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Author/Creator Povysil, Gundula

1. Casual Genetic Variants in Stillbirth. Issue 2 (February 2021)

Authors:
Stanley, Kate E.; Giordano, Jessica; Thorsten, Vanessa; Buchovecky, Christie; Thomas, Amanda; Ganapathi, Mythily; Liao, Jun; Dharmadhikari, Avinash V.; Revah-Politi, Anya; Ernst, Michelle; Lippa, Natalie; Holmes, Halie; Povysil, Gundula; Hostyk, Joseph; Parker, Corette B.; Goldenberg, Robert; Saa...
Journal:
Obstetrical & gynecological survey
Issue:
Volume 76:Issue 2(2021)
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Record Type:
Journal Article
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2. Clinical and Genetic Characteristics of CKD Patients with High-Risk APOL1 Genotypes. Issue 5 (9th May 2023)

Authors:
Elliott, Mark D.; Marasa, Maddalena; Cocchi, Enrico; Vena, Natalie; Zhang, Jun Y.; Khan, Atlas; Krishna Murthy, Sarath; Bheda, Shiraz; Milo Rasouly, Hila; Povysil, Gundula; Kiryluk, Krzysztof; Gharavi, Ali G.
Journal:
Journal of the American Society of Nephrology
Issue:
Volume 34:Issue 5(2023)
Page Start:
909
Record Type:
Journal Article
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3. CSGALNACT1‐congenital disorder of glycosylation: A mild skeletal dysplasia with advanced bone age. Issue 3 (3rd December 2019)

Authors:
Mizumoto, Shuji; Janecke, Andreas R.; Sadeghpour, Azita; Povysil, Gundula; McDonald, Marie T.; Unger, Sheila; Greber‐Platzer, Susanne; Deak, Kristen L.; Katsanis, Nicholas; Superti‐Furga, Andrea; Sugahara, Kazuyuki; Davis, Erica E.; Yamada, Shuhei; Vodopiutz, Julia
Journal:
Human mutation
Issue:
Volume 41:Issue 3(2020)
Page Start:
655
Record Type:
Journal Article
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8. Utility of whole genome sequencing in assessing risk and clinically relevant outcomes for pulmonary fibrosis. Issue 6 (22nd December 2022)

Authors:
Zhang, David; Newton, Chad A.; Wang, Binhan; Povysil, Gundula; Noth, Imre; Martinez, Fernando J.; Raghu, Ganesh; Goldstein, David; Garcia, Christine Kim
Journal:
European respiratory journal
Issue:
Volume 60:Issue 6(2022)
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Record Type:
Journal Article
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