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Noa Zunz Henig
Observed names:
Henig, Noa,
N. Zunz Henig,
Noa Henig,
Noa Z. Henig
Observed institutions:
Tel Aviv University,
Tel Aviv Sourasky Medical Center
OpenAlex ID:
A5031244264
Exome sequencing as first‐tier test for fetuses with severe central nervous system structural anomalies
2022
·
Y. Yaron
, V. Ofen Glassner
, et al.
·
Ultrasound in Obstetrics and Gynecology
·
81
Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease
2023
·
Daniel G. Calame
, Tianyu Guo
, et al.
·
The American Journal of Human Genetics
·
43
PDF
De novo variants in ATP2B1 lead to neurodevelopmental delay
2022
·
Meer Jacob Rahimi
, Nicole Urban
, et al.
·
The American Journal of Human Genetics
·
24
MSL2 variants lead to a neurodevelopmental syndrome with lack of coordination, epilepsy, specific dysmorphisms, and a distinct episignature
2024
·
Remzi Karayol
, Maria Carla Borroto
, et al.
·
The American Journal of Human Genetics
·
16
PDF
Biallelic loss of EMC10 leads to mild to severe intellectual disability
2022
·
Rauan Kaiyrzhanov
, Clarissa Rocca
, et al.
·
Annals of Clinical and Translational Neurology
·
16
PDF
CD55-deficiency in Jews of Bukharan descent is caused by the Cromer blood type Dr(a−) variant
2022
·
Alina Kurolap
, David Hagin
, et al.
·
Human Genetics
·
10
PDF
Non‐immune hydrops fetalis caused by PIEZO1 compound heterozygous deletions detected only by exome sequencing
2022
·
Sivan Reytan
, Noa Zunz Henig
, et al.
·
Prenatal Diagnosis
·
4
De novo variants in ATP2B1 lead to neurodevelopmental delay
2025
·
Meer Jacob Rahimi
, Nicole Urban
, et al.
·
The American Journal of Human Genetics
Monoallelic variation in DHX9 , the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease
2023
·
Daniel G. Calame
, Tianyu Guo
, et al.
·
medRxiv
PDF
eP345: Community data-driven approach for generating cross-ethnic population carrier screening panel
2022
·
Yaron Einhorn
, Moshe Einhorn
, et al.
·
Genetics in Medicine
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Works count:
11
Citation count:
194
H-index:
6
I10-index:
6
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