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Connection

Pall Melsted to Humans

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This is a "connection" page, showing publications Pall Melsted has written about Humans.
Pall Melsted
Connection Strength
0.213
Humans
  1. GraphTyper2 enables population-scale genotyping of structural variation using pangenome graphs. Nat Commun. 2019 11 27; 10(1):5402.
    View in: PubMed
    Score: 0.023
  2. Gene-based burden tests of rare germline variants identify six cancer susceptibility genes. Nat Genet. 2024 Nov; 56(11):2422-2433.
    View in: PubMed
    Score: 0.008
  3. Sequence variants influencing the regulation of serum IgG subclass levels. Nat Commun. 2024 Sep 14; 15(1):8054.
    View in: PubMed
    Score: 0.008
  4. Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency. Nat Genet. 2024 Sep; 56(9):1804-1810.
    View in: PubMed
    Score: 0.008
  5. Start codon variant in LAG3 is associated with decreased LAG-3 expression and increased risk of autoimmune thyroid disease. Nat Commun. 2024 Jul 09; 15(1):5748.
    View in: PubMed
    Score: 0.008
  6. Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis. Nat Genet. 2023 Dec; 55(12):2149-2159.
    View in: PubMed
    Score: 0.007
  7. Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura. Nat Genet. 2023 Nov; 55(11):1843-1853.
    View in: PubMed
    Score: 0.007
  8. Large-scale plasma proteomics comparisons through genetics and disease associations. Nature. 2023 Oct; 622(7982):348-358.
    View in: PubMed
    Score: 0.007
  9. Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria. Commun Biol. 2023 07 10; 6(1):703.
    View in: PubMed
    Score: 0.007
  10. Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality. Nat Commun. 2023 06 10; 14(1):3453.
    View in: PubMed
    Score: 0.007
  11. Multiomics study of nonalcoholic fatty liver disease. Nat Genet. 2022 11; 54(11):1652-1663.
    View in: PubMed
    Score: 0.007
  12. Effect of booster vaccination against Delta and Omicron SARS-CoV-2 variants in Iceland. Nat Commun. 2022 09 28; 13(1):5701.
    View in: PubMed
    Score: 0.007
  13. HLA alleles, disease severity, and age associate with T-cell responses following infection with SARS-CoV-2. Commun Biol. 2022 09 06; 5(1):914.
    View in: PubMed
    Score: 0.007
  14. The sequences of 150,119 genomes in the UK Biobank. Nature. 2022 07; 607(7920):732-740.
    View in: PubMed
    Score: 0.007
  15. Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset. Ann Rheum Dis. 2022 08; 81(8):1085-1095.
    View in: PubMed
    Score: 0.007
  16. Reconstruction of a large-scale outbreak of SARS-CoV-2 infection in Iceland informs vaccination strategies. Clin Microbiol Infect. 2022 Jun; 28(6):852-858.
    View in: PubMed
    Score: 0.007
  17. Large-scale integration of the plasma proteome with genetics and disease. Nat Genet. 2021 12; 53(12):1712-1721.
    View in: PubMed
    Score: 0.007
  18. Genetic variants associated with platelet count are predictive of human disease and physiological markers. Commun Biol. 2021 09 27; 4(1):1132.
    View in: PubMed
    Score: 0.006
  19. Molecular benchmarks of a SARS-CoV-2 epidemic. Nat Commun. 2021 06 15; 12(1):3633.
    View in: PubMed
    Score: 0.006
  20. The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis. Commun Biol. 2021 06 09; 4(1):706.
    View in: PubMed
    Score: 0.006
  21. Loss-of-Function Variants in the Tumor-Suppressor Gene PTPN14 Confer Increased Cancer Risk. Cancer Res. 2021 04 15; 81(8):1954-1964.
    View in: PubMed
    Score: 0.006
  22. Lifelong Reduction in LDL (Low-Density Lipoprotein) Cholesterol due to a Gain-of-Function Mutation in LDLR. Circ Genom Precis Med. 2021 02; 14(1):e003029.
    View in: PubMed
    Score: 0.006
  23. Humoral Immune Response to SARS-CoV-2 in Iceland. N Engl J Med. 2020 10 29; 383(18):1724-1734.
    View in: PubMed
    Score: 0.006
  24. FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid disease. Nature. 2020 08; 584(7822):619-623.
    View in: PubMed
    Score: 0.006
  25. Spread of SARS-CoV-2 in the Icelandic Population. N Engl J Med. 2020 06 11; 382(24):2302-2315.
    View in: PubMed
    Score: 0.006
  26. Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank. Commun Biol. 2020 03 17; 3(1):129.
    View in: PubMed
    Score: 0.006
  27. A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy. Nat Commun. 2019 04 16; 10(1):1777.
    View in: PubMed
    Score: 0.005
  28. Insights into imprinting from parent-of-origin phased methylomes and transcriptomes. Nat Genet. 2018 11; 50(11):1542-1552.
    View in: PubMed
    Score: 0.005
  29. Graphtyper enables population-scale genotyping using pangenome graphs. Nat Genet. 2017 Nov; 49(11):1654-1660.
    View in: PubMed
    Score: 0.005
  30. Diversity in non-repetitive human sequences not found in the reference genome. Nat Genet. 2017 Apr; 49(4):588-593.
    View in: PubMed
    Score: 0.005
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.