The DOI matches its Crossref record; 50 of the 50 references it cites were found in a registry or an index.
Colocalization of GWAS and eQTL Signals Detects Target Genes
Open accessPublished version of a preprint
Abstract
The vast majority of genome-wide association study (GWAS) risk loci fall in non-coding regions of the genome. One possible hypothesis is that these GWAS risk loci alter the individual's disease risk through their effect on gene expression in different tissues. In order to understand the mechanisms driving a GWAS risk locus, it is helpful to determine which gene is affected in specific tissue types. For example, the relevant gene and tissue could play a role in the disease mechanism if the same variant responsible for a GWAS locus also affects gene expression. Identifying whether or not the same variant is causal in both GWASs and expression quantitative trail locus (eQTL) studies is challenging because of the uncertainty induced by linkage disequilibrium and the fact that some loci harbor multiple causal variants. However, current methods that address this problem assume that each locus contains a single causal variant. In this paper, we present eCAVIAR, a probabilistic method that has several key advantages over existing methods. First, our method can account for more than one causal variant in any given locus. Second, it can leverage summary statistics without accessing the individual genotype data. We use both simulated and real datasets to demonstrate the utility of our method. Using publicly available eQTL data on 45 different tissues, we demonstrate that eCAVIAR can prioritize likely relevant tissues and target genes for a set of glucose- and insulin-related trait loci.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Modern human genetics methods, such as genetic colocalization163 and Mendelian randomization164, can also be used to test causality in ageing clock models.”
From Measuring biological age using omics data (2022) · cites this paper as [163]
In the citing paper
“One colocalization method originally proposed by Plagnol et al 112 frames shared causality as the null hypothesis and rejection of this would indicate violation of IV condition 2, i.e. that there are no common causes of the instrument and the outcome.112–114”
From Mendelian randomization (2022) · cites this paper as [114]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
The Wellcome Trust Case Control Consortium, Management Committee, Burton, P. R., Clayton, D. G., Cardon, L. R., Craddock, N., Deloukas, P., Duncanson, A., Kwiatkowski, D. P., McCarthy, M. I., et al. (2007) · Nature · doi:10.1038/nature05911 · Cited by 9,442
A map of human genome variation from population-scale sequencing.
The 1000 Genomes Project Consortium (2010) · Nature · doi:10.1038/nature09534 · Cited by 7,877
An integrated map of genetic variation from 1,092 human genomes
The 1000 Genomes Project Consortium (2012) · Nature · doi:10.1038/nature11632 · Cited by 7,711
The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans
The GTEx Consortium, Ardlie, K. G., Deluca, D. S., Segrè, A. V., Sullivan, T. J., Young, T. R., Gelfand, E. T., Trowbridge, C. A., Maller, J. B., Tukiainen, T., et al. (2015) · Science · doi:10.1126/science.1262110 · Cited by 5,062
Self-citationGiambartolomei, C., Vukcevic, D., Schadt, E. E., Franke, L., Hingorani, A. D., Wallace, C., & Plagnol, V. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004383 · Cited by 4,261
Integrating common and rare genetic variation in diverse human populations
The International HapMap 3 Consortium (2010) · Nature · doi:10.1038/nature09298 · Cited by 3,026
