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News - Revision history
2026-04-05T20:03:56Z
Revision history for this page on the wiki
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http://statgen.us/index.php?title=News&diff=1395&oldid=prev
Serveradmin: Blanked the page
2022-02-24T03:27:41Z
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<td colspan='2' style="background-color: white; color:black; text-align: center;">← Older revision</td>
<td colspan='2' style="background-color: white; color:black; text-align: center;">Revision as of 03:27, 24 February 2022</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l1" >Line 1:</td>
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<tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div><del style="font-weight: bold; text-decoration: none;">* '''07/10/2020 [new paper]''' Gao's fine-mapping method paper is published online at [https://rss.onlinelibrary.wiley.com/doi/10.1111/rssb.12388 JRSS-B].</del></div></td><td colspan="2"> </td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td></tr>
<tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div><del style="font-weight: bold; text-decoration: none;">* '''06/23/2020 [new paper]''' Isabelle's paper, ''Autosomal Dominantly Inherited GREB1L Variants in Individuals with Profound Sensorineural Hearing Impairment'', is published online at [https://www.mdpi.com/2073-4425/11/6/687 Genes]. Congrats Isabelle, Thashi and Anu!</del></div></td><td colspan="2"> </td></tr>
<tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div><del style="font-weight: bold; text-decoration: none;"></del></div></td><td colspan="2"> </td></tr>
<tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div><del style="font-weight: bold; text-decoration: none;">* '''05/14/2020 [funding]''' Congrats to Gao for receiving a fund from Thompson Family Foundation Program for Accelerated Medicines Exploration in Alzheimer’s Disease and Related Disorders of The Nervous System.</del></div></td><td colspan="2"> </td></tr>
<tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div><del style="font-weight: bold; text-decoration: none;"></del></div></td><td colspan="2"> </td></tr>
<tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div><del style="font-weight: bold; text-decoration: none;">* '''10/03/2019 [new paper]''' Linhai's paper, ''A Rare Variant Nonparametric Linkage Method for Nuclear and Extended Pedigrees with Application to Late-Onset Alzheimer Disease via WGS Data'', is published online at [https://www.sciencedirect.com/science/article/pii/S0002929719303453 American Journal of Human Genetics]. Good work, Linhai!</del></div></td><td colspan="2"> </td></tr>
<tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div><del style="font-weight: bold; text-decoration: none;"></del></div></td><td colspan="2"> </td></tr>
<tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div><del style="font-weight: bold; text-decoration: none;">* '''09/27/2019 [new paper]''' Imen's paper, ''Disparities in Discovery of Pathogenic Variants for Autosomal Recessive Non-Syndromic Hearing Impairment by Ancestry'', is published online at [https://www.nature.com/articles/s41431-019-0417-2 European Journal of Human Genetics]. Congratulations to Imen and Isabelle!</del></div></td><td colspan="2"> </td></tr>
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Serveradmin
http://statgen.us/index.php?title=News&diff=1175&oldid=prev
Serveradmin at 22:14, 16 July 2020
2020-07-16T22:14:58Z
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<td colspan='2' style="background-color: white; color:black; text-align: center;">Revision as of 22:14, 16 July 2020</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l1" >Line 1:</td>
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<tr><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>* '''07/10/2020 [new paper]''' Gao's fine-mapping method paper is published online at [https://rss.onlinelibrary.wiley.com/doi/10.1111/rssb.12388 JRSS-B].</div></td><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>* '''07/10/2020 [new paper]''' Gao's fine-mapping method paper is published online at [https://rss.onlinelibrary.wiley.com/doi/10.1111/rssb.12388 JRSS-B].</div></td></tr>
<tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div><del style="font-weight: bold; text-decoration: none;"></del></div></td><td colspan="2"> </td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>* '''06/23/2020 [new paper]''' Isabelle's paper, ''Autosomal Dominantly Inherited GREB1L Variants in Individuals with Profound Sensorineural Hearing Impairment'', is published online at [https://www.mdpi.com/2073-4425/11/6/687 Genes]. Congrats Isabelle, Thashi and Anu!</div></td><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>* '''06/23/2020 [new paper]''' Isabelle's paper, ''Autosomal Dominantly Inherited GREB1L Variants in Individuals with Profound Sensorineural Hearing Impairment'', is published online at [https://www.mdpi.com/2073-4425/11/6/687 Genes]. Congrats Isabelle, Thashi and Anu!</div></td></tr>
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Serveradmin
http://statgen.us/index.php?title=News&diff=1174&oldid=prev
Serveradmin at 21:57, 16 July 2020
2020-07-16T21:57:58Z
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<td colspan='2' style="background-color: white; color:black; text-align: center;">Revision as of 21:57, 16 July 2020</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l1" >Line 1:</td>
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<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">* '''07/10/2020 [new paper]''' Gao's fine-mapping method paper is published online at [https://rss.onlinelibrary.wiley.com/doi/10.1111/rssb.12388 JRSS-B].</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"></ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"></ins></div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>* '''06/23/2020 [new paper]''' Isabelle's paper, ''Autosomal Dominantly Inherited GREB1L Variants in Individuals with Profound Sensorineural Hearing Impairment'', is published online at [https://www.mdpi.com/2073-4425/11/6/687 Genes]. Congrats Isabelle, Thashi and Anu!</div></td><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>* '''06/23/2020 [new paper]''' Isabelle's paper, ''Autosomal Dominantly Inherited GREB1L Variants in Individuals with Profound Sensorineural Hearing Impairment'', is published online at [https://www.mdpi.com/2073-4425/11/6/687 Genes]. Congrats Isabelle, Thashi and Anu!</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td></tr>
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Serveradmin
http://statgen.us/index.php?title=News&diff=1159&oldid=prev
Serveradmin at 15:08, 24 June 2020
2020-06-24T15:08:31Z
<p></p>
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<td colspan='2' style="background-color: white; color:black; text-align: center;">← Older revision</td>
<td colspan='2' style="background-color: white; color:black; text-align: center;">Revision as of 15:08, 24 June 2020</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l1" >Line 1:</td>
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<tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>* '''06/23/2020 [paper <del class="diffchange diffchange-inline">published</del>]''' Isabelle's paper, ''Autosomal Dominantly Inherited GREB1L Variants in Individuals with Profound Sensorineural Hearing Impairment'', is published online at [https://www.mdpi.com/2073-4425/11/6/687 Genes]. Congrats Isabelle, Thashi and Anu!</div></td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>* '''06/23/2020 [<ins class="diffchange diffchange-inline">new </ins>paper]''' Isabelle's paper, ''Autosomal Dominantly Inherited GREB1L Variants in Individuals with Profound Sensorineural Hearing Impairment'', is published online at [https://www.mdpi.com/2073-4425/11/6/687 Genes]. Congrats Isabelle, Thashi and Anu!</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>* '''05/14/2020 [funding]''' Congrats to Gao for receiving a fund from Thompson Family Foundation Program for Accelerated Medicines Exploration in Alzheimer’s Disease and Related Disorders of The Nervous System.</div></td><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>* '''05/14/2020 [funding]''' Congrats to Gao for receiving a fund from Thompson Family Foundation Program for Accelerated Medicines Exploration in Alzheimer’s Disease and Related Disorders of The Nervous System.</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td></tr>
<tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>* '''10/03/2019 [paper <del class="diffchange diffchange-inline">published</del>]''' Linhai's paper, ''A Rare Variant Nonparametric Linkage Method for Nuclear and Extended Pedigrees with Application to Late-Onset Alzheimer Disease via WGS Data'', is published online at [https://www.sciencedirect.com/science/article/pii/S0002929719303453 American Journal of Human Genetics]. Good work, Linhai!</div></td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>* '''10/03/2019 [<ins class="diffchange diffchange-inline">new </ins>paper]''' Linhai's paper, ''A Rare Variant Nonparametric Linkage Method for Nuclear and Extended Pedigrees with Application to Late-Onset Alzheimer Disease via WGS Data'', is published online at [https://www.sciencedirect.com/science/article/pii/S0002929719303453 American Journal of Human Genetics]. Good work, Linhai!</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td></tr>
<tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>* '''09/27/2019 [paper <del class="diffchange diffchange-inline">published</del>]''' Imen's paper, ''Disparities in Discovery of Pathogenic Variants for Autosomal Recessive Non-Syndromic Hearing Impairment by Ancestry'', is published online at [https://www.nature.com/articles/s41431-019-0417-2 European Journal of Human Genetics]. Congratulations to Imen and Isabelle!</div></td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>* '''09/27/2019 [<ins class="diffchange diffchange-inline">new </ins>paper]''' Imen's paper, ''Disparities in Discovery of Pathogenic Variants for Autosomal Recessive Non-Syndromic Hearing Impairment by Ancestry'', is published online at [https://www.nature.com/articles/s41431-019-0417-2 European Journal of Human Genetics]. Congratulations to Imen and Isabelle!</div></td></tr>
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Serveradmin
http://statgen.us/index.php?title=News&diff=1158&oldid=prev
Serveradmin at 15:08, 24 June 2020
2020-06-24T15:08:04Z
<p></p>
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<td colspan='2' style="background-color: white; color:black; text-align: center;">← Older revision</td>
<td colspan='2' style="background-color: white; color:black; text-align: center;">Revision as of 15:08, 24 June 2020</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l1" >Line 1:</td>
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<tr><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>* '''06/23/2020 [paper published]''' Isabelle's paper, ''Autosomal Dominantly Inherited GREB1L Variants in Individuals with Profound Sensorineural Hearing Impairment'', is published online at [https://www.mdpi.com/2073-4425/11/6/687 Genes]. Congrats Isabelle, Thashi and Anu!</div></td><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>* '''06/23/2020 [paper published]''' Isabelle's paper, ''Autosomal Dominantly Inherited GREB1L Variants in Individuals with Profound Sensorineural Hearing Impairment'', is published online at [https://www.mdpi.com/2073-4425/11/6/687 Genes]. Congrats Isabelle, Thashi and Anu!</div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"></ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">* '''05/14/2020 [funding]''' Congrats to Gao for receiving a fund from Thompson Family Foundation Program for Accelerated Medicines Exploration in Alzheimer’s Disease and Related Disorders of The Nervous System.</ins></div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>* '''10/03/2019 [paper published]''' Linhai's paper, ''A Rare Variant Nonparametric Linkage Method for Nuclear and Extended Pedigrees with Application to Late-Onset Alzheimer Disease via WGS Data'', is published online at [https://www.sciencedirect.com/science/article/pii/S0002929719303453 American Journal of Human Genetics]. Good work, Linhai!</div></td><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>* '''10/03/2019 [paper published]''' Linhai's paper, ''A Rare Variant Nonparametric Linkage Method for Nuclear and Extended Pedigrees with Application to Late-Onset Alzheimer Disease via WGS Data'', is published online at [https://www.sciencedirect.com/science/article/pii/S0002929719303453 American Journal of Human Genetics]. Good work, Linhai!</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>* '''09/27/2019 [paper published]''' Imen's paper, ''Disparities in Discovery of Pathogenic Variants for Autosomal Recessive Non-Syndromic Hearing Impairment by Ancestry'', is published online at [https://www.nature.com/articles/s41431-019-0417-2 European Journal of Human Genetics]. Congratulations to Imen and Isabelle!</div></td><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>* '''09/27/2019 [paper published]''' Imen's paper, ''Disparities in Discovery of Pathogenic Variants for Autosomal Recessive Non-Syndromic Hearing Impairment by Ancestry'', is published online at [https://www.nature.com/articles/s41431-019-0417-2 European Journal of Human Genetics]. Congratulations to Imen and Isabelle!</div></td></tr>
