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COsegregation of VARiants in Panel of Genes (COVAR)

• Source: Study of Family COsegregation of Nucleotide VARiants in the Panel of Genes to Validate Their Use in Genetic Counseling

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Genetics of Mendelian Forms of Young Onset Alzheimer Disease (GMAJ)

• Source: Genetics of Mendelian Forms of Young Onset Alzheimer Disease. Identification of Novel Genetic Causes of AD Are of Importance in Completing the Mechanisms of the Amyloid Hypothesis. This Project is

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Genetic and Inflammatory Markers in Cardiovascular Disease (GEM) Registry (GEM)

• Authors : University of California, San Francisco

• Source: Genetic and Inflammatory Markers in Cardiovascular Disease (GEM) Registry

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A gene frequency model for QTL mapping using Bayesian inference

• Authors : He, Wei; Fernando, Rohan L; Dekkers, Jack CM

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Insulin, Androgen, and Risk in African-American Women

• Source: Falkner B. The role of cardiovascular reactivity as a mediator of hypertension in African Americans. Semin Nephrol. 1996 Mar;16(2):117-25.Sumner AE, Kushner H, Tulenko TN, et al: The

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The Measurement of Mood Variability and Sustained Attention in Women With Alcohol Dependence.

• Authors : Saskatoon Health Region

• Source: The Measurement of Mood Variability and Sustained Attention in Women With Alcohol Dependence.

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Exome sequencing identifies a mutation in TMC1 as a novel cause of autosomal recessive nonsyndromic hearing loss

• Authors : Hu, Jiongjiong; Liu, Fei; Xia, Wenjun

Subjects: Deafness; Ear; Transmembrane channel-like 1

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Darier's disease: a new paradigm for genetic studies in psychiatric disorders

• Authors : Cordeiro Júnior, Quirino; Werebe, Daniela Meshulam; Vallada, Homero

Subjects: Darier's disease; Depression; Psychiatry

• Source: Sao Paulo Medical Journal. November 2000 118(6)

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A novel mutation in C5L2 gene was associated with hyperlipidemia and retinitis pigmentosa in a Chinese family

• Authors : Qu, Ling-hui; Jin, Xin; Li, Liang-mao

Subjects: C5L2; Mutation; Retinitis pigmentosa

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