Michael C O'Donovan

Biochemistry, Genetics and Molecular BiologyMedicine

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

39.2Author DataRank

Indexed papers

7in 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 7 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.

Analysis of protein-coding genetic variation in 60,706 humans

Nature(2016)10.1038/nature19057

Top 1%

13.0DataRank

Top 1%10410 citations

Monkol Lek, Konrad J. Karczewski, Eric V. Minikel, Kaitlin E. Samocha, Iain Mathieson +76 more

Papers

Driven by 81 papers — median percentile 97. Top paper: “Analysis of protein-coding genetic variation in 60,706 humans”.

Analysis of protein-coding genetic variation in 60,706 humans

Nature(2016)10.1038/nature19057

Top 1%

13.0DataRank

Top 1%10410 citations

Monkol Lek, Konrad J. Karczewski, Eric V. Minikel, Kaitlin E. Samocha, Iain Mathieson +76 more

A map of human genome variation from population-scale sequencing

Nature(2010)10.1038/nature09534

Top 2%

9.1DataRank

Top 2%8109 citations

Min Hu, Yuan Chen, Matthew N. Bainbridge, Richard M. Durbin, Si Quang Le +319 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

Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects

Nature Communications(2018)10.1038/s41467-018-06159-4

Top 3%

6.6DataRank

Top 3%260 citations

Yossi Farjoun, Ilya Shlyakhter, Olga Krasheninina, Hyun Min Kang, Daniel P. Howrigan +16 more

Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains

Nature Genetics(2023)10.1038/s41588-022-01285-8

N/A

6.1DataRank · unranked

775 citations

G. Bragi Walters, Georgios Athanasiadis, Raymond K. Walters, Karen Therrien, Trine Tollerup Nielsen +81 more

Evidence that duplications of 22q11.2 protect against schizophrenia

Molecular Psychiatry(2013)10.1038/mp.2013.156

N/A

5.8DataRank · unranked

188 citations

James T.R. Walters, J T R Walters, K D Chambert, Dragan M. Švrakić, J Szatkiewicz +53 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

Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

Nature Communications(2018)10.1038/s41467-018-04668-w

N/A

3.7DataRank · unranked

109 citations

Sanni Ruotsalainen, Robert E. Handsaker, Maris Alver, Jonathan M. Bloom, Timothy Poterba +442 more

Meta-analysis of genome-wide association studies confirms a susceptibility locus for knee osteoarthritis on chromosome 7q22

Annals of the Rheumatic Diseases(2011)10.1136/ard.2010.132787

N/A

3.6DataRank · unranked

148 citations

Ana M. Valdes, Unnur Styrkarsdottir, YanYan Zhu, Ingrid Meulenbelt, Rik J Lories +94 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

Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

Nature Neuroscience(2016)10.1038/nn.4404

N/A

3.3DataRank · unranked

113 citations

Giulio Genovese, Daniel P. Howrigan, Andrea Byrnes, Mitja I Kurki, Seyedeh M. Zekavat +31 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

DNA methylation meta-analysis reveals cellular alterations in psychosis and markers of treatment-resistant schizophrenia

eLife(2021)10.7554/elife.58430

N/A

2.8DataRank · unranked

144 citations

Emma Dempster, Georgina Mansell, Joe Burrage, Nick Bass, Marc M. Bohlken +41 more

An open resource of structural variation for medical and population genetics

bioRxiv (Cold Spring Harbor Laboratory)(2019)10.1101/578674

Top 9%

2.2DataRank

Top 9%44 citations

Harrison Brand, Konrad J. Karczewski, Xuefang Zhao, Jessica Alföldi, Laurent C. Francioli +37 more

PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses

The American Journal of Human Genetics(2007)10.1086/519795

N/A

1.6DataRank · unranked

35753 citations

Preben Bo Mortensen, Kathe Todd-Brown, Lori Thomas, Manuel A.R. Ferreira, David Bender +12 more

2013 ESH/ESC Guidelines for the management of arterial hypertension

European Heart Journal(2013)10.1093/eurheartj/eht151

N/A

1.4DataRank · unranked

13664 citations

Robert Fagard, Krzysztof Narkiewicz, Josep Redón, Alberto Zanchetti, Michael Böhm +86 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

