Diagnostic tests for the detection of motor neuropathy

SLC1A1 marker for anxiety disorder

Single nucleotide polymorphism associated with stroke susceptibility

Methods for diagnosing and characterizing breast cancer and susceptibility to breast cancer

Methods and kits for detecting single nucleotide polymorphisms of chromosome implicated in premature canities

Parkinson's disease-related disease compositions and methods

Diagnostic markers of hypertension and methods of use thereof

Gene variants and use thereof

Genetic polymorphisms associated with cardiovascular disorders and drug response, methods of detection and uses thereof

Method for treatment of cardiovascular and metabolic diseases and detecting the risk of the same

METHODS AND SYSTEMS FOR FACILITATING THE DIAGNOSIS AND TREATMENT OF SCHIZOPHRENIA

ERCC2 polymorphisms

Mutations in NOD2 are associated with fibrostenosing disease in patients with Crohn's disease

Agronomically elite soybeans with high beta-conglycinin content

Method for detecting a risk of cardiovascular disease

Chromosome 1p36 polymorphisms and low bone mineral density

Genes from chromosomes 3, 5 and 11 involved in premature canities

Novel genes and markers associated to type 2 diabetes mellitus

Tumor suppressor designated TS10Q23.3

Arrays of nucleic acid probes for analyzing biotransformation genes

Tumor suppressor designated TS10q23.3

Marker for a Psychosis or a Mood Disorder

Polymorphism in the macrophage migration inhibitory factor (MIF) gene as marker for prostate cancer

Methods of selection, reporting and analysis of genetic markers using broad-based genetic profiling applications

Computer systems and methods for inferring casuality from cellular constituent abundance data

Method for assessing trait anxiety by determining cholinergic status

Diagnostic and therapeutic target for macular degeneration

Multiplex assays for inferring ancestry

CYP19A1 polymorphisms

Metalloproteinase gene polymorphism in copd

Fine mapping of chromosome 17 quantitative trait loci and use of same for marker assisted selection

Gene sequence variations with utility in determining the treatment of neurological or psychiatric disease

Compositions, methods and systems for inferring bovine breed

Use of polymorphisms in human OATP-C associated with an effect on statin pharmacokinetics in humans in statin therapy

Method for detecting large mutations and duplications using control amplification comparisons to paralogous genes

Compositions and methods for the inference of pigmentation traits

Methods for treatment of age-related macular degeneration

Variants of the ADAM 12 gene

Glutathione S-transferase sequence variants

Method and kit for detecting a risk of coronary heart disease

Dairy cattle breeding for improved milk production traits in cattle

Method of treating patients with a mucinous glycoprotein (MUC-1) vaccine

Nephrin gene and protein

Methods and compositions for vitamin K epoxide reductase

Methods, uses and compositions for determining redisposition to cancers by identifying specific genotypes of CYP1B1 gene

Selecting animals for desired genotypic or potential phenotypic properties

Methods for selecting medications

Compositions and methods for spinocerebellar ataxia

Selecting animals for parentally imprinted traits

Genetic variants in the TCF7L2 gene as diagnostic markers for risk of type 2 diabetes mellitus

Identification of the genetic determinants of the polymorphic CYP3A5 expression

Polynucleotide comprising single-nucleotide polymorphism associated with colorectal cancer, microarray and diagnostic kit comprising the same, and method of diagnosing colorectal cancer using the same

Susceptibility genes for age-related maculopathy (ARM) on chromosome 10q26

Methods and compositions for assessment of pulmonary function and disorders

Methods for detecting genetic haplotypes by interaction with probes

Identification of genes involved in angiogenesis, and development of an angiogenesis diagnostic chip to identify patients with impaired angiogenesis

Methods of analysis of polymorphisms and uses thereof

Association between markers in the leptin gene and carcass traits in commercial feedlot steer and heifers

Porcine polymorphisms and methods for detecting them

Methods and compositions for assessment of pulmonary function and disorders

Genetic predictor for clinical use of drugs used in the treatment of neurological conditions

Methods for determining glutathione S-transferase theta-1 genotype

Method of diagnosis of obesity

Multiple SNP for diagnosing cardiovascular disease, microarray and kit comprising the same, and method of diagnosing cardiovascular disease using the same

