Michael J. Owen

Biochemistry, Genetics and Molecular Biology

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

13.4Author DataRank

Indexed papers

9in 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 9 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 79 papers — median percentile 97. Top paper: “Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel”.

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

A structural variation reference for medical and population genetics

Nature(2020)10.1038/s41586-020-2287-8

Top 3%

6.7DataRank

Top 3%1180 citations

Harrison Brand, Konrad J. Karczewski, Xuefang Zhao, Jessica Alföldi, Laurent C. Francioli +201 more

Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes

Nature Communications(2020)10.1038/s41467-019-12438-5

N/A

5.6DataRank · unranked

143 citations

James Zou, Beryl B. Cummings, Jessica Alföldi, Laurent C. Francioli, Laura D. Gauthier +174 more

Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals

Nature Communications(2020)10.1038/s41467-019-10717-9

N/A

5.2DataRank · unranked

191 citations

Konrad J. Karczewski, Xiaolei Zhang, Sonia Chothani, Miriam J. Smith, D. Gareth Evans +181 more

The effect of LRRK2 loss-of-function variants in humans

Nature Medicine(2020)10.1038/s41591-020-0893-5

N/A

4.9DataRank · unranked

114 citations

Irina M. Armean, Aaron Kleinman, Jamie L. Marshall, Eric V. Minikel, Julia K. Goodrich +214 more

Underlying Genetic Models of Inheritance in Established Type 2 Diabetes Associations

American Journal of Epidemiology(2009)10.1093/aje/kwp145

N/A

4.0DataRank · unranked

67 citations

Lorraine Southam, David Altshuler, Kristin G. Ardlie, Inês Barroso, Michael Boehnke +27 more

Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia

Nature Genetics(2022)10.1038/s41588-022-01034-x

N/A

3.5DataRank · unranked

214 citations

Daniel P. Howrigan, Sinéad B. Chapman, Rolf Adolfsson, Nick Bass, Douglas Blackwood +42 more

Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns

Nature Communications(2019)10.1038/s41467-019-10461-0

N/A

2.8DataRank · unranked

151 citations

Gökçen Eraslan, Christian M. Page, Jari Lahti, Marius Lahti-Pulkkinen, Esa Hämäläinen +233 more

Genetic comorbidity between major depression and cardio‐metabolic traits, stratified by age at onset of major depression

American Journal of Medical Genetics Part B Neuropsychiatric Genetics(2020)10.1002/ajmg.b.32807

N/A

1.6DataRank · unranked

65 citations

Jonathan R. I. Coleman, Shing Wan Choi, Héléna A. Gaspar, Mark J. Adams, David M. Howard +43 more

The mutational constraint spectrum quantified from variation in 141,456 humans

Nature(2020)10.1038/s41586-020-2308-7

N/A

1.4DataRank · unranked

9958 citations

Laurent C. Francioli, Grace Tiao, Beryl B. Cummings, Jessica Alföldi, Qingbo S. Wang +187 more

Mapping Subcortical Brain Alterations in 22q11.2 Deletion Syndrome: Effects of Deletion Size and Convergence With Idiopathic Neuropsychiatric Illness

American Journal of Psychiatry(2020)10.1176/appi.ajp.2019.19060583

N/A

1.4DataRank · unranked

89 citations

Boris A. Gutman, Daqiang Sun, Julio E. Villalón‐Reina, Anjanibhargavi Ragothaman, Dmitry Isaev +50 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

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

Nature(2011)10.1038/nature10251

N/A

1.2DataRank · unranked

2729 citations

Stephen Sawcer, Garrett Hellenthal, Matti Pirinen, Chris C. A. Spencer, Nikolaos A. Patsopoulos +241 more

Defining the role of common variation in the genomic and biological architecture of adult human height

Nature Genetics(2014)10.1038/ng.3097

N/A

1.1DataRank · unranked

2093 citations

Emilio Rodríguez-Ruiz, The PAGE Consortium, Diana O. Perkins, Tonu Esko, Jian Yang +479 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

The genetic architecture of type 2 diabetes

Nature(2016)10.1038/nature18642

N/A

1.1DataRank · unranked

1106 citations

Menachem Fromer, Tanya M. Teslovich, Anubha Mahajan, Vineeta Agarwala, Kyle J. Gaulton +334 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

