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Author/Creator Maslen, Cheryl L.

1. Associations of Age and Sex With Marfan Phenotype: The National Heart, Lung, and Blood Institute GenTAC (Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions) Registry. (June 2017)

Authors:
Roman, Mary J.; Devereux, Richard B.; Preiss, Liliana R.; Asch, Federico M.; Eagle, Kim A.; Holmes, Kathryn W.; LeMaire, Scott A.; Maslen, Cheryl L.; Milewicz, Dianna M.; Morris, Shaine A.; Prakash, Siddharth K.; Pyeritz, Reed E.; Ravekes, William J.; Shohet, Ralph V.; Song, Howard K.; Weinsaft, ...
Journal:
Circulation
Issue:
Volume 10:Number 3(2017)
Page Start:
Record Type:
Journal Article
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2. Autosomal and X chromosome structural variants are associated with congenital heart defects in Turner syndrome: The NHLBI GenTAC registry. Issue 12 (8th September 2016)

Authors:
Prakash, Siddharth K.; Bondy, Carolyn A.; Maslen, Cheryl L.; Silberbach, Michael; Lin, Angela E.; Perrone, Laura; Limongelli, Giuseppe; Michelena, Hector I.; Bossone, Eduardo; Citro, Rodolfo; Lemaire, Scott A.; Body, Simon C.; Milewicz, Dianna M.
Journal:
American journal of medical genetics
Issue:
Volume 170:Issue 12(2016)
Page Start:
3157
Record Type:
Journal Article
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3. Bicuspid and unicuspid aortic valves: Different phenotypes of the same disease? Insight from the GenTAC Registry. (14th August 2017)

Authors:
Krepp, Joseph M.; Roman, Mary J.; Devereux, Richard B.; Bruce, Adrienne; Prakash, Siddharth K.; Morris, Shaine A.; Milewicz, Dianna M.; Holmes, Kathryn W.; Ravekes, William; Shohet, Ralph V.; Pyeritz, Reed E.; Maslen, Cheryl L.; Kroner, Barbara L.; Eagle, Kim A.; Preiss, Liliana; Asch, Federico M.
Journal:
Congenital heart disease
Issue:
Volume 12:Number 6(2017)
Page Start:
740
Record Type:
Journal Article
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6. GenTAC registry report: Gender differences among individuals with genetically triggered thoracic aortic aneurysm and dissection1. Issue 4 (26th February 2013)

Authors:
Holmes, Kathryn W.; Maslen, Cheryl L.; Kindem, Mark; Kroner, Barbara L.; Song, Howard K.; Ravekes, William; Dietz, H.C.; Weinsaft, Jonathan W.; Roman, Mary J.; Devereux, Richard B.; Pyeritz, Reed E.; Bavaria, Joseph; Milewski, Karianna; Milewicz, Dianna; LeMaire, Scott A.; Hendershot, Tabitha; Ea...
Journal:
American journal of medical genetics
Issue:
Volume 161:Issue 4(2013:Apr.)
Page Start:
779
Record Type:
Journal Article
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7. Identification of novel rare copy number variants associated with sporadic tetralogy of Fallot and clinical implications. Issue 5 (2nd August 2022)

Authors:
He, Guo‐Wei; Maslen, Cheryl L.; Chen, Huan‐Xin; Hou, Hai‐Tao; Bai, Xiao‐Yan; Wang, Xiu‐Li; Liu, Xiao‐Cheng; Lu, Wan‐Li; Chen, Xin‐Xin; Chen, Wei‐Dan; Xing, Quan‐Sheng; Wu, Qin; Wang, Jun; Yang, Qin
Journal:
Clinical genetics
Issue:
Volume 102:Issue 5(2022)
Page Start:
391
Record Type:
Journal Article
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8. Proceedings from the Turner Resource Network symposium: The crossroads of health care research and health care delivery. (29th April 2015)

Authors:
Backeljauw, Philippe F.; Bondy, Carolyn; Chernausek, Steven D.; Cernich, Joseph T.; Cole, David A.; Fasciano, Laura P.; Foodim, Joan; Hawley, Scott; Hong, David S.; Knickmeyer, Rebecca C.; Kruszka, Paul; Lin, Angela E.; Lippe, Barbara M.; Lorigan, Gary A.; Maslen, Cheryl L.; Mauras, Nelly; Page, ...
Journal:
American journal of medical genetics
Issue:
Volume 167:Number 9(2015:Sep.)
Page Start:
1962
Record Type:
Journal Article
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