlagnol, VincentIllig, ThomasJónsson, Pálmi VLambert, Jean-CharlesLangford, CordeliaLees, AndrewLichtner, PeterLimousin, PatriciaLopez, GriselLorenz, DeliaMcNeill, AlisdairHernandez, Dena GMoorby, CatrionaMoore, MatthewMorris, Huw RMorrison, Karen EMudanohwo, EseO'Sullivan, Sean SPearson, JustinPerlmutter, Joel SPétursson, HjörvarPollak, PierreSharma, ManuPost, BartPotter, SimonRavina, BernardRevesz, TamasRiess, OlafRivadeneira, FernandoRizzu, PatriziaRyten, MinaSawcer, StephenSchapira, Anthony
Geissler, J M, Schulte, C, Berg, D & International Parkinson Disease Genomics Consortium members 2017, 'No genetic association between attention-deficit/hyperactivity disorder (ADHD) and Parkinson’s disease in nine ADHD candidate SNPs', ADHD Attention Deficit and Hyperactivity Disorders, vol. 9, no. 2, pp. 121-127. https://doi.org/10.1007/s12402-017-0219-8
ADHD Attention Deficit and Hyperactivity Disorders 9(2), 121-127 (2017). doi:10.1007/s12402-017-0219-8
Attention Deficit and Hyperactivity Disorders, 9, 2, pp. 121-127
Academic Journal
Iwaki H; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.; Data Tecnica International, Glen Echo, Maryland, USA.; Blauwendraat C; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.; Leonard HL; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.; Data Tecnica International, Glen Echo, Maryland, USA.; Makarious MB; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.; Kim JJ; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.; Liu G; School of Medicine, Sun Yat-sen University, Guangzhou, China.; Advanced Center for Parkinson's Disease Research, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, USA.; Precision Neurology Program, Harvard Medical School, Brigham and Women's Hospital, Boston, Massachusetts, USA.; Maple-Grødem J; The Norwegian Centre for Movement Disorders, Stavanger University Hospital, Stavanger, Norway.; Department of Chemistry, Bioscience and Environmental Engineering, University in Stavanger, Stavanger, Norway.; Corvol JC; Assistance-Publique Hôpitaux de Paris, ICM, INSERM UMRS 1127, CNRS 7225, ICM, Department of Neurology and CIC Neurosciences, Pitié-Salpêtrière Hospital, Paris, France.; Pihlstrøm L; Department of Neurology, Oslo University Hospital, Oslo, Norway.; van Nimwegen M; Department of Neurology, Donders Institute for Brain, Cognition, and Behaviour, Radboud University Medical Centre, Nijmegen, the Netherlands.; Smolensky L; The Michael J. Fox Foundation for Parkinson's Research, New York, New York, USA.; Amondikar N; The Michael J. Fox Foundation for Parkinson's Research, New York, New York, USA.; Hutten SJ; The Michael J. Fox Foundation for Parkinson's Research, New York, New York, USA.; Frasier M; The Michael J. Fox Foundation for Parkinson's Research, New York, New York, USA.; Nguyen KH; Translational Genome Sciences, Biogen, Cambridge, Massachusetts, USA.; Rick J; Department of Neurology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.; Eberly S; Department of Biostatistics and Computational Biology, University of Rochester, Rochester, New York, USA.; Faghri F; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.; Auinger P; Department of Neurology, Center for Health + Technology, University of Rochester, Rochester, New York, USA.; Scott KM; Department of Clinical Neurosciences, University of Cambridge, John van Geest Centre for Brain Repair, Cambridge, UK.; Wijeyekoon R; Department of Clinical Neurosciences, University of Cambridge, John van Geest Centre for Brain Repair, Cambridge, UK.; Van Deerlin VM; Department of Pathology and Laboratory Medicine, Center for Neurodegenerative Disease Research, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA.; Hernandez DG; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.; Gibbs RJ; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.; Day-Williams AG; Flagship Labs 60 Inc, Cambridge, Massachusetts, USA.; Statistical Genetics, Biogen, Cambridge, Massachusetts, USA.; Brice A; Institut du cerveau et de la moelle épinière ICM, Paris, France.; Sorbonne Université SU, Paris, France.; INSERM UMR1127, Paris, France.; Alves G; The Norwegian Centre for Movement Disorders, Stavanger University Hospital, Stavanger, Norway.; Department of Chemistry, Bioscience and Environmental Engineering, University in Stavanger, Stavanger, Norway.; Department of Neurology, Stavanger University Hospital, Stavanger, Norway.; Noyce AJ; Preventive Neurology Unit, Wolfson Institute of Preventive Medicine, Queen Mary University of London, London, UK.; Department of Clinical and Movement Neurosciences, UCL Institute of Neurology, London, UK.; Tysnes OB; Department of Neurology, Haukeland University Hospital, Bergen, Norway.; Department of Clinical Medicine, University of Bergen, Bergen, Norway.; Evans JR; Department of Neurology, Nottingham University NHS Trust, Nottingham, UK.; Breen DP; Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, Scotland, UK.; Anne Rowling Regenerative Neurology Clinic, University of Edinburgh, Edinburgh, UK.; Usher Institute of Population Health Sciences and Informatics, University of Edinburgh, Edinburgh, UK.; Estrada K; Translational Genome Sciences, Biogen, Cambridge, Massachusetts, USA.; Wegel CE; Department of Medical and Molecular Genetics, Indiana University, Indianapolis, Indiana, USA.; Danjou F; Institut du cerveau et de la moelle épinière ICM, Paris, France.; Simon DK; Department of Neurology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.; Harvard Medical School, Boston, Massachusetts, USA.; Andreassen OA; NORMENT; Institute of Clinical Medicine, University of Oslo, Oslo, Norway.; Division of Mental Health and Addiction, Oslo University Hospital, Oslo, Norway.; Ravina B; Voyager Therapeutics, Cambridge, Massachusetts, USA.; Department of Neurology, University of Rochester School of Medicine, Rochester, New York, USA.; Toft M; Department of Neurology, Oslo University Hospital, Oslo, Norway.; Institute of Clinical Medicine, University of Oslo, Oslo, Norway.; Heutink P; German Center for Neurodegenerative Diseases-Tubingen, Tuebingen, Germany.; HIH Tuebingen, Tuebingen, Germany.; Bloem BR; Department of Neurology, Donders Institute for Brain, Cognition, and Behaviour, Radboud University Medical Centre, Nijmegen, the Netherlands.; Weintraub D; Department of Psychiatry, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.; Department of Veterans Affairs, Philadelphia, Pennsylvania, USA.; Barker RA; Department of Clinical Neurosciences and WT-MRC Cambridge Stem Cell Institute, University of Cambridge, Cambridge, UK.; Williams-Gray CH; Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.; van de Warrenburg BP; Department of Neurology, Donders Institute for Brain, Cognition, and Behaviour, Radboud University Medical Centre, Nijmegen, the Netherlands.; Van Hilten JJ; Department of Neurology, Leiden University Medical Center, Leiden, the Netherlands.; Scherzer CR; Advanced Center for Parkinson's Disease Research, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, USA.; Precision Neurology Program, Harvard Medical School, Brigham and Women's Hospital, Boston, Massachusetts, USA.; Singleton AB; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.; Nalls MA; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.; Data Tecnica International, Glen Echo, Maryland, USA.
