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/vufind/Search/Results?lookfor=%22Leo%2C+Paul+J%22&type=Person&page=4
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PubPharm (88)
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
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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
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33
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
| 2016
von
Prince, R.
|
Fu, X.
|
Uitterlinden, A.
| +30
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34
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
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35
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
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36
The Connecticut Mental Health Center: Celebrating 50 Years of a Successful Partnership Between the State and Yale University
enthalten in:
Psychiatric services
| 2016
von
Steiner, J.
|
Anez-Nava, L.
|
Baranoski, M.
| +17
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37
The Connecticut Mental Health Center: Celebrating 50 Years of a Successful Partnership Between the State and Yale University
enthalten in:
Psychiatric services
| 2016
von
Steiner, J.
|
Anez-Nava, L.
|
Baranoski, M.
| +17
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38
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
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39
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
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40
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
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Human molecular genetics
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American journal of human genetics
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Meta-Analysis
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HLA-B27 Antigen
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WNT16 protein, human
3
Wnt Proteins
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Cytoplasmic Dyneins
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DNA-Binding Proteins
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DYNC2H1 protein, human
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EC 2.7.11.1
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EC 3.6.4.2
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Extracellular Matrix Proteins
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Fibrillin-1
2
Fryns syndrome
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Glycoproteins
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HUMAN ASSOCIATION STUDIES
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Intracellular Signaling Peptides and Proteins
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Erscheinungszeitraum
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2000-
10
1900-1999
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