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  • Jeffery M Vance
2012

Tyrosine hydroxylase gene: Another piece of the genetic puzzle of Parkinson's disease

Bademci, G., Vance, J. M. & Wang, L., Jun 1 2012, In : CNS and Neurological Disorders - Drug Targets. 11, 4, p. 469-481 13 p.

Research output: Contribution to journalArticle

12 Scopus citations

Gene expression profiles in Parkinson disease prefrontal cortex implicate FOXO1 and genes under its transcriptional regulation

Dumitriu, A., Latourelle, J. C., Hadzi, T. C., Pankratz, N., Garza, D., Miller, J. P., Vance, J. M., Foroud, T., Beach, T. G. & Myers, R. H., Jun 1 2012, In : PLoS Genetics. 8, 6, e1002794.

Research output: Contribution to journalArticle

40 Scopus citations
2019

Genome-wide brain DNA methylation analysis suggests epigenetic reprogramming in Parkinson disease

Young, J. I., Sivasankaran, S. K., Wang, L., Ali, A., Mehta, A., Davis, D. A., Dykxhoorn, D. M., Petito, C. K., Beecham, G. W., Martin, E. R., Mash, D. C., Pericak-Vance, M., Scott, W. K., Montine, T. J. & Vance, J. M., Aug 1 2019, In : Neurology: Genetics. 5, 4, 342.

Research output: Contribution to journalArticle

Open Access
1 Scopus citations
2013
12 Scopus citations
2016

Identification of TMEM230 mutations in familial Parkinson's disease

Deng, H. X., Shi, Y., Yang, Y., Ahmeti, K. B., Miller, N., Huang, C., Cheng, L., Zhai, H., Deng, S., Nuytemans, K., Corbett, N. J., Kim, M. J., Deng, H., Tang, B., Yang, Z., Xu, Y., Chan, P., Huang, B., Gao, X. P., Song, Z. & 14 others, Liu, Z., Fecto, F., Siddique, N., Foroud, T., Jankovic, J., Ghetti, B., Nicholson, D. A., Krainc, D., Melen, O., Vance, J. M., Pericak-Vance, M. A., Ma, Y. C., Rajput, A. H. & Siddique, T., Jul 1 2016, In : Nature Genetics. 48, 7, p. 733-739 7 p.

Research output: Contribution to journalArticle

88 Scopus citations
2018

Variants in chondroitin sulfate metabolism genes in thrombotic storm

Nuytemans, K., Ortel, T. L., Gomez, L., Hofmann, N., Alves, N., Dueker, N., Beecham, A., Whitehead, P., Hahn Estabrooks, S., Kitchens, C. S., Erkan, D., Brandão, L. R., James, A. H., Kulkarni, R., Manco-Johnson, M. J., Pericak-Vance, M. A. & Vance, J. M., Jan 1 2018, In : Thrombosis Research. 161, p. 43-51 9 p.

Research output: Contribution to journalArticle

2012

What should the genome-wide significance threshold be? Empirical replication of borderline genetic associations

Panagiotou, O. A., Ioannidis, J. P. A., Hirschhorn, J. N., Abecasis, G. R., Frayling, T. M., McCarthy, M. I., Lindgren, C. M., Beaty, T. H., Eriksson, N., Polychronakos, C., Kathirensan, S., Plenge, R. M., Spritz, R., Payami, H., Martin, E. R., Vance, J. M., Su, W. H., Chang, Y. S., Bei, J. X., Zeng, Y. X. & 12 others, Paré, G., Faraone, S. V., Neale, B., Anney, R. J., Traynor, B. J., Scherag, A., Hebebrand, J., Hinney, A., Froguel, P., Meyre, D., Chanock, S. J. & Kesheng, W., Feb 1 2012, In : International Journal of Epidemiology. 41, 1, p. 273-286 14 p., dyr178.

