Gabriel Cuellar Partida
Gabriel Cuellar Partida
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Common genetic variants influence human subcortical brain structures
DP Hibar, JL Stein, ME Renteria, A Arias-Vasquez, S Desrivières, ...
Nature 520 (7546), 224-229, 2015
Rare and low-frequency coding variants alter human adult height
E Marouli, M Graff, C Medina-Gomez, KS Lo, AR Wood, TR Kjaer, RS Fine, ...
Nature 542 (7640), 186-190, 2017
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
V Turcot, Y Lu, HM Highland, C Schurmann, AE Justice, RS Fine, ...
Nature genetics 50 (1), 26-41, 2018
Novel genetic loci associated with hippocampal volume
DP Hibar, HHH Adams, N Jahanshad, G Chauhan, JL Stein, E Hofer, ...
Nature communications 8 (1), 1-12, 2017
Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma
PG Hysi, CY Cheng, H Springelkamp, S Macgregor, JNC Bailey, ...
Nature genetics 46 (10), 1126-1130, 2014
Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept
B Franke, JL Stein, S Ripke, V Anttila, DP Hibar, KJE Van Hulzen, ...
Nature neuroscience 19 (3), 420-431, 2016
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
MS Tedja, R Wojciechowski, PG Hysi, N Eriksson, NA Furlotte, ...
Nature genetics 50 (6), 834-848, 2018
Novel genetic loci underlying human intracranial volume identified through genome-wide association
HHH Adams, DP Hibar, V Chouraki, JL Stein, PA Nyquist, ME Rentería, ...
Nature neuroscience 19 (12), 1569-1582, 2016
Epigenetic priors for identifying active transcription factor binding sites
G Cuellar-Partida, FA Buske, RC McLeay, T Whitington, WS Noble, ...
Bioinformatics 28 (1), 56-62, 2012
New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
H Springelkamp, AI Iglesias, A Mishra, R Höhn, R Wojciechowski, ...
Human molecular genetics 26 (2), 438-453, 2017
Genetic architecture of subcortical brain structures in 38,851 individuals
CL Satizabal, HHH Adams, DP Hibar, CC White, MJ Knol, JL Stein, ...
Nature genetics 51 (11), 1624-1636, 2019
Association of vitamin D levels and risk of ovarian cancer: a Mendelian randomization study
JS Ong, G Cuellar-Partida, Y Lu, Australian Ovarian Cancer Study, ...
International journal of epidemiology 45 (5), 1619-1630, 2016
ARHGEF12 influences the risk of glaucoma by increasing intraocular pressure
H Springelkamp, AI Iglesias, G Cuellar-Partida, N Amin, KP Burdon, ...
Human molecular genetics 24 (9), 2689-2699, 2015
Assessing the genetic predisposition of education on myopia: a mendelian randomization study
G Cuellar‐Partida, Y Lu, PF Kho, AW Hewitt, HE Wichmann, S Yazar, ...
Genetic epidemiology 40 (1), 66-72, 2016
Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia
M Miyake, K Yamashiro, Y Tabara, K Suda, S Morooka, H Nakanishi, ...
Nature communications 6 (1), 1-9, 2015
Genome-wide association study identifies 48 common genetic variants associated with handedness
G Cuellar-Partida, JY Tung, N Eriksson, E Albrecht, F Aliev, ...
Nature human behaviour 5 (1), 59-70, 2021
Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases
AI Iglesias, A Mishra, V Vitart, Y Bykhovskaya, R Höhn, H Springelkamp, ...
Nature communications 9 (1), 1-11, 2018
Shared genetics underlying epidemiological association between endometriosis and ovarian cancer
Y Lu, G Cuellar-Partida, JN Painter, DR Nyholt, ...
Human molecular genetics 24 (20), 5955-5964, 2015
Genome-wide in silico prediction of gene expression
RC McLeay, T Lesluyes, G Cuellar Partida, TL Bailey
Bioinformatics 28 (21), 2789-2796, 2012
WNT10A exonic variant increases the risk of keratoconus by decreasing corneal thickness
G Cuellar-Partida, H Springelkamp, SEM Lucas, S Yazar, AW Hewitt, ...
Human molecular genetics 24 (17), 5060-5068, 2015
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