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Edward R. Oliver, Ph.D. - Publications

Affiliations: 
2005 University of Michigan, Ann Arbor, Ann Arbor, MI 
Area:
Genetics
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17 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Didier RA, Martin-Saavedra JS, Oliver ER, DeBari SE, Bilaniuk LT, Howell LJ, Moldenhauer JS, Adzick NS, Heuer GG, Coleman BG. Fetal Intraventricular Hemorrhage in Open Neural Tube Defects: Prenatal Imaging Evaluation and Perinatal Outcomes. Ajnr. American Journal of Neuroradiology. PMID 32943419 DOI: 10.3174/Ajnr.A6745  0.336
2020 Weiss DA, Oliver ER, Borer JG, Kryger JV, Roth EB, Groth TW, Shukla AR, Mitchell ME, Canning DA, Victoria T. Key anatomic findings on fetal ultrasound and MRI in the prenatal diagnosis of bladder and cloacal exstrophy. Journal of Pediatric Urology. PMID 32773250 DOI: 10.1016/J.Jpurol.2020.07.024  0.301
2020 Oliver ER, Maturen KE, Feldstein VA, Poder L, Shipp TD, Simpson L, Strachowski LM, Sussman BL, Weber TM, Winter T, Glanc P. ACR Appropriateness Criteria® Assessment of Gravid Cervix. Journal of the American College of Radiology : Jacr. 17: S26-S35. PMID 32370970 DOI: 10.1016/J.Jacr.2020.01.032  0.31
2020 Poder L, Weinstein S, Maturen KE, Feldstein VA, Mackenzie DC, Oliver ER, Shipp TD, Strachowski LM, Sussman BL, Wang EY, Weber TM, Whitcomb BP, Glanc P. ACR Appropriateness Criteria® Placenta Accreta Spectrum Disorder. Journal of the American College of Radiology : Jacr. 17: S207-S214. PMID 32370965 DOI: 10.1016/J.Jacr.2020.01.031  0.318
2019 Shipp TD, Zelop CM, Maturen KE, Deshmukh SP, Dudiak KM, Henrichsen TL, Oliver ER, Poder L, Sadowski EA, Simpson L, Weber TM, Winter T, Glanc P. ACR Appropriateness Criteria Growth Disturbances-Risk of Fetal Growth Restriction. Journal of the American College of Radiology : Jacr. 16: S116-S125. PMID 31054738 DOI: 10.1016/J.Jacr.2019.02.009  0.323
2019 Oliver ER, DeBari SE, Adams SE, Didier RA, Horii SC, Victoria T, Hedrick HL, Adzick NS, Howell LJ, Moldenhauer JS, Coleman BG. Congenital diaphragmatic hernia sacs: prenatal imaging and associated postnatal outcomes. Pediatric Radiology. PMID 30635693 DOI: 10.1007/S00247-018-04334-9  0.303
2018 Didier RA, DeBari SE, Oliver ER, Gebb JS, Howell LJ, Hedrick HL, Adzick NS, Coleman BG. Secondary Imaging Findings Aid in Prenatal Diagnosis and Characterization of Congenital Diaphragmatic Hernia: Role of an Abnormal Orientation of Vascular Structures and Gallbladder Position. Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine. PMID 30244484 DOI: 10.1002/Jum.14823  0.336
2018 Oliver ER, DeBari SE, Horii SC, Pogoriler JE, Victoria T, Khalek N, Howell LJ, Adzick NS, Coleman BG. Congenital Lobar Overinflation: A Rare Enigmatic Lung Lesion on Prenatal Ultrasound and Magnetic Resonance Imaging. Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine. PMID 30208226 DOI: 10.1002/Jum.14801  0.304
2017 Oliver ER, Coleman BG, DeBari SE, Victoria T, Looney DM, Horii SC, Moldenhauer JS, Langer JE, Howell LJ, Pawel BR, Adzick NS. Fetal Lymphatic Malformations: More Variable Than We Think? Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine. PMID 28127788 DOI: 10.7863/Ultra.16.04071  0.302
2016 Azour L, Besa C, Lewis S, Kamath A, Oliver ER, Taouli B. The gravid uterus: MR imaging and reporting of abnormal placentation. Abdominal Radiology (New York). PMID 27472936 DOI: 10.1007/S00261-016-0752-5  0.337
2013 Kaplan MC, Coleman BG, Shaylor SD, Howell LJ, Oliver ER, Horii SC, Adzick NS. Sonographic features of rare posterior fetal neck masses of vascular origin. Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine. 32: 873-80. PMID 23620330 DOI: 10.7863/Ultra.32.5.873  0.303
2012 Prasov L, Masud T, Khaliq S, Mehdi SQ, Abid A, Oliver ER, Silva ED, Lewanda A, Brodsky MC, Borchert M, Kelberman D, Sowden JC, Dattani MT, Glaser T. ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous. Human Molecular Genetics. 21: 3681-94. PMID 22645276 DOI: 10.1093/Hmg/Dds197  0.621
2004 Oliver ER, Saunders TL, Tarlé SA, Glaser T. Ribosomal protein L24 defect in belly spot and tail (Bst), a mouse Minute. Development (Cambridge, England). 131: 3907-20. PMID 15289434 DOI: 10.1242/Dev.01268  0.614
2004 Adamska M, MacDonald BT, Sarmast ZH, Oliver ER, Meisler MH. En1 and Wnt7a interact with Dkk1 during limb development in the mouse. Developmental Biology. 272: 134-44. PMID 15242796 DOI: 10.1016/J.Ydbio.2004.04.026  0.305
2001 Tucker P, Laemle L, Munson A, Kanekar S, Oliver ER, Brown N, Schlecht H, Vetter M, Glaser T. The eyeless mouse mutation (ey1) removes an alternative start codon from the Rx/rax homeobox gene. Genesis (New York, N.Y. : 2000). 31: 43-53. PMID 11668677 DOI: 10.1002/Gene.10003  0.605
2001 Vincent A, Billingsley G, Priston M, Williams-Lyn D, Sutherland J, Glaser T, Oliver E, Walter MA, Heathcote G, Levin A, Héon E. Phenotypic heterogeneity of CYP1B1: mutations in a patient with Peters' anomaly. Journal of Medical Genetics. 38: 324-6. PMID 11403040 DOI: 10.1136/Jmg.38.5.324  0.642
2000 Lauderdale JD, Wilensky JS, Oliver ER, Walton DS, Glaser T. 3' deletions cause aniridia by preventing PAX6 gene expression Proceedings of the National Academy of Sciences of the United States of America. 97: 13755-13759. PMID 11087823 DOI: 10.1073/Pnas.240398797  0.616
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