19 results match your criteria: "Naif Arab University of Security Sciences[Affiliation]"

A methylation panel of 10 CpGs for accurate age inference via stepwise conditional epigenome-wide association study.

Int J Legal Med

December 2024

Department of Forensic Sciences, College of Criminal Justice, Naif Arab University of Security Sciences, Riyadh, 11452, Kingdom of Saudi Arabia.

Estimating individual age from DNA methylation at age associated CpG sites may provide key information facilitating forensic investigations. Systematic marker screening and feature selection play a critical role in ensuring the performance of the final prediction model. In the discovery stage, we screened for 811876 CpGs from whole blood of 2664 Chinese individuals ranging from 18 to 83 years of age based on a stepwise conditional epigenome-wide association study (SCEWAS).

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Analysis of blood methylation quantitative trait loci in East Asians reveals ancestry-specific impacts on complex traits.

Nat Genet

May 2024

CAS Key Laboratory of Computational Biology, Shanghai Institute of Nutrition and Health, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai, China.

Methylation quantitative trait loci (mQTLs) are essential for understanding the role of DNA methylation changes in genetic predisposition, yet they have not been fully characterized in East Asians (EAs). Here we identified mQTLs in whole blood from 3,523 Chinese individuals and replicated them in additional 1,858 Chinese individuals from two cohorts. Over 9% of mQTLs displayed specificity to EAs, facilitating the fine-mapping of EA-specific genetic associations, as shown for variants associated with height.

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Searching across-cohort relatives in 54,092 GWAS samples via encrypted genotype regression.

PLoS Genet

January 2024

Center for Reproductive Medicine, Department of Genetic and Genomic Medicine, and Clinical Research Institute, Zhejiang Provincial People's Hospital, People's Hospital of Hangzhou Medical College, Hangzhou, Zhejiang, China.

Explicitly sharing individual level data in genomics studies has many merits comparing to sharing summary statistics, including more strict QCs, common statistical analyses, relative identification and improved statistical power in GWAS, but it is hampered by privacy or ethical constraints. In this study, we developed encG-reg, a regression approach that can detect relatives of various degrees based on encrypted genomic data, which is immune of ethical constraints. The encryption properties of encG-reg are based on the random matrix theory by masking the original genotypic matrix without sacrificing precision of individual-level genotype data.

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Background: The immune responses to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are crucial in maintaining a delicate balance between protective effects and harmful pathological reactions that drive the progression of coronavirus disease 2019 (COVID-19). T cells play a significant role in adaptive antiviral immune responses, making it valuable to investigate the heterogeneity and diversity of SARS-CoV-2-specific T cell responses in COVID-19 patients with varying disease severity.

Methods: In this study, we employed high-throughput T cell receptor (TCR) β repertoire sequencing to analyze TCR profiles in the peripheral blood of 192 patients with COVID-19, including those with moderate, severe, or critical symptoms, and compared them with 81 healthy controls.

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Coronavirus disease 2019 (COVID-19) caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) may lead to life-threatening respiratory symptoms. Understanding the genetic basis of the prognosis of COVID-19 is important for risk profiling of potentially severe symptoms. Here, we conducted a genome-wide epistasis study of COVID-19 severity in 2243 patients with severe symptoms and 12,612 patients with no or mild symptoms from the UK Biobank, followed by a replication study in an independent Spanish cohort (1416 cases, 4382 controls).

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Genetic diversity and forensic application of Y-filer STRs in four major ethnic groups of Pakistan.

BMC Genomics

November 2022

Department of Anthropology and Ethnology, Institute of Anthropology, School of Sociology and Anthropology, Xiamen University, Xiamen, China.

Article Synopsis
  • The study examined 17 Y-chromosomal STRs in 493 unrelated individuals from four Pakistani ethnic groups: Baloch, Pathan, Punjabi, and Sindhi, to analyze forensic parameters and genetic structure.
  • Eighty-two distinct haplotypes were identified, with haplotype diversity values ranging from 0.9906 in Baloch to 0.9957 in Pathans, indicating significant genetic variation within these groups.
  • The results suggest that these populations share genetic similarities with Central Asian and Northern Indian regions, and the low gene diversity may be influenced by endogamy practices.
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Article Synopsis
  • The text discusses a correction made to the findings presented in the article with the DOI: 10.3389/fgene.2021.760760.
  • The correction addresses specific errors or inaccuracies that were identified after the original publication.
  • This ensures that the scientific community has access to accurate information and maintains the integrity of the reported research.
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Article Synopsis
  • * This study analyzed mutation rates in 9379 pairs of men across 30 RM Y-STRs and found significant differences in mutation rates compared to standard Y-STRs, revealing higher differentiation rates among more distantly related individuals.
  • * The results indicate that RM Y-STRs can accurately predict the degree of patrilineal relatedness, with potential to greatly enhance forensic Y-chromosome analysis compared to traditional methods.
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  • * Rapidly mutating Y-STRs (RM Y-STRs) have higher mutation rates and can better differentiate male lineages, especially in endogamous groups, than traditional Y-STRs.
  • * This study analyzed 861 male pairs from Punjabi endogamous pedigrees, observing varying mutation frequencies, with overall differentiation rates averaging 59.46%, and updated mutation rates for RM Y-STRs based on father-son pair data.
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Article Synopsis
  • The study investigates the genetic basis of facial hair traits in Punjabi males from Pakistan by examining 16 specific genetic variations (SNPs) that may influence features like monobrows, eyebrow thickness, and beard thickness.
  • Significant associations were found for particular SNPs: rs365060 in EDAR and rs12597422 in FTO related to monobrows, rs6684877 in MACF1 linked to eyebrow thickness, and rs9654415 and rs7702331 in LOC105379031 connected to beard thickness.
  • The findings highlight potential differences in genetic associations for facial hair traits across different ethnic groups and regions, suggesting further research is needed for validation but having implications for forensic studies
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Background: Xibe is the fifth largest minority population of Liaoning province. Predominately they live in Liaoning province (69.52%), followed by Xinjiang (18.

