The Institute for Clinical and Experimental Research® is focused on the development of new diagnostic assays in a wide range of disciplines. Researchers at the institute regularly publish in respected, peer-reviewed journals, give presentations at national and international organizations, author books and book chapters, and develop new tests.

There are 104 total entries for the year 2018.

Rivera-Muñoz EA, Milko LV, Harrison SM, Azzariti DR, Kurtz CL, Lee K, Mester JL, Weaver MA, Currey E, Craigen W, Eng C, Funke B, Hegde M, Hershberger RE, Mao R, Steiner RD, Vincent LM, Martin CL, Plon SE, Ramos E, Rehm HL, Watson M, Berg JS. ClinGen Variant Curation Expert Panel experiences and standardized processes for disease and gene-level specification of the ACMG/AMP guidelines for sequence variant interpretation.​  Human Mutation. 39(11):1614-1622.

Benefield RJ, Slechta ES, Gast CM, Spivak ES, Hanson KE, Alexander DP. Comparison of the drug-drug interaction potential of daptomycin in combination with rifampin in healthy adult volunteers.​  Antimicrobial Agents and Chemotherapy. 62(12).

Riggs ER, Nelson T, Merz A, Ackley T, Bunke B, Collins CD, Collinson MN, Fan Y, Goodenberger ML, Golden DM, Haglund-Hazy L, Krgovic D, Lamb AN, Lewis Z, Li G, Liu Y, Meck J, Neufeld-Kaiser W, Runke CL, Sanmann JN, Stavropoulos DJ, Strong E, Su M, Tayeh MK, Vokac NK, Thorland EC, Andersen EF, Martin, CL. Copy Number Variant Discrepancy Resolution Using the ClinGen Dosage Sensitivity Map Results in Updated Clinical Interpretations in ClinVar.​  Human Mutation. 39(11):1650-1659.

Couturier B, Riley T, Gowans J, Couturier MR. Direct-from-stool testing for shiga-toxins by an immunochromatographic assay is insensitive for detection of shigatoxigenic E. coli.​  Journal of Clinical Microbiology. 56(12).

Yuzyuk T, Balakrishnan B, Schwarz EL, De Biase I, Hobert J, Longo N, Mao R, Lai K, Pasquali M. Effect of genotype on galactose-1-phosphate in classic galactosemia patients.​  Molecular Genetics and Metabolism. 125(3):258-265.

Crist RA, Heikal NM, Rodgers GM, Grenache DG, Smock KJ. Evaluation of a new commercial method for von Willebrand factor multimeric analysis.​  International Jounal of Laboratory Hematologyr. 40(5):586-591.

Pegalajar-Jurado A, Schriefer ME, Welch RJ, Couturier MR, MacKenzie T, Clark RJ, Ashton LV, Delorey MJ, Molins CR. Evaluation of Modified Two-Tiered Testing Algorithms for Lyme Disease Laboratory Diagnosis Using Well-Characterized Serum Samples.​  Journal of Clinical Microbiology. 56(8).

Wooderchak-Donahue WL, Johnson P, McDonald J, Blei F, Berenstein A, Sorscher M, Mayer J, Scheuerle AE, Lewis T, Grimmer JF, Richter GT, Steeves MA, Lin AE, . Expanding the Clinical and Molecular Findings in RASA1 Capillary Malformation-Arteriovenous Malformation.​  European Journal of Human Genetics. 26(10):1521-1536.


Yuzyuk T, Wilson A, Mao R, Pasquali M . Galactose-1-phosphate uridyltransferase activities in different genotypes: a retrospective analysis of 927 samples.​ Journal of Applied Laboratory Medicine. 222-230.

Wooderchak-Donahue WL, McDonald J, Farrell A, Akay G, Velinder M, Johnson P, VanSant-Webb C, Margraf R, Briggs E, Whitehead KJ, Thomson J, Lin AE, Pyeritz RE, Marth G, Bayrak-Toydemir P. Genome sequencing reveals a deep intronic splicing ACVRL1 mutation hotspot in Hereditary Haemorrhagic Telangiectasia.​  Journal of Medical Genetics. 55(12):824-830.

