Stanley F Nelson

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 4

Top Topics

Single Molecule

Duchenne Muscular Dystrophy

Intellectual Disability

Top Venues

EMBO molecular medicine

Human molecular genetics

Genetics in medicine : official journal of the American College of Medical Genetics

Communications biology

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

Publications

Samantha Wong, Yu Xuan Tan, Abigail Yi Ting Loh, Kiat-Yi Tan, Hane Lee, Zainab Aziz, Stanley F Nelson, Engin Özkan, Hülya Kayserili, Nathalie Escande-Beillard, Bruno Reversade
RAF1 deficiency causes a lethal syndrome that underscores RTK signaling during embryogenesis. EMBO molecular medicine (2023)
Franziska Paul, Calista Ng, Umar Bin Mohamad Sahari, Shahriar Nafissi, Yalda Nilipoor, Ali Reza Tavasoli, Carine Bonnard, Pui-Mun Wong, Nasrinsadat Nabavizadeh, Umut Altunoğlu, Mehrdad A Estiar, Charles B L M Majoie, Hane Lee, Stanley F Nelson, Ziv Gan Or, Guy A Rouleau, Paul P Van Veldhoven, Rami Massie, Raoul C Hennekam, Ariana Kariminejad, Bruno Reversade
RABENOSYN separation-of-function mutations uncouple endosomal recycling from lysosomal degradation, causing a distinct Mendelian disorder. Human molecular genetics 31 (21) (2022)
Deirdre D Scripture-Adams, Kevin N Chesmore, Florian Barthelemy, Richard T Wang, Shirley Nieves-Rodriguez, Derek W Wang, Ekaterina I Mokhonova, Emilie D Douine, Jijun Wan, Isaiah Little, Laura N Rabichow, Stanley F Nelson, M Carrie Miceli
Single nuclei transcriptomics of muscle reveals intra-muscular cell dynamics linked to dystrophin loss and rescue. Communications biology 5 (1) (2022)
Hane Lee, Alden Y Huang, Lee-Kai Wang, Amanda J Yoon, Genecee Renteria, Ascia Eskin, Rebecca H Signer, Naghmeh Dorrani, Shirley Nieves-Rodriguez, Jijun Wan, Emilie D Douine, Jeremy D Woods, Esteban C Dell'Angelica, Brent L Fogel, Martin G Martin, Manish J Butte, Neil H Parker, Richard T Wang, Perry B Shieh, Derek A Wong, Natalie Gallant, Kathryn E Singh, Y Jane Tavyev Asher, Janet S Sinsheimer, Deborah Krakow, Sandra K Loo, Patrick Allard, Jeanette C Papp, null null, Christina G S Palmer, Julian A Martinez-Agosto, Stanley F Nelson
Diagnostic utility of transcriptome sequencing for rare Mendelian diseases. Genetics in medicine : official journal of the American College of Medical Genetics 22 (3) (2019)