Alina Kurolap
18PUBLICATIONS
71CO-AUTHORS
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Publications (18)
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|Apr 09, 2025
LSM1 c.231+4A>C hotspot variant is associated with a novel neurodevelopmental syndrome: first patient cohort.Sivan Reytan Miron, Alina Kurolap, Bassam Abu-Libdeh
|Dec 23, 2024
Impaired Wnt/Planar Cell Polarity Signaling in Yellow Nail Syndrome.Alina Kurolap, Chofit Chai Gadot, Orly Eshach Adiv
|May 08, 2024
Expanded targeted preconception screening panel in Israel: findings and insights.Adi Reches, Vered Ofen Glassner, Nurit Goldstein
|Feb 01, 2024
PUF60 loss-of-function with normal cognition should be considered in the differential diagnosis of Klippel-Feil syndrome.Michal Yacobi Bach, Sivan Reytan Miron, Alina Kurolap
|Nov 01, 2023
Corin and Left Atrial Cardiomyopathy, Hypertension, Arrhythmia, and Fibrosis.Hagit Baris Feldman, Chofit Chai Gadot, David Zahler
|Aug 28, 2023
SMARCC1 is a susceptibility gene for congenital hydrocephalus with an autosomal dominant inheritance mode and incomplete penetrance.Noa Hourvitz, Alina Kurolap, Adi Mory
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Frequent Collaborators
3 joint publications
Yuval Yaron
2 joint publications
Gustavo Malinger
2 joint publications
Karina Krajden Haratz
2 joint publications
Lena Sagi-Dain
1 joint publications
Jan A Smeitink
1 joint publications
Maciej J Szukszto
1 joint publications
Tzung-Chien Hsieh
1 joint publications
Wen-Hann Tan
1 joint publications
Karin Weiss
1 joint publications
Ariel F Martinez
