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Dina Vojinovic
Dina Vojinovic
Erasmus MC, Rotterdam, the Netherlands
Verified email at erasmusmc.nl
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Cited by
Year
The TREAT‐NMD DMD Global Database: analysis of more than 7,000 Duchenne muscular dystrophy mutations
CL Bladen, D Salgado, S Monges, ME Foncuberta, K Kekou, K Kosma, ...
Human mutation 36 (4), 395-402, 2015
7152015
Relationship between gut microbiota and circulating metabolites in population-based cohorts
D Vojinovic, D Radjabzadeh, A Kurilshikov, N Amin, C Wijmenga, ...
Nature communications 10 (1), 5813, 2019
2212019
Clinical outcomes in Duchenne muscular dystrophy: a study of 5345 patients from the TREAT-NMD DMD global database
Z Koeks, CL Bladen, D Salgado, E Van Zwet, O Pogoryelova, ...
Journal of neuromuscular diseases 4 (4), 293-306, 2017
1652017
A large-scale multi-ancestry genome-wide study accounting for smoking behavior identifies multiple significant loci for blood pressure
YJ Sung, TW Winkler, L de Las Fuentes, AR Bentley, MR Brown, AT Kraja, ...
The American Journal of Human Genetics 102 (3), 375-400, 2018
1492018
Metabolomic profiles predict individual multidisease outcomes
T Buergel, J Steinfeldt, G Ruyoga, M Pietzner, D Bizzarri, D Vojinovic, ...
Nature medicine 28 (11), 2309-2320, 2022
1342022
Multi-ancestry genome-wide gene–smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids
AR Bentley, YJ Sung, MR Brown, TW Winkler, AT Kraja, I Ntalla, ...
Nature genetics 51 (4), 636-648, 2019
1162019
Multiancestry genome-wide association study of lipid levels incorporating gene-alcohol interactions
PS De Vries, MR Brown, AR Bentley, YJ Sung, TW Winkler, I Ntalla, ...
American journal of epidemiology 188 (6), 1033-1054, 2019
1012019
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries
MF Feitosa, AT Kraja, DI Chasman, YJ Sung, TW Winkler, I Ntalla, X Guo, ...
PloS one 13 (6), e0198166, 2018
962018
Common genetic variation indicates separate causes for periventricular and deep white matter hyperintensities
NJ Armstrong, KA Mather, M Sargurupremraj, MJ Knol, R Malik, ...
Stroke 51 (7), 2111-2121, 2020
842020
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity
TO Kilpeläinen, AR Bentley, R Noordam, YJ Sung, K Schwander, ...
Nature communications 10 (1), 376, 2019
812019
Meta-analysis of epigenome-wide association studies of cognitive abilities
RE Marioni, AF McRae, J Bressler, E Colicino, E Hannon, S Li, D Prada, ...
Molecular psychiatry 23 (11), 2133-2144, 2018
782018
Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration
R Noordam, MM Bos, H Wang, TW Winkler, AR Bentley, TO Kilpeläinen, ...
Nature communications 10 (1), 5121, 2019
702019
Integration of epidemiologic, pharmacologic, genetic and gut microbiome data in a drug–metabolite atlas
J Liu, L Lahousse, MG Nivard, M Bot, L Chen, JB van Klinken, CS Thesing, ...
Nature medicine 26 (1), 110-117, 2020
632020
Intellectual ability in the duchenne muscular dystrophy and dystrophin gene mutation location
MV Rasic, D Vojinovic, J Pesovic, G Mijalkovic, V Lukic, J Mladenovic, ...
Balkan Journal of Medical Genetics 17 (2), 25-35, 2014
602014
Multiethnic exome-wide association study of subclinical atherosclerosis
P Natarajan, JC Bis, LF Bielak, AJ Cox, M Dörr, MF Feitosa, ...
Circulation: Cardiovascular Genetics 9 (6), 511-520, 2016
582016
Microbiomics, metabolomics, predicted metagenomics, and hepatic steatosis in a population‐based study of 1,355 adults
LJM Alferink, D Radjabzadeh, NS Erler, D Vojinovic, C Medina‐Gomez, ...
Hepatology 73 (3), 968-982, 2021
542021
Association of common genetic variants with brain microbleeds: a genome-wide association study
MJ Knol, D Lu, M Traylor, HHH Adams, JRJ Romero, AV Smith, ...
Neurology 95 (24), e3331-e3343, 2020
532020
Rare, low frequency and common coding variants in CHRNA5 and their contribution to nicotine dependence in European and African Americans
E Olfson, NL Saccone, EO Johnson, LS Chen, R Culverhouse, K Doheny, ...
Molecular psychiatry 21 (5), 601-607, 2016
502016
Association of variants in HTRA1 and NOTCH3 with MRI-defined extremes of cerebral small vessel disease in older subjects
A Mishra, G Chauhan, MH Violleau, D Vojinovic, X Jian, JC Bis, S Li, ...
Brain 142 (4), 1009-1023, 2019
492019
A multi-ancestry genome-wide study incorporating gene–smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure
YJ Sung, L de Las Fuentes, TW Winkler, DI Chasman, AR Bentley, ...
Human molecular genetics 28 (15), 2615-2633, 2019
442019
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