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• Abelson Murine Leukemia Viral Oncogene Homolog 1 (ABL1) Variant Testing in Acquired Tyrosine Kinase Inhibitor (TKI) Resistance – View Report
• AlloMap – View Report
• Alpha-1-Antitrypsin Deficiency (AATD) – View Report
• Alpha-Thalassemia – View Report
• Alport Syndrome – View Report
• Amyotrophic Lateral Sclerosis (ALS; Lou Gehrig’s Disease) – View Report
• Anaplastic Lymphoma Kinase (ALK) Gene Rearrangement Testing in Non-Small Cell Lung Cancer (NSCLC) – View Report
• Angelman Syndrome (AS) – View Report
• Angiotensin-Converting Enzyme (ACE) Insertion/Deletion (I/D) Polymorphism Testing – View Report
• Angiotensin Receptor 1 (AGTR1) c.1166A>C Polymorphism Testing for Essential Hypertension – View Report
• APC-Associated Polyposis Conditions – View Report
• Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy (ARVD/C) – View Report
• Ashkenazi Jewish Genetic Screening Panel – View Report
• Autosomal Dominant Spinocerebellar Ataxia – View Report
• BCR-ABL – View Report
• Beta-2 Adrenergic Receptor (ADRB2) Testing – View Report
• Beta-Thalassemia – View Report
• Biotinidase (BTD) Gene Sequencing – View Report
• BRAF p.Val600Glu (V600E) – View Report
• BRCA1 and BRCA2 Rearrangements – View Report
• BRCA1/BRCA2 Sequence Variant Analysis (Breast Cancer) – View Report
• BRCA1/BRCA2 Sequence Variant Analysis (Ovarian Cancer) – View Report
• Brugada Syndrome (BrS) – View Report
• CADASIL – View Report
• Cadherin 1 (E-cadherin; CDH1) – View Report
• CancerTYPE ID® – View Report
• Carnitine Palmitoyltransferase II (CPTII; CPT2) Deficiency – View Report
• Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) – View Report
• CDKN2A Testing – View Report
• Celiac Disease – View Report
• Cerebral Cavernous Malformations (CCM) – View Report
• Charcot-Marie-Tooth Disease Type 1A (PMP22) – View Report
• Charcot-Marie-Tooth Neuropathy, Type 1 (CMT1) – View Report
• Chemokine CC Motif Receptor 5 (CCR5) CCR5-∆32 Polymorphism – View Report
• Chromosome 22q11.2 Deletion Syndrome – View Report
• COL1A1 and COL1A2 Testing – View Report
• Collagen Type VI-Related Disorders – View Report
• ColoSure™ – View Report
• Comparative Genomic Hybridization (CGH) Microarray – View Report
• Complement Factor 4 (CFH) p.Tyr402His and ARMS p.Ala69Ser Polymorphism Testing for Susceptibility to Age-Related Macular Degeneration (ARMD) – View Report
• Corus™ CAD – View Report
• Counsyl Universal Genetic Test – View Report
• Cyclin D1-Immunoglobulin Heavy Chain (CCND1-IGH@) Translocation Testing – View Report
• CYP2C19 Variant Testing – View Report
• CYP2C9 and VKORC1 Variant Testing – View Report
• CYP2D6 Genotyping – View Report
• Cystic Fibrosis Transmembrane Regulator (CFTR) – View Report
• Cytochrome P450 1A2 (CYP1A2) – View Report
• Cytochrome P450 21A2 (CYP21A2) Testing – View Report
• Cytochrome P450 3A4 (CYP3A4) – View Report
• Cytochrome P450 3A5 (CYP3A5) Testing – View Report
• Cytochrome P450 (CYP450) Genotyping to Predict Response to Antipsychotic Medications – View Report
• DecisionDx-GBM – View Report
• DecisionDx-UM – View Report
• deCODE BreastCancer™ – View Report
• deCODE MI™ – View Report
• deCODE ProstateCancer™ – View Report
• Dentatorubral-Pallidoluysian Atrophy (DRPLA) – View Report
• DNA Polymerase Gamma (POLG)-Related Disorders – View Report
• Early-Onset Familial Alzheimer Disease (EOFAD) – View Report
• Ehlers-Danlos Syndrome (EDS) Classic Type – View Report
• Ehlers-Danlos Syndrome (EDS) Type IV – View Report
• Epidermal Growth Factor Receptor (EGFR) Analysis – View Report
• Epidermal Growth Factor Receptor (EGFR) Gene Amplification Analysis by Fluorescence in situ Hybridization (FISH) – View Report
• Episodic Ataxia (EA) – View Report
• ERCC1 – View Report
• Estrogen Receptor (ESR1) and Progesterone Receptor (PGR) Testing – View Report
• Facioscapulohumeral Muscular Dystrophy (FSHMD) – View Report
• Factor V (F5) HR2 Haplotype Testing – View Report
• Factor VII (F7) p.Arg353Gln Polymorphism Testing – View Report
• Factor V Leiden – View Report
• Factor XI Deficiency – View Report
• Factor XIIIA1 (F13A1) p.Val34Leu Polymorphism Testing – View Report
• Familial Dilated Cardiomyopathy (FDC) – View Report
• Familial Hemophagocytic Lymphohistiocytosis (FHL) – View Report
• Familial Hypertrophic Cardiomyopathy (FHCM) – View Report
• Familial Mediterranean Fever (FMF) – View Report
• Familial Transthyretin Amyloidosis (Familial TTR Amyloidosis) – View Report
• Fibrinogen-Beta (FGB) c.-455G>A Polymorphism Testing – View Report
• Fibroblast Growth Factor Receptor 3 (FGFR3) Testing – View Report
• FIP1L1-PDGFRA Fusion Gene Testing – View Report
• FMR1 Testing – View Report
• Forkhead Box Protein G1 (FOXG1) – View Report
• Fragile X Syndrome (FMR1) – View Report
• Friedreich Ataxia (FRDA) – View Report
• Galactose-1-Phosphate Uridylyltransferase (GALT) Testing – View Report
• Generalized Epilepsy with Febrile Seizures Plus (GEFS+) – View Report
• Genetic and Molecular Testing for Diagnosis and Prognosis in Acute Myeloid Leukemia (AML) – View Report
• Genomic Microarray Testing for Hematological Oncology Indications – View Report
• GJB2 (Connexin 26) and GJB6 (Connexin 30) Sequence Variant Analysis – View Report
• Hemophilia A – View Report
• Hereditary Hemorrhagic Telangiectasia (HHT) – View Report
• Hereditary Neuralgic Amyotrophy – View Report
• Hereditary Pancreatitis – View Report
• Hereditary Paraganglioma-Pheochromocytoma Syndromes (PGL/PCC) – View Report
• Hereditary Pulmonary Arterial Hypertension – View Report
• Hereditary Spastic Paraplegia (HSP) – View Report
• HERmark Breast Cancer Assay – View Report
• HFE-Associated Hemochromatosis – View Report
• H/I™ (HOXB13:IL17BR) Gene Expression Ratio – View Report
• HLA-B27 Testing – View Report
• HLA-B*5701 Screening – View Report
• Human Leukocyte Antigen (HLA) Genotyping – View Report
• Human Platelet Antigen (HPA) Genotyping – View Report
• Hunter Syndrome – View Report
• Huntington Disease – View Report
• Immunoglobulin Gene (IGHV@ and IGKV@) – View Report
• Immunoglobulin Heavy Variable Group (IgHV) Gene Testing – View Report

View more: Reports: J-R | Reports: S-Z