Bernie Devlin

58.5k total citations · 5 hit papers
196 papers, 16.2k citations indexed

About

Bernie Devlin is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Bernie Devlin has authored 196 papers receiving a total of 16.2k indexed citations (citations by other indexed papers that have themselves been cited), including 112 papers in Genetics, 62 papers in Molecular Biology and 39 papers in Cognitive Neuroscience. Recurrent topics in Bernie Devlin's work include Genetic Associations and Epidemiology (61 papers), Autism Spectrum Disorder Research (35 papers) and Genomic variations and chromosomal abnormalities (29 papers). Bernie Devlin is often cited by papers focused on Genetic Associations and Epidemiology (61 papers), Autism Spectrum Disorder Research (35 papers) and Genomic variations and chromosomal abnormalities (29 papers). Bernie Devlin collaborates with scholars based in United States, Canada and United Kingdom. Bernie Devlin's co-authors include Kathryn Roeder, Neil Risch, Mária Kovács, Norman C. Ellstrand, Silviu‐Alin Bacanu, Larry Wasserman, Stephen W. Scherer, Lambertus Klei, Andrew G. Stephenson and Robert E. Ferrell and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Bernie Devlin

192 papers receiving 15.5k citations

Hit Papers

5 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.

Genomic Control for Association Studies

1999 1.9k citations Bernie Devlin, Kathryn Roeder Biometrics profile →
Mutations in SDHD , a Mitochondrial Complex II Gene, in Hereditary Paraganglioma

2000 1.3k citations Bora E. Baysal, David Myssiorek et al. Science profile →
A Comparison of Linkage Disequilibrium Measures for Fine-Scale Mapping

1995 813 citations Bernie Devlin, Neil Risch profile →
Most genetic risk for autism resides with common variation

2014 774 citations Lambertus Klei, Stephan Sanders et al. profile →
Testing for an Unusual Distribution of Rare Variants

2011 432 citations Bernie Devlin, Kathryn Roeder et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Bernie Devlin United States	66	7.5k	5.1k	2.5k	1.9k	1.3k	196	16.2k
Kenneth K. Kídd United States	81	10.0k 1.3×	7.1k 1.4×	1.7k 0.7×	2.5k 1.3×	2.1k 1.5×	389	24.1k
Jonathan Flint United Kingdom	84	10.1k 1.3×	7.7k 1.5×	3.9k 1.5×	2.5k 1.3×	1.6k 1.2×	302	27.3k
Pamela Sklar United States	17	15.3k 2.0×	8.3k 1.6×	1.1k 0.5×	590 0.3×	1.2k 0.9×	23	26.3k
Grant W. Montgomery Australia	75	11.3k 1.5×	7.8k 1.5×	1.0k 0.4×	839 0.4×	946 0.7×	507	26.1k
Nicholas J. Schork United States	94	10.9k 1.4×	10.9k 2.1×	1.7k 0.7×	1.5k 0.8×	1.6k 1.2×	460	32.3k
Lon R. Cardon United Kingdom	74	13.6k 1.8×	8.9k 1.7×	1.4k 0.6×	1.5k 0.8×	1.2k 0.9×	188	28.2k
D.B. Bender United States	21	12.9k 1.7×	6.7k 1.3×	3.1k 1.2×	369 0.2×	778 0.6×	33	24.6k
Jürg Ott United States	74	8.5k 1.1×	10.6k 2.1×	1.4k 0.6×	1.3k 0.6×	1.2k 0.9×	343	25.1k
Moshe Szyf Canada	89	5.3k 0.7×	16.0k 3.1×	1.6k 0.7×	4.2k 2.2×	1.1k 0.8×	327	31.1k
Shaun Purcell United States	53	22.3k 3.0×	11.7k 2.3×	2.1k 0.8×	1.0k 0.5×	2.0k 1.5×	136	39.1k

Countries citing papers authored by Bernie Devlin

Since Specialization

Citations

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

Fields of papers citing papers by Bernie Devlin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bernie Devlin

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Mahjani, Behrang, Lambertus Klei, Henrik Larsson, et al.. (2023). Direct additive genetics and maternal effect contribute to the risk of Tourette disorder. Journal of Neurology Neurosurgery & Psychiatry. 94(8). 638–642. 2 indexed citations

Sloofman, Laura, Lindsay Liang, Enrico Mossotto, et al.. (2022). Spatiotemporal and genetic regulation of A-to-I editing throughout human brain development. Cell Reports. 41(5). 111585–111585. 12 indexed citations

