Method for the Prediction of Adverse Drug Responses to Stains

Method and device for the in vitro detection of polycystic ovarian syndrome (pcos) and pathologies involving cardiovascular risk

HUMAN OBESITY SUSCEPTIBILITY GENE ENCODING A MEMBER OF THE NEUREXIN FAMILY AND USES THEREOF

MSMB-gene based diagnosis, staging and prognosis of prostate cancer

COMPOSITIONS AND METHODS FOR DIAGNOSING AND TREATING MACULAR DEGENERATION

Genetic polymorphisms for identifying individuals at risk for drug-induced vestibular dysfunction

Human single nucleotide polymorphisms in ion channels and other proteins

Haplotypes and polymorphisms linked to human thiopurine s-methyltransferase deficiencies

GENETIC POLYMORPHISMS ASSOCIATED WITH ALZHEIMER'S DISEASE, METHODS OF DETECTION AND USES THEREOF

Human Niemann Pick C1-Like 1 Gene (NPC1L1) Polymorphisms and Methods of Use Thereof

DIAGNOSTICS AND THERAPEUTICS FOR CARDIOVASCULAR DISORDERS

Methods for predicting the response of multiple sclerosis patients to interferon therapy and diagnosing multiple sclerosis

Markers for metabolic syndrome

Detection of mutations in a gene associated with resistance to viral infection

Methods and systems for medical sequencing analysis

TRANSCRIPTION FACTOR ARNTL2 GENE AND EXPRESSION PRODUCTS THEREOF USED IN THE DIAGNOSIS, PREVENTION, AND TREATMENT OF TYPE 1 DIABETES

GENEMAP OF THE HUMAN GENES ASSOCIATED WITH CROHN'S DISEASE

Use of the ornithine transcarbamylase (), as a marker for diagnosing brain damages

GENETIC POLYMORPHISMS AND SUBSTANCE DEPENDENCE

Probe for detecting ABL gene mutation and uses thereof

Toll-like receptor 2 (tlr-2) haplotypes predict outcome of patients

Gray leaf spot tolerant maize and methods of production

Loci associated charcoal rot drought complex tolerance in soybean

Loci associated charcoal rot drought complex tolerance in soybean

Loci associated charcoal rot drought complex tolerance in soybean

Diagnostics for Aging-Related Dermatologic Disorders

METHOD FOR INCREASING THE SALTWATER TOLERANCE OF A FISH

DIAGNOSTICS AND THERAPEUTICS FOR EARLY-ONSET MENOPAUSE

Identification of Genetic Variants Associated with Increased Severity of Pulmonary Disease

Genetic polymorphisms associated with psoriasis, methods of detection and uses thereof

Genetic polymorphisms associated with rheumatoid arthritis, methods of detection and uses thereof

Genetic Analysis in Racing Animals

Novel genes and markers in essential arterial hypertension

Pharmaceutical and therapeutic applications relating to a type 9 adenylyl cyclase Polymorphism in asthma and reversible bronchial obstruction

COAGULATION FACTOR III POLYMORPHISMS ASSOCIATED WITH PREDICTION OF SUBJECT OUTCOME AND RESPONSE TO THERAPY

DIAGNOSIS AND TREATMENT OF TYPE 1 DIABETES

Resistance Genes

GENETIC MARKERS FOR SCD OR SCA THERAPY SELECTION

DIAGNOSTIC KITS AND METHODS FOR SCD OR SCA THERAPY SELECTION

Predicting and diagnosing patients with autoimmune disease

Genetic polymorphisms associated with liver fibrosis, methods of detection and uses thereof

Single Nucelotide Polymorphism (SNP)

Complement factor H for diagnosis of age-related macular degeneration

QUANTITATIVE TEST TO DETECT DISEASE PROGRESSION MARKERS OF EPITHELIAL OVARIAN CANCER PATIENTS

Detection of mutations in a gene associated with resistance to viral infection, OAS1

Biomarkers for Identifying Efficacy of Tegaserod in Patients with Chronic Constipation

Association of Single Nucleotide Polymorphisms in the CBFA2T1 and DECR1 Genes with Performance and Carcass Merit of Beef Cattle

