Suchergebnisse - "Leo, Paul J"

PubPharm (47)

21

The Connecticut Mental Health Center : Celebrating 50 Years of a Successful Partnership Between the State and Yale University

enthalten in: Psychiatric services (Washington, D.C.) | 2016

von Steiner, J. | Anez-Nava, L. | Baranoski, M. | +17

22

Mutations in LTBP3 cause acromicric dysplasia and geleophysic dysplasia

enthalten in: Journal of medical genetics | 2016

von McInerney-Leo, A. | Le Goff, C. | Leo, P. | +11

23

Fryns Syndrome Associated with Recessive Mutations in PIGN in two Separate Families

enthalten in: Human mutation | 2016

von McInerney-Leo, A. | Harris, J. | Gattas, M. | +11

CommentIn: Hum Mutat. 2016 Jul;37(7):621. - PMID 27300081

24

Mutations in human C2CD3 cause skeletal dysplasia and provide new insights into phenotypic and cellular consequences of altered C2CD3 function

enthalten in: Scientific reports | 2016

von Cortés, C. | McInerney-Leo, A. | Vogel, I. | +10

25

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

26

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

27

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

28

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

29

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

30

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