Research output: Contribution to journalArticle

140 Scopus citations
2018

Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's disease

Hui, K. Y., Fernandez-Hernandez, H., Hu, J., Schaffner, A., Pankratz, N., Hsu, N. Y., Chuang, L. S., Carmi, S., Villaverde, N., Li, X., Rivas, M., Levine, A. P., Bao, X., Labrias, P. R., Haritunians, T., Ruane, D., Gettler, K., Chen, E., Li, D., Schiff, E. R. & 31 others, Pontikos, N., Barzilai, N., Brant, S. R., Bressman, S., Cheifetz, A. S., Clark, L. N., Daly, M. J., Desnick, R. J., Duerr, R. H., Katz, S., Lencz, T., Myers, R. H., Ostrer, H., Ozelius, L., Payami, H., Peter, Y., Rioux, J. D., Segal, A. W., Scott, W. K., Silverberg, M. S., Vance, J. M., Ubarretxena-Belandia, I., Foroud, T., Atzmon, G., Pe'er, I., Ioannou, Y., McGovern, D. P. B., Yue, Z., Schadt, E. E., Cho, J. H. & Peter, I., Jan 10 2018, In : Science Translational Medicine. 10, 423, eaai7795.

Research output: Contribution to journalArticle

59 Scopus citations
2012

Derivation of autism spectrum disorder-specific induced pluripotent stem cells from peripheral blood mononuclear cells

DeRosa, B. A., Van Baaren, J. M., Dubey, G. K., Lee, J. M., Cuccaro, M., Vance, J. M., Pericak-Vance, M. A. & Dykxhoorn, D. M., May 10 2012, In : Neuroscience Letters. 516, 1, p. 9-14 6 p.

Research output: Contribution to journalArticle

44 Scopus citations
2011

Thrombotic storm revisited: Preliminary diagnostic criteria suggested by the thrombotic storm study group

Kitchens, C. S., Erkan, D., Brando, L. R., Hahn, S., James, A. H., Kulkarni, R., Pericak-Vance, M. A., Vance, J. M. & Ortel, T. L., Apr 1 2011, In : American Journal of Medicine. 124, 4, p. 290-296 7 p.

Research output: Contribution to journalArticle

26 Scopus citations
2017

Early-onset Alzheimer disease and candidate risk genes involved in endolysosomal transport

Kunkle, B. W., Vardarajan, B. N., Naj, A. C., Whitehead, P. L., Rolati, S., Slifer, S., Carney, R. M., Cuccaro, M., Vance, J. M., Gilbert, J., Wang, L. S., Farrer, L. A., Reitz, C., Haines, J. L., Beecham, G. W., Martin, E. R., Schellenberg, G. D., Mayeux, R. P. & Pericak-Vance, M. A., Sep 1 2017, In : JAMA Neurology. 74, 9, p. 1113-1122 10 p.

Research output: Contribution to journalArticle

8 Scopus citations
2012

A recurrent loss-of-function alanyl-tRNA synthetase (AARS) mutation in patients with charcot-marie-tooth disease type 2N (CMT2N)

McLaughlin, H. M., Sakaguchi, R., Giblin, W., Wilson, T. E., Biesecker, L., Lupski, J. R., Talbot, K., Vance, J. M., Zuchner, S. L., Lee, Y. C., Kennerson, M., Hou, Y. M., Nicholson, G. & Antonellis, A., Jan 1 2012, In : Human Mutation. 33, 1, p. 244-253 10 p.

Research output: Contribution to journalArticle

54 Scopus citations
2016

Overlap between Parkinson disease and Alzheimer disease in ABCA7 functional variants

Nuytemans, K., Maldonado, L., Ali, A., John-Williams, K., Beecham, G. W., Martin, E. R., Scott, W. K. & Vance, J. M., Feb 1 2016, In : Neurology: Genetics. 2, 1, e44.

Research output: Contribution to journalArticle

10 Scopus citations
2019

The Puerto Rico Alzheimer disease initiative (PRADI): A multisource ascertainment approach

Feliciano-Astacio, B. E., Celis, K., Ramos, J., Rajabli, F., Adams, L. D., Rodriguez, A., Rodriguez, V., Bussies, P. L., Sierra, C., Manrique, P., Mena, P. R., Grana, A., Prough, M., Hamilton-Nelson, K. L., Feliciano, N., Chinea, A., Acosta, H., McCauley, J. L., Vance, J. M., Beecham, G. W. & 2 others, Pericak-Vance, M. A. & Cuccaro, M. L., Jan 1 2019, In : Frontiers in Genetics. 10, JUN, 538.