Microduplications of 16p11.2 are associated with schizophrenia

Nature Genetics(2009)10.1038/ng.474

N/A

0.990DataRank · unranked

733 citations

Kenneth S. Kendler, Manfred Kayser, Anjene M Addington, Jon McClellan, Milica Pejović-Milovančević +66 more

Genome-wide analyses of smoking behaviors in schizophrenia: Findings from the Psychiatric Genomics Consortium

Journal of Psychiatric Research(2021)10.1016/j.jpsychires.2021.02.027

N/A

0.893DataRank · unranked

16 citations

Tim B. Bigdeli, Stephan Ripke, Silviu‐Alin Bacanu, Pablo V. Gejman, Douglas F. Levinson +16 more

Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia

Human Molecular Genetics(2007)10.1093/hmg/ddm323

N/A

0.892DataRank · unranked

381 citations

D. Gumus, Ivan Nikolov, L. Georgieva, M. Sari, F. Erdogan +13 more

The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability

Nature Genetics(2017)10.1038/ng.3903

N/A

0.826DataRank · unranked

246 citations

David M. Hougaard, Mandy Johnstone, Nicholas Bass, Jaana Suvisaari, Minna Torniainen +21 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

Transcript expression-aware annotation improves rare variant interpretation

Nature(2020)10.1038/s41586-020-2329-2

N/A

0.796DataRank · unranked

201 citations

Konrad J. Karczewski, Ditte Demontis, Eleanor G. Seaby, Nicholas A. Watts, Moriel Singer-Berk +177 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

Evaluating drug targets through human loss-of-function genetic variation

Nature(2020)10.1038/s41586-020-2267-z

N/A

0.779DataRank · unranked

179 citations

Konrad J. Karczewski, Hilary C. Martin, Beryl B. Cummings, Nicola Whiffin, Daniel R. Rhodes +150 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

0.773DataRank · unranked

25 citations

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

Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum

The American Journal of Human Genetics(2018)10.1016/j.ajhg.2018.05.002

N/A

0.713DataRank · unranked

115 citations

F. Kyle Satterstrom, Seyedeh M. Zekavat, Indraniel Das, Mitja I Kurki, Claire Churchhouse +45 more

Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder

Molecular Psychiatry(2021)10.1038/s41380-020-01006-9

N/A

0.686DataRank · unranked

22 citations

Fernando S. Goes, Adam E. Locke, Duncan S. Palmer, Weiqing Wang, Sarah Cohen‐Woods +71 more

Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD

Nature Communications(2023)10.1038/s41467-023-43776-0

N/A

0.657DataRank · unranked

24 citations

Belinda Wang, Vanessa Drury, Sam Drake, Nawei Sun, Hasan Alkhairo +63 more

Pharmacogenomics: A road ahead for precision medicine in psychiatry

Neuron(2021)10.1016/j.neuron.2021.09.011

N/A

0.650DataRank · unranked

75 citations

Michael J. Owen, James Walters, Antonio F. Pardiñas

A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants

medRxiv(2020)10.1101/2020.01.14.20017426

N/A

0.629DataRank · unranked

14 citations

Joanne Doherty, Richard Anney, Kevin M. Antshel, Carrie E. Bearden, Raphael Bernier +26 more

Cognitive deficits in childhood, adolescence and adulthood in 22q11.2 deletion syndrome and association with psychopathology

Translational Psychiatry(2020)10.1038/s41398-020-0736-7

N/A

0.614DataRank · unranked

59 citations

Samuel J. R. A. Chawner, Thérèse van Amelsvoort, Ann Swillen, Claudia Vingerhoets, Elfi Vergaelen +5 more

A transgenic T cell receptor restores thymocyte differentiation in interleukin‐7 receptor α chain‐deficient mice

European Journal of Immunology(1997)10.1002/eji.1830270115

N/A

0.593DataRank · unranked

51 citations

Susan V. Outram, Jennifer Buckland, Michael J. Owen, Tessa Crompton

Rare CNVs and phenome-wide profiling highlight brain structural divergence and phenotypical convergence

Nature Human Behaviour(2023)10.1038/s41562-023-01541-9

N/A

0.588DataRank · unranked

28 citations

Kuldeep Kumar, Karin Saltoun, Claudia Modenato, Clara Moreau, Sandra Martin‐Brevet +27 more

