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	<title>Genetic Disease Foundation &#187; GDF News</title>
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	<link>http://www.geneticdiseasefoundation.org</link>
	<description>Hope Through Knowledge</description>
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		<title>GDF&#8217;s “Raise Your Glass&#8221; Event a Big Success</title>
		<link>http://www.geneticdiseasefoundation.org/2011/12/gdfs-%e2%80%9craise-your-glass-event-a-big-success/</link>
		<comments>http://www.geneticdiseasefoundation.org/2011/12/gdfs-%e2%80%9craise-your-glass-event-a-big-success/#comments</comments>
		<pubDate>Tue, 13 Dec 2011 05:42:34 +0000</pubDate>
		<dc:creator>GDF</dc:creator>
				<category><![CDATA[GDF News]]></category>

		<guid isPermaLink="false">http://www.geneticdiseasefoundation.org/?p=1073</guid>
		<description><![CDATA[Over 130 people attended the GDF's Raise Your Glass event, raising over $25,000 to help fund genetic disease research and education. ]]></description>
			<content:encoded><![CDATA[<p><a href="http://www.geneticdiseasefoundation.org/wp-content/uploads/2011/12/party1.jpg"><img class="aligncenter size-full wp-image-1084" title="GDF Raise Your Glass Event" src="http://www.geneticdiseasefoundation.org/wp-content/uploads/2011/12/party1.jpg" alt="" width="600" height="445" /></a></p>
<p>More than 130 people attended Genetic Disease Foundations’s recent wine tasting event “Raise Your Glass,” which raised more than $25,000 to help fund research and education towards the prevention and treatment of genetic diseases.  Held on November 14 at the Glass Houses at Manhattan’s Chelsea Art Towers, the event featured wine tasting stations around the room offering a selection from Robert Mondavi Winery, SIMI, Coppola, Brancott, Mumm Napa, Chateau St. Michelle, Antinori, Main St. Winery, Carmen, Alta Luna and Rocca delle Macie.  While enjoying the wines and lovely sunset views, guests learned about GDF’s Know Your Genes public service campaign through a video, new brochures and presentations.</p>
<p>Adding to the evening’s entertainment, more than a dozen donated raffle prizes were given out including a five-course tasting dinner for two with wine pairing at Gravy; a Flywheel spin package; catered dinner for four from Paul Evans Caterers; a wine basket from Premier Cru Wine Merchants; two tickets to the Rachel Ray Show; a Cake Boss package; a Sarah Oliver handbag; two tickets to the Westminster Dog Show at Madison Square Garden; two tickets to the opening day of the 2012 US OPEN Tennis Tournament and tour of facility; and a beauty treatment and products from Stephen Knoll Salon.</p>
<p>GDF extends special thanks to Genzyme Personalized Genetic Health and all those who helped make the event a success.</p>
<p><strong>About the Genetic Disease Foundation</strong></p>
<p>The GDF is affiliated with the <a href="http://www.mssm.edu/departments-and-institutes/genetics-and-genomic-sciences">Mount Sinai School of Medicine’s Department of Genetics and Genomics Sciences</a>, one of the largest medical genetics centers in the United States, whose faculty lead the country in clinical research to improve prenatal diagnosis, carrier screening, genetic counseling methods and therapies for genetic diseases.</p>
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		<title>The Leta Lindley Prader-Willi Classic</title>
		<link>http://www.geneticdiseasefoundation.org/2011/05/the-leta-lindley-prader-willi-classic/</link>
		<comments>http://www.geneticdiseasefoundation.org/2011/05/the-leta-lindley-prader-willi-classic/#comments</comments>
		<pubDate>Thu, 26 May 2011 03:18:57 +0000</pubDate>
		<dc:creator>GDF</dc:creator>
				<category><![CDATA[GDF News]]></category>

