Author

Andrea Paras

Northwestern University

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Alena Jahodová· 1 shared Allan BayatiD· 1 shared Allyn McConkie‐RoselliD· 1 shared Anita DattaiD· 1 shared Anju ShuklaiD· 1 shared Barbara K. BurtoniD· 1 shared Brenda E. PorteriD· 1 shared Christina FengeriD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenetic & Genomic Medicine

Alena Jahodová

Mutual co-authors in cluster

Author profile →

1 paper

Recent·Most cited

Missense variants in the voltage sensing and pore domain of KCNH5 cause neurodevelopmental phenotypes including epilepsy

Hannah C. Happ, Lynette Grant Sadleir, Matthew Zemel, Guillem de Valles‐Ibáñez, Michael S. Hildebrand, Allyn McConkie‐Rosell, Marie McDonald, Halie J. May, Tristan T. Sands, Vimla S. Aggarwal, Christopher J. Elder, Timothy J. Feyma, Allan Bayat, Rikke Steensbjerre Møller, Christina Fenger, , Gemma L. Carvill

The paper reports a cohort of 17 patients with pathogenic KCNH5 variants causing neurodevelopmental disorders and epilepsy, identifying genotype-phenotype correlations.

medRxiv · Apr 26, 2022 · PreprintGenetic & Genomic Medicine