Scholar: Haley Eidem

Haley Eidem

integRATE: a desirability-based data integration framework for the prioritization of candidate genes across heterogeneous omics and its application to preterm birth

  • Haley R Eidem, Jacob L Steenwyk, Jennifer H Wisecaver, John A Capra, Patrick Abbot, Antonis Rokas
  • BMC Med Genomics, 10.1186/s12920-018-0426-y
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Correction: Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth

  • Johanna M Huusko, Minna K Karjalainen, Britney E Graham, …, Kelli K Ryckman, Mikko Hallman, Louis J Muglia
  • PLoS Genet, 10.1371/journal.pgen.1007673
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The transformative potential of an integrative approach to pregnancy

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Comprehensive RNA profiling of villous trophoblast and decidua basalis in pregnancies complicated by preterm birth following intra-amniotic infection

  • William E Ackerman, Irina A Buhimschi, Haley R Eidem, …, Taryn L Summerfield, Mark B Landon, Catalin S Buhimschi
  • Placenta, 10.1016/j.placenta.2016.05.010
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Comparing human and macaque placental transcriptomes to disentangle preterm birth pathology from gestational age effects

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Integrating Diverse Types of Genomic Data to Identify Genes that Underlie Adverse Pregnancy Phenotypes

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GEneSTATION 1.0: a synthetic resource of diverse evolutionary and functional genomic data for studying the evolution of pregnancy-associated tissues and phenotypes

  • Mara Kim, Brian A Cooper, Rohit Venkat, …, Patrick Abbot, Antonis Rokas, Kriston L McGary
  • Nucleic Acids Res, 10.1093/nar/gkv1137
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Gestational tissue transcriptomics in term and preterm human pregnancies: a systematic review and meta-analysis

  • Haley R Eidem, William E Ackerman, Kriston L McGary, Patrick Abbot, Antonis Rokas
  • BMC Med Genomics, 10.1186/s12920-015-0099-8
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Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq study

  • Flavia M Facio, Haley Eidem, Tyler Fisher, …, Kimberly A Kaphingst, Leslie G Biesecker, Barbara B Biesecker
  • Eur J Hum Genet, 10.1038/ejhg.2012.179
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Effects of informed consent for individual genome sequencing on relevant knowledge

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