Julien Bryois

28.4k total citations · 2 hit papers
27 papers, 1.7k citations indexed

About

Julien Bryois is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Julien Bryois has authored 27 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 14 papers in Genetics and 3 papers in Neurology. Recurrent topics in Julien Bryois's work include Genetic Associations and Epidemiology (13 papers), Single-cell and spatial transcriptomics (8 papers) and Bioinformatics and Genomic Networks (4 papers). Julien Bryois is often cited by papers focused on Genetic Associations and Epidemiology (13 papers), Single-cell and spatial transcriptomics (8 papers) and Bioinformatics and Genomic Networks (4 papers). Julien Bryois collaborates with scholars based in United States, Sweden and United Kingdom. Julien Bryois's co-authors include Patrick F. Sullivan, Nathan Skene, Jens Hjerling‐Leffler, Ana B. Muñoz‐Manchado, Sten Linnarsson, Gerome Breen, Jeanne E. Savage, Daniëlle Posthuma, Philip R. Jansen and Kyoko Watanabe and has published in prestigious journals such as Science, Nature Communications and Neuron.

In The Last Decade

Julien Bryois

24 papers receiving 1.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways

2018 405 citations Mats Nagel, Philip R. Jansen et al. Nature Genetics profile →
Genetic identification of brain cell types underlying schizophrenia

2018 326 citations Nathan Skene, Julien Bryois et al. Nature Genetics profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Julien Bryois United States	17	797	735	186	162	150	27	1.7k
Ann M. Manzardo United States	27	613 0.8×	900 1.2×	327 1.8×	215 1.3×	214 1.4×	84	1.8k
Janice M. Fullerton Australia	25	533 0.7×	665 0.9×	269 1.4×	221 1.4×	215 1.4×	65	1.9k
Jubao Duan United States	22	1.2k 1.5×	682 0.9×	216 1.2×	113 0.7×	361 2.4×	72	2.2k
Geòrgia Escaramís Spain	27	858 1.1×	301 0.4×	201 1.1×	167 1.0×	245 1.6×	61	2.2k
Adriana Lori United States	22	522 0.7×	257 0.3×	165 0.9×	239 1.5×	112 0.7×	58	1.7k
Henriette Raventós Costa Rica	22	457 0.6×	487 0.7×	303 1.6×	159 1.0×	172 1.1×	75	1.6k
Juan Pablo López Canada	24	787 1.0×	308 0.4×	116 0.6×	168 1.0×	191 1.3×	53	1.8k
Gilles Maussion Canada	22	903 1.1×	430 0.6×	226 1.2×	250 1.5×	255 1.7×	36	1.8k
Amanda Mitchell United States	23	1.3k 1.6×	591 0.8×	341 1.8×	70 0.4×	248 1.7×	59	2.3k
Lourdes Martorell Spain	22	594 0.7×	410 0.6×	209 1.1×	146 0.9×	255 1.7×	82	1.8k

Countries citing papers authored by Julien Bryois

Since Specialization

Citations

This map shows the geographic impact of Julien Bryois'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 Julien Bryois with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Julien Bryois more than expected).

Fields of papers citing papers by Julien Bryois

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Julien Bryois. 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 Julien Bryois. The network helps show where Julien Bryois may publish in the future.

Co-authorship network of co-authors of Julien Bryois

This figure shows the co-authorship network connecting the top 25 collaborators of Julien Bryois. A scholar is included among the top collaborators of Julien Bryois based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Julien Bryois. Julien Bryois is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Gaur, Pallavi, Julien Bryois, Daniela Calini, et al.. (2025). Single-nucleus and spatial transcriptomic profiling of human temporal cortex and white matter reveals key associations with AD pathology. Nature Communications. 16(1). 10395–10395.

Rietschel, Marcella, et al.. (2024). Conditional GWAS analysis to identify disorder-specific SNPs for psychiatric disorders. UNC Libraries.

