Author

Mariam M. AlEissa

University College LondonORCID 0000-0002-2355-4036Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 3 Assay:GWAS summary statistics· 3 Organism:human· 3 Approach:statistical model· 3 Research Focus:polygenic risk· 2 Assay:scRNA-seq· 2 Approach:Bayesian inference· 1 Assay:clinical cohort / trial· 1

Frequent Co-Authors

Alessia FiorentinoiD· 3 shared Jakob GroveiD· 3 shared Jonas Bybjerg‐GrauholmiD· 3 shared Nelson B. FreimeriD· 3 shared Nicholas James BassiD· 3 shared Tim B. BigdeliiD· 3 shared Andreas J. ForstneriD· 2 shared David CurtisiD· 2 shared

Activity by Year

2021-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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Curved chords = mutual co-authorship

3 shared papersGenetic & Genomic Medicine

Alessia FiorentinoORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Mapping genomic loci prioritises genes and implicates synaptic biology in schizophrenia

Vassily Trubetskoy, Antonio F. Pardiñas, Ting Qi, Georgia Panagiotaropoulou, Swapnil Awasthi, Tim B. Bigdeli, Julien Bryois, Chia‐Yen Chen, Charlotte A. Dennison, Lynsey S. Hall, Max Lam, Kyoko Watanabe, Oleksandr Frei, Tian Ge, Janet C Harwood, , Elliot S. Gershon

A genome-wide association study of 69,369 schizophrenia cases and 236,642 controls identifies 270 risk loci, prioritizes 130 genes, and links common and rare risk variants to neuronal synaptic biology.

Nature · Apr 8, 2022Peer-reviewedGenetic & Genomic Medicine✦ In-depth digest

Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia

Tarjinder Singh, Timothy Poterba, David Curtis, Huda Akil, Mariam M. AlEissa, Jack D. Barchas, Nicholas James Bass, Tim B. Bigdeli, Gerome D. Breen, Evelyn J. Bromet, P.F. Buckley, William E. Bunney, Jonas Bybjerg‐Grauholm, William Byerley, Sinéad B. Chapman, , David St Clair

Exomes of 24,248 schizophrenia cases and 97,322 controls implicate ultra-rare damaging variants in 10 genes, including GRIN2A and GRIA3, with odds ratios of 3 to 50.

Nature · Apr 8, 2022Peer-reviewedGenetic & Genomic Medicine✦ In-depth digest

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

Niamh Mullins, Andreas J. Forstner, Kevin Sean O’Connell, Brandon J. Coombes, Jonathan R. I. Coleman, Zhen Qiao, Thomas D. Als, Tim B. Bigdeli, Sigrid Børte, Julien Bryois, Alexander W. Charney, Ole Kristian Drange, Michael J. Gandal, Saskia P. Hagenaars, Masashi Ikeda, , Janos L. Kalman

Meta-analysis of 41,917 European-ancestry bipolar disorder cases versus 371,549 controls yields 64 risk loci (33 novel), neuronal and synaptic gene enrichment, and 15 eQTL-prioritized genes.

Nature Genetics · May 17, 2021Peer-reviewedGenetic & Genomic Medicine✦ In-depth digest