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Author Details
Full Name
Susana Eyheramendy
Affiliation
Universidad Adolfo Ibanez
ORCID
Career Start Year
2007
Papers
26
H Index
14
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36844456
New insights from GWAS on BMI-related growth traits in a longitudinal cohort of admixed children with Native American and European ancestry.
iScience
2023
34047840
Novel loci and Mapuche genetic ancestry are associated with pubertal growth traits in Chilean boys.
Hum Genet
2021
34786538
Screening of COVID-19 cases through a Bayesian network symptoms model and psychophysical olfactory test.
iScience
2021
34345942
Correction to: Novel loci and mapuche genetic ancestry are associated with pubertal growth traits in Chilean boys.
Hum Genet
2021
32614437
Postadmixture Selection on Chileans Targets Haplotype Involved in Pigmentation, Thermogenesis and Immune Defense against Pathogens.
Genome Biol Evol
2020
31915828
A Polygenic Risk Score Suggests Shared Genetic Architecture of Voice Break With Early Markers of Pubertal Onset in Boys.
J Clin Endocrinol Metab
2020
30765821
Whole Genome Sequence, Variant Discovery and Annotation in Mapuche-Huilliche Native South Americans.
Sci Rep
2019
31384924
Adaptation to Extreme Environments in an Admixed Human Population from the Atacama Desert.
Genome Biol Evol
2019
28132020
Simultaneous Modeling of Disease Status and Clinical Phenotypes To Increase Power in Genome-Wide Association Studies.
Genetics
2017
25778948
Genetic structure characterization of Chileans reflects historical immigration patterns.
Nat Commun
2015
22581622
Genome-wide association mapping with longitudinal data.
Genet Epidemiol
2012
23151256
APOA5 Q97X mutation identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous family.
BMC Med Genet
2012
21686131
Effect of genome-wide simultaneous hypotheses tests on the discovery rate.
Int J Mol Epidemiol Genet
2011
21909115
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
Nature
2011
21909110
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.
Nat Genet
2011
21082022
Genome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension.
PLoS Genet
2010
19304780
Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations.
Hum Mol Genet
2009
20031576
Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts.
Circ Cardiovasc Genet
2009
19430483
Genome-wide association study identifies eight loci associated with blood pressure.
Nat Genet
2009
19347040
Polymorphisms in the WNK1 gene are associated with blood pressure variation and urinary potassium excretion.
PLoS One
2009
19562039
Targeting 160 candidate genes for blood pressure regulation with a genome-wide genotyping array.
PLoS One
2009
18391950
Identification of ten loci associated with height highlights new biological pathways in human growth.
Nat Genet
2008
18842065
SLC2A9 is a high-capacity urate transporter in humans.
PLoS Med
2008
17095708
A model-based approach to capture genetic variation for future association studies.
Genome Res
2007
17943122
A second generation human haplotype map of over 3.1 million SNPs.
Nature
2007
17943131
Genome-wide detection and characterization of positive selection in human populations.
Nature
2007
1 - 26 of 26
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London NorthWest Healthcare NHS Trust
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