Assessing brain aneurysms

POLYNUCLEOTIDES ASSOCIATED WITH AGE-RELATED MACULAR DEGENERATION AND METHODS FOR EVALUATING PATIENT RISK

Simplified Method of Determining Predisposition to Scoliosis

Genetic variant of the annexin A5 gene

Dopamine D2 receptor gene variants

IDENTIFICATION OF GENETIC MARKERS ASSOCIATED WITH PARKINSON DISEASE

METHODS AND PRODUCTS RELATED TO GENOTYPING AND DNA ANALYSIS

Prognostic and diagnostic method for disease therapy

IL-1 gene cluster, insulin resistance and coronary artery disease associated polymorphisms and haplotypes and methods of using same

ALPK1 GENE VARIANTS IN DIAGNOSIS RISK OF GOUT

Polymorphic Nucleic Acids Associated With Colorectal Cancer And Uses Thereof

Association of SNPs with fat deposition and fatty acid composition

Method of evaluating drug sensitivity by analyzing GIRK channel genes

Methods for Individualizing Cardiovascular Disease Treatment Protocols Based on Beta-1 Adrenergic Receptor Haplotype

METHOD FOR ADMINISTERING ANTICOAGULATION THERAPY

Method for Detecting Large Mutations and Duplications Using Control Amplification Comparisons to Paralogous Genes

Methods for identifying an individual at increased risk of developing coronary artery disease

Mitochondrial DNA variants associated with metabolic syndrome

GENEMAP OF THE HUMAN GENES ASSOCIATED WITH CROHN'S DISEASE

Bone/joint disease sensitivity gene and use thereof

DIAGNOSTIC METHODS AND AGENTS

Methods of identifying individuals at risk of perioperative bleeding, renal dysfunction or stroke

Methods and Compositions for Goss' Wilt Resistance in Corn

BIOCHEMICAL AND GENETIC ANALYSIS FOR PREDICTION OF BREAST CANCER RISK

Methods and Compositions for Haploid Mapping

Methods and compositions for gray leaf spot resistance in corn

Methods and compositions for selecting soybean plants resistant to southern root knot nematode

Method of prognosing and diagnosing hereditary spastic paraplegia, mutant nucleic acid molecules and polypeptides

Genetic variation in pro-melanin-concentrating hormone gene affects carcass traits in cattle

POLYMORPHISMS IN MGST3 ARE ASSOCIATED WITH ELEVATED ALAT LEVELS AFTER XIMELAGATRAN TREATMENT

METHOD OF DETECTING HUMAN CYTOCHROME P450 (CYP) 2D6 GENE MUTATION

Methods to identify soybean aphid resistant quantitative trait loci in soybean and compositions thereof

Primers for amplifying and detecting the beta 2 adrenergic receptor gene

Detecting disease association with aberrant glycogen synthase kinase 3beta expression

ESTROGEN RECEPTOR ALLELES THAT ARE PREDICTIVE OF INCREASED SUSCEPTIBILITY TO BONE FRACTURE

ASSOCIATION BETWEEN HLA-DRBI*07 ALLELE AND SUSCEPTIBILY TO INCREASED LEVELS OF ALAT FOLLOWING XIMELAGATRAN ADMINISTRATION

METHODS AND COMPOSITIONS FOR IDENTIFYING A SUBJECT WITH AN INCREASED RISK OF GRAM NEGATIVE BACTERIAL INFECTION

Methods and compositions for correlating genetic markers with multiple sclerosis

Genetic Markers Associated with Scoliosis and Uses Thereof

Method of Determining Predisposition to Scoliosis and Uses Thereof

Method for identifying maize plants with RCG1 gene conferring resistance to colletotrichum infection

GENETIC VARIANTS ON CHR 15Q24 AS MARKERS FOR USE IN DIAGNOSIS, PROGNOSIS AND TREATMENT OF EXFOLIATION SYNDROME AND GLAUCOMA

GENETIC MODELS FOR STRATIFICATION OF CANCER RISK

POLYMORPHISMS IN PON1 ARE ASSOCIATED WITH ELEVATED ALANINE AMINOTRANSFERASE LEVELS AFTER XIMELAGATRAN OR TACRINE ADMINISTRATION

