Forbes D Porter

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 14

Top Venues

International journal of molecular sciences

Journal of inherited metabolic disease

Biology open

Journal of neuroinflammation

National Institutes of Health

Washington University in St. Louis (PHD)

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

Affiliation History

National Institutes of Health

United States

Senior Investigator and Clinical Director :: NICHD

Education History

Washington University in St. Louis

United States

PHD

Publications

Nicole Y Farhat, Derek Alexander, Kyli McKee, James Iben, Jorge L Rodriguez-Gil, Christopher A Wassif, Niamh X Cawley, William E Balch, Forbes D Porter
Sterol O-Acyltransferase 1 ( SOAT1 ): A Genetic Modifier of Niemann-Pick Disease, Type C1. International journal of molecular sciences 25 (8) (2024)
Nicole Y Farhat, Derek Alexander, Kyli McKee, James Iben, Jorge L Rodriguez-Gil, Christopher A Wassif, Niamh X Cawley, William E Balch, Forbes D Porter
Sterol O-Acyltransferase 1 ( SOAT1 ): A Genetic Modifier of Niemann-Pick Disease, Type C1. International journal of molecular sciences 25 (8) (2024)
Aishwarya Selvaraman, Samar Rahhal, Simona Bianconi, Tristan Furnary, Forbes D Porter
Assessing Postnatal Mortality in Smith-Lemli-Opitz Syndrome. American journal of medical genetics. Part A (2024)
Avani V Mylvara, Alana L Gibson, Tansy Gu, Cristin D Davidson, Art A Incao, Katerina Melnyk, Dominick Pierre-Jacques, Stephanie M Cologna, Charles P Venditti, Forbes D Porter, William J Pavan
Optimization of systemic AAV9 gene therapy in Niemann-Pick disease type C1 mice. bioRxiv : the preprint server for biology (2024)
Nicole Y Farhat, Derek Alexander, Kyli McKee, James Iben, Jorge L Rodriguez-Gil, Christopher A Wassif, Niamh X Cawley, William E Balch, Forbes D Porter
Sterol O-Acyltransferase 1 ( SOAT1 ): A Genetic Modifier of Niemann-Pick Disease, Type C1. International journal of molecular sciences 25 (8) (2024)
Nouf N Laqtom, Wentao Dong, Uche N Medoh, Andrew L Cangelosi, Vimisha Dharamdasani, Sze Ham Chan, Tenzin Kunchok, Caroline A Lewis, Ivonne Heinze, Rachel Tang, Christian M Grimm, An N Dang Do, Forbes D Porter, Alessandro Ori, David M Sabatini, Monther Abu-Remaileh
CLN3 is required for the clearance of glycerophosphodiesters from lysosomes. Nature 609 (7929) (2022)
Niamh X Cawley, Anna T Lyons, Daniel Abebe, Rachel Luke, Julia Yerger, Rebecca Telese, Christopher A Wassif, Richard K Wilson, Forbes D Porter
Complex N-Linked Glycosylation: A Potential Modifier of Niemann-Pick Disease, Type C1 Pathology. International journal of molecular sciences 23 (9) (2022)
Julia Yerger, Antony C Cougnoux, Craig B Abbott, Rachel Luke, Tannia S Clark, Niamh X Cawley, Forbes D Porter, Cristin D Davidson
Phenotype assessment for neurodegenerative murine models with ataxia and application to Niemann-Pick disease, type C1. Biology open 11 (4) (2022)
Elaine Tierney, Alan T Remaley, Audrey Thurm, Leah R Jager, Christopher A Wassif, Lisa E Kratz, Richard K Wilson, Irena Bukelis, Geeta Sarphare, Eun Sol Jung, Boudewien Brand, Kelly K Noah, Forbes D Porter
Sterol and lipid analyses identifies hypolipidemia and apolipoprotein disorders in autism associated with adaptive functioning deficits. Translational psychiatry 11 (1) (2021)
Antony C Cougnoux, Julia C Yerger, Mason Fellmeth, Jenny Serra-Vinardell, Kyle Martin, Fatemeh Navid, James Iben, Christopher A Wassif, Niamh X Cawley, Forbes D Porter
Single Cell Transcriptome Analysis of Niemann-Pick Disease, Type C1 Cerebella. International journal of molecular sciences 21 (15) (2020)
Alexandria Colaco, Ecem Kaya, Elias Adriaenssens, Lianne C Davis, Stefania Zampieri, María E Fernández-Suárez, Chong Y Tan, Patrick B Deegan, Forbes D Porter, Antony Galione, Bruno Bembi, Andrea Dardis, Frances Mary Platt
Mechanistic convergence and shared therapeutic targets in Niemann-Pick disease. Journal of inherited metabolic disease 43 (3) (2019)
Antony Cougnoux, Rebecca A Drummond, Mason Fellmeth, Fatemeh Navid, Amanda L Collar, James Iben, Ashok B Kulkarni, James Pickel, Raphael Schiffmann, Christopher A Wassif, Niamh X Cawley, Michail S Lionakis, Forbes D Porter
Unique molecular signature in mucolipidosis type IV microglia. Journal of neuroinflammation 16 (1) (2019)
Wei-Chia Tseng, Hannah E Loeb, Wuhong Pei, Chon-Hwa Tsai-Morris, Lisha Xu, Celine V Cluzeau, Christopher A Wassif, Benjamin Feldman, Jason W Sinclair, William J Pavan, Forbes D Porter
Modeling Niemann-Pick disease type C1 in zebrafish: a robust platform for in vivo screening of candidate therapeutic compounds. Disease models & mechanisms 11 (9) (2018)
Christopher A Wassif, Lisa Kratz, Susan E Sparks, Courtney Wheeler, Simona Bianconi, Andrea L Gropman, Karim A Calis, Richard I Kelley, Elaine Tierney, Forbes D Porter
A placebo-controlled trial of simvastatin therapy in Smith-Lemli-Opitz syndrome. Genetics in medicine : official journal of the American College of Medical Genetics 19 (3) (2016)

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Publication Activity (10 Years)

Top Topics

Top Venues

Forbes D Porter