| human | Q5 |
| P8189 | National Library of Israel J9U ID | 987007307135505171 |
| P496 | ORCID iD | 0000-0002-8460-1502 |
| P214 | VIAF ID | 298343501 |
| P108 | employer | Tel Aviv University | Q319239 |
| P106 | occupation | researcher | Q1650915 |
| Q43029588 | A likelihood method for detecting trait-dependent shifts in the rate of molecular evolution |
| Q45944935 | A machine learning approach for predicting CRISPR-Cas9 cleavage efficiencies and patterns underlying its mechanism of action. |
| Q45964330 | A machine-learning approach for predicting B-cell epitopes. |
| Q125926814 | A non‐homogeneous model of chromosome‐number evolution to reveal shifts in the transition patterns across the phylogeny |
| Q33677595 | An evolutionary analysis of lateral gene transfer in thymidylate synthase enzymes |
| Q57053528 | Body sizes and diversification rates of lizards, snakes, amphisbaenians and the tuatara |
| Q100730730 | COVID-19 pandemic-related lockdown: response time is more important than its strictness |
| Q35561866 | Clumpak: a program for identifying clustering modes and packaging population structure inferences across K. |
| Q39776544 | ConSurf 2016: an improved methodology to estimate and visualize evolutionary conservation in macromolecules |
| Q56879918 | ConSurf: Using Evolutionary Data to Raise Testable Hypotheses about Protein Function |
| Q34497994 | Dioecy does not consistently accelerate or slow lineage diversification across multiple genera of angiosperms |
| Q33265689 | Epitope mapping using combinatorial phage-display libraries: a graph-based algorithm |
| Q30380632 | Epitopia: a web-server for predicting B-cell epitopes. |
| Q57053482 | Erratum: Sex determination, longevity, and the birth and death of reptilian species |
| Q96219685 | Heterogeneity in the rate of molecular sequence evolution substantially impacts the accuracy of detecting shifts in diversification rates |
| Q39228983 | Increased growth in sunflower correlates with reduced defences and altered gene expression in response to biotic and abiotic stress |
| Q38404852 | Karyotypic changes through dysploidy persist longer over evolutionary time than polyploid changes |
| Q38770777 | Macroevolutionary synthesis of flowering plant sexual systems |
| Q51387507 | Methods for studying polyploid diversification and the dead end hypothesis: a reply to Soltis et al. (2014). |
| Q62659220 | Model selection may not be a mandatory step for phylogeny reconstruction |
| Q56879924 | Probabilistic Methods and Rate Heterogeneity |
| Q31140943 | Selecton: a server for detecting evolutionary forces at a single amino-acid site |
| Q28597844 | Sex determination, longevity, and the birth and death of reptilian species |
| Q21092698 | Sex determination: why so many ways of doing it? |
| Q34893298 | Synonymous site conservation in the HIV-1 genome |
| Q92348862 | TRY plant trait database - enhanced coverage and open access |
| Q51392051 | The Chromosome Counts Database (CCDB) - a community resource of plant chromosome numbers. |
| Q62659224 | The global biogeography of polyploid plants |
| Q39537676 | Whole-genome duplication as a key factor in crop domestication |
| Q57277882 | “Not Just One Common Sense”: Gramsci's Common Sense and Laclau and Mouffe's Radical Democratic Politics |
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