The NHGRI GWAS Catalog, a curated resource of SNP-trait associations
Welter, D., MacArthur, J., Morales, J., Burdett, T., Hall, P., Junkins, H., Klemm, A., Flicek, P., Manolio, T., Hindorff, L., et al. (2014) · Nucleic Acids Research · doi:10.1093/nar/gkt1229 · Cited by 2,707
Integrative approaches for large-scale transcriptome-wide association studies
Gusev, A., Ko, A., Shi, H., Bhatia, G., Chung, W., Penninx, B. W. J. H., Jansen, R., de Geus, E. J. C., Boomsma, D. I., Wright, F. A., et al. (2016) · Nature Genetics · doi:10.1038/ng.3506 · Cited by 2,479
Visscher, P. M., Brown, M. A., McCarthy, M. I., & Yang, J. (2012) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2011.11.029 · Cited by 2,425
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
DIAGRAM Consortium, Dupuis, J., GIANT Consortium, Global BPgen Consortium, Anders Hamsten on behalf of Procardis Consortium, the MAGIC investigators, Langenberg, C., Prokopenko, I., Saxena, R., Soranzo, N., et al. (2010) · Nature Genetics · doi:10.1038/ng.520 · Cited by 2,166
Flagged first, then by citations
Cited by
Sorted by citations
Items 601–700 of 716
Sayer, J. A. (2018) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.734486771.793554174
Desch, K. C. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.736847106.793570169
Okamoto, J., Wang, L., Yin, X., Luca, F., Piqué-Regi, R., Helms, A. S., Im, H. K., Morrison, J., & Wen, X. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.07.19.500651
Khan, A. H., Bagley, J. R., LaPierre, N., Gonzalez‐Figueroa, C., Spencer, T. C., Choudhury, M., Xiao, X. G., Eskin, E., Jentsch, J. D., & Smith, D. J. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.11.10.516062
Self-citationWang, B., Lu, D., Zhang, C., Xu, N., Qiu, S., Bai, Y., Hu, B., & Qin, Z. S. (2022) · IEEE International Conference on Bioinformatics and Biomedicine (BIBM) · doi:10.1109/bibm55620.2022.9995232
Nguyen, D. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.03.22.533756
Data from Smoking Modifies Pancreatic Cancer Risk Loci on 2q21.3
Mocci, E., Kundu, P., Wheeler, W. M., Arslan, A. A., Freeman, L. E. B., Bracci, P. M., Brennan, P., Canzian, F., Du, M., Gallinger, S., et al. (2023) · doi:10.1158/0008-5472.c.6513538.v1
Dupuis, T., Anjana, R. M., Srinivasan, S., Dawed, A. Y., Melhem, A. L., Bigossi, M., Taylor, A., Adedire, E. T., Jebarani, S., Sartori, A., et al. (2023) · medRxiv · doi:10.1101/2023.05.04.23289501
Statistical methods for gene selection and genetic association studies
Cao, X. (2023) · Digital Commons - Michigan Tech (Michigan Technological University) · doi:10.37099/mtu.dc.etdr/1575
Prediction of transcription factor binding using epigenomics and genome variation data
Baumgarten, N. (2023) · Publication Server of Goethe University Frankfurt am Main (Goethe University Frankfurt) · doi:10.21248/gups.82138
Liu, Y., Liu, X., Zheng, Z., Ma, T., Liu, Y., Long, H., Cheng, H., Fang, M., Gong, J., Li, X., et al. (2020) · Figshare · doi:10.6084/m9.figshare.13076493
Self-citationLiu, Y., Liu, X., Zheng, Z., Ma, T., Liu, Y., Long, H., Cheng, H., Fang, M., Gong, J., Li, X., et al. (2020) · Figshare · doi:10.6084/m9.figshare.13076475
Self-citationLiu, Y., Liu, X., Zheng, Z., Ma, T., Liu, Y., Long, H., Cheng, H., Fang, M., Gong, J., Li, X., et al. (2020) · Figshare · doi:10.6084/m9.figshare.13076487
Self-citationLiu, Y., Liu, X., Zheng, Z., Ma, T., Liu, Y., Long, H., Cheng, H., Fang, M., Gong, J., Li, X., et al. (2020) · Figshare · doi:10.6084/m9.figshare.13076496
Self-citationSun, B., & Chen, L. (2023) · Figshare · doi:10.6084/m9.figshare.23665392