</table>
Serveradmin
http://statgen.us/index.php?title=News&diff=1157&oldid=prev
Serveradmin at 15:04, 24 June 2020
2020-06-24T15:04:58Z
<p></p>
<table class='diff diff-contentalign-left'>
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<td colspan='2' style="background-color: white; color:black; text-align: center;">← Older revision</td>
<td colspan='2' style="background-color: white; color:black; text-align: center;">Revision as of 15:04, 24 June 2020</td>
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<tr><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>* '''06/23/2020 [paper published]''' Isabelle's paper, ''Autosomal Dominantly Inherited GREB1L Variants in Individuals with Profound Sensorineural Hearing Impairment'', is published online at [https://www.mdpi.com/2073-4425/11/6/687 Genes]. Congrats Isabelle, Thashi and Anu!</div></td><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>* '''06/23/2020 [paper published]''' Isabelle's paper, ''Autosomal Dominantly Inherited GREB1L Variants in Individuals with Profound Sensorineural Hearing Impairment'', is published online at [https://www.mdpi.com/2073-4425/11/6/687 Genes]. Congrats Isabelle, Thashi and Anu!</div></td></tr>
<tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div><del style="font-weight: bold; text-decoration: none;"></del></div></td><td colspan="2"> </td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>* '''10/03/2019 [paper published]''' Linhai's paper, ''A Rare Variant Nonparametric Linkage Method for Nuclear and Extended Pedigrees with Application to Late-Onset Alzheimer Disease via WGS Data'', is published online at [https://www.sciencedirect.com/science/article/pii/S0002929719303453 American Journal of Human Genetics]. Good work, Linhai!</div></td><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>* '''10/03/2019 [paper published]''' Linhai's paper, ''A Rare Variant Nonparametric Linkage Method for Nuclear and Extended Pedigrees with Application to Late-Onset Alzheimer Disease via WGS Data'', is published online at [https://www.sciencedirect.com/science/article/pii/S0002929719303453 American Journal of Human Genetics]. Good work, Linhai!</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>* '''09/27/2019 [paper published]''' Imen's paper, ''Disparities in Discovery of Pathogenic Variants for Autosomal Recessive Non-Syndromic Hearing Impairment by Ancestry'', is published online at [https://www.nature.com/articles/s41431-019-0417-2 European Journal of Human Genetics]. Congratulations to Imen and Isabelle!</div></td><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>* '''09/27/2019 [paper published]''' Imen's paper, ''Disparities in Discovery of Pathogenic Variants for Autosomal Recessive Non-Syndromic Hearing Impairment by Ancestry'', is published online at [https://www.nature.com/articles/s41431-019-0417-2 European Journal of Human Genetics]. Congratulations to Imen and Isabelle!</div></td></tr>
</table>
Serveradmin
http://statgen.us/index.php?title=News&diff=1156&oldid=prev
Serveradmin at 15:04, 24 June 2020
2020-06-24T15:04:45Z
<p></p>
<table class='diff diff-contentalign-left'>
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<td colspan='2' style="background-color: white; color:black; text-align: center;">Revision as of 15:04, 24 June 2020</td>