Research output: Contribution to journalArticle

Open Access
2014

Detecting genetic interactions in pathway-based genome-wide association studies

Huang, A., Martin, E. R., Vance, J. M. & Cai, X., Jan 1 2014, In : Genetic Epidemiology. 38, 4, p. 300-309 10 p.

Research output: Contribution to journalArticle

10 Scopus citations
2015

Global and local ancestry in African-Americans: Implications for Alzheimer's disease risk

Hohman, T. J., Cooke-Bailey, J. N., Reitz, C., Jun, G., Naj, A., Beecham, G. W., Liu, Z., Carney, R. M., Vance, J. M., Cuccaro, M., Rajbhandary, R., Vardarajan, B. N., Wang, L. S., Valladares, O., Lin, C. F., Larson, E. B., Graff-Radford, N. R., Evans, D., De Jager, P. L., Crane, P. K. & 33 others, Buxbaum, J. D., Murrell, J. R., Raj, T., Ertekin-Taner, N., Logue, M. W., Baldwin, C. T., Green, R. C., Barnes, L. L., Cantwell, L. B., Fallin, M. D., Go, R. C. P., Griffith, P., Obisesan, T. O., Manly, J. J., Lunetta, K. L., Kamboh, M. I., Lopez, O. L., Bennett, D. A., Hardy, J., Hendrie, H. C., Hall, K. S., Goate, A. M., Lang, R., Byrd, G. S., Kukull, W. A., Foroud, T. M., Farrer, L. A., Martin, E. R., Pericak-Vance, M. A., Schellenberg, G. D., Mayeux, R., Haines, J. L. & Thornton-Wells, T. A., 2015, (Accepted/In press) In : Alzheimer's and Dementia.

Research output: Contribution to journalArticle

9 Scopus citations
2011

Vitamin D Receptor Gene as a Candidate Gene for Parkinson Disease

Butler, M. W., Burt, A., Edwards, T. L., Zuchner, S. L., Scott, W. K., Martin, E. R., Vance, J. M. & Wang, L., Mar 1 2011, In : Annals of Human Genetics. 75, 2, p. 201-210 10 p.

Research output: Contribution to journalArticle

77 Scopus citations

Comparison of three targeted enrichment strategies on the Solid sequencing platform

Hedges, D. J., Guettouche, T., Yang, S., Bademci, G., Diaz, A., Andersen, A., Hulme, W. F., Linker, S., Mehta, A., Edwards, Y. J. K., Beecham, G. W., Martin, E. R., Pericak-Vance, M. A., Zuchner, S. L., Vance, J. M. & Gilbert, J., May 12 2011, In : PLoS One. 6, 4, e18595.

Research output: Contribution to journalArticle

60 Scopus citations
2014

A Recurrent Loss-of-Function Alanyl-tRNA Synthetase (AARS) Mutation in Patients with Charcot-Marie-Tooth Disease Type 2N (CMT2N)

Mclaughlin, H. M., Sakaguchi, R., Giblin, W., Wilson, T. E., Biesecker, L., Lupski, J. R., Talbot, K., Vance, J. M., Zuchner, S. L., Lee, Y. C., Kennerson, M., Hou, Y. M., Nicholson, G. & Antonellis, A., Jan 1 2014, In : Human Mutation. 35, 4, p. 512-512 1 p.

Research output: Contribution to journalArticle

1 Scopus citations
2012

Clinical causes and treatment of the thrombotic storm

Ortel, T. L., Kitchens, C. S., Erkan, D., Brandão, L. R., Hahn, S., James, A. H., Kulkarni, R., Manco-Johnson, M. J., Pericak-Vance, M. A. & Vance, J. M., Dec 1 2012, In : Expert Review of Hematology. 5, 6, p. 553-559 7 p.