Methods for predicting late onset Alzheimer disease in an individual

Genetic polymorphisms associated with myocardial infarction and uses thereof

Method to optimize drug selection, dosing and evaluation and to help predict therapeutic response and toxicity from immunosuppressant therapy

Novel Methods and Devices for Evaluating Poisons

Method for diagnosing myocardial infarction

Computer systems and methods for inferring causality from cellullar constituent abundance data

Genetic test for the identification of carriers of complex vertebral malformations in cattle

Markers associated with the therapeutic efficacy of glatiramer acetate

Method of analyzing breast cancer susceptibility and resistance

Methods and compositions for the correlation of single nucleotide polymorphisms in the vitamin K epoxide reductase gene and warfarin dosage

Methods of treatment of type 2 diabetes

Methods of diagnosis

Physiogenomic method for predicting clinical outcomes of treatments in patients

Pathogenic gene for coronary artery disease

Association of snps in the comt locus and neighboring loci with schizophrenia, bipolar disorder, breast cancer and colorectal cancer

Haplotype structures of chromosome 21

Arrays of nucleic acid probes for analyzing biotransformation genes

Genetic basis of Alzheimer's disease and diagnosis and treatment thereof

Polynucleotides and methods for making plants resistant to fungal pathogens

Polynucleotides and methods for making plants resistant to fungal pathogens

Polynucleotides and methods for making plants resistant to fungal pathogens

Genetic polymorphisms associated with coronary heart disease, methods of detection and uses thereof

SNPs in 5' regulatory region of MDR1 gene

Methods for identifying risk of breast cancer and treatments thereof

Reagents and methods for diagnosis of attention deficit hyperactivity disorder

Methods to predict ederma as a side effect of drug treatment

Human genomic polymorphisms

Genetic markers in the HLA-C gene associated with an adverse hematological response to drugs

Method for determining predisposition to a physiological reaction in a patient

Screening for alzheimer's disease

Genetic markers in the CSF2RB gene associated with an adverse hematological response to drugs

Biallelic markers for use in constructing a high density disequilibrium map of the human genome

Genetic markers in the HLA-DQBI gene associated with an adverse hematological response to drugs

Genetic markers of schizophrenia spectrum disorders in the sulfotransferase 4a (sult4a) gene

Methods for treatment with bucindolol based on genetic targeting

Method for detecting adverse reaction susceptibility to an HMG CoA reductase inhibitor

Genetic variants predicting warfarin sensitivity

NTRK1 genetic markers associated with progression of Alzheimer's disease

Genetic marker for coronary artery disease

Hsan II related gene and expression products and uses thereof

Parkinson's disease susceptibility haptotype as a tool for genetic screening

Pharmacogenetic DME detection assay methods and kits

Detection methods for disorders of the lung

Novel coding sequence haplotypes of the human BRCA2 gene

LDLR genetic markers associated with age of onset of Alzheimer's Disease

Methods of diagnosing cardiovascular disease

Use of a gene mutation in the human gnas gene for predicting risks of diseases, courses of the disease and for predicting the response to disease therapies

Method of judging inflammatory disease

Disease risk estimating method fusing sequence polymorphisms in a specific region of chromosome 19

Genetic marker for coronary artery disease

Screens for altered immune response capability

Marker gene

Methods and compositions for treating and diagnosing mood disorders, schizophrenia, and neuro-psychiatric disorders

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

Methods of identifying metastatic potential in cancer

Diagnostic and therapeutic means for kidney stone related pathologies

Identification of a gene causing the most common form of Bardet-Biedl syndrome and uses thereof

Method and kit for detecting a risk of essential arterial hypertension

Method and kit for detecting a risk of acute myocardial infarction

Methods of assessing the risk for the development of sporadic prostate cancer

Identification of genetic markers associated with parkinson disease

Methods for detection of pathogens in red blood cells

Risk prediction for hypertension, elevated plasma triglyceride and metabolic syndrome

Methods and compositions relating to COL2A1 gene mutations and osteonecrosis

Administration of FGF2 for treamtent of anxiety

Polymorphic Plasminogen genes and uses thereof

Thymidylate synthase polymorphisms for use in screening for cancer susceptibility