		<guid isPermaLink="false">http://www.geneticdiseasefoundation.org/?p=929</guid>
		<description><![CDATA[The 2011 Leta Lindley Prader-Willi Classic was a tremendous success and a majority of the $100,000 raised at the event will directly support the GDF. ]]></description>
			<content:encoded><![CDATA[<p><a href="http://www.geneticdiseasefoundation.org/wp-content/uploads/2011/05/leta-lindley-prader-willi_classic_check.jpg"><img class="size-full wp-image-937" title="leta-lindley-prader-willi_classic_check" src="http://www.geneticdiseasefoundation.org/wp-content/uploads/2011/05/leta-lindley-prader-willi_classic_check.jpg" alt="" width="600" height="354" /></a></p>
<p>May 17, 2011, New York &#8212; The Genetic Disease Foundation (GDF) received a check for more than $50,000 from proceeds of the 2011 Leta Lindley Prader-Willi Classic held in January.  The annual event with LPGA Tour Professional Leta Lindley is organized by Josilyn’s Faith Foundation headed by Director Ira Levine and President Michael Levine, whose daughter Josilyn is battling Prader-Willi Syndrome.</p>
<p>Pictured above at the check presentation (from l to r):  Dr. Robert Desnick, Dean of the Dept. of Genetics &#038; Genomics Sciences at Mount Sinai Medical Center, GDF Medical Advisory Board; Dr. Andrew Sharp, Senior Faculty in the Dept. of Genetics &#038; Genomics Sciences at Mount Sinai Medical Center, GDF Medical Advisory Board; Michael Levine; Ira Levine; Dr. Jamie Bassel, GDF Board of Directors &#038; Medical Advisory Board. </p>
<p>The weekend-long Classic was well-attended and raised over $100,000 for genetic disease research and education.  It began on Friday evening with an opening cocktail party featuring a lively auction.  On Saturday, 125 players participated in Saturday’s LPGA Pro Am event on The Champion Course at the beautiful PGA National Resort and Spa. At the luncheon that followed, Dr. Sharp presented a lecture on the latest research trying to unlock the mysteries of genetic disorders like Prader-Willi.</p>
<p>The 2012 Classic promises to be even better. Mark your calendar now for January 13, 14 and 15, 2012. On Friday there will be a Gala Dinner and Auction; Saturday brings the The Leta Lindley Classic; and on Sunday there will be a “Speed Six” Golf tournament with a clinic for children and a special opportunity for participants to play one-on-one with an LPGA marquee professional partner.</p>
<p>Visit the <a href="http://www.pwclassic.com/">Leta Lindley Prader-Willi Classic website</a> for more information.</p>
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		<title>New Website KnowYourGenes.org Provides Information About How to Benefit From Latest Advances in Genetics</title>
		<link>http://www.geneticdiseasefoundation.org/2011/03/new-website-www-knowyourgenes-org-provides-information-about-how-to-benefit-from-latest-advances-in-genetics/</link>
		<comments>http://www.geneticdiseasefoundation.org/2011/03/new-website-www-knowyourgenes-org-provides-information-about-how-to-benefit-from-latest-advances-in-genetics/#comments</comments>
		<pubDate>Thu, 10 Mar 2011 05:00:30 +0000</pubDate>
		<dc:creator>GDF</dc:creator>
				<category><![CDATA[GDF News]]></category>

