Karina Krajden Haratz

29PUBLICATIONS
54CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Comparative language studiesFrench languageCentral nervous systemNeurogenetics
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Publications (29)

|Feb 12, 2026
Early diagnosis of fetal ganglionic eminence cysts: imaging, outcome and genetic associations, revealing role of mitochondrial dysfunction.

R Birnbaum, G Malinger, H Miremberg

|Aug 23, 2025
Prenatal evaluation, diagnosis and management of fetal corpus callosal abnormalities: international Delphi consensus.

R Corroenne, D Paladini, I Papastefanou

|May 05, 2025
Transvaginal ultrasound assessment of corpus callosal length in the fetus: multicenter cross-sectional study.

D Paladini, S Parodi, H Xie

|Dec 19, 2024
Relationship between prenatal ultrasound signs and genetic abnormalities for fetal malformations of cortical development.

JunYa Chen, Rong Zhu, Hong Pan

|Oct 05, 2024
Prenatal Diagnosis of a KIDINS220 De Novo Heterozygous Variant in a Fetus With a Complex CNS Anomaly.

Hadas Miremberg, Roee Birnbaum, Dorin Trigubov

|Feb 17, 2024
A de novo pathogenic variant in DHX30 gene in a fetus with isolated dysgenesis of the corpus callosum.

Karina Krajden Haratz, Gustavo Malinger, Uri Erlik

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Frequent Collaborators

19 joint publications

Gustavo Malinger

15 joint publications

Roee Brinbaum

5 joint publications

Dario Paladini

5 joint publications

Liat Gindes