Search results - ORA - Oxford University Research Archive

1 - 9 of 9

1

Journal article

A phenome-wide association study of a lipoprotein associated phospholipase A2 loss-of-function variant in 90 000 Chinese adults

Millwood, I, Bennett, D, Walters, R, et al.
2016-06-01

2

Journal article

Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes

Newbury, D, Pettigrew, K, Frinton, E, et al.
2016-06-14

3

Thesis

Genome mapping of malaria resistance genes: the host ligands of PfEMP1

Fry, A
2009-09-07

4

Journal article

The importance of context: uncovering species- and tissue-specific effects of genetic risk variants for type 2 diabetes

Thomsen, S, McCarthy, M, Gloyn, A
2016-01-01

5

Journal article

Characterisation of the opposing effects of G6PD deficiency on cerebral malaria and severe malarial anaemia

Clarke, G, Rockett, K, Kivinen, K, et al.
2017-01-09

6

Journal article

Heritable components of the human fecal microbiome are associated with visceral fat

Beaumont, M, Goodrich, J, Jackson, M, et al.
2016-09-26

7

Journal article

Genetic association analysis reveals differences in the contribution of NOD2 variants to the clinical phenotypes of orofacial granulomatosis

Mentzer, A, Nayee, S, Omar, Y, et al.
2016-06-10

8

Journal article

Reassessing the association: evaluation of a polyalanine deletion variant of RUNX2 in non-syndromic sagittal and metopic craniosynostosis

Walton, IS, McCann, E, Weber, A, et al.
2024-05-17

9

Journal article

Reassessing the association: Evaluation of a polyalanine deletion variant of RUNX2 in non‐syndromic sagittal and metopic craniosynostosis

Walton, IS, McCann, E, Weber, A, et al.
2024-05-17

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