Jeffrey L. Neul

Also affiliated with John F. Kennedy Center for the Performing Arts, Kennedy Center, Vanderbilt Health, Vanderbilt University Medical Center

Biochemistry, Genetics and Molecular BiologyNeurosciencePsychologyMedicine

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

1.0Author DataRank

Indexed papers

4in 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 4 indexed papers 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 variants paired with phenotype: A rich resource for brain gene curation

Genetics in Medicine(2023)10.1016/j.gim.2023.101035

Top 35%

0.557DataRank

Top 35%11 citations

Juliann M. Savatt, Taylor I. Bingaman, Molly Good, Alexis Morgan, Caitlin Cooney +37 more

Papers

Driven by 35 papers — median percentile 37. Top paper: “Trofinetide for the treatment of Rett syndrome: a randomized phase 3 study”.

Trofinetide for the treatment of Rett syndrome: a randomized phase 3 study

Nature Medicine(2023)10.1038/s41591-023-02398-1

N/A

4.2DataRank · unranked

190 citations

Alan K. Percy, Tim A. Benke, Elizabeth Berry‐Kravis, Daniel G. Glaze, Eric D. Marsh +5 more

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

Anxiety-like behavior and anxiolytic treatment in the Rett syndrome natural history study

Journal of Neurodevelopmental Disorders(2022)10.1186/s11689-022-09432-2

N/A

0.897DataRank · unranked

45 citations

Jennifer L. Stallworth, Aubin E. Joy, Rebekah E. Dixon, Alexandra E. Scott, Arthur Beisang +16 more

Clinical variants paired with phenotype: A rich resource for brain gene curation

Genetics in Medicine(2023)10.1016/j.gim.2023.101035

Top 35%

0.557DataRank

Top 35%11 citations

Juliann M. Savatt, Taylor I. Bingaman, Molly Good, Alexis Morgan, Caitlin Cooney +37 more

Modeling antisense oligonucleotide therapy in MECP2 duplication syndrome human iPSC-derived neurons reveals gene expression programs responsive to MeCP2 levels

Human Molecular Genetics(2024)10.1093/hmg/ddae135

N/A

0.383DataRank · unranked

10 citations

Yehezkel Sztainberg, Alexander J. Trostle, Harini P Tirumala, Ying‐Wooi Wan, Caroline L Harrop +10 more

The Brain Gene Registry: a data snapshot

Journal of Neurodevelopmental Disorders(2024)10.1186/s11689-024-09530-3

Top 48%

0.373DataRank

Top 48%11 citations

Levi Kaster, Catherine Sancimino, Siddharth Srivastava, Sophie Molholm, Aditi Gupta +58 more

Natural history of epilepsy in FOXG1 Syndrome

Epilepsy Research(2025)10.1016/j.eplepsyres.2025.107644

Top 78%

0.104DataRank

Top 78%1 citations

Benjamin Rees, Holly Dubbs, Mollie Lesser, Lucas E. Morgan, Tim A. Benke +4 more

Rett Syndrome and MECP2 Duplication Syndrome: Disorders of MeCP2 Dosage

Neuropsychiatric Disease and Treatment(2022)10.2147/ndt.s371483

N/A

0DataRank · unranked

83 citations

Jeffrey L. Neul, Bridget E. Collins

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

Anthropometric Measures Correspond with Functional Motor Outcomes in Females with Rett Syndrome

The Journal of Pediatrics(2022)10.1016/j.jpeds.2022.01.009

N/A

0DataRank · unranked

16 citations

Suzanne Geerts, Fran Annese, Jeffrey L. Neul, Tim A. Benke, Eric D. Marsh +11 more

Behavioral and brain anatomical analysis of Foxg1 heterozygous mice

PLoS ONE(2022)10.1371/journal.pone.0266861

N/A

0DataRank · unranked

9 citations

Rebekah Farmer, Jonathan K. Merritt, Zeljka Miletic Lanaghan, Mark D. Does, Karthik Ramadass +4 more

