Although previous studies have found that a large percentage of hair colour variation is explained by heritable factors, previous
genetic studies only identified a dozen or so hair colour genes.
But this was a prediction based on
genetic studies only.
Not exact matches
Cases of identical twins separated at birth who were outlined in this
study indicated that
only one third of our ability to think creatively is
genetic.
However, this
study only included kids at high - risk for celiac (based on
genetic markers or a first - degree relative with the disease), so it might not apply to the general population.
Several
studies have also attempted to understand the role of breastfeeding on IQ, and although some authors conclude that the observed advantage of breastfeeding on IQ is related
only to
genetic and socioenvironmental factors, a recent meta - analysis showed that after adjustment for appropriate key co-factors, breastfeeding was associated with significantly higher scores for cognitive development than formula feeding.6 Longer duration of breastfeeding has also been positively associated with intelligence in adulthood.22 We also observed the benefits of long - term breastfeeding on mental indices, along with the indirect benefit of balancing the impact of exposure to p, p ′ DDE after adjustment for some socioeconomic variables.
Stepfathers are widespread not
only in modern industrial societies but also in subsistence - level societies as well.6, 51,52 Many
studies have found that, compared with resident biological fathers, stepfathers invest less in the children who live with them, both in the United States37, 39,53 and other cultures.54 - 56 Stepchildren are more likely to have emotional and behavioural problems than resident
genetic offspring, 39,40 although there is evidence that children who have close relationships with their stepfathers have better outcomes.41, 57
Study have been made, pregnancy is not the
only way or symptom to get stretch marks, because
genetic history do play role with stretch mark appearing.
Of the thousands of ancestral variants reintroduced into modern humans,
only 41 have been linked in
genetic studies to diseases, such as skin conditions and neurological and psychiatric disorders, he said.
One high - profile recent
study suggested that each
genetic component entered Europe by way of a separate migration and that they
only came together in most Europeans in the past 5000 years.
Of all four groups
studied,
only those at high
genetic risk for Alzheimer's who did not exercise experienced a decrease in hippocampal volume (3 %) over the 18 - month period.
The authors note that while the sample size of the meta - analyses was large (123,132 to 260,861 participants in different
studies), they used
only GWAS summary statistics and can not estimate all
genetic variance factors; some
studies also used different methodologies.
Widschwendter, who led the
study, said: «Our work provides clear evidence that it is not
only genetic alterations which trigger and lead to cancer but that epigenetic alteration can also be the initiating step.»
Burt has made a career
studying «selfish
genetic elements,» parasitic pieces of DNA or RNA that exist
only to propagate themselves.
«We don't know why
only a fraction of individuals with
genetic risk factors for celiac disease actually become gluten intolerant,» said Peter Green, MD, the Phyllis and Ivan Seidenberg Professor of Medicine at Columbia University Medical Center (CUMC), Director of the Celiac Disease Center at Columbia University and co-author on the
study.
Currently
only a handful of known
genetic mutations have been found to account for about 10 percent of glaucoma, says Liu, corresponding author of the
study in the journal Human Molecular Genetics.
They reached out to clinicians worldwide to identify patients with arhinia — before this
study only 80 cases had been reported during the past century — and gathered samples for
genetic sequencing.
«Our
study is the first to provide empirical evidence that artificial insemination with long - stored spermatozoa is not
only possible but also beneficial to the
genetic diversity of an endangered species,» said David Wildt, lead author, senior scientist and head of the Center for Species Survival at SCBI.
Mayer and McHugh also appear to be data snooping when they reference
only one of six
studies in the peer - reviewed literature of the past 16 years that employ proper probability - sampling methods, «and it just so happens to be the one with the lowest estimate of
genetic influence of the entire set,» Hamer says.
In a meta - analysis of
studies that linked
genetic markers to cultural heritage in North and Central America, Iceland, Australia, Africa and New Guinea, they found that
only Y - chromosome DNA reflected the cultural origins of the local language.
«In this sense, pending the collection of new samples of this new Mediterranean Osedax species to
study its morphological characteristics, the
only differences that we have been able to determine in relation to other species are
genetic,» notes Sergi Taboada.
He omits, for example, the
studies showing that children who are abused or neglected are
only slightly more likely to become delinquent than children who are not: once again the difference may be caused by
genetic inheritance rather than by the parents» maltreatment.
«It is amazing to me that more than 100 years after the discovery of
genetic recombination in flies, we are
only starting to understand just how these events are distributed,» says R. Scott Hawley, Ph.D., an investigator at the Stowers Institute and senior author of the
study.
With the aim of
studying the history and
genetic diversity of the species, analysis was conducted on the genomes of another ten Iberian lynxes from Doñana and Sierra Morena, the
only two surviving populations on the Iberian Peninsula, which have been isolated from each other for decades.
Their traditionally low - budget science, which needs
only pencil and paper to tally shared traits in the classical twin
studies, has entered the high - tech world of
genetic epidemiology, which traces the power of genes to influence the health of populations.
