Publications

  1. Thilagar BP, Ghosh AK, Nguyen J, Theiler RN, Wick MJ, Hurt RT, Razonable RR, Ganesh R. Anti-Spike Monoclonal Antibody Therapy in Pregnant Women With Mild-to-Moderate Coronavirus Disease 2019 (COVID-19). Obstet Gynecol 2022 Apr 1; 139 (4):616-618 Epub 2022 Jan 13
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  2. Theiler RN, Wick M, Mehta R, Weaver AL, Virk A, Swift M. Pregnancy and birth outcomes after SARS-CoV-2 vaccination in pregnancy. Am J Obstet Gynecol MFM. 2021 Nov; 3 (6):100467 Epub 2021 Aug 20
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  3. Alrahmani L, Gonzalez Suarez ML, Cousin MA, Moyer AM, Willrich MAV, White WM, Wick MJ, Tostrud LJ, Narang K, Garovic VD. Quantitative Alterations in Complement Alternative Pathway and Related Genetic Analysis in Severe Phenotype Preeclampsia. Kidney360. 2021 Sep 30; 2 (9):1463-1472 Epub 2021 June 30
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  4. Tischkowitz M, Balmana J, Foulkes WD, James P, Ngeow J, Schmutzler R, Voian N, Wick MJ, Stewart DR, Pal T, ACMG Professional Practice and Guidelines Committee. Management of individuals with germline variants in PALB2: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG). Genet Med. 2021 Aug; 23 (8):1416-1423 Epub 2021 May 11
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  5. Enninga EAL, Jang JS, Hur B, Johnson EL, Wick MJ, Sung J, Chakraborty R. Maternal obesity is associated with phenotypic alterations in fetal immune cells by single-cell mass cytometry. Am J Reprod Immunol. 2021 Mar; 85 (3):e13358 Epub 2020 Nov 04
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  6. Samadder NJ, Riegert-Johnson D, Boardman L, Rhodes D, Wick M, Okuno S, Kunze KL, Golafshar M, Uson PLS Jr, Mountjoy L, Ertz-Archambault N, Patel N, Rodriguez EA, Lizaola-Mayo B, Lehrer M, Thorpe CS, Yu NY, Esplin ED, Nussbaum RL, Sharp RR, Azevedo C, Klint M, Hager M, Macklin-Mantia S, Bryce AH, Bekaii-Saab TS, Sekulic A, Stewart AK. Comparison of Universal Genetic Testing vs Guideline-Directed Targeted Testing for Patients With Hereditary Cancer Syndrome. JAMA Oncol. 2021 Feb 1; 7 (2):230-237
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  7. Daly MB, Pal T, Berry MP, Buys SS, Dickson P, Domchek SM, Elkhanany A, Friedman S, Goggins M, Hutton ML, Karlan BY, Khan S, Klein C, Kohlmann W, Kurian AW, Laronga C, Litton JK, Mak JS, Menendez CS, Merajver SD, Norquist BS, Offit K, Pederson HJ, Reiser G, Senter-Jamieson L, Shannon KM, Shatsky R, Visvanathan K, Weitzel JN, Wick MJ, Wisinski KB, Yurgelun MB, Darlow SD, Dwyer MA, CGC//CGC//LCGC//CGC//CGC. Genetic/Familial High-Risk Assessment: Breast, Ovarian, and Pancreatic, Version 2.2021, NCCN Clinical Practice Guidelines in Oncology. J Natl Compr Canc Netw. 2021 Jan 6; 19 (1):77-102 Epub 2021 Jan 06
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  8. Ferrer A, Starosta RT, Ranatunga W, Ungar D, Kozicz T, Klee E, Rust LM, Wick M, Morava E. Fetal glycosylation defect due to ALG3 and COG5 variants detected via amniocentesis: Complex glycosylation defect with embryonic lethal phenotype. Mol Genet Metab. 2020 Dec; 131 (4):424-429 Epub 2020 Nov 07
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  9. Ballout RA, Dickerson C, Wick MJ, Al-Sweel N, Openshaw AS, Srivastava S, Swanson LC, Bramswig NC, Kuechler A, Hong B, Fleming LR, Curry K, Robertson SP, Andersen EF, El-Hattab AW. Int22h1/Int22h2-mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features. Hum Mutat. 2020 Jul; 41 (7):1238-1249 Epub 2020 Mar 12
