Peter Holmans

102.8k citations
377 papers · 74.2k · 36 hit papers · h-index 110

Impact in

    • Tryptophan and brain disorders
  • Genetics top 0.01%
    • Genetic Associations and Epidemiology
    • Genetics and Neurodevelopmental Disorders
    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases

Papers in

    • Genetic Associations and Epidemiology 177
    • Genomic variations and chromosomal abnormalities 60
    • Genetics and Neurodevelopmental Disorders 52
    • Genomics and Rare Diseases 41
    • Genetic Mapping and Diversity in Plants and Animals 24
    • Genetic Neurodegenerative Diseases 43

Peter Holmans

368 papers receiving 72.5k citations

Peter Holmans's Hit Papers

Genomics yields biological and phenotypic insights into bipolar disorder 2025 · 65 citations
650+3+6Years since publication50010001.5k2.0k

Peers

Peter Holmans
Comparison fields: 5 of 220
  • Biological Psychiatry 3.6k
  • Genetics 29.3k
  • Psychiatry and Mental health 9.2k
  • Neurology 4.7k
  • Cellular and Molecular Neuroscience 8.4k
Replace Markus Maria Nöthen with:
Markus Maria Nöthen Germany
Hreinn Stefánsson Iceland
Aarno V. Palotie Finland
Michael C. O’Donovan United Kingdom
Joseph D. Buxbaum United States
Michael Gill Ireland
Michael Owen United Kingdom
Patrick F Sullivan United States
Ole A. Andreassen Norway
Hakon Hakonarson United States
Peter Holmans relative to Markus Maria Nöthen Germany Markus Maria Nöthen's profile →
Citations per field
00.5×1.5×
Markus Maria Nöthen · 1×
Citations per year

Countries citing papers authored by Peter Holmans

Since Specialization
Citations

This map shows the geographic impact of Peter Holmans's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Peter Holmans with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter Holmans more than expected).

Fields of papers citing papers by Peter Holmans

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peter Holmans. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Peter Holmans. The network helps show where Peter Holmans may publish in the future.

Co-authors

The 25 scholars most cited alongside Peter Holmans, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Peter Holmans Line = papers co-authored together Peter Holmans links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 377 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
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20077865
2
Biological insights from 108 schizophrenia-associated genetic loci
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20146062
3
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
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20133446
4
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease
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20092879
5
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
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20192087
6
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease
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20111656
7
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
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20221614
8
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
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20191602
9
Analysis of shared heritability in common disorders of the brain
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20181441
10
New insights into the genetic etiology of Alzheimer’s disease and related dementias
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20221436
11
Gene-Wide Analysis Detects Two New Susceptibility Genes for Alzheimer's Disease
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20141332
12
De novo mutations in schizophrenia implicate synaptic networks
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20141284
13
Genome-wide association analysis identifies 13 new risk loci for schizophrenia
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20131231
14
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants
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20071188
15
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4
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20111099
16
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
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20181079
17
Genome-wide association study identifies 30 loci associated with bipolar disorder
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20191065
18
Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder
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20081024
19
Common variants on chromosome 6p22.1 are associated with schizophrenia
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2009971
20
Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders
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2019965

About Peter Holmans

Peter Holmans is a scholar working on Genetics, Cellular and Molecular Neuroscience, Psychiatry and Mental health, Molecular Biology and Physiology, having authored 377 papers that have together received 74.2k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (177 papers), Genomic variations and chromosomal abnormalities (60 papers), Genetics and Neurodevelopmental Disorders (52 papers), Genetic Neurodegenerative Diseases (43 papers), Genomics and Rare Diseases (41 papers), Alzheimer's disease research and treatments (34 papers), Bioinformatics and Genomic Networks (32 papers) and Genetic Mapping and Diversity in Plants and Animals (24 papers). The work is most often cited by research in Biological Psychiatry (3.6k citations), Genetics (29.3k citations), Psychiatry and Mental health (9.2k citations), Neurology (4.7k citations) and Cellular and Molecular Neuroscience (8.4k citations). Peter Holmans has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Michael C. O’Donovan, Michael Owen, Nick J. Craddock, Valentina Moskvina, Kirov George, Nigel M. Williams, Peter McGuffin, Lesley Jones, Lisa Anne Jones and Anita Thapar. Their work appears in journals such as Molecular Psychiatry, Human Molecular Genetics, American Journal of Medical Genetics Part B Neuropsychiatric Genetics, Nature Genetics and The American Journal of Human Genetics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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