Robert S Molday

ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 21

Top Venues

Disease models & mechanisms

Diagnostics (Basel, Switzerland)

International journal of molecular sciences

Human mutation

University of British Columbia

University of Pennsylvania (PHD)

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

Affiliation History

University of British Columbia Jan 01 1985

Canada

Professor :: Biochemistry and Molecular Biology

University of British Columbia Jan 01 1980 - Dec 31 1985

Canada

Associate Professor :: Biochemistry and Molecular Biology

University of British Columbia Faculty of Medicine Oct 01 1975 - Jan 01 1980

Canada

Assistant Professor :: Biochemistry and Molecular Biology

Education History

University of Pennsylvania Sep 05 1967 - May 29 1971

United States

PHD :: Biology

Georgetown University Sep 05 1965 - Jun 18 1967

United States

MSC :: Chemistry

University of Pennsylvania Sep 05 1961 - May 24 1965

United States

BSC :: Chemistry

Publications

Eli Matsell, Jens Peter Andersen, Robert S Molday
Functional and In-silico analysis of ATP8A2 and other P4-ATPase variants associated with human genetic diseases. Disease models & mechanisms (2024)
Eli Matsell, Jens Peter Andersen, Robert S Molday
Functional and in silico analysis of ATP8A2 and other P4-ATPase variants associated with human genetic diseases. Disease models & mechanisms 17 (6) (2024)
Davide Piccolo, Christina Zarouchlioti, James Bellingham, Rosellina Guarascio, Kalliopi Ziaka, Robert S Molday, Michael E Cheetham
A Proximity Complementation Assay to Identify Small Molecules That Enhance the Traffic of ABCA4 Misfolding Variants. International journal of molecular sciences 25 (8) (2024)
Hanna De Bruyn, Megan Johnson, Madelyn Moretti, Saleh Ahmed, Mircea Mujat, James D Akula, Tomislav Glavan, Ivana Mihalek, Sigrid Aslaksen, Laurie L Molday, Robert S Molday, Bruce A Berkowitz, Anne B Fulton
The Surviving, Not Thriving, Photoreceptors in Patients with ABCA4 Stargardt Disease. Diagnostics (Basel, Switzerland) 14 (14) (2024)
Davide Piccolo, Christina Zarouchlioti, James Bellingham, Rosellina Guarascio, Kalliopi Ziaka, Robert S Molday, Michael E Cheetham
A Proximity Complementation Assay to Identify Small Molecules That Enhance the Traffic of ABCA4 Misfolding Variants. International journal of molecular sciences 25 (8) (2024)
Hanna De Bruyn, Megan Johnson, Madelyn Moretti, Saleh Ahmed, Mircea Mujat, James D Akula, Tomislav Glavan, Ivana Mihalek, Sigrid Aslaksen, Laurie L Molday, Robert S Molday, Bruce A Berkowitz, Anne B Fulton
The Surviving, Not Thriving, Photoreceptors in Patients with ABCA4 Stargardt Disease. Diagnostics (Basel, Switzerland) 14 (14) (2024)
Eli Matsell, Jens Peter Andersen, Robert S Molday
Functional and in silico analysis of ATP8A2 and other P4-ATPase variants associated with human genetic diseases. Disease models & mechanisms 17 (6) (2024)
Eli Matsell, Jens Peter Andersen, Robert S Molday
Functional and in silico analysis of ATP8A2 and other P4-ATPase variants associated with human genetic diseases. Disease models & mechanisms 17 (6) (2024)
Eli Matsell, Jens Peter Andersen, Robert S Molday
Functional and in silico analysis of ATP8A2 and other P4-ATPase variants associated with human genetic diseases. Disease models & mechanisms 17 (6) (2024)
Davide Piccolo, Christina Zarouchlioti, James Bellingham, Rosellina Guarascio, Kalliopi Ziaka, Robert S Molday, Michael E Cheetham
A Proximity Complementation Assay to Identify Small Molecules That Enhance the Traffic of ABCA4 Misfolding Variants. International journal of molecular sciences 25 (8) (2024)
Hanna De Bruyn, Megan Johnson, Madelyn Moretti, Saleh Ahmed, Mircea Mujat, James D Akula, Tomislav Glavan, Ivana Mihalek, Sigrid Aslaksen, Laurie L Molday, Robert S Molday, Bruce A Berkowitz, Anne B Fulton