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  10. Pal T, Agnese D, Daly M, La Spada A, Litton J, Wick M, Klugman S, Esplin ED, Jarvik GP, Professional Practice and Guidelines Committee. Points to consider: is there evidence to support BRCA1/2 and other inherited breast cancer genetic testing for all breast cancer patients? A statement of the American College of Medical Genetics and Genomics (ACMG). Genet Med. 2020 Apr; 22 (4):681-685 Epub 2019 Dec 13
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  11. Daly MB, Pilarski R, Yurgelun MB, Berry MP, Buys SS, Dickson P, Domchek SM, Elkhanany A, Friedman S, Garber JE, Goggins M, Hutton ML, Khan S, Klein C, Kohlmann W, Kurian AW, Laronga C, Litton JK, Mak JS, Menendez CS, Merajver SD, Norquist BS, Offit K, Pal T, Pederson HJ, Reiser G, Shannon KM, Visvanathan K, Weitzel JN, Wick MJ, Wisinski KB, Dwyer MA, Darlow SD. NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Breast, Ovarian, and Pancreatic, Version 1.2020. J Natl Compr Canc Netw. 2020 Apr; 18 (4):380-391
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  12. Helbig KL, Lauerer RJ, Bahr JC, Souza IA, Myers CT, Uysal B, Schwarz N, Gandini MA, Huang S, Keren B, Mignot C, Afenjar A, Billette de Villemeur T, Heron D, Nava C, Valence S, Buratti J, Fagerberg CR, Soerensen KP, Kibaek M, Kamsteeg EJ, Koolen DA, Gunning B, Schelhaas HJ, Kruer MC, Fox J, Bakhtiari S, Jarrar R, Padilla-Lopez S, Lindstrom K, Jin SC, Zeng X, Bilguvar K, Papavasileiou A, Xing Q, Zhu C, Boysen K, Vairo F, Lanpher BC, Klee EW, Tillema JM, Payne ET, Cousin MA, Kruisselbrink TM, Wick MJ, Baker J, Haan E, Smith N, Sadeghpour A, Davis EE, Katsanis N, Corbett MA, MacLennan AH, Gecz J, Biskup S, Goldmann E, Rodan LH, Kichula E, Segal E, Jackson KE, Asamoah A, Dimmock D, McCarrier J, Botto LD, Filloux F, Tvrdik T, Cascino GD, Klingerman S, Neumann C, Wang R, Jacobsen JC, Nolan MA, Snell RG, Lehnert K, Sadleir LG, Anderlid BM, Kvarnung M, Guerrini R, Friez MJ, Lyons MJ, Leonhard J, Kringlen G, Casas K, El Achkar CM, Smith LA, Rotenberg A, Poduri A, Sanchis-Juan A, Carss KJ, Rankin J, Zeman A, Raymond FL, Blyth M, Kerr B, Ruiz K, Urquhart J, Hughes I, Banka S, Hedrich UBS, Scheffer IE, Helbig I, Zamponi GW, Lerche H, Mefford HC, Task Force for Neonatal Genomics//Deciphering Developmental Disorders Study. De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias. Am J Hum Genet. 2018 Nov 1; 103 (5):666-678 Epub 2018 Oct 18
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  13. Allyse MA, Wick MJ. Noninvasive Prenatal Genetic Screening Using Cell-free DNA. JAMA. 2018 Aug 14; 320 (6):591-592
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  14. Gammon BL, Otto L, Wick M, Borowski K, Allyse M. Implementing Group Prenatal Counseling for Expanded Noninvasive Screening Options. J Genet Couns. 2018 Aug; 27 (4):894-901 Epub 2017 Dec 15
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  15. Swanson CL, Kumar A, Maharaj JM, Kemppainen JL, Thomas BC, Weinhold MR, Slaby KM, Mara KC, Wick MJ, Bakkum-Gamez JN. Increasing genetic counseling referral rates through bundled interventions after ovarian cancer diagnosis. Gynecol Oncol. 2018 Apr; 149 (1):121-126 Epub 2018 Feb 03
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  16. Rose NC, Wick M. Carrier screening for single gene disorders. Semin Fetal Neonatal Med. 2018 Apr; 23 (2):78-84 Epub 2017 June 29
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  17. Ainsworth AJ, Holman MA, Codsi E, Wick M. Use of Genetic Testing after Abnormal Screening Ultrasound: A Descriptive Cohort Study. Gynecol Obstet Invest. 2018; 83 (5):466-470 Epub 2017 Nov 20
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  18. Wick MJ, Trinidad CM. ACOG Practice Bulletin No. 187. Neural Tube Defects (Replaces Practice Bulletin Number 44, July 2003) Obstetrics and Gynecology. 2017; 6(130):e279-e290.