Research output: Contribution to journalArticle

13 Scopus citations
2019

Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Alzheimer Disease Genetics Consortium (ADGC), European Alzheimer’s Disease Initiative (EADI), Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium (CHARGE), & Genetic and Environmental Risk in AD/Defining Genetic, Polygenic and Environmental Risk for Alzheimer’s Disease Consortium (GERAD/PERADES), Mar 1 2019, In : Nature genetics. 51, 3, p. 414-430 17 p.

Research output: Contribution to journalArticle

92 Scopus citations
2018

Convergent Pathways in Idiopathic Autism Revealed by Time Course Transcriptomic Analysis of Patient-Derived Neurons

Derosa, B. A., El Hokayem, J., Artimovich, E., Garcia-Serje, C., Phillips, A. W., Van Booven, D., Nestor, J. E., Wang, L., Cuccaro, M. L., Vance, J. M., Pericak-Vance, M. A., Cukier, H. N., Nestor, M. W. & Dykxhoorn, D. M., Dec 1 2018, In : Scientific Reports. 8, 1, 8423.

Research output: Contribution to journalArticle

16 Scopus citations
2014

Absence of C9ORF72 expanded or intermediate repeats in autopsy-confirmed Parkinson's disease

Nuytemans, K., Inchausti, V., Beecham, G. W., Wang, L., Dickson, D. W., Trojanowski, J. Q., Lee, V. M. Y., Mash, D. C., Frosch, M. P., Foroud, T. M., Honig, L. S., Montine, T. J., Dawson, T. M., Martin, E. R., Scott, W. K. & Vance, J. M., Jan 1 2014, In : Movement Disorders. 29, 6, p. 827-830 4 p.

Research output: Contribution to journalArticle

18 Scopus citations
2011

Mutation screening of mitofusin 2 in Charcot-Marie-Tooth disease type 2

McCorquodale, D. S., Montenegro, G., Peguero, A., Carlson, N., Speziani, F., Price, J., Taylor, S. W., Melanson, M., Vance, J. M. & Zuchner, S. L., Jul 1 2011, In : Journal of Neurology. 258, 7, p. 1234-1239 6 p.

Research output: Contribution to journalArticle

26 Scopus citations
2016

hVMAT2: A Target of Individualized Medication for Parkinson’s Disease

Xiong, N., Li, N., Martin, E. R., Yu, J., Li, J., Liu, J., Lee, D. Y. W., Isacson, O., Vance, J. M., Qing, H., Wang, T. & Lin, Z., May 2 2016, (Accepted/In press) In : Neurotherapeutics. p. 1-12 12 p.

Research output: Contribution to journalArticle

4 Scopus citations
2013

Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease

Nuytemans, K., Bademci, G., Inchausti, V., Dressen, A., Kinnamon, D. D., Mehta, A., Wang, L., Zuchner, S. L., Beecham, G. W., Martin, E. R., Scott, W. K. & Vance, J. M., Mar 12 2013, In : Neurology. 80, 11, p. 982-989 8 p.

Research output: Contribution to journalArticle

50 Scopus citations
2011

Exome sequencing allows for rapid gene identification in a Charcot-Marie-Tooth family

Montenegro, G., Powell, E., Huang, J., Speziani, F., Edwards, Y. J. K., Beecham, G. W., Hulme, W., Siskind, C., Vance, J. M., Shy, M. & Zuchner, S. L., Mar 1 2011, In : Annals of Neurology. 69, 3, p. 464-470 7 p.

Research output: Contribution to journalArticle

93 Scopus citations
2012

Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDgene database

Lill, C. M., Roehr, J. T., McQueen, M. B., Kavvoura, F. K., Bagade, S., Schjeide, B. M. M., Schjeide, L. M., Meissner, E., Zauft, U., Allen, N. C., Liu, T., Schilling, M., Anderson, K. J., Beecham, G. W., Berg, D., Biernacka, J. M., Brice, A., DeStefano, A. L., Do, C. B., Eriksson, N. & 34 others, Factor, S. A., Farrer, M. J., Foroud, T., Gasser, T., Hamza, T., Hardy, J. A., Heutink, P., Hill-Burns, E. M., Klein, C., Latourelle, J. C., Maraganore, D. M., Martin, E. R., Martinez, M., Myers, R. H., Nalls, M. A., Pankratz, N., Payami, H., Satake, W., Scott, W. K., Sharma, M., Singleton, A. B., Stefansson, K., Toda, T., Tung, J. Y., Vance, J. M., Wood, N. W., Zabetian, C. P., Young, P., Tanzi, R. E., Khoury, M. J., Zipp, F., Lehrach, H., Ioannidis, J. P. A. & Bertram, L., Mar 1 2012, In : PLoS Genetics. 8, 3, e1002548.

