Iqbal, Sumaiya

Predicting functional effects of missense variants in voltage-gated sodium and calcium channels

Heyne, H. O., Baez-Nieto, D., Iqbal, S., Palmer, D. S., Brunklaus, A., May, P., Collaborative, E., Johannesen, K. M., Lauxmann, S., Lemke, J. R., et al. (2020) · Science Translational Medicine

Ion channel regulation and functionGenomics and Rare Diseases

Cited by 140

Genomics 2 Proteins portal: A resource and discovery tool for linking genetic screening outputs to protein sequences and structures

Kwon, S., Safer, J., Nguyen, D. T., Hoksza, D., May, P., Arbesfeld, J. A., Rubin, A. F., Campbell, A. J., Burgin, A., & Iqbal, S. (2024) · Nature Methods

Genomics and Rare DiseasesProtein Structure and Dynamics

Cited by 29

MAVISp: A Modular Structure-Based Framework for Protein Variant Effects

Arnaudi, M., Utichi, M., Degn, K., Tiberti, M., Beltrame, L., Krzesińska, K., Sánchez-Izquierdo Besora, P., Kiachaki, E., Scrima, S., Bauer, L., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory)

Genomics and Rare DiseasesProtein Structure and Dynamics

Cited by 20

Characterizing proteomic and transcriptomic features of missense variants in amyotrophic lateral sclerosis genes

Dilliott, A. A., Rouleau, G. A., Iqbal, S., & Farhan, S. M. K. (2022) · Brain

Amyotrophic Lateral Sclerosis ResearchGenomics and Rare Diseases

Cited by 8

Characterizing proteomic and transcriptomic features of missense variants in amyotrophic lateral sclerosis genes

Dilliott, A. A., Kwon, S., Rouleau, G. A., Iqbal, S., & Farhan, S. M. K. (2023) · Brain

Amyotrophic Lateral Sclerosis ResearchGenomics and Rare Diseases

Cited by 8