Methods and compositions for the diagnosis and treatment of schizophrenia

Roles for dual endothelin-1/angiotensin II receptor (Dear) in hypertension and angiogenesis

Involvement of a Novel Nuclear-Encoded Mitochondrial Poly(A) Polymerase PAPD1 in Extreme Obesity-Related Phenotypes in Mammals

DIAGNOSTICS AND THERAPEUTICS FOR OSTEOPOROSIS

ORAL CANCER MARKERS AND THEIR DETECTION

METHODS AND COMPOSITIONS RELATING TO THE PHARMACOGENETICS OF DIFFERENT GENE VARIANTS

Methods and Compositions for Treating Ocular Disorders

Genetic markers of schizophrenia

SUSCEPTIBILITY TO BONE DAMAGE

HUMAN AUTISM SUSCEPTIBILITY GENE ENCODING A KINASE AND USES THEREOF

Polymorphic Cd24 Genotypes that are Predictive of Multiple Sclerosis Risk and Progression

Methods for detecting a cyclophilin B SNP associated with HERDA

Polymorphism in the Apo(a) gene predict responsiveness to acetylsalicylic acid treatment

Compositions and Methods for Inferring an Adverse Effect in Response to a Drug Treatment

Identification of Gene Associated with Reading Disability and Uses Therefor

Novel Missense Mutations and Single Nucleotide Polymorphisms in the Rabphillin-3A-Like Gene and Uses Thereof

Methods and Compositions For Correlating Ccl3l1/Ccr5 Genotypes With Disorders

Methods for selecting initial doses of psychotropic medications based on a CYP2D6 genotype

Dairy cattle breeding for improved milk production traits in cattle

Method of Administering a Therapeutic

Genetic Markers Associated with Endometriosis and Use Thereof

GENETIC MARKER FOR INCREASED RISK FOR OBESITY-RELATED DISORDERS

Method and Apparatus for Using SLC2A10 Genetic Polymorphisms for Determining Peripheral Vascular Disease in Patients with Type-2 Diabetes

Genetic polymorphisms associated with liver fibrosis, methods of detection and uses thereof

Methods and Kits for Predicting Liver Fibrosis Progression Rate in Chronic Hepatitis C Patients

Susceptibility Gene for Myocardial Infarction, Stroke, Paod and Methods of Treatment

METHODS AND KITS BASED ON UGT1A7 PROMOTER POLYMORPHISM

Human sweet and umami taste receptor variants

Genetic polymorphisms associated with neurodegenerative diseases, methods of detection and uses thereof

Methods and Compositions for Assessment of Pulmonary Function and Disorders

Human Obesity Susceptibility Gene Encoding a Taste Receptor and Uses Thereof

Methods and compositions for screening and treatment of disorders of blood glucose regulation

Inherited Mitochondrial Dna Mutations in Cancer

Method for Personalized Diet Design for Females of Asian Origin

Methods for detecting an increased risk for coronary heart disease

Common allele on chromosome 9 associated with coronary heart disease

Compositions, methods and systems for inferring bovine breed or trait

Schizophrenia, Schizoaffective Disorder and Bipolar Disorder Susceptibility Gene Mutation and Applications to Their Diagnosis and Treatment

Chromosome 5 Genetic Variants Related to Dyslexia

Methods and compositions for selecting soybean plants resistant to phytophthora root rot

Method for determining the risk of developing a neurological disease

DIABETES GENE

Variants in complement regulatory genes predict age-related macular degeneration

Utility of SNP markers associated with major soybean plant maturity and growth habit genomic regions

Method Evolved for Recognition and Testing of Age Related Macular Degeneration (Mert-Armd)

IL-GENE CLUSTER AND ASSOCIATED INFLAMMATORY POLYMORPHISMS AND HAPLOTYPES

IL-1 GENE CLUSTER AND ASSOCIATED INFLAMMATORY POLYMORPHISMS AND HAPLOTYPES

IL-1 GENE CLUSTER AND ASSOCIATED INFLAMMATORY POLYMORPHISMS AND HAPLOTYPES

Genetic markers for assessing risk of premature birth resulting from preterm premature rupture of membranes

