Myra J Wick, MD, PhD

  • 1010 Citations
  • 15 Scopus h-Index
19962019
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Research Output 1996 2019

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Article
2018
8 Citations (Scopus)

De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias

Deciphering Developmental Disorders Study, Nov 1 2018, In : American Journal of Human Genetics. 103, 5, p. 666-678 13 p.

Research output: Contribution to journalArticle

Megalencephaly
Dyskinesias
Brain Diseases
Contracture
S 6
5 Citations (Scopus)

Increasing genetic counseling referral rates through bundled interventions after ovarian cancer diagnosis

Swanson, C. L., Kumar, A., Maharaj, J. M., Kemppainen, J. L., Thomas, B. C., Weinhold, M. R., Slaby, K. M., Mara, K. C., Wick, M. J. & Bakkum-Gamez, J. N., Jan 1 2018, (Accepted/In press) In : Gynecologic Oncology.

Research output: Contribution to journalArticle

Genetic Counseling
Ovarian Neoplasms
Referral and Consultation
Genetic Testing
Genetic Templates
2017
3 Citations (Scopus)

Carrier screening for single gene disorders

Rose, N. C. & Wick, M. J., 2017, (Accepted/In press) In : Seminars in Fetal and Neonatal Medicine.

Research output: Contribution to journalArticle

Inborn Genetic Diseases
Newborn Infant
Genes
Phenylketonurias
History
4 Citations (Scopus)

Implementing Group Prenatal Counseling for Expanded Noninvasive Screening Options

Gammon, B. L., Otto, L., Wick, M. J., Borowski, K. & Allyse, M., Dec 15 2017, (Accepted/In press) In : Journal of Genetic Counseling. p. 1-8 8 p.

Research output: Contribution to journalArticle

Prenatal Diagnosis
Counseling
Genetic Counseling
Pregnant Women
Decision Making
5 Citations (Scopus)

Offering Prenatal Screening in the Age of Genomic Medicine: A Practical Guide

Allyse, M., Aypar, U., Bonhomme, N., Darilek, S., Dougherty, M., Farrell, R., Grody, W., Highsmith, W. E. J., Michie, M., Nunes, M., Otto, L., Pabst, R., Palomaki, G., Runke, C., Sharp, R. R., Skotko, B., Stoll, K. & Wick, M. J., Jul 1 2017, In : Journal of Women's Health. 26, 7, p. 755-761 7 p.

Research output: Contribution to journalArticle

Prenatal Diagnosis
Medicine
Medical Genetics
Genetic Testing
Gynecology

Use of Genetic Testing after Abnormal Screening Ultrasound: A Descriptive Cohort Study

Ainsworth, A. J., Holman, M. A., Codsi, E. & Wick, M. J., Nov 20 2017, (Accepted/In press) In : Gynecologic and Obstetric Investigation.

Research output: Contribution to journalArticle

Genetic Testing
Prenatal Diagnosis
Amniocentesis
Cohort Studies
Aneuploidy
1 Citation (Scopus)
Genetic Testing
Genomics
Prenatal Diagnosis
Practice Guidelines
Guidelines
2016
3 Citations (Scopus)

Current recommendations: Screening for Mendelian disorders

Rose, N. C. & Wick, M. J., Feb 1 2016, In : Seminars in Perinatology. 40, 1, p. 23-28 6 p.

Research output: Contribution to journalArticle

Phenylketonurias
Technology
Genes
85 Citations (Scopus)

Genetic/familial high-risk assessment: Breast and ovarian, version 2.2015 Featured updates to the NCCN guidelines

Daly, M. B., Pilarski, R., Axilbund, J. E., Berry, M., Buys, S. S., Crawford, B., Farmer, M., Friedman, S., Garber, J. E., Khan, S., Klein, C., Kohlmann, W., Kurian, A., Litton, J. K., Madlensky, L., Marcom, P. K., Merajver, S. D., Offit, K., Pal, T., Rana, H. & 12 others, Reiser, G., Robson, M. E., Shannon, K. M., Swisher, E., Voian, N. C., Weitzel, J. N., Whelan, A., Wick, M. J., Wiesner, G. L., Dwyer, M., Kumar, R. & Darlow, S., Feb 1 2016, In : JNCCN Journal of the National Comprehensive Cancer Network. 14, 2, p. 153-162 10 p.

