Karoline Kuchenbaecker

12.4k total citations · 1 hit paper
28 papers, 962 citations indexed

About

Karoline Kuchenbaecker is a scholar working on Genetics, Psychiatry and Mental health and Molecular Biology. According to data from OpenAlex, Karoline Kuchenbaecker has authored 28 papers receiving a total of 962 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 4 papers in Psychiatry and Mental health and 3 papers in Molecular Biology. Recurrent topics in Karoline Kuchenbaecker's work include Genetic Associations and Epidemiology (17 papers), BRCA gene mutations in cancer (6 papers) and Genetic and phenotypic traits in livestock (3 papers). Karoline Kuchenbaecker is often cited by papers focused on Genetic Associations and Epidemiology (17 papers), BRCA gene mutations in cancer (6 papers) and Genetic and phenotypic traits in livestock (3 papers). Karoline Kuchenbaecker collaborates with scholars based in United Kingdom, United States and Germany. Karoline Kuchenbaecker's co-authors include Muhammad Ayub, Segun Fatumo, Alicia R. Martin, Ananyo Choudhury, Tinashe Chikowore, Antonis C. Antoniou, Nasim Mavaddat, Douglas F. Easton, Alex Cunningham and Daniel I. Swerdlow and has published in prestigious journals such as Nature Medicine, Nature Communications and Bioinformatics.

In The Last Decade

Karoline Kuchenbaecker

26 papers receiving 949 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.

A roadmap to increase diversity in genomic studies

2022 276 citations Segun Fatumo, Tinashe Chikowore et al. Nature Medicine profile →

Peers

Karoline Kuchenbaecker

GENET

PHYSI

PHEOH

Heather Mason‐Suares United States

Longda Jiang Australia

Maiken E. Gabrielsen Norway

Nina Mars Finland

Diane T. Smelser United States

Eric A. W. Slob United Kingdom

Wes Spiller United Kingdom

Jennifer Malinowski United States

Paula Abreu United States

Akl C. Fahed United States

Heather Mason‐Suares United States

Karoline Kuchenbaecker

454 ×0.8

GENET

370 ×1.6

92 ×0.8

116 ×1.3

PHYSI

157 ×1.8

PHEOH

Citations per year, relative to Karoline Kuchenbaecker Karoline Kuchenbaecker (= 1×) peers Heather Mason‐Suares

Countries citing papers authored by Karoline Kuchenbaecker

Since Specialization

Citations

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

Fields of papers citing papers by Karoline Kuchenbaecker

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karoline Kuchenbaecker

This figure shows the co-authorship network connecting the top 25 collaborators of Karoline Kuchenbaecker. A scholar is included among the top collaborators of Karoline Kuchenbaecker 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 Karoline Kuchenbaecker. Karoline Kuchenbaecker 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

Kuchenbaecker, Karoline, et al.. (2026). Ancestral diversity in complex disease genetics: from discovery to translation. Nature Reviews Genetics.

Thu, Nguyễn Thị Hoài, Yoonsu Cho, Alona Sosinsky, et al.. (2025). Equity in cancer genomics in the UK: a cross-sectional analysis of a national cancer cohort. The Lancet Oncology. 26(7). 971–980. 1 indexed citations

Adams, Mark J., Yixiang Jiang, C Tian, et al.. (2024). Polygenic prediction of major depressive disorder and related traits in African ancestries UK Biobank participants. Molecular Psychiatry. 30(1). 151–157. 2 indexed citations

Levey, Daniel F., Olga Giannakopoulou, Joseph D. Deak, et al.. (2023). Genome-wide association studies and cross-population meta-analyses investigating short and long sleep duration. Nature Communications. 14(1). 6059–6059. 17 indexed citations

Meng, Xiangrui, Olga Giannakopoulou, Daniel F. Levey, et al.. (2023). 17. ANCESTRY-AWARE MIXED MODEL GWAS OF MAJOR DEPRESSION CHARTS A PATH FOR INCLUSIVE AND DIVERSE GENETIC RESEARCH. European Neuropsychopharmacology. 75. S65–S66. 1 indexed citations