Detection methods

Marker mapping and resistance gene associations in soybean

Novel allelic variant of CYP2C19 associated with drug metabolism

Method for detecting the risk of and for treatment of type 2 diabetes

Marker at the androgen receptor gene for determining breast cancer susceptibility

Selecting animals for desired genotypic or potential phenotypic properties

Forensic identification

Detecting genotypes associated with congenital adrenal hyperplasia

Transforming growth factor beta 1 (TGFβ1) haplotypes and prediction of susceptibility for immunological disorders

Genetic polymorphisms associated with liver fibrosis

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

Susceptibility gene for myocardial infarction, stroke, and PAOD, methods of treatment

Association of single nucleotide polymorphisms in PPARgamma with osteoporosis

Method of diagnosis of inclusion body myopathy-paget bone disease-frontotemporal dementia syndrome

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

Methods and compositions for determining responsiveness to antibody therapy

Methods and compositions for the diagnosis of Cornelia de Lange Syndrome

Responsiveness to therapy for liver disorders

Use of HLA-G genotyping in immune-mediated conditions

Susceptibility gene for human stroke; methods of treatment

Methods and systems for inferring bovine traits

Diagnostics and therapeutics for diseases associated with an IL-1 inflammatory haplotype

Methods for coupling resistance alleles in tomato

Sulfotransferase SULT2A1 sequence variants

APOE genetic markers associated with age of onset of Alzheimer's disease

Methods for identifying subjects at risk of melanoma and treatments thereof

Genetic polymorphisms associated with cardiovascular disorders and drug response, methods of detection and uses thereof

Methods of preventing or treating recurrence of myocardial infarction

Methods for identifying risk of breast cancer and treatments thereof

Polymorphisms in the region of the human hemochromatosis gene

Haplotype markers for diagnosing susceptibility to immunological conditions

Treatment with cytokines

LRPAP1 genetic markers associated with galantamine

Methods, kits and pharmaceutical compositions for diagnosing, delaying onset of, preventing and/or treating osteoporosis

Compositions for inferring bovine traits

Cytogenetically determined diagnosis and prognosis of proliferative disorders

Method of detecting an increased susceptibility to breast cancer

Method for diagnosing or predicting susceptibility to psychiatric disorders

APOC1 genetic markers associated with age of onset of Alzheimer's Disease

SLC5A7 genetic markers associated with age of onset of Alzheimer's disease

CDK5 genetic markers associated with galantamine response

CHRNA9 genetic markers associated with progression of Alzheimer's disease

NTRK1 genetic markers associated with age of onset of Alzheimer's Disease

Method of detecting and predicting bronchodilatory response to beta agonist

Diagnosis of abnormal blood conditions based on polymorphisms in the glycoprotein VI gene

ACE2 activation for treatment of heart, lung and kidney disease and hypertension

Diagnosis and treatment of herpes simplex virus diseases

Real-time polymerase chain reaction-based genotyping assay for chemokine receptor (CXCR2) single nucleotide polymorphism

APOA4 genetic markers associated with progression of Alzheimer's disease

NTRK2 genetic markers associated with progression of Alzheimer's disease

EPHX2 Genetic markers associated with galantamine

Compositions and methods for viral resistance genes

Diagnosing predisposition to fat deposition and associated conditions

Methods for identifying risk of melanoma and treatments thereof

Nucleic acid encoding a retinoblastoma binding protein (RBP-7) and polymorphic markers associated with said nucleic acid

Oligonucleotides antibodies and kits including same for treating prostate cancer and determining predisposition thereto

Detection of predisposition to osteoporosis

Chromosome 6 and 9 genes involved in premature canities

Identification of fat and lean phenotypes in chickens using molecular markers

Human type II diabetes gene - Kv channel-interacting protein (KChIP1) located on chromosome 5

Methods for identifying risk of breast cancer and treatments thereof

Novel PRKAG3 alleles and use of the same as genetic markers for reproductive and meat quality traits