Fine-mapping genomic loci refines bipolar disorder risk genes

Nature Neuroscience(2025)10.1038/s41593-025-01998-z

N/A

0.572DataRank · unranked

22 citations

Ashvin Ravi, Georgia Panagiotaropoulou, Brian M. Schilder, Jack Humphrey, Alice Braun +95 more

Genetic Heterogeneity Shapes Brain Connectivity in Psychiatry

Biological Psychiatry(2022)10.1016/j.biopsych.2022.08.024

N/A

0.505DataRank · unranked

28 citations

Annabelle Harvey, Kuldeep Kumar, Guillaume Huguet, Sebastian Urchs, Élise Douard +24 more

Subcortical Brain Alterations in Carriers of Genomic Copy Number Variants

American Journal of Psychiatry(2023)10.1176/appi.ajp.20220304

N/A

0.500DataRank · unranked

27 citations

Claudia Modenato, Clara Moreau, Christopher R. K. Ching, Annabelle Harvey, Sandra Martin‐Brevet +35 more

Brain functional connectivity mirrors genetic pleiotropy in psychiatric conditions

Brain(2022)10.1093/brain/awac315

N/A

0.483DataRank · unranked

24 citations

Kuldeep Kumar, Annabelle Harvey, Guillaume Huguet, Sebastian Urchs, Laura M. Schultz +21 more

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

Source‐based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome

Human Brain Mapping(2024)10.1002/hbm.26553

N/A

0.385DataRank · unranked

6 citations

Christopher R. K. Ching, Anne S. Bassett, Leila Kushan, Kevin M. Antshel, Thérèse van Amelsvoort +42 more

Impaired oxysterol-liver X receptor signaling underlies aberrant cortical neurogenesis in a stem cell model of neurodevelopmental disorder

Cell Reports(2024)10.1016/j.celrep.2024.113946

N/A

0.373DataRank · unranked

11 citations

Claudia Tamburini, Emily Stonelake, Robert Andrews, Jeremy Hall, Michael J. Owen +4 more

Exome sequencing in bipolar disorder reveals shared risk gene AKAP11 with schizophrenia

medRxiv(2021)10.1101/2021.03.09.21252930

N/A

0.366DataRank · unranked

7 citations

Daniel P. Howrigan, Sinéad B. Chapman, Rolf Adolfsson, Nick Bass, Douglas Blackwood +41 more

Assessing the validity of a self-reported clinical diagnosis of schizophrenia

Schizophrenia(2024)10.1038/s41537-024-00526-5

N/A

0.330DataRank · unranked

8 citations

Sophie E. Legge, Amy Lynham, Sophie E. Smart, Leon Hubbard, Ellie R. Daniel +7 more

Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia

Molecular Psychiatry(2023)10.1038/s41380-023-02009-y

N/A

0.311DataRank · unranked

5 citations

Yingjie Zhao, M. Reza Jabalameli, Nha Nguyen, Joydeep Mitra, Ann Swillen +15 more

A novel Alzheimer disease locus located near the gene encoding tau protein

UNC Libraries(2020)10.17615/7php-8b80

N/A

0.292DataRank · unranked

6 citations

Thomas Bird, DeStefano, Hanon, Tárraga, Allan I. Levey +95 more

Fine-mapping genomic loci refines bipolar disorder risk genes

medRxiv(2024)10.1101/2024.02.12.24302716

N/A

0.292DataRank · unranked

6 citations

Ashvin Ravi, Georgia Panagiotaropoulou, Brian M. Schilder, Jack Humphrey, Alice Braun +95 more

Beyond the Global Brain Differences: Intraindividual Variability Differences in 1q21.1 Distal and 15q11.2 BP1-BP2 Deletion Carriers

Biological Psychiatry(2023)10.1016/j.biopsych.2023.08.018

N/A

0.292DataRank · unranked

6 citations

Tobias Kaufmann, Dennis van der Meer, Oleksandr Frei, Ingrid Agartz, David Ames +95 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

Using rare genetic mutations to revisit structural brain asymmetry

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.04.17.537199

N/A

0.241DataRank · unranked

4 citations

Kuldeep Kumar, Kimia Shafighi, Karin Saltoun, Claudia Modenato, Clara Moreau +25 more

