Sökning: "haplotypes disorder"

Visar resultat 1 - 5 av 18 avhandlingar innehållade orden haplotypes disorder.

  1. 1. Genes of the serotonergic system and susceptibility to psychiatric disorders : a gene-based haplotype approach

    Författare :Ghazal Zaboli; Karolinska Institutet; Karolinska Institutet; []
    Nyckelord :Borderline Personality Disorder; Candidate genes; Case-control; Depression; Gene-based haplotypes; Linkage Disequilibrium; Schizophrenia; SNP.;

    Sammanfattning : Psychiatric disorders are complex, non-mendelian disorders. Complex disorders are ultimately determined by a number of genetic and environmental factors, and the effect of each factor may be obscured or confounded by others. LÄS MER

  2. 2. The genetic contribution to stroke in northern Sweden

    Författare :Tomas Janunger; Dan Holmberg; Holger Luthman; Umeå universitet; []
    Nyckelord :MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES; Northern Sweden; stroke; genetics; genome wide scan; association; 5q13; 9q31-33; Medical genetics; Medicinsk genetik; medicinsk genetik; Medical Genetics;

    Sammanfattning : Stroke is a common multi factorial cerebrovascular disorder with a large impact on global health. It is a disorder primarily associated with old age but environmental factors, lifestyle choices and medical history are all important for the risk of developing the disorder. LÄS MER

  3. 3. Gene-environment factors in depressive disorders with a focus on circadian genes

    Författare :Louise Sjöholm; Karolinska Institutet; Karolinska Institutet; []
    Nyckelord :;

    Sammanfattning : Depressive disorders have a multifactorial etiology, where both environmental and genetic risk factors contribute. Depression is characterized by a depressed mood and accompanied by e.g. loss of interest and pleasure, disturbed sleep and appetite and difficulties in concentrating. LÄS MER

  4. 4. Mapping trait genes in dogs : using the dog as a model organism

    Författare :Izabella Baranowska Körberg; Sveriges lantbruksuniversitet; Sveriges lantbruksuniversitet; []
    Nyckelord :NATURVETENSKAP; NATURAL SCIENCES;

    Sammanfattning : Understanding the genetic background of a given phenotypic trait or disease has long intrigued scientists. Model organisms can be employed when it is not feasible or possible to find trait causality in human cohorts. LÄS MER

  5. 5. Identification of susceptibility genes for dyslexia

    Författare :Heidi Anthoni; Karolinska Institutet; Karolinska Institutet; []
    Nyckelord :;

    Sammanfattning : Developmental dyslexia, also known as specific reading disability, is characterized by persistent difficulties in learning to read and spell in spite of adequate intelligence, education, social environment, and normal senses. It is the most common learning disability affecting 5-10% of school-aged children. LÄS MER