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Association of DNA Methylation Markers with C-reactive protein in
African Americans
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Genome-Wide Burden of Copy Number Variations in Schizophrenia and
Bipolar I Disorder: A case-control study
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22q11 Deletion Syndrome: B-cell Gene Expression Profiles and
Potential Links to ASD and Schizophrenia
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Genome-wide identification of DNA methylation associated with
Systolic and Diastolic Blood Pressures among African Americans
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Maternal Folic Acid Supplementation and Congenital Heart Defects in
Down Syndrome
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Sex-Specific Differential DNA Methylation Related to Cigarette Smoking in African Americans
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Refining the roles of genetic, environmental, and endogenous factors in Factor VIII activity levels.
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Effects of Low Calcium, Immune, and Endocrine Factors on Maladaptive Behavioral Problems in Patients with 22q11 Deletion Syndrome
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Genome-wide association study in two populations to determine genetic variants associated with Toxoplasma gondii infection and relationship to schizophrenia risk.
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Genome-wide association study of hemodynamic response to mental stress
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Factors Affecting Fabry Disease Diagnosis in Relatives of an Identified Proband
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Polygenic Risk Scores and Schizophrenia: Association with Gender and Age of Onset in an Ashkenazi Jewish Population
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Diabetes-related DNA Methylation of TXNIP Independently Associated with Inflammation
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Epigenetic Associations of Circulating Interleukin 6 among People with HIV
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Pilot investigation of treatment effect modification by vitamin D binding protein isoforms on calcium and vitamin D effects on biomarkers of risk for colorectal cancer in the normal-appearing colorectal mucosa of colorectal adenoma patients
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Transmission patterns of extensively drug-resistant tuberculosis in South Africa: a network approach
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Association between Maternal Depression during Pregnancy and Newborn DNA Methylation
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Associations between Neighborhood-Level Factors and DNA Methylation in Breast Tumor Tissue: Using Social Epigenomics to Explore Cancer Disparities
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The Association between Maternal Occupation and Down Syndrome: A Report from the National Down Syndrome Project
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Metabolomic alterations in Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS) premutation carriers
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