Gareth Baynam

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 1%percentile

5.2Author DataRank

Indexed papers

2in 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 2 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.

The Human Phenotype Ontology in 2024: phenotypes around the world

Nucleic Acids Research(2023)10.1093/nar/gkad1005

Top 6%

3.9DataRank

Top 6%387 citations

Nicolas A Matentzoglu, Ben D Coleman, Eunice B Addo-Lartey, Anna V. Anagnostopoulos, Joel Anderton +95 more

Papers

Driven by 20 papers — median percentile 89. Top paper: “The Human Phenotype Ontology in 2024: phenotypes around the world”.

The Human Phenotype Ontology in 2024: phenotypes around the world

Nucleic Acids Research(2023)10.1093/nar/gkad1005

Top 6%

3.9DataRank

Top 6%387 citations

Nicolas A Matentzoglu, Ben D Coleman, Eunice B Addo-Lartey, Anna V. Anagnostopoulos, Joel Anderton +95 more

The GA4GH Phenopacket schema defines a computable representation of clinical data

Nature Biotechnology(2022)10.1038/s41587-022-01357-4

N/A

2.4DataRank · unranked

111 citations

Michael Baudis, Gareth Baynam, J. Beckmann, Sergi Beltrán, Orion J. Buske +62 more

The case for open science: rare diseases

JAMIA Open(2020)10.1093/jamiaopen/ooaa030

N/A

2.2DataRank · unranked

63 citations

Peter N. Robinson, William A. Gahl, Paul Avillach, Gareth Baynam, Helene Cederroth +20 more

Survival of infants born with esophageal atresia among 24 international birth defects surveillance programs

Birth Defects Research(2021)10.1002/bdr2.1891

Top 17%

1.2DataRank

Top 17%30 citations

Gareth Baynam, Jorieke E. H. Bergman, Eva Bermejo, Lorenzo D. Botto, Mark A. Canfield +24 more

The GA4GH Phenopacket schema: A computable representation of clinical data for precision medicine

medRxiv(2021)10.1101/2021.11.27.21266944

N/A

0.631DataRank · unranked

14 citations

Michael Baudis, Gareth Baynam, J. Beckmann, Sergi Beltrán, Tiffany J. Callahan +42 more

An evaluation of GPT models for phenotype concept recognition

BMC Medical Informatics and Decision Making(2024)10.1186/s12911-024-02439-w

N/A

0.550DataRank · unranked

38 citations

Harry Caufield, Dylan Gration, Gareth Baynam, Melissa A Haendel, Peter N. Robinson +3 more

Advancing diagnosis and research for rare genetic diseases in Indigenous peoples

Nature Genetics(2024)10.1038/s41588-023-01642-1

N/A

0.416DataRank · unranked

15 citations

Daria Julkowska, Sarah Bowdin, Azure Hermes, Christopher R. McMaster, Elissa Prichep +20 more

Deletion of ERF and CIC causes abnormal skull morphology and global developmental delay

Molecular Case Studies(2021)10.1101/mcs.a005991

N/A

0.241DataRank · unranked

4 citations

Ana S.A. Cohen, Cathryn Poulton, Tina Duelund Hjortshøj, Moe Akahira‐Azuma, Geetu Mendiratta +10 more

An evaluation of GPT models for phenotype concept recognition

arXiv (Cornell University)(2023)10.48550/arxiv.2309.17169

N/A

0.104DataRank · unranked

1 citations

Harry Caufield, Dylan Gration, Gareth Baynam, Melissa A Haendel, Peter N. Robinson +3 more

FastHPOCR: pragmatic, fast, and accurate concept recognition using the human phenotype ontology

Bioinformatics(2024)10.1093/bioinformatics/btae406

N/A

0DataRank · unranked

12 citations

Dylan Gration, Gareth Baynam, Peter N. Robinson, Tudor Groza

Fatal Perinatal Mitochondrial Cardiac Failure Caused by Recurrent De Novo Duplications in the ATAD3 Locus

Med(2020)10.1016/j.medj.2020.06.004

N/A

0DataRank · unranked

72 citations

Alison G. Compton, Yoshihito Kishita, Daniella H. Hock, AnneMarie E. Welch, Sumudu S. C. Amarasekera +40 more

A 3D Clinical Face Phenotype Space of Genetic Syndromes Using a Triplet-Based Singular Geometric Autoencoder

IEEE Access(2024)10.1109/access.2024.3524428

N/A

0DataRank · unranked

1 citations

Eduarda Caldeira, Harold Matthews, Michiel Vanneste, Nele Nauwelaers, Meng Yuan +10 more

The Deep Genome Project

Genome biology(2020)10.1186/s13059-020-1931-9

N/A

0DataRank · unranked

44 citations

David J. Adams, Gareth Baynam, Arthur L. Beaudet, Fátima Bosch, Kym M. Boycott +39 more

Genotype–phenotype correlations and novel molecular insights into the DHX30 -associated neurodevelopmental disorders

medRxiv(2020)10.1101/2020.09.24.20196097

N/A

0DataRank · unranked

0 citations

Nghi Dang, Hannes Huber, Jaclyn B. Murry, Jeff Abramson, Thorsten Althoff +60 more

Large-scale open-source three-dimensional growth curves for clinical facial assessment and objective description of facial dysmorphism

Scientific Reports(2021)10.1038/s41598-021-91465-z

N/A

0DataRank · unranked

42 citations

R. Palmer, Gareth Baynam, Oliver Quarrell, Ophir D. Klein, Richard A. Spritz +10 more

Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders

Genome Medicine(2021)10.1186/s13073-021-00900-3

N/A

0DataRank · unranked

31 citations

Nghi Dang, Hannes Huber, Jaclyn B. Murry, Jeff Abramson, Thorsten Althoff +60 more

Multi-Scale Part-Based Syndrome Classification of 3D Facial Images

IEEE Access(2022)10.1109/access.2022.3153357

N/A

0DataRank · unranked

12 citations

Harold Matthews, Nele Nauwelaers, Michiel Vanneste, Shunwang Gong, Giorgos Bouritsas +9 more

Refining nosology by modelling variation among facial phenotypes: the RASopathies

Journal of Medical Genetics(2022)10.1136/jmedgenet-2021-108366

N/A

0DataRank · unranked

10 citations

Michiel Vanneste, Kaitlin Katsura, David Aponte, Michael A. Patton, Peter Hammond +7 more

A 3D Clinical Face Phenotype Space of Genetic Syndromes using a Triplet-Based Singular Geometric Autoencoder

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.12.27.521999

N/A

0DataRank · unranked

5 citations

Eduarda Caldeira, Harold Matthews, Michiel Vanneste, Nele Nauwelaers, Meng Yuan +11 more

Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype–phenotype correlations and common mechanisms

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63247

N/A

0DataRank · unranked

41 citations

Justin Blair, Batsal Devkota, Sierra Fortunato, Dinah Clark, Audrey Lawrence +92 more

Gareth Baynam

Indexed papers

Top data-sharing exemplar

Papers