Timothy Feyma

Also affiliated with Gillette Children's Specialty Healthcare

Biochemistry, Genetics and Molecular BiologyNeuroscienceMedicine

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 11 papers. Top paper: “Top caregiver concerns in Rett syndrome and related disorders: data from the US natural history study”.

Top caregiver concerns in Rett syndrome and related disorders: data from the US natural history study

Journal of Neurodevelopmental Disorders(2023)10.1186/s11689-023-09502-z

N/A

1.6DataRank · unranked

57 citations

Tim A. Benke, Eric D. Marsh, Bernhard Suter, Lori Silveira, Cary Fu +12 more

Safety and feasibility of transcranial direct current stimulation stratified by corticospinal organization in children with hemiparesis

European Journal of Paediatric Neurology(2023)10.1016/j.ejpn.2023.01.013

N/A

0.470DataRank · unranked

11 citations

Daniel H. Lench, Ellen N. Sutter, Jesse L. Kowalski, Sunday M. Francis, Gregg Meekins +4 more

Analysis of X‐inactivation status in a Rett syndrome natural history study cohort

Molecular Genetics & Genomic Medicine(2022)10.1002/mgg3.1917

N/A

0DataRank · unranked

23 citations

Kameryn M. Butler, Fatima Abidi, Jennifer Gass, Arthur Beisang, Timothy Feyma +14 more

Neurodevelopmental and Epilepsy Phenotypes in Individuals With Missense Variants in the Voltage-Sensing and Pore Domains of KCNH5

Neurology(2022)10.1212/wnl.0000000000201492

N/A

0DataRank · unranked

24 citations

Lynette G. Sadleir, Matthew Zemel, Guillem de Valles‐Ibáñez, Michael S. Hildebrand, Allyn McConkie‐Rosell +50 more

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

medRxiv(2022)10.1101/2022.04.26.22274147

N/A

0DataRank · unranked

0 citations

Lynette G. Sadleir, Matthew Zemel, Guillem de Valles‐Ibáñez, Michael S. Hildebrand, Allyn McConkie‐Rosell +49 more

Parental perspectives of episodic irritability in an ultra-rare genetic disorder associated with NACC1

Orphanet Journal of Rare Diseases(2023)10.1186/s13023-023-02891-3

N/A

0DataRank · unranked

5 citations

Allyn McConkie‐Rosell, Nicole Walley, Vikas Bhambhani, Timothy Feyma, Undiagnosed Diseases Network +5 more

Anodal Contralesional tDCS Enhances CST Excitability Bilaterally in an Adolescent with Hemiparetic Cerebral Palsy: A Brief Report

Developmental Neurorehabilitation(2023)10.1080/17518423.2023.2193626

N/A

0DataRank · unranked

0 citations

Ellen N. Sutter, Samuel T. Nemanich, Linda E. Krach, Gregg Meekins, Timothy Feyma +2 more

Clinical Features and Disease Progression in Older Individuals with Rett Syndrome

Genes(2024)10.3390/genes15081107

N/A

0DataRank · unranked

8 citations

Tim A. Benke, Eric D. Marsh, Bernhard Suter, Cary Fu, Robin C. Ryther +9 more

Damaging de novo missense variants inEEF1A2lead to a developmental and degenerative epileptic‐dyskinetic encephalopathy

Human Mutation(2020)10.1002/humu.24015

N/A

0DataRank · unranked

40 citations

Katherine L. Helbig, Candace T. Myers, Marcello Scala, Robert Huether, Sara A. Lewis +40 more

Hyperkinetic Movement Disorder Caused by the Recurrent c. 892C >T NACC1 Variant

Movement Disorders Clinical Practice(2024)10.1002/mdc3.14051

N/A

0DataRank · unranked

4 citations

Salla M. Kangas, Estrella López‐Martín, Timothy Feyma, Fernando Scaglia, Beatriz Martínez–Delgado +7 more

Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders

Genome Medicine(2021)10.1186/s13073-021-00870-6

N/A

0DataRank · unranked

117 citations

Tianyun Wang, Kendra Hoekzema, Jill A. Rosenfeld, Pengfei Liu, Hui Guo +95 more