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Marion Verp

TitleASSOCIATE PROFESSOR
InstitutionUniversity of Chicago
DepartmentObstetrics & Gynecology
AddressChicago IL 60637
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    Collapse Bibliographic 
    Collapse selected publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    1. Guindalini RSC, Zheng Y, Abe H, Whitaker K, Yoshimatsu TF, Walsh T, Schacht D, Kulkarni K, Sheth D, Verp MS, Bradbury AR, Churpek J, Obeid E, Mueller J, Khramtsova G, Liu F, Raoul A, Cao H, Romero IL, Hong S, Livingston R, Jaskowiak N, Wang X, Debiasi M, Pritchard CC, King MC, Karczmar G, Newstead GM, Huo D, Olopade OI. Intensive Surveillance with Biannual Dynamic Contrast-Enhanced Magnetic Resonance Imaging Downstages Breast Cancer in BRCA1 Mutation Carriers. Clin Cancer Res. 2019 Mar 15; 25(6):1786-1794. PMID: 30154229.
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    2. Yamaguchi K, Schacht D, Newstead GM, Bradbury AR, Verp MS, Olopade OI, Abe H. Breast cancer detected on an incident (second or subsequent) round of screening MRI: MRI features of false-negative cases. AJR Am J Roentgenol. 2013 Nov; 201(5):1155-63. PMID: 24147491.
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    3. Bradbury AR, Ibe CN, Dignam JJ, Cummings SA, Verp M, White MA, Artioli G, Dudlicek L, Olopade OI. Uptake and timing of bilateral prophylactic salpingo-oophorectomy among BRCA1 and BRCA2 mutation carriers. Genet Med. 2008 Mar; 10(3):161-166. PMID: 18344704.
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    4. Chapa JB, Hibbard JU, Weber EM, Abramowicz JS, Verp MS. Prenatal diagnosis of methotrexate embryopathy. Obstet Gynecol. 2003 May; 101(5 Pt 2):1104-7. PMID: 12738117.
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    5. Cheng Y, Verp MS, Knutel T, Hibbard JU. Mucopolysaccharidosis type VII as a cause of recurrent non-immune hydrops fetalis. J Perinat Med. 2003; 31(6):535-7. PMID: 14711113.
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    6. Aldrich C, Verp MS, Walker MA, Ober C. A null mutation in HLA-G is not associated with preeclampsia or intrauterine growth retardation. J Reprod Immunol. 2000 May; 47(1):41-8. PMID: 10779589.
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    7. Verp MS. Maternal serum alpha-fetoprotein and anal atresia. Prenat Diagn. 1999 Jul; 19(7):689-90. PMID: 10419625.
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    8. Gabrielian K, Oganesian A, Patel SC, Verp MS, Ernest JT. Cellular response in rabbit eyes after human fetal RPE cell transplantation. Graefes Arch Clin Exp Ophthalmol. 1999 Apr; 237(4):326-35. PMID: 10208266.
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    9. Gabrielian K, Oganesian A, Farrokh-Siar L, Rezai KA, Verp MS, Patel SC, Ernest JT. Growth of human fetal retinal pigment epithelium as microspheres. Graefes Arch Clin Exp Ophthalmol. 1999 Mar; 237(3):241-8. PMID: 10090588.
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    10. Heckerling PS, Verp MS, Albert N. Patient or physician preferences for decision analysis: the prenatal genetic testing decision. Med Decis Making. 1999 Jan-Mar; 19(1):66-77. PMID: 9917022.
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    11. Ober C, Aldrich C, Rosinsky B, Robertson A, Walker MA, Willadsen S, Verp MS, Geraghty DE, Hunt JS. HLA-G1 protein expression is not essential for fetal survival. Placenta. 1998 Mar-Apr; 19(2-3):127-32. PMID: 9548178.
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    12. Heckerling PS, Verp MS, Albert N. The role of physician preferences in the choice of amniocentesis or chorionic villus sampling for prenatal genetic testing. Genet Test. 1998; 2(1):61-6. PMID: 10464598.
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    13. Mahowald MB, Verp MS, Anderson RR. Genetic counseling: clinical and ethical challenges. Annu Rev Genet. 1998; 32:547-59. PMID: 9928491.
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    14. Digiovanni LM, Quinlan MP, Verp MS. Choroid plexus cysts: infant and early childhood developmental outcome. Obstet Gynecol. 1997 Aug; 90(2):191-4. PMID: 9241291.
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    15. Heckerling PS, Verp MS, Albert N. Prenatal testing for limb reduction defects. How patients' views affect their choice of CVS. J Reprod Med. 1997 Feb; 42(2):114-20. PMID: 9058348.
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    16. Kubota T, Aradhya S, Macha M, Smith AC, Surh LC, Satish J, Verp MS, Nee HL, Johnson A, Christan SL, Ledbetter DH. Analysis of parent of origin specific DNA methylation at SNRPN and PW71 in tissues: implication for prenatal diagnosis. J Med Genet. 1996 Dec; 33(12):1011-4. PMID: 9004133.
