Gholson J. Lyon

Also affiliated with City University of New York, New York State Office for People With Developmental Disabilities

Biochemistry, Genetics and Molecular BiologyMedicinePsychology

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 2%percentile

4.2Author 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 →

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

Phen2Gene: rapid phenotype-driven gene prioritization for rare diseases

NAR Genomics and Bioinformatics(2020)10.1093/nargab/lqaa032

Top 7%

3.3DataRank

Top 7%87 citations

James M. Havrilla, Fang Li, Ying Chen, Jacqueline Peng, Cong Liu +8 more

Papers

Driven by 37 papers — median percentile 61. Top paper: “Phen2Gene: rapid phenotype-driven gene prioritization for rare diseases”.

Phen2Gene: rapid phenotype-driven gene prioritization for rare diseases

NAR Genomics and Bioinformatics(2020)10.1093/nargab/lqaa032

Top 7%

3.3DataRank

Top 7%87 citations

James M. Havrilla, Fang Li, Ying Chen, Jacqueline Peng, Cong Liu +8 more

Sex Differences in Natural History and Health Outcomes Among Individuals With Tic Disorders

Neurology(2025)10.1212/wnl.0000000000210249

Top 39%

0.492DataRank

Top 39%11 citations

Lori B. Chibnik, Natasha Tracy, Lisa Osiecki, Cathy L. Budman, Daniëlle C. Cath +10 more

Genome-Wide Association Study Meta-Analysis of 9619 Cases With Tic Disorders

Biological Psychiatry(2024)10.1016/j.biopsych.2024.07.025

Top 44%

0.421DataRank

Top 44%13 citations

Matthew Halvorsen, Jakob Grove, Bergrún Ásbjörnsdóttir, Pétur Lúðvígsson, Ólafur Thorarensen +93 more

Synaptic processes and immune-related pathways implicated in Tourette syndrome

Translational Psychiatry(2021)10.1038/s41398-020-01082-z

N/A

0DataRank · unranked

58 citations

Dongmei Yu, Jae Hoon Sul, Alden Y. Huang, Cornelia Illmann, Lisa Osiecki +66 more

Is Persistent Motor or Vocal Tic Disorder a Milder Form of Tourette Syndrome?

Movement Disorders(2021)10.1002/mds.28593

N/A

0DataRank · unranked

45 citations

Daniel A. Stevens, Sang‐Wahn Koo, Alexa Valko, O. Joseph Bienvenu, Cathy B. Budman +26 more

Elevated common variant genetic risk for tourette syndrome in a densely-affected pedigree

Molecular Psychiatry(2021)10.1038/s41380-021-01277-w

N/A

0DataRank · unranked

10 citations

Jin Szatkiewicz, Poorva Mudgal, Dongmei Yu, H.N. Aschauer, Gil Atzmon +94 more

Naa12 compensates for Naa10 in mice in the amino-terminal acetylation pathway

eLife(2021)10.7554/elife.65952

N/A

0DataRank · unranked

14 citations

Mi-Ni Lee, Max J. Dörfel, Seungwoon Seo, Leah Gottlieb, Thomas Papazyan +24 more

SvAnna: efficient and accurate pathogenicity prediction for coding and regulatory structural variants in long-read genome sequencing

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.07.14.452267

N/A

0DataRank · unranked

2 citations

Julius O.B. Jacobsen, Parithi Balachandran, Qihui Zhu, Feyza Yilmaz, Justin T Reese +9 more

SvAnna: efficient and accurate pathogenicity prediction of coding and regulatory structural variants in long-read genome sequencing

Genome Medicine(2022)10.1186/s13073-022-01046-6

N/A

0DataRank · unranked

42 citations

Julius O.B. Jacobsen, Parithi Balachandran, Qihui Zhu, Feyza Yilmaz, Justin T Reese +9 more

KBG syndrome: videoconferencing and use of artificial intelligence driven facial phenotyping in 25 new patients

European Journal of Human Genetics(2022)10.1038/s41431-022-01171-1

N/A

0DataRank · unranked

31 citations

Jiyeon Park, Edward Yi, Elaine Marchi, Tzung‐Chien Hsieh, Yana Kibalnyk +10 more

Expanding the Phenotypic spectrum of NAA10 -related neurodevelopmental syndrome and NAA15 -related neurodevelopmental syndrome

medRxiv(2022)10.1101/2022.08.22.22279061

N/A

0DataRank · unranked

7 citations

Marall Vedaie, Travis Besheim, Agnes Park, Elaine Marchi, Leah Gottlieb +19 more

PhenoScore: AI-based phenomics to quantify rare disease and genetic variation

medRxiv(2022)10.1101/2022.10.24.22281480

N/A

0DataRank · unranked

6 citations

Max Hinne, Kim M. G. Truijen, Lia Goltstein, Jeroen van Reeuwijk, Nicole de Leeuw +26 more

