The University of Chicago Header Logo

Connection

Pall Melsted to Genetic Predisposition to Disease

Back to Details
This is a "connection" page, showing publications Pall Melsted has written about Genetic Predisposition to Disease.
Pall Melsted
Connection Strength
0.535
Genetic Predisposition to Disease
  1. 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: 0.115
  2. 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: 0.113
  3. FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid disease. Nature. 2020 08; 584(7822):619-623.
    View in: PubMed
    Score: 0.085
  4. A genome-wide association meta-analysis links hidradenitis suppurativa to common and rare sequence variants causing disruption of the Notch and Wnt/ß-catenin signaling pathways. J Am Acad Dermatol. 2025 Apr; 92(4):761-772.
    View in: PubMed
    Score: 0.029
  5. A partial loss-of-function variant in STAT6 protects against type 2 asthma. J Allergy Clin Immunol. 2025 Jan; 155(1):228-235.
    View in: PubMed
    Score: 0.029
  6. Sequence variants influencing the regulation of serum IgG subclass levels. Nat Commun. 2024 09 14; 15(1):8054.
    View in: PubMed
    Score: 0.029
  7. Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency. Nat Genet. 2024 Sep; 56(9):1804-1810.
    View in: PubMed
    Score: 0.028
  8. 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: 0.024
  9. 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: 0.023
  10. 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: 0.022
  11. 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: 0.021
  12. Diversity in non-repetitive human sequences not found in the reference genome. Nat Genet. 2017 Apr; 49(4):588-593.
    View in: PubMed
    Score: 0.017
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.