  19. Ainsworth A, Holman , M, Codsi , E, Wick MJ. Use of Genetic Testing after Abnormal Screening Ultrasound Gynecologic and Obstetric Investigation. 2017.
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  20. Allyse M, Wick MJ. What do the new American College of Medical Genetics and Genomics (ACMG) guidelines mean for the provision of non-invasive prenatal genetic screening? J Obstet Gynaecol. 2017 Aug; 37 (6):795-798 Epub 2017 Apr 01
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  21. Allyse M, Aypar U, Bonhomme N, Darilek S, Dougherty M, Farrell R, Grody W, Highsmith WE, Michie M, Nunes M, Otto L, Pabst R, Palomaki G, Runke C, Sharp RR, Skotko B, Stoll K, Wick M. Offering Prenatal Screening in the Age of Genomic Medicine: A Practical Guide. J Womens Health (Larchmt). 2017 Jul; 26 (7):755-761 Epub 2017 Apr 07
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  22. Daly MB, Pilarski R, Berry M, Buys SS, Farmer M, Friedman S, Garber JE, Kauff ND, Khan S, Klein C, Kohlmann W, Kurian A, Litton JK, Madlensky L, Merajver SD, Offit K, Pal T, Reiser G, Shannon KM, Swisher E, Vinayak S, Voian NC, Weitzel JN, Wick MJ, Wiesner GL, Dwyer M, Darlow S. NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2017. J Natl Compr Canc Netw. 2017 Jan; 15 (1):9-20
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  23. Boczek NJ, Sigafoos AN, Zimmermann MT, Maus RL, Cousin MA, Blackburn PR, Urrutia R, Clark KJ, Patterson MC, Wick MJ, Klee EW. Functional characterization of a GFAP variant of uncertain significance in an Alexander disease case within the setting of an individualized medicine clinic. Clin Case Rep. 2016 Sep; 4 (9):885-95 Epub 2016 Aug 15
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  24. Lazaridis KN, Schahl KA, Cousin MA, Babovic-Vuksanovic D, Riegert-Johnson DL, Gavrilova RH, McAllister TM, Lindor NM, Abraham RS, Ackerman MJ, Pichurin PN, Deyle DR, Gavrilov DK, Hand JL, Klee EW, Stephens MC, Wick MJ, Atkinson EJ, Linden DR, Ferber MJ, Wieben ED, Farrugia G, Individualized Medicine Clinic Members. Outcome of Whole Exome Sequencing for Diagnostic Odyssey Cases of an Individualized Medicine Clinic: The Mayo Clinic Experience. Mayo Clin Proc. 2016 Mar; 91: (3)297-307.
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  25. Wick MJ, Borowski KS. Genetics: Counseling, Testing, and Diagnosis. ACOG Clinical Updates in Women's Health Care.2016;XV:(Number 2)1-62.
