Suchergebnisse - "Leo, Paul J"

PubPharm (47)

11

Genome-wide association study in Turkish and Iranian populations identify rare familial Mediterranean fever gene (MEFV) polymorphisms associated with ankylosing spondylitis

enthalten in: PLoS genetics | 2019

von Li, Z. | Akar, S. | Yarkan, H. | +27

12

Comprehensive genetic screening : The prevalence of maturity-onset diabetes of the young gene variants in a population-based childhood diabetes cohort

enthalten in: Pediatric diabetes | 2019

von Johnson, S. | Ellis, J. | Leo, P. | +13

13

HLA and KIR Associations of Cervical Neoplasia

enthalten in: The Journal of infectious diseases | 2018

von Bao, X. | Hanson, A. | Madeleine, M. | +31

14

Genome-wide association study of extreme high bone mass : Contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genes

enthalten in: Bone | 2018

von Gregson, C. | Newell, F. | Leo, P. | +17

15

Correction : Defining the genetic susceptibility to cervical neoplasia-A genome-wide association study

enthalten in: PLoS genetics | 2018

von Leo, P. | Madeleine, M. | Wang, S. | +28

ErratumFor: PLoS Genet. 2017 Aug 14;13(8):e1006866. - PMID 28806749

16

Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in Chinese

enthalten in: Genome medicine | 2017

von Gratten, J. | Zhao, Q. | Benyamin, B. | +35

17

Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis

enthalten in: Nature communications | 2017

von Benyamin, B. | He, J. | Zhao, Q. | +61

18

NAD Deficiency, Congenital Malformations, and Niacin Supplementation

enthalten in: The New England journal of medicine | 2017

von Shi, H. | Enriquez, A. | Rapadas, M. | +30

CommentIn: Nat Rev Endocrinol. 2017 Oct 11;13(11):630-631. - PMID 29019348

19

Defining the genetic susceptibility to cervical neoplasia-A genome-wide association study

enthalten in: PLoS genetics | 2017

von Leo, P. | Madeleine, M. | Wang, S. | +28

ErratumIn: PLoS Genet. 2018 Mar 1;14 (3):e1007257. - PMID 29494589

20

Homozygous variant in C21orf2 in a case of Jeune syndrome with severe thoracic involvement : Extending the phenotypic spectrum

enthalten in: American journal of medical genetics. Part A | 2017

von McInerney-Leo, A. | Wheeler, L. | Marshall, M. | +6