Zhou XA, Louissaint A, Wenzel A, Yang J, Martinez-Escala ME, Moy AP, Morgan EA, Paxton CN, Hong B, Andersen EF, Guitart J, Behdad A, Cerroni L, Weinstock DM, Choi J. Genomic Analyses Identify Recurrent Alterations in Immune Evasion Genes in Diffuse Large B Cell Lymphoma, Leg Type .​  Journal of Investigative Dermatology. 138(11):2365-2376.

Warren JS, Tracy CM, Miller MR, Makaju A, Szulik MW, Oka SI, Yuzyuk TN, Cox JE, Kumar A, Lozier BK, Wang L, Llana JG, Sabry AD, Cawley KM, Barton DW, Han YH, Boudina S, Fiehn O, Tucker HO, Zaitsev AV, Franklin S. Histone methyltransferase Smyd1 regulates mitochondrial energetics in the heart.​  Proceedings of the National Academy of Sciences of the United States of America. 115(33):E7871-E7880.

Delgado JC, Lázár-Molnár E. HLA in Transplantation and Beyond.​  Clinics in Laboratory Medicine. 38(4):xi-xii.

Mathison BA, Couturier MC. Human Dirofilariasis. ASCP Case Reports. 43116.

Profaizer T, Kumánovics A. Human Leukocyte Antigen Typing by Next-Generation Sequencing.​  Clinics in Laboratory Medicine. 38(4):565-578.

Chu Y, Lee S, Shah T, Yin C, Barth M, Miles RR, Ayello J, Morris E, Harrison L, Van de Ven C, Galardy P, Goldman SC, Lim MS, Hermiston M, McAllister-Lucas LM, Giulino-Roth L, Perkins SL, Cairo MS. Ibrutinib significantly inhibited Bruton's tyrosine kinase (BTK) phosphorylation,in-vitro proliferation and enhanced overall survival in a preclinical Burkitt lymphoma (BL) model.​  Oncoimmunology. 8(1):e1512455.

Tiburcio PDB, Xiao B, Chai Y, Asper S, Tripp SR, Gillespie DL, Jensen RL, Huang LE. IDH1R132H is intrinsically tumor-suppressive but functionally attenuated by the glutamate-rich cerebral environment.​  Oncotarget. 9(80):35100-35113.

Buss BA, Baures TJ, Yoo M, Hanson KE, Alexander DP, Benefield RJ, Spivak ES. Impact of a Multiplex PCR Assay for Bloodstream Infections With and Without Antimicrobial Stewardship Intervention at a Cancer Hospital.​  Open Forum Infectious Diseases. 5(10):ofy258.

Kushnir MM, Clarke NJ, Rockwood AL. Mass Spectrometry Tietz Fundamentals of Clinical Chemistry, Eighth Edition. 201-214.

Smy L, Straseski JA. Measuring estrogens in women, men, and children: Recent advances 2012-2017.​  Clinical Biochemistry. 62:11-23.

Baker VL, Gracia C, Glassner MJ, Schnell VL, Doody K, Coddington CC, Shin SS, Marshall LA, Alper MM, Morales AJ, Pavone ME, Behera MA, Zbella EA, Shapiro BS, Straseski JA, Broyles DL. Multicenter evaluation of the Access AMH antimüllerian hormone assay for the prediction of antral follicle count and poor ovarian response to controlled ovarian stimulation.​  Fertility and Sterility. 110(3):506-513.e3.

Streiff MB, Holmstrom B, Angelini D, Ashrani A, Bockenstedt PL, Chesney C, Fanikos J, Fenninger RB, Fogerty AE, Gao S, Goldhaber SZ, Gundabolu K, Hendrie P, Lee AI, Lee JT, Mann J, McMahon B, Millenson MM, Morton C, Ortel TL, Ozair S, Paschal R, Shattil S, Siddiqi T, Smock KJ, Soff G, Wang TF, Williams E, Zakarija A, Hammond L, Dwyer MA, Engh AM. NCCN Guidelines Insights: Cancer-Associated Venous Thromboembolic Disease, Version 2.2018.​  Journal of the National Comprehensive Cancer Network. 16(11):1289-1303.