Diagnostic tests for the detection of peripheral neuropathy

Human schizophrenia gene

Genes from Chromosome 3, 5 and 11 involved in premature canities

Leptin promoter polymorphisms and uses thereof

Estrogen receptor alleles that are predictive of increased susceptibility to bone fracture

Application of kiaa0172 gene to treatment and diagnosis of diseases and drug discovery

Haplotypes of the FCER1A gene

Human Type II diabetes gene - Kv channel-interacting protein (KChIP1) located on chromosome 5

Characterization of CYP 2D6 genotypes

Methods for identifying risk of breast cancer and treatments thereof

Gene sequence variances in genes related to folate metabolism having utility in determining the treatment of disease

Method for determining the risk of developing a neurological disease

Identification of genetic forms of a gene that leads to high risk for parkinson disease

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

Methods of detecting Charcot-Marie Tooth disease type 2A

Kruppel-like factor 6 ( KLF6), a tumor suppressor protein, and diagnostics, therapeutics, and screening based on this protein

Methods of identifying genetic risk for and evaluating treatment of alzheimer's disease by determining single nucleotide polymorphisms

Diagnostic markers of mood disorders and methods of use thereof

Polymorphic olfactory receptor genes and arrays, kits and methods utilizing information derived therefrom for genetic typing of individuals

Genetic markers for bone mass

Polycystic kidney disease gene and uses thereof

Gout related genetic locus

Susceptibility gene for human stroke: method of treatment

Methods to predict patient responsiveness to tyrosine kinase inhibitors

PG-3 and biallelic markers thereof

Association of TSPYL polymorphisms with SIDDT syndrome

Real-time polymerase chain reaction-based genotyping assay for beta2-adrenergic receptor single nucleotide polymorphism

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

Estrogen receptor gene variation and disease

Apparatus and methods for parallel processing of micro-volume liquid reactions

Tumor suppressor designated TS10q23.3

Methods of diagnosing renal and cardiovascular disease

Susceptibility locus for schizophrenia

Genetic analysis for stratification of cancer risk

Methods and reagents for modulating cholesterol levels

Genetic polymorphisms in the prostate-specific antigen gene promoter

Mutations in WNT-frizzled signaling pathways associated with osteoarthritis

Method for detecting growth hormone variations in humans, the variations and their uses

Glaucoma therapeutics and diagnostics

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

Human mitochondrial dna polymorphisms, haplogroups, associations with physiological conditions, and genotyping arrays

Diagnostics and therapeutics for arterial wall disruptive disorders

Methods for identifying risk of breast cancer and treatments thereof

Gene sequence variances in genes related to folate metabolism having utility in determining the treatment of disease

Detection of neurodegenerative diseases

Method for detecting cell proliferative disorders

T cell regulatory genes associated with immune disease

Diagnostics and therapeutics for osteoporosis

Method for determining susceptibility to heart disease by screening polymorphisms in the vitamin D receptor gene

Diagnostics and therapeutics for early-onset menopause

Methods for identifying risk of breast cancer and treatments thereof

Gene and methods for diagnosing neuropsychiatric disorders and treating such disorders

Methods for diagnosing schizophrenia by detecting a polymorphism in the KalphaM1 gene

Chemical compounds

Insulin-like growth factor-1 receptor (IGF-1R) polymorphic alleles and use of the same to identify DNA markers for reproductive longevity

Macular degeneration diagnostics and therapeutics

Methods for identifying risk of breast cancer and treatments thereof

CHRNA2 genetic markers associated with galantamine response

Method for detecting subjects having Paget's disease of bone

Diagnostic test kit for determining a predisposition for breast and ovarian cancer, materials and methods for such determination

Detection of polymorphisms in the human 5-lipoxygenase gene

Genes and polymorphisms on chromosome 10 associated with Alzheimer's disease and other neurodegenerative diseases

Mutations in the KCNE1 gene encoding human minK which cause arrhythmia susceptibility thereby establishing KCNE1 as an LQT gene

Screening methods and sequences relating thereto

Diagnostic methods for cardiovascular disease, low hdl-cholesterol levels, and high triglyceride levels

Molecular markers linked to disease resistance in soybean

Resistance alleles in soybean

Molecular structure of RHD negative