Research output: Contribution to journalArticle

Ovarian Neoplasms
Breast
Risk Management
Genetic Testing
Guidelines
52 Citations (Scopus)

Outcome of Whole Exome Sequencing for Diagnostic Odyssey Cases of an Individualized Medicine Clinic: The Mayo Clinic Experience

Lazaridis, K. N., Schahl, K. A., Cousin, M. A., Babovic-Vuksanovic, D., Riegert-Johnson, D. L., Gavrilova, R. M., McAllister, T. M., Lindor, N. M., Abraham, R. S., Ackerman, M. J., Pichurin, P. N., Deyle, D. R., Gavrilov, D. K., Hand, J. L., Klee, E. W., Stephens, M. C., Wick, M. J., Atkinson, E. J., Linden, D. R., Ferber, M. J. & 19 others, Wieben, E. D., Farrugia, G., Baudhuin, L. M., Beck, S. A., Beek, G. J., Go, R. S., Guthrie, K. J., Hovan, M. J., Hunt, K. S., Kemppainen, J. L., Kruisselbrink, T. M., McCormick, J. B., McLaughlin, B. M., Murphree, M. I., Niewold, T. B., Oglesbee, D., Reed, A., Thibodeau, S. N. & Thorland, E. C., Mar 1 2016, In : Mayo Clinic Proceedings. 91, 3, p. 297-307 11 p.

Research output: Contribution to journalArticle

Exome
Precision Medicine
Inborn Genetic Diseases
Insurance Coverage
Medicaid
2014
55 Citations (Scopus)

Clinical characteristics of ovarian cancer classified by BRCA1, BRCA2, and RAD51C status

Cunningham, J. M., Cicek, M., Larson, N., Davila, J., Wang, C., Larson, M. C., Song, H., Dicks, E. M., Harrington, P., Wick, M. J., Winterhoff, B. J., Hamidi, H., Konecny, G. E., Chien, J., Bibikova, M., Fan, J. B., Kalli, K. R., Lindor, N. M., Fridley, B. L., Pharoah, P. P. D. & 1 others, Goode, E. L., Feb 7 2014, In : Scientific Reports. 4, 4026.

Research output: Contribution to journalArticle

Ovarian Neoplasms
Homologous Recombination
Germ-Line Mutation
Phenotype
Epigenomics
21 Citations (Scopus)

Predicting vaginal birth after cesarean section: A cohort study

Tessmer-Tuck, J. A., El-Nashar, S. A., Racek, A. R., Lohse, C. M., Famuyide, A. O. & Wick, M. J., 2014, In : Gynecologic and Obstetric Investigation. 77, 2, p. 121-126 6 p.

Research output: Contribution to journalArticle

Vaginal Birth after Cesarean
Cesarean Section
Cohort Studies
Trial of Labor
Logistic Models
7 Citations (Scopus)

Pregnancy in an individual with mild Smith-Lemli-Opitz syndrome

Ellingson, M. S., Wick, M. J., White, W. M., Raymond, K. M., Saenger, A. K., Pichurin, P. N., Wassif, C. A., Porter, F. D. & Babovic-Vuksanovic, D., 2014, In : Clinical Genetics. 85, 5, p. 495-497 3 p.

Research output: Contribution to journalArticle

Smith-Lemli-Opitz Syndrome
Pregnancy
2013
33 Citations (Scopus)

Challenging and complex decisions in the management of the BRCA mutation carrier

Stan, D. L., Shuster, L. T., Wick, M. J., Swanson, C. L., Pruthi, S. & Bakkum-Gamez, J. N., Oct 1 2013, In : Journal of Women's Health. 22, 10, p. 825-834 10 p.

Research output: Contribution to journalArticle

Ovarian Neoplasms
Ovariectomy
Breast Neoplasms
Menopause
Mutation
80 Citations (Scopus)

Long QT syndrome-associated mutations in intrauterine fetal death

Crotti, L., Tester, D. J., White, W. M., Bartos, D. C., Insolia, R., Besana, A., Kunic, J. D., Will, M. L., Velasco, E. J., Bair, J. J., Ghidoni, A., Cetin, I., Van Dyke, D. L., Wick, M. J., Brost, B., Delisle, B. P., Facchinetti, F., George, A. L., Schwartz, P. J. & Ackerman, M. J., Apr 10 2013, In : JAMA - Journal of the American Medical Association. 309, 14, p. 1473-1482 10 p.

