Peter Holmans

Biochemistry, Genetics and Molecular BiologyNeuroscience

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

6.9Author DataRank

Indexed papers

5in 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 5 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.

Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

Nature Communications(2015)10.1038/ncomms9111

Top 3%

6.7DataRank

Top 3%386 citations

Bryan Howie, Shane McCarthy, Yasin Memari, Klaudia Walter, Josine L. Min +234 more

Papers

Driven by 42 papers — median percentile 63. Top paper: “Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology”.

Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

Nature Genetics(2021)10.1038/s41588-021-00857-4

N/A

8.4DataRank · unranked

1610 citations

Andreas J. Forstner, Kevin S. O’Connell, Brandon J. Coombes, Jonathan R. I. Coleman, Zhen Qiao +95 more

Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

Nature Communications(2015)10.1038/ncomms9111

Top 3%

6.7DataRank

Top 3%386 citations

Bryan Howie, Shane McCarthy, Yasin Memari, Klaudia Walter, Josine L. Min +234 more

Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets

JAMA Neurology(2021)10.1001/jamaneurol.2020.5257

N/A

4.5DataRank · unranked

205 citations

David Zhang, Sebastian Guelfi, Claudia Manzoni, Leon Hubbard, Regina Hertfelder Reynolds +85 more

Biological insights from 108 schizophrenia-associated genetic loci

Nature(2014)10.1038/nature13595

N/A

1.3DataRank · unranked

8042 citations

Stephan Ripke, Aiden Corvin, Jesse R. Dixon, Kai-How Farh, Peter Holmans +284 more

Rare chromosomal deletions and duplications increase risk of schizophrenia

Nature(2008)10.1038/nature07239

N/A

1.1DataRank · unranked

1503 citations

Michael C O'Donovan, Catherine H. Wilson, Manfred Kayser, Pentti J. Tienari, Aiden Corvin +72 more

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

Nature Genetics(2016)10.1038/ng.3725

N/A

1.1DataRank · unranked

1129 citations

Daniel P. Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S. Greer +267 more

Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

Cell Genomics(2023)10.1016/j.xgen.2023.100356

N/A

1.0DataRank · unranked

43 citations

Maxwell A. Sherman, Giulio Genovese, Thomas G. Gilgenast, Tushar Kamath, S.J. Burris +95 more

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia

Molecular Psychiatry(2011)10.1038/mp.2011.154

N/A

1.0DataRank · unranked

874 citations

A J Pocklington, D Ivanov, Samuel A. Rose, Andrew McQuillin, Hywel Williams +46 more

Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome

Nature Communications(2021)10.1038/s41467-021-26280-1

N/A

0.808DataRank · unranked

217 citations

Demis A. Kia, Mona M. Almramhi, Sara Bandres-Ciga, Chris Finan, Alastair J. Noyce +170 more

A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts

Biological Psychiatry(2021)10.1016/j.biopsych.2021.04.018

N/A

0.801DataRank · unranked

207 citations

Jian Zeng, Joana Revez, Ying Wang, Zhili Zheng, Tian Ge +95 more

Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia

Neuron(2015)10.1016/j.neuron.2015.04.022

N/A

0.799DataRank · unranked

205 citations

Elliott Rees, James T.R. Walters, Jun Han, David H. Kavanagh, Kimberly D. Chambert +9 more

Investigating the Contribution of Common Genetic Variants to the Risk and Pathogenesis of ADHD

American Journal of Psychiatry(2012)10.1176/appi.ajp.2011.11040551

N/A

0.790DataRank · unranked

193 citations

Marian Hamshere, Peter Holmans, Kate Langley, Irina Zaharieva, Ziarah Hawi +7 more

Genomics yields biological and phenotypic insights into bipolar disorder

Nature(2025)10.1038/s41586-024-08468-9

N/A

0.775DataRank · unranked

174 citations

Maria Koromina, Tracey van der Veen, Toni Boltz, Friederike S. David, Jessica Yang +95 more

Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion

Molecular Psychiatry(2020)10.1038/s41380-020-0654-3

N/A

0.738DataRank · unranked

136 citations

Worrawat Engchuan, Matthew S. Hestand, Tracy Heung, Aaron M. Holleman, H. Richard Johnston +95 more

Genetic modifiers of Huntington disease differentially influence motor and cognitive domains

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.03.004

N/A

0.721DataRank · unranked

121 citations

Yuan Huang, Michael Orth, Tammy Gillis, Jacqueline Siciliano, Eunpyo Hong +23 more