Neuropsychiatric copy number variants exert shared effects on human brain structure

medRxiv(2020)10.1101/2020.04.15.20056531

N/A

0.208DataRank · unranked

3 citations

Kuldeep Kumar, Clara Moreau, Sandra Martin‐Brevet, Guillaume Huguet, Catherine Schramm +27 more

Genetic predisposition to myeloproliferative neoplasms implicates hematopoietic stem cell biology

bioRxiv (Cold Spring Harbor Laboratory)(2019)10.1101/790626

N/A

0.188DataRank · unranked

2 citations

Satish K. Nandakumar, Xiaotian Liao, Alexander G. Bick, Christel M. Middeldorp, Marcin Tabaka +30 more

Subcortical brain alterations in carriers of genomic copy number variants

medRxiv(2023)10.1101/2023.02.14.23285913

N/A

0.165DataRank · unranked

2 citations

Claudia Modenato, Clara Moreau, Christopher R. K. Ching, Annabelle Harvey, Sandra Martin‐Brevet +36 more

DLG2 knockout reveals neurogenic transcriptional programs underlying neuropsychiatric disorders and cognition

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.01.10.898676

N/A

0.165DataRank · unranked

2 citations

Daniel D’Andrea, Mark O. Collins, Elliott Rees, Tom G. J. Steward, Ying Zhu +13 more

Rare Maternally Inherited Coding Variants on Chromosome X Carry Predominantly Male Risk in Autism, Tourette Syndrome, and Attention-deficit/Hyperactivity Disorder

medRxiv(2022)10.1101/2022.09.22.22280248

N/A

0.104DataRank · unranked

1 citations

Belinda Wang, Vanessa Drury, Sam Drake, Nawei Sun, Hasan Alkhairo +16 more

Penetrance of Neurodevelopmental Copy Number Variants Is Associated With Variations in Cortical Morphology

Biological Psychiatry Cognitive Neuroscience and Neuroimaging(2025)10.1016/j.bpsc.2025.05.010

N/A

0.104DataRank · unranked

1 citations

Ida E. Sønderby, George Kirov, Abdel Abdellaoui, Ingrid Agartz, David Ames +95 more

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

UNC Libraries(2020)10.17615/pbds-w495

N/A

0DataRank · unranked

0 citations

David Craig, Liming Qu, Jonathan L. Haines, Taniesha Morgan, Mark A. Sager +95 more

Contributors

Genomic and Personalized Medicine(2013)10.1016/b978-0-12-382227-7.00124-5

N/A

0DataRank · unranked

0 citations

Minhaz Uddin Ahmed, Sun Hee Ahn, R. Rand Allingham, Jude Alsarraj, Matthew L. Anderson +228 more

Striatal dopaminergic alterations in individuals with copy number variants at the 22q11.2 genetic locus and their implications for psychosis risk: a [18F]-DOPA PET study

Molecular Psychiatry(2021)10.1038/s41380-021-01108-y

N/A

0DataRank · unranked

32 citations

Céline Devroye, Mariasole Ciampoli, Mattia Veronese, Abhishekh H. Ashok, Robert A. McCutcheon +11 more

Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium

UNC Libraries(2020)10.17615/k3vg-tb84

N/A

0DataRank · unranked

0 citations

Stacy Steinberg, Johannes H. Smit, Tim B. Bigdeli, Kāri Stefánsson, Stefan Kloiber +71 more

No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study

UCL Discovery (University College London)(2020)10.17615/snbr-qh40

N/A

0DataRank · unranked

0 citations

Kung‐Yee Liang, Per Hoffman, Stefan Herms, Gary Donohoe, Luba Kalaydjieva +94 more

Fine-mapping reveals novel alternative splicing of the dopamine transporter

UNC Libraries(2020)10.17615/sbyt-hc58

N/A

0DataRank · unranked

0 citations

Pramod Thomas, Joel Wood, Michael Chen, A. Javier Lopez, Annie Watson +21 more

Reciprocal Duplication of the Williams-Beuren Syndrome Deletion on Chromosome 7q11.23 Is Associated with Schizophrenia

UNC Libraries(2020)10.17615/8m0s-na92

N/A

0DataRank · unranked

0 citations

John A. McGrath, Pamela Sklar, Gerald Nestadt, David J. Cutler, Paula Wolyniec +25 more

Genomic Stratification of Clozapine Prescription Patterns Using Schizophrenia Polygenic Scores