Sun, B., & Chen, L. (2023) · Figshare · doi:10.6084/m9.figshare.23665383
Liu, Y., Liu, X., Zheng, Z., Ma, T., Liu, Y., Long, H., Cheng, H., Fang, M., Gong, J., Li, X., et al. (2020) · Figshare · doi:10.6084/m9.figshare.13076484
Self-citationSun, B., & Chen, L. (2023) · Figshare · doi:10.6084/m9.figshare.23665380
Liu, Y., Liu, X., Zheng, Z., Ma, T., Liu, Y., Long, H., Cheng, H., Fang, M., Gong, J., Li, X., et al. (2020) · Figshare · doi:10.6084/m9.figshare.13076478
Self-citationSun, B., & Chen, L. (2023) · Figshare · doi:10.6084/m9.figshare.23665389
Liu, Y., Liu, X., Zheng, Z., Ma, T., Liu, Y., Long, H., Cheng, H., Fang, M., Gong, J., Li, X., et al. (2020) · Figshare · doi:10.6084/m9.figshare.13076469
Self-citationLiu, Y., Liu, X., Zheng, Z., Ma, T., Liu, Y., Long, H., Cheng, H., Fang, M., Gong, J., Li, X., et al. (2020) · Figshare · doi:10.6084/m9.figshare.13076490
Self-citationAdolphe, C., Xue, A., Fard, A. T., Genovesi, L. A., Yang, J., & Wainwright, B. J. (2021) · Figshare · doi:10.6084/m9.figshare.13727596
Liu, Y., Liu, X., Zheng, Z., Ma, T., Liu, Y., Long, H., Cheng, H., Fang, M., Gong, J., Li, X., et al. (2020) · Figshare · doi:10.6084/m9.figshare.13076472
Self-citationMendelian randomization Identifies RSPO3 in Serum as a Potential Target for EndometriosisPreprint
Guo, W., Zhong, Z., Yang, X., Ou, T., Zhang, D., Liu, Y., Zhang, Y., & Xiong, Y. (2024) · Research Square · doi:10.21203/rs.3.rs-4265646/v1
Kumar, R., Venkatesh, R., & Ritchie, M. D. (2024) · PubMed Central
Current molecular understanding of peripheral arterial disease
Adkar, S. S., & Leeper, N. J. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-13593-4.00006-8
Blüher, S., Rajcsanyi, L. S., Zheng, Y., Giuranna, J., & Hinney, A. (2024) · Springer eBooks · doi:10.1007/978-3-662-58895-6_6
Molecular Genetics of Primary Open-Angle Glaucoma
Aboobakar, I. F., Wiggs, J. L., & Segrè, A. V. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-13820-1.00144-4
Self-citationeQTL in diseased colon tissue identifies novel target genes associated with IBDPreprint
Nishiyama, N. C., Silverstein, S., Darlington, K., Ng, M. M. K., Clough, K., Bauer, M. J., Beasley, C., Bharadwaj, A., Ganesan, R., Kapadia, M. R., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.10.14.618229
Kuksa, P. P., Ionita, M., Carter, L., Cifello, J., Clark, K., Valladares, O., Leung, Y. Y., & Wang, L. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.10.30.621077
Hsiao, Y., Li, H., Xue, C. C., Chong, C. C. Y., Zhu, E., Yuan, Q., Yu, M., Cheung, C. M. G., Fan, Q., Sabanayagam, C., et al. (2025) · SSRN Electronic Journal · doi:10.2139/ssrn.5126663
Liu, C., Zhang, C., & Glatt, S. J. (2025) · Psychiatric Clinics of North America · doi:10.1016/j.psc.2025.01.002 · Cited by 1
Hu, X., Luo, B., Li, Y., Wang, Y., & Wang, J. (2025) · Research Square · doi:10.21203/rs.3.rs-5881486/v1
Zhang, G., Hao, J., Ren, Q., Guan, J., Li, Q., Bai, T., & Wang, K. (2025) · Journal of Affective Disorders · doi:10.1016/j.jad.2025.119647
Differing Genetics of Saline and Cocaine Self‐Administration in the Hybrid Mouse Diversity Panel
Khan, A. H., Bagley, J. R., LaPierre, N., Gonzalez‐Figueroa, C., Spencer, T. C., Choudhury, M., Xiao, X. G., Eskin, E., Jentsch, D., & Smith, D. J. (2025) · Genes Brain & Behavior · doi:10.1111/gbb.70029
Self-citationOverlap between COPD genetic association results and transcriptional quantitative trait loci
Saferali, A., Kim, W., Chase, R., Vollmers, C., Silverman, E. K., Cho, M., Castaldi, P. J., & Hersh, C. P. (2025) · Human Genetics and Genomics Advances · doi:10.1016/j.xhgg.2025.100493