Judkins AJ, MacQueen BC, Christensen RD, Comstock J, Mao R, Flores-Daboub J. Non-Immune Hydrops, Hypotonia, Encephalopathy, and Liver Failure with Novel Compound Heterozygous AHCY Mutations.​  Neonatology. 114(4):337-340.

Melber DJ, Andreasen TS, Mao R, Tvrdik T, Miller CE, Moore TR, Woelkers DA, Lamale-Smith LM. Novel mutation in CCBE 1 as a cause of recurrent hydrops fetalis from Hennekam lymphangiectasia-lymphedema syndrome-1.​  Clinical Case Reports. 6(12):2358-2363.

Hiemenz MC, Ostrow DG, Busse TM, Buckley J, Maglinte DT, Bootwalla M, Done J, Ji J, Raca G, Ryutov A, Xu X, Zhen CJ, Conroy JM, Hazard FK, Deignan JL, Rogers B, Treece AL, Parham DM, Gai X, Judkins AR, Triche TJ, Biegel JA. OncoKidsSM: A Comprehensive Next-Generation Sequencing Panel for Pediatric Malignancies.​  The Journal of Molecular Diagnostics. 20(6):765-776.

Cairo M, Auperin A, Perkins SL, Pinkerton R, Harrison L, Goldman S, Patte C. Overall survival of children and adolescents with mature B cell non-Hodgkin lymphoma who had refractory or relapsed disease during or after treatment with FAB/LMB 96: A report from the FAB/LMB 96 study group.​  British Journal of Haematology. 182(6):859-869.

Kushnir M, Peterson L, Strathmann F. Parathyroid hormone related protein concentration in human serum and CSF correlates with age.​  Medicine Innovates.

Tashi T, Swierczek S, Kim SJ, Salama ME, Song J, Heikal N, King KY, Hickman K, Litton S, Prchal JT. Pegylated interferon Alfa-2a and hydroxyurea in polycythemia vera and essential thrombocythemia: differential cellular and molecular responses.​  Leukemia. 32(8):1830-1833.

MacQueen BC, Christensen RD, Yost CC, Gordon PV, Baer VL, Schlaberg R, Lowe J. Reference intervals for stool calprotectin in preterm neonates and their utility for the diagnosis of necrotizing enterocolitis.​  Journal of Perinatol. 38(10):1379-1385.

Klee GG, Ichihara K, Ozarda Y, Baumann NA, Straseski J, Bryant SC, Wood-Wentz CM. Reference Intervals: Comparison of Calculation Methods and Evaluation of Procedures for Merging Reference Measurements From Two US Medical Centers.​  American Journal of Clinical Pathology. 150(6):545-554.

Harrison SM, Dolinksy JS, Chen W, Collins CD, Das S, Deignan JL, Garber KB, Garcia J, Jarinova O, Knight Johnson AE, Koskenvuo JW, Lee H, Mao R, Mar-Heyming R, McFaddin AS, Moyer K, Nagan N, Rentas S, Santani AB, Seppälä EH, Shirts BH, Tidwell T, Topper S, Vincent LM, Vinette K, Rehm HL; ClinGen Sequence Variant Inter-Laboratory Discrepancy Resolution Working Group. Scaling resolution of variant classification differences in ClinVar between 41 clinical laboratories through an outlier approach.​  Human Mutation. 39(11):1641-1649.

Smith KA, Merrigan SD, Johnson-Davis KL. Selecting a Structural Analog as an Internal Standard for the Quantification of 6-Methylmercaptopurine by LC-MS/MS.​  The Journal of Applied Laboratory Medicine.

Mollaoglu G, Jones A, Wait SJ, Mukhopadhyay A, Jeong S, Arya R, Camolotto SA, Mosbruger TL, Stubben CJ, Conley CJ, Bhutkar A, Vahrenkamp JM, Berrett KC, Cessna MH, Lane TE, Witt BL, Salama ME, Gertz J, Jones . The Lineage-Defining Transcription Factors SOX2 and NKX2-1 Determine Lung Cancer Cell Fate and Shape the Tumor Immune Microenvironment.​  Immunity. 49(4):764-779.e9.

