Patrick May

Biochemistry, Genetics and Molecular BiologyComputer Science

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

2.1Author 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.

Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers

Movement Disorders(2023)10.1002/mds.29337

Top 25%

0.809DataRank

Top 25%28 citations

Elise A. Lucotte, Cloé Domenighetti, Matthew H. Law, Mark M. Iles, Kevin M. Brown +89 more

Papers

Driven by 34 papers — median percentile 70. Top paper: “Genetic evaluation of dementia with Lewy bodies implicates distinct disease subgroups”.

Genetic evaluation of dementia with Lewy bodies implicates distinct disease subgroups

Brain(2021)10.1093/brain/awab402

N/A

1.4DataRank · unranked

66 citations

Zalak Shah, Ruth Chia, Sandra E. Black, Ziv Gan‐Or, Julia Keith +81 more

Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals

Nature Communications(2023)10.1038/s41467-023-39539-6

N/A

1.2DataRank · unranked

56 citations

David Lewis‐Smith, Ryan L. Collins, Lisa‐Marie Niestroj, Shridhar Parthasarathy, Julie Xian +94 more

Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers

Movement Disorders(2023)10.1002/mds.29337

Top 25%

0.809DataRank

Top 25%28 citations

Elise A. Lucotte, Cloé Domenighetti, Matthew H. Law, Mark M. Iles, Kevin M. Brown +89 more

Critical Assessment of MetaProteome Investigation (CAMPI): a multi-laboratory comparison of established workflows

Nature Communications(2021)10.1038/s41467-021-27542-8

N/A

0.729DataRank · unranked

128 citations

Benoît J. Kunath, Kay Schallert, Stephanie Serena Schäpe, Paul E. Abraham, Jean Armengaud +40 more

SLC6A1 variant pathogenicity, molecular function and phenotype: a genetic and clinical analysis

Brain(2023)10.1093/brain/awad292

Top 30%

0.660DataRank

Top 30%23 citations

Eduardo Pérez‐Palma, Tobias Brünger, Ludovica Montanucci, Cornelius Gati, Chiara Klöckner +41 more

Genomics 2 Proteins portal: a resource and discovery tool for linking genetic screening outputs to protein sequences and structures

Nature Methods(2024)10.1038/s41592-024-02409-0

Top 32%

0.626DataRank

Top 32%21 citations

Jordan Safer, Duyen T. Nguyen, David Hoksza, Patrick May, Jeremy A. Arbesfeld +5 more

Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.04.009

N/A

0.617DataRank · unranked

60 citations

Gundula Povysil, Ryan S. Dhindsa, Kate E. Stanley, Andrew S. Allen, Yen‐Chen Anne Feng +95 more

Data-driven historical characterization of epilepsy-associated genes

European Journal of Paediatric Neurology(2022)10.1016/j.ejpn.2022.12.005

N/A

0.542DataRank · unranked

36 citations

Eduardo Pérez‐Palma, Javier A. López-Rivera, Alina Ivaniuk, Patrick May, Rikke S. Møller +2 more

Systematic characterization of human gut microbiome-secreted molecules by integrated multi-omics

ISME Communications(2021)10.1038/s43705-021-00078-0

N/A

0.503DataRank · unranked

15 citations

Antoine Malabirade, Javier Ramiro‐Garcia, Janine Habier, Jean‐Pierre Trezzi, Samantha L. Peters +11 more

The Interaction between HLA‐DRB1 and Smoking in Parkinson's Disease Revisited

Movement Disorders(2022)10.1002/mds.29133

N/A

0.416DataRank · unranked

15 citations

Venceslas Douillard, Pierre‐Emmanuel Sugier, Ashwin Ashok Kumar Sreelatha, Claudia Schulte, Sandeep Grover +75 more