Compositions and Methods for Treating Schizophrenia and Related Disorders

Human Obesity Susceptibility Genes Encoding Peptide Hormones and Uses Thereof

Sirtuin polymorphisms and methods of use thereof

Glutathione S-transferase sequence variants

GENETIC SCREENING FOR PREDICTING ANTIDEPRESSANT DRUG RESPONSE BASED ON THE MONOAMINE TRANSPORTER GENE POLYMORPHISM COMBINATION

Polymorphisms in the Fcgr2b Promoter and Uses Thereof

Leptin promoter polymorphisms and uses thereof

Methods of macromolecular analysis using nanochannel arrays

Fibroblast growth factor (FGF23) polypeptides

Genetic polymorphisms associated with coronary events and drug response, methods of detection and uses thereof

Method for improving neoadjuvant chemotherapy

Method for HLA typing

NOVEL HUMAN GENE FUNCTIONALLY RELATED TO DYSLEXIA

Compositions and methods for increasing bone mineralization

SINGLE NUCLEOTIDE POLYMORPHISMS ASSOCIATED WITH SUSCEPTIBILITY TO CARDIOVASCULAR DISEASE

Methods for treatment with bucindolol based on genetic targeting

Dog Periodontitis

Method for diagnosing or predicting susceptibility to optic neuropathy

Single nucleotide polymorphisms and the identification of lactose intolerance

Test for determining blood type in the cat

Screening methods and sequences relating thereto

Methods and materials for identifying polymorphic variants, diagnosing susceptibilities, and treating disease

Methods for detecting age-related macular degeneration

SNP DETECTION AND OTHER METHODS FOR CHARACTERIZING AND TREATING BIPOLAR DISORDER AND OTHER AILMENTS

Identification marker responsive to interferon therapy for renal cell cancer

Methods of Analysis of Polymorphisms and Uses Thereof

Human Obesity Susceptibility Gene Encoding a Potassium Voltage-Gated Channel and Uses Thereof

Methods and Compositions for Inferring Eye Color and Hair Color

Human Autism Susceptibility Gene Encoding Prkcb1 and Uses Thereof

Methods and compositions for genetically detecting improved milk production traits in cattle

DIAGNOSTICS AND THERAPEUTICS FOR DISEASES ASSOCIATED WITH AN IL-1 INFLAMMATORY HAPLOTYPE

Polymorphisms in mitochondrial transcription factor A ("TFAM") gene and their associations with carcass traits

Compositions and methods for increasing bone mineralization

Asthma Susceptibility Locus

Methods for Identifying a Patient as a Candidate for Treatment with a Long Acting Beta Agonist and for Predicting a Patient's Response to Long Acting Beta2 Agonist Therapy by Analysing Polymorphisms in the Beta2-Adrenergic Receptor Gene

Polymorphisms in the urocortin 3 gene and their associations with marbling and subcutaneous fat depth in beef cattle

METHOD FOR PERSONALIZED DIET DESIGN

Methods of detecting prostate cancer using BAP28-related biallelic markers

METHODS AND COMPOSITIONS FOR DIAGNOSING AND TREATING PROSTATE CANCER

CDK5 genetic markers associated with galantamine response

Method to identify disease resistant quantitative trait loci in soybean and compositions thereof

Association of Single Nucleotide Polymorphisms, Dairy Form and Productive Life

Methods and reagents for treatment and diagnosis of vascular disorders and age-related macular degeneration

Diagnostics and Therapeutics of Neurological Disease

Methods of diagnosis and treatment for asthma, allergic rhinitis and other respiratory diseases based on haplotype association

HLA alleles associated with adverse drug reactions and methods for detecting such

Process for prognosis of disease using gene GNA11

gene polymorphisms are associated with susceptibility to idiopathic scoliosis

IDENTIFICATION OF SOYBEANS HAVING RESISTANCE TO PHYTOPHTHORA SOJAE

DIAGNOSTICS AND THERAPEUTICS FOR ARTERIAL WALL DISRUPTIVE DISORDERS

Diagnostics And Therapeutics For Diseases Associated With An Il-1 Inflammatory Haplotype