Cooper, Claudia, Joseph Hayes, Andrew McQuillin, et al.. (2023). Investigating the association between schizophrenia and distance visual acuity: Mendelian randomisation study. BJPsych Open. 9(2). e33–e33. 2 indexed citations

Wang, Baihan, Leun J. Otten, Katja Schulze, et al.. (2023). Is auditory processing measured by the N100 an endophenotype for psychosis? A family study and a meta-analysis. Psychological Medicine. 54(8). 1559–1572. 3 indexed citations

Hodgson, Sam, Qin Qin Huang, Neneh Sallah, et al.. (2022). Integrating polygenic risk scores in the prediction of type 2 diabetes risk and subtypes in British Pakistanis and Bangladeshis: A population-based cohort study. PLoS Medicine. 19(5). e1003981–e1003981. 33 indexed citations

Mueller, Stefanie H., et al.. (2022). Mendelian randomization analyses implicate biogenesis of translation machinery in human aging. Genome Research. 32(2). 258–265. 9 indexed citations

10.

Huang, Qin Qin, Neneh Sallah, Bhavi Trivedi, et al.. (2022). Transferability of genetic loci and polygenic scores for cardiometabolic traits in British Pakistani and Bangladeshi individuals. Nature Communications. 13(1). 4664–4664. 34 indexed citations

11.

Mukadam, Naaheed, Olga Giannakopoulou, Nicholas Bass, Karoline Kuchenbaecker, & Andrew McQuillin. (2022). Genetic risk scores and dementia risk across different ethnic groups in UK Biobank. PLoS ONE. 17(12). e0277378–e0277378. 6 indexed citations

12.

Fatumo, Segun, Tinashe Chikowore, Ananyo Choudhury, et al.. (2022). A roadmap to increase diversity in genomic studies. Nature Medicine. 28(2). 243–250. 276 indexed citations breakdown →

13.

Farmaki, Aliki‐Eleni, Victoria Garfield, Sophie V. Eastwood, et al.. (2021). Type 2 diabetes risks and determinants in second-generation migrants and mixed ethnicity people of South Asian and African Caribbean descent in the UK. Diabetologia. 65(1). 113–127. 14 indexed citations

14.

Bhat, Anjali, Haritz Irizar, Johan H. Thygesen, et al.. (2021). Transcriptome-wide association study reveals two genes that influence mismatch negativity. Cell Reports. 34(11). 108868–108868. 9 indexed citations

15.

Gilly, Arthur, Lorraine Southam, Dániel Süveges, et al.. (2018). Very low-depth whole-genome sequencing in complex trait association studies. Bioinformatics. 35(15). 2555–2561. 60 indexed citations

16.

Mamakou, Vasiliki, Sophie Hackinger, Eleni Zengini, et al.. (2018). Combination therapy as a potential risk factor for the development of type 2 diabetes in patients with schizophrenia: the GOMAP study. BMC Psychiatry. 18(1). 249–249. 4 indexed citations

17.

Prins, Bram P., Karoline Kuchenbaecker, Yanchun Bao, et al.. (2017). Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations. Scientific Reports. 7(1). 11008–11008. 67 indexed citations

18.

Swerdlow, Daniel I., Karoline Kuchenbaecker, Sonia Shah, et al.. (2016). Selecting instruments for Mendelian randomization in the wake of genome-wide association studies. International Journal of Epidemiology. 45(5). 1600–1616. 213 indexed citations

19.

Kuchenbaecker, Karoline, Jacques Simard, Kenneth Offit, et al.. (2016). Abstract 2598: Predicting breast and ovarian cancer risks for BRCA1 and BRCA2 mutation carriers using polygenic risk scores. Cancer Research. 76(14_Supplement). 2598–2598. 1 indexed citations

20.

Holmes, Michael V., Sonia Shah, Aspasia Angelakopoulou, et al.. (2009). Complex disease genetics: present and future translational applications. Genome Medicine. 1(11). 104–104. 2 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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