Phenotypic variability and Gastrointestinal Manifestations/Interventions for growth in Ogden syndrome (also known as NAA10 -related Syndrome)

medRxiv(2022)10.1101/2022.03.16.22272517

N/A

0DataRank · unranked

4 citations

Elaine Marchi, Maureen Gavin, Karen Amble, Gholson J. Lyon, Katherine Sandomirsky

PhenoScore quantifies phenotypic variation for rare genetic diseases by combining facial analysis with other clinical features using a machine-learning framework

Nature Genetics(2023)10.1038/s41588-023-01469-w

N/A

0DataRank · unranked

77 citations

Max Hinne, Kim M. G. Truijen, Lia Goltstein, Jeroen van Reeuwijk, Nicole de Leeuw +28 more

Expanding the phenotypic spectrum of NAA10-related neurodevelopmental syndrome and NAA15-related neurodevelopmental syndrome

European Journal of Human Genetics(2023)10.1038/s41431-023-01368-y

N/A

0DataRank · unranked

52 citations

Marall Vedaie, Travis Beisheim, Agnes Park, Elaine Marchi, Leah Gottlieb +19 more

Genome-Wide Association Study Points to Novel Locus for Gilles de la Tourette Syndrome

Biological Psychiatry(2023)10.1016/j.biopsych.2023.01.023

N/A

0DataRank · unranked

31 citations

Apostolia Topaloudi, Pritesh Jain, Zhiyu Yang, Dongmei Yu, Petros Kolovos +94 more

Studying Long QT Syndrome Caused by NAA10 Genetic Variants Using Patient-Derived Induced Pluripotent Stem Cells

Circulation(2023)10.1161/circulationaha.122.061864

N/A

0DataRank · unranked

16 citations

Yiyang Wu, Mengcheng Shen, Sophia Zhang, Joe Z. Zhang, Chun Liu +5 more

Phenotypic variability and gastrointestinal manifestations/interventions for growth in NAA10‐related neurodevelopmental syndrome

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63152

N/A

0DataRank · unranked

9 citations

Elaine Marchi, Maureen Gavin, Karen Amble, Gholson J. Lyon, Katherine Sandomirsky

Evaluating possible maternal effect lethality and genetic background effects in Naa10 knockout mice

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.04.27.538618

N/A

0DataRank · unranked

1 citations

Joseph Longo, Andrew Garcia, Fatima Inusa, Elaine Marchi, Daniel Shi +7 more

The Challenge of Examining Social Determinants of Health in People Living With Tourette Syndrome

Pediatric Neurology(2024)10.1016/j.pediatrneurol.2024.02.008

N/A

0DataRank · unranked

9 citations

Samuel J. Carr, Angela Essa, Lisa Osiecki, Daniel T. Lackland, Jenifer H. Voeks +14 more

Longitudinal adaptive behavioral outcomes in Ogden syndrome by seizure status and therapeutic intervention

American Journal of Medical Genetics Part A(2024)10.1002/ajmg.a.63651

N/A

0DataRank · unranked

9 citations

Carolina Christ, Elaine Marchi, Randie Harpell, Gholson J. Lyon, Rikhil Makwana

Ophthalmic manifestations of NAA10 ‐related and NAA15 ‐related neurodevelopmental syndromes: Analysis of cortical visual impairment and refractive errors

American Journal of Medical Genetics Part A(2024)10.1002/ajmg.a.63821

N/A

0DataRank · unranked

6 citations

Agnes Park, Elaine Marchi, Andrea Gropman, Matthew T. Whitehead, Gholson J. Lyon +1 more

Evaluating possible maternal effect lethality and genetic background effects in Naa10 knockout mice

PLoS ONE(2024)10.1371/journal.pone.0301328

N/A

0DataRank · unranked

3 citations

Joseph Longo, Andrew Garcia, Fatima Inusa, Elaine Marchi, Daniel Shi +7 more

Sex Differences in People with Tourette Syndrome and Persistent Motor or Vocal Tic Disorder in the Tourette Association of America International Consortium for Genetics Database

medRxiv(2024)10.1101/2024.01.07.24300816

N/A

0DataRank · unranked

10 citations

Lori B. Chibnik, Natasha Tracy, Lisa Osiecki, Cathy L. Budman, Daniëlle C. Cath +10 more