Biological Psychiatry(2022)10.1016/j.biopsych.2022.07.014

N/A

0DataRank · unranked

27 citations

Sophie E. Legge, Leon Hubbard, Isabella Willcocks, Kevin S. O’Connell, Robert L. Smith +10 more

Pathogenic mis-splicing of CPEB4 in schizophrenia

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.09.22.508890

N/A

0DataRank · unranked

1 citations

Antonio F. Pardiñas, Alberto Parras, Ivó H. Hernández, María Santos‐Galindo, Sara Picó +12 more

Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS and sporadic congenital heart disease

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.09.30.507111

N/A

0DataRank · unranked

0 citations

Yujue Wang, Lijie Shi, Donna M. McDonald‐McGinn, T. Blaine Crowley, Daniel E. McGinn +45 more

Pathogenic Mis-splicing of CPEB4 in Schizophrenia

Biological Psychiatry(2023)10.1016/j.biopsych.2023.03.010

N/A

0DataRank · unranked

27 citations

Antonio F. Pardiñas, Alberto Parras, Ivó H. Hernández, María Santos‐Galindo, Sara Picó +13 more

Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS

npj Genomic Medicine(2023)10.1038/s41525-023-00363-y

N/A

0DataRank · unranked

12 citations

Yujue Wang, Lijie Shi, Donna M. McDonald‐McGinn, T. Blaine Crowley, Daniel E. McGinn +47 more

Assessing the validity of a self-reported clinical diagnosis of schizophrenia

medRxiv(2023)10.1101/2023.12.06.23299622

N/A

0DataRank · unranked

4 citations

Sophie E. Legge, Amy Lynham, Sophie E. Smart, Leon Hubbard, Ellie R. Daniel +7 more

Challenges in Multi-Task Learning for fMRI-Based Diagnosis: Benefits for Psychiatric Conditions and CNVs Would Likely Require Thousands of Patients

PsyArXiv (OSF Preprints)(2023)10.31234/osf.io/srmx7

N/A

0DataRank · unranked

0 citations

Clara Moreau, Kuldeep Kumar, Guillaumeaf, Sebastian Urchs, Hanad Sharmarke +17 more

Using rare genetic mutations to revisit structural brain asymmetry

Nature Communications(2024)10.1038/s41467-024-46784-w

N/A

0DataRank · unranked

8 citations

Kuldeep Kumar, Kimia Shafighi, Karin Saltoun, Claudia Modenato, Clara Moreau +25 more

Challenges in multi-task learning for fMRI-based diagnosis: Benefits for psychiatric conditions and CNVs would likely require thousands of patients

Imaging Neuroscience(2024)10.1162/imag_a_00222

N/A

0DataRank · unranked

3 citations

Clara Moreau, Kuldeep Kumar, Guillaume Huguet, Sebastian Urchs, Hanad Sharmarke +17 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

Identifying genetic differences between bipolar disorder and major depression through multiple genome-wide association analyses

The British Journal of Psychiatry(2025)10.1192/bjp.2024.125

N/A

0DataRank · unranked

5 citations

Kajsa-Lotta Georgii Hellberg, Jonathan R. I. Coleman, Darsol Seok, János Kálmán, Philip B. Mitchell +49 more

Cortical differences across psychiatric disorders and associated common and rare genetic variants

medRxiv(2025)10.1101/2025.04.16.25325971

N/A

0DataRank · unranked

2 citations

Zhijie Liao, Jakub Kopál, Clara Moreau, Christopher R. K. Ching, Claudia Modenato +30 more

A large-scale multi-ancestry genome-wide association study of chronic prostatitis/chronic pelvic pain syndrome in men

Nature Communications(2026)10.1038/s41467-025-64954-2

Top 100%

0DataRank

Top 100%0 citations

Adam X. Maihofer, Caroline M. Nievergelt, Daniel Dochtermann, Armand Gerstenberger, Thomas Whisenant +8 more

Copy number variants reveal divergent genetic and diagnostic cortical signatures across psychiatric disorders

10.21203/rs.3.rs-9246968/v1

N/A

0DataRank · unranked

0 citations

Zhijie Liao, Jakub Kopál, Clara Moreau, Christopher Ching, Claudia Modenato +29 more

Michael J. Owen

Indexed papers

Top data-sharing exemplar

Papers