Association of Body Mass Index and Parkinson Disease

Neurology(2024)10.1212/wnl.0000000000209620

N/A

0.385DataRank · unranked

12 citations

Pierre‐Emmanuel Sugier, Ashwin Ashok Kumar Sreelatha, Claudia Schulte, Sandeep Grover, Berta Portugal +72 more

Association of cardiovascular disease management drugs with Lewy body dementia: a case–control study

Brain Communications(2023)10.1093/braincomms/fcad346

N/A

0.292DataRank · unranked

6 citations

Brian Moroz, Sara Sáez-Atiénzar, Ruth Chia, Elizabeth K. Cahoon, Clifton L. Dalgard +93 more

Pathogenic paralogous variants can be used to apply the ACMG PS1 and PM5 variant interpretation criteria

medRxiv(2023)10.1101/2023.08.22.23294353

N/A

0.269DataRank · unranked

5 citations

Alina Ivaniuk, Eduardo Pérez‐Palma, Ludovica Montanucci, Stacey Cohen, Lacey Smith +6 more

Synergistic effect of short- and long-read sequencing on functional meta-omics

10.1101/2021.04.22.440869

N/A

0.136DataRank · unranked

1 citations

Susheel Bhanu Busi, Benoît J. Kunath, Laura de Nies, Magdalena Calusinska, Rashi Halder +4 more

Conserved patterns across ion channels correlate with variant pathogenicity and clinical phenotypes

Brain(2022)10.1093/brain/awac305

N/A

0DataRank · unranked

26 citations

Eduardo Pérez‐Palma, Ludovica Montanucci, Michael Nothnagel, Rikke S. Møller, Stéphanie Schorge +8 more

Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With KCNC2 Pathogenic Variants

Neurology(2022)10.1212/wnl.0000000000200660

N/A

0DataRank · unranked

21 citations

Simone Seiffert, Manuela Pendziwiat, Annika Rademacher, Tobias Brünger, Ulrike B. S. Hedrich +43 more

Loss-of-function variants in the KCNQ5 gene are implicated in genetic generalized epilepsies

EBioMedicine(2022)10.1016/j.ebiom.2022.104244

N/A

0DataRank · unranked

21 citations

Julian Schubert, Josua Kegele, Audrey Labalme, Miaomiao Mao, Jacqueline Heighway +17 more

Delineation of functionally essential protein regions for 242 neurodevelopmental genes

Brain(2022)10.1093/brain/awac381

N/A

0DataRank · unranked

17 citations

Tobias Brünger, Eduardo Pérez‐Palma, Marie Macnee, Andreas Brunklaus, Mark J. Daly +5 more

Association of ultra‐rare coding variants with genetic generalized epilepsy: A case–control whole exome sequencing study

Epilepsia(2022)10.1111/epi.17166

N/A

0DataRank · unranked

13 citations

Joshua E. Motelow, Kate E. Stanley, Dheeraj Reddy Bobbili, Ryan S. Dhindsa, Patrick May +3 more

Dairy Intake and Parkinson's Disease: A Mendelian Randomization Study

Movement Disorders(2022)10.1002/mds.28902

N/A

0DataRank · unranked

45 citations

Pierre‐Emmanuel Sugier, Ashwin Ashok Kumar Sreelatha, Claudia Schulte, Sandeep Grover, Océane Mohamed +74 more

Genome-wide structural variant analysis identifies risk loci for non-Alzheimer’s dementias

Cell Genomics(2023)10.1016/j.xgen.2023.100316

N/A

0DataRank · unranked

32 citations

Ruth Chia, Jinhui Ding, Memoona Rasheed, Masashi Fujita, Vilas Menon +88 more

Loss-of-function variants in the KCNQ5 gene are associated with genetic generalized epilepsies

medRxiv(2021)10.1101/2021.04.20.21255696

N/A

0DataRank · unranked

3 citations

Julian Schubert, Josua Kegele, Audrey Labalme, Miaomiao Mao, Jacqueline Heighway +17 more