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<tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>* '''<del class="diffchange diffchange-inline">2019</del>/10/<del class="diffchange diffchange-inline">03 </del>[paper published]''' <del class="diffchange diffchange-inline">Our </del>paper, ''A Rare Variant Nonparametric Linkage Method for Nuclear and Extended Pedigrees with Application to Late-Onset Alzheimer Disease via WGS Data'', is published online at [https://www.sciencedirect.com/science/article/pii/S0002929719303453 American Journal of Human Genetics].</div></td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>* '''<ins class="diffchange diffchange-inline">06</ins>/<ins class="diffchange diffchange-inline">23/2020 [paper published]''' Isabelle's paper, ''Autosomal Dominantly Inherited GREB1L Variants in Individuals with Profound Sensorineural Hearing Impairment'', is published online at [https://www.mdpi.com/2073-4425/11/6/687 Genes]. Congrats Isabelle, Thashi and Anu!</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins class="diffchange diffchange-inline">* '''</ins>10/<ins class="diffchange diffchange-inline">03/2019 </ins>[paper published]''' <ins class="diffchange diffchange-inline">Linhai's </ins>paper, ''A Rare Variant Nonparametric Linkage Method for Nuclear and Extended Pedigrees with Application to Late-Onset Alzheimer Disease via WGS Data'', is published online at [https://www.sciencedirect.com/science/article/pii/S0002929719303453 American Journal of Human Genetics]. <ins class="diffchange diffchange-inline">Good work, Linhai!</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins class="diffchange diffchange-inline">* '''09/27/2019 [paper published]''' Imen's paper, ''Disparities in Discovery of Pathogenic Variants for Autosomal Recessive Non-Syndromic Hearing Impairment by Ancestry'', is published online at [https://www.nature.com/articles/s41431-019-0417-2 European Journal of Human Genetics]. Congratulations to Imen and Isabelle!</ins></div></td></tr>
</table>
Serveradmin
http://statgen.us/index.php?title=News&diff=993&oldid=prev
Serveradmin at 02:19, 21 January 2020
2020-01-21T02:19:04Z
<p></p>
<table class='diff diff-contentalign-left'>
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<td colspan='2' style="background-color: white; color:black; text-align: center;">← Older revision</td>
<td colspan='2' style="background-color: white; color:black; text-align: center;">Revision as of 02:19, 21 January 2020</td>
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<tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>* '''2019/10/03 [paper <del class="diffchange diffchange-inline">accepted</del>]'''Our paper, ''A Rare Variant Nonparametric Linkage Method for Nuclear and Extended Pedigrees with Application to Late-Onset Alzheimer Disease via WGS Data'', is published online at [https://www.sciencedirect.com/science/article/pii/S0002929719303453 American Journal of Human Genetics].</div></td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>* '''2019/10/03 [paper <ins class="diffchange diffchange-inline">published</ins>]''' Our paper, ''A Rare Variant Nonparametric Linkage Method for Nuclear and Extended Pedigrees with Application to Late-Onset Alzheimer Disease via WGS Data'', is published online at [https://www.sciencedirect.com/science/article/pii/S0002929719303453 American Journal of Human Genetics].</div></td></tr>
</table>
Serveradmin
http://statgen.us/index.php?title=News&diff=992&oldid=prev
Serveradmin at 02:18, 21 January 2020
2020-01-21T02:18:48Z
<p></p>
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<td colspan='2' style="background-color: white; color:black; text-align: center;">Revision as of 02:18, 21 January 2020</td>
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</table>
Serveradmin
http://statgen.us/index.php?title=News&diff=981&oldid=prev
Serveradmin: Created page with "* '''2019/10/03 '''Our paper, ''A Rare Variant Nonparametric Linkage Method for Nuclear and Extended Pedigrees with Application to Late-Onset Alzheimer Disease via WGS Data'..."
2020-01-07T18:45:24Z
<p>Created page with "* '''2019/10/03 '''Our paper, ''A Rare Variant Nonparametric Linkage Method for Nuclear and Extended Pedigrees with Application to Late-Onset Alzheimer Disease via WGS Data'..."</p>
<p><b>New page</b></p><div>* '''2019/10/03 '''Our paper, ''A Rare Variant Nonparametric Linkage Method for Nuclear and Extended Pedigrees with Application to Late-Onset Alzheimer Disease via WGS Data'', is published online at [https://www.sciencedirect.com/science/article/pii/S0002929719303453 American Journal of Human Genetics].</div>
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