Lázár-Molnár E, Snyder M. The Role of Human Leukocyte Antigen in Celiac Disease Diagnostics.​  Clinics in Laboratory Medicine. 38(4):655-668.

Whitfield KC, Bourassa MW, Adamolekun B, Bergeron G, Bettendorff L, Brown KH, Cox L, Fattal-Valevski A, Fischer PR, Frank EL, Hiffler L, Hlaing LM, Jefferds ME, Kapner H, Kounnavong S, Mousavi MPS, Roth DE, Tsaloglou MN, Wieringa F, Combs GF Jr.. Thiamine deficiency disorders: diagnosis, prevalence, and a roadmap for global control programs.​  Annals of the New York Academy of Sciences. 1430(1):3-43.

McDonald J, Wooderchak-Donahue WL, Henderson K, Paul E, Morris A, Bayrak-Toydemir P. Tissue-specific mosaicism in hereditary hemorrhagic telangiectasia: Implications for genetic testing in families.​  American Journal of Medical Genetics. Part A. 176(7):1618-1621.

Merzianu M, Groman A, Hutson A, Cotta C, Brynes RK, Orazi A, Reddy V, Teruya-Feldstein J, Amre R, Balasubramanian M, Brandao G, Cherian S, Courville E, Czuchlewski D, Fan G, Grier D, Hoehn D, Inamdar KV, Juskevicius R, Kaur P, Lazarchick J, Lewis MR, Miles RR, Myers JB, Nasr M, Qureishi HN, Olteanu H, Robu VG, Salaru G, Vajpayee N, Vos J, Zhang L, Zhang S, Aye L, Brega E, Coad JE, Grantham J, Ivelja S, McKenna R, Sultan K, Wilding G, Hutchison R, Peterson L, Cheney RT. Trends in Bone Marrow Sampling and Core Biopsy Specimen Adequacy in the United States and Canada: A Multicenter Study.​  American Journal of Clinical Pathology. 150(5):393-405.

Miller HK, Binder AM, Peterson A, Theel ES, Volpe JM, Couturier MR, Cherry CC, Kersh GJ. Trends in Q fever serologic testing by immunofluorescence from four large reference laboratories in the United States, 2012-2016.​  Scientific Reports. 8(1):16670.

Sirohi D, Smith SC, Agarwal N, Maughan BL. Unclassified renal cell carcinoma: diagnostic difficulties and treatment modalities.​  Research and Reports in Urology. 10:205-217.

Zastrow DB, Baudet H, Shen W, Thomas A, Si Y, Weaver MA, Lager AM, Liu J, Mangels R, Dwight SS, Wright MW, Dobrowolski SF, Eilbeck K, Enns GM, Feigenbaum A, Lichter-Konecki U, Lyon E, Pasquali M, Watson M, Blau N, Steiner RD, Craigen WJ, Mao R; ClinGen Inborn Errors of Metabolism Working Group. Unique aspects of sequence variant interpretation for inborn errors of metabolism (IEM): The ClinGen IEM Working Group and the Phenylalanine Hydroxylase Gene.​  Human Mutation. 39(11):1569-1580.

Powers JL, Rasmussen NN, Hurst D, Strathmann FG. Up in Smoke: Uncovering a Lack of Evidence for Proton Pump Inhibitors as a Source of Tetrahydrocannibol Immunoassay False Positives.​  Pain Medicine. 19(11):2196-2200.

Waggoner D, Wain KE, Dubuc AM, Conlin L, Hickey SE, Lamb AN, Martin CL, Morton CC, Rasmussen K, Schuette JL, Schwartz S, Miller DT; ACMG Professional Practice and Guidelines Committee. Yield of additional genetic testing after chromosomal microarray for diagnosis of neurodevelopmental disability and congenital anomalies: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).​  Genetics in Medicine. 20(10):1105-1113.

