Fine Mapping Genomic Regions Associated with Endometriosis Risk

Fine Mapping Genomic Regions Associated with Endometriosis Risk

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς:	Montgomery, G, Luong, H, Jones, L, Fung, J, Painter, J, Zondervan, K, Nyholt, DR, Rogers, P
Μορφή:	Journal article
Έκδοση:	2014

Παρόμοια τεκμήρια

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No evidence for genetic association with the let-7 microRNA-binding site or other common KRAS variants in risk of endometriosis.
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The search for genes contributing to endometriosis risk.
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High-density fine-mapping of a chromosome 10q26 linkage peak suggests association between endometriosis and variants close to CYP2C19.
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High-density fine-mapping of a chromosome 10q26 linkage peak suggests association between endometriosis and variants close to CYP2C19
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Beyond endometriosis genome-wide association study: from genomics to phenomics to the patient
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High-density fine-mapping of a chromosome 10q26 linkage peak suggests association between endometriosis and variants close to CYP2C19
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Genome-wide association meta-analysis identifies new endometriosis risk loci.
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Common variants in the CYP2C19 gene are associated with susceptibility to endometriosis
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Common variants in the CYP2C19 gene are associated with susceptibility to endometriosis.
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Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis.
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The future for genetic studies in reproduction.
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Significant evidence of one or more susceptibility loci for endometriosis with near-Mendelian inheritance on chromosome 7p13-15.
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Genome-wide association analysis identifies 27 novel loci associated with uterine leiomyomata revealing common genetic origins with endometriosis
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Endometriosis
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