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

Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects

bioRxiv (Cold Spring Harbor Laboratory)(2018)10.1101/269316

Top 16%

1.3DataRank

Top 16%34 citations

Yossi Farjoun, David Larson, Olga Krasheninina, Hyun Min Kang, Daniel P. Howrigan +19 more

Partitioning heritability by functional annotation using genome-wide association summary statistics

Nature Genetics(2015)10.1038/ng.3404

N/A

1.2DataRank · unranked

3020 citations

Hilary K. Finucane, Anders D. Børglum, The RACI Consortium, Brendan K Bulik-Sullivan, Alexander Gusev +22 more

Clinical use of current polygenic risk scores may exacerbate health disparities

Nature Genetics(2019)10.1038/s41588-019-0379-x

N/A

1.2DataRank · unranked

2850 citations

Masahiro Kanai, Yoichiro Kamatani, Karen L. Mohlke, Michael C O'Donovan, Coleen Damcott +1 more

Patterns and rates of exonic de novo mutations in autism spectrum disorders

Nature(2012)10.1038/nature11011

N/A

1.1DataRank · unranked

1794 citations

Yan Kou, Li Liu, Avi Ma’ayan, Kaitlin E. Samocha, Aniko Sabo +60 more

Efficient Bayesian mixed-model analysis increases association power in large cohorts

Nature Genetics(2015)10.1038/ng.3190

N/A

1.1DataRank · unranked

1781 citations

George Tucker, Brendan K Bulik-Sullivan, Bjarni J. Vilhjálmsson, Hilary K. Finucane, Rany M. Salem +9 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

A framework for the interpretation of de novo mutation in human disease

Nature Genetics(2014)10.1038/ng.3050

N/A

1.1DataRank · unranked

1119 citations

Elise B Robinson, Stephan J. Sanders, Christine Stevens, Aniko Sabo, Lauren M. McGrath +25 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

Extremely low-coverage sequencing and imputation increases power for genome-wide association studies

Nature Genetics(2012)10.1038/ng.2283

N/A

0.868DataRank · unranked

326 citations

Nicholas Mancuso, Paul J. McLaren, Kiran Garimella, Noah Zaitlen, Alexandra P. Lewis +23 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

Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants

Nature Neuroscience(2019)10.1038/s41593-019-0527-8

N/A

0.815DataRank · unranked

228 citations

F. Kyle Satterstrom, Tarjinder Singh, Emilie M. Wigdor, Jurgen Del‐Favero, Ditte Demontis +17 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

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

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

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

Current clinical use of polygenic scores will risk exacerbating health disparities

bioRxiv (Cold Spring Harbor Laboratory)(2018)10.1101/441261

N/A

0.568DataRank · unranked

43 citations

Masahiro Kanai, Yoichiro Kamatani, Karen L. Mohlke, Michael C O'Donovan, Coleen Damcott +1 more

The Psychiatric Genomics Consortium: discoveries and directions

The Lancet Psychiatry(2025)10.1016/s2215-0366(25)00124-5

N/A

0.505DataRank · unranked

28 citations

Cynthia M. Bulik, Dawit Abebe, Ole A. Andreassen, Elizabeth G. Atkinson, Karmel W. Choi +34 more

ASD and ADHD have a similar burden of rare protein-truncating variants

bioRxiv (Cold Spring Harbor Laboratory)(2018)10.1101/277707

N/A

0.434DataRank · unranked

17 citations

Tarjinder Singh, Emilie M. Wigdor, Jurgen Del‐Favero, Ditte Demontis, Christine Stevens +18 more

Recommendations for defining treatment outcomes in major psychiatric disorders using real-world data

The Lancet Psychiatry(2025)10.1016/s2215-0366(25)00061-6

N/A

0.406DataRank · unranked

14 citations

Sophie E. Smart, Guðmundur Einarsson, Anders Kämpe, Lina Jönsson, Maris Alver +25 more

Examining sex differences in neurodevelopmental and psychiatric genetic risk in anxiety and depression

PLoS ONE(2021)10.1371/journal.pone.0248254

N/A

0.406DataRank · unranked

14 citations

Kimiya Asjadi, Leon Hubbard, Kimberley Kendall, Antonio F. Pardiñas, Bradley Jermy +20 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