Research output: Contribution to journalArticle

Long QT Syndrome
Fetal Death
Mutation
Romano-Ward Syndrome
Exome
2011
3 Citations (Scopus)

Primary appendiceal mucinous adenocarcinoma in two first-degree relatives: Case report and review

Racek, A. R., Rabe, K. G., Wick, M. J., Psychogios, A. & Lindor, N. M., May 4 2011, In : Hereditary Cancer in Clinical Practice. 9, 1, 1.

Research output: Contribution to journalArticle

Appendiceal Neoplasms
Mucinous Adenocarcinoma
Siblings
DNA Mismatch Repair
Gastrointestinal Neoplasms
2003
43 Citations (Scopus)

Graft-vs-host disease after solid organ transplant

Gulbahce, H. E., Brown, C. A., Wick, M. J., Segall, M. & Jessurun, J., Apr 1 2003, In : American Journal of Clinical Pathology. 119, 4, p. 568-573 6 p.

Research output: Contribution to journalArticle

Graft vs Host Disease
Transplants
Organ Transplantation
Blood Transfusion
Chimerism

Graft-vs-host disease after solid organ transplant

Gulbahce, H. E., Brown, C. A., Wick, M. J., Segall, M. & Jessurun, J., Apr 1 2003, In : American Journal of Clinical Pathology. 119, 4, p. 568-573 6 p.

Research output: Contribution to journalArticle

Graft vs Host Disease
Transplants
Organ Transplantation
Blood Transfusion
Chimerism
2002
49 Citations (Scopus)

Childhood-onset ataxia: Testing for large CAG-repeats in SCA2 and SCA7

Mao, R., Aylsworth, A. S., Potter, N., Wilson, W. G., Breningstall, G., Wick, M. J., Babovic-Vuksanovic, D., Nance, M., Patterson, M. C., Gomez, C. M. & Snow, K., Jul 15 2002, In : American Journal of Medical Genetics. 110, 4, p. 338-345 8 p.

Research output: Contribution to journalArticle

Ataxia
Polymerase Chain Reaction
Cerebellar Ataxia
Oligonucleotide Probes
Sepharose
28 Citations (Scopus)

The molecular characterization of fatal infectious mononucleosis

Wick, M. J., Woronzoff-Dashkoff, K. P. & McGlennen, R. C., 2002, In : American Journal of Clinical Pathology. 117, 4, p. 582-588 7 p.

Research output: Contribution to journalArticle

Infectious Mononucleosis
Human Herpesvirus 4
Gene Rearrangement
Fatal Outcome
T-Lymphocyte Gene Rearrangement
2000
9 Citations (Scopus)

Diagnosis of human papillomavirus gynecologic infections

Wick, M. J., 2000, In : Clinics in Laboratory Medicine. 20, 2, p. 271-287 17 p.

Research output: Contribution to journalArticle

Papillomavirus Infections
Testing
Viruses
Papanicolaou Test
Assays
1999
80 Citations (Scopus)

Analysis of a very large trinucleotide repeat in a patient with juvenile Huntington's disease

Nance, M. A., Mathias-Hagen, V., Breningstall, G., Wick, M. J. & McGlennen, R. C., Jan 15 1999, In : Neurology. 52, 2, p. 392-394 3 p.

Research output: Contribution to journalArticle

Trinucleotide Repeat Expansion
Trinucleotide Repeats
Huntington Disease
Molecular Biology
Alleles
1 Citation (Scopus)

DNA sequence analysis of Hb Leiden [β6(A3) or β7(A4) Glu→0]

Hoyer, J., Wick, M. J., Snow, K., Finkelstein, W. & Fairbanks, V. F., 1999, In : Hemoglobin. 23, 3, p. 299-301 3 p.

Research output: Contribution to journalArticle

DNA sequences
hemoglobin Leiden
1 Citation (Scopus)

Genetic testing of banked umbilical cord blood.

Wick, M. J., Clay, M. E., Eastlund, T., Vawter, D. E., McGlennen, R. & McCullough, J., 1999, In : Cytotherapy. 1, 4, p. 275-278 4 p.