Martins TB, Heikal N, Miller J, Willis R, Schmidt RL, Tebo AE. Assessment of Diagnostic Methods for the Detection of Anticardiolipin and Anti-βeta2 glycoprotein I Antibodies in Patients under Evaluation for Antiphospholipid Syndrome.​ Clinica Chimica Acta. 485:7-13.

Xu X, Bryke C, Sukhanova M, Huxley E, Dash DP, Dixon-Mciver A, Fang M, Griepp PT, Hodge JC, Iqbal A, Jeffries S, Kanagal-Shamanna R, Quintero-Rivera F, Shetty S, Slovak ML, Yenamandra A, Lennon PA, Raca G. Assessing copy number abnormalities and copy-neutral loss-of-heterozygosity across the genome as best practice in diagnostic evaluation of acute myeloid leukemia: An evidence-based review from the cancer genomics consortium (CGC) myeloid neoplasms working group.​  Cancer Genetics. 228-229:218-235.

Kanagal-Shamanna R, Hodge JC, Tucker T, Shetty S, Yenamandra A, Dixon-McIver A, Bryke C, Huxley E, Lennon PA, Raca G, Xu X, Jeffries S, Quintero-Rivera F, Greipp PT, Slovak ML, Iqbal MA, Fang M. Assessing copy number aberrations and copy neutral loss of heterozygosity across the genome as best practice: An evidence based review of clinical utility from the cancer genomics consortium (CGC) working group for myelodysplastic syndrome, myelodysplastic/myeloproliferative and myeloproliferative neoplasms.​ Cancer Genetics. 228-229:197-217.

Gibbins K, Tebo A, Nielsen S, Branch D. Antiphospholipid Antibodies in Women with Severe Preeclampsia and Placental Insufficiency: A Case-Control Study. ​  Lupus. 27(12):1903-1910.

Wu J, Tian W, Tian G, Sumner K, Hutchinson DT, Ji Y. An investigation of PIK3CA mutations in isolated macrodactyly.​  The Journal of Hand Surgery, European Volume. 43(7):756-760.

Deschamps R, Savatovsky J, Vignal C, Fisselier M, Imbard A, Wolf B, Procter M, Gout O. Adult-onset biotinidase deficiency: two individuals with severe, but reversible optic neuropathy.​  Journal of Neurology, Neurosurgery, and Psychiatry. 89(9):1009-1010.

Christensen RD, Agarwal AM, George TI, Bhutani VK, Yaish HM. Acute neonatal bilirubin encephalopathy in the State of Utah 2009-2018.​  Blood Cells, Molecules and Diseases. 72:10-13.

Timbrook TT, Spivak ES, Hanson KE. Current and Future Opportunities for Rapid Diagnostics in Antimicrobial Stewardship.​ The Medical Clinics of North America. 102(5):899-911.

Corean J, Li KD. A Rare Case of ALK-Positive Large B-Cell Lymphoma with CD33 Expression. Case Reports in Hematology. 2018:5320590.

Owen WE, Hunsaker JJH, Genzen JR. Alpha-fetoprotein in pericardial, peritoneal, and pleural fluids: A body fluid matrix evaluation. Clinical Biochemistry. 56:109-112.

Peterson LK, Jaskowski TD, La`ulu SL, Tebo AE. Antibodies to Small Ubiquitin-like Modifier Activating Enzyme are Associated with a Diagnosis of Dermatomyositis: Results from an Unselected Cohort. Immunologic Research. 66(3):431-436.

Hellwig S, Nix DA, Gligorich KM, O'Shea JM, Thomas A, Fuertes CL, Bhetariya PJ, Marth GT, Bronner MP, Underhill HR. Automated size selection for short cell-free DNA fragments enriches for circulating tumor DNA and improves error correction during next generation sequencing​. PLoS One. 13(7): e0197333. July 2018.

Yuzyuk T, Viau K, Andrews A, Pasquali M, Longo N. Biochemical changes and clinical outcomes in 34 patients with classic galactosemia. Journal of Inherited Metabolic Disease. 41(2):197-208.

Genzen JR, Burnham CD, Felder RA, Hawker CD, Lippi G, Palmer OMP. Challenges and Opportunities in Implementing Total Laboratory Automation. Clinical Chemistry. 64(2):259-264.

