Author details

Full Name

Yossi Farjoun

Affiliation

ORCID

Career Start Year

2008

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
38057664	A genomic mutational constraint map using variation in 76,156 human genomes.	Nature	2024
36805566	Proteome-wide Mendelian randomization implicates nephronectin as an actionable mediator of the effect of obesity on COVID-19 severity.	Nat Metab	2023
37794074	Alternative splicing in lung influences COVID-19 severity and respiratory diseases.		2023
36773317	Increasing serum iron levels and their role in the risk of infectious diseases: a Mendelian randomization approach.	Int J Epidemiol	2023
36635386	Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases.	Nat Genet	2023
37069249	Circulating proteins to predict COVID-19 severity.	Sci Rep	2023
37009933	Predicting ExWAS findings from GWAS data: a shorter path to causal genes.	Hum Genet	2023
36271419	Dehydration is associated with production of organic osmolytes and predicts physical long-term symptoms after COVID-19: a multicenter cohort study.	Crit Care	2022
36376796	Correction: The dynamic changes and sex differences of 147 immune-related proteins during acute COVID-19 in 580 individuals.	Clin Proteomics	2022
34373650	Addendum: The mutational constraint spectrum quantified from variation in 141,456 humans.	Nature	2021
33536625	Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans.	Nature	2021
32728101	Detecting sample swaps in diverse NGS data types using linkage disequilibrium.	Nat Commun	2020
31830260	Lean and deep models for more accurate filtering of SNP and INDEL variant calls.	Bioinformatics	2020
32461654	The mutational constraint spectrum quantified from variation in 141,456 humans.	Nature	2020
33293579	A validated lineage-derived somatic truth data set enables benchmarking in cancer genome analysis.	Commun Biol	2020
29360107	Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.	Sci Data	2018
30013044	A synthetic-diploid benchmark for accurate variant-calling evaluation.	Nat Methods	2018
30279509	Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects.	Nat Commun	2018
29739332	Characterization and remediation of sample index swaps by non-redundant dual indexing on massively parallel sequencing platforms.	BMC Genomics	2018
29257133	Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.	Sci Data	2017
28341696	A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.	Diabetes	2017
27826357	Systematic comparison of monoclonal versus polyclonal antibodies for mapping histone modifications by ChIP-seq.	Epigenetics Chromatin	2016
27195107	Recommendations for open data science.	GigaScience	2016
27398621	The genetic architecture of type 2 diabetes.	Nature	2016
24584071	Loss-of-function mutations in SLC30A8 protect against type 2 diabetes.	Nat Genet	2014
21728547	Aggregation according to classical kinetics: from nucleation to coarsening.		2011
19113125	Exhaustion of nucleation in a closed system.		2008