Articles with public access mandates - Zoltán KutalikLearn more
Not available anywhere: 9
Review
Mendelian randomization to assess causality between uromodulin, blood pressure and chronic kidney disease
B Ponte, MC Sadler, E Olinger, P Vollenweider, M Bochud, ...
Kidney international 100 (6), 1282-1291, 2021
Mandates: Swiss National Science Foundation, British Heart Foundation, UK Medical …
Review
Using instrumental variables to estimate the attributable fraction
E Dahlqwist, Z Kutalik, A Sjölander
Statistical methods in medical research 29 (8), 2063-2073, 2020
Mandates: Swiss National Science Foundation, Swedish Research Council, UK Medical …
Review
Heterogeneity in obesity: genetic basis and metabolic consequences
J Sulc, TW Winkler, IM Heid, Z Kutalik
Current diabetes reports 20, 1-8, 2020
Mandates: Swiss National Science Foundation, Federal Ministry of Education and …
Review
Dysregulation of a long noncoding RNA reduces leptin leading to a leptin-responsive form of obesity
OS Dallner, JM Marinis, YH Lu, K Birsoy, E Werner, G Fayzikhodjaeva, ...
Nature medicine 25 (3), 507-516, 2019
Mandates: US National Institutes of Health, Swedish Research Council
Review
Genetic and clinic predictors of new onset diabetes mellitus after transplantation
N Saigi-Morgui, L Quteineh, PY Bochud, S Crettol, Z Kutalik, NJ Mueller, ...
The pharmacogenomics journal 19 (1), 53-64, 2019
Mandates: Swiss National Science Foundation
Review
48th European Mathematical Genetics Meeting (EMGM) 2020: Lausanne, Switzerland, April 16–17, 2020
Z Kutalik, M Robinson
Mandates: European Commission
Review
Novel method to estimate the phenotypic variation explained by genome‐wide association studies reveals large fraction of the missing heritability
Z Kutalik, J Whittaker, D Waterworth, GIANT consortium, JS Beckmann, ...
Genetic epidemiology 35 (5), 341-349, 2011
Mandates: Swiss National Science Foundation
Review
Genome-wide association study identifies new HLA class II haplotypes strongly protective against narcolepsy
H Hor, Z Kutalik, Y Dauvilliers, A Valsesia, GJ Lammers, ...
Nature genetics 42 (9), 786-789, 2010
Mandates: Swiss National Science Foundation
Review
Penetrance of marked cognitive impairment in older male carriers of the FMR1 gene premutation
M Sevin, Z Kutalik, S Bergman, M Vercelletto, P Renou, E Lamy, ...
Journal of Medical Genetics 46 (12), 818-824, 2009
Mandates: Swiss National Science Foundation
Available somewhere: 304
Review
SMIM1 absence is associated with reduced energy expenditure and excess weight
L Stefanucci, C Moslemi, AR Tomé, S Virtue, G Bidault, NS Gleadall, ...
Med, 2024
Mandates: National Institute for Health Research, UK
Review
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits
JM Keaton, Z Kamali, T Xie, A Vaez, A Williams, SB Goleva, A Ani, ...
Nature genetics, 1-14, 2024
Mandates: National Institute for Health Research, UK
Review
Leveraging large-scale biobank EHRs to enhance pharmacogenetics of cardiometabolic disease medications
MC Sadler, A Apostolov, C Cevallos, DM Ribeiro, RB Altman, Z Kutalik
medRxiv, 2024
Mandates: Chan Zuckerberg Initiative
Review
The human-specific BOLA2 duplication modifies iron homeostasis and anemia predisposition in chromosome 16p11. 2 autism patients
RA Philpott, Z Kutalik, MD Fleming, EE Eichler, A Reymond
Mandates: European Commission
Review
DNA methylation may partly explain psychotropic drug-induced metabolic side effects: results from a prospective 1-month observational study
C Dubath, E Porcu, A Delacrétaz, C Grosu, N Laaboub, M Piras, ...
Clinical Epigenetics 16 (1), 36, 2024
Mandates: Swiss National Science Foundation
Review
PheWAS-based clustering of Mendelian Randomisation instruments reveals distinct mechanism-specific causal effects between obesity and educational attainment
L Darrous, G Hemani, G Davey Smith, Z Kutalik
Nature Communications 15 (1), 1420, 2024
Mandates: Swiss National Science Foundation, Wellcome Trust
Review
Rare copy-number variants as modulators of common disease susceptibility
C Auwerx, M Jõeloo, MC Sadler, N Tesio, S Ojavee, CJ Clark, R Mägi, ...
Genome Medicine 16 (1), 5, 2024
Mandates: Swiss National Science Foundation, European Commission
Review
Disentangling mechanisms behind the pleiotropic effects of proximal 16p11. 2 BP4-5 CNVs
C Auwerx, S Moix, Z Kutalik, A Reymond
medRxiv, 2024.03. 20.24304613, 2024
Mandates: European Commission
Review
MR-link-2: pleiotropy robust cis Mendelian randomization validated in four independent gold-standard datasets of causality
A van der Graaf, R Warmerdam, CMP Auwerx, eQTLGen Consortium, ...
medRxiv, 2024.01. 22.24301400, 2024
Mandates: Swiss National Science Foundation, British Heart Foundation, Chief Scientist …
Review
Breaking down causes, consequences, and mediating effects of age-related telomere shortening on human health
S Moix, MC Sadler, Z Kutalik, C Auwerx
medRxiv, 2024.01. 12.24301196, 2024
Mandates: Swiss National Science Foundation
Review
Novel discoveries and enhanced genomic prediction from modelling genetic risk of cancer age-at-onset
ES Maksimova, SE Ojavee, K Läll, MC Sadler, R Mägi, Z Kutalik, ...
eLife 12, 2023
Mandates: Swiss National Science Foundation
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