Follow
Maria Loreto Munoz Venegas
Title
Cited by
Cited by
Year
Validity of (ultra-) short recordings for heart rate variability measurements
ML Munoz, A Van Roon, H Riese, C Thio, E Oostenbroek, I Westrik, ...
PloS one 10 (9), e0138921, 2015
3212015
A decade of genome-wide association studies for coronary artery disease: The challenges ahead
HS Jeanette Erdmann, Thorsten Kessler, Loretto Munoz
Cardiovascular Research, 2018
3192018
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants
KG Aragam, T Jiang, A Goel, S Kanoni, BN Wolford, DS Atri, EM Weeks, ...
Nature genetics 54 (12), 1803-1815, 2022
1892022
Genetic loci associated with heart rate variability and their effects on cardiac disease risk
IM Nolte, ML Munoz, V Tragante, AT Amare, R Jansen, A Vaez, ...
Nature communications 8 (1), 15805, 2017
1322017
Transfrontal three‐dimensional visualization of midline cerebral structures
F Vinals, M Munoz, R Naveas, A Giuliano
Ultrasound in Obstetrics and Gynecology: The Official Journal of the …, 2007
772007
Genome-wide association meta-analysis of coronary artery disease and periodontitis reveals a novel shared risk locus
M Munz, GM Richter, BG Loos, S Jepsen, K Divaris, S Offenbacher, ...
Scientific reports 8 (1), 13678, 2018
472018
QCGWAS: A flexible R package for automated quality control of genome-wide association results.
PJ van der Most, A Vaez, BP Prins, ML Munoz, H Snieder, BZ Alizadeh, ...
Bioinformatics, 2014
332014
Heritability and genetic correlations of heart rate variability at rest and during stress in the Oman Family Study
ML Muņoz, D Jaju, S Voruganti, S Albarwani, A Aslani, R Bayoumi, ...
Journal of hypertension 36 (7), 1477-1485, 2018
182018
Identifying genetic variants for heart rate variability in the acetylcholine pathway
H Riese, LM Munoz, CA Hartman, X Ding, S Su, AJ Oldehinkel, ...
PLoS One 9 (11), e112476, 2014
162014
Heritability of ambulatory and beat-to-beat office blood pressure in large multigenerational Arab pedigrees: the ‘Oman Family study’
S Albarwani, ML Munoz, VS Voruganti, D Jaju, VS Al-Yahyaee, SG Rizvi, ...
Twin Research and Human Genetics 15 (6), 753-758, 2012
152012
Impact of depression and psychosocial treatment on heart rate variability in patients with type 2 diabetes mellitus: an exploratory analysis based on the HEIDIS trial
V Zimmermann-Schlegel, B Wild, P Nawroth, S Kopf, W Herzog, ...
Experimental and Clinical Endocrinology & Diabetes 127 (06), 367-376, 2019
142019
Association of Genetic Variation at AQP4 Locus with Vascular Depression
AL Westermair, M Munz, A Schaich, S Nitsche, B Willenborg, ...
Biomolecules 8 (4), 164, 2018
142018
Heritability and genetic correlations of obesity indices with ambulatory and office beat-to-beat blood pressure in the Oman Family Study
T Man, IM Nolte, D Jaju, ZAM Al-Anqoudi, ML Muņoz, MO Hassan, ...
Journal of hypertension 38 (8), 1474-1480, 2020
132020
Heritability and genetic and environmental correlations of heart rate variability and baroreceptor reflex sensitivity with ambulatory and beat-to-beat blood pressure
T Man, H Riese, D Jaju, ML Muņoz, MO Hassan, S Al-Yahyaee, ...
Scientific reports 9 (1), 1664, 2019
112019
Iris Westrik, Eco JC De Geus, Ron Gansevoort, Joop Lefrandt, Ilja M. Nolte, and Harold Snieder. 2015. Validity of (Ultra-) Short recordings for heart rate variability measurements
ML Munoz, A Van Roon, H Riese, C Thio, E Oostenbroek
PloS one 10 (9), e0138921, 2015
72015
Deficiency of ZC3HC1 increases vascular smooth muscle cell migration, proliferation and neointima formation following injury
R Aherrahrou, T Reinberger, J Werner, M Otto, J Al-Hasani, ...
bioRxiv, 2021
22021
Genome-wide association study of over one million participants identifies 49 novel loci associated with coronary artery disease
KG Aragam, T Jiang, S Kanoni, G Anuj, B Wolford, I Surakka, C Grace, ...
Circulation 140 (Suppl_1), A15391-A15391, 2019
22019
Chapter 4: The Genetics of Coronary Heart Disease
ML Erdmann, Jeanette and Munoz Venegas
Genetic Causes of Cardiac Disease, 2019
12019
The genetics of heart rate variability
MLM Venegas
12016
Deficiency of ZC3HC1 modulates vascular smooth muscle cell phenotype and increases neointima formation
R Aherrahrou, T Reinberger, J Werner, M Otto, J Al-Hasani, ...
bioRxiv, 2021.09. 29.462212, 2021
2021
The system can't perform the operation now. Try again later.
Articles 1–20