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Comparison study of genetic tests for ASD finds CMA with highest detection rate

The Autism Consortium, an innovative research, clinical and family collaboration dedicated to catalyzing research and enhancing clinical care for families with autism spectrum disorders (ASDs), announced today that the results of its comparison study of genetic testing methods for autism spectrum disorders is available from the journal Pediatrics through early online release in their eFirst pages today and will appear in the journal's April issue.

15 Mar 2010

ATS releases new clinical policy statement on CCHS

The American Thoracic Society has released a new official clinical policy statement on congenital central hypoventilation syndrome (CCHS), a disorder of respiratory and autonomic nervous system (ANS) regulation. The ANS regulates reflexive acts, including heart rate and blood pressure, digestion, body temperature and pain perception.

15 Mar 2010

New molecule effective against lice

French medical researchers from the AP-HP (Henri Mondor Hospital and Avicenne Hospital) and Inserm (Unit 738 "Models and methods for therapeutic evaluation of chronic illnesses" and CIC 202, at Tours) have recently demonstrated the effectiveness of a new molecule in the fight against lice. Faced with the emergence of increasing resistance to conventional treatments by these parasites, this new medication represents a real therapeutic alternative which is effective in 95% of cases.

12 Mar 2010

Whole genome sequencing of entire family beneficial

The Institute for Systems Biology (ISB) has analyzed the first whole genome sequences of a human family of four. The findings of a project funded through a partnership between ISB and the University of Luxembourg was published online today by Science on its Science Express website. It demonstrates the benefit of sequencing entire families, including lowering error rates, identifying rare genetic variants and identifying disease-linked genes.

11 Mar 2010

ISB uses Complete Genomics’ service to sequence genomes of four family members suffer from Miller syndrome

Complete Genomics Inc., a third-generation human genome sequencing company, today announced that the Institute for Systems Biology employed Complete Genomics’ human genome sequencing service to sequence a family quartet to determine the depth of genetic information possible in analyzing a full family’s sequence, and to verify the gene responsible for Miller syndrome, a rare craniofacial disorder.

11 Mar 2010

WHO and UN partners join hands to eliminate discrimination against women

Thirty years after the adoption of the Convention on the Elimination of All Forms of Discrimination against Women (CEDAW), many girls and women still do not have equal opportunities to realize rights recognized by law.

11 Mar 2010

USF study: HHV-6 causes permanent infection by inserting its DNA into human chromosomes

Human herpesvirus 6 (HHV-6) infects nearly 100 percent of humans in early childhood, and the infection then lasts for the rest of a person's life. Now, a team led by Peter Medveczky, MD, a professor in the Department of Molecular Medicine at the University of South Florida, has discovered that in some individuals, HHV-6 causes such a permanent infection by inserting or "integrating" its DNA into human chromosomes.

9 Mar 2010

Scientists discover genetic cause of Quebec Platelet Disorder

For some Canadians, any cut such as from dental work or surgery can cause days or more of bleeding. Although they are not hemophiliacs, for some an ordinary bruise can balloon into the size of an orange.

4 Mar 2010

MetLife data indicates middle boomers should be treated as separate demographic groups

For decades, American Baby Boomers have been characterized as a bloc of people who think and act as one monolithic generation. However, recent data from the MetLife Mature Market Institute®, show that Young, Middle and Older Boomers grew up during disparate “eras” and are now at different stages in their lives. They should, perhaps, be treated as separate demographic groups.

4 Mar 2010

Colonoscopy screening recommended for people with family history of colon cancer

A family history of colon cancer, also known as colorectal cancer or CRC, puts people at higher than average risk for developing the disease.

2 Mar 2010

Ten steps to help caregivers take care of themselves

Faced with the need to provide daily care, often to family members with special needs or disabilities, caregivers tend to overlook their own short- and long-term personal and financial needs, putting at risk their own health and security.

24 Feb 2010

Genetic link between schizophrenia and autism may help study effectiveness of drugs for both illnesses

A genetic link between schizophrenia and autism is enabling researchers to study the effectiveness of drugs used to treat both illnesses.