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    17. Christian SL, Smith AC, Macha M, Black SH, Elder FF, Johnson JM, Resta RG, Surti U, Suslak L, Verp MS, Ledbetter DH. Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicism. Prenat Diagn. 1996 Apr; 16(4):323-32. PMID: 8734806.
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    18. Verp MS, Heckerling PS. Use of decision analysis to evaluate patients' choices of diagnostic prenatal test. Am J Med Genet. 1995 Sep 25; 58(4):337-44. PMID: 8533842.
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    19. Giannoni F, Chou SC, Skarosi SF, Verp MS, Field FJ, Coleman RA, Davidson NO. Developmental regulation of the catalytic subunit of the apolipoprotein B mRNA editing enzyme (APOBEC-1) in human small intestine. J Lipid Res. 1995 Aug; 36(8):1664-75. PMID: 7595088.
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    20. Heckerling PS, Verp MS, Hadro TA. Preferences of pregnant women for amniocentesis or chorionic villus sampling for prenatal testing: comparison of patients' choices and those of a decision-analytic model. J Clin Epidemiol. 1994 Nov; 47(11):1215-28. PMID: 7722557.
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    21. Heckerling PS, Verp MS. A cost-effectiveness analysis of amniocentesis and chorionic villus sampling for prenatal genetic testing. Med Care. 1994 Aug; 32(8):863-80. PMID: 8057700.
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    22. Hanlon-Lundberg KM, Verp MS, Loy G. Posterior urethral valves in successive generations. Am J Perinatol. 1994 Jan; 11(1):37-9. PMID: 8155208.
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    23. Marcus P, Verp MS. Menetrier disease in a child of a consanguineous union. Am J Med Genet. 1993 Dec 01; 47(8):1231-2. PMID: 8123171.
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    24. Blakemore K, Filkins K, Luthy DA, Platt LD, Medearis AL, Carlson D, Priest J, Korotkin J, Verp MS, Padilla LM, et al. Cook obstetrics and gynecology catheter multicenter chorionic villus sampling trial: comparison of birth defects with expected rates. Am J Obstet Gynecol. 1993 Oct; 169(4):1022-6. PMID: 8238113.
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    25. Burton BK, Prins GS, Verp MS. A prospective trial of prenatal screening for Down syndrome by means of maternal serum alpha-fetoprotein, human chorionic gonadotropin, and unconjugated estriol. Am J Obstet Gynecol. 1993 Sep; 169(3):526-30. PMID: 7690522.
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    26. Verp MS, Sibul M, Billstrand C, Bellen G, Hsu M, Ober C. Maternal-fetal histocompatibility in intrauterine growth retarded and normal weight babies. Am J Reprod Immunol. 1993 May; 29(4):195-8. PMID: 8397808.
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    27. Ditzian-Kadanoff R, Garon J, Verp MS, Zilberstein M. Gamma delta T cells in human decidua. Am J Obstet Gynecol. 1993 Mar; 168(3 Pt 1):831-6. PMID: 8096118.
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    28. Verp MS, Harrison HH, Ober C, Oliveri D, Amarose AP, Lindgren V, Talerman A. Chimerism as the etiology of a 46,XX/46,XY fertile true hermaphrodite. Fertil Steril. 1992 Feb; 57(2):346-9. PMID: 1735486.
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    29. Verp MS, Ober C, Oliveri DR, Israel J. Delayed diagnosis of pseudohermaphroditism on stored blood spot. Lancet. 1991 Apr 27; 337(8748):1037. PMID: 1673185.
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    30. Heckerling PS, Verp MS. Genetic risk and early versus late prenatal testing. Lancet. 1991 Feb 09; 337(8737):363. PMID: 1671254.
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    31. Heckerling PS, Verp MS. Amniocentesis or chorionic villus sampling for prenatal genetic testing: a decision analysis. J Clin Epidemiol. 1991; 44(7):657-70. PMID: 2066746.
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    32. Talerman A, Verp MS, Senekjian E, Gilewski T, Vogelzang N. True hermaphrodite with bilateral ovotestes, bilateral gonadoblastomas and dysgerminomas, 46,XX/46,XY karyotype, and a successful pregnancy. Cancer. 1990 Dec 15; 66(12):2668-72. PMID: 2249209.
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    33. Teng B, Verp M, Salomon J, Davidson NO. Apolipoprotein B messenger RNA editing is developmentally regulated and widely expressed in human tissues. J Biol Chem. 1990 Nov 25; 265(33):20616-20. PMID: 2243107.
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    34. Verp MS, Unger NL. Chorionic chromosome abnormalities and intrauterine growth retardation. J Perinatol. 1990 Mar; 10(1):52-4. PMID: 2313394.
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    35. Verp MS. Pulmonary artery agenesis. Am J Obstet Gynecol. 1989 Dec; 161(6 Pt 1):1746-7. PMID: 2603937.
