Kimberly Goodspeed
12PUBLICATIONS
35CO-AUTHORS
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Publications (12)
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|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
|Sep 23, 2022
SLC13A5 Deficiency Disorder: From Genetics to Gene Therapy.Kimberly Goodspeed, Judy S Liu, Kimberly L Nye
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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
1 joint publications
Rikke S Møller
1 joint publications
Megan Bone
1 joint publications
Andrea Lowden
1 joint publications
Peter V Sguigna
1 joint publications
Peter Tsai
1 joint publications
Yuliya Voskobiynyk
