Pall Melsted to Genetic Predisposition to Disease
This is a "connection" page, showing publications Pall Melsted has written about Genetic Predisposition to Disease.
Connection Strength
0.532
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Gene-based burden tests of rare germline variants identify six cancer susceptibility genes. Nat Genet. 2024 Nov; 56(11):2422-2433.
Score: 0.128
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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.
Score: 0.126
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FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid disease. Nature. 2020 08; 584(7822):619-623.
Score: 0.095
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Sequence variants influencing the regulation of serum IgG subclass levels. Nat Commun. 2024 Sep 14; 15(1):8054.
Score: 0.032
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Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency. Nat Genet. 2024 Sep; 56(9):1804-1810.
Score: 0.032
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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.
Score: 0.027
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The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis. Commun Biol. 2021 06 09; 4(1):706.
Score: 0.025
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Loss-of-Function Variants in the Tumor-Suppressor Gene PTPN14 Confer Increased Cancer Risk. Cancer Res. 2021 04 15; 81(8):1954-1964.
Score: 0.025
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Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank. Commun Biol. 2020 03 17; 3(1):129.
Score: 0.023
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Diversity in non-repetitive human sequences not found in the reference genome. Nat Genet. 2017 Apr; 49(4):588-593.
Score: 0.019