		<guid isPermaLink="false">http://www.geneticdiseasefoundation.org/?p=878</guid>
		<description><![CDATA[GDF launches a new resource for adults &#038; parents-to-be]]></description>
			<content:encoded><![CDATA[<h3><strong>Resource for Adults &amp; Parents-to-Be as Scientists Crack Codes of Genetic Diseases</strong></h3>
<p><strong>NEW YORK, NY, Jan. 25, 2011</strong> &#8212; The Genetic Disease Foundation (GDF) has launched KnowYourGenes.org, a new online resource for people who wish to know more about how genetics can benefit their health and the health of their families. <a href="http://www.knowyourgenes.org">Knowyourgenes.org</a> is an easy-to-understand- and-navigate site where people can sort through the latest information about what tests are available and how results can be used to prevent, prepare for, or manage disease.</p>
<p>Speedy advances in genetic research mean that more gene mutations are being linked with specific diseases, more diagnostic tools are available to pinpoint previously-unidentifiable illnesses, and new treatments are being developed.</p>
<p>“The KnowYourGenes.org site may be helpful to anyone interested in exploring their genetics as part of family planning, to potentially identify a disease in themselves or a loved one, or to know more about what their hereditary risks may be,” explains Elisa Ross, president of GDF. “There are now more than 10,000 recorded genetic diseases that are passed on through generations, including widely recognized conditions and rare disorders.”</p>
<p>The website consists of three sections:</p>
<p><strong>1) <em>&#8220;Genetic Testing &amp; Pregnancy&#8221;</em></strong> is for adults/couples who plan to have children and may want to know their risk of carrying gene abnormalities that can be passed on. For example, an infant disease like Tay-Sachs is rare, but members of certain ethnic groups are more likely to carry the gene mutation and may wish to undergo screening (see www.knowyourgenes.org for more details).</p>
<p><strong>2) <em>&#8220;Know Your Family History&#8221;</em></strong> is a guide to understanding individual family history – how to gather information to tell if you may be at risk for any number of illnesses (like diabetes or heart disease)</p>
<p><strong>3) <em>&#8220;What is Genetic Testing?&#8221;</em></strong> covers types of tests, their purpose, how they’re conducted, and more.</p>
<p>Additional information includes “Genes 101” on the basics, a list of genetic diseases, how to find a certified genetic counselor, and a quiz to help determine who should be tested. Cost and privacy are also addressed.</p>
<p>The site was created partly in response to a survey conducted by GDF, in which the majority of respondents said they saw benefit to genetic testing, but nearly 80% said they’d never talked with their doctor about genetic screening.</p>
<p>GDF would like to encourage more conversations between doctors and patients about genetic testing and more visits to genetic counselors.</p>
<p>“We believe that number can change if people are more informed about the potential benefits of ‘knowing their genes,’” said Ms. Ross. “All of us at the GDF have had personal experience with genetic disease, and we’re pleased to bring this resource to help people understand how genetic advances can help them manage their health.”</p>
<p>For more information, visit <a href="http://www.KnowYourGenes.org">www.KnowYourGenes.org</a>.</p>
<p><strong>About The Genetic Disease Foundation</strong></p>
<p>The Genetic Disease Foundation (GDF) is a 501(c)(3) not-for-profit organization established in 1997 by patients and families affected by genetic disorders. The Foundation’s mission is to support research, education and the prevention of genetic diseases.</p>
<p>The Genetic Disease Foundation is affiliated with the Mount Sinai School of Medicine&#8217;s Department of Genetics and Genomic Sciences, whose faculty lead the country in clinical research to improve prenatal diagnosis, carrier screening, genetic counseling methods, and therapies for genetic diseases.</p>
<p><strong>CONTACT:</strong></p>
<p><a href="mailto:sue.preziotti@yahoo.com">Sue Preziotti</a>, 917-647-1590<br />
<a href="mailto:loriebroser@gmail.com">Lorie Broser</a>, 917-589-4876</p>
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		<title>GDF Supports Mount Sinai Gene Sequencer Purchases</title>
		<link>http://www.geneticdiseasefoundation.org/2010/08/gdf-supports-mount-sinai-gene-sequencer-purchases/</link>
		<comments>http://www.geneticdiseasefoundation.org/2010/08/gdf-supports-mount-sinai-gene-sequencer-purchases/#comments</comments>
		<pubDate>Mon, 23 Aug 2010 02:46:28 +0000</pubDate>
		<dc:creator>GDF</dc:creator>
				<category><![CDATA[GDF News]]></category>
		<category><![CDATA[Mount Sinai News]]></category>
		<category><![CDATA[gene sequencing]]></category>
		<category><![CDATA[Mount Sinai School of Medicine]]></category>
		<category><![CDATA[research]]></category>

		<guid isPermaLink="false">http://www.geneticdiseasefoundation.org/?p=749</guid>
		<description><![CDATA[The GDF recently donated $600,000 to the Mount Sinai Department of Genetics and Genomics to assist with the purchase of two state-of-the-art gene sequencers.]]></description>
			<content:encoded><![CDATA[<p><img class="aligncenter size-full wp-image-830" title="GDF Board with Dr. Desnick" src="http://www.geneticdiseasefoundation.org/wp-content/uploads/2010/08/gdf-board-with-dr-desnick.jpg" alt="" width="550" height="367" /></p>
<p>This spring GDF donated funds to assist with the purchase of two state-of-the-art gene sequencers for Mount Sinai&#8217;s Department of Genetics and Genomics. The Illumina GXII NextGen Sequencers were purchased by combining a grant from the National Institutes of Health with a $600,000 grant from the GDF. These machines help expand Mount Sinai&#8217;s research capabilities in many ways, including:</p>
<ul>
<li>disease gene discovery</li>
<li>analysis of gene expression (number of copies of all genes made in normal and diseased cells)</li>
<li>analysis of the elements that control gene expression, as well as the ability to sequence a person’s whole genome</li>
</ul>
<p>Already, both machines are working at full capacity and have dramatically increased the department’s capabilities. With this purchase Mount Sinai will be one of only four research institutions in the country with this level of sophisticated equipment allowing the department to expand further into the field of genomics.</p>
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		<title>New Jersey GDF Comedy Night Raises Over $6,000</title>
		<link>http://www.geneticdiseasefoundation.org/2010/08/new-jersey-gdf-comedy-night-raises-over-6000/</link>
		<comments>http://www.geneticdiseasefoundation.org/2010/08/new-jersey-gdf-comedy-night-raises-over-6000/#comments</comments>
		<pubDate>Mon, 23 Aug 2010 02:45:42 +0000</pubDate>
		<dc:creator>GDF</dc:creator>
				<category><![CDATA[GDF News]]></category>
		<category><![CDATA[Special Events]]></category>