Liew M, Rowe LR, Szankasi P, Paxton CN, Kelley T, Toydemir RM, Salama ME. Characterizing atypical BCL6 signal patterns detected by digital fluorescence in situ hybridization (FISH) analysis. Annals of Laboratory Medicine. 38(6):619-622.

Biswas A, Leon ME, Drew P, Fernandez-Bussy S, Furtado LV, Jantz MA, Mehta HJ. Clinical performance of endobronchial ultrasound-guided transbronchial needle aspiration for assessing programmed death ligand-1 expression in nonsmall cell. Diagnostic Cytopathology. 46(5):378-383.

Ji Y, Si Y, McMillin GA, Lyon E. Clinical pharmacogenomics testing in the era of next generation sequencing: challenges and opportunities for precision medicine. Expert Review of Molecular Diagnostics. 18(5):411-421.

Lin DC, Genzen JR Concordance analysis of paired cancer antigen (CA) 15-3 and 27.29 testing. Breast Cancer Research and Treatment. 167(1):269-276.

Russell CW, Fleming BA, Jost CA, Tran A, Stenquist AT, Wambaugh MA, Bronner MP, Mulvey MA. Context-Dependent Requirements for FimH and Other Canonical Virulence Factors in Gut Colonization by Extraintestinal Pathogenic Escherichia coli. The Medical Clinics of North America. 86(3).

Timbrook TT, Spivak ES, Hanson KE Current and Future Opportunities for Rapid Diagnostics in Antimicrobial Stewardship. The Medical Clinics of North America. 102(5):899-911.

Wabuyele SL, Colby JM, McMillin GA. Detection of Drug-Exposed Newborns. Therapeutic Drug Monitoring. 40(2):166-185.

Shen W, Paxton CN, Szankasi P, Longhurst M, Schumacher JA, Frizzell KA, Sorrells SM, Clayton AL, Jattani RP, Patel JL, Toydemir R, Kelley TW, Xu X. Detection of genome-wide copy number variants in myeloid malignancies using next-generation sequencing. Journal of Clinical Pathology. 71(4):372-378.

Wu F, Scroggin TL, Metz TD, McMillin GA. Development of A Liquid Chromatography-Tandem Mass Spectrometry Method for the Simultaneous Determination of Four Cannabinoids in Umbilical Cord Tissue. Journal of Analytical Toxicology. 42(1):42-48.

Lu J, Genzen JR, Grenache DG. Development of an enzymatic assay to measure lactate in perchloric acid-precipitated cerebrospinal fluid.​ Clinica Chimica Acta. 483:142-144.

Hagiya AS, Etman A, Siddiqi IN, Cen S, Matcuk GR Jr, Brynes RK, Salama ME. Digital image analysis agrees with visual estimates of adult bone marrow trephine biopsy cellularity.​ International Journal of Laboratory Hematology. 40(2):209-2144.

​​Schmidt RL, LoPresti J, McDermott MT MD, Zick SM, Straseski JA. D. Does Reverse Triiodothyronine Testing Have Clinical Utility? An Analysis of Practice Variation Based on Data from a National Reference Laboratory.  Thyroid. 28(7):842-848. July 2018.

McMillin GA. Drug Detection in Urine for Evaluating Exposures. The Journal of Applied Laboratory Medicine. 2(4):648-53.

​​Górska A, Peter S, Willmann M, Autenrieth I, Schlaberg R, Huson DH. Dynamics of the human gut phageome during antibiotic treatment.  Computational Biology and Chemistry. 274:420-427.

​​Bailey EB, Merriman J, Maughan B, Poole A, Tantravahi SK, Agarwal AM, Batten JA, Patel SB, Pal SK, Stenehjem DD, Agarwal N.Effect of treatment dose reductions in the setting of hand-foot syndrome on survival outcomes in patients with metastatic renal cell carcinoma treated with. Journal of Oncology Pharmacy Practice. 24(3):190-197.

