Single Nucleotide Polymorphisms News and Research

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Analysis reveals novel insights into Indian genetic heritage of people living in present-day Thailand

A new genetic analysis reveals novel insights into the genetic heritage of people living in Thailand in the present day, which suggest the potential importance of past migrations in spreading Indian culture to the region.

18 Feb 2022

Oligodendrocyte plays major role in the development of multiple sclerosis, says study

A team of international researchers revealed that oligodendrocytes, a kind of central nervous system cell, may play a different function in the progression of MS.

2 Feb 2022

Study elucidates the role of genomics in obsessive-compulsive disorder

According to recent research carried out by the researchers from the Icahn School of Medicine at Mount Sinai, both rare and commonly seen differences in the DNA letters threaded along an individual’s chromosomes can elucidate about a third of the risk for being diagnosed with obsessive-compulsive disorder (OCD).

19 Nov 2021

New research center brings advancements in genomic medicine to admixed individuals

One way to make health care more personalized is to use a person's DNA sequence -; or genome -; to predict their risk of disease. But as the field of precision medicine grows, so have concerns that we may be leaving a large fraction of Americans out.

From UC San Diego 13 Oct 2021

Study identifies C9orf72 repeat expansion using novel genetic marker

Research offers a new genetic tool to pinpoint C9orf72 repeat expansion-carrying frontotemporal lobar degeneration from huge population-based cohorts.

25 Aug 2021

New CRISPR-SNP-Chip technology detects single-point mutations without amplification

The CRISPR-Chip technology was first introduced in 2019 by Dr. Kiana Aran, an Assistant Professor at Keck Graduate Institute (KGI).

6 Apr 2021

Gender difference accounts for major psychiatric disorders

According to an analysis of sex variations in the genetics of bipolar disorder, schizophrenia, and major depressive disorders.

24 Mar 2021

Unusual DNA folding leads to higher mutation rates

DNA sequences that can fold into shapes other than the classic double helix tend to have higher mutation rates than other regions in the human genome.

From Penn State University 10 Feb 2021

Researchers discover genetic factors underlying diabetic retinopathy

In a quest to find the genetic factors that are fundamental to diabetic retinopathy, scientists from the University of Illinois Chicago (UIC) have also discovered a new method that can be employed as a template to investigate other types of diseases.

8 Dec 2020

Study shows how genetic variability may shape mathematical performance in children

According to a study, DNA variation in a gene is linked to early anatomical variations in a region of the brain that plays a crucial role in quantity representation.

26 Oct 2020

Inherited variation in GATA3 gene associated with relapse in children with leukemia

Scientists at St. Jude Children's Research Hospital are investigating the inherited genetics of childhood leukemia and how particular gene variations can affect treatment outcomes. The research showed that an inherited variation in the GATA3 gene strongly influences early response to chemotherapy and is linked to relapse in children with acute lymphoblastic leukemia (ALL).

14 Sep 2020

New genotyping chip could boost coral conservation efforts

Coral conservation efforts could get a boost from a newly developed genotyping "chip"--the first of its kind for corals.

26 Aug 2020

Novel technology can minimize errors in DNA testing

Today's DNA testing is highly accurate, but errors still occur due to the limited genetic information accessible with current technologies. These errors can have serious impact on people's lives.

18 Aug 2020

NIH-supported research delineates how genetic variations cause atopic dermatitis

New research supported by the National Institutes of Health delineates how two relatively common variations in a gene called KIF3A are responsible for an impaired skin barrier that allows increased water loss from the skin, promoting the development of atopic dermatitis, commonly known as eczema.

17 Aug 2020

New findings help to better understand the genetics of neuropsychiatric disorders

A new study led by NorthShore University HealthSystem (NorthShore) and the University of Chicago took a novel approach to identifying SNPs influencing the risk of neuropsychiatric disorders like schizophrenia, bipolar and major depressive disorder, the institutions announced today.

5 Aug 2020

Single Nucleotide Polymorphisms News and Research

Analysis reveals novel insights into Indian genetic heritage of people living in present-day Thailand

Oligodendrocyte plays major role in the development of multiple sclerosis, says study

Study elucidates the role of genomics in obsessive-compulsive disorder

New research center brings advancements in genomic medicine to admixed individuals

Study identifies C9orf72 repeat expansion using novel genetic marker

New CRISPR-SNP-Chip technology detects single-point mutations without amplification

Gender difference accounts for major psychiatric disorders

Unusual DNA folding leads to higher mutation rates

Researchers discover genetic factors underlying diabetic retinopathy

Study shows how genetic variability may shape mathematical performance in children

Inherited variation in GATA3 gene associated with relapse in children with leukemia

New genotyping chip could boost coral conservation efforts

Novel technology can minimize errors in DNA testing

NIH-supported research delineates how genetic variations cause atopic dermatitis

New findings help to better understand the genetics of neuropsychiatric disorders

New technique increases the precision of gene editing

Study shows microbiome can determine the wound healing process

Genetic variation in taste receptors could help inform food production

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Revolutionizing Mass Spectrometry: A Deep Dive into Plasmion’s SICRIT® Technology

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