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Researchers identify over 2,000 genetic signals linked to blood pressure in study of over 1 million people

Researchers identify over 2,000 genetic signals linked to blood pressure in study of over 1 million people
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Scientists discover over 100 new genomic regi

<p>National Institutes of Health researchers and collaborators have discovered over 100 new regions of the human genome, also known as genomic loci, that appear to influence a person’s blood pressure. Results of the study also point to several specific genomic loci that may be relevant to iron metabolism and a type of cellular receptor known as adrenergic receptors. </p>

<p>The study, published in Nature Genetics, is one of the largest such genomic studies of blood pressure to date, including data from over 1 million participants and laying the groundwork for researchers to better understand how blood pressure is regulated. Such insights could point to potential new drug targets. </p>

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Researchers identify over 2,000 genetic signals linked to blood pressure in study of over one million people

Researchers identify over 2,000 genetic signals linked to blood pressure in study of over one million people
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Over 2,000 Genetic Signals Tied to Blood Pressure: Study

Over 2,000 Genetic Signals Tied to Blood Pressure: Study
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Cognitively Healthy Centenarians; Seizures and COVID Vax; New AAN Statement

News and commentary from the world of neurology and neuroscience

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Study finds 2,000 genetic signals that influence blood pressure

Study finds 2,000 genetic signals that influence blood pressure
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FMD - Researchers identify over 2,000 genetic signals linked to blood pressure in study of over 1 million people

FMD - Researchers identify over 2,000 genetic signals linked to blood pressure in study of over 1 million people
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After 25 Years, Researchers Uncover Genetic Cause of Rare Neurological Disease

Spinocerebellar ataxia 4 is a devastating progressive movement disorder. A multinational study has now conclusively identified the genetic difference that cause

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After 25 Years, Researchers Uncover Genetic Cause of Rare Neurological Disease

Spinocerebellar ataxia 4 is a severe progressive movement disease that can begin as early as the late teens. Now, a multinational research team led by University of Utah researchers has conclusively identified the genetic difference that causes the disease, bringing answers to families and opening the door to future treatments.

Utah , United-states , Hamburg , Germany , Salt-lake-valley , Eppendorf , Nordrhein-westfalen , University-of-utah , K-pattie-figueroa , Sophia-friesen , Stefan-pulst , Veterans-administration-medical-center

Analysis identifies 50 new genomic regions associated with kidney cancer risk

Analysis identifies 50 new genomic regions associated with kidney cancer risk
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