The Surviving, Not Thriving, Photoreceptors in Patients with ABCA4 Stargardt Disease. Diagnostics (Basel, Switzerland) 14 (14) (2024)
Eli Matsell, Jens Peter Andersen, Robert S Molday
Functional and in silico analysis of ATP8A2 and other P4-ATPase variants associated with human genetic diseases. Disease models & mechanisms 17 (6) (2024)
Myrthe J van Dijk, Brigitte A van Oirschot, Alexander N Harrison, Steffen M Recktenwald, Min Qiao, Amaury Stommen, Anne-Sophie Cloos, Juliette Vanderroost, Romano Terrasi, Kuntal Dey, Jennifer Bos, Minke A E Rab, Anna Yu Bogdanova, Giampaolo Minetti, Giulio G Muccioli, Donatienne Tyteca, Stéphane Egée, Lars Kaestner, Robert S Molday, Eduard J van Beers, Richard van Wijk
A novel missense variant in ATP11C is associated with reduced red blood cell phosphatidylserine flippase activity and mild hereditary hemolytic anemia. American journal of hematology (2023)
Francesco Tadini-Buoninsegni, Stine A Mikkelsen, Louise S Mogensen, Rikke Holm, Robert S Molday, Jens Peter Andersen
Electrogenic reaction step and phospholipid translocation pathway of the mammalian P4-ATPase ATP8A2. FEBS letters (2022)
Jessica Fernandes Scortecci, Laurie L Molday, Susan B Curtis, Fabian A Garces, Pankaj Panwar, Filip Van Petegem, Robert S Molday
Cryo-EM structures of the ABCA4 importer reveal mechanisms underlying substrate binding and Stargardt disease. Nature communications 12 (1) (2021)
Tao Li, Diankun Yu, Hayeon C Oak, Beika Zhu, Li Wang, Xueqiao Jiang, Robert S Molday, Arnold Kriegstein, Xianhua Piao
Phospholipid-flippase chaperone CDC50A is required for synapse maintenance by regulating phosphatidylserine exposure. The EMBO journal 40 (21) (2021)
Daisuke Ennishi, Shannon Healy, Ali Bashashati, Saeed Saberi, Christoffer Hother, Anja Mottok, Fong Chun Chan, Lauren Chong, Libin Abraham, Robert Kridel, Merrill Boyle, Barbara Meissner, Tomohiro Aoki, Katsuyoshi Takata, Bruce W Woolcock, Elena Viganò, Michael R Gold, Laurie L Molday, Robert S Molday, Adele Telenius, Michael Y Li, Nicole Wretham, Nancy Dos Santos, Mark Wong, Natasja N Viller, Robert A Uger, Gerben Duns, Abigail Baticados, Angel Madero, Brianna N Bristow, Pedro Farinha, Graham W Slack, Susana Ben-Neriah, Daniel Lai, Allen W Zhang, Sohrab Salehi, Hennady P Shulha, Derek S Chiu, Sara Mostafavi, Alina S Gerrie, Da Wei Huang, Christopher Rushton, Diego R Villa, Laurie H Sehn, Kerry J Savage, Andrew J Mungall, Andrew P Weng, Marcel B Bally, Ryan D Morin, Gabriela V Cohen Freue, Louis M Staudt, Joseph M Connors, Marco A Marra, Sohrab P Shah, Randy D Gascoyne, David W Scott, Christian Steidl
TMEM30A loss-of-function mutations drive lymphomagenesis and confer therapeutically exploitable vulnerability in B-cell lymphoma. Nature medicine 26 (4) (2020)
Susan B Curtis, Laurie L Molday, Fabian A Garces, Robert S Molday
Functional analysis and classification of homozygous and hypomorphic ABCA4 variants associated with Stargardt macular degeneration. Human mutation 41 (11) (2020)
Hanbin Choi, Jens Peter Andersen, Robert S Molday
Expression and functional characterization of missense mutations in ATP8A2 linked to severe neurological disorders. Human mutation 40 (12) (2019)
Angela Y Liou, Laurie L Molday, Jiao Wang, Jens Peter Andersen, Robert S Molday
Identification and functional analyses of disease-associated P4-ATPase phospholipid flippase variants in red blood cells. The Journal of biological chemistry 294 (17) (2019)
Robert S Molday, Andrew F X Goldberg
Peripherin diverts ciliary ectosome release to photoreceptor disc morphogenesis. The Journal of cell biology 216 (5) (2017)

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Publication Activity (10 Years)

Top Topics

Top Venues

Robert S Molday