Dimitri J Stavropoulos (D J Stavropoulos, Dimitri James Stavropoulos)

Years Active: 2017-2021
Publications (10 Years): 3

This page only lists publications with an associated author ORCID identifier.

Publications

Justin O Szot, Anne M Slavotinek, Karen Chong, Oliver Brandau, Marjan M Nezarati, Anna M Cueto-González, Millan S Patel, W Patrick Devine, Shannon Rego, Alicia P Acyinena, Patrick Shannon, Diane Myles-Reid, Susan I Blaser, Tim VAN Mieghem, Halenur Yavuz-Kienle, Heyko Skladny, Kristen Miller, Miereia D T Riera, Silvia A Martínez, Eduardo F Tizzano, Lucie Dupuis, Dimitri J Stavropoulos, Vanda McNiven, Roberto Mendoza-Londono, Alison M Elliott, null null, Robert S Phillips, Gavin Chapman, Sally L Dunwoodie
New cases that expand the genotypic and phenotypic spectrum of Congenital NAD Deficiency Disorder. Human mutation 42 (7) (2021)
Erin Rooney Riggs, Tristan Nelson, Andrew Merz, Todd Ackley, Brian Bunke, Christin D Collins, Morag N Collinson, Yao-Shan Fan, McKinsey L Goodenberger, Denae M Golden, Linda Haglund-Hazy, Danijela Krgovic, Allen N Lamb, Zoe Lewis, Guang Li, Yajuan Liu, Jeanne Meck, Whitney Neufeld-Kaiser, Cassandra K Runke, Jennifer N Sanmann, Dimitri J Stavropoulos, Emma Strong, Meng Su, Marwan K Tayeh, Nadja Kokalj Vokac, Erik C Thorland, Erica Andersen, Christa L Martin
Copy number variant discrepancy resolution using the ClinGen dosage sensitivity map results in updated clinical interpretations in ClinVar. Human mutation 39 (11) (2019)
A Noor, S Bogatan, N Watkins, W S Meschino, Dimitri J Stavropoulos
Disruption of YWHAE gene at 17p13.3 causes learning disabilities and brain abnormalities. Clinical genetics 93 (2) (2017)

Dimitri J Stavropoulos.css-eqlu8i{font-size:small;padding-left:4px;} (D J Stavropoulos, Dimitri James Stavropoulos)