Critical Assessment of Metaproteome Investigation (CAMPI): A Multi-Lab Comparison of Established Workflows

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.03.05.433915

N/A

0DataRank · unranked

12 citations

Benoît J. Kunath, Kay Schallert, Stephanie Serena Schäpe, Paul E. Abraham, Jean Armengaud +40 more

Mendelian Randomisation Study of Smoking, Alcohol, and Coffee Drinking in Relation to Parkinson’s Disease

Journal of Parkinson s Disease(2021)10.3233/jpd-212851

N/A

0DataRank · unranked

81 citations

Pierre‐Emmanuel Sugier, Ashwin Ashok Kumar Sreelatha, Claudia Schulte, Sandeep Grover, Océane Mohamed +74 more

Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture

Nature Genetics(2021)10.1038/s41588-021-00785-3

N/A

0DataRank · unranked

487 citations

Marya S. Sabir, Sara Bandrés‐Ciga, Sara Sáez-Atiénzar, Regina Hertfelder Reynolds, Emil K. Gustavsson +95 more

Dopamine pathway and Parkinson’s risk variants are associated with levodopa-induced dyskinesia

medRxiv(2023)10.1101/2023.08.28.23294610

N/A

0DataRank · unranked

0 citations

Sara Bandrés‐Ciga, Bart Ferwerda, Maria Teresa Periñan Tocino, Dìaz R. Belloso, Pilar Gómez‐Garre +32 more

Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into the complex genetic architecture

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.06.185066

N/A

0DataRank · unranked

7 citations

Marya S. Sabir, Sara Bandrés‐Ciga, Sara Sáez-Atiénzar, Regina Hertfelder Reynolds, Emil K. Gustavsson +95 more

Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy

Brain(2020)10.1093/brain/awaa085

N/A

0DataRank · unranked

32 citations

Felicitas Becker, Heba Morsy, Miriam Schmidts, Katia Hardies, Beyhan Tüysüz +40 more

Dopamine Pathway and Parkinson's Risk Variants Are Associated with Levodopa‐Induced Dyskinesia

Movement Disorders(2024)10.1002/mds.29960

N/A

0DataRank · unranked

11 citations

Sara Bandrés‐Ciga, Bart Ferwerda, Maria Teresa Periñan Tocino, Dìaz R. Belloso, Pilar Gómez‐Gil +32 more

Genomics 2 Proteins portal: A resource and discovery tool for linking genetic screening outputs to protein sequences and structures

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.01.02.573913

N/A

0DataRank · unranked

5 citations

Jordan Safer, Duyen T. Nguyen, David Hoksza, Patrick May, Jeremy A. Arbesfeld +5 more

Conserved missense variant pathogenicity and correlated phenotypes across paralogous genes

Research Square(2024)10.21203/rs.3.rs-5434140/v1

N/A

0DataRank · unranked

0 citations

Alina Ivanuk, Eduardo Pérez‐Palma, Ludovica Montanucci, Stacey Cohen, Lacey Smith +6 more

Genome-wide association meta-analyses of drug-resistant epilepsy

EBioMedicine(2025)10.1016/j.ebiom.2025.105675

N/A

0DataRank · unranked

12 citations

Andreja Avberšek, Remi Stevelink, Helena Martins Custodio, Siwei Chen, Doug Speed +88 more

USP25 in genetic generalized epilepsy: a gene under scrutiny

Brain(2025)10.1093/brain/awaf406

N/A

0DataRank · unranked

1 citations

Jill R. Murrell, Anna J. Prentice, Ingo Helbig, Holger Lerche, Patrick May +90 more

Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects

Brain(2020)10.1093/brain/awaa171

N/A

0DataRank · unranked

81 citations

Eduardo Pérez‐Palma, Daniel P. Howrigan, Yadi Zhou, Feixiong Cheng, Elmo Saarentaus +86 more

Patrick May

Indexed papers

Top data-sharing exemplar

Papers