Kimberly Goodspeed

13PUBLICATIONS
40CO-AUTHORS
Neurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)Infant and child healthEpigenetics (incl. genome methylation and epigenomics)Systems physiology
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Publications (13)

|Oct 06, 2026
Beyond Seizure Management in a Developmental Epileptic Encephalopathy: Expanding the SLC6A1 Neurodevelopmental Disorder Phenotype.

|Mar 13, 2026
Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant Classification.

Tobias Brünger, Ilona Krey, Suyeon Kim

|Dec 22, 2024
Developmental phenotype and quality of life in SLC13A5 citrate transporter disorder.

Can Ozlu, Raegan M Adams, Rayann M Solidum

|Oct 26, 2024
Sleep Abnormalities in SLC13A5 Citrate Transporter Disorder.

Raegan M Adams, Can Ozlu, Lauren E Bailey

|Jul 28, 2023
Patient-derived SLC6A1 variant S295L results in an epileptic phenotype similar to haploinsufficient mice.

Britta E Lindquist, Yuliya Voskobiynyk, Kimberly Goodspeed

|Jun 02, 2023
Electroencephalographic (EEG) Biomarkers in Genetic Neurodevelopmental Disorders.

Kimberly Goodspeed, Dallas Armstrong, Alison Dolce

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Frequent Collaborators

2 joint publications

Rachel M Bailey

2 joint publications

Brenda E Porter

2 joint publications

Kimberly Nye

2 joint publications

Tanya L Brown