🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Bernhard Suter

Baylor College of Medicine

ORCID: 0000-0002-0127-7322

Also affiliated with Texas Children's Hospital

Biochemistry, Genetics and Molecular BiologyNeurosciencePsychology

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 5%percentile
0.424Author DataRank

Indexed papers

3in 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 3 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 →

Top data-sharing exemplar

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

Pangenome discovery of missing autism variants

medRxiv(2025)10.1101/2025.07.21.25331932
Top 63%
0.216DataRank
Top 63%3 citations

Jiadong Lin, Michelle D. Noyes, Young-Jun Kwon, Isaac Wong, Nidhi Koundinya +23 more

Papers

Driven by 21 papers — median percentile 35. 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

Structural variant allelic heterogeneity in MECP2 duplication syndrome provides insight into clinical severity and variability of disease expression

Genome Medicine(2024)10.1186/s13073-024-01411-7
N/A
0.474DataRank · unranked
17 citations

Jesse D. Bengtsson, Sameer S. Bajikar, Christopher M. Grochowski, Ming Yin Lun, Mira Gandhi +38 more

Pangenome discovery of missing autism variants

medRxiv(2025)10.1101/2025.07.21.25331932
Top 63%
0.216DataRank
Top 63%3 citations

Jiadong Lin, Michelle D. Noyes, Young-Jun Kwon, Isaac Wong, Nidhi Koundinya +23 more

Using the linear references from the pangenome to discover missing autism variants

Nature Communications(2026)10.1038/s41467-026-68378-4
Top 65%
0.208DataRank
Top 65%3 citations

Jiadong Lin, Michelle D. Noyes, Young-Jun Kwon, Isaac Wong, Nidhi Koundinya +252 more

Content Validation of Clinician-Reported Items for a Severity Measure for CDKL5 Deficiency Disorder

Journal of Child Neurology(2021)10.1177/08830738211019576
N/A
0DataRank · unranked
27 citations

Judith Weisenberg, Elia Pestana‐Knight, Eric D. Marsh, Bernhard Suter, Rajsekar R. Rajaraman +10 more

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

Epileptic spasms in CDKL5 deficiency disorder: Delayed treatment and poor response to first‐line therapies

Epilepsia(2023)10.1111/epi.17630
N/A
0DataRank · unranked
11 citations

Scott Demarest, Elia Pestana‐Knight, Ahsan N. Moosa, Xiaoming Zhang, José R. Pérez‐Pérez +17 more

The development, content and response process validation of a caregiver-reported severity measure for CDKL5 deficiency disorder

Epilepsy Research(2023)10.1016/j.eplepsyres.2023.107231
N/A
0DataRank · unranked
8 citations

Alexandra T. Mackie, Jacinta Saldaris, Helen Leonard, Peter Jacoby, Eric D. Marsh +11 more

Generation of five induced pluripotent stem cell lines from patients with MECP2 Duplication Syndrome

Stem Cell Research(2023)10.1016/j.scr.2023.103292
N/A
0DataRank · unranked
2 citations

Gerarda Cappuccio, Jennifer L. Sheppard, Magdalena Delacruz, Jesse D. Bengtsson, Claudia M.B. Carvalho +9 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

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

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
0DataRank · unranked
10 citations

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

Adapting a measure of gross motor skills for individuals with CDKL5 deficiency disorder: A psychometric study

Epilepsy Research(2024)10.1016/j.eplepsyres.2024.107287
N/A
0DataRank · unranked
7 citations

Peter Jacoby, Eric D. Marsh, Bernhard Suter, Helen Leonard, Heather E. Olson +9 more

Psychometric evaluation of clinician‐ and caregiver‐reported clinical severity assessments for individuals with CDKL5 deficiency disorder

Epilepsia(2024)10.1111/epi.18094
N/A
0DataRank · unranked
5 citations

Peter Jacoby, Jenny Downs, Eric D. Marsh, Helen Leonard, Elia Pestana‐Knight +10 more

Sensory experiences questionnaire unravels differences in sensory profiles between MECP2‐related disorders

Autism Research(2024)10.1002/aur.3112
N/A
0DataRank · unranked
5 citations

Davut Pehli̇van, Muharrem Ak, Holly K. Harris, Ariel M. Lyons‐Warren, Bernhard Suter

Modification of a parent-report sleep scale for individuals with CDKL5 deficiency disorder: a psychometric study

Journal of Clinical Sleep Medicine(2024)10.5664/jcsm.11244
N/A
0DataRank · unranked
4 citations

Scott Demarest, Peter Jacoby, Heather E. Olson, Kiran Maski, Elia Pestana‐Knight +9 more

Deletions in the CDKL5 5′ untranslated region lead to CDKL5 deficiency disorder

American Journal of Medical Genetics Part A(2024)10.1002/ajmg.a.63843
N/A
0DataRank · unranked
2 citations

Ralph D. Hector, Lindsay C. Swanson, Aubrie Soucy Verran, Emma Sherrill, Zoë Frazier +20 more

Excessive Formation and Stabilization of Dendritic Spine Clusters in the MECP2-Duplication Syndrome Mouse Model of Autism

eNeuro(2020)10.1523/eneuro.0282-20.2020
N/A
0DataRank · unranked
14 citations

Jiyoung Park, Bernhard Suter, Huda Y. Zoghbi, Stelios M. Smirnakis, Ryan T. Ash

Beyond Seizures as an Outcome Measure: A Global Severity Scoring System for CDKL5 Deficiency Disorder

Brain and Behavior(2025)10.1002/brb3.71061
Top 100%
0DataRank
Top 100%0 citations

Eric D. Marsh, Scott Demarest, Jacinta Saldaris, Helen Leonard, Heather E. Olson +9 more