Publisher: Wiley-Liss Country of Publication: United States NLM ID: 8610688 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1531-8257 (Electronic) Linking ISSN: 08853185 NLM ISO Abbreviation: Mov Disord Subsets: MEDLINE
Academic Journal
Klebe, StephanGolmard, Jean-LouisNalls, Michael ASaad, MohamadSingleton, Andrew BBras, Jose MHardy, JohnSimon-Sanchez, JavierHeutink, PeterKuhlenbäumer, GregorCharfi, RimKlein, ChristineHagenah, JohannGasser, ThomasWurster, IsabelLesage, SuzanneLorenz, DeliaDeuschl, GüntherDurif, FranckPollak, PierreDamier, PhilippeTison, FrançoisDurr, AlexandraAmouyel, PhilippeLambert, Jean-CharlesTzourio, ChristopheMaubaret, CéciliaCharbonnier-Beaupel, FannyTahiri, KhadijaVidailhet, MarieMartinez, MariaBrice, AlexisCorvol, Jean-ChristopheAgid, YAnheim, MBonnet, A-MBorg, MBrice, A.Broussolle, ECorvol, J-CDamier, Ph.Destée, A.Durr, ADurif, FKlebe, SLohmann, EMartinez, MPenet, CPollak, PKrack, PRascol, OTison, FTranchant, CVérin, MViallet, FPlagnol, VincentBras, Jose MHernandez, Dena GSharma, ManuSheerin, Una-MarieSaad, MohamadSimón-Sánchez, JavierSchulte, ClaudiaLesage, SuzanneSveinbjörnsdóttir, SigurlaugAmouyel, PhilippeArepalli, SampathBand, GavinBarker, Roger ABellinguez, CélineBen-Shlomo, YoavBerendse, Henk WBerg, DanielaBhatia, Kailashde Bie, Rob MABiffi, AlessandroBloem, BasBochdanovits, ZoltanBonin, MichaelBrockmann, KathrinBrooks, JanetBurn, David JCharlesworth, GavinChen, HongleiChinnery, Patrick FChong, SeanClarke, Carl ECookson, Mark RCooper, J MarkCorvol, Jean ChristopheCounsell, CarlDamier, PhilippeDartigues, Jean-FrançoisDeloukas, PanosDexter, David Tvan Dijk, Karin DDillman, AllissaDurif, FrankEdkins, SarahEvans, Jonathan RFoltynie, ThomasFreeman, ColinGao, JianjunGardner, MichelleGibbs, RaphaelGoate, AlisonGray, EmmaGuerreiro, RitaGústafsson, ÓmarHarris, ClareHellenthal, Garrettvan Hilten, Jacobus JHofman, AlbertHollenbeck, AlbertHolton, JaniceHu, MicheleHuang, XuemeiHuber, HeikoHudson, GavinHunt, Sarah EHuttenlocher, JohannaIllig, ThomasJónsson, Pálmi VLangford, CordeliaLees, AndrewLichtner, PeterLimousin, PatriciaLopez, GriselLorenz, DeliaMcNeill, AlisdairMoorby, CatrionaMorris, HuwMorrison, Karen EMudanohwo, EseOʼSullivan, Sean SPearson, JustinPearson, RichardPerlmutter, Joel SPétursson, HjörvarPirinen, MattiPollak, PierrePost, BartPotter, SimonRavina, BernardRevesz, TamasRiess, OlafRivadeneira, FernandoRizzu, PatriziaRyten, MinaSawcer, StephenSchapira, AnthonyScheffer, HansShaw, KarenShoulson, IraSidransky, Ellende Silva, RohanSmith, ColinSpencer, Chris CAStefánsson, HreinnSteinberg, StacyStockton, Joanna DStrange, AmySu, ZhanTalbot, KevinTanner, Carlie MTashakkori-Ghanbaria, AvazehTison, FrançoisTrabzuni, DaniahTraynor, Bryan JUitterlinden, GVandrovcova, JanaVelseboer, DaanVidailhet, MarieVukcevic, DamjanWalker, Robertvan de Warrenburg, BartWeale, Michael EWickremaratchi, MirdhuWilliams, NigelWilliams-Gray, Caroline HWinder-Rhodes, SophieMartinez, MariaDonnelly, PeterHardy, JohnHeutink, PeterBrice, AlexisGasser, ThomasWood, Nicholas WSingleton, Andrew B
Journal of Neurology, Neurosurgery & Psychiatry. Jun 01, 2013 84(6):666-673
Academic Journal
Iwaki H; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.; Data Tecnica International, Glen Echo, Maryland, USA.; Blauwendraat C; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.; Leonard HL; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.; Data Tecnica International, Glen Echo, Maryland, USA.; Kim JJ; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.; Liu G; School of Medicine, Sun Yat-sen University, Guangzhou, Guangdong, China.; Advanced Center for Parkinson's Disease Research, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, USA.; Precision Neurology Program, Harvard Medical School, Brigham and Women's Hospital, Boston, Massachusetts, USA.; Maple-Grødem J; The Norwegian Centre for Movement Disorders, Stavanger University Hospital, Stavanger, Norway.; Department of Chemistry, Bioscience and Environmental Engineering, University in Stavanger, Stavanger, Norway.; Corvol JC; Assistance-Publique Hôpitaux de Paris, ICM, INSERM UMRS 1127, CNRS 7225, ICM, Department of Neurology and CIC Neurosciences, Pitié-Salpêtrière Hospital, Paris, France.; Pihlstrøm L; Department of Neurology, Oslo University Hospital, Oslo, Norway.; van Nimwegen M; Radboud University Medical Centre, Donders Institute for Brain, Cognition, and Behaviour; Department of Neurology, Nijmegen, The Netherlands.; Hutten SJ; The Michael J. Fox Foundation for Parkinson's Research, New York, New York, USA.; Nguyen KH; Translational Genome Sciences, Biogen, Cambridge, Massachusetts, USA.; Rick J; Department of Neurology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.; Eberly