24 Feb 2010

Ways of stem cells division linked to development of cancer

Changes in the way that stem cells divide in the gut could lead to cancer, according to a new study funded by the Bobby Moore Fund for Cancer Research UK.

20 Feb 2010

Six states to study sickle cell disease and thalassemias in national pilot project

Medical researchers are developing a new surveillance system to determine the number of patients diagnosed with a family of inherited blood disorders known as hemoglobinopathies, including sickle cell disease, thalassemias, and hemoglobin E disease.

19 Feb 2010

Meda publishes 2009 year-end report

“The Meda Group expects to achieve sales of about SEK 13,000 million and an EBITDA of about SEK 4,200 million for full-year 2009.”

16 Feb 2010

First-quarter fiscal 2010 results announced by Agilent Technologies

Agilent Technologies Inc. today reported revenues of $1.21 billion for the first fiscal quarter ended Jan. 31, 2010, 4 percent above one year ago. First quarter GAAP net income was $79 million, or $0.22 per diluted share. Last year’s first quarter GAAP net income was $64 million, or $0.18 per share.

12 Feb 2010

Quebec transplantation: 431 people receive 499 organs from 138 deceased donors

Owing to the generosity of Quebecers, 499 organs from 138 deceased donors in 2009 were transplanted into 431 recipients. Though there were 13 fewer donors than in 2008, Québec posted an average of more than 3.6 transplanted organs per deceased donor in 2009, placing the province among the leaders in Canada and even North America. "We're particularly proud of the sustained collaboration of professionals in hospitals in 2009," says Louis Beaulieu, chief executive officer of Québec-Transplant, the organization responsible for coordinating the organ donation process.

11 Feb 2010

HairDX introduces improved genetic baldness test, incorporates maternal and paternal influences

HairDX, developer of the first genetic test for predicting the risk of male and female pattern hair loss (Androgenetic Alopecia) today announced it is now able to provide doctors with an improved prediction by looking at genetic variants inherited from the mother combined with the risk for baldness attributed by the father.

10 Feb 2010

Around seven in every thousand morbidly obese people are missing part of their DNA

A small but significant proportion of morbidly obese people are missing a section of their DNA, according to research published today in Nature. The authors of the study, from Imperial College London and ten other European Centres, say that missing DNA such as that identified in this research may be having a dramatic effect on some people's weight.

4 Feb 2010

Study indicates dogs make excellent models for studying human genetic disorders

In the new Swedish-Finnish study, published in Nature Genetics, the researchers identified five loci that predispose to an SLE-related disease in Nova Scotia duck tolling retrievers.

31 Jan 2010

Inherit News and Research

Comparison study of genetic tests for ASD finds CMA with highest detection rate

ATS releases new clinical policy statement on CCHS

New molecule effective against lice

Whole genome sequencing of entire family beneficial

ISB uses Complete Genomics’ service to sequence genomes of four family members suffer from Miller syndrome

WHO and UN partners join hands to eliminate discrimination against women

USF study: HHV-6 causes permanent infection by inserting its DNA into human chromosomes

Scientists discover genetic cause of Quebec Platelet Disorder

MetLife data indicates middle boomers should be treated as separate demographic groups

Colonoscopy screening recommended for people with family history of colon cancer

Ten steps to help caregivers take care of themselves

Genetic link between schizophrenia and autism may help study effectiveness of drugs for both illnesses

Ways of stem cells division linked to development of cancer

Six states to study sickle cell disease and thalassemias in national pilot project

Meda publishes 2009 year-end report

First-quarter fiscal 2010 results announced by Agilent Technologies

Quebec transplantation: 431 people receive 499 organs from 138 deceased donors

HairDX introduces improved genetic baldness test, incorporates maternal and paternal influences

Around seven in every thousand morbidly obese people are missing part of their DNA

Study indicates dogs make excellent models for studying human genetic disorders

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