Suchergebnisse - "Leo, Paul J"

PubPharm (53)

31

Identification of IDUA and WNT16 Phosphorylation-Related Non-Synonymous Polymorphisms for Bone Mineral Density in Meta-Analyses of Genome-Wide Association Studies

enthalten in: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research | 2016

von Niu, T. | Liu, N. | Yu, X. | +30

32

Exome-wide study of ankylosing spondylitis demonstrates additional shared genetic background with inflammatory bowel disease

enthalten in: NPJ genomic medicine | 2016

von Robinson, P. | Leo, P. | Pointon, J. | +83

33

Novel TBK1 truncating mutation in a familial amyotrophic lateral sclerosis patient of Chinese origin

enthalten in: Neurobiology of aging | 2015

von Williams, K. | McCann, E. | Fifita, J. | +7

34

Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture

enthalten in: Nature | 2015

von Zheng, H. | Forgetta, V. | Hsu, Y. | +100

35

Identification of a novel FGFRL1 MicroRNA target site polymorphism for bone mineral density in meta-analyses of genome-wide association studies

enthalten in: Human molecular genetics | 2015

von Niu, T. | Liu, N. | Zhao, M. | +31

36

Major histocompatibility complex associations of ankylosing spondylitis are complex and involve further epistasis with ERAP1

enthalten in: Nature communications | 2015

von Cortes, A. | Pulit, S. | Leo, P. | +45

37

Compound heterozygous mutations in RIPPLY2 associated with vertebral segmentation defects

enthalten in: Human molecular genetics | 2015

von McInerney-Leo, A. | Sparrow, D. | Harris, J. | +9

38

Genetic determinants of heel bone properties : genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium

enthalten in: Human molecular genetics | 2014

von Moayyeri, A. | Hsu, Y. | Karasik, D. | +98

39

Multistage genome-wide association meta-analyses identified two new loci for bone mineral density

enthalten in: Human molecular genetics | 2014

von Zhang, L. | Choi, H. | Estrada, K. | +53

40

Whole exome sequencing is an efficient and sensitive method for detection of germline mutations in patients with phaeochromcytomas and paragangliomas

enthalten in: Clinical endocrinology | 2014

von McInerney-Leo, A. | Marshall, M. | Gardiner, B. | +7

CommentIn: Clin Endocrinol (Oxf). 2014 Jan;80(1):23-4. - PMID 24168015