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  1. No Access

    Article

    Common sequence variants on 20q11.22 confer melanoma susceptibility

    Brown et al. report results of a genome-wide association study for melanoma. Their screen, which used a pooling strategy, identified common variants on 20q11.22 associated with melanoma susceptibility. In two sep...

    Kevin M Brown, Stuart MacGregor, Grant W Montgomery, David W Craig in Nature Genetics (2008)

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    Article

    Evidence for linkage of a new region (11p14) to eczema and allergic diseases

    Asthma, allergic rhinitis (AR) and atopic dermatitis also called eczema are allergic co-morbidites, which are likely to depend on pleiotropic genetic effects as well as on specific genetic factors. After a pre...

    Michel Guilloud-Bataille, Emmanuelle Bouzigon, Isabella Annesi-Maesano in Human Genetics (2008)

  3. Article

    Open Access

    A two-step multiple-marker strategy for genome-wide association studies

    Genome-wide association studies raise study-design and analytical issues that are still being debated. Among them, stands the issue of reducing the number of markers to be genotyped without loss of efficiency ...

    Hugues Aschard, Mickaël Guedj, Florence Demenais in BMC Proceedings (2007)

  4. No Access

    Article

    Evidence for a pleiotropic QTL on chromosome 5q13 influencing both time to asthma onset and asthma score in French EGEA families

    Although many genome screens have been conducted for asthma as a binary trait, there is limited information regarding the genetic factors underlying variation of asthma expression. Phenotypes related to variab...

    Emmanuelle Bouzigon, Ayse Ulgen, Marie-Hélène Dizier, Valérie Siroux in Human Genetics (2007)

  5. Article

    Open Access

    Using an age-at-onset phenotype with interval censoring to compare methods of segregation and linkage analysis in a candidate region for elevated systolic blood pressure

    Genetic studies of complex disorders such as hypertension often utilize families selected for this outcome, usually with information obtained at a single time point. Since age-at-onset for diagnosed hypertensi...

    Karen A Kopciuk, Laurent Briollais, Florence Demenais, Shelley B Bull in BMC Genetics (2003)

  6. No Access

    Article

    Dissecting the loci controlling fetal haemoglobin production on chromosomes 11p and 6q by the regressive approach

    The Changes in the type of haemoglobin (Hb) produced during embryonic, fetal and adult life, have served as a paradigm for understanding the developmental regulation of human genes. A genetically determined pe...

    Jamie E. Craig, Jacques Rochette, Chris A. Fisher, David J. Weatherall in Nature Genetics (1996)

  7. No Access

    Article

    Congenital glaucoma: Genetic models

    Modes of inheritance of congenital glaucoma have been studied. Two methods of analysis, complex segregation analysis and frequency of congenital glaucoma in second- and third-degree relatives, did not permit o...

    Florence Demenais, Catherine Bonaïti, Marie-Louise Briard, Josué Feingold in Human Genetics (1979)

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