S; Department of Biostatistics and Computational Biology, University of Rochester, Rochester, New York, USA.; Faghri F; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.; Department of Computer Science, University of Illinois Urbana-Champaign, Champaign, Illinois, USA.; Auinger P; Department of Neurology, Center for Health + Technology, University of Rochester, Rochester, New York, USA.; Scott KM; Department of Clinical Neurosciences, University of Cambridge, John van Geest Centre for Brain Repair, Cambridge, United Kingdom.; Wijeyekoon R; Department of Clinical Neurosciences, University of Cambridge, John van Geest Centre for Brain Repair, Cambridge, United Kingdom.; Van Deerlin VM; Department of Pathology and Laboratory Medicine, Center for Neurodegenerative Disease Research, Parelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA.; Hernandez DG; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.; Gibbs JR; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.; Chitrala KN; Laboratory of Epidemiology and Population Sciences, National Institute on Aging, National Institutes of Health, Baltimore, Maryland, USA.; Day-Williams AG; Flagship Labs 60 Inc, Cambridge, Massachusetts, USA.; Statistical Genetics, Biogen, Cambridge, Massachusetts, USA.; Brice A; Institut du cerveau et de la moelle épinière ICM, Paris, France.; Sorbonne Université SU, Paris, France.; INSERM UMR1127, Paris, France.; Alves G; The Norwegian Centre for Movement Disorders, Stavanger University Hospital, Stavanger, Norway.; Department of Chemistry, Bioscience and Environmental Engineering, University in Stavanger, Stavanger, Norway.; Department of Neurology, Stavanger University Hospital, Stavanger, Norway.; Noyce AJ; Preventive Neurology Unit, Wolfson Institute of Preventive Medicine, Queen Mary University of London, London, United Kingdom.; Department of Clinical and Movement Neurosciences, UCL Institute of Neurology, London, United Kingdom.; Tysnes OB; Department of Neurology, Haukeland University Hospital, Bergen, Norway.; University of Bergen, Bergen, Norway.; Evans JR; Department of Neurology, Nottingham University NHS Trust, Nottingham, United Kingdom.; Breen DP; Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, Scotland.; Anne Rowling Regenerative Neurology Clinic, University of Edinburgh, Edinburgh, Scotland.; Usher Institute of Population Health Sciences and Informatics, University of Edinburgh, Edinburgh, Scotland.; Estrada K; Translational Genome Sciences, Biogen, Cambridge, Massachusetts, USA.; Wegel CE; Department of Medical and Molecular Genetics, Indiana University, Indianapolis, Indiana, USA.; Danjou F; Institut du cerveau et de la moelle épinière ICM, Paris, France.; Simon DK; Department of Neurology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.; Harvard Medical School, Boston, Massachusetts, USA.; Andreassen O; NORMENT, Institute of Clinical Medicine, University of Oslo, Oslo, Norway, Norway.; Division of Mental Health and Addiction, Oslo University Hospital, Oslo, Norway, Norway.; Ravina B; Voyager Therapeutics, Cambridge, Massachusetts, USA.; Department of Neurology, University of Rochester School of Medicine, Rochester, New York, USA.; Toft M; Department of Neurology, Oslo University Hospital, Oslo, Norway.; Institute of Clinical Medicine, University of Oslo, Oslo, Norway.; Heutink P; German Center for Neurodegenerative Diseases-Tubingen, Tuebingen, Germany.; HIH Tuebingen, Tubingen, Tuebingen, Germany.; Bloem BR; Radboud University Medical Centre, Donders Institute for Brain, Cognition, and Behaviour; Department of Neurology, Nijmegen, The Netherlands.; Weintraub D; Department of Psychiatry, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.; Department of Veterans Affairs, Philadelphia, Pennsylvania, USA.; Barker RA; Department of Clinical Neurosciences, University of Cambridge, Cambridge, United Kingdom.; Williams-Gray CH; Department of Clinical Neurosciences, University of Cambridge, Cambridge, United Kingdom.; van de Warrenburg BP; Radboud University Medical Centre, Donders Institute for Brain, Cognition, and Behaviour; Department of Neurology, Nijmegen, The Netherlands.; Van Hilten JJ; Department of Neurology, Leiden University Medical Center, Leiden, The Netherlands.; Scherzer CR; Advanced Center for Parkinson's Disease Research, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, USA.; Precision Neurology Program, Harvard Medical School, Brigham and Women's Hospital, Boston, Massachusetts, USA.; Singleton AB; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.; Nalls MA; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.; Data Tecnica International, Glen Echo, Maryland, USA.
