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Laura Portas
Laura Portas
Research Associate, Imperial College London
Verified email at imperial.ac.uk
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Cited by
Year
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations
A Köttgen, E Albrecht, A Teumer, V Vitart, J Krumsiek, C Hundertmark, ...
Nature genetics 45 (2), 145-154, 2013
5062013
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
C Pattaro, A Teumer, M Gorski, AY Chu, M Li, V Mijatovic, M Garnaas, ...
Nature communications 7 (1), 10023, 2016
4722016
Seventy-five genetic loci influencing the human red blood cell
P Van Der Harst, W Zhang, I Mateo Leach, A Rendon, N Verweij, J Sehmi, ...
Nature 492 (7429), 369-375, 2012
3832012
Genome analyses of> 200,000 individuals identify 58 loci for chronic inflammation and highlight pathways that link inflammation and complex disorders
S Ligthart, A Vaez, U Võsa, MG Stathopoulou, PS De Vries, BP Prins, ...
The American Journal of Human Genetics 103 (5), 691-706, 2018
3532018
Genome-wide association and functional follow-up reveals new loci for kidney function
C Pattaro, A Köttgen, A Teumer, M Garnaas, CA Böger, C Fuchsberger, ...
PLoS genetics 8 (3), e1002584, 2012
2102012
Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error
CY Cheng, M Schache, MK Ikram, TL Young, JA Guggenheim, V Vitart, ...
The American Journal of Human Genetics 93 (2), 264-277, 2013
1772013
Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations
CM O'Seaghdha, H Wu, Q Yang, K Kapur, I Guessous, AM Zuber, ...
PLoS genetics 9 (9), e1003796, 2013
1712013
Analysis of 12,517 inhabitants of a Sardinian geographic isolate reveals that predispositions to thrombocytopenia and thrombocytosis are inherited traits
G Biino, CL Balduini, L Casula, P Cavallo, S Vaccargiu, D Parracciani, ...
Haematologica 96 (1), 96, 2011
1662011
Meta-analysis of gene–environment-wide association scans accounting for education level identifies additional loci for refractive error
Q Fan, VJM Verhoeven, R Wojciechowski, VA Barathi, PG Hysi, ...
Nature communications 7 (1), 11008, 2016
1362016
A three-generation study on the association of tobacco smoking with asthma
S Accordini, L Calciano, A Johannessen, L Portas, B Benediktsdóttir, ...
International journal of epidemiology 47 (4), 1106-1117, 2018
1262018
Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium
VJM Verhoeven, PG Hysi, SM Saw, V Vitart, A Mirshahi, JA Guggenheim, ...
Human genetics 131, 1467-1480, 2012
1032012
Hearing function and thresholds: a genome-wide association study in European isolated populations identifies new loci and pathways
G Girotto, N Pirastu, R Sorice, G Biino, H Campbell, AP d'Adamo, ...
Journal of medical genetics 48 (6), 369-374, 2011
872011
Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function
DI Chasman, C Fuchsberger, C Pattaro, A Teumer, CA Böger, K Endlich, ...
Human molecular genetics 21 (24), 5329-5343, 2012
772012
Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with …
D Stambolian, R Wojciechowski, K Oexle, M Pirastu, X Li, LJ Raffel, ...
Human molecular genetics 22 (13), 2754-2764, 2013
752013
Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci
CL Simpson, R Wojciechowski, K Oexle, F Murgia, L Portas, X Li, ...
PloS one 9 (9), e107110, 2014
602014
Genetic variants associated with circulating parathyroid hormone
C Robinson-Cohen, PL Lutsey, ME Kleber, CM Nielson, BD Mitchell, ...
Journal of the American Society of Nephrology 28 (5), 1553-1565, 2017
572017
Modulation of genetic associations with serum urate levels by body-mass-index in humans
JE Huffman, E Albrecht, A Teumer, M Mangino, K Kapur, T Johnson, ...
PloS one 10 (3), e0119752, 2015
462015
Common variants in Mendelian kidney disease genes and their association with renal function
A Parsa, C Fuchsberger, A Koettgen, CM O’Seaghdha, C Pattaro, ...
Journal of the American Society of Nephrology 24 (12), 2105-2117, 2013
412013
A population-based study of an Italian genetic isolate reveals that mean platelet volume is not a risk factor for thrombosis
G Biino, L Portas, F Murgia, S Vaccargiu, D Parracciani, M Pirastu, ...
Thrombosis research 129 (4), e8-e13, 2012
382012
Lung development genes and adult lung function
L Portas, M Pereira, SO Shaheen, AB Wyss, SJ London, PGJ Burney, ...
American journal of respiratory and critical care medicine 202 (6), 853-865, 2020
262020
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