Publications by authors named "Nadra Samra"

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Exploring the unique characteristics of genes with dual autosomal dominant and recessive inheritance: mechanisms, phenotypes and candidate identification.
Shlomit Ezer, Tal Sido, Jonathan Rips, Ronit Hoffman Lipschuetz, Adina Fuchs, Nadra Samra

J Med Genet· October 2025

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From trauma to resilience: psychological and epigenetic adaptations in the third generation of holocaust survivors.
Guy Oren, Anat Shoshani, Nadra Nasser Samra, Willem Jmi Verbeke, Pascal Vrticka

Sci Rep· July 2025

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Targeting CD38 immunometabolic checkpoint improves metabolic fitness and cognition in a mouse model of Alzheimer's disease.
Javier María Peralta Ramos, Giulia Castellani, Denise Kviatcovsky, Tommaso Croese, Afroditi Tsitsou-Kampeli, Nadra Samra

Nat Commun· April 2025

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Correction: The genetic landscape of Lynch syndrome in the Israeli population.
Aasem Abu Shtaya, Sofia Naftaly Nathan, Inbal Kedar, Eitan Friedman, Elizabeth Half, Nadra Nasser Samra

Fam Cancer· March 2025

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The long-term associations of childhood parental loss with attachment, creativity, and epigenetic regulation.
Adi Shapira Dvilansky, Hodaya Zadok, Anat Shoshani, Nadra Nasser Samra, Willem Verbeke

Sci Rep· February 2025

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The genetic landscape of Lynch syndrome in the Israeli population.
Aasem Abu Shtaya, Sofia Naftaly Nathan, Inbal Kedar, Eitan Friedman, Elizabeth Half, Nadra Nasser Samra

Fam Cancer· November 2024

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Lisch Epithelial Corneal Dystrophy Is Caused by Heterozygous Loss-of-Function Variants in MCOLN1.
Karynne Patterson, Jessica X Chong, Doug D Chung, Walter Lisch, Carol L Karp, Nadra Naser Samra

Am J Ophthalmol· February 2024

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National Rapid Genome Sequencing in Neonatal Intensive Care.
Daphna Marom, Adi Mory, Sivan Reytan-Miron, Yam Amir, Alina Kurolap, Nadra Nasser Samra

JAMA Netw Open· February 2024

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Exome sequencing links the SUMO protease SENP7 with fatal arthrogryposis multiplex congenita, early respiratory failure and neutropenia.
Nadra Samra, Nicolette S Jansen, Ilham Morani, Reli Rachel Kakun, Rinat Zaid

J Med Genet· November 2023

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Familial Early-Onset Alzheimer's Caused by Novel Genetic Variant and APP Duplication: A Cross-Sectional Study.
Limor Kalfon, Rotem Paz, Hadas Raveh-Barak, Areef Salama, Nadra Samra

Curr Alzheimer Res· January 2023

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variants of cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway.
Maria Asif, Emrah Kaygusuz, Marwan Shinawi, Anna Nickelsen, Tzung-Chien Hsieh, Nadra Nasser Samra

HGG Adv· July 2022

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Congenital Hypotonia: Cracking a SAGA of consanguineous kindred harboring four genetic variants.
Limor Kalfon, Meirav Baydany, Nadra Samra, Nawaf Heno, Zvi Segal

Mol Genet Genomic Med· January 2022

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Hypoadrenalism as the Single Presentation of Autoimmune Polyglandular Syndrome Type 1.
Nadim H Nasser, Nadra G Samra, Deeb D Naccache

J Endocr Soc· December 2021

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RBL2 bi-allelic truncating variants cause severe motor and cognitive impairment without evidence for abnormalities in DNA methylation or telomeric function.
Nadra Samra, Shir Toubiana, Hilde Yttervik, Aya Tzur-Gilat, Ilham Morani

J Hum Genet· November 2021

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Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1.
Zippora Brownstein, Suleyman Gulsuner, Tom Walsh, Fábio T A Martins, Shahar Taiber, Nadra Samra

Clin Genet· October 2020

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The yield of full BRCA1/2 genotyping in Israeli Arab high-risk breast/ovarian cancer patients.
Rinat Bernstein-Molho, Inbal Barnes-Kedar, Mark D Ludman, Gili Reznik, Hagit Baris Feldman, Nadra Nasser Samra

Breast Cancer Res Treat· November 2019

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Phospholipase A2-activating protein is associated with a novel form of leukoencephalopathy.
Tzipora C Falik Zaccai, David Savitzki, Yifat Zivony-Elboum, Thierry Vilboux, Eric C Fitts, Nadra Samra

Brain· February 2017

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