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机译:鉴定帕金森病的新风险基因座,因果洞察力和遗传风险:基因组关联研究的荟萃分析
NIA Lab Neurogenet NIH Bethesda MD 20892 USA;
NIA Lab Neurogenet NIH Bethesda MD 20892 USA;
Univ Queensland Inst Mol Biosci Brisbane Qld Australia;
23andMe Sunnyvale CA USA;
NIA Lab Neurogenet NIH Bethesda MD 20892 USA;
Genentech Inc Dept Human Genet San Francisco CA USA;
UCL Queen Sq Inst Neurol Dept Mol Neurosci London England;
UCL Queen Sq Inst Neurol Dept Mol Neurosci London England;
UCL Queen Sq Inst Neurol Dept Mol Neurosci London England;
Univ Queensland Queensland Brain Inst Brisbane Qld Australia;
UCL Queen Sq Inst Neurol Dept Neurodegenerat Dis London England;
Baylor Coll Med Dept Neurol Houston TX 77030 USA;
Univ Maryland Sch Med Dept Neurol Baltimore MD 21201 USA;
Univ Tubingen Dept Neurodegenerat Dis Hertie Inst Clin Brain Res Tubingen Germany;
Univ Tubingen Dept Neurodegenerat Dis Hertie Inst Clin Brain Res Tubingen Germany;
Univ Tubingen Ctr Genet Epidemiol Inst Clin Epidemiol &
Appl Biometry Tubingen Germany;
McGill Univ Dept Human Genet Montreal PQ Canada;
Oslo Univ Hosp Dept Neurol Oslo Norway;
Univ Oulu Dept Neurol Inst Clin Med Oulu Finland;
NIA Lab Neurogenet NIH Bethesda MD 20892 USA;
NIA Lab Neurogenet NIH Bethesda MD 20892 USA;
NIA Lab Neurogenet NIH Bethesda MD 20892 USA;
NIA Lab Neurogenet NIH Bethesda MD 20892 USA;
NIA Lab Neurogenet NIH Bethesda MD 20892 USA;
NINDS NIH Bldg 36 Rm 4D04 Bethesda MD 20892 USA;
UCL Queen Sq Inst Neurol Dept Mol Neurosci London England;
Inst Natl Sante &
Rech Med Unite Mixte Rech 1220 Toulouse France;
Inst Natl Sante &
Rech Med CNRS U1127 UMR 7225 Paris France;
Inst Natl Sante &
Rech Med CNRS U1127 UMR 7225 Paris France;
Baylor Coll Med Dept Neurol Houston TX 77030 USA;
Univ Maryland Sch Med Dept Neurol Baltimore MD 21201 USA;
NINDS NIH Bldg 36 Rm 4D04 Bethesda MD 20892 USA;
Univ Helsinki Clin Neurosci Neurol Helsinki Finland;
Univ Oulu Dept Neurol Inst Clin Med Oulu Finland;
Oslo Univ Hosp Dept Neurol Oslo Norway;
Oslo Univ Hosp Div Mental Hlth &
Addict Oslo Norway;
Genentech Inc Dept Human Genet San Francisco CA USA;
Inst Natl Sante &
Rech Med CNRS U1127 UMR 7225 Paris France;
Univ Queensland Queensland Brain Inst Brisbane Qld Australia;
McGill Univ Dept Human Genet Montreal PQ Canada;
Univ Tubingen Dept Neurodegenerat Dis Hertie Inst Clin Brain Res Tubingen Germany;
Univ Tubingen Dept Neurodegenerat Dis Hertie Inst Clin Brain Res Tubingen Germany;
Baylor Coll Med Dept Neurol Houston TX 77030 USA;
UCL Queen Sq Inst Neurol Dept Mol Neurosci London England;
23andMe Sunnyvale CA USA;
UCL Queen Sq Inst Neurol Dept Mol Neurosci London England;
UCL Queen Sq Inst Neurol Dept Clin &
Movement Neurosci London England;
Univ Queensland Inst Mol Biosci Brisbane Qld Australia;
Univ Queensland Queensland Brain Inst Brisbane Qld Australia;
Genentech Inc Dept Human Genet San Francisco CA USA;
NIA Lab Neurogenet NIH Bethesda MD 20892 USA;
机译:鉴定帕金森病的新风险基因座,因果洞察力和遗传风险:基因组关联研究的荟萃分析
机译:插入序列变异体以鉴定帕金森氏病的遗传风险:全基因组关联研究的荟萃分析。
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机译:探索血压的遗传性缺失:新型血压表型的全基因组关联研究。
机译:序列的归责识别的遗传风险帕金森病变:全基因组关联研究进行了荟萃分析
机译:综合鉴定孢子克雷托茨菲尔特 - 雅各疾病的新风险基因座和因果见解:一种基因组关联研究