A Natural History of NAA15 -related Neurodevelopmental Disorder Through Adolescence

medRxiv(2024)10.1101/2024.04.20.24306120

N/A

0DataRank · unranked

7 citations

Carolina Christ, Rahi Patel, Elaine Marchi, Randie Harpell, Gholson J. Lyon +1 more

Ophthalmic Manifestations of NAA10-Related and NAA15-Related Neurodevelopmental Syndrome: Analysis of Cortical Visual Impairment and Refractive Errors

medRxiv(2024)10.1101/2024.02.01.24302161

N/A

0DataRank · unranked

6 citations

Agnes Park, Elaine Marchi, Andrea Gropman, Matthew T. Whitehead, Gholson J. Lyon +1 more

Longitudinal Adaptive Behavioral Outcomes in Ogden Syndrome by Seizure Status and Therapeutic Intervention

medRxiv(2024)10.1101/2024.02.23.24303144

N/A

0DataRank · unranked

4 citations

Carolina Christ, Elaine Marchi, Randie Harpell, Gholson J. Lyon, Rikhil Makwana

Neuroanatomical Features of NAA10- and NAA15-Related Neurodevelopmental Syndromes

medRxiv(2024)10.1101/2024.06.24.24309433

N/A

0DataRank · unranked

4 citations

Rikhil Makwana, Carolina Christ, Elaine Marchi, Nathaniel Ung, Randie Harpell +5 more

A repository of Ogden syndrome patient derived iPSC lines and isogenic pairs by X-chromosome screening and genome-editing

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.09.28.615067

N/A

0DataRank · unranked

1 citations

Tom Rusielewicz, Yu-Ren Chen, Brigham J. Hartley, Dayna McKenzie, Matthew Yim +16 more

DNA-binding affinity and specificity determine the phenotypic diversity in BCL11B-related disorders

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2024.12.012

N/A

0DataRank · unranked

6 citations

Anja Barešić, Iván K. Chinn, Jonathan May, Anu Goenka, Kate Chandler +91 more

The Cardiovascular Manifestations and Management Recommendations for Ogden Syndrome

Pediatric Cardiology(2025)10.1007/s00246-025-03877-7

N/A

0DataRank · unranked

3 citations

Rahi Patel, Rosemary O’Neill, Elaine Marchi, Gholson J. Lyon, Rikhil Makwana

HYPK ‐Related Neurodevelopmental Syndrome: Case Report of Intellectual Disability, Developmental Delay, and Dysmorphic Features

Clinical Genetics(2025)10.1111/cge.70039

N/A

0DataRank · unranked

1 citations

Rikhil Makwana, Elaine Marchi, Ziyi Fan, Erin Falsey, Beatriz Menéndez +6 more

Natural History of NAA15‐Related Neurodevelopmental Disorder Through Adolescence

American Journal of Medical Genetics Part A(2025)10.1002/ajmg.a.64009

N/A

0DataRank · unranked

1 citations

Carolina Christ, Rahi Patel, Elaine Marchi, Randie Harpell, Gholson J. Lyon +1 more

The Cardiovascular Manifestations and Management Recommendations for Ogden Syndrome

medRxiv(2025)10.1101/2025.02.11.25321331

N/A

0DataRank · unranked

1 citations

Rahi Patel, Rosemary O’Neill, Elaine Marchi, Gholson J. Lyon, Rikhil Makwana

DNA-binding affinity and specificity determine the phenotypic diversity in BCL11B-related disorders

UNC Libraries(2025)10.17615/dy6f-xt03

N/A

0DataRank · unranked

0 citations

Benjamin Cogné, Rachel Rabin, E Kessler, Céline Chappé, Melanie Brügger +92 more

Synaptic processes and immune-related pathways implicated in Tourette Syndrome

medRxiv(2020)10.1101/2020.04.24.20047845

N/A

0DataRank · unranked

7 citations

Dongmei Yu, Jae Hoon Sul, Alden Y. Huang, Cornelia Illmann, Lisa Osiecki +59 more

Naa12 compensates for Naa10 in mice in the amino-terminal acetylation pathway

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.12.19.422860

N/A

0DataRank · unranked

0 citations

Mi-Ni Lee, Max J. Dörfel, Seungwoon Seo, Leah Gottlieb, Thomas Papazyan +24 more

Gholson J. Lyon

Indexed papers

Top data-sharing exemplar

Papers