檢索結果 - Edwin S. Iversen
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Association between DNA Damage Response and Repair Genes and Risk of Invasive Serous Ovarian Cancer 由 Joellen M. Schildkraut, Edwin S. Iversen, Melanie A. Wilson, Merlise A. Clyde, Patricia G. Moorman, Rachel T. Palmieri, Regina S. Whitaker, Rex C. Bentley, Jeffrey R. Marks, Andrew Berchuck
出版 2010Artigo -
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Probing Structure-Function Relationships in Missense Variants in the Carboxy-Terminal Region of BRCA1 由 Renato S. Carvalho, Renata B. V. Abreu, Aneliya Velkova, Sylvia M. Marsillac, Renato Santos Rodarte, Guilherme Suarez‐Kurtz, Edwin S. Iversen, Álvaro N.A. Monteiro, Marcelo A. Carvalho
出版 2014Artigo -
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Methylation variation at<i>IGF2</i>differentially methylated regions and maternal folic acid use before and during pregnancy 由 Cathrine Hoyo, Amy Murtha, Joellen M. Schildkraut, Randy L. Jirtle, Wendy Demark‐Wahnefried, Michele R. Forman, Edwin S. Iversen, Joanne Kurtzberg, Francine Overcash, Zhiqing Huang, Susan K. Murphy
出版 2011Artigo -
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Depression in pregnancy, infant birth weight and DNA methylation of imprint regulatory elements 由 Ying Liu, Susan K. Murphy, Amy Murtha, Bernard F. Fuemmeler, Joellen M. Schildkraut, Zhiqing Huang, Francine Overcash, Joanne Kurtzberg, Randy L. Jirtle, Edwin S. Iversen, Michele R. Forman, Cathrine Hoyo
出版 2012Artigo -
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Functional assays provide a robust tool for the clinical annotation of genetic variants of uncertain significance 由 Nicholas T. Woods, Rebekah Baskin, Volha A. Golubeva, Ankita Jhuraney, Giuliana De-Gregoriis, Tereza Vaclová, David E. Goldgar, Fergus J. Couch, Marcelo A. Carvalho, Edwin S. Iversen, Álvaro N.A. Monteiro
出版 2016Artigo -
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A Systematic Genetic Assessment of 1,433 Sequence Variants of Unknown Clinical Significance in the BRCA1 and BRCA2 Breast Cancer–Predisposition Genes 由 Douglas F. Easton, Amie M. Deffenbaugh, Dmitry Pruss, Cynthia Frye, Richard Wenstrup, Kristina Allen‐Brady, Sean V. Tavtigian, Álvaro N.A. Monteiro, Edwin S. Iversen, Fergus J. Couch, David E. Goldgar
出版 2007Artigo
相關主題
Biology
Genetics
Gene
Medicine
Cancer
Internal medicine
Ovarian cancer
Computational biology
Genotype
Oncology
Single-nucleotide polymorphism
Bioinformatics
Gene expression
Serous fluid
Genome-wide association study
Cancer research
Computer science
DNA methylation
Missense mutation
Mutation
Environmental health
Methylation
Odds ratio
Phenotype
Population
SNP
Breast cancer
Pregnancy
Biochemistry
Carcinogenesis