Dan E. Arking
Dan E. Arking
Professor, Genetic Medicine, Johns Hopkins University
Email verificata su jhmi.edu - Home page
Citata da
Citata da
Transactivation of miR-34a by p53 broadly influences gene expression and promotes apoptosis
TC Chang, EA Wentzel, OA Kent, K Ramachandran, M Mullendore, ...
Molecular cell 26 (5), 745-752, 2007
Association between microdeletion and microduplication at 16p11. 2 and autism
LA Weiss, Y Shen, JM Korn, DE Arking, DT Miller, R Fossdal, ...
New England Journal of Medicine 358 (7), 667-675, 2008
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
GB Ehret, PB Munroe, KM Rice, M Bochud, AD Johnson, DI Chasman, ...
Nature 478 (7367), 103-109, 2011
Widespread microRNA repression by Myc contributes to tumorigenesis
TC Chang, D Yu, YS Lee, EA Wentzel, DE Arking, KM West, CV Dang, ...
Nature genetics 40 (1), 43-50, 2008
Dysregulation of TGF-β activation contributes to pathogenesis in Marfan syndrome
ER Neptune, PA Frischmeyer, DE Arking, L Myers, TE Bunton, B Gayraud, ...
Nature genetics 33 (3), 407-411, 2003
Genome-wide association study of blood pressure and hypertension
D Levy, GB Ehret, K Rice, GC Verwoert, LJ Launer, A Dehghan, ...
Nature genetics 41 (6), 677-687, 2009
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
SH Lee, S Ripke, BM Neale, SV Faraone, SM Purcell, RH Perlis, ...
Nature genetics 45 (9), 984-995, 2013
New loci associated with kidney function and chronic kidney disease
A Kttgen, C Pattaro, CA Bger, C Fuchsberger, M Olden, NL Glazer, ...
Nature genetics 42 (5), 376, 2010
Analysis of shared heritability in common disorders of the brain
V Anttila, B Bulik-Sullivan, HK Finucane, RK Walters, J Bras, L Duncan, ...
Science 360 (6395), 2018
From vulnerable plaque to vulnerable patient—part III: executive summary of the Screening for Heart Attack Prevention and Education (SHAPE) Task Force report
M Naghavi, E Falk, HS Hecht, MJ Jamieson, S Kaul, D Berman, Z Fayad, ...
The American journal of cardiology 98 (2), 2-15, 2006
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways
RA Scott, V Lagou, RP Welch, E Wheeler, ME Montasser, R Mgi, ...
Nature genetics 44 (9), 991-1005, 2012
Genomic alterations in cultured human embryonic stem cells
A Maitra, DE Arking, N Shivapurkar, M Ikeda, V Stastny, K Kassauei, G Sui, ...
Nature genetics 37 (10), 1099-1103, 2005
A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism
DE Arking, DJ Cutler, CW Brune, TM Teslovich, K West, M Ikeda, A Rea, ...
The American Journal of Human Genetics 82 (1), 160-164, 2008
A genome-wide linkage and association scan reveals novel loci for autism
LA Weiss, DE Arking
Nature 461 (7265), 802-808, 2009
Multiple loci associated with indices of renal function and chronic kidney disease
A Kttgen, NL Glazer, A Dehghan, SJ Hwang, R Katz, M Li, Q Yang, ...
Nature genetics 41 (6), 712-717, 2009
Meta-analysis identifies six new susceptibility loci for atrial fibrillation
PT Ellinor, KL Lunetta, CM Albert, NL Glazer, MD Ritchie, AV Smith, ...
Nature genetics 44 (6), 670-675, 2012
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization
DE Arking, A Pfeufer, W Post, WHL Kao, C Newton-Cheh, M Ikeda, K West, ...
Nature genetics 38 (6), 644-651, 2006
Genomewide association studies: history, rationale, and prospects for psychiatric disorders
Psychiatric GWAS Consortium Coordinating Committee
American Journal of Psychiatry 166 (5), 540-556, 2009
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence
JE Savage, PR Jansen, S Stringer, K Watanabe, J Bryois, CA De Leeuw, ...
Nature genetics 50 (7), 912-919, 2018
Association of human aging with a functional variant of klotho
DE Arking, A Krebsova, M Macek, A Arking, IS Mian, L Fried, A Hamosh, ...
Proceedings of the National Academy of Sciences 99 (2), 856-861, 2002
Il sistema al momento non pu eseguire l'operazione. Riprova pi tardi.
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