Kenneth H. Fischbeck

Also affiliated with National Institute of Neurological Disorders and Stroke

NeuroscienceMedicineBiochemistry, Genetics and Molecular Biology

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 3%percentile

1.2Author DataRank

Indexed papers

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Clinical and Molecular Aspects of Senataxin Mutations in Amyotrophic Lateral Sclerosis 4

Annals of Neurology(2020)10.1002/ana.25681

Top 18%

1.2DataRank

Top 18%37 citations

Aneesh Patankar, Joshua Amaya, Jason A. Watts, Dongjun Li, Prisila Ramirez +4 more

Papers

Driven by 22 papers — median percentile 82. Top paper: “Clinical and Molecular Aspects of Senataxin Mutations in Amyotrophic Lateral Sclerosis 4”.

Clinical and Molecular Aspects of Senataxin Mutations in Amyotrophic Lateral Sclerosis 4

Annals of Neurology(2020)10.1002/ana.25681

Top 18%

1.2DataRank

Top 18%37 citations

Aneesh Patankar, Joshua Amaya, Jason A. Watts, Dongjun Li, Prisila Ramirez +4 more

A novel variant in the spatacsin gene causing SPG11 in a Malian family

Journal of the Neurological Sciences(2020)10.1016/j.jns.2020.116675

N/A

0DataRank · unranked

12 citations

Kékouta Dembélé, Salimata Diarra, Lassana Cissé, Oumar Samassékou, A Bocoum +5 more

Nucleic acid therapeutics in neurodevelopmental disease

Current Opinion in Genetics & Development(2020)10.1016/j.gde.2020.05.022

N/A

0DataRank · unranked

11 citations

Kenneth H. Fischbeck, Audrey M. Winkelsas

Linking epigenetic dysregulation, mitochondrial impairment, and metabolic dysfunction in SBMA motor neurons

JCI Insight(2020)10.1172/jci.insight.136539

N/A

0DataRank · unranked

29 citations

Ester Masati, Eric Bunker, Alec R. Nickolls, Parisorn Thepmankorn, Kory R. Johnson +5 more

Exercise intervention leads to functional improvement in a patient with spinal and bulbar muscular atrophy

Journal of Rehabilitation Medicine – Clinical Communications(2020)10.2340/20030711-1000041

N/A

0DataRank · unranked

1 citations

Jayaraj Joseph, Vincent Shieh, Angela Kokkinis, A Acevedo, Kenneth H. Fischbeck +3 more

Combinatorial treatment for spinal muscular atrophy

Journal of Neurochemistry(2020)10.1111/jnc.14974

N/A

0DataRank · unranked

21 citations

Kenneth H. Fischbeck, Angelo Poletti

Variants in ATP6V0A1 cause progressive myoclonus epilepsy and developmental and epileptic encephalopathy

Brain Communications(2021)10.1093/braincomms/fcab245

N/A

0DataRank · unranked

32 citations

Mitra Forouhan, Maria Lieto, Ambre J. Sala, Ruth Ellerington, Janel O. Johnson +53 more

Improving the efficacy of exome sequencing at a quaternary care referral centre: novel mutations, clinical presentations and diagnostic challenges in rare neurogenetic diseases

Journal of Neurology Neurosurgery & Psychiatry(2021)10.1136/jnnp-2020-325437

N/A

0DataRank · unranked

22 citations

Nathan Sarkar, Joyce Lu, Mallory Owen, Alice B. Schindler, Peter A. Calabresi +13 more

Dynamic Balance in Spinal and Bulbar Muscular Atrophy: Relationship between Strength and Performance of Forward Lunge, Step Up and Over, and Step Quick Turn

Rehabilitation Research and Practice(2021)10.1155/2021/2540324

N/A

0DataRank · unranked

1 citations

Ashwini Sansare, Vincent Shieh, Joshua G. Woolstenhulme, Julie Rekant, Rafael Jiménez‐Silva +6 more

Friedreich ataxia in a family from Mali, West Africa

(2021)10.22541/au.161414432.28217723/v1

N/A

0DataRank · unranked

0 citations

Lassana Cissé, Hamidou O Bah, Oumar Samassékou, Assiatou Simaga, Abdoulaye Taméga +12 more