  26. Rose NC, Wick M. Current recommendations: Screening for Mendelian disorders. Semin Perinatol. 2016 Feb; 40 (1):23-8 Epub 2015 Dec 17
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  27. Daly MB, Pilarski R, Axilbund JE, Berry M, Buys SS, Crawford B, Farmer M, Friedman S, Garber JE, Khan S, Klein C, Kohlmann W, Kurian A, Litton JK, Madlensky L, Marcom PK, Merajver SD, Offit K, Pal T, Rana H, Reiser G, Robson ME, Shannon KM, Swisher E, Voian NC, Weitzel JN, Whelan A, Wick MJ, Wiesner GL, Dwyer M, Kumar R, Darlow S. Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2015. J Natl Compr Canc Netw. 2016 Feb; 14 (2):153-62
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  28. Cao Y, Hoppman NL, Kerr SE, Sattler CA, Borowski KS, Wick MJ, Highsmith WE, Aypar U. False Negative Cell-Free DNA Screening Result in a Newborn with Trisomy 13. Case Rep Genet. 2016; 2016:7397405 Epub 2016 Feb 22
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  29. Cunningham JM, Cicek MS, Larson NB, Davila J, Wang C, Larson MC, Song H, Dicks EM, Harrington P, Wick M, Winterhoff BJ, Hamidi H, Konecny GE, Chien J, Bibikova M, Fan JB, Kalli KR, Lindor NM, Fridley BL, Pharoah PP, Goode EL. Clinical characteristics of ovarian cancer classified by BRCA1, BRCA2, and RAD51C status. Sci Rep. 2014 Feb 7; 4:4026 Epub 2014 Feb 07
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  30. Tessmer-Tuck JA, El-Nashar SA, Racek AR, Lohse CM, Famuyide AO, Wick MJ. Predicting vaginal birth after cesarean section: a cohort study. Gynecol Obstet Invest. 2014; 77 (2):121-6 Epub 2014 Feb 11
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  31. Stan DL, Shuster LT, Wick MJ, Swanson CL, Pruthi S, Bakkum-Gamez JN. Challenging and complex decisions in the management of the BRCA mutation carrier. J Womens Health (Larchmt). 2013 Oct; 22 (10):825-34 Epub 2013 Aug 29
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  32. Crotti L, Tester DJ, White WM, Bartos DC, Insolia R, Besana A, Kunic JD, Will ML, Velasco EJ, Bair JJ, Ghidoni A, Cetin I, Van Dyke DL, Wick MJ, Brost B, Delisle BP, Facchinetti F, George AL, Schwartz PJ, Ackerman MJ. Long QT syndrome-associated mutations in intrauterine fetal death. JAMA. 2013 Apr 10; 309(14):1473-82.
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  33. Wick JB, Johnson KJ, O'Brien J, Wick MJ. Second-Trimester Diagnosis of Triploidy: A Series of Four Cases. Am J Perinatol Rep. 2012 Dec 31; 2(1).
  34. Racek AR, Rabe KG, Wick MJ, Psychogios A, Lindor NM. Primary appendiceal mucinous adenocarcinoma in two first-degree relatives: case report and review. Hered Cancer Clin Pract. 2011 May 4; 9 (1):1 Epub 2011 May 04
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  35. Wick JM, Grotthus JL, Gressick BA, Thao J, Julson JL. Effects of passive smoke on high density lipoprotein cholesterol in college aged individuals Journal of Undergraduate Kinesiology Research. 2008; 3(2):26-33.
  36. Gulbahce HE, Brown CA, Wick M, Segall M, Jessurun J. Graft-vs-host disease after solid organ transplant. Am J Clin Pathol. 2003 Apr; 119(4):568-73.
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  37. Mao R, Aylsworth AS, Potter N, Wilson WG, Breningstall G, Wick MJ, Babovic-Vuksanovic D, Nance M, Patterson MC, Gomez CM, Snow K. Childhood-onset ataxia: testing for large CAG-repeats in SCA2 and SCA7. Am J Med Genet. 2002 Jul 15; 110(4):338-45.
