Keren Machol
6PUBLICATIONS
38CO-AUTHORS
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Publications (6)
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|Nov 05, 2021
Molecular alterations due to Col5a1 haploinsufficiency in a mouse model of classic Ehlers-Danlos syndrome.Keren Machol, Urszula Polak, Monika Weisz-Hubshman
|Jan 14, 2021
Evidence that FGFRL1 contributes to congenital diaphragmatic hernia development in humans.Yoel Gofin, Laura Palmer Mackay, Keren Machol
|Feb 04, 2020
Deficient histone H3 propionylation by BRPF1-KAT6 complexes in neurodevelopmental disorders and cancer.Kezhi Yan, Justine Rousseau, Keren Machol
|Dec 27, 2019
Hearing loss in individuals with osteogenesis imperfecta in North America: Results from a multicenter study.Keren Machol, Trevor D Hadley, Jake Schmidt
|Oct 04, 2019
Widening of the genetic and clinical spectrum of Lamb-Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency.Ash Zawerton, Cyril Mignot, Ashley Sigafoos
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Frequent Collaborators
2 joint publications
Kirsty McWalter
2 joint publications
Daryl A Scott
1 joint publications
Patrick R Blackburn
1 joint publications
Zehua Zhu
1 joint publications
Daphné Lehalle
1 joint publications
Sophie Nambot
1 joint publications
Christèle Dubourg
1 joint publications
Lynne M Bird
1 joint publications
Emily Fassi
1 joint publications
Anthony Vandersteen