Pall Melsted to Genome-Wide Association Study
This is a "connection" page, showing publications Pall Melsted has written about Genome-Wide Association Study.
Connection Strength
0.905
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Sequence variants influencing the regulation of serum IgG subclass levels. Nat Commun. 2024 09 14; 15(1):8054.
Score: 0.126
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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: 0.125
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Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis. Nat Genet. 2023 12; 55(12):2149-2159.
Score: 0.118
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Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria. Commun Biol. 2023 07 10; 6(1):703.
Score: 0.116
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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: 0.106
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Missense variants in FRS3 affect body mass index in populations of diverse ancestries. Nat Commun. 2025 Mar 25; 16(1):2694.
Score: 0.033
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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.
Score: 0.032
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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: 0.031
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Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura. Nat Genet. 2023 11; 55(11):1843-1853.
Score: 0.030
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Multiomics study of nonalcoholic fatty liver disease. Nat Genet. 2022 11; 54(11):1652-1663.
Score: 0.028
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Large-scale integration of the plasma proteome with genetics and disease. Nat Genet. 2021 12; 53(12):1712-1721.
Score: 0.026
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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: 0.024
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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: 0.023
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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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A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy. Nat Commun. 2019 04 16; 10(1):1777.
Score: 0.022
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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