Behavioral and imaging analysis of Foxg1 heterozygous mice

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.03.29.486318

N/A

0DataRank · unranked

0 citations

Rebekah Lifer, Jonathan K. Merritt, Zeljka Miletic Lanaghan, Mark D. Does, Karthik Ramadass +4 more

A review of the Rett Syndrome Behaviour Questionnaire and its utilization in the assessment of symptoms associated with Rett syndrome

Frontiers in Pediatrics(2023)10.3389/fped.2023.1229553

N/A

0DataRank · unranked

31 citations

Jeffrey L. Neul, Tim A. Benke, Eric D. Marsh, Daniel G. Glaze, Alan K. Percy

Distribution of hand function by age in individuals with Rett syndrome

Annals of the Child Neurology Society(2023)10.1002/cns3.20038

N/A

0DataRank · unranked

12 citations

Tim A. Benke, Eric D. Marsh, Jane B. Lane, David N. Lieberman, Steven A. Skinner +11 more

Parental age effects and Rett syndrome

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63396

N/A

0DataRank · unranked

3 citations

Lauren M. Baggett, Raymond Caylor, Alan K. Percy, Jeffrey L. Neul, Jane B. Lane +8 more

Top Caregiver Concerns in Rett syndrome and related disorders: data from the US Natural History Study

Research Square(2023)10.21203/rs.3.rs-2566253/v1

N/A

0DataRank · unranked

14 citations

Tim A. Benke, Eric D. Marsh, Bernhard Suter, Lori Silveira, Cary Fu +4 more

Rett syndrome: The Natural History Study journey

Annals of the Child Neurology Society(2024)10.1002/cns3.20086

N/A

0DataRank · unranked

11 citations

Tim A. Benke, Eric D. Marsh, Jeffrey L. Neul, Alan K. Percy

Burden of illness in Rett syndrome: initial evaluation of a disorder-specific caregiver survey

Orphanet Journal of Rare Diseases(2024)10.1186/s13023-024-03313-8

N/A

0DataRank · unranked

10 citations

Alan K. Percy, Jeffrey L. Neul, Jenny Downs, Helen Leonard, Paige Nues +12 more

International workshop: what is needed to ensure outcome measures for Rett syndrome are fit-for-purpose for clinical trials? June 7, 2023, Nashville, USA

Trials(2024)10.1186/s13063-024-08678-6

N/A

0DataRank · unranked

9 citations

Dominique C. Pichard, Walter E. Kaufmann, Joseph P. Horrigan, Melissa Raspa, Gillian S. Townend +17 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

Clinical and genetic delineation of autosomal recessive and dominant ACTL6B-related developmental brain disorders

Genetics in Medicine(2024)10.1016/j.gim.2024.101251

N/A

0DataRank · unranked

4 citations

Tania Quirin, Clarissa Rocca, Stéphanie Efthymiou, Antonella Riva, Dana Marafi +95 more

Normalized Clinical Severity Scores Reveal a Correlation between X Chromosome Inactivation and Disease Severity in Rett Syndrome

Genes(2024)10.3390/genes15050594

N/A

0DataRank · unranked

8 citations

Xiaolan Fang, Raymond Caylor, Steven A. Skinner, Michael J. Friez, Alan K. Percy +2 more

Potentiation of the muscarinic acetylcholine receptor 1 modulates neurophysiological features in a mouse model of Rett syndrome

Neurotherapeutics(2024)10.1016/j.neurot.2024.e00384

N/A

0DataRank · unranked

4 citations

Kelly Weiss, Kathryn Baugh, Mac Meadows, Colleen M. Niswender, Jeffrey L. Neul +1 more

Rett syndrome diagnostic odyssey: Limitations of NextGen sequencing

American Journal of Medical Genetics Part A(2024)10.1002/ajmg.a.63725

N/A

0DataRank · unranked

3 citations

Katie Angione, Emily K. Forbes, Mikayla Stoecker, Margarita Sáenz, Jeffrey L. Neul +5 more

