To evaluate the shared
genetic etiology of type 2 diabetes (T2D) and coronary heart disease (CHD), we conducted a genome - wide, multi-ancestry study of genetic variation for both diseases in up to 265,678 subjects for T2D and 260,365 subjects for CHD.
Results indicate a common
genetic etiology of psoriasis and obesity.
This study highlights the shared
genetic etiology of many canine and human genetic disorders, and provides new tools to investigate PRA mechanisms while the beloved dogs benefit from genetic testing.
Not exact matches
It has been estimated that 5 % to 10 %
of infants who die from SIDS have novel mutations in the cardiac sodium or potassium channel genes that result in long QT syndrome as well as in other genes that regulate channel function.44 A recent report described important new molecular and functional evidence that implicates specific SCN5A (sodium channel gene) β subunits in SIDS pathogenesis.47 The identification
of polymorphisms in genes pertinent to the embryologic origin
of the autonomic nervous system in SIDS cases also lends support to the hypothesis that a
genetic predisposition contributes to the
etiology of SIDS.
The new study quadruples the number
of known
genetic risk factors for Fuchs dystrophy, and helps explain its
genetic etiology.
We are currently focusing our efforts on an exceptional resource
of laboratory mouse strains with proven Mendelian disorders with unknown
genetic etiology, strains stewarded by the Mouse Mutant Resource at The Jackson Laboratory for over 50 years.
Dr. Torkamani's research covers a broad range
of areas centered on the use
of genomic technologies to identify the
genetic etiology and underlying mechanisms
of human disease in order to define precision therapies for diseased individuals.
Until now the following parameters have been identified with the
etiology of colorectal cancer
genetic mutations, inflammatory processes, diet, and the gut microbes.
As an example, skeletal malformations and dysplasias, often detected through routine prenatal ultrasound examination, constitute a phenotypic finding in more than 300 syndromic and non-syndromic disorders and their
genetic etiology may be due to a wide variety
of genetic aberrations, ranging from copy number variations to single gene mutations.
In the current work, researchers led by John B. Harley, M.D., Ph.D., director
of the Center for Autoimmune Genomics and
Etiology (CAGE) at Cincinnati Children's Hospital Medical Center, with his colleagues Matthew T. Weirauch, Ph.D., and Leah C. Kottyan, Ph.D., also
of CAGE, wondered whether
genetic analysis could further explain the relationship between EBV infection and lupus.
Dr. Mullegama: My research focuses on understanding the
genetic etiology and phenotype
of rare neurodevelopmental
genetic disorders.
It is classified as a distinct primary cardiomyopathy with a
genetic etiology and may be an isolated finding or may also be associated with other forms
of structural congenital heart disease (Jenni et al., 2001).
Previous studies suggest that
genetic and environmental factors play a role in the
etiology of ASD.1 - 3
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of emphysema: Mutations in telomere genes uncover a distinct
genetic etiology and common mechanism for pathogenesis.
Although both scientists and lay people alike may frequently identify a single dietary element as the cause
of chronic disease (eg, saturated fat causes heart disease and salt causes high blood pressure), evidence gleaned over the past 3 decades now indicates that virtually all so - called diseases
of civilization have multifactorial dietary elements that underlie their
etiology, along with other environmental agents and
genetic susceptibility.
Perhaps for this reason, the
etiology of ASD is not well defined and the combinations
of environmental and
genetic factors that protect against or increase risk
of developing autism are not well understood.
Numerous twin studies have examined the
genetic and environmental
etiology of reading comprehension, though it is likely that etiological estimates are influenced by unidentified sample conditions
Type 2 diabetes has a complex
etiology and is caused by a combination
of genetic factors and environmental interactions, and risk increases with aging (11,12).
Etiology of this tumor is largely unknown;
genetic, physiologic, and molecular influences have all been implemented in possible causative factors1.
Our pedigree analysis included Swedish vallhund dogs examined in seven different countries, spanning three continents, and was highly suggestive
of a
genetic etiology and an autosomal recessive mode
of inheritance.
Altogether our results add more evidence for shared
etiology and mechanisms
of OCD in dogs and humans [6], and suggest that both environmental and
genetic factors affect compulsive behaviour.
This is most likely because diseases like CM and syringomyelia have a complex
etiology and disease expression probably occurs when there is a threshold combination
of genetic and environmental factors.
Although an independent replication
of this
genetic finding is required, it provides further support that overlapping
etiologies may lead to compulsive behaviours across species.
We investigated the temporal pattern
of genetic and environmental
etiology of PA during this crucial developmental period.
Together with evidence that GAD and depression co-occur more often with one another than with other disorders20, 57 and have shared
genetic etiology, 58,59 this lends support to the notion
of grouping these disorders more closely than is currently reflected in the DSM - IV.
Genetic and Environmental
Etiology of the Relationship Between Childhood Hyperactivity / Inattention and Conduct Problems in a South Korean Twin Sample.
However, the precise
genetic polymorphisms implicated in the
etiology of antisocial behaviors remain elusive.
Genetic factors in the
etiology of criminal behavior.
Opportunities to refine phenotypes through an understanding
of their
genetic influences will be important to characterize
genetic and environmental
etiologies.
The
etiology of conduct disorder involves an interaction
of genetic / constitutional, familial and social factors.
A longitudinal behavioral
genetic analysis
of the
etiology of aggressive and nonaggressive antisocial behavior
Molecular
genetic findings support the thesis that dopaminergic, serotonergic, and noradrenergic neurotransmission pathways account for the
etiology of this complex disease.
The
genetic - environmental
etiology of parents» perceptions and self - assessed behaviours towards their 5 - month - old infants in a large twin and singleton sample
Our goals were (1) to compare the trajectory
of depressive symptoms among boys and girls from childhood into adolescence; (2) to analyze the role
of genetic, shared, and unique environmental factors in depression among prepubertal and pubertal male and female twins; and (3) to investigate a possible common
etiology between liability to depression and one salient index
of the child's environment: past - year life events.
Considering the complexity
of mental illnesses
etiology, which involves multiple interacting
genetic, environmental and biological factors; large effect sizes are unlikely to be detected; therefore the magnitude
of the associations described in this community - based study are noteworthy and possibly indicative
of clinical relevance.