Research output: Contribution to journalArticle

356 Scopus citations
2013

Genomic Signatures of a Global Fitness Index in a Multi-Ethnic Cohort of Women

Rampersaud, E., Nathanson, L., Farmer, J., Meshbane, K., Belton, R. L., Dressen, A., Cuccaro, M., Musto, A., Daunert, S., Deo, S. K., Hudson, N., Vance, J. M., Seo, D. M., Mendez, A. J., Dykxhoorn, D. M., Pericak-Vance, M. A. & Goldschmidt-Clermont, P., Mar 1 2013, In : Annals of Human Genetics. 77, 2, p. 147-157 11 p.

Research output: Contribution to journalArticle

4 Scopus citations
2011

Whole-exome sequencing links a variant in DHDDS to retinitis pigmentosa

Zuchner, S. L., Dallman, J., Wen, R., Beecham, G. W., Naj, A., Farooq, A., Kohli, M. A., Whitehead, P. L., Hulme, W., Konidari, I., Edwards, Y. J. K., Cai, G., Peter, I., Seo, D. M., Buxbaum, J. D., Haines, J. L., Blanton, S. H., Young, J., Alfonso, E. C., Vance, J. M. & 2 others, Lam, B. L. & Pericak-Vance, M. A., Feb 11 2011, In : American Journal of Human Genetics. 88, 2, p. 201-206 6 p.

Research output: Contribution to journalArticle

107 Scopus citations
2017

Generation of disease-specific autopsy-confirmed iPSCs lines from postmortem isolated Peripheral Blood Mononuclear Cells

Belle, K., Shabazz, F. S., Nuytemans, K., Davis, D. A., Ali, A., Young, J., Scott, W. K., Mash, D. C., Vance, J. M. & Dykxhoorn, D. M., Jan 10 2017, In : Neuroscience Letters. 637, p. 201-206 6 p.

Research output: Contribution to journalArticle

1 Scopus citations
2012

Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12

Montenegro, G., Rebelo, A. P., Connell, J., Allison, R., Babalini, C., D'Aloia, M., Montieri, P., Schüle, R., Ishiura, H., Price, J., Strickland, A., Gonzalez, M. A., Baumbach-Reardon, L., Deconinck, T., Huang, J., Bernardi, G., Vance, J. M., Rogers, M. T., Tsuji, S., De Jonghe, P. & 5 others, Pericak-Vance, M. A., Schöls, L., Orlacchio, A., Reid, E. & Zuchner, S. L., Feb 1 2012, In : Journal of Clinical Investigation. 122, 2, p. 538-544 7 p.

Research output: Contribution to journalArticle

91 Scopus citations
2011

A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism

Hussman, J. P., Chung, R. H., Griswold, A., Jaworski, J. M., Salyakina, D., Ma, D., Konidari, I., Whitehead, P. L., Vance, J. M., Martin, E. R., Cuccaro, M., Gilbert, J., Haines, J. L. & Pericak-Vance, M. A., Dec 1 2011, In : Molecular Autism. 2, 1, 1.

Research output: Contribution to journalArticle

102 Scopus citations
2015

Genome-wide linkage analyses of non-Hispanic white families identify novel loci for familial late-onset Alzheimer's disease

Kunkle, B. W., Jaworski, J., Barral, S., Vardarajan, B., Beecham, G. W., Martin, E. R., Cantwell, L. S., Partch, A., Bird, T. D., Raskind, W. H., Destefano, A. L., Carney, R. M., Cuccaro, M., Vance, J. M., Farrer, L. A., Goate, A. M., Foroud, T., Mayeux, R. P., Schellenberg, G. D., Haines, J. L. & 1 others, Pericak-Vance, M. A., 2015, (Accepted/In press) In : Alzheimer's and Dementia.

