Dena Hernandez

发表

Genomic Variation in Seven Khoe-San Groups Reveals Adaptation and Complex African History

Mattias Jakobsson, Flora Jay, Michael G. B. Blum, 2012, Science.

A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)

Mark I. McCarthy, Luigi Ferrucci, Kara Stevens, 2008, PLoS genetics.

Correction: Corrigendum: Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis

Christian Gieger, Thomas Meitinger, Andres Metspalu, 2015, Nature Communications.

A meta-analysis of four genome-wide association studies of survival to age 90 years or older: the Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium.

Sudha Seshadri, Ralph B D'Agostino, Vilmundur Gudnason, 2010, The journals of gerontology. Series A, Biological sciences and medical sciences.

Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes.

Luigi Ferrucci, Sven Bergmann, Vincent Mooser, 2008, American journal of human genetics.

Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium

Christian Gieger, Ming-Huei Chen, Luigi Ferrucci, 2009, Nature Genetics.

Discovery and Refinement Supplementary

Christian Gieger, Cisca Wijmenga, Inês Barroso, 2015 .

CUBN is a gene locus for albuminuria.

Sylvia Stracke, Ming-Huei Chen, Luigi Ferrucci, 2011, Journal of the American Society of Nephrology : JASN.

Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals.

Sonja W. Scholz, John Hardy, Mar Matarin, 2007, Human molecular genetics.

Genetic Variants in Novel Pathways Influence Blood Pressure and Cardiovascular Disease Risk

Christian Gieger, Xiaofeng Zhu, Paolo Vineis, 2011, Nature.

A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release

Sonja W. Scholz, Scott Silliman, Carl D Langefeld, 2007, The Lancet Neurology.

Genome-wide physical activity interactions in adiposity. A meta-analysis of 200,452 adults

Claude Bouchard, Christian Gieger, Tuija Tammelin, 2017 .

Genome-Wide Association Study of White Blood Cell Count in 16,388 African Americans: the Continental Origins and Genetic Epidemiology Network (COGENT)

Yusuke Nakamura, Yukinori Okada, David Couper, 2011, PLoS genetics.

α-synuclein gene haplotypes are associated with Parkinson’s disease

Matthew J. Farrer, John Hardy, Mariza de Andrade, 2001 .

Mutation at the SCA17 locus is not a common cause of parkinsonism.

John Hardy, Bernard Ravina, Melissa Hanson, 2003, Parkinsonism & related disorders.

Genome-wide screen identifies rs646776 near sortilin as a regulator of progranulin levels in human plasma.

Allissa Dillman, Ronald C Petersen, Mark R Cookson, 2010, American journal of human genetics.

Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic risk.

Peter Holmans, Alexandra Durr, Manu Sharma, 2013, JAMA neurology.

Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

Christian Gieger, Jingyuan Fu, Thomas Meitinger, 2011, Nature Genetics.

Deletion at ITPR1 Underlies Ataxia in Mice and Spinocerebellar Ataxia 15 in Humans

Paola Giunti, Sonja W. Scholz, Elsdon Storey, 2007, PLoS genetics.

Early‐onset Parkinson's disease caused by a compound heterozygous DJ‐1 mutation

Vincenzo Bonifati, John Hardy, Peter Heutink, 2003, Annals of neurology.

Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease

Tatiana Foroud, Nathan Pankratz, Shushant Jain, 2005, The Lancet.