Suchergebnisse - "Leo, Paul J"

PubPharm (38)

1

Proteome profiling of salivary small extracellular vesicles in glioblastoma patients

enthalten in: Cancer | 2023

von Müller Bark, J. | Trevisan França de Lima, L. | Zhang, X. | +6

2

Reducing exacerbations in children and adults with primary ciliary dyskinesia using erdosteine and/or azithromycin therapy (REPEAT trial) : study protocol for a multicentre, double-blind, double-dummy, 2×2 partial factorial, randomised controlled trial

enthalten in: BMJ open respiratory research | 2022

von Chang, A. | Morgan, L. | Duncan, E. | +22

3

Germline ERBB3 mutation in familial non-small-cell lung carcinoma : expanding ErbB's role in oncogenesis

enthalten in: Human molecular genetics | 2021

von McInerney-Leo, A. | Chew, H. | Inglis, P. | +17

4

Polygenic Risk Scores have high diagnostic capacity in ankylosing spondylitis

enthalten in: Annals of the rheumatic diseases | 2021

von Li, Z. | Wu, X. | Leo, P. | +100

ErratumIn: Ann Rheum Dis. 2021 Nov;80(11):e187. - PMID 34642186

5

A KCNK16 mutation causing TALK-1 gain of function is associated with maturity-onset diabetes of the young

enthalten in: JCI insight | 2021

von Graff, S. | Johnson, S. | Leo, P. | +10

6

Multiple Endocrine Tumors Associated with Germline MAX Mutations : Multiple Endocrine Neoplasia Type 5?

enthalten in: The Journal of clinical endocrinology and metabolism | 2021

von Seabrook, A. | Harris, J. | Velosa, S. | +17

7

Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice

enthalten in: Human molecular genetics | 2020

von Martin, E. | Enriquez, A. | Sparrow, D. | +31

8

Compound heterozygous mutations in FBN1 in a large family with Marfan syndrome

enthalten in: Molecular genetics & genomic medicine | 2020

von McInerney-Leo, A. | West, J. | Wheeler, L. | +6

9

Genetic susceptibility to cervical neoplasia

enthalten in: Papillomavirus research (Amsterdam, Netherlands) | 2019

von Brown, M. | Leo, P.

10

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