New insights on the genetic etiology of Alzheimer’s and related dementia

medRxiv(2020)10.1101/2020.10.01.20200659

N/A

0.677DataRank · unranked

90 citations

Fahri Küçükali, Iris E. Jansen, Víctor Andrade, Sonia Moreno–Grau, Najaf Amin +95 more

Genetic and Functional Analyses Point to FAN1 as the Source of Multiple Huntington Disease Modifier Effects

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.05.012

N/A

0.652DataRank · unranked

76 citations

Eun Pyo Hong, Jun Wan Shin, Michael J. Chao, Jacob M. Loupe, Tammy Gillis +12 more

Huntington’s disease age at motor onset is modified by the tandem hexamer repeat in TCERG1

npj Genomic Medicine(2022)10.1038/s41525-022-00317-w

N/A

0.649DataRank · unranked

21 citations

Branduff McAllister, Mia McDade‐Kumar, G. Bernhard Landwehrmeyer, Michael Orth, Anne Rosser +13 more

Genome-wide association identifies the first risk loci for psychosis in Alzheimer disease

Molecular Psychiatry(2021)10.1038/s41380-021-01152-8

N/A

0.637DataRank · unranked

69 citations

Lambertus Klei, Byron Creese, Janet Harwood, Elise A. Weamer, Lora McClain +39 more

Genetic modifiers of somatic expansion and clinical phenotypes in Huntington’s disease highlight shared and tissue-specific effects

Nature Genetics(2025)10.1038/s41588-025-02191-5

N/A

0.578DataRank · unranked

46 citations

Jong-Min Lee, Zachariah L. McLean, Kevin Correia, Jun Wan Shin, Sujin Lee +38 more

The relationship between case–control differential gene expression from brain tissue and genetic associations in schizophrenia

American Journal of Medical Genetics Part B Neuropsychiatric Genetics(2023)10.1002/ajmg.b.32931

N/A

0.466DataRank · unranked

13 citations

Anton Schulmann, Peter Holmans, Michael C O'Donovan, Marquis P. Vawter, Nicholas E. Clifton

Whole-exome sequencing analysis identifies risk genes for schizophrenia

Nature Communications(2025)10.1038/s41467-025-62429-y

N/A

0.446DataRank · unranked

15 citations

Peter Holmans, Darren Cameron, Detelina Grozeva, Rebecca Sims, Julie Williams +6 more

Comparison of autism domains across thirty rare variant genotypes

EBioMedicine(2025)10.1016/j.ebiom.2024.105521

N/A

0.312DataRank · unranked

7 citations

Samuel J. R. A. Chawner, Leila Kushan, Carrie E. Bearden, Jennifer G. Mullé, Rebecca M. Pollak +18 more

A polygenic resilience score moderates the genetic risk for schizophrenia: Replication in 18,090 cases and 28,114 controls from the Psychiatric Genomics Consortium

American Journal of Medical Genetics Part B Neuropsychiatric Genetics(2023)10.1002/ajmg.b.32957

N/A

0.312DataRank · unranked

7 citations

Manuel Mattheisen, Tiffany A. Greenwood, Ming T. Tsuang, Howard J. Edenberg, Peter Holmans +3 more

Developmental profile of psychiatric risk associated with voltage-gated cation channel activity

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.10.19.345801

N/A

0.269DataRank · unranked

5 citations

Leonardo Collado‐Torres, Emily E. Burke, Antonio F. Pardiñas, Janet Harwood, Arianna Di Florio +8 more

The timing and impact of psychiatric, cognitive and motor abnormalities in Huntington’s disease

ORCA Online Research @Cardiff (Cardiff University)(2020)10.1101/2020.05.26.116798

Top 70%

0.150DataRank

Top 70%1 citations

James F. Gusella, G. Bernhard Landwehrmeyer, Jong-Min Lee, Marcy E. MacDonald, Michael Orth +6 more

Genomic dimensions deconstruct the clinical heterogeneity of bipolar disorder

medRxiv(2025)10.1101/2025.06.23.25330155

N/A

0.104DataRank · unranked

1 citations

Markos Tesfaye, Jessica Yang, Toni Boltz, Friederike S. David, Shane Crinion +95 more

Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept

Faculty of Health; Institute of Health and Biomedical Innovation(2020)10.17615/4xr8-gp35

N/A

0.104DataRank · unranked

1 citations

Simon E. Fisher, William Byerley, Jens R. Wendland, Nick Craddock, Luigi Ferrucci +95 more