«
Studies focused
only on additive effects often explain just a fraction of the
genetic basis of many traits.
That's the
only way to get ES cells with the
genetic signatures of patients whose diseases they want to
study.
Only one gene — TCF4 — has been successfully associated with Fuchs dystrophy in
genetic studies.
Neanderthal
genetic material is found in
only small amounts in the genomes of modern humans because, after interbreeding, natural selection removed large numbers of weakly deleterious Neanderthal gene variants, according to a
study by Ivan Juric and colleagues at the University of California, Davis, published November 8th, 2016 in PLOS Genetics.
Although specific microbial halogenation reactions have been recognized for decades and the link between the dehalogenation of anthropogenic halogenated contaminants in laboratory cultures and contaminated field sites has been well established,
only a few
studies specifically looked at pristine ecosystems and the
genetic potential for microbial degradation of naturally occurring organohalogens, Kappler says.
Despite the size of this
study, the new
genetic findings likely explain
only about 3 percent of autism's
genetic roots, researchers behind the new
study noted.
Morgan Fullerton, lead author of the
study, added: «Unlike the majority of
studies using
genetic mouse models, we haven't deleted an entire protein; we have
only made a very minor
genetic mutation, equivalent to what might be seen in humans, thus highlighting the very precise way metformin lowers blood sugar in Type 2 Diabetes»
This bank of living tumour cells allowed the team to
study not
only the genetics of the cells, but also how
genetic mutations in the mitochondria — which drive energy production in the cell — caused changes in the cell's metabolism.
Previous
studies that used
only information from
genetic analyses of current species have suggested that birds arose anywhere from 72 million to 170 million years ago.
«Since our
study only looked at common gene variants, the total
genetic overlap between the disorders is likely higher,» explained Naomi Wray, Ph.D., University of Queensland, Brisbane, Australia, who co-led the multi-site
study by the Cross Disorders Group of the Psychiatric Genomics Consortium (PGC), which is supported by the NIH's National Institute of Mental Health (NIMH).
Genetic studies of drug response are often based
only on memory of the response rather than systematically recorded data.
This
study opens up new avenues for the role of purified resveratrol in preventing cancer, but suggests that it may
only be effective for people with a specific
genetic make - up, particular diets and lifestyles.
In the second
study, another of Worobey's graduate students, Marlea Gemmel, analyzed HIV - 1
genetic material obtained from lymph tissue collected in 1960 from the University of Kinshasa pathology department in the Democratic Republic of the Congo —
only the second HIV sequence predating 1976 deciphered to date.
In their recent paper, the researchers not
only looked at the
genetic code, but also
studied how gene activity varied between the two populations.
Anthropologists and geneticists know that populations throughout the world migrated from Africa more than 60,000 years ago (see diagram), and that the human genome is at its most diverse in our continent of origin, but previous
studies have
only scratched the surface of African
genetic diversity.
The low amount of
genetic diversity in the current population, which is descended from
only 14
genetic founders from the captive flock, was already well known, but this was the first
study to show that there was substantial
genetic diversity in the historical population.
«In the space of just five years, reasonably affordable
studies using DNA sequencing have advanced from using
only a handful of
genetic markers to more than 2,000 — an unbelievable amount of DNA,» adds Simison.
Only one question concerned NCRR: Genome institute scientist Shawn Burgess asked what will happen to the center's fruit fly and yeast stock resources for
genetic studies.
«This shows that the risk of developing type 2 diabetes is not
only genetic, but also epigenetic,» said Charlotte Ling, who led the
study.
The
study, published online Oct. 17 in Molecular Psychiatry, shows that
only male mice with the autism - associated
genetic deletion have abnormal reward - learning behavior.
She
studies South American flies that can look exactly the same and can be distinguished
only by
genetic analysis.
A startling new
study of fragile X syndrome — the most common cause of inherited mental retardation as well as a leading
genetic cause of autism — indicates that not
only can malformed nerves be repaired but that behavior can be restored to normal, or nearly so.
Valentina Coia explains further: «The first hypothesis could not be ruled out given that the
study considered
only 85 modern comparison samples from the K1 lineage — the
genetic lineage that also includes that of Ötzi — which comprised few samples from Europe and especially none from the eastern Alps, which are home to populations that presumably have a
genetic continuity with the Iceman.
«This important
study not
only adds more
genetic risk factors to the list of those known for testicular germ cell tumours — the most common cancer in young men — but also adds detail to the emerging picture of testicular cancer as a strongly heritable disease.
The fusion of these two genes was observed in just three percent of tumors
studied, so any therapy based on this particular
genetic aberration would apply to
only a small subset of glioblastoma patients.
Deep Sequencing of Influenza A Virus from a Human Challenge
Study Reveals a Selective Bottleneck and
Only Limited Intrahost
Genetic Diversification.