Publisher: Wiley-Liss Country of Publication: United States NLM ID: 8610688 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1531-8257 (Electronic) Linking ISSN: 08853185 NLM ISO Abbreviation: Mov Disord Subsets: MEDLINE
Academic Journal
Neurol Genet
Neurology / Genetics 5(4), e348 (2019). doi:10.1212/NXG.0000000000000348
Neurology. Genetics, 5, 4
Neurology: Genetics
Iwaki, H, Blauwendraat, C, Leonard, H L, Liu, G, Maple-grødem, J, Corvol, J, Pihlstrøm, L, Van Nimwegen, M, Hutten, S J, Nguyen, K H, Rick, J, Eberly, S, Faghri, F, Auinger, P, Scott, K M, Wijeyekoon, R, Van Deerlin, V M, Hernandez, D G, Day-williams, A G, Brice, A, Alves, G, Noyce, A J, Tysnes, O, Evans, J R, Breen, D P, Estrada, K, Wegel, C E, Danjou, F, Simon, D K, Ravina, B, Toft, M, Heutink, P, Bloem, B R, Weintraub, D, Barker, R A, Williams-gray, C H, Van De Warrenburg, B P, Van Hilten, J J, Scherzer, C R, Singleton, A B & Nalls, M A 2019, ' Genetic risk of Parkinson disease and progression: An analysis of 13 longitudinal cohorts ', Neurology Genetics, vol. 5, no. 4, pp. e348 . https://doi.org/10.1212/NXG.0000000000000348
Academic Journal
Consortium, Coffee and Caffeine GeneticsCornelis, Marilyn CRenstrom, FridaRasheed, AsifMason, Marc AZonderman, Alan BFranke, LudeKristal, Bruce SConsortium, International Parkinson’s Disease GenomicsConsortium, North American Brain ExpressionConsortium, UK Brain ExpressionKarjalainen, JuhaReed, Danielle RNgwa, Julius SWestra, Harm-JanEvans, Michele KSaleheen, DanishHarris, Tamara BDedoussis, GeorgeCurhan, GaryStumvoll, MichaelBeilby, JohnPasquale, Louis RFeenstra, BjarkeHuikari, VilleBandinelli, StefaniaOrdovas, Jose MChan, Andrew TPeters, UlrikeOhlsson, ClaesGieger, ChristianMartin, Nicholas GWaldenberger, MelanieSiscovick, David SRaitakari, OlliCavadino, AlanaEriksson, Johan GMitchell, PaulHunter, David JKraft, PeterRimm, Eric BBoomsma, Dorret IBorecki, Ingrid BLoos, Ruth JfWareham, Nicholas JVollenweider, PeterNolte, Ilja MCaporaso, NeilGrabe, Hans JörgenNeuhouser, Marian LWolffenbuttel, Bruce HrHu, Frank BHyppönen, ElinaJärvelin, Marjo-RiittaCupples, L AdrienneFranks, Paul WRidker, Paul MTeumer, Alexandervan Duijn, Cornelia MHeiss, GerardoMetspalu, AndresNorth, Kari EIngelsson, ErikNettleton, Jennifer Avan Dam, Rob MChasman, Daniel INalls, Michael APlagnol, VincentYu, KaiHernandez, Dena GSharma, ManuSheerin, Una-MarieSaad, MohamadSimón-Sánchez, JavierSchulte, ClaudiaLesage, SuzanneSveinbjörnsdóttir, SigurlaugArepalli, SampathBarker, RogerMarques-Vidal, PedroBen-Shlomo, YoavBerendse, Henk WBerg, DanielaBhatia, Kailashde Bie, Rob M ABiffi, AlessandroBloem, BasBochdanovits, ZoltanBonin, MichaelBras, M.Rawal, RajeshBrockmann, KathrinBrooks, JanetBurn, David JCharlesworth, GavinChen, HongleiChinnery, Patrick FChong, SeanClarke, Carl ECookson, Mark RCooper, J MarkManichaikul, AniCorvol, Jean ChristopheCounsell, CarlDamier, PhilippeDartigues, Jean-FrançoisDeloukas, PanosDeuschl, GüntherDexter, David Tvan Dijk, Karin DDillman, AllissaDurif, FrankByrne, Enda MWojczynski, Mary KDürr, AlexandraEdkins, SarahEvans, Jonathan RFoltynie, ThomasDong, JingGardner, MichelleGibbs, J RaphaelGoate, AlisonGray, EmmaGuerreiro, RitaVink, Jacqueline MHarris, Clarevan Hilten, Jacobus JHofman, AlbertHollenbeck, AlbertHolton, JaniceHu, MicheleHuang, XuemeiHershey, Milton SWurster, IsabelMätzler, WalterZhao, Jing HuaHudson, GavinHunt, Sarah EHuttenlocher, JohannaIllig, ThomasMünchen, Helmholtz ZentrumJónsson, Pálmi VLambert, Jean-CharlesLangford, CordeliaLees, AndrewLichtner, PeterBurlutsky, GeorgeLimousin, PatriciaLopez, GriselLorenz, DeliaMcNeill, AlisdairMoorby, CatrionaMoore, MatthewMorris, Huw RMorrison, Karen EO' Sullivan, Sean SLahti, JariPearson, JustinPerlmutter, Joel SPétursson, HjörvarPollak, PierrePotter, SimonRavina, BernardRevesz, TamasRiess, OlafRivadeneira, FernandoRizzu, PatriziaMikkilä, VeraRyten, MinaSawcer, StephenSchapira, AnthonyScheffer, HansShaw, KarenSidransky, EllenSmith, ColinSpencer, Chris