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

Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

Nature Communications(2020)10.1038/s41467-020-15236-6

Top 57%

0.275DataRank

Top 57%2 citations

Sanni Ruotsalainen, Robert E. Handsaker, Maris Alver, Jonathan M. Bloom, Timothy Poterba +442 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

Large-scale analysis of DNA methylation identifies cellular alterations in blood from psychosis patients and molecular biomarkers of treatment-resistant schizophrenia

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.04.05.026211

N/A

0.104DataRank · unranked

1 citations

Emma Dempster, Georgina Mansell, Joe Burrage, Nick Bass, Marc M. Bohlken +41 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

Extremely low-coverage sequencing and imputation increases power for genome-wide association studies

UNC Libraries(2020)10.17615/haws-ma91

N/A

0DataRank · unranked

0 citations

Nicholas Mancuso, Paul J. McLaren, Kiran Garimella, Noah Zaitlen, Alexandra P. Lewis +19 more

Genome-wide Association Analysis of Parkinson’s Disease and Schizophrenia Reveals Shared Genetic Architecture and Identifies Novel Risk Loci

Biological Psychiatry(2020)10.1016/j.biopsych.2020.01.026

N/A

0DataRank · unranked

104 citations

Alexey Shadrin, Shahram Bahrami, Iris Broce, Martin Tesli, Oleksandr Frei +17 more

Hypothesis-driven candidate genes for schizophrenia compared to genome-wide association results

UNC Libraries(2020)10.17615/wy8g-pq41

N/A

0DataRank · unranked

5 citations

P. F. Sullivan, Y. Kim, Michael C O'Donovan, P. Sklar, A. L. Collins

Mapping genomic loci prioritises genes and implicates synaptic biology in schizophrenia

medRxiv(2020)10.1101/2020.09.12.20192922

N/A

0DataRank · unranked

345 citations

James Walters, Michael C O'Donovan, Stephan Ripke

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

0DataRank · unranked

5 citations

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

0DataRank · unranked

2 citations

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

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

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

All SNPs Are Not Created Equal: Genome-Wide Association Studies Reveal a Consistent Pattern of Enrichment among Functionally Annotated SNPs

UNC Libraries(2020)10.17615/e1kj-ax40

N/A

0DataRank · unranked

0 citations

Ole A. Andreassen, Wesley K. Thompson, Michael C O'Donovan, J. Cooper Roddey, Patrick F. Sullivan +7 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

0DataRank · unranked

0 citations

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

An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype

UNC Libraries(2020)10.17615/jcdv-pt45

N/A

0DataRank · unranked

0 citations

Wei Zhao, Cathryn M. Lewis, Thomas G. Schulze, Philip L. De Jager, Markus M. Nöthen +95 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

Investigating Direct and Indirect Genetic Effects in Attention-Deficit/Hyperactivity Disorder Using Parent-Offspring Trios

Biological Psychiatry(2022)10.1016/j.biopsych.2022.06.008

N/A

0DataRank · unranked

28 citations

Matthew Wray, Sharifah Shameem Agha, Katie Lewis, Richard Anney, Michael C O'Donovan +3 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

Early manifestations of genetic liability for ADHD, autism and schizophrenia at ages 18 and 24 months

JCPP Advances(2022)10.1002/jcv2.12093

N/A

0DataRank · unranked

22 citations

Esther Tobarra Sánchez, Evie Stergiakouli, Alexandra Havdahl, Kate Tilling, Michael C O'Donovan +4 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

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

0DataRank · unranked

1 citations

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

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

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

0DataRank · unranked

13 citations

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

Examining the association between exposome score for schizophrenia and cognition in schizophrenia, siblings, and healthy controls: Results from the EUGEI study

Psychiatry Research(2023)10.1016/j.psychres.2023.115184

N/A

0DataRank · unranked

10 citations

Thanavadee Prachason, Gamze Erzın, Lotta-Katrin Pries, Natascia Brondino, Pierluigi Politi +44 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

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

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

N/A

0DataRank · unranked

8 citations

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

Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder

UNC Libraries(2024)10.17615/gad3-dw62

N/A

0DataRank · unranked

0 citations

R.S. Kahn, Gonçalo R. Abecasis, Neil Risch, Andrew McQuillin, Aiden Corvin +71 more

Michael C O'Donovan

Indexed papers

Top data-sharing exemplar

Papers