Beate Glaser

2.4k total citations
18 papers, 760 citations indexed

About

Beate Glaser is a scholar working on Genetics, Molecular Biology and Clinical Psychology. According to data from OpenAlex, Beate Glaser has authored 18 papers receiving a total of 760 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 8 papers in Molecular Biology and 3 papers in Clinical Psychology. Recurrent topics in Beate Glaser's work include Congenital heart defects research (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Beate Glaser is often cited by papers focused on Congenital heart defects research (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Beate Glaser collaborates with scholars based in United Kingdom, Ireland and United States. Beate Glaser's co-authors include Michael O’Donovan, Michael J. Owen, Nigel Williams, George Kirov, Kieran C. Murphy, Marianne van den Bree, Katherine H. Shelton, George Davey Smith, Stephen Monks and Hywel Williams and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and American Journal of Psychiatry.

In The Last Decade

Beate Glaser

18 papers receiving 730 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Beate Glaser United Kingdom 13 436 374 107 100 87 18 760
Kathleen Hodgkinson Canada 15 428 1.0× 505 1.4× 79 0.7× 97 1.0× 128 1.5× 23 1.0k
Line Olsen Denmark 13 392 0.9× 192 0.5× 50 0.5× 91 0.9× 112 1.3× 17 868
Lin Xie United States 21 809 1.9× 330 0.9× 44 0.4× 65 0.7× 37 0.4× 42 1.3k
Wendy Gold Australia 14 413 0.9× 370 1.0× 46 0.4× 52 0.5× 146 1.7× 37 879
Amirthagowri Ambalavanan Canada 15 335 0.8× 348 0.9× 39 0.4× 65 0.7× 77 0.9× 31 795
Juan M. Peralta United States 17 321 0.7× 472 1.3× 62 0.6× 227 2.3× 140 1.6× 59 1.1k
William J. Cutter United Kingdom 12 212 0.5× 305 0.8× 58 0.5× 86 0.9× 276 3.2× 16 659
L. Giuffra United States 12 201 0.5× 393 1.1× 39 0.4× 149 1.5× 110 1.3× 23 797
Karola Rehnström Finland 14 257 0.6× 432 1.2× 67 0.6× 62 0.6× 256 2.9× 21 760
Muhammad Mahajnah Israel 16 391 0.9× 281 0.8× 41 0.4× 83 0.8× 59 0.7× 55 831

Countries citing papers authored by Beate Glaser

Since Specialization
Citations

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

Fields of papers citing papers by Beate Glaser

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Beate Glaser

This figure shows the co-authorship network connecting the top 25 collaborators of Beate Glaser. A scholar is included among the top collaborators of Beate Glaser 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 Beate Glaser. Beate Glaser is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Glaser, Beate, A. E. Ades, Sarah J. Lewis, et al.. (2010). Perinatal folate-related exposures and risk of psychotic symptoms in the ALSPAC birth cohort. Schizophrenia Research. 120(1-3). 177–183. 14 indexed citations
2.
Glaser, Beate, Katherine H. Shelton, & Marianne van den Bree. (2010). The Moderating Role of Close Friends in the Relationship Between Conduct Problems and Adolescent Substance Use. Journal of Adolescent Health. 47(1). 35–42. 59 indexed citations
3.
Medland, Sarah E., Tetyana Zayats, Beate Glaser, et al.. (2010). A Variant in LIN28B Is Associated with 2D:4D Finger-Length Ratio, a Putative Retrospective Biomarker of Prenatal Testosterone Exposure. The American Journal of Human Genetics. 86(4). 519–525. 71 indexed citations
4.
Glaser, Beate, David Gunnell, Nicholas J. Timpson, et al.. (2010). Age- and puberty-dependent association between IQ score in early childhood and depressive symptoms in adolescence. Psychological Medicine. 41(2). 333–343. 24 indexed citations
5.
Ruano, Dina, Gonçalo R. Abecasis, Beate Glaser, et al.. (2010). Functional Gene Group Analysis Reveals a Role of Synaptic Heterotrimeric G Proteins in Cognitive Ability. The American Journal of Human Genetics. 86(2). 113–125. 85 indexed citations
6.
Glaser, Beate & Peter Holmans. (2009). Comparison of Methods for Combining Case-Control and Family-Based Association Studies. Human Heredity. 68(2). 106–116. 8 indexed citations
7.
Azuma, Rayna, Eileen Daly, Linda Campbell, et al.. (2009). Visuospatial working memory in children and adolescents with 22q11.2 deletion syndrome; an fMRI study. Journal of Neurodevelopmental Disorders. 1(1). 46–60. 27 indexed citations
8.
Williams, Nigel, Hywel Williams, Elisa Majounie, et al.. (2008). Analysis of copy number variation using quantitative interspecies competitive PCR. Nucleic Acids Research. 36(17). e112–e112. 7 indexed citations
9.
Williams, Nigel, Beate Glaser, Nadine Norton, et al.. (2007). Strong evidence that GNB1L is associated with schizophrenia. Human Molecular Genetics. 17(4). 555–566. 44 indexed citations
10.
Glaser, Beate, Ivan Nikolov, Daniel Chubb, et al.. (2007). Analyses of single marker and pairwise effects of candidate loci for rheumatoid arthritis using logistic regression and random forests. BMC Proceedings. 1(S1). S54–S54. 8 indexed citations
11.
Hamshere, Marian L., Ricardo Segurado, Valentina Moskvina, et al.. (2007). Large-scale linkage analysis of 1302 affected relative pairs with rheumatoid arthritis. BMC Proceedings. 1(S1). S100–S100. 2 indexed citations
12.
Segurado, Ricardo, Marian L. Hamshere, Beate Glaser, et al.. (2007). Combining linkage data sets for meta-analysis and mega-analysis: the GAW15 rheumatoid arthritis data set. BMC Proceedings. 1(S1). S104–S104. 5 indexed citations
13.
Glaser, Beate, Valentina Moskvina, George Kirov, et al.. (2006). Analysis of ProDH, COMT and ZDHHC8 risk variants does not support individual or interactive effects on schizophrenia susceptibility. Schizophrenia Research. 87(1-3). 21–27. 34 indexed citations
14.
Paylor, Richard, Beate Glaser, Annalisa Mupo, et al.. (2006). Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: Implications for 22q11 deletion syndrome. Proceedings of the National Academy of Sciences. 103(20). 7729–7734. 225 indexed citations
15.
Glaser, Beate, George Kirov, Nicholas J. Bray, et al.. (2005). Identification of a potential Bipolar risk haplotype in the gene encoding the winged-helix transcription factor RFX4. Molecular Psychiatry. 10(10). 920–927. 21 indexed citations
16.
Williams, Hywel, Beate Glaser, Nigel Williams, et al.. (2005). No Association Between Schizophrenia and Polymorphisms in COMT in Two Large Samples. American Journal of Psychiatry. 162(9). 1736–1738. 65 indexed citations
17.
Green, Elaine, Gareth Elvidge, Nick Jacobsen, et al.. (2004). Localization of Bipolar Susceptibility Locus by Molecular Genetic Analysis of the Chromosome 12q23-q24 Region in Two Pedigrees With Bipolar Disorder and Darier’s Disease. American Journal of Psychiatry. 162(1). 35–42. 39 indexed citations
18.
Glaser, Beate, George Kirov, Elaine Green, Nick Craddock, & Michael J. Owen. (2004). Linkage disequilibrium mapping of bipolar affective disorder at 12q23‐q24 provides evidence for association at CUX2 and FLJ32356. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 132B(1). 38–45. 22 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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