C AStefánsson, HreinnBettella, FrancescoLemaitre, Rozenn NStockton, Joanna DStrange, AmyTalbot, KevinTanner, M.Tashakkori-Ghanbaria, AvazehTison, FrançoisTrabzuni, DaniahTraynor, Bryan JUitterlinden, André GVelseboer, DaanEriksson, JoelVidailhet, MarieWalker, Robertvan de Warrenburg, BartWickremaratchi, MirdhuWilliams, NigelWilliams-Gray, Caroline HWinder-Rhodes, SophieStefánsson, KáriMartinez, MariaSabatier, PaulMusani, Solomon KWood, Nicholas WHardy, JohnHeutink, PeterBrice, AlexisGasser, ThomasSingleton, Andrew BSingleton, AndrewCookson, MarkHernandez, DenaTanaka, ToshikoNalls, MichaelZonderman, AlanFerrucci, LuigiJohnson, RobertLongo, DanO'Brien, RichardTraynor, BryanTroncoso, JuanEsko, TõnuGeller, Frankvan der Brug, MarcelZielke, RonaldWeale, MichaelRamasamy, AdaikalavanBox, P. O.Luan, Jian'anHui, JennieMägi, ReedikDimitriou, MariaGarcia, Melissa EHo, Weang-KeeWright, Margaret JRose, Lynda MMagnusson, Patrik KePedersen, Nancy LCouper, DavidOostra, Ben AIkram, Mohammad ArfanTiemeier, Henning WUitterlinden, Andre Gvan Rooij, Frank JaBarroso, InêsJohansson, IngegerdGanna, AndreaXue, LutingKaakinen, MarikaMilani, LiliPower, ChrisSnieder, HaroldStolk, Ronald PBaumeister, Sebastian EBiffar, ReinerGu, FangyiBastardot, FrançoisPaynter, NinaKutalik, ZoltánJacobs, David RForouhi, Nita GMihailov, EvelinLind, LarsLindgren, CeciliaMichaëlsson, KarlMorris, AndrewJensen, MajkenKhaw, Kay-TeeMonda, Keri LLuben, Robert NWang, Jie JinMännistö, SatuPerälä, Mia-MariaKähönen, MikaLehtimäki, TerhoViikari, JormaMozaffarian, DariushMukamal, KennethPsaty, Bruce MAmin, NajafDöring, AngelaHeath, Andrew CMontgomery, Grant WDahmen, NorbertCarithers, TeresaTucker, Katherine LBoyd, Heather AMelbye, MadsTreur, Jorien LFischer, KristaMellström, DanHottenga, Jouke JanProkopenko, IngaTönjes, AnkeKanoni, StavroulaLorentzon, MattiasHouston, Denise KLiu, YongmeiDanesh, John
Berendse, H W, Dijk, K D V & IFGC (International FTD-Genomics Consortium), IPDGC (The International Parkinson Disease Genomics Consortium) 2015, 'Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption', Molecular Psychiatry, vol. 20, no. 5, pp. 647-656. https://doi.org/10.1038/mp.2014.107
Molecular psychiatry 20(5), 647-656 (2014). doi:10.1038/mp.2014.107
Molecular Psychiatry, 20, 5, pp. 647-656
Molecular Psychiatry, 20, 5, pp. 647-56
Molecular Psychiatry
Academic Journal
Nalls, Mike APankratz, NathanSchulte, ClaudiaDurif, FrankDürr, AlexandraEdkins, SarahEvans, Jonathan RFoltynie, ThomasDong, JingGardner, MichelleGibbs, J RaphaelGoate, AlisonGray, EmmaKeller, Margaux FGuerreiro, RitaHarris, Clarevan Hilten, Jacobus JHofman, AlbertHollenbeck, AlbertHolton, JaniceHu, MicheleHuang, XuemeiWurster, IsabelMätzler, WalterArepalli, SampathHudson, GavinHunt, Sarah EHuttenlocher, JohannaIllig, ThomasJónsson, Pálmi VLambert, Jean-CharlesLangford, CordeliaLees, AndrewLichtner, PeterLimousin, PatriciaLetson, ChristopherLopez, GriselLorenz, DeliaMcNeill, AlisdairMoorby, CatrionaMoore, MatthewMorris, Huw RMorrison, Karen EMudanohwo, EseO'Sullivan, Sean SPearson, JustinEdsall, ConnorPerlmutter, Joel SPétursson, HjörvarPollak, PierrePost, BartPotter, SimonRavina, BernardRevesz, TamasRiess, OlafRivadeneira, FernandoRizzu, PatriziaStefansson, HreinnRyten, MinaSawcer, StephenSchapira, AnthonyScheffer, HansShaw, KarenShoulson, IraSidransky, EllenSmith, ColinSpencer, Chris C AStefánsson, HreinnLiu, XinminBettella, FrancescoStockton, Joanna DStrange, AmyTalbot, KevinTanner, Carlie MTashakkori-Ghanbaria, AvazehTison, FrançoisTrabzuni, DaniahTraynor, Bryan JUitterlinden, André GPliner, HannahVelseboer, DaanVidailhet, MarieWalker, Robertvan de Warrenburg, BartWickremaratchi, MirdhuWilliams, NigelWilliams-Gray, Caroline HWinder-Rhodes, SophieStefánsson, KáriMartinez, MariaLee, Joseph HWood, Nicholas WHardy, JohnBrice, AlexisSingleton, Andrew BFactor, S.Higgins, D.Evans, S.Shill, H.Stacy, M.Danielson, J.Cheng, RongMarlor, L.Williamson, K.Jankovic, J.Hunter, C.Simon, D.Ryan, P.Scollins, L.Saunders-Pullman, R.Boyar, K.Costan-Toth, C.Lill, Christina