Research output: Contribution to journalArticle

10 Scopus citations
2018

Ancestral origin of ApoE ε4 Alzheimer disease risk in Puerto Rican and African American populations

Rajabli, F., Feliciano, B. E., Celis, K., Hamilton-Nelson, K. L., Whitehead, P. L., Adams, L. D., Bussies, P. L., Manrique, C. P., Rodriguez, A., Rodriguez, V., Starks, T., Byfield, G. E., Sierra Lopez, C. B., McCauley, J. L., Acosta, H., Chinea, A., Kunkle, B. W., Reitz, C., Farrer, L. A., Schellenberg, G. D. & 8 others, Vardarajan, B. N., Vance, J. M., Cuccaro, M., Martin, E. R., Haines, J. L., Byrd, G. S., Beecham, G. W. & Pericak-Vance, M. A., Dec 1 2018, In : PLoS Genetics. 14, 12, e1007791.

Research output: Contribution to journalArticle

Open Access
8 Scopus citations
2011

Genomic medicine and neurology

Vance, J. M. & Tekin, D., Apr 1 2011, In : CONTINUUM Lifelong Learning in Neurology. 17, 2, p. 249-267 19 p.

Research output: Contribution to journalArticle

3 Scopus citations
2016

GWAS analysis implicates NF-κB-mediated induction of inflammatory T cells in multiple sclerosis

Hussman, J. P., Beecham, A. H., Schmidt, M., Martin, E. R., McCauley, J. L., Vance, J. M., Haines, J. L. & Pericak-Vance, M. A., Jun 9 2016, (Accepted/In press) In : Genes and Immunity.

Research output: Contribution to journalArticle

22 Scopus citations

ABCA7 frameshift deletion associated with Alzheimer disease in African Americans

Cukier, H. N., Kunkle, B. W., Vardarajan, B. N., Rolati, S., Hamilton-Nelson, K. L., Kohli, M. A., Whitehead, P. L., Dombroski, B. A., Van Booven, D., Lang, R., Dykxhoorn, D. M., Farrer, L. A., Cuccaro, M., Vance, J. M., Gilbert, J., Beecham, G. W., Martin, E. R., Carney, R. M., Mayeux, R., Schellenberg, G. D. & 3 others, Byrd, G. S., Haines, J. L. & Pericak-Vance, M. A., Jun 1 2016, In : Neurology: Genetics. 2, 3, e79.

Research output: Contribution to journalArticle

19 Scopus citations

Segregation of a rare TTC3 variant in an extended family with late-onset Alzheimer disease

Kohli, M. A., Cukier, H. N., Hamilton-Nelson, K. L., Rolati, S., Kunkle, B. W., Whitehead, P. L., Zuchner, S. L., Farrer, L. A., Martin, E. R., Beecham, G. W., Haines, J. L., Vance, J. M., Cuccaro, M., Gilbert, J., Schellenberg, G. D., Carney, R. M. & Pericak-Vance, M. A., Feb 1 2016, In : Neurology: Genetics. 2, 1, e41.

Research output: Contribution to journalArticle

18 Scopus citations
2017

Targeted sequencing of ABCA7 identifies splicing, stop-gain and intronic risk variants for Alzheimer disease

Kunkle, B. W., Carney, R. M., Kohli, M. A., Naj, A. C., Hamilton-Nelson, K. L., Whitehead, P. L., Wang, L., Lang, R., Cuccaro, M., Vance, J. M., Byrd, G. S., Beecham, G. W., Gilbert, J., Martin, E. R., Haines, J. L. & Pericak-Vance, M. A., May 10 2017, In : Neuroscience Letters. 649, p. 124-129 6 p.

