Author

Chaim Jalas

ORCID 0000-0002-3788-0924Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Chaim Jalas1 paper

Biology Disciplines

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Genetic & Genomic Medicine· 2 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Assay:whole-exome sequencing· 2 Research Focus:benchmarking· 1 Research Focus:fine-mapping· 1 Research Focus:GWAS / association mapping· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Benjamin GläseriD· 2 shared Gil AtzmoniD· 2 shared Laurent BeaugerieiD· 2 shared Maria Teresa AbreuiD· 2 shared Martti A. FärkkiläiD· 2 shared Mikko HiltuneniD· 2 shared Stacey GabrieliD· 2 shared Tariq AhmadiD· 2 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenomics

Benjamin GläserORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJun 23, 2025

PGT-A Mosaicism Reporting Lacks Clinical Predictive Value: Evidence from a Multisite, Double-Blinded Study with Independent Validation Across 15,315 Single-Embryo Transfers

P. Gill, Xin Tao, Yiping Zhan…·Antonio Capalbo

This study shows that reporting mosaicism in PGT-A based on intermediate copy number (ICN) does not improve clinical outcomes in embryo selection.

DOI 10.1101/2025.06.23.25329758

humanstatistical model

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GenomicsNature GeneticsPeer-reviewedDec 6, 2023

Inferring compound heterozygosity from large-scale exome sequencing data

Michael H. Guo, Laurent C. Francioli, Sarah L. Stenton…·Bong-Jo Kim

The paper develops a method to infer compound heterozygosity from exome sequencing data, achieving high accuracy in phasing rare variants for recessive disease diagnosis.

36 citationstop 2%

humanwhole-exome sequencing

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Genetic & Genomic MedicineNature GeneticsPeer-reviewedAug 29, 2022

Sequencing of over 100,000 individuals identifies multiple genes and rare variants associated with Crohns disease susceptibility

Aleksejs Sazonovs, Christine R. Stevens, Guhan Ram Venkataraman…·Rasha Shawky

The paper identifies ten new genes with coding variants linked to Crohn's disease risk using sequencing data from over 30,000 patients and 80,000 controls.

197 citationstop 1%

humanwhole-exome sequencing

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