Phenotyping Down syndrome: discovery and predictive modelling with electronic medical records

Journal of Intellectual Disability Research(2024)10.1111/jir.13124

Top 100%

0DataRank

Top 100%0 citations

Cailey I. Kerley, Alexandra P. Key, Angie Maxwell‐Horn, Quinn S. Wells, Jeffrey L. Neul +3 more

MeCP2 prevents against sustained ketamine-induced synaptic depression at inhibitory synapses

iScience(2025)10.1016/j.isci.2025.112485

N/A

0DataRank · unranked

2 citations

Abigael R. Weit, Ege T. Kavalali, Jeffrey L. Neul, Lisa M. Monteggia, Michelle K. Piazza

Symptom Onset in Classic Rett Syndrome: Analysis of Initial Clinical Severity Scale Entries

Annals of the Child Neurology Society(2025)10.1002/cns3.70017

N/A

0DataRank · unranked

1 citations

Jeffrey L. Neul, Amitha Ananth, Tim A. Benke, Eric D. Marsh, Alan K. Percy

Loss of MeCP2 Function Across Several Neuronal Populations Impairs Breathing Response to Acute Hypoxia

Frontiers in Neurology(2020)10.3389/fneur.2020.593554

N/A

0DataRank · unranked

20 citations

Teng-Wei Huang, José A. Herrera, Rodney C. Samaco, Christopher M. McGraw, Diana Parra +7 more

Trajectory of skill acquisition, loss, and regain in females with classic Rett syndrome

Research Square(2025)10.21203/rs.3.rs-8245192/v1

N/A

0DataRank · unranked

0 citations

Tim A. Benke, Eric D. Marsh, Sarika U. Peters, Cary Fu, Jonathan K. Merritt +2 more

Metabolic Signatures Differentiate Rett Syndrome From Unaffected Siblings

Frontiers in Integrative Neuroscience(2020)10.3389/fnint.2020.00007

N/A

0DataRank · unranked

44 citations

Steven A. Skinner, Fran Annese, Jane B. Lane, Peter Heydemann, Mary Jones +4 more

Pharmacological read-through of R294X Mecp2 in a novel mouse model of Rett syndrome

Human Molecular Genetics(2020)10.1093/hmg/ddaa102

N/A

0DataRank · unranked

29 citations

Bridget E. Collins, Kirsty R. Erickson, Hong‐Wei Dong, Jeffrey L. Neul, Jonathan K. Merritt

Cortisol profiles and clinical severity in MECP2 duplication syndrome

Journal of Neurodevelopmental Disorders(2020)10.1186/s11689-020-09322-5

N/A

0DataRank · unranked

3 citations

Cary Fu, Jeffrey L. Neul, Douglas A. Granger, Sarika U. Peters

Current neurologic treatment and emerging therapies in CDKL5 deficiency disorder

Journal of Neurodevelopmental Disorders(2021)10.1186/s11689-021-09384-z

N/A

0DataRank · unranked

48 citations

Carolyn I. Daniels, Isabel Haviland, Lindsay C. Swanson, Caitlin Greene, Anne Marie M. Denny +14 more

Safety and efficacy of genetic MECP2 supplementation in the R294X mouse model of Rett syndrome

Genes Brain & Behavior(2021)10.1111/gbb.12739

N/A

0DataRank · unranked

24 citations

Jonathan K. Merritt, Kirsty R. Erickson, Jeffrey L. Neul, Bridget E. Collins

Recommendations by the ClinGen Rett/Angelman‐like expert panel for gene‐specific variant interpretation methods

Human Mutation(2021)10.1002/humu.24302

N/A

0DataRank · unranked

16 citations

Lora Jh Bean, Izabela Karbassi, Katelynn Beattie, Thierry Bienvenu, Hope Bonin +13 more

Jeffrey L. Neul

Indexed papers

Top data-sharing exemplar

Papers