Elon Pras

5PUBLICATIONS
47CO-AUTHORS
Medical mycologyGene expression (incl. microarray and other genome-wide approaches)Developmental genetics (incl. sex determination)Cardiovascular medicine and haematology not elsewhere classifiedEpigenetics (incl. genome methylation and epigenomics)
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Publications (5)

|Jun 05, 2025
Prophylactic colchicine for familial Mediterranean fever: response rates revisited.

A Wiener, Y Shinar, E Pras

|Oct 28, 2020
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

|Jan 30, 2019
Prenatal diagnosis for de novo mutations: Experience from a tertiary center over a 10-year period.

Ori Eyal, Michal Berkenstadt, Haike Reznik-Wolf

|Jun 30, 2018
SMYD1 is the underlying gene for the AnWj-negative blood group phenotype.

Vered Yahalom, Nir Pillar, Yingying Zhao

|Jul 20, 2016
Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects.

Amos J Simon, Atar Lev, Yong Zhang

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Frequent Collaborators

2 joint publications

Noam Shomron

1 joint publications

A Wiener

1 joint publications

Y Shinar

1 joint publications

Ortal Barel