Touil, Hanane, Tina Roostaei, Daniela Calini, et al.. (2023). A structured evaluation of cryopreservation in generating single-cell transcriptomes from cerebrospinal fluid. Cell Reports Methods. 3(7). 100533–100533. 8 indexed citations

Bryois, Julien, et al.. (2023). Mapping human adult hippocampal neurogenesis with single-cell transcriptomics: Reconciling controversy or fueling the debate?. Neuron. 111(11). 1714–1731.e3. 47 indexed citations

Bryois, Julien, Daniela Calini, Will Macnair, et al.. (2022). Cell-type-specific cis-eQTLs in eight human brain cell types identify novel risk genes for psychiatric and neurological disorders. Nature Neuroscience. 25(8). 1104–1112. 106 indexed citations

Koopmans, Frank, Miguel A. Gonzalez‐Lozano, Hanna C. A. Lammertse, et al.. (2022). Dysregulation of Synaptic and Developmental Transcriptomic/Proteomic Profiles upon Depletion of MUNC18-1. eNeuro. 9(6). ENEURO.0186–22.2022. 5 indexed citations

Nölle, Anna, Daniela Calini, Julien Bryois, et al.. (2021). Enrichment of Glial Cells From Human Post-mortem Tissue for Transcriptome and Proteome Analysis Using Immunopanning. Frontiers in Cellular Neuroscience. 15. 772011–772011. 3 indexed citations

Byrne, Enda M., Zhihong Zhu, Ting Qi, et al.. (2020). Conditional GWAS analysis to identify disorder-specific SNPs for psychiatric disorders. Molecular Psychiatry. 26(6). 2070–2081. 44 indexed citations

Yılmaz, Zeynep, Christopher Hübel, Julien Bryois, et al.. (2020). Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa. Yearbook of pediatric endocrinology. 3 indexed citations

10.

Halvorsen, Matthew, Ruth Huh, Nikolay Oskolkov, et al.. (2020). Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia. Nature Communications. 11(1). 1842–1842. 42 indexed citations

11.

Rossi, Mark A., Marcus L. Basiri, Jenna A. McHenry, et al.. (2019). Obesity remodels activity and transcriptional state of a lateral hypothalamic brake on feeding. Science. 364(6447). 1271–1274. 112 indexed citations

12.

Hill, W. David, Neil M Davies, Stuart J. Ritchie, et al.. (2019). Genome-wide analysis identifies molecular systems and 149 genetic loci associated with income. Nature Communications. 10(1). 5741–5741. 110 indexed citations

13.

Moslem, Mohsen, Julien Bryois, Harriet Rönnholm, et al.. (2019). Single cell analysis of autism patient with bi-allelic NRXN1-alpha deletion reveals skewed fate choice in neural progenitors and impaired neuronal functionality. Experimental Cell Research. 383(1). 111469–111469. 38 indexed citations

14.

Nagel, Mats, Philip R. Jansen, Sven Stringer, et al.. (2018). Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. Nature Genetics. 50(7). 920–927. 405 indexed citations breakdown →

15.

Skene, Nathan, Julien Bryois, Trygve E. Bakken, et al.. (2018). Genetic identification of brain cell types underlying schizophrenia. Nature Genetics. 50(6). 825–833. 326 indexed citations breakdown →

16.

Coleman, Jonathan R. I., Julien Bryois, Héléna A. Gaspar, et al.. (2018). Biological annotation of genetic loci associated with intelligence in a meta-analysis of 87,740 individuals. Molecular Psychiatry. 24(2). 182–197. 41 indexed citations

17.

Kim, Y, Paola Giusti‐Rodríguez, James J. Crowley, et al.. (2017). Comparative genomic evidence for the involvement of schizophrenia risk genes in antipsychotic effects. Molecular Psychiatry. 23(3). 708–712. 18 indexed citations

18.

Bryois, Julien, Alfonso Buil, Pedro G. Ferreira, et al.. (2017). Time-dependent genetic effects on gene expression implicate aging processes. Genome Research. 27(4). 545–552. 26 indexed citations

19.

Bryois, Julien, Alfonso Buil, David M. Evans, et al.. (2014). Cis and Trans Effects of Human Genomic Variants on Gene Expression. PLoS Genetics. 10(7). e1004461–e1004461. 93 indexed citations

20.

Hens, Korneel, Alina Isakova, Andreas Massouras, et al.. (2011). Automated protein-DNA interaction screening of Drosophila regulatory elements. Nature Methods. 8(12). 1065–1070. 67 indexed citations

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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