Kristen Park

Also affiliated with Epilepsy Foundation, University of Colorado Denver

MedicineBiochemistry, Genetics and Molecular BiologyNeuroscience

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 17 papers. Top paper: “Diagnostic utility of DNA methylation analysis in genetically unsolved pediatric epilepsies and CHD2 episignature refinement”.

Diagnostic utility of DNA methylation analysis in genetically unsolved pediatric epilepsies and CHD2 episignature refinement

Nature Communications(2024)10.1038/s41467-024-50159-6

N/A

0.489DataRank · unranked

25 citations

Cassandra Rastin, Soham Sengupta, Helen E. Pennington, Sophie Russ-Hall, Amy Schneider +50 more

Unrecognized Focal Nonmotor Seizures in Adolescents Presenting to Emergency Departments

Neurology(2024)10.1212/wnl.0000000000209389

N/A

0.312DataRank · unranked

7 citations

Monica Ferrer, Jacob Pellinen, Hadley T. Greenwood, Dennis Dlugos, Kristen Park +4 more

Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition

Research Square(2023)10.21203/rs.3.rs-3317938/v1

N/A

0.241DataRank · unranked

4 citations

Ghayda Mirzaa, Keqin Yan, Raissa Relator, Sara Timpano, Binnaz Yalcin +57 more

Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition

Nature Communications(2025)10.1038/s41467-025-64838-5

N/A

0.241DataRank · unranked

4 citations

Keqin Yan, Raissa Relator, Mathieu Lévesque, P.S. Jayasinghe, Sara Timpano +61 more

Androgens mediate sexual dimorphism in Pilarowski-Bjornsson Syndrome

medRxiv(2025)10.1101/2025.05.06.25326635

N/A

0.165DataRank · unranked

2 citations

Eirny Tholl Thorolfsdottir, Ilana M. Nodelman, Sara Tholl Halldorsdottir, Stefania Benónísdóttir, Malak Alghamdi +64 more

Tob Regulates the Timing of Sleep Onset at Night inDrosophila

Journal of Neuroscience(2024)10.1523/jneurosci.0389-23.2024

N/A

0.104DataRank · unranked

1 citations

Sang‐Soo Lee, Kristen Park, Ian D. Blum, Qiang Liu, Anuradha Mehta +9 more

Clinical and functional consequences of GRIA variants in patients with neurological diseases

Cellular and Molecular Life Sciences(2023)10.1007/s00018-023-04991-6

N/A

0DataRank · unranked

19 citations

Riley E. Perszyk, Nana Liu, Yuchen Xu, Subhrajit Bhattacharya, Gil Shaulsky +25 more

Astroglial Calcium Signaling Encodes Sleep Need in Drosophila

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.04.187906

N/A

0DataRank · unranked

4 citations

Mehmet F. Keleş, El‐Sayed Baz, Emily L. Han, Kristen Park, Skylar Luu +7 more

Plural molecular and cellular mechanisms of pore domain KCNQ2 encephalopathy

eLife(2024)10.7554/elife.91204

N/A

0DataRank · unranked

3 citations

Emma C. Thompson, Anuraag Madabushi, Kristen Park, Heun Soh, Nissi Varghese +20 more

Somatic variants in diverse genes leads to a spectrum of focal cortical malformations

UNC Libraries(2024)10.17615/98hm-r135

N/A

0DataRank · unranked

0 citations

Peter Canoll, Anne F. Buckley, Gretchen K. Von Allmen, Hyun Yong Koh, Gerald A. Grant +20 more

The effect of TERT promoter mutation on predicting meningioma outcomes: a multi-institutional cohort analysis

The Lancet Oncology(2025)10.1016/s1470-2045(25)00422-x

N/A

0DataRank · unranked

11 citations

Ruchit V. Patel, Yang Feng, Hia S. Ghosh, Miguel A. Millares Chavez, Joseph O’Brien +36 more

Diagnostic Utility of Genome-wide DNA Methylation Analysis in Genetically Unsolved Developmental and Epileptic Encephalopathies and Refinement of a CHD2 Episignature

medRxiv(2023)10.1101/2023.10.11.23296741

N/A

0DataRank · unranked

1 citations

Cassandra Rastin, Soham Sengupta, Helen E. Pennington, Sophie Russ-Hall, Amy Schneider +48 more

Kinetically Stabilizing Mutations in Beta Tubulins Create Isotype-Specific Brain Malformations

Frontiers in Cell and Developmental Biology(2021)10.3389/fcell.2021.765992

N/A

0DataRank · unranked

29 citations

Katelyn J. Hoff, Linnea C. Wethekam, Nicholas Stence, Margarita Sáenz, Jeffrey K. Moore +1 more

Somatic mutation involving diverse genes leads to a spectrum of focal cortical malformations

medRxiv(2021)10.1101/2021.12.22.21267563

N/A

0DataRank · unranked

4 citations

Meethila Gade, Edward Yang, Hyun Yong Koh, Nicole M. Walley, Anne F. Buckley +18 more

Loss of Grin2a Causes a Transient Delay in the Electrophysiological Maturation of Hippocampal Parvalbumin Interneurons: A Possible Mechanism for Transient Seizure Burden in Patients with Null GRIN2A Variants

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.12.29.474447

N/A

0DataRank · unranked

3 citations

Anna Vlachos, Chiara Klöckner, Ilona Krey, Tue G. Banke, Nima Shariatzadeh +14 more

Somatic variants in diverse genes leads to a spectrum of focal cortical malformations

Brain(2022)10.1093/brain/awac117

N/A

0DataRank · unranked

78 citations

Meethila Gade, Edward Yang, Hyun Yong Koh, Jinfeng Lü, Nicole M Walley +20 more

Loss of Grin2a causes a transient delay in the electrophysiological maturation of hippocampal parvalbumin interneurons

Communications Biology(2023)10.1038/s42003-023-05298-9

N/A

0DataRank · unranked

38 citations

Anna Vlachos, Chiara Klöckner, Ilona Krey, Tue G. Banke, Nima Shariatzadeh +14 more