Body BA, Beard MA, Slechta ES, Hanson KE, Barker AP, Babady NE, McMillen T, Tang YW, Brown-Elliott BA, Iakhiaeva E, Vasireddy R, Vasireddy S, Smith T, Wallace RJ Jr, Turner S, Curtis L, Butler-Wu S, Rychert J. Evaluation of the Vitek MS v3.0 Matrix-Assisted Laser Desorption Ionization--Time of Flight Mass Spectrometry System for Identification of Mycobacterium and Nocardia species.  Journal of Clinical Microbiology. Vol. 56, No. 6.

Jannetto PJ, Bratanow NC, Clark WA, Hamill-Ruth RJ, Hammett-Stabler CA, Huestis MA, Kassed CA, McMillin GA, Melanson SE, Langman LJ. Executive Summary: American Association of Clinical Chemistry Laboratory Medicine Practice Guideline - Using Clinical Laboratory Tests to Monitor Drug Therapy. The Journal of Applied Laboratory Medicine. 2(4):489-526.

Wei X, Calvo-Vidal MN, Chen S, Wu G, Revuelta MV, Sun J, Zhang J, Walsh MF, Nichols KE, Joseph V, Snyder C, Vachon CM, McKay JD, Wang SP, Jayabalan DS, Jacobs. Germline mutations in lysine specific demethylase 1 (LSD1/KDM1A) confer susceptibility to multiple myeloma. Cancer Research. 78(10):2747-2759.

Paul L, Comstock J, Edes K, Schlaberg R. Gestational Psittacosis Resulting in Neonatal Death Identified by Next-Generation RNA Sequencing of Postmortem, Formalin-Fixed Lung Tissue. Open Forum Infectious Diseases. 5(8):ofy172.

Tharkar-Promod S, Johnson DP, Bennett SE, Dennis EM, Banowsky BG, Jones SS, Shearstone JR, Quayle SN, Min C, Jarpe M, Mosbruger T, Pomicter AD, Miles RR. HDAC1,2 inhibition and doxorubicin impair Mre11-dependent DNA repair and DISC to override BCR-ABL1-driven DSB repair in Philadelphia chromosome-positive B-. Leukemia. 32(1):49-60.

Bliss J, Bouhenia M, Hale P, Couturier BA, Iyer AS, Rumunu J, Martin S, Wamala JF, Abubakar A, Sack DA, Luquero FJ, Couturier MR, Azman AS, Leung DT. High Prevalence of Shigella or Enteroinvasive Escherichia coli Carriage among Residents of an Internally Displaced Persons Camp in South Sudan. The American Journal of Tropical Medicine and Hygiene. 98(2):595-597.

La'ulu SL, Kalp KJ, Straseski JA. How Low Can You Go? Analytical Performance of Five Automated​ Testosterone Immunoassays. Clinical Biochemistry. 58:64-71.

Yuzyuk T, Lozier B, Schwarz EL, Viau K, Kish-Trier E, De Biase I. Intra-individual variability of long-chain fatty acids (C12-C24) in plasma and red blood cells. Modern Pathology. 31(4):643-651.

Caliskan A, Kohlmann WK, Affolter KE, Downs-Kelly E, Kanth P, Bronner MP. Intramucosal lipomas of the colon implicate Cowden syndrome Modern Pathology. 31(4):643-651.

Pasquali M, Yu C, Coffee B. Laboratory diagnosis of galactosemia: a technical standard and guideline of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 20(1):3-11

Hunsaker JJH, La'ulu SL, Wyness SP, Genzen JR. Lipemic interference of ceruloplasmin assays - An evaluation of lipid removal methods. Clinica Chimica Acta. 480:71-78.

Spörndly-Neesa E, Boberg J, Ekstedt E, Holm L, Fakhrzadeh A, Dunderd L, Kushnir MM, Lejonklou MH, Lind M. Low-dose exposure to Bisphenol A during development has limited effects on male​ ​reproduction in prepubertal and aging Fischer 344 rats. Reproductive Toxicology. 81:196-206.

Lloyd I, Chadwick B. Lymphoepithelioma-like Carcinoma of the Uterine Cervix: Cytomorphologic Features and Diagnostic Pitfalls by Liquid-Based Cytology. Diagnostic Cytopathology. 46(5):443-446.