Research output: Contribution to journalArticle

4 Scopus citations
2011

Convergence of mirna expression profiling, α-synuclein interacton and GWAS in Parkinson's disease

Martins, M., Rosa, A., Guedes, L. C., Fonseca, B. V., Gotovac, K., Violante, S., Mestre, T., Coelho, M., RosaMá, M. M., Martin, E. R., Vance, J. M., Outeiro, T. F., Wang, L., Borovecki, F., Ferreira, J. J. & Oliveira, S. A., Oct 7 2011, In : PLoS One. 6, 10, e25443.

Research output: Contribution to journalArticle

137 Scopus citations
2014
5 Scopus citations
3 Scopus citations
2019

Author Correction: Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (Nature Genetics, (2019), 51, 3, (414-430), 10.1038/s41588-019-0358-2)

Alzheimer Disease Genetics Consortium (ADGC), The European Alzheimer’s Disease Initiative (EADI), Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium (CHARGE) & Genetic and Environmental Risk in AD/Defining Genetic, Polygenic and Environmental Risk for Alzheimer’s Disease Consortium (GERAD/PERADES), Sep 1 2019, In : Nature genetics. 51, 9, p. 1423-1424 2 p.

Research output: Contribution to journalComment/debate

Open Access
2018

2017 year in review and message from the editors to our reviewers

Pulst, S. M., Johnson, N. E., Pandolfo, M., Roos, R. P. & Vance, J. M., Feb 1 2018, In : Neurology: Genetics. 4, 1, e221.

Research output: Contribution to journalReview article

2016

2016 in review and message from the Editors to Our Reviewers

Pulst, S. M., Johnson, N. E., Durr, A., Pandolfo, M., Roos, R. P. & Vance, J. M., Jan 1 2016, In : Neurology: Genetics. 3, 1, e132.

Research output: Contribution to journalReview article

2019

Motivations for participation in Parkinson disease genetic research among hispanics versus non-hispanics

Nuytemans, K., Manrique, C. P., Uhlenberg, A., Scott, W. K., Cuccaro, M. L., Luca, C., Singer, C. & Vance, J. M., Jan 1 2019, In : Frontiers in Genetics. 10, JUN, 658.

Research output: Contribution to journalComment/debate

Open Access
2013

C9orf72 intermediate repeat copies are a significant risk factor for parkinson disease

Nuytemans, K., Bademci, G., Kohli, M. M., Beecham, G. W., Wang, L., Young, J., Nahab, F., Martin, E. R., Gilbert, J., Benatar, M. G., Haines, J. L., Scott, W. K., Zuchner, S. L., Pericak-Vance, M. A. & Vance, J. M., Sep 1 2013, In : Annals of Human Genetics. 77, 5, p. 351-363 13 p.

Research output: Contribution to journalArticle

46 Scopus citations
2016

DNA variants in CACNA1C modify Parkinson disease risk only when Vitamin D level is deficient

Wang, L., Maldonado, L., Beecham, G. W., Martin, E. R., Evatt, M. L., Ritchie, J. C., Haines, J. L., Zabetian, C. P., Payami, H., Pericak-Vance, M. A., Vance, J. M. & Scott, W. K., Jun 1 2016, In : Neurology: Genetics. 2, 3, e72.

Research output: Contribution to journalArticle

4 Scopus citations
2015

PARK10 is a major locus for sporadic neuropathologically confirmed Parkinson disease

Beecham, G. W., Dickson, D. W., Scott, W. K., Martin, E. R., Schellenberg, G., Nuytemans, K., Larson, E. B., Buxbaum, J. D., Trojanowski, J. Q., Van Deerlin, V. M., Hurtig, H. I., Mash, D. C., Beach, T. G., Troncoso, J. C., Pletnikova, O., Frosch, M. P., Ghetti, B., Foroud, T. M., Honig, L. S., Marder, K. & 12 others, Vonsattel, J. P., Goldman, S. M., Vinters, H. V., Ross, O. A., Wszolek, Z. K., Wang, L., Dykxhoorn, D. M., Pericak-Vance, M. A., Montine, T. J., Leverenz, J. B., Dawson, T. M. & Vance, J. M., Mar 10 2015, In : Neurology. 84, 10, p. 972-980 9 p.

Research output: Contribution to journalArticle

28 Scopus citations