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Author/Creator MacCarrick, Gretchen

1. A mutation update on the LDS‐associated genes TGFB2/3 and SMAD2/3. Issue 5 (6th March 2018)

Authors:
Schepers, Dorien; Tortora, Giada; Morisaki, Hiroko; MacCarrick, Gretchen; Lindsay, Mark; Liang, David; Mehta, Sarju G.; Hague, Jennifer; Verhagen, Judith; van de Laar, Ingrid; Wessels, Marja; Detisch, Yvonne; van Haelst, Mieke; Baas, Annette; Lichtenbelt, Klaske; Braun, Kees; van der Linde, Denis...
Journal:
Human mutation
Issue:
Volume 39:Issue 5(2018)
Page Start:
621
Record Type:
Journal Article
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2. At the Heart of the Pregnancy: What Prenatal and Cardiovascular Genetic Counselors Need to Know about Maternal Heart Disease. Issue 4 (10th March 2017)

Authors:
Morales, Ana; Allain, Dawn C.; Arscott, Patricia; James, Emily; MacCarrick, Gretchen; Murray, Brittney; Tichnell, Crystal; Shikany, Amy R.; Spencer, Sara; Fitzgerald‐Butt, Sara M.; Kushner, Jessica D.; Munn, Christi; Smith, Emily; Spoonamore, Katherine G.; Tandri, Harikrishna S.; Kay, W. Aaron
Journal:
Journal of genetic counseling
Issue:
Volume 26:Issue 4(2017)
Page Start:
669
Record Type:
Journal Article
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3. Blood pressure in adults with short stature skeletal dysplasias. Issue 1 (15th November 2019)

Authors:
Hoover‐Fong, Julie; Alade, Adekemi Yewande; Ain, Michael; Berkowitz, Ivor; Bober, Michael; Carter, Erin; Hecht, Jacqueline; Hoerschemeyer, Dan; Krakow, Debra; MacCarrick, Gretchen; Mackenzie, William G.; Mendoza, Roberto; Okenfuss, Ericka; Popplewell, Deirdre; Raggio, Cathleen; Schulze, Kerry; Mc...
Journal:
American journal of medical genetics
Issue:
Volume 182:Issue 1(2020)
Page Start:
150
Record Type:
Journal Article
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4. Blood pressure in adults with short stature skeletal dysplasias. Issue 1 (15th November 2019)

Authors:
Hoover‐Fong, Julie; Alade, Adekemi Yewande; Ain, Michael; Berkowitz, Ivor; Bober, Michael; Carter, Erin; Hecht, Jacqueline; Hoerschemeyer, Dan; Krakow, Debra; MacCarrick, Gretchen; Mackenzie, William G.; Mendoza‐Londono, Roberto; Okenfuss, Ericka; Popplewell, Deirdre; Raggio, Cathleen; Schulze, K...
Journal:
American journal of medical genetics
Issue:
Volume 182:Issue 1(2020)
Page Start:
150
Record Type:
Journal Article
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5. Erratum to: At the Heart of the Pregnancy: What Prenatal and Cardiovascular Genetic Counselors Need to Know about Maternal Heart Disease. Issue 4 (4th May 2017)

Authors:
Morales, Ana; Allain, Dawn C.; Arscott, Patricia; James, Emily; MacCarrick, Gretchen; Murray, Brittney; Tichnell, Crystal; Shikany, Amy R.; Spencer, Sara; Fitzgerald‐Butt, Sara M.; Kushner, Jessica D.; Munn, Christi; Smith, Emily; Spoonamore, Katherine G.; Tandri, Harikrishna S.; Aaron Kay, W.
Journal:
Journal of genetic counseling
Issue:
Volume 26:Issue 4(2017)
Page Start:
689
Record Type:
Journal Article
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6. Loeys–Dietz syndrome caused by 1q41 deletion including TGFB2 is associated with a neurodevelopmental phenotype. Issue 7 (15th April 2022)

Authors:
Fry, Deanna; Groepper, Daniel; MacCarrick, Gretchen; Demo, Erin M.; Thomas, Matthew J.; Wilkes, Margaret J.; Lyons, Michael J.; Tucker, Megan E.; Steding, Catherine; Fleischer, Julie
Journal:
American journal of medical genetics
Issue:
Volume 188:Issue 7(2022)
Page Start:
2237
Record Type:
Journal Article
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8. Recruitment, retention, and adherence in a clinical trial: The Pediatric Heart Network's Marfan Trial experience. (December 2020)

Authors:
Hamstra, Michelle S; Pemberton, Victoria L; Dagincourt, Nicholas; Hollenbeck-Pringle, Danielle; Trachtenberg, Felicia L; Cnota, James F; Atz, Andrew M; Cappella, Elizabeth; De Nobele, Sylvia; Grima, Josephine; King, Martha; Korsin, Rosalind; Lambert, Linda M; MacNeal, Meghan K; Markham, Larry W; ...
Journal:
Clinical trials
Issue:
Volume 17:Number 6(2020)
Page Start:
684
Record Type:
Journal Article
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9. ROBO4 variants predispose individuals to bicuspid aortic valve and thoracic aortic aneurysm. (January 2019)

Authors:
Gould, Russell; Aziz, Hamza; Woods, Courtney; Seman-Senderos, Manuel; Sparks, Elizabeth; Preuss, Christoph; Wünnemann, Florian; Bedja, Djahida; Moats, Cassandra; McClymont, Sarah; Rose, Rebecca; Sobreira, Nara; Ling, Hua; MacCarrick, Gretchen; Kumar, Ajay; Luyckx, Ilse; Cannaerts, Elyssa; Verstra...
Journal:
Nature genetics
Issue:
Volume 51:Number 1(2019)
Page Start:
42
Record Type:
Journal Article
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10. Sleep disordered breathing in Marfan syndrome: Value of standard screening questionnaires. Issue 1 (10th November 2019)

Authors:
Sowho, Mudiaga O.; Patil, Susheel; Schneider, Hartmut; MacCarrick, Gretchen; Kirkness, Jason P.; Wolfe, Lisa F.; Sterni, Laura; Cistulli, Peter A.; Neptune, Enid R.
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 8:Issue 1(2020)
Page Start:
n/a
Record Type:
Journal Article
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