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    36. Verp MS, Rosinsky B, Sheikh Z, Amarose AP. Non-mosaic trisomy 16 confined to villi. Lancet. 1989 Oct 14; 2(8668):915-6. PMID: 2571827.
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    37. Verp MS, Sheikh Z, Amarose AP, Cibils LA. Cystic hygroma and 45,X/46,XY mosaicism. Am J Med Genet. 1989 Jul; 33(3):402-4. PMID: 2679092.
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    38. Verp MS. Urinary tract abnormalities in hand-foot-genital syndrome. Am J Med Genet. 1989 Apr; 32(4):555. PMID: 2774004.
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    39. Verp MS, Ismail MA, Sheikh Z. Fetal urinary tract obstruction and trisomy 18 mosaicism. A case report. J Reprod Med. 1988 Apr; 33(4):391-2. PMID: 3285006.
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    40. Verp MS, Rosinsky B, Le Beau MM, Martin AO, Kaplan R, Wallemark CB, Otano L, Simpson JL. Growth disadvantage of 45,X and 46,X,del(X)(p11) fibroblasts. Clin Genet. 1988 Apr; 33(4):277-85. PMID: 3359684.
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    41. Verp MS, Bombard AT, Simpson JL, Elias S. Parental decision following prenatal diagnosis of fetal chromosome abnormality. Am J Med Genet. 1988 Mar; 29(3):613-22. PMID: 3377004.
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    42. Verp MS, Amarose AP. Chromosomal mosaicism of trisomy 7 restricted to chorionic villi. Am J Med Genet. 1987 Sep; 28(1):221. PMID: 3674111.
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    43. Verp MS, Amarose AP. Inflammatory bowel disease and X chromosome abnormalities. A case report. J Reprod Med. 1987 Jun; 32(6):466-8. PMID: 3612638.
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    44. Verp MS, Simpson JL. Abnormal sexual differentiation and neoplasia. Cancer Genet Cytogenet. 1987 Apr; 25(2):191-218. PMID: 3548944.
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    45. Verp MS, Amarose AP, Esterly JR, Moawad AH. Mosaic trisomy 7 and renal dysplasia. Am J Med Genet. 1987 Jan; 26(1):139-43. PMID: 3812554.
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    46. Verp MS, Milunsky A, Simpson JL, Graham A, Sabbagha R. Elevated alpha-fetoprotein and acetylcholinesterase associated with hydrocele. Am J Med Genet. 1984 Dec; 19(4):651-2. PMID: 6083726.
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    47. Verp MS, Radvany RM, Green D, Conneally PM, Patel VA, Martin AO, Simpson JL. Linkage analysis in von Willebrand disease. Clin Genet. 1983 Dec; 24(6):434-8. PMID: 6606506.
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    48. Verp MS, Cohen MR, Simpson JL. Necessity of formal genetic screening in artificial insemination by donor. Obstet Gynecol. 1983 Oct; 62(4):474-9. PMID: 6888826.
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    49. Verp MS, Simpson JL, Elias S, Carson SA, Sarto GE, Feingold M. Heritable aspects of uterine anomalies. I. Three familial aggregates with Müllerian fusion anomalies. Fertil Steril. 1983 Jul; 40(1):80-5. PMID: 6862042.
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    50. Verp MS, Simpson JL, Martin AO. Hypostatic ulcers in 47,XXY Klinefelter's syndrome. J Med Genet. 1983 Apr; 20(2):100-1. PMID: 6842542.
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    51. Verp MS, Rzeszotarski MS, Martin AO, Simpson JL. Relationship between Y-chromosome length and first-trimester spontaneous abortions. Am J Obstet Gynecol. 1983 Feb 15; 145(4):433-8. PMID: 6824036.
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    52. Verp MS, Elias S, Simpson JL. Further comments on amniocentesis in twin gestations. Am J Med Genet. 1983 Feb; 14(2):397-8. PMID: 6837636.
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    53. Elias S, Verp MS. Prenatal diagnosis of genetic disorders. Obstet Gynecol Annu. 1983; 12:79-102. PMID: 6346164.
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    54. Simpson JL, Verp MS. The prenatal diagnosis of genetic disorders. Clin Obstet Gynecol. 1982 Dec; 25(4):635-58. PMID: 6761024.
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    55. Simpson JL, Martin AO, Verp MS, Elias S, Patel VA. Hypermodal cells in amniotic fluid cultures: frequency, interpretation, and clinical significance. Am J Obstet Gynecol. 1982 Jun 01; 143(3):250-8. PMID: 7081343.
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    56. Verp MS, Gerbie AB. Amniocentesis for prenatal diagnosis. Clin Obstet Gynecol. 1981 Dec; 24(4):1007-21. PMID: 6800677.
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    57. Verp M, Karpatkin S. Effect of plasma, steroids, or steroid products on the adhesion of human opsonized thrombocytes to human leukocytes. J Lab Clin Med. 1975 Mar; 85(3):478-86. PMID: 804027.
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