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  38. Wick MJ, Woronzoff-Dashkoff KP, McGlennen RC. The molecular characterization of fatal infectious mononucleosis. Am J Clin Pathol. 2002 Apr; 117(4):582-8.
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  39. Rowsell EH, Wick MJ. Molecular detection of multiple endocrine neoplasia type 2. Methods Mol Med. 2001; 49:243-62
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  40. Wick MJ. Diagnosis of human papillomavirus gynecologic infections. Clin Lab Med. 2000 Jun; 20(2):271-87, vi.
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  41. Hoyer JD, Wick MJ, Snow K, Finkelstein W, Fairbanks VF. DNA sequence analysis of Hb Leiden [beta6(A3) or beta7(A4) Glu-->0]. Hemoglobin. 1999 Aug; 23 (3):299-301
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  42. Nance M, Matthias Hagen VL, Brenningstall G, Wick MJ, McGlennen RC. Analysis of a very large trinucleotide repeat in a patient with juvenile Huntington's Disease. Neurology. 1999; 52:392-5.
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  43. Hoyer JD, Wick MJ, Thibodeau SN, Kechteiger KS, Cook JD, Fairbanks VF. Hb Silver Springs [beta 131(H9)Gln-->His], a new hemoglobin variant found in six African-Americans. Hemoglobin. 1998 Jan; 22 (1):37-44
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  44. Hoyer JD, Wick MJ, Thibodeau SN, Viker KA, Conner R, Fairbanks VF. Hb Tak confirmed by DNA analysis: not expressed as thalassemia in a Hb Tak/Hb E compound heterozygote. Hemoglobin. 1998 Jan; 22 (1):45-52
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  45. Wick MJ, Matthias Hagen VL, Day JW, Gomez CM, McGlennen RC. Long Range Polymerase Chain Reaction-Based Diagnosis of Friedreich Ataxia in the Clinical Molecular Diagnostics Laboratory. Molecular Diagnosis. 1998; 3:3-9.
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  46. Lindor NM, Valdes MG, Wick M, Thibodeau SN, Jalal S. De novo 16p deletion: ATR-16 syndrome. Am J Med Genet. 1997 Nov 12; 72(4):451-4.
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  47. Wick MJ. Clinical and molecular aspects of multiple endocrine neoplasia. Clinics in Laboratory Medicine.1997;17:((1)):39-57.
  48. Cunningham JM, Shan A, Wick MJ, McDonnell SK, Schaid DJ, Tester DJ, Qian J, Takahashi S, Jenkins RB, Bostwick DG, Thibodeau SN. Allelic imbalance and microsatellite instability in prostatic adenocarcinoma. Cancer Res. 1996 Oct 1; 56(19):4475-82.
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  49. Oda RP, Wick MJ, Rueckert LM, Lust JA, Landers JP. Evaluation of capillary electrophoresis in polymer solutions with laser-induced fluorescence detection for the automated detection of T-cell gene rearrangements in lymphoproliferative disorders. Electrophoresis. 1996 Sep; 17 (9):1491-8
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  50. Zembower DE, Neudauer CL, Wick MJ, Ames MM. Peptide boronic acids. Versatile synthetic ligands for affinity chromatography of serine proteinases. Int J Pept Protein Res. 1996 May; 47 (5):405-13
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  51. Ames MM, Kinder DH, Wick MJ. Mechanism-based serine protease inhibitors as potential antitumor agents: cellular targets. J Cell Biochem Suppl. 1991; (15G):139.
  52. Westphal SA, Mariash CN, Wick M, Oppenheimer JH. Hypercortisolism due to an autonomously functioning pituitary adenoma: limitations in diagnostic test procedures. J Clin Endocrinol Metab. 1988 Nov; 67(5):1105-10.
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  53. Errede LA, Kueker MJ, Tiers GVD, Vanbogar JW. Polymer drying time studies of desorption from liquid saturated poly(styrene-co-divinylbenzene) microparticles. J Polym Sci [Polym Chem Ed] 1988; 26(12):3375-3389.