Cognitive Decline in Alzheimer’s Disease Is Not Associated with APOE

Journal of Alzheimer s Disease(2021)10.3233/jad-210685

N/A

0DataRank · unranked

9 citations

the Alzheimer’s Disease Neuroimaging Initiative, Ganna Leonenko, Dobril Ivanov, Alun Meggy, Iain Marshall +5 more

Modification of Huntington’s disease by short tandem repeats

Brain Communications(2024)10.1093/braincomms/fcae016

N/A

0DataRank · unranked

12 citations

Eliana Marisa Ramos, N. Ahmad Aziz, Thomas H. Massey, Branduff McAllister, S. V. Lobanov +16 more

Posttranscriptional regulation of FAN1 by miR-124-3p at rs3512 underlies onset-delaying genetic modification in Huntington’s disease

Proceedings of the National Academy of Sciences(2024)10.1073/pnas.2322924121

N/A

0DataRank · unranked

10 citations

Eun Pyo Hong, Yukyeong Lee, Zachariah L. McLean, Emanuela Elezi, Ramee Lee +15 more

Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders

UNC Libraries(2024)10.17615/4nb8-at41

N/A

0DataRank · unranked

0 citations

David Curtis, Jennifer Sambrook, Robin Murray, David St Clair, Trevor Cole +54 more

Monocyte-specific changes in gene expression implicate LACTB2 and PLIN2 in Alzheimer’s disease

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.06.05.136275

N/A

0DataRank · unranked

0 citations

Ganna Leonenko, Rebecca Sims, Valentina Escott‐Price, Julie Williams, Peter Holmans +1 more

Association Analysis of Chromosome X to Identify Genetic Modifiers of Huntington’s Disease

Journal of Huntington s Disease(2021)10.3233/jhd-210485

N/A

0DataRank · unranked

8 citations

Michael J. Chao, Thomas H. Massey, Branduff McAllister, S. V. Lobanov, Lesley Jones +12 more

A Novel Method to Disentangle Tightly Linked Risk and Resilience Genes for Brain Disorders: Application to Alzheimer’s Disease

medRxiv(2025)10.1101/2025.02.26.25322962

N/A

0DataRank · unranked

1 citations

Jonathan Hess, Jiahui Hou, Valentina Escott‐Price, Christine Fennema‐Notestine, William S. Kremen +8 more

FAN1 nuclease activity affects CAG expansion and age at onset of Huntington’s disease

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.04.13.439716

N/A

0DataRank · unranked

3 citations

Jasmine Donaldson, Caroline S. Binda, Sophie Powell, Uroosa Chughtai, Gareth Edwards +29 more

Developmental Profile of Psychiatric Risk Associated With Voltage-Gated Cation Channel Activity

Biological Psychiatry(2021)10.1016/j.biopsych.2021.03.009

N/A

0DataRank · unranked

25 citations

Leonardo Collado‐Torres, Emily E. Burke, Antonio F. Pardiñas, Janet Harwood, Arianna Di Florio +8 more

Huntington’s disease age at motor onset is modified by the tandem hexamer repeat in TCERG1

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.07.16.452643

N/A

0DataRank · unranked

1 citations

Branduff McAllister, Mia McDade‐Kumar, G. Bernhard Landwehrmeyer, Michael Orth, Anne Rosser +13 more

Huntington’s Disease Pathogenesis: Two Sequential Components

Journal of Huntington s Disease(2021)10.3233/jhd-200427

N/A

0DataRank · unranked

114 citations

Marcy E. MacDonald, Vanessa C. Wheeler, Lesley Jones, Peter Holmans, Michael Orth +6 more

Exome sequencing of individuals with Huntington’s disease implicates FAN1 nuclease activity in slowing CAG expansion and disease onset

Nature Neuroscience(2022)10.1038/s41593-022-01033-5

N/A

0DataRank · unranked

92 citations

Jasmine Donaldson, Caroline S. Binda, Sophie Powell, Uroosa Chughtai, Gareth Edwards +29 more

Genetic modifiers of Huntington’s disease differentially influence motor and cognitive domains

medRxiv(2022)10.1101/2022.01.03.22268687

N/A

0DataRank · unranked

1 citations

Yuan Huang, Michael Orth, Tammy Gillis, Jacqueline Siciliano, Eunpyo Hong +23 more

Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases

UNC Libraries(2020)10.17615/vqrj-3e30

N/A

0DataRank · unranked

0 citations

Patrick F. Sullivan, Chongzhi Zang, David Collier, Hailiang Huang, Eli A. Stahl +24 more

Peter Holmans

Indexed papers

Top data-sharing exemplar

Papers