Compositions and Methods For Determining and Predicting Treatment Responses For Depression and Anxiety

Genetic polymorphisms associated with psoriasis, methods of detection and uses thereof

GENES ASSOCIATED WITH OBESITY

GENES ASSOCIATED WITH COPD

GENES ASSOCIATED WITH MIGRAINE

GENES ASSOCIATED WITH RHEUMATOID ARTHRITIS

GENES ASSOCIATED WITH UNIPOLAR DEPRESSION

Forensic identification

Method for the Prediction of the Risk Potential for Cancerous Diseases and Inflammatory Intestinal Diseases and Corresponding Tests

Compositions and methods for obesity screening using polymorphisms in NPY2R

Methods for treatment with bucindolol based on genetic targeting

Leptin and Growth Hormone Receptor Gene Markers Associated with Rearing, Carcass Traits and Productive Life in Cattle

Maize polymorphisms and methods of genotyping

Variants of the Serotonin Transporter

MOLECULAR HAPLOTYPING OF GENOMIC DNA

Methods for the identification, evaluation and treatment of patients having CC-Chemokine receptor 2 (CCR-2) mediated disorders

Inbred corn line DE811ASR(BC5)

Method for cancer detection and monitoring

Polymorphisms in ABCB1 associated with a lack of clinical response to medicaments

Nucleic acid molecules correlated with the Rhesus weak D phenotype

Polycystic xidney disease PKD2 gene and uses thereop

Genetic polymorphisms associated with Alzheimer's disease, methods of detection and uses thereof

Identification of Snps Associated with Hyperlipidemia, Dyslipidemia and Defective Carbohydrate Metabolism

ENA-78 Gene Polymorphisms and Protein Concentrations as Diagnostic and Prognostic Tools

NPH6 nucleic acids and proteins

Genetic polymorphisms in the prostate-specific antigen gene promoter

Method of haplotype-based genetic analysis for determining risk for developing insulin resistance, coronary artery disease and other phenotypes

IRF-5 HAPLOTYPES IN SYSTEMIC LUPUS ERYTHEMATOSUS

Prediction and prophylactic treatment of type 1 diabetes

Protein C And Endothelial Protein C Receptor Polymorphisms As Indicators Of Subject Outcome

Corn variety DE811ASR(BC5)

Method Of Evaluating Drug Sensitivity By Analyzing The Mu-Opioid Receptor Gene

Detecting fetal chromosomal abnormalities using tandem single nucleotide polymorphisms

METHODS AND APPARATUS FOR GENOTYPING

Use Of A Genetic Modification In The Human Gnaq Gene For Predicting Risk Of Disease, The Course Of Disease, And Reaction To Treatments

Haplotype Markers And Methods Of Using The Same To Determine Response To Treatment

Polynucleotides and methods for making plants resistant to fungal pathogens

Polynucleotide

GENETIC MODELS FOR STRATIFICATION OF CANCER RISK

Association of gene expression and psychiatric disoders

WARFARIN DOSAGE PREDICTION

Calpastatin markers for fertility and longevity

Novel Target for Antiderpressant Therapy

Identifying a high oil phenotype in maize by detecting a marker locus genetically linked with a QTL6 region

Methods and compositions for genetic markers for autism

Genes and markers in type 2 diabetes and obesity

Thrombomodulin (Thbd) Haplotypes Predict Outcome

Methods of diagnosing susceptibility to myocardial infarction and screening for an LTA4H haplotype

Polymorphisms in fatty acid binding protein 4 (''FABP4'') gene and their associations with carcass traits

Polymorphisms in the Epidermal Growth Factor Receptor Gene Promoter

Mutant sodium channel Na1.7 nucleic acid methods

Chromosome 5 Genetic Variants Related To Dyslexia

Methods and compositions for producing vitamin K dependent proteins

Compositions and methods for viral resistance genes

Estimation method, human estrogen receptor alpha gene, genomic DNA, and diagnostic marker

Compositions related to the quantitative trait locus 6 (QTL6) in maize and methods of use