MConsortium, International Parkinson's Disease GenomicsOhmann, E.Sudarsky, L.Joubert, C.Friedman, J.Chou, K.Fernandez, H.Lannon, M.Galvez-Jimenez, N.Podichetty, A.Thompson, K.Group, Parkinson's StudyLewitt, P.DeAngelis, M.O'Brien, C.Seeberger, L.Dingmann, C.Judd, D.Marder, K.Fraser, J.Harris, J.Bertoni, J.23andMePeterson, C.Rezak, M.Medalle, G.Chouinard, S.Panisset, M.Hall, J.Poiffaut, H.Calabrese, V.Roberge, P.Wojcieszek, J.GenePDBelden, J.Jennings, D.Marek, K.Mendick, S.Reich, S.Dunlop, B.Jog, M.Horn, C.Uitti, R.Turk, M.Consortium, NeuroGenetics ResearchAjax, T.Mannetter, J.Sethi, K.Carpenter, J.Dill, B.Hatch, L.Ligon, K.Narayan, S.Blindauer, K.Abou-Samra, K.Genomics, Hussman Institute of HumanPetit, J.Elmer, L.Aiken, E.Davis, K.Schell, C.Wilson, S.Velickovic, M.Koller, W.Phipps, S.Feigin, A.Investigator, Ashkenazi Jewish DatasetGordon, M.Hamann, J.Licari, E.Marotta-Kollarus, M.Shannon, B.Winnick, R.Simuni, T.Videnovic, A.Kaczmarek, A.Williams, K.Epidemiology, Cohorts for Health and Aging Research in GeneticWolff, M.Rao, J.Cook, M.Fernandez, M.Kostyk, S.Hubble, J.Campbell, A.Reider, C.Seward, A.Camicioli, R.Consortium, North American Brain ExpressionCarter, J.Nutt, J.Andrews, P.Morehouse, S.Stone, C.Mendis, T.Grimes, D.Alcorn-Costa, C.Gray, P.Haas, K.Consortium, United Kingdom Brain ExpressionVendette, J.Sutton, J.Hutchinson, B.Young, J.Rajput, A.Klassen, L.Shirley, T.Manyam, B.Simpson, P.Whetteckey, J.Do, Chuong BConsortium, Greek Parkinson's DiseaseWulbrecht, B.Truong, D.Pathak, M.Frei, K.Luong, N.Tra, T.Tran, A.Vo, J.Lang, A.Kleiner- Fisman, G.Group, Alzheimer Genetic AnalysisNieves, A.Johnston, L.So, J.Podskalny, G.Giffin, L.Atchison, P.Allen, C.Martin, W.Wieler, M.Suchowersky, O.Ikram, M ArfanFurtado, S.Klimek, M.Hermanowicz, N.Niswonger, S.Shults, C.Fontaine, D.Aminoff, M.Christine, C.Diminno, M.Hevezi, J.Ioannidis, John P ADalvi, A.Kang, U.Richman, J.Uy, S.Sahay, A.Gartner, M.Schwieterman, D.Hall, D.Hadjigeorgiou, Georgios MLeehey, M.Culver, S.Derian, T.Demarcaida, T.Thurlow, S.Rodnitzky, R.Dobson, J.Lyons, K.Pahwa, R.Gales, T.Bis, Joshua CThomas, S.Shulman, L.Weiner, W.Dustin, K.Singer, C.Zelaya, L.Tuite, P.Hagen, V.Rolandelli, S.Schacherer, R.Kosowicz, J.Gordon, P.Werner, J.Serrano, C.Roque, S.Kurlan, R.Berry, D.Gardiner, I.Hauser, R.Sanchez-Ramos, J.Zesiewicz, T.Delgado, H.Price, K.Rodriguez, P.Wolfrath, S.Pfeiffer, R.Davis, L.Pfeiffer, B.Dewey, R.Hayward, B.Johnson, A.Meacham, M.Estes, B.Walker, F.Hunt, V.O'Neill, C.Marder, KarenRacette, B.Swisher, L.Dijamco, CheriConley, Emily DrabantDorfman, ElizabethTung, Joyce YHinds, David AMountain, Joanna LWojcicki, AnneLew, M.Hernandez, Dena GFiske, BrianKlein, C.Golbe, L.Growdon, J.Wooten, G. F.Watts, R.Guttman, M.Sutherland, MargaretGoldwurm, S.Saint-Hilaire, M. H.Baker, K.Litvan, I.Nicholson, G.Nance, M.Drasby, E.Isaacson, S.Burn, D.Xiromerisiou, GeorgiaPramstaller, P.Al-hinti, J.Moller, A.Sherman, S.Roxburgh, R.Slevin, J.Perlmutter, J.Mark, M. H.Huggins, N.Pezzoli, G.Myers, Richard HMassood, T.Itin, I.Corbett, A.Chinnery, P.Ostergaard, K.Snow, B.Cambi, F.Kay, D.Samii, A.Clark, Lorraine NAgarwal, P.Roberts, J. W.Higgins, D. S.Molho, EricRosen, AmiMontimurro, J.Martinez, E.Griffith, A.Kusel, V.Yearout, D.Stefansson, KariZabetian, C.Clark, L. N.Liu, X.Lee, J. H.Taub, R ChengLouis, E. D.Cote, L. J.Waters, C.Hardy, John AFord, B.Fahn, S.Vance, Jeffery MBeecham, Gary WMartin, Eden RNuytemans, KarenPericak-Vance, Margaret AHaines, Jonathan LDeStefano, AnitaSeshadri, SudhaHeutink, PeterChoi, Seung HoanFrank, SamuelPsaty, Bruce MRice, KennethLongstreth, W. T.Ton, Thanh G NJain, Samayvan Duijn, Cornelia MChen, HongleiVerlinden, Vincent JKoudstaal, Peter JSingleton, AndrewCookson, MarkHernandez, DenaDillman, AllissaNalls, MichaelZonderman, AlanFerrucci, LuigiJohnson, RobertLongo, DanO'Brien, RichardTraynor, BryanTroncoso, Juanvan der