J Paul Taylor

12PUBLICATIONS
63CO-AUTHORS
Medical infection agents (incl. prions)Gene and molecular therapyStructure and dynamics of materialsMedical molecular engineering of nucleic acids and proteinsNeurology and neuromuscular diseases
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Publications (12)

|Jun 17, 2026
A mutation in the nuclear speckle and splicing factor SRRM2 is associated with multisystem proteinopathy and causes dysregulation of synapse-associated genes.

|Nov 24, 2025
Preclinical evaluation of antisense oligonucleotide therapy in a mouse model of HNRNPH2-related neurodevelopmental disorder.

Ane Korff, Xiaojing Yang, Ozan Ozdemir

|Mar 11, 2024
Tunable metastability of condensates reconciles their dual roles in amyloid fibril formation.

Tapojyoti Das, Fatima K Zaidi, Mina Farag

|Jan 29, 2024
Identification of small molecule inhibitors of G3BP-driven stress granule formation.

Brian D Freibaum, James Messing, Haruko Nakamura

|Jan 30, 2023
A new Karyopherin-β2 binding PY-NLS epitope of HNRNPH2 is linked to neurodevelopmental disorders.

Abner Gonzalez, Hong Joo Kim, Brian D Freibaum

|Apr 28, 2022
Heterozygous frameshift variants in HNRNPA2B1 cause early-onset oculopharyngeal muscular dystrophy.

Hong Joo Kim, Payam Mohassel, Sandra Donkervoort

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Frequent Collaborators

8 joint publications

Hong Joo Kim

3 joint publications

Brian D Freibaum

2 joint publications

Rohit V Pappu

2 joint publications

Brian A Maxwell