Publications by authors named "Noa Henig"

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De novo variants in ATP2B1 lead to neurodevelopmental delay.
Meer Jacob Rahimi, Nicole Urban, Meret Wegler, Heinrich Sticht, Michael Schaefer, Noa Henig

Am J Hum Genet· December 2025

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The zinc-finger transcription factor Sfp1 imprints specific classes of mRNAs and links their synthesis to cytoplasmic decay.
Moran Kelbert, Antonio Jordán-Pla, Lola de Miguel-Jiménez, José García-Martínez, Michael Selitrennik, Noa Henig

Elife· October 2024

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MSL2 variants lead to a neurodevelopmental syndrome with lack of coordination, epilepsy, specific dysmorphisms, and a distinct episignature.
Remzi Karayol, Maria Carla Borroto, Sadegheh Haghshenas, Anoja Namasivayam, Jack Reilly, Noa Henig

Am J Hum Genet· July 2024

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Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease.
Daniel G Calame, Tianyu Guo, Chen Wang, Lillian Garrett, Angad Jolly, Noa Zunz Henig

Am J Hum Genet· August 2023

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Biallelic loss of EMC10 leads to mild to severe intellectual disability.
Rauan Kaiyrzhanov, Clarissa Rocca, Mohnish Suri, Sughra Gulieva, Maha S Zaki, Noa Z Henig

Ann Clin Transl Neurol· July 2022

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De novo variants in ATP2B1 lead to neurodevelopmental delay.
Meer Jacob Rahimi, Nicole Urban, Meret Wegler, Heinrich Sticht, Michael Schaefer, Noa Henig

Am J Hum Genet· May 2022

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NEBNext Direct: A Novel, Rapid, Hybridization-Based Approach for the Capture and Library Conversion of Genomic Regions of Interest.
Amy B Emerman, Sarah K Bowman, Andrew Barry, Noa Henig, Kruti M Patel

Curr Protoc Mol Biol· July 2017

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Interferon-beta induces distinct gene expression response patterns in human monocytes versus T cells.
Noa Henig, Nili Avidan, Ilana Mandel, Elsebeth Staun-Ram, Elizabeta Ginzburg

PLoS One· November 2013

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