Raymond K. Walters

38.1k total citations · 2 hit papers
18 papers, 1.6k citations indexed

About

Raymond K. Walters is a scholar working on Genetics, Epidemiology and Psychiatry and Mental health. According to data from OpenAlex, Raymond K. Walters has authored 18 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 3 papers in Epidemiology and 3 papers in Psychiatry and Mental health. Recurrent topics in Raymond K. Walters's work include Genetic Associations and Epidemiology (14 papers), Genetic and phenotypic traits in livestock (5 papers) and Genetic Mapping and Diversity in Plants and Animals (4 papers). Raymond K. Walters is often cited by papers focused on Genetic Associations and Epidemiology (14 papers), Genetic and phenotypic traits in livestock (5 papers) and Genetic Mapping and Diversity in Plants and Animals (4 papers). Raymond K. Walters collaborates with scholars based in United States, Netherlands and United Kingdom. Raymond K. Walters's co-authors include Benjamin M. Neale, Simon Gravel, Mark J. Daly, Alicia R. Martin, Christopher R. Gignoux, Eimear E. Kenny, Genevieve L. Wojcik, Carlos D. Bustamante, Robbee Wedow and James J. Lee and has published in prestigious journals such as Nature Genetics, Bioinformatics and American Journal of Psychiatry.

In The Last Decade

Raymond K. Walters

16 papers receiving 1.6k citations

Hit Papers

Human Demographic History Impacts Genetic Risk Prediction... 2017 2026 2020 2023 2017 2017 250 500 750
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.

  1. Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations
    2017 784 citations Alicia R. Martin, Christopher R. Gignoux et al. The American Journal of Human Genetics profile →
  2. Multi-trait analysis of genome-wide association summary statistics using MTAG
    2017 538 citations Patrick Turley, Raymond K. Walters et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Raymond K. Walters United States 9 1.1k 359 166 153 102 18 1.6k
Aysu Okbay Netherlands 12 705 0.6× 229 0.6× 209 1.3× 90 0.6× 75 0.7× 22 1.2k
Jack Euesden United Kingdom 10 659 0.6× 251 0.7× 169 1.0× 106 0.7× 170 1.7× 15 1.3k
Roseann E. Peterson United States 17 546 0.5× 207 0.6× 162 1.0× 112 0.7× 287 2.8× 51 1.2k
Lea K. Davis United States 26 811 0.7× 603 1.7× 131 0.8× 165 1.1× 202 2.0× 105 2.1k
Delilah Zabaneh United Kingdom 14 729 0.7× 282 0.8× 97 0.6× 148 1.0× 51 0.5× 20 1.4k
Alexander I. Young United Kingdom 14 891 0.8× 245 0.7× 307 1.8× 71 0.5× 132 1.3× 19 1.5k
Timothy Shin Heng Mak Hong Kong 13 784 0.7× 375 1.0× 91 0.5× 189 1.2× 327 3.2× 22 1.7k
Laurence J Howe United Kingdom 14 623 0.6× 246 0.7× 94 0.6× 105 0.7× 68 0.7× 25 1.1k
Lorenza Nisticò Italy 22 1.4k 1.3× 371 1.0× 130 0.8× 183 1.2× 76 0.7× 55 2.4k
Robbee Wedow United States 8 563 0.5× 198 0.6× 209 1.3× 58 0.4× 89 0.9× 18 1.1k

Countries citing papers authored by Raymond K. Walters

Since Specialization
Citations

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

Fields of papers citing papers by Raymond K. Walters

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Raymond K. Walters. 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 Raymond K. Walters. The network helps show where Raymond K. Walters may publish in the future.

