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Perez Botero, Juliana

0000-0002-3674-4170

Mayo Clinic

Division of Hematology, Department of Medicine, Mayo Clinic, Rochester, MN, USA.

Citations 9

Phenotypic heterogeneity associated with germline GATA2 haploinsufficiency: a comprehensive kindred study
Haddox, Candace L. , Carr, Ryan M. , Abraham, Roshini S. , Botero, Juliana Perez , Rodriguez, Vilmarie , Pardanani, Animesh , Patnaik, Mrinal M. , Perez Botero, Juliana , Haddox, Candace L , Carr, Ryan M

Leukemia & Lymphoma | June 27, 2019 | Volume: 60 | Issue: 13 | Pages: 3282-3286

10.1080/10428194.2019.1633630 Get It

Factor IX Gene (F9) Genotyping Trends and Spectrum of Mutations Identified: A Reference Laboratory Experience
Botero, Juliana Perez , Coon, Lea M., Majerus, Julie A. , Chen, Dong , Pruthi, Rajiv K. , Perez Botero, Juliana , Chen, Dong

Seminars in Thrombosis and Hemostasis | September 14, 2017 | Volume: 44 | Issue: 03 | Pages: 287-292

10.1055/s-0037-1605567 Get It

AbstractIn hemophilia B (HB), factor IX gene (F9) genotyping is used for molecular confirmation of affected individuals, for carrier testing, to facilitate the identification of those at risk for anaphylaxis/inhibitors (associated with large deletions), and to assist in assigning disease severity. Owing to test costs, optimal test utilization involves pre/post-test counseling and appropriate patient and test selection (e.g., mutation screening [F9MS] vs. known mutation [F9KM] testing). This article aims to review the trends and outcomes of F9-genotyping orders and describe the spectrum of variants identified in a sample of individuals in our reference laboratory. We performed a retrospective review of consecutive orders submitted to the Special Coagulation DNA Diagnostic Laboratory, Mayo Clinic, between 2012 and 2015. A total of 133 orders (38%) were identified for men: 118 (88%) were F9MS and 15 (12%) were F9KM. Thirteen orders (10%) were cancelled. A total of 209 orders were identified for women: 178 (85%) were F9MS and 31 (15%) were F9KM. Thirty-seven orders (18%) were cancelled and 30% of the tests performed yielded negative results. A total of 164 samples (47%) were received without clinical information. Seventeen previously unreported variants were identified. F9 genotyping provides useful information for HB management; however, 18% of our orders were cancelled and almost half were received without relevant clinical information, thus reaffirming the need for ongoing scrutiny of submitted orders. Optimal patient and test selection is important as is the accurate interpretation of variants identified. Most of the pathogenic variants identified were point mutations, with very few large deletions, consistent with the literature.
Coagulation abnormalities and haemostatic surgical outcomes in 142 patients with Noonan syndrome
Botero, Juliana Perez , Ho, Thanh P. , Rodriguez, Vilmarie , Khan, Shakila P. , Pruthi, Rajiv K. , Patnaik, Mrinal M. , Perez Botero, Juliana

Haemophilia | May 18, 2017 | Volume: 23 | Issue: 3 | Pages: No page available

10.1111/hae.13225 Get It

Clinical spectrum and clonal evolution in germline syndromes with predisposition to myeloid neoplasms
Botero, Juliana Perez , Ho, Thanh P. , Kenderian, Saad S. , Gangat, Naseema , Tefferi, Ayalew , Abraham, Roshini S. , Nguyen, Phuong L., Oliveira, Jennifer L. , He, Rong , Chen, Dong , Viswanatha, David S., Rodriguez, Vilmarie , Khan, Shakila P. , Patnaik, Mrinal M. , Herrick, Jennifer L. , Perez Botero, Juliana , Viswanatha, David, Hogan, William J. , Kenderian, Saad Sirop , Chen, Dong

British Journal of Haematology | May 9, 2017 | Volume: 182 | Issue: 1 | Pages: 141-145

10.1111/bjh.14746 Get It

Diagnostic Testing Approaches for Activated Protein C Resistance and Factor V Leiden
Botero, Juliana Perez , Majerus, Julie A. , Strege, Ann K., Johnson, Ryan D., Pruthi, Rajiv K. , Chen, Dong , Perez Botero, Juliana

American Journal of Clinical Pathology | February 15, 2017 | Volume: 147 | Issue: 6 | Pages: 604-610

10.1093/ajcp/aqx033 Get It

AbstractObjectivesTo analyze the economic impact of testing for activated protein C resistance (APC-R) due to factor V Leiden (FVL) mutation with APC-R with reflexive FVL genotyping (algorithmic approach) or genotyping alone.MethodsOptumLabs Data Warehouse (OLDW) data were used to assess testing approaches. Insurance claims for APC-R and FVL in 2013 were compared with the Mayo Clinic database. Centers for Medicare & Medicaid Services diagnostic fee schedules were used to assign costs.ResultsOf 19.3 million OLDW-covered individuals, 74,242 (0.385%) received 75,608 tests: APC-R, 2,265 (2.9%); FVL genotyping, 70,619 (90.1%); and both APC-R and FVL, 2,724 (7.0%). In total, 1,317 tests were performed at Mayo Clinic: APC-R with reflex FVL (1,256; 95.4%) and FVL alone (61; 4.6%). Costs per evaluated individual and per total population (person/year) in OLDW and algorithmic approach were $83.77 vs $36.38 and $0.32 vs $0.14, respectively.ConclusionsThe cost-optimized algorithmic approach reduces health care costs.
Clinical characteristics and platelet phenotype in a family withRUNX1mutated thrombocytopenia
Botero, Juliana Perez , Chen, Dong , Cousin, Margot A. , Majerus, Julie A. , Coon, Lea M., Kruisselbrink, Teresa , Klee, Eric W. , Pruthi, Rajiv K. , Patnaik, Mrinal M. , Perez Botero, Juliana, Kruisselbrink, Teresa M, Lazaridis, Konstantinos N. , Perez Botero, Juliana , Chen, Dong

Leukemia & Lymphoma | December 9, 2016 | Volume: 58 | Issue: 8 | Pages: 1963-1967

10.1080/10428194.2016.1265118 Get It

Grey platelet syndrome misdiagnosed as ITP
Botero, Juliana Perez , Im, Roeun, Chen, Dong , Patnaik, Mrinal M. , Perez Botero, Juliana, Perez Botero, Juliana , Chen, Dong

British Journal of Haematology | May 13, 2016 | Volume: 173 | Issue: 5 | Pages: 662-662

10.1111/bjh.14079 Get It

von Willebrand disease type1/type 2N compound heterozygotes: diagnostic and management challenges
Botero, Juliana Perez , Pruthi, Rajiv K. , Nichols, William L., Ashrani, Aneel A. , Patnaik, Mrinal M. , Perez Botero, Juliana, Perez Botero, Juliana

British Journal of Haematology | March 12, 2016 | Volume: 176 | Issue: 6 | Pages: 994-997

10.1111/bjh.14028 Get It

Successful treatment with thalidomide of a patient with congenital factor V deficiency and factor V inhibitor with recurrent gastrointestinal bleeding from small bowel arteriovenous malformations
Botero, Juliana Perez , Burns, Daniel J.P. , Thompson, Carrie A. , Pruthi, Rajiv K. , Perez Botero, Juliana

Haemophilia | November 22, 2012 | Volume: 19 | Issue: 1 | Pages: No page available

10.1111/hae.12066 Get It