Hoffman, Gabriel E., Andrew E. Jaffe, Michael J. Gandal, et al.. (2022). Comment on: What genes are differentially expressed in individuals with schizophrenia? A systematic review. Molecular Psychiatry. 28(2). 523–525. 7 indexed citations

Roeder, Kathryn, et al.. (2021). An approach to gene-based testing accounting for dependence of tests among nearby genes. Briefings in Bioinformatics. 22(6). 2 indexed citations

Piantadosi, Sean C., Lora McClain, Lambertus Klei, et al.. (2021). Transcriptome alterations are enriched for synapse-associated genes in the striatum of subjects with obsessive-compulsive disorder. Translational Psychiatry. 11(1). 171–171. 17 indexed citations

Belyeu, Jonathan R., Harrison Brand, Harold Wang, et al.. (2021). De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 families. The American Journal of Human Genetics. 108(4). 597–607. 50 indexed citations

Wang, Jiebiao, Bernie Devlin, & Kathryn Roeder. (2019). Using multiple measurements of tissue to estimate subject- and cell-type-specific gene expression. Bioinformatics. 36(3). 782–788. 20 indexed citations

Melhem, Nadine, Frank A. Middleton, Kathryn McFadden, et al.. (2011). Copy Number Variants for Schizophrenia and Related Psychotic Disorders in Oceanic Palau: Risk and Transmission in Extended Pedigrees. Biological Psychiatry. 70(12). 1115–1121. 23 indexed citations

Howrigan, Daniel P., N. M. Laird, Jordan W. Smoller, Bernie Devlin, & Matthew B. McQueen. (2011). Using linkage information to weight a genome‐wide association of bipolar disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 156(4). 462–471. 6 indexed citations

10.

Calkins, Monica E., Ping G. Tepper, Ruben C. Gur, et al.. (2010). Project Among African-Americans to Explore Risks for Schizophrenia (PAARTNERS): Evidence for Impairment and Heritability of Neurocognitive Functioning in Families of Schizophrenia Patients. American Journal of Psychiatry. 167(4). 459–472. 50 indexed citations

11.

Klei, Lambertus, et al.. (2010). Using ancestry matching to combine family‐based and unrelated samples for genome‐wide association studies. Statistics in Medicine. 29(28). 2932–2945. 5 indexed citations

12.

Kaye, Walter H., Cynthia M. Bulik, Katherine Plotnicov, et al.. (2008). The genetics of anorexia nervosa collaborative study: Methods and sample description. International Journal of Eating Disorders. 41(4). 289–300. 33 indexed citations

13.

Mansour, Hader, Joel Wood, Kodavali V. Chowdari, et al.. (2005). Association study of eight circadian genes with bipolar I disorder, schizoaffective disorder and schizophrenia. Genes Brain & Behavior. 5(2). 150–157. 221 indexed citations

14.

Mansour, Hader, Joel Wood, Michael E. Thase, et al.. (2005). Circadian Phase Variation in Bipolar I Disorder. Chronobiology International. 22(3). 571–584. 164 indexed citations

15.

Devlin, Bernie, Kathryn Roeder, & Larry Wasserman. (2003). Analysis of multilocus models of association. Genetic Epidemiology. 25(1). 36–47. 60 indexed citations

16.

Bacanu, Silviu‐Alin, Bernie Devlin, Kodavali V. Chowdari, et al.. (2002). Linkage analysis of Alzheimer disease with psychosis. Neurology. 59(1). 118–120. 45 indexed citations

17.

Roeder, Kathryn, et al.. (2000). Haplotype Fine Mapping by Evolutionary Trees. The American Journal of Human Genetics. 66(2). 659–673. 45 indexed citations

18.

Baysal, Bora E., Evert M. van Schothorst, David Myssiorek, et al.. (1999). Repositioning the hereditary paraganglioma critical region on chromosome band 11q23. Human Genetics. 104(3). 219–225. 46 indexed citations

19.

Devlin, Bernie, Neil Risch, & Kathryn Roeder. (1993). Statistical Evaluation of DNA Fingerprinting: a Critique of the NRC's Report. Science. 259(5096). 748–749. 40 indexed citations

20.

Roeder, Kathryn, Bernie Devlin, & Bruce G. Lindsay. (1989). Application of Maximum Likelihood Methods to Population Genetic Data for the Estimation of Individual Fertilities. Biometrics. 45(2). 363–363. 79 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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