Browse by UCL people
Group by: Type | Date
Jump to: Article
Number of items: 7.
Article
Huang, J;
Howie, B;
McCarthy, S;
Memari, Y;
Walter, K;
Min, JL;
Danecek, P;
... Soranzo, N; + view all
(2015)
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel.
Nature Communications
, 6
(811)
10.1038/ncomms9111.
|
Karaman, I;
Ferreira, DL;
Boulangé, CL;
Kaluarachchi, MR;
Herrington, D;
Dona, AC;
Castagné, R;
... Ebbels, TM; + view all
(2016)
Workflow for Integrated Processing of Multicohort Untargeted 1H NMR Metabolomics Data in Large-Scale Metabolic Epidemiology.
Journal of Proteome Research
, 15
(12)
pp. 4188-4194.
10.1021/acs.jproteome.6b00125.
|
Moayyeri, A;
Cheung, CL;
Tan, KCB;
Morris, JA;
Cerani, A;
Mohney, RP;
Richards, JB;
... Menni, C; + view all
(2018)
Metabolomic Pathways to Osteoporosis in Middle-Aged Women: A Genome-Metabolome-Wide Mendelian Randomization Study.
Journal of Bone and Mineral Research
, 33
(4)
pp. 643-650.
10.1002/jbmr.3358.
|
Schmidts, M;
Hou, Y;
Cortés, CR;
Mans, DA;
Huber, C;
Boldt, K;
Patel, M;
... Witman, GB; + view all
(2015)
TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport.
Nature Communications
, 6
, Article 7074. 10.1038/ncomms8074.
|
Schumann, G;
Liu, C;
O'Reilly, P;
Gao, H;
Song, P;
Xu, B;
Ruggeri, B;
... Elliott, P; + view all
(2016)
KLB is associated with alcohol drinking, and its gene product beta-Klotho is necessary for FGF21 regulation of alcohol preference.
Proceedings of the National Academy of Sciences of the United States of America
, 113
(50)
pp. 14372-14377.
10.1073/pnas.1611243113.
|
Surendran, P;
Drenos, F;
Young, R;
Warren, H;
Cook, JP;
Manning, AK;
Grarup, N;
... Munroe, PB; + view all
(2016)
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension.
Nature Genetics
, 48
(10)
pp. 1151-1161.
10.1038/ng.3654.
|
Walter, K;
Min, JL;
Huang, J;
Crooks, L;
Memari, Y;
McCarthy, S;
Perry, JRB;
... Zhang, W; + view all
(2015)
The UK10K project identifies rare variants in health and disease.
Nature
, 526
(7571)
pp. 82-90.
10.1038/nature14962.
|