| Year |
Citation |
Score |
| 2018 |
Eidem HR, Steenwyk JL, Wisecaver JH, Capra JA, Abbot P, Rokas A. integRATE: a desirability-based data integration framework for the prioritization of candidate genes across heterogeneous omics and its application to preterm birth. Bmc Medical Genomics. 11: 107. PMID 30453955 DOI: 10.1186/S12920-018-0426-Y |
0.757 |
|
| 2018 |
Huusko JM, Karjalainen MK, Graham BE, Zhang G, Farrow EG, Miller NA, Jacobsson B, Eidem HR, Murray JC, Bedell B, Breheny P, Brown NW, Bødker FL, Litterman NK, Jiang PP, et al. Correction: Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth. Plos Genetics. 14: e1007673. PMID 30212495 DOI: 10.1371/Journal.Pgen.1007673 |
0.555 |
|
| 2018 |
Huusko JM, Karjalainen MK, Graham BE, Zhang G, Farrow EG, Miller NA, Jacobsson B, Eidem HR, Murray JC, Bedell B, Breheny P, Brown NW, Bødker FL, Litterman NK, Jiang PP, et al. Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth. Plos Genetics. 14: e1007394. PMID 30001343 DOI: 10.1371/Journal.Pgen.1007394 |
0.605 |
|
| 2017 |
Eidem HR, McGary KL, Capra JA, Abbot P, Rokas A. The transformative potential of an integrative approach to pregnancy. Placenta. 57: 204-215. PMID 28864013 DOI: 10.1016/J.Placenta.2017.07.010 |
0.781 |
|
| 2016 |
Ackerman WE, Buhimschi IA, Eidem HR, Rinker DC, Rokas A, Rood K, Zhao G, Summerfield TL, Landon MB, Buhimschi CS. Comprehensive RNA profiling of villous trophoblast and decidua basalis in pregnancies complicated by preterm birth following intra-amniotic infection. Placenta. 44: 23-33. PMID 27452435 DOI: 10.1016/J.Placenta.2016.05.010 |
0.746 |
|
| 2016 |
Eidem HR, Rinker DC, Ackerman WE, Buhimschi IA, Buhimschi CS, Dunn-Fletcher C, Kallapur SG, Pavličev M, Muglia LJ, Abbot P, Rokas A. Comparing human and macaque placental transcriptomes to disentangle preterm birth pathology from gestational age effects. Placenta. 41: 74-82. PMID 27208410 DOI: 10.1016/J.Placenta.2016.03.006 |
0.743 |
|
| 2015 |
Hirbo J, Eidem H, Rokas A, Abbot P. Integrating Diverse Types of Genomic Data to Identify Genes that Underlie Adverse Pregnancy Phenotypes. Plos One. 10: e0144155. PMID 26641094 DOI: 10.1371/Journal.Pone.0144155 |
0.672 |
|
| 2015 |
Kim M, Cooper BA, Venkat R, Phillips JB, Eidem HR, Hirbo J, Nutakki S, Williams SM, Muglia LJ, Capra JA, Petren K, Abbot P, Rokas A, McGary KL. GEneSTATION 1.0: a synthetic resource of diverse evolutionary and functional genomic data for studying the evolution of pregnancy-associated tissues and phenotypes. Nucleic Acids Research. PMID 26567549 DOI: 10.1093/Nar/Gkv1137 |
0.612 |
|
| 2015 |
Eidem HR, Ackerman WE, McGary KL, Abbot P, Rokas A. Gestational tissue transcriptomics in term and preterm human pregnancies: a systematic review and meta-analysis. Bmc Medical Genomics. 8: 27. PMID 26044726 DOI: 10.1186/S12920-015-0099-8 |
0.788 |
|
| 2015 |
Eidem HR, McGary KL, Rokas A. Shared Selective Pressures on Fungal and Human Metabolic Pathways Lead to Divergent yet Analogous Genetic Responses. Molecular Biology and Evolution. 32: 1449-55. PMID 25681382 DOI: 10.1093/Molbev/Msv034 |
0.74 |
|
| 2015 |
Ackerman W, Buhimschi I, Eidem H, Rinker D, Rokas A, Rood K, Zhao G, Summerfield T, Landon M, Buhimschi C. 274: Next generation sequencing (RNA-seq) of the human decidual and placental villous transcriptomes in intra-amniotic infection (IAI) induced preterm birth (PTB) American Journal of Obstetrics and Gynecology. 212: S149-S150. DOI: 10.1016/J.Ajog.2014.10.320 |
0.736 |
|
| 2015 |
Ackerman W, Buhimschi I, Eidem H, Rinker D, Rokas A, Millen KR, Summerfield T, Zhao G, Shellhaas C, Landon M, Buhimschi C. 115: A comprehensive analysis of the human decidual and placental villous transcriptomes in women with preeclampsia (PE) using next generation sequencing (RNA-seq) American Journal of Obstetrics and Gynecology. 212: S75. DOI: 10.1016/J.Ajog.2014.10.161 |
0.728 |
|
| 2013 |
Facio FM, Eidem H, Fisher T, Brooks S, Linn A, Kaphingst KA, Biesecker LG, Biesecker BB. Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq study European Journal of Human Genetics. 21: 261-265. PMID 22892536 DOI: 10.1038/Ejhg.2012.179 |
0.314 |
|
| 2012 |
Chan B, Facio FM, Eidem H, Hull SC, Biesecker LG, Berkman BE. Genomic inheritances: disclosing individual research results from whole-exome sequencing to deceased participants' relatives. American Journal of Bioethics. 12: 1-8. PMID 22974017 DOI: 10.1080/15265161.2012.699138 |
0.349 |
|
| 2012 |
Kaphingst KA, Facio FM, Cheng M, Brooks S, Eidem H, Linn A, Biesecker BB, Biesecker LG. Effects of informed consent for individual genome sequencing on relevant knowledge. Clinical Genetics. 82: 408-415. PMID 22694298 DOI: 10.1111/J.1399-0004.2012.01909.X |
0.315 |
|
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