Brug, MarcelZielke, RonaldSaad, MohamadHoulden, HenryWeale, MichaelRamasamy, AdaikalavanKara, EleannaDardiotis, EfthimiosPayami, HaydehTsimourtou, VanaSpanaki, CleanthePlaitakis, AndreasBozi, MariaStefanis, LeonidasVassilatis, DimitrisKoutsis, GeorgiosPanas, MariosLunnon, KatieLupton, MichellePowell, JohnParkkinen, LauraAnsorge, OlafScott, William KGasser, ThomasBertram, LarsEriksson, NicholasForoud, TatianaDeStefano, Anita LPlagnol, VincentSharma, ManuSheerin, Una-MarieSimón-Sánchez, JavierLesage, SuzanneSveinbjörnsdóttir, SigurlaugBarker, RogerBen-Shlomo, YoavBerendse, Henk WBerg, DanielaBhatia, Kailashde Bie, Rob M ABiffi, AlessandroBloem, BasBochdanovits, ZoltanBonin, MichaelBras, JoseBras, Jose MBrockmann, KathrinBrooks, JanetBurn, David JCharlesworth, GavinChinnery, Patrick FChong, SeanClarke, Carl ECookson, Mark RCooper, J MarkCorvol, Jean ChristopheCounsell, CarlDamier, PhilippeDartigues, Jean-FrançoisDeloukas, PanosDeuschl, GüntherDexter, David Tvan Dijk, Karin D
Nat Genet
Berendse, H W, GenePD, NeuroGenetics Research Consortium (NGRC), Hussman Institute of Human Genomics (HIHG), The Ashkenazi Jewish Dataset Investigator, Cohorts for Health and Aging Research in Genetic Epidemiology (CHARGE), North American Brain Expression Consortium (NABEC), United Kingdom Brain Expression Consortium (UKBEC), Greek Parkinson’s Disease Consortium, Alzheimer Genetic Analysis Group, International Parkinson’s Disease Genomics Consortium (IPDGC), Parkinson’s Study Group (PSG) Parkinson’s Research: The Organized GENetics Initiative (PROGENI) & 23andMe 2014, 'Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease', Nature Genetics, vol. 46, no. 9, pp. 989-993. https://doi.org/10.1038/ng.3043
Nature genetics 46(9), 989-993 (2014). doi:10.1038/ng.3043
Nature Genetics, 46, 9, pp. 989-93
Nature Genetics
Nature Genetics, vol 46, iss 9
Academic Journal
Nalls, Mike ASaad, MohamadMorris, Huw RMudanohwo, EseO'Sullivan, Sean SPearson, JustinPerlmutter, Joel SPétursson, HjörvarPollak, PierrePost, BartPotter, SimonRavina, BernardRevesz, TamasWilliams, NigelRiess, OlafRivadeneira, FernandoRizzu, PatriziaRyten, MinaSawcer, StephenSchapira, AnthonyScheffer, HansShaw, KarenShoulson, IraSidransky, EllenGasser, ThomasSmith, ColinSpencer, Chris C AStefánsson, HreinnSteinberg, StacyStockton, Joanna DStrange, AmyTalbot, KevinTanner, Carlie MTashakkori-Ghanbaria, AvazehTison, FrançoisHeutink, PeterTrabzuni, DaniahTraynor, Bryan JUitterlinden, André GVelseboer, DaanVidailhet, MarieWalker, Robertvan de Warrenburg, BartWickremaratchi, MirdhuWilliams-Gray, Caroline HWood, NickWinder-Rhodes, SophieStefánsson, KáriMartinez, MariaHardy, JohnBrice, AlexisSingleton, Andrew BWood, Nicholas WDonnelly, PeterBarroso, InesBlackwell, Jenefer MBramon, ElviraBrown, Matthew ACasas, Juan PCorvin, AidenDeloukas, PanosDuncanson, AudreyJankowski, JanuszMarkus, Hugh SMathew, Christopher GPalmer, N. A.Plomin, RobertRautanen, AnnaSawcer, Stephen JTrembath, Richard CViswanathan, Ananth CBand, GavinBellenguez, CélineFreeman, ColinHellenthal, GarrettGiannoulatou, EleniPirinen, MattiPearson, RichardSu, ZhanVukcevic, DamjanConsortium, International Parkinson's Disease GenomicsLangford, CordeliaHunt, Sarah EEdkins, SarahGwilliam, RhianBlackburn, HannahBumpstead, Suzannah JDronov, SergeGillman, MatthewGray, EmmaHammond, Naomi2, Wellcome Trust Case Control ConsortiumJayakumar, AlagurevathiMcCann, Owen TLiddle, JenniferPotter, Simon CRavindrarajah, RadhiRicketts, MichelleWaller, MatthewWeston, PaulWidaa, SaraWhittaker, PamelaNoyce, Alastair JConsortium, North American Brain ExpressionMcCarthy, Mark ICookson, Mark RConsortium, United Kingdom Brain ExpressionGibbs, J RaphaelHernandez, Dena GDillman, AllissaNalls, Michael AZonderman, Alan BArepalli, SampathFerrucci, LuigiJohnson, RobertLongo, Dan LO'Brien, RichardNalls, MikeTraynor, BryanTroncoso, Juanvan der Brug, MarcelZielke, Ronald HWeale, Michael ERamasamy, AdaikalavanPlagnol, VincentWalker, RoberSharma, ManuSheerin, Una-MarieSimón-Sánchez, JavierSchulte, ClaudiaKeller, Margaux