M. Alvarado

发表

Genetic Services in the KP Southern California Region: Delivering the Promises of Tomorrow Today.

M. Jamehdor, M. Alvarado, N. Shinno, 2006, The Permanente journal.

Comparison of two Lynch screening strategies in endometrial cancer in a California health system.

E. Hoodfar, M. Armstrong, C. Powell, 2020, Gynecologic oncology.

Next-generation universal hereditary cancer screening: implementation of an automated hereditary cancer screening program for patients with advanced cancer undergoing tumor sequencing in a large HMO

J. Goff, R. Haque, T. Hoffman, 2022, Familial Cancer.

Prevalence of mutations in a diverse cohort of 3162 women tested via the same multigene cancer panel in a managed care health plan

R. Haque, G. Tiller, Joanie Chung, 2020, Journal of Community Genetics.

Demographic differences in the utilization of clinical and direct-to-consumer genetic testing.

Nikki M. Carroll, E. McGlynn, A. Burnett-Hartman, 2019, Journal of genetic counseling.

Return of Research-Related Genetic Test Results and Genetic Discrimination Concerns: Facilitators and Barriers of Genetic Research Participation in Diverse Groups

Nikki M. Carroll, E. McGlynn, A. Burnett-Hartman, 2020, Public Health Genomics.

Medical Genetics and Genetic Counseling in Chile

K. Álvarez, Sonia Margarit, G. Lay-Son, 2013, Journal of Genetic Counseling.

Feasibility, patient compliance and acceptability of ovarian cancer surveillance using two serum biomarkers and Risk of Ovarian Cancer Algorithm compared to standard ultrasound and CA 125 among women with BRCA mutations.

S. Skates, L. Kushi, Wenqing Jiang, 2020, Gynecologic oncology.

Patterns of care and outcomes of risk reducing surgery in women with pathogenic variants in non-BRCA and Lynch syndrome ovarian cancer susceptibility genes.

C. Walsh, I. Cass, B. Rimel, 2023, Gynecologic oncology.

Survival Outcomes in BRCA1 or BRCA2 Mutation Carriers and the Influence of Triple-Negative Breast Cancer Subtype

J. Tyczynski, C. Telford, R. Haque, 2018 .

Miller-Dieker Syndrome: Detection of a Cryptic Chromosome Translocation Using In Situ Hybridization in a Family With Multiple Affected Offspring

P. Jacob, H. Bass, M. Jamehdor, 1993 .

Prevalence of mutations in a diverse cohort of 3162 women tested via the same multigene cancer panel in a managed care health plan

R. Haque, G. Tiller, M. Alvarado, 2020, Journal of Community Genetics.

Development of a longitudinal two-biomarker algorithm for early detection of ovarian cancer in women with BRCA mutations.

S. Skates, Wenqing Jiang, R. Haque, 2020, Gynecologic oncology.

Evaluation of an automated process for disclosure of negative noninvasive prenatal test results

B. Bejjani, D. Bulpitt, S. Bhatt, 2019, Journal of genetic counseling.