		<guid isPermaLink="false">http://www.geneticdiseasefoundation.org/?p=763</guid>
		<description><![CDATA[Over one hundred supporters enjoyed a night of laughs and good times in Pine Brook, NJ to raise money for the GDF.]]></description>
			<content:encoded><![CDATA[<p><a href="http://www.geneticdiseasefoundation.org/wp-content/uploads/2010/08/nj-comedy-event.jpg"><img src="http://www.geneticdiseasefoundation.org/wp-content/uploads/2010/08/nj-comedy-event.jpg" alt="New Jersey GDF Comedy Event" title="New Jersey GDF Comedy Event" width="465" height="336" class="aligncenter size-full wp-image-772" /></a></p>
<p>Special thanks go to Andrea Trombino for organizing an amazing event at Suppa’s Restaurant and the Comedy Shoppe in Pine Brook, NJ. About one hundred friends and family of the GDF gathered to share laughs, drinks and great food.</p>
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		<title>GDF Charity Ride Raises over $44,000</title>
		<link>http://www.geneticdiseasefoundation.org/2010/08/gdf-charity-ride-raises-over-44000/</link>
		<comments>http://www.geneticdiseasefoundation.org/2010/08/gdf-charity-ride-raises-over-44000/#comments</comments>
		<pubDate>Mon, 23 Aug 2010 02:34:39 +0000</pubDate>
		<dc:creator>GDF</dc:creator>
				<category><![CDATA[GDF News]]></category>
		<category><![CDATA[Special Events]]></category>
		<category><![CDATA[fundraising]]></category>

		<guid isPermaLink="false">http://www.geneticdiseasefoundation.org/?p=755</guid>
		<description><![CDATA[Thanks to everyone for a hugely successful Know Your Genes, Know Your Zone charity ride in NYC!]]></description>
			<content:encoded><![CDATA[<div>
<p>Thank you to everyone who supported our Know Your Genes, Know Your Zone charity ride. <a href="http://www.ridethezone.com/">Ride the Zone</a>, New York’s premiere indoor cycling studio, was an incredible location for this wildly successful event. The event raised over $44,000, exceeding everyone’s wildest expectations. We are so thankful to everyone who rode, sponsored and/or cheered on the riders. Special thanks to GDF Board Member Carrie Green for leading this effort!</p>
</div>
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		<title>Open Position: Part-time Director</title>
		<link>http://www.geneticdiseasefoundation.org/2009/12/open-position-part-time-director/</link>
		<comments>http://www.geneticdiseasefoundation.org/2009/12/open-position-part-time-director/#comments</comments>
		<pubDate>Tue, 08 Dec 2009 02:25:55 +0000</pubDate>
		<dc:creator>GDF</dc:creator>
				<category><![CDATA[GDF News]]></category>

		<guid isPermaLink="false">http://www.geneticdiseasefoundation.org/?p=389</guid>
		<description><![CDATA[The GDF is looking to hire a part-time Director. ]]></description>
			<content:encoded><![CDATA[<p>The Genetic Disease Foundation is looking to hire a part-time Director to help with administration, communications and development. <a href="http://www.geneticdiseasefoundation.org/job-part-time-director/"><br />
</a></p>
<p><strong><em>Update: This position has been filled</em></strong>.</p>
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		<title>Welcome to the new GDF Web site!</title>
		<link>http://www.geneticdiseasefoundation.org/2009/09/elcome-to-the-new-gdf-web-site/</link>
		<comments>http://www.geneticdiseasefoundation.org/2009/09/elcome-to-the-new-gdf-web-site/#comments</comments>
		<pubDate>Mon, 28 Sep 2009 16:28:46 +0000</pubDate>
		<dc:creator>GDF</dc:creator>
				<category><![CDATA[GDF News]]></category>

		<guid isPermaLink="false">http://www.geneticdiseasefoundation.org/?p=119</guid>
		<description><![CDATA[Learn about the newly designed GDF Web site.]]></description>
			<content:encoded><![CDATA[<p>We&#8217;re thrilled to announce the launch of the new Genetic Disease Foundation Web site. This new site has been designed to make it easier for you to learn about our organization and the people behind it, stay updated on GDF and genetic disease-related news and learn how you can help us fulfill our mission to support education and research for treatment and cures for genetic diseases.</p>
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