FLesage, SuzanneSveinbjörnsdóttir, SigurlaugBarker, RogerBen-Shlomo, YoavBerendse, Henk WBerg, DanielaBhatia, Kailashde Bie, Rob M ABiffi, AlessandroSchrag, AnetteBloem, BasBochdanovits, ZoltanBonin, MichaelBras, Jose MBrockmann, KathrinBrooks, JanetBurn, David JCharlesworth, GavinChen, HongleiChinnery, Patrick FBestwick, Jonathan PChong, SeanClarke, Carl ECooper, J MarkCorvol, Jean ChristopheCounsell, CarlDamier, PhilippeDartigues, Jean-FrançoisDeuschl, GüntherDexter, David Tvan Dijk, Karin DDurif, FrankDürr, AlexandraEvans, Jonathan RFoltynie, ThomasGao, JianjunGardner, MichelleGoate, AlisonGuerreiro, RitaGústafsson, ÓmarHarris, Clarevan Hilten, Jacobus JHofman, AlbertHollenbeck, AlbertHolton, JaniceHu, MicheleHuang, XuemeiHuber, HeikoHudson, GavinHuttenlocher, JohannaIllig, ThomasJónsson, Pálmi VLambert, Jean-CharlesLees, AndrewLichtner, PeterLimousin, PatriciaLopez, GriselLorenz, DeliaMcNeill, AlisdairMoorby, CatrionaMoore, MatthewMorrison, Karen E
Human molecular genetics 23(3), 831-841 (2013). doi:10.1093/hmg/ddt465
Human Molecular Genetics, 23, 3, pp. 831-41
Academic Journal
Mittag, FlorianBüchel, FinjaGibbs, J RaphaelPearson, JustinPerlmutter, Joel SPétursson, HjörvarPollak, PierrePotter, SimonRavina, BernardRevesz, TamasRiess, OlafRivadeneira, FernandoRizzu, PatriziaLesage, SuzanneRyten, MinaSawcer, StephenSchapira, AnthonyScheffer, HansShaw, KarenSidransky, EllenSmith, ColinSpencer, Chris C AStefánsson, HreinnSteinberg, StacyBrice, AlexisStockton, Joanna DStrange, AmyTalbot, KevinTanner, Carlie MTashakkori-Ghanbaria, AvazehTison, FrançoisTrabzuni, DaniahTraynor, Bryan JUitterlinden, André GVelseboer, DaanHeutink, PeterVidailhet, MarieWalker, Robertvan de Warrenburg, BartWickremaratchi, MirdhuWilliams, NigelWilliams-Gray, Caroline HWinder-Rhodes, SophieStefánsson, KáriMartinez, MariaHardy, JohnSingleton, Andrew BWood, Nicholas WZell, AndreasGasser, ThomasSaad, MohamadSharma, ManuConsortium, International Parkinson’s Disease GenomicsNalls, Michael APlagnol, VincentSheerin, Una-MarieSimón-Sánchez, JavierSveinbjörnsdóttir, SigurlaugArepalli, SampathJahn, AndreasBarker, RogerBen-Shlomo, YoavBerendse, Henk WBerg, DanielaBhatia, Kailashde Bie, Rob M ABiffi, AlessandroBloem, BasBochdanovits, ZoltanBonin, MichaelSchulte, ClaudiaBras, Jose MBrockmann, KathrinBrooks, JanetBurn, David JCharlesworth, GavinChen, HongleiChinnery, Patrick FChong, SeanClarke, Carl ECookson, Mark RCooper, J MarkCorvol, Jean ChristopheCounsell, CarlDamier, PhilippeDartigues, Jean-FrançoisDeloukas, PanosDeuschl, GüntherDexter, David Tvan Dijk, Karin DDillman, AllissaDurif, FrankDürr, AlexandraEdkins, SarahEvans, Jonathan RFoltynie, ThomasGao, JianjunGardner, MichelleGoate, AlisonGray, EmmaNalls, Mike AGuerreiro, RitaGústafsson, ÓmarHarris, Clarevan Hilten, Jacobus JHofman, AlbertHollenbeck, AlbertHolton, JaniceHu, MicheleHuang, XuemeiHershey, Milton SKeller, MargauxHuber, HeikoHudson, GavinHunt, Sarah EHuttenlocher, JohannaIllig, ThomasJónsson, Pálmi VLambert, Jean-CharlesLangford, CordeliaLees, AndrewLichtner, PeterHernandez, Dena GMünchen, Helmholtz ZentrumLimousin, PatriciaLopez, GriselLorenz, DeliaMcNeill, AlisdairMoorby, CatrionaMoore, MatthewMorris, Huw RMorrison, Karen EO'Sullivan, Sean S
Mittag, F, Buchel, F, Saad, M, Jahn, A, Schulte, C, Bochdanovits, Z, Simon-Sanchez, J, Nalls, M A, Keller, M, Hernandez, D G, Gibbs, J R, Lesage, S, Brice, A, Heutink, P, Martinez, M, Wood, N W, Hardy, J, Singleton, A B, Zell, A, Gasser, T & Sharma, M 2012, 'Use of support vector machines for disease risk prediction in genome-wide association studies: Concerns and opportunities', Human Mutation, vol. 33, no. 12, pp. 1708-1718. https://doi.org/10.1002/humu.22161
Human mutation 33(12), 1708-1718 (2012). doi:10.1002/humu.22161
Human Mutation, Vol. 33, No 12 (2012) pp. 1708-18
검색 결과 제한하기
제한된 항목
[AR] Evans, Jonathan R
발행연도 제한
-
학술DB(Database Provider)
저널명(출판물, Title)
출판사(Publisher)
자료유형(Source Type)
주제어
언어