Jessica Alföldi
Genetics · 2011–2023
A researcher in the Science corpus: 19 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 322 citations into it
- Computational Biology & Bioinformatics — 38 citations into it
Whom Jessica Alföldi trusts
Their strongest outbound trust, strongest first, inferred from their citations.
- James Y. Zou (in Genetics)
Papers from Jessica Alföldi's perspective
Ordered by how strongly the researchers Jessica Alföldi trusts endorse each paper. Same corpus, a different order for every researcher.
- The human genome browser at UCSC.
- A Fast and Symmetric DUST Implementation to Mask Low-Complexity DNA Sequences (J. Comput. Biol.)
- Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes.
- Ultraconserved Elements in the Human Genome (Science)
- Distinguishing protein-coding and noncoding genes in the human genome (Proceedings of the National Academy of Sciences of the United States of America)
- Upstream open reading frames cause widespread reduction of protein expression and are polymorphic among humans (Proceedings of the National Academy of Sciences of the United States of America)
- High-Resolution CRISPR Screens Reveal Fitness Genes and Genotype-Specific Cancer Liabilities. (Cell)
- Haplotype-based variant detection from short-read sequencing
- Salmon: fast and bias-aware quantification of transcript expression using dual-phase inference
- KEGG: Kyoto Encyclopedia of Genes and Genomes (Nucleic Acids Res.)
Their papers
- Progressive Cactus is a multiple-genome aligner for the thousand-genome era (2020) — 445 citations
- The mutational constraint spectrum quantified from variation in 141,456 humans (2020) — 8,441 citations
- The genome of the green anole lizard and a comparative analysis with birds and mammals (2011) — 645 citations
- Variation across 141,456 human exomes and genomes reveals the spectrum of loss-of-function intolerance across human protein-coding genes (2019) — 1,088 citations
- FEELnc: a tool for long non-coding RNA annotation and its application to the dog transcriptome (2017) — 433 citations
- Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2019) — 162 citations
- A genomic mutational constraint map using variation in 76,156 human genomes (2023) — 1,228 citations
- A genome-wide mutational constraint map quantified from variation in 76,156 human genomes (2022) — 258 citations
- Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes (2020) — 126 citations
- A structural variation reference for medical and population genetics (2020) — 876 citations
- Transcript expression-aware annotation improves rare variant discovery and interpretation (2019) — 26 citations
- Human loss-of-function variants suggest that partial LRRK2 inhibition is a safe therapeutic strategy for Parkinson’s disease (2019) — 13 citations
- Evaluating potential drug targets through human loss-of-function genetic variation (2019) — 22 citations
- Evaluating drug targets through human loss-of-function genetic variation (2019) — 168 citations
- An open resource of structural variation for medical and population genetics (2019) — 76 citations
- Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes (2019) — 3 citations
- The genomic substrate for adaptive radiation in African cichlid fish (2014) — 934 citations
- Mammalian Y chromosomes retain widely expressed dosage-sensitive regulators (2014) — 603 citations
- A high-resolution map of human evolutionary constraint using 29 mammals (2011) — 867 citations