Biallelic and de novo variants in ATP6V0A1 cause progressive myoclonus epilepsy and developmental and epileptic encephalopathy

medRxiv(2021)10.1101/2021.06.01.21257500

N/A

0DataRank · unranked

0 citations

Mitra Forouhan, Maria Lieto, Ambre J. Sala, Ruth Ellerington, Janel O. Johnson +21 more

Altered SYNJ2BP-mediated mitochondrial-ER contacts in motor neuron disease

Neurobiology of Disease(2022)10.1016/j.nbd.2022.105832

N/A

0DataRank · unranked

15 citations

Ester Masati, Amber Lopez, Eric Bunker, Allison Snyder, Nancy A. Edwards +4 more

GJB1 variants in Charcot‐Marie‐Tooth disease X‐linked type 1 in Mali

Journal of the Peripheral Nervous System(2022)10.1111/jns.12486

N/A

0DataRank · unranked

5 citations

Seybou Hassane Diallo, Lassana Cissé, Mamadou Karembé, Salimata Diallo, Thomas Coulibaly +8 more

Pentanucleotide Repeat Insertions in RAI1 Cause Benign Adult Familial Myoclonic Epilepsy Type 8

Movement Disorders(2023)10.1002/mds.29654

N/A

0DataRank · unranked

24 citations

Mohamed E. Dembélé, Monnat Pongpanich, Lassana Cissé, Chalurmpon Srichomthong, Alassane Baneye Maīga +15 more

Patient-Reported Impact of Symptoms in Spinal and Bulbar Muscular Atrophy

Neurology Clinical Practice(2023)10.1212/cpj.0000000000200213

N/A

0DataRank · unranked

3 citations

Angela Kokkinis, Christine Zizzi, Nuran Dilek, Kenneth H. Fischbeck, Chad Heatwole +2 more

AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia

Neurobiology of Disease(2024)10.1016/j.nbd.2024.106537

N/A

0DataRank · unranked

5 citations

Saikat Ghosh, Lassana Cissé, Thomas Coulibaly, Abdoulaye Yalcouyé, George G. Harmison +20 more

A Novel Splice Site Variant in COL6A1 Causes Ullrich Congenital Muscular Dystrophy in a Consanguineous Malian Family

Molecular Genetics & Genomic Medicine(2024)10.1002/mgg3.70032

N/A

0DataRank · unranked

2 citations

I.S. Pamanta, Salia Bamba, Lassana Cissé, Salimata Diarra, Sidi Touré +11 more

Genetic profile of progressive myoclonic epilepsy in Mali reveals novel findings

Frontiers in Neurology(2024)10.3389/fneur.2024.1455467

N/A

0DataRank · unranked

1 citations

Salia Bamba, Seybou Hassane Diallo, Weizhen Ji, M Dembélé, Abdoulaye Yalcouyé +18 more

271st ENMC international workshop: Towards a unifying effort to fight Kennedy's disease. 20-22 October 2023, Hoofddorp, Netherlands

Neuromuscular Disorders(2024)10.1016/j.nmd.2024.03.003

N/A

0DataRank · unranked

0 citations

P.-F. Pradat, Linda Greensmith, Manuela Basso, Marco Bertolotti, Marco Bertolotti +24 more

Evaluation of Sensory and Motor Function in Spinal and Bulbar Muscular Atrophy Using Quiet Stance and Reactive Postural Control

Neurology International(2025)10.3390/neurolint17060079

N/A

0DataRank · unranked

1 citations

Ashwini Sansare, Allison C. Niemic, Rafael Jiménez‐Silva, Joshua G. Woolstenhulme, Galen O. Joe +6 more

Molecular pathogenesis of spinal bulbar muscular atrophy (Kennedy's disease) and avenues for treatment

Current Opinion in Neurology(2020)10.1097/wco.0000000000000856

N/A

0DataRank · unranked

20 citations

Kenneth H. Fischbeck, Christopher Grunseich

Identifying Clinical Measures Related to Falls in Ambulatory Patients with Spinal and Bulbar Muscular Atrophy

Neurology International(2025)10.3390/neurolint17060080

N/A

0DataRank · unranked

0 citations

Allison C. Niemic, Rafael Jiménez‐Silva, Joshua G. Woolstenhulme, Galen O. Joe, Uma Jacobs +6 more

Kenneth H. Fischbeck

Indexed papers

Top data-sharing exemplar

Papers