Genetics Research
rs7984966
Population Frequencies12
African
T 0.66471C 0.33529TT 0.44676TC/CT 0.435891CC 0.117348pop=42,506
African American
T 0.66564C 0.33436TT 0.448108TC/CT 0.435056CC 0.116836pop=41,066
African Others
T 0.6382C 0.3618TT 0.408333TC/CT 0.459722CC 0.131944pop=1,440
Asian
T 0.9429C 0.0571TT 0.889686TC/CT 0.106518CC 0.003797pop=9,482
East Asian
T 0.9532C 0.0468TT 0.908456TC/CT 0.089396CC 0.002148pop=7,450
European
T 0.757826C 0.242174TT 0.575802TC/CT 0.364048CC 0.06015pop=287,050
Latin American 1
T 0.6918C 0.3082TT 0.479851TC/CT 0.423976CC 0.096173pop=5,906
Latin American 2
T 0.86207C 0.13793TT 0.74338TC/CT 0.237379CC 0.019242pop=10,498
Other
T 0.78122C 0.21878TT 0.618388TC/CT 0.325672CC 0.055941pop=11,834
Other Asian
T 0.9055C 0.0945TT 0.820866TC/CT 0.169291CC 0.009843pop=2,032
South Asian
T 0.8772C 0.1228TT 0.773249TC/CT 0.207807CC 0.018944pop=3,484
Studies20
Unread Studies20 ▼
1
Dr. Rónai Zsolt „Genetikai polimorfizmusok vizsgálata: A génvariációk molekuláris hatásától a komplex jellegek örökletes hátteréig” című az MTA doktora címre pályázó disszertációja …
2
Attention-Deficit/Hyperactive Disorder (ADHD) is the neurodevelopmental disorder which commonly occurs in children with the prevalence ranging from 3.4% to 7.2%. It …
3
Complex diseases impact millions of people worldwide, caused by a variety of genetic and environmental factors. Genome-wide association studies have done an adequate job of …
4
… Najsilniejszy związek zaobserwowano pomiędzy polimorfizmem genu receptora serotoniny HTR2A (rs7984966) i zmiennym czasem reakcji. Autorzy przypuszczają, że w tym wypadku …
5
… The strongest correlation was observed for the rs7984966 SNP in the serotonin receptor gene (HTR2A) and RTV. The authors suggest overlapping genetic associations between ADHD …
6
Neuropsychiatric disorders are common and heritable diseases that have a large burden on societies around the world. Multiple genomic studies have identified novel candidate genes …
7
2018. Tese (Doutorado em Genética)–Programa de Pós Graduação em Genética, Universidade Federal do Rio de Janeiro, 2018. O efavirenz (EFV) é amplamente utilizado na terapia …
8
A Perturbação de Hiperatividade/Défice de Atenção (PHDA) é atualmente vista como uma lifespan disorder, isto é, uma perturbação de caráter permanente, cuja génese é multifatorial, …
9
… e o alelo T do rs7984966), o HTR1B (que codifica o recetor de serotonina 1B), o HTR2A [polimorfismo de nucleótido único (SNP – single nucleotide polymorphism) rs7984966 no gene …
10
Several genome‐wide association studies ( GWASs ) in Caucasian populations have identified 12 loci that are significantly associated with migraine. More evidence suggests that …
11
So far, associations between serotonergic neurotransmission pathways and suicidality have been reported. The aim of our study was to investigate the role of genetic polymorphisms …
12
… The strongest association was observed for the rs7984966 SNP in the serotonin receptor gene (HTR2A), and RTV (P = 0.007; unadjusted for multiple testing). Mediation analysis …
13
The amygdala plays a critical role in emotion processing and psychiatric disorders associated with emotion dysfunction. Accumulating evidence suggests that amygdala structure is …
14
… The polymorphism rs7322347 was in strong LD with rs7984966 as well (chromosomal distance: 19343 bp), although to a lesser extent than with rs6314. In addition, prominently high …
15
The present thesis uses data collected from four studies. The research described in chapter 2 utilised data from the Twins' Early Development Study (TEDS); an ongoing general …
16
Migraine is a painful temporarily incapacitating disorder that affects an estimated 12% of the general population including 18% of adult women and 6% of adult men. The disorder …
17
… Analysis of HTR2A- The analysis showed significant associations between HTR2A rs1745837, rs1328684, rs7984966 and membership in the high anxiety trajectory versus low+ …
18
Epidemiological studies, such as family, twin, and adoption studies, demonstrate the presence of a heritable component to both attempted and completed suicide. Some of this …
19
A Perturbação de Hiperatividade/Défice de Atenção (PHDA) é atualmente vista como uma lifespan disorder, isto é, uma perturbação de caráter permanente, cuja génese é multifatorial, …
20
In order to evaluate the contribution of 19 serotonin‐related genes to the susceptibility to migraine in a Spanish population we performed a case–control association study of 122 single …
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