Research output: Contribution to journalArticle

Neonatal Screening
Blood Banks
Mass Screening
Genetic Testing
Fetal Blood
1998
10 Citations (Scopus)

Hb Silver Springs [β131(H9)Gln→His], a new hemoglobin variant found in six African-Americans

Hoyer, J., Wick, M. J., Thibodeau, S. N., Kechteiger, K. S., Cook, J. D. & Fairbanks, V. F., 1998, In : Hemoglobin. 22, 1, p. 37-44 8 p.

Research output: Contribution to journalArticle

Codon
African Americans
Hemoglobins
Substitution reactions
High performance liquid chromatography
15 Citations (Scopus)

Hb Tak confirmed by DNA analysis: Not expressed as thalassemia in a Hb Tak/Hb E compound heterozygote

Hoyer, J., Wick, M. J., Thibodeau, S. N., Viker, K. A., Conner, R. & Fairbanks, V. F., 1998, In : Hemoglobin. 22, 1, p. 45-52 8 p.

Research output: Contribution to journalArticle

Thalassemia
Heterozygote
DNA
Elongation
Amino Acids
1 Citation (Scopus)

Long range polymerase chain reaction-based diagnosis of friedreich ataxia in the clinical molecular diagnostics laboratory

Wick, M. J., Matthias Hagen, V. L., Day, J. W., Gomez, C. M. & McGlennen, R. C., 1998, In : Molecular Diagnosis. 3, 1, p. 3-9 7 p.

Research output: Contribution to journalArticle

Friedreich Ataxia
Molecular Pathology
Polymerase Chain Reaction
Alleles
Trinucleotide Repeats
1997
9 Citations (Scopus)

Clinical and molecular aspects of multiple endocrine neoplasia

Wick, M. J., 1997, In : Clinics in Laboratory Medicine. 17, 1, p. 39-57 19 p.

Research output: Contribution to journalArticle

Multiple Endocrine Neoplasia
Clinical laboratories
Proto-Oncogenes
Mutation
Risk assessment
16 Citations (Scopus)

De novo 16p deletion: ATR-16 syndrome

Lindor, N. M., Valdes, M. G., Wick, M. J., Thibodeau, S. N. & Jalal, S., Nov 12 1997, In : American Journal of Medical Genetics. 72, 4, p. 451-454 4 p.

Research output: Contribution to journalArticle

Thalassemia
Globins
Chromosomes, Human, Pair 16
Chromosome Deletion
Densitometry
1996
163 Citations (Scopus)

Allelic imbalance and microsatellite instability in prostatic adenocarcinoma

Cunningham, J. M., Shan, A., Wick, M. J., McDonnell, S. K., Schaid, D. J., Tester, D. J., Qian, J., Takahashi, S., Jenkins, R. B., Bostwick, D. G. & Thibodeau, S. N., Oct 1 1996, In : Cancer Research. 56, 19, p. 4475-4482 8 p.

Research output: Contribution to journalArticle

Allelic Imbalance
Microsatellite Instability
Adenocarcinoma
Chromosomes, Human, Pair 16
Tumor Suppressor Genes
15 Citations (Scopus)

Evaluation of capillary electrophoresis in polymer solutions with laser-induced fluorescence detection for the automated detection of T-cell gene rearrangements in lymphoproliferative disorders

Oda, R. P., Wick, M. J., Rueckert, L. M., Lust, J. A. & Landers, J. P., Sep 1996, In : Electrophoresis. 17, 9, p. 1491-1498 8 p.

Research output: Contribution to journalArticle

T-Lymphocyte Gene Rearrangement
Capillary electrophoresis
T-cells
Lymphoproliferative Disorders
Capillary Electrophoresis
10 Citations (Scopus)

Peptide boronic acids Versatile synthetic ligands for affinity chromatography of serine proteinases

Zembower, D. E., Neudauer, C. L., Wick, M. J. & Ames, M. M., 1996, In : International Journal of Peptide and Protein Research. 47, 5, p. 405-413 9 p.

Research output: Contribution to journalArticle

Boronic Acids
Affinity chromatography
Chymotrypsin
Serine Proteases
Affinity Chromatography