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Are Roma People Descended from the Punjab Region of Pakistan: A Y-Chromosomal Perspective.

Genes (Basel)

March 2022

Department of Anthropology and Ethnology, Institute of Anthropology, School of Sociology and Anthropology, Xiamen University, Xiamen 361000, China.

Article Synopsis
  • Gypsies, also known as Roma or untouchables, are a distinct ethnic group in Pakistan, characterized by their nomadic lifestyle and unique living conditions in tent houses.
  • A study on 285 unrelated Roma individuals in Punjab used genetic analysis to reveal high allelic diversity and demonstrated a close genetic relationship between Pakistani Roma and those from Romania.
  • The research indicated significant gene flow and historical migration patterns from Pakistan to India and Europe, showcasing the marked genetic diversity within the Roma population.
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Article Synopsis
  • The Xinjiang Uyghur Autonomous Region in China is home to nearly 50 ethnic groups, with the majority being Uyghur, Han, Kazakh, and Hui, representing 97.33% of the population.
  • In a study, researchers analyzed genetic data from 2,121 samples across these four major ethnic groups, using advanced STR analysis techniques, revealing various genetic diversity metrics.
  • The genetic findings highlighted distinct affinity and relationships among populations based on linguistic, ethnic, and geographical contexts, with no significant departures from Hardy-Weinberg equilibrium observed.
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The study aimed to screen for gene mutations among Saudi women with Ovarian Cancer. The study included 298 Saudi women with epithelial ovarian cancers (EOC). DNA sequence analysis was employed to screen for the mutations.

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Honey and its nutritional and anti-inflammatory value.

BMC Complement Med Ther

January 2021

Department of Technology and Natural Resources, Faculty of Applied Sciences and Technology, Universiti Tun Hussein Onn Malaysia, 86400, Pagoh, Johor, Malaysia.

Inflammation is the main key role in developing chronic diseases including cancer, cardiovascular diseases, diabetes, arthritis, and neurodegenerative diseases which possess a huge challenge for treatment. With massively compelling evidence of the role played by nutritional modulation in preventing inflammation-related diseases, there is a growing interest into the search for natural functional foods with therapeutic and preventive actions. Honey, a nutritional healthy product, is produced mainly by two types of bees: honeybee and stingless bee.

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Prostate cancer (PCa) is a challenging polygenic disease because the genes that cause PCa remain largely elusive and are affected by several causal factors. Consequently, research continuously strives to identify a genetic marker which could be used as an indicator to predict the most vulnerable (i.e.

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The World Health Organization (WHO) recognized a novel coronavirus as the causative agent of a new form of pneumonia. It was subsequently named COVID-19 and reported as the source of a respiratory disease occurrence starting in December 2019 in Wuhan, Hubei Province, China. It has been affirmed a public health emergency of international significance by the World Health Organization.

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Commentary Regarding the Effect of Long Term Use of Finasteride on Saudi Women.

Asian Pac J Cancer Prev

August 2020

Department of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia.

In the following commentary, we provided discussions regarding an article bublished by Albasher et al. (2020) concerning the effects of long-term use of finasteride on women. They reported some adverse effects, including abnormal levels in the steroid hormones, irregular menstrual cycles, and heavy menstrual bleeding.

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Induction of Chronic Subclinical Systemic Inflammation in Sprague-Dawley Rats Stimulated by Intermittent Bolus Injection of Lipopolysaccharide.

Arch Immunol Ther Exp (Warsz)

December 2019

Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, 43400, UPM Serdang, Selangor, Malaysia.

Chronic subclinical systemic inflammation has a key role in stimulating several chronic conditions associated with cardiovascular diseases, cancer, rheumatoid arthritis, diabetes, and neurodegenerative diseases. Hence, developing in vivo models of chronic subclinical systemic inflammation are essential to the study of the pathophysiology and to measure the immunomodulatory agents involved. Male Sprague-Dawley rats were subjected to intraperitoneal, intermittent injection with saline, or lipopolysaccharide (LPS) (0.

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