Rychert J, Slechta ES, Barker AP, Miranda E, Babady NE, Tang Y, Wiederhold N, Sutton D, Hanson KE. Multi-center evaluation of the VITEK MS v3.0 system for the identification of filamentous fungi. Journal of Clinical Microbiology. 56(2).

Philip B, Yu DX, Silvis MR, Shin CH, Robinson JP, Robinson GL, Welker AE, Angel SN, Tripp SR, Sonnen JA, VanBrocklin MW, Gibbons RJ, Looper RE, Colman H, Holmen SL. Mutant IDH1 Promotes Glioma Formation In Vivo. Cell Reports. 2018;23(5):1553-1564.

Johnson DN, Furtado LV, Long BC, Zhen CJ, Wurst M, Mujacic I, Kadri S, Segal JP, Antic T, Cipriani NA.  Noninvasive Follicular Thyroid Neoplasms With Papillary-Like Nuclear Features (NIFTPs) Are Genetically and Biologically Similar to Adenomatous Nodules and Distinct From Papillary Thyroid Carcinomas With Extensive Follicular Growth. Archives of Pathology and Laboratory Medicine. 142(7):838-850. July 2018.

Margraf RL, Durtschi J, Krock B, Newcomb TM, Bonkowsky J, Voelkerding KV, Bayrak-Toydemir P, Lutz RE, Swoboda KJ.  Novel PLP1 Mutations Identified with Next-Generation Sequencing Expand the Spectrum of PLP1-Associated Leukodystrophy Clinical Phenotypes. Child Neurology Open. 5:2329048X18789282. July 2018.

Kushnir MM, Peterson LK, Strathmann FG. Parathyroid Hormone Related Protein Concentration in Human Serum and CSF Correlates with Age. Clinical Biochemistry. 2018;52:56-60.

Castanon A, Pierre G, Willis R, Harris NE, Papalardo E, Romay-Penabad Z, Schleh A, Jajoria P, Smikle M, DeCeulaer K, Tebo A, Jaskowski T, Guerra MM, Branch DW. Performance Evaluation And Clinical Associations Of Immunoassays That Detect Antibodies To Negatively-Charged Phospholipids Other Than Cardiolipin. American Journal of Clinical Pathology. 149(5):401-411.

Erickson JA, Grenache DG. ​Performance Evaluation of a Serum S-100B ELISA for Use with Cerebrospinal Fluid.​ The Journal of Applied Laboratory Medicine. 2:811-813.

McMillin GA, Wadelius M, Pratt VM. ​Pharmacogenetics.​ Tietz Textbook of Clinical Chemistry and Molecular Diagnostics. 6th Ed., Chapter 54 (Electronic Only).

McMillin GA. ​Pharmacogenetics of opioid use and implications for pain management - are we ready?.​ The Journal of Applied Laboratory Medicine. 2(4)481-4.

Karner KH, Inamdar KV. ​Plasma cell myeloma mimicking classical Hodgkin lymphoma in the bone marrow.​ International Journal of Hematology. 107(2):127-128.

Shen W, Young BA, Bosworth M, Wright KE, Lamb AN, Ji Y. ​Prenatal detection of uniparental disomy of chromosome 2 carrying a CHRND pathogenic variant that causes lethal multiple pterygium syndrome.​ Clinical Genetics. 93(6):1248-1249.

Scroggin TL, McMillin GA. ​Quantitation of Cocaine and Metabolites, Barbiturates, and Phencyclidine in Meconium by Liquid Chromatography Tandem Mass Spectrometry.​ Journal of Analytical Toxicology. 42(3):177-182.

Genzen JR, Murray DL, Abel G, Meng QH, Baltaro RJ, Rhoads DD, Delgado JC, Souers RJ, Bashleben C, Keren DF, Ansari MQ. ​Screening and Diagnosis of Monoclonal Gammopathies: An International Survey of Laboratory Practice.​ Archives of Pathology and Laboratory Medicine. 142(4):507-515.

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