Single Nucleotide Polymorphisms as Prognostic Tool to Diagnose Adverse Drug Reactions (Adr) and Drug Efficacy

IL-1 gene cluster and associated inflammatory polymorphisms and haplotypes

Method of judging risk for onset of drug-induced granulocytopenia

Markers for addiction

Dep2 and its uses in major depressive disorder and other related disorders

DEP2 and its uses in major depressive disorder and other related disorders

Genetic polymorphisms in the corticotropin-releasing hormone (CRH) gene as markers for improving beef marbling score and/or subcutaneous fat depth

Genetic polymorphisms associated with Alzheimer's Disease, methods of detection and uses thereof

Diagnostic methods for pain sensitivity and chronicity and for tetrahydrobiopterin-related disorders

Identification of a novel gene underlying familial spastic paraplegia

Methods and Compositions for Autism Risk Assessment

Use Of Genetic Polymorphisms To Predict Drug-Induced Hepatotoxicity

GENETIC VARIANTS OF HUMAN INOSITOL POLYPHOSPHATE-4-PHOSPHATASE, TYPE I (INPP4A) USEFUL FOR PREDICTION AND THERAPY OF IMMUNOLOGICAL DISORDER

Methods for identification of alport syndrome

Method and Kit for Predicting Adverse Side Effects of Paclitaxel Therapy

Methods for detecting ovarian cancer and anticipating chemotherapy response

Association of PDE4D allelic variants with stroke

Human Autism Predisposition Gene Encoding a Transcription Factor and Uses Thereof

Method of determining the susceptibility of a subject to developing insulin-dependent diabetes

Novel genes and markers associated with high-density lipoprotein-cholesterol (HDL-C)

Polymorphisms in growth hormone receptor, ghrelin, leptin, neuropeptide Y, and uncoupling protein 2 genes and their associations with measures of performance and carcass merit in beef cattle

Angiogenesis pathway gene polymorphisms for therapy selection

12 kb sequence immediately adjacent to and upstream of the AKT1 gene locus containing multiple genetic variations associated with changes in metabolic syndrome, and methods of use

Method for non-invasive prenatal diagnosis

Human single nucleotide polymorphisms associated with dose-dependent weight gain and methods of use thereof

Assay For Bipolar Affective Disorder

Method of diagnosis of obesity

Hepoxilins and modulators of ichthyin for treatment skin disorders

Methods and compositions for vitamin K epoxide reductase

Human MLR single nucleotide polymorphisms associated with dose-dependent congestive heart failure and methods of use thereof

Use of single nucleotide polymorphism in the coding region of the porcine leptin receptor gene to enhance pork production

Lafora's disease gene

Genetic markers of food allergy

Alterations in the copy number of the SULT1A1 gene

WDR36 Gene Alterations and Glaucoma

Method for identifying progressive rod-cone degeneration in dogs

Cystic fibrosis transmembrane conductance regulator gene mutations

Use of genetic polymorphisms that associate with efficacy of treatment of inflammatory disease

Detection of mutations in a gene associated with resistance to viral infection, OAS1

LSAMP Gene Associated With Cardiovascular Disease

Method for detecting gene specifying allergic predisposition

Association of polymorphic kinase anchor proteins with cardiac phenotypes and related methods

Usages of MTHFR gene polymorphisms in predicting homocysteine level, disease risk, and treatment effects and related methods and kit

Method and markers for determining the genotype of horned/polled cattle

Human autism susceptibility gene and uses thereof

Use of KIAA0172 gene in treatment and diagnosis of diseases as well as in pharmaceutical development

Polynucleotide associated with a colon cancer comprising single nucleotide polymorphism, microarray and diagnostic kit comprising the same and method for diagnosing a colon cancer using the polynucleotide

Bovine gene missense mutations and uses thereof

Methods of diagnosing or prognosticating age-related macular degeneration

METHODS OF USING IL-21

Detection of mutations in a gene associated with resistance to viral infection, OAS2 and OAS3

Inversion on chromosome 8p23 is a risk factor for anxiety disorders, depression and bipolar disorders

Marker assisted best linear unbiased prediction (ma-blup): software adaptions for large breeding populations in farm animal species