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Komla-Ebri, Davide
60
results:
Search for persons
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Format
Online (58)
Print (2)
Mediatypes
Books (2)
Articles (Online) (17)
Bookchapter (Online) (1)
OpenAccess-fulltext (40)
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italian (2)
english (54)
Sorted by: Relevance
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?
1
Hypochondroplasia gain-of-function mutation in FGFR3 causes..:
Loisay, Léa
;
Komla-Ebri, Davide
;
Morice, Anne
...
JCI Insight. 8 (2023) 12 - p. , 2023
Link:
https://doi.org/10.1172/..
?
2
Publisher Correction: Accelerating functional gene discover..:
Butterfield, Natalie C.
;
Curry, Katherine F.
;
Steinberg, Julia
...
Nature Communications. 12 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1038/..
?
3
Osteocyte transcriptome mapping identifies a molecular land..:
Youlten, Scott E.
;
Kemp, John P.
;
Logan, John G.
...
Nature Communications. 12 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1038/..
?
4
Osteoclasts recycle via osteomorphs during RANKL-stimulated..:
McDonald, Michelle M.
;
Khoo, Weng Hua
;
Ng, Pei Ying
...
Cell. 184 (2021) 7 - p. 1940 , 2021
Link:
https://doi.org/10.1016/..
?
5
Accelerating functional gene discovery in osteoarthritis:
Butterfield, Natalie C.
;
Curry, Katherine F.
;
Steinberg, Julia
...
Nature Communications. 12 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1038/..
?
6
Osteoclasts recycle via osteomorphs during RANKL-stimulated..:
McDonald, Michelle M.
;
Khoo, Weng Hua
;
Ng, Pei Ying
...
Cell. 184 (2021) 5 - p. 1330-1347.e13 , 2021
Link:
https://doi.org/10.1016/..
?
7
Mitoguardin-2 deficiency results in severe osteoporosis:
Komla-Ebri, Davide
;
Pollard, Andrea S.
;
Sparkes, Penny C.
...
Bone Reports. 13 (2020) - p. 100646 , 2020
Link:
https://doi.org/10.1016/..
?
8
Functional validation of the osteoporosis GWAS candidate FU..:
Watts, Laura
;
Freudenthal, Bernard
;
Butterfield, Natalie C.
...
Bone Reports. 13 (2020) - p. 100554 , 2020
Link:
https://doi.org/10.1016/..
?
9
Identification of 153 new loci associated with heel bone mi..:
Kemp, John P
;
Morris, John A
;
Medina-Gomez, Carolina
...
Nature Genetics. 49 (2017) 10 - p. 1468-1475 , 2017
Link:
https://doi.org/10.1038/..
?
10
Meckel's and condylar cartilages anomalies in achondroplasi..:
Biosse Duplan, Martin
;
Komla-Ebri, Davide
;
Heuzé, Yann
...
Human Molecular Genetics. , 2016
Link:
https://doi.org/10.1093/..
?
11
FGFR3 mutation causes abnormal membranous ossification in a..:
Di Rocco, Federico
;
Biosse Duplan, Martin
;
Heuzé, Yann
...
Human Molecular Genetics. 23 (2014) 11 - p. 2914-2925 , 2014
Link:
https://doi.org/10.1093/..
?
12
Author Correction: An atlas of genetic influences on osteop..:
23andMe Research Team
;
Morris, John A.
;
Kemp, John P.
...
Nature Genetics. 51 (2019) 5 - p. 920-920 , 2019
Link:
https://doi.org/10.1038/..
?
13
An atlas of genetic influences on osteoporosis in humans an..:
23andMe Research Team
;
Morris, John A.
;
Kemp, John P.
...
Nature Genetics. 51 (2018) 2 - p. 258-266 , 2018
Link:
https://doi.org/10.1038/..
?
14
Hypochondroplasia gain-of-function mutation in FGFR3 causes..:
Loisay, Léa
;
Komla-Ebri, Davide
;
Morice, Anne
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10371252/. , 2023
Link:
http://www.ncbi.nlm.nih...
?
15
Publisher Correction: Accelerating functional gene discover..:
Butterfield, Natalie C
;
Curry, Katherine F
;
Steinberg, Julia
...
https://www.repository.cam.ac.uk/handle/1810/341479. , 2022
Link:
https://www.repository.c..
1-15