M.A. Pericak-Vance - Hussman Institute for Human Genomics, University of Miami, Miller School of Medicine, Miami, FL, USA

基本信息

浏览量：55

职业迁徙

个人简介

暂无内容

研究兴趣

论文共 414 篇作者统计合作学者相似作者

按年份排序按引用量排序主题筛选期刊级别筛选合作者筛选合作机构筛选

Increased APOEε4 expression is associated with reactive A1 astrocytes and the difference in Alzheimer Disease risk from diverse ancestral backgrounds

A. J. Griswold,K. Celis, P. Bussies,F. Rajabli, P. Whitehead, K. Hamilton-Nelson,G. W. Beecham, D. M. Dykxhoorn,K. Nuytemans,L. Wang,O. K. Gardner, D. Dorfsman,

biorxiv（2020）

引用1浏览0引用

Genetic overlap between Alzheimer's disease and Parkinson's disease at the MAPT locus

R S Desikan,A J Schork,Y Wang,A Witoelar, M Sharma, L K McEvoy,D Holland,J B Brewer,C-H Chen,W K Thompson,D Harold, J Williams,

Molecular psychiatryno. 12 (2015): 1588-95

引用122浏览0WOS引用

122

Parkinson disease loci in the mid-western Amish

M. F. Davis, A. C. Cummings, L. N. D’Aoust,L. Jiang,D. R. Velez Edwards, R. Laux, L. Reinhart-Mercer, D. Fuzzell,W. K. Scott,M. A. Pericak-Vance, S. L. Lee,J. L. Haines

Human genetics（2013）

引用13浏览0WOS引用

ASSOCIATION STUDIES ARTICLES

G Coppola, S Chinnathambi, JJY Lee, BA Dombroski, MC Baker, AI Soto-Ortolaza,SE Lee, E Klein, AY Huang, R Sears, JR Lane, AM Karydas,

Human Molecular Geneticsno. 15 (2012)

引用0浏览0引用

Mutation screening of spastin, atlastin, and REEP1 in hereditary spastic paraplegia

DS McCorquodale III,U Ozomaro,J Huang,G Montenegro,A Kushman,L Citrigno,J Price,F Speziani,MA Pericak-Vance,S Züchner

CLINICAL GENETICS（2011）

引用44浏览0WOS引用

Emprirically Defining Autism-Epilepsy Phenotypes

M. L. Cuccaro, K. L. Hamilton, J. R. Gilbert,M. A. Pericak-Vance, R. F. Tuchmann

ANNALS OF NEUROLOGY（2010）

引用0浏览0引用

Genome-wide association study for late-onset Alzheimer's disease in the Mid-Western U.S. Amish

A.C. Cummings,L. Jiang,D. Velez Edwards,R. Laux,L.L. McFarland,P.J. Gallins,L. Caywood,M. Creason,D. Fuzzell,C. Knebusch,M.G. Tramontana,M.A. Slifer,

Alzheimer's & Dementia: The Journal of the Alzheimer's Association（2010）

引用0浏览0EI引用

Localization of cloned unique DNA to three different regions of chromosome 19: screen for linkage probes for myotonic dystrophy

L. H. Yamaoka,R. J. Bartlett,D. A. Ross, G. H. Fey,D. H. Ledbetter,G. Bruns,M. A. Pericak-vance, M. H. Herbstreith,A. D. Roses

JOURNAL OF NEUROGENETICS（2009）

引用17浏览0WOS引用

Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis

J L McCauley, R L Zuvich, Y Bradford, S J Kenealy, N Schnetz-Boutaud,S G Gregory,S L Hauser,J R Oksenberg,D P Mortlock,M A Pericak-Vance,J L Haines

Genes & Immunityno. 7 (2009): 624-630

引用8浏览0WOSNATURE引用

Multiple rare SAPAP3 missense variants in trichotillomania and OCD

S Züchner,J R Wendland,A E Ashley-Koch,A L Collins,K N Tran-Viet,K Quinn,K C Timpano,M L Cuccaro,M A Pericak-Vance,D C Steffens,K R Krishnan,G Feng,

MOLECULAR PSYCHIATRY（2009）

引用150浏览0WOSNATURE引用

150

加载更多

作者统计

合作学者

合作机构

D-Core

合作者
学生
导师

暂无相似学者，你可以通过学者研究领域进行搜索筛选

数据免责声明

页面数据均来自互联网公开来源、合作出版商和通过AI技术自动分析结果，我们不对页面数据的有效性、准确性、正确性、可靠性、完整性和及时性做出任何承诺和保证。若有疑问，可以通过电子邮件方式联系我们：report@aminer.cn