Hélène Choquet to Mutation
This is a "connection" page, showing publications Hélène Choquet has written about Mutation.
Connection Strength
1.115
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Genetic and functional characterization of PCSK1. Methods Mol Biol. 2011; 768:247-53.
Score: 0.360
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Genome-wide Genotyping of Cerebral Cavernous Malformation Type 1 Individuals to Identify Genetic Modifiers of Disease Severity. Methods Mol Biol. 2020; 2152:77-84.
Score: 0.168
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A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci. Nat Commun. 2018 06 11; 9(1):2278.
Score: 0.151
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Cytochrome P450 and matrix metalloproteinase genetic modifiers of disease severity in Cerebral Cavernous Malformation type 1. Free Radic Biol Med. 2016 Mar; 92:100-109.
Score: 0.128
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Genetics of cerebral cavernous malformations: current status and future prospects. J Neurosurg Sci. 2015 Sep; 59(3):211-20.
Score: 0.121
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Heterozygous mutations causing partial prohormone convertase 1 deficiency contribute to human obesity. Diabetes. 2012 Feb; 61(2):383-90.
Score: 0.096
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No major contribution of TCF7L2 sequence variants to maturity onset of diabetes of the young (MODY) or neonatal diabetes mellitus in French white subjects. Diabetologia. 2007 Jan; 50(1):214-6.
Score: 0.067
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Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and human. Nature. 2012 Feb 19; 483(7389):350-4.
Score: 0.024