Co-authorship network of co-authors of Raymond K. Walters

This figure shows the co-authorship network connecting the top 25 collaborators of Raymond K. Walters. A scholar is included among the top collaborators of Raymond K. Walters 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 Raymond K. Walters. Raymond K. Walters 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.
Carey, Caitlin E., Rebecca Shafee, Robbee Wedow, et al.. (2024). Principled distillation of UK Biobank phenotype data reveals underlying structure in human variation. Nature Human Behaviour. 8(8). 1599–1615. 8 indexed citations
2.
Walters, Raymond K., Tetyana Zayats, & Jan Haavik. (2023). GENETICS OF ADHD AND ITS UTILITY IN SCIENCE AND CLINIC. European Neuropsychopharmacology. 75. S20–S21.
3.
Carey, Caitlin E., Robbee Wedow, Nikolas Baya, et al.. (2023). Patterns of item nonresponse behaviour to survey questionnaires are systematic and associated with genetic loci. Nature Human Behaviour. 7(8). 1371–1387. 14 indexed citations
4.
5.
Hatoum, Alexander S., Emma C. Johnson, Sarah M. C. Colbert, et al.. (2021). The addiction risk factor: A unitary genetic vulnerability characterizes substance use disorders and their associations with common correlates. Neuropsychopharmacology. 47(10). 1739–1745. 63 indexed citations
6.
Walters, Raymond K., Ditte Demontis, Stephen V. Faraone, Anders D. Børglum, & Benjamin M. Neale. (2019). Increasing Trans-Ethnic Diversity In Genome-Wide Association Meta-Analysis Of ADHD. European Neuropsychopharmacology. 29. S722–S723. 1 indexed citations
7.
Klein, Marieke, Raymond K. Walters, Ditte Demontis, et al.. (2019). Genetic Markers of ADHD-Related Variations in Intracranial Volume. American Journal of Psychiatry. 176(3). 228–238. 48 indexed citations
8.
Walters, Raymond K., Benjamin M. Neale, Howard J. Edenberg, Joel Gelernter, & Amit Agrawal. (2019). GENOME-WIDE META-ANALYSIS OF >14,000 ALCOHOL DEPENDENT INDIVIDUALS HIGHLIGHTS PSYCHIATRIC COMORBIDITIES. European Neuropsychopharmacology. 29. S802–S802. 1 indexed citations
9.
Walters, Raymond K., Michel G. Nivard, Matthijs D. van der Zee, et al.. (2019). EXPLORING SEX DIFFERENCES IN THE GENETICS OF UK BIOBANK PHENOTYPES. European Neuropsychopharmacology. 29. S56–S56. 1 indexed citations
10.
Kim, Hyo‐Won, et al.. (2019). SU6HYPERACTIVITY SYMPTOM IS PREDICTED BY AGE-OF-MENARCHE POLYGENIC RISK SCORE IN ADHD CHILDREN. European Neuropsychopharmacology. 29. S1271–S1271. 1 indexed citations
11.
Lescai, Francesco, Kyle Satterstrom, Thomas D. Als, et al.. (2019). LARGE META-ANALYSIS OF SCANDINAVIAN EXOME SEQUENCING STUDIES OF SCHIZOPHRENIA. European Neuropsychopharmacology. 29. S813–S813. 1 indexed citations
12.
Turley, Patrick, Raymond K. Walters, Omeed Maghzian, et al.. (2017). Multi-trait analysis of genome-wide association summary statistics using MTAG. Nature Genetics. 50(2). 229–237. 538 indexed citations breakdown →
13.
Martin, Alicia R., Christopher R. Gignoux, Raymond K. Walters, et al.. (2017). Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations. The American Journal of Human Genetics. 100(4). 635–649. 784 indexed citations breakdown →
14.
Walters, Raymond K., Charles Laurin, & Gitta H. Lubke. (2014). Epi2Loc: An R Package to Investigate Two-Locus Epistatic Models. Twin Research and Human Genetics. 17(4). 272–278. 3 indexed citations
15.
Beek, Jenny H. D. A. van, Gitta H. Lubke, Marleen H. M. de Moor, et al.. (2014). Heritability of liver enzyme levels estimated from genome-wide SNP data. European Journal of Human Genetics. 23(9). 1223–1228. 11 indexed citations
16.
Walters, Raymond K., Charles Laurin, & Gitta H. Lubke. (2014). EpiPen: An R Package to Investigate Two-Locus Epistatic Models. Twin Research and Human Genetics. 17(4). 1 indexed citations
17.
Lubke, Gitta H., Jouke‐Jan Hottenga, Raymond K. Walters, et al.. (2012). Estimating the Genetic Variance of Major Depressive Disorder Due to All Single Nucleotide Polymorphisms. Biological Psychiatry. 72(8). 707–709. 88 indexed citations
18.
Walters, Raymond K., Charles Laurin, & Gitta H. Lubke. (2012). An integrated approach to reduce the impact of minor allele frequency and linkage disequilibrium on variable importance measures for genome-wide data. Bioinformatics. 28(20). 2615–2623. 13 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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