Disentangling the multi-omics layers of complex traits: Celiac disease as a model
Cerqueira, J. X. D. M. (2025) · Advances in genetics · doi:10.1016/bs.adgen.2025.07.001
Gu, J., Fuller, C., Carbonetto, P. S., He, X., Zheng, J., & Li, H. (2025) · eLife · doi:10.7554/elife.107957
Gu, J., Fuller, C., Carbonetto, P. S., He, X., Zheng, J., & Li, H. (2025) · eLife · doi:10.7554/elife.107957.1
Siddiqui, M. K., Dupuis, T., Anjana, R. M., Dawed, A. Y., Bigossi, M., Srinivasan, S., Hodgson, S., Adedire, E. T., Taylor, A., Jebarani, S., et al. (2025) · Communications Medicine · doi:10.1038/s43856-025-01076-2
Li, Z., & Chen, L. (2025) · Genome biology · doi:10.1186/s13059-025-03767-4
Yu, L., Zhe, W., jin, P., Niu, Y., & Jiang, L. (2025) · medRxiv · doi:10.1101/2025.10.04.25337327
Lin, X., Zheng, Q., Ma, J., Ouyang, W., & Chen, B. (2025) · Medicine · doi:10.1097/md.0000000000045102
Mo, S., Wang, J., Li, X., Xie, Y., Yang, L., & Yang, K. (2025) · Journal of Asthma · doi:10.1080/02770903.2025.2580995
Self-citationAdvancing risk gene discovery across the allele frequency spectrum
Caballero, M., & Mahjani, B. (2026) · Human Genetics and Genomics Advances · doi:10.1016/j.xhgg.2026.100599
Sharma, M., & Wheeler, H. E. (2025) · G3 Genes Genomes Genetics · doi:10.1093/g3journal/jkaf277
Additional file 1 of Estimating colocalization probability from limited summary statistics
King, E. A., Dunbar, F., Davis, J. W., & Degner, J. F. (2021) · Figshare · doi:10.6084/m9.figshare.14608489
Ludwig‐Słomczyńska, A. H., Seweryn, M. T., Kapusta, P., Pitera, E., Mantaj, U., Cyganek, K., Gutaj, P., Dobrucka, Ł., Wender-Ożegowska, E., Małecki, M. T., et al. (2021) · Figshare · doi:10.6084/m9.figshare.13620034
Sun, B., & Chen, L. (2023) · Figshare · doi:10.6084/m9.figshare.23665377
Ludwig‐Słomczyńska, A. H., Seweryn, M. T., Kapusta, P., Pitera, E., Mantaj, U., Cyganek, K., Gutaj, P., Dobrucka, Ł., Wender-Ożegowska, E., Małecki, M. T., et al. (2021) · Figshare · doi:10.6084/m9.figshare.13620055
Sun, B., & Chen, L. (2023) · Figshare · doi:10.6084/m9.figshare.23665395
Aygün, N., Liang, D., Crouse, W. L., Keele, G. R., Love, M. I., & Stein, J. L. (2024) · Figshare · doi:10.6084/m9.figshare.26592971
Bone, W. P., Siewert, K. M., Jha, A., Klarin, D. M., Damrauer, S. M., Chang, K.-M., Tsao, P. S., Assimes, T. L., Ritchie, M. D., & Voight, B. F. (2021) · Figshare · doi:10.6084/m9.figshare.13719193
Ludwig‐Słomczyńska, A. H., Seweryn, M. T., Kapusta, P., Pitera, E., Mantaj, U., Cyganek, K., Gutaj, P., Dobrucka, Ł., Wender-Ożegowska, E., Małecki, M. T., et al. (2021) · Figshare · doi:10.6084/m9.figshare.13620073
Zhang, Y., Quick, C., Yu, K., Barbeira, A., Luca, F., Piqué-Regi, R., Kyung Im, H., & Wen, X. (2020) · Figshare · doi:10.6084/m9.figshare.12940576
Ludwig‐Słomczyńska, A. H., Seweryn, M. T., Kapusta, P., Pitera, E., Mantaj, U., Cyganek, K., Gutaj, P., Dobrucka, Ł., Wender-Ożegowska, E., Małecki, M. T., et al. (2021) · Figshare · doi:10.6084/m9.figshare.13620049
Ludwig‐Słomczyńska, A. H., Seweryn, M. T., Kapusta, P., Pitera, E., Mantaj, U., Cyganek, K., Gutaj, P., Dobrucka, Ł., Wender-Ożegowska, E., Małecki, M. T., et al. (2021) · Figshare · doi:10.6084/m9.figshare.13620061
Yang, C., Fagan, A. M., Perrin, R. J., Rhinn, H., Harari, O., & Cruchaga, C. (2023) · Figshare · doi:10.6084/m9.figshare.22605292
Aygün, N., Liang, D., Crouse, W. L., Keele, G. R., Love, M. I., & Stein, J. L. (2024) · Figshare · doi:10.6084/m9.figshare.26592974
Additional file 1 of MARS: leveraging allelic heterogeneity to increase power of association testing
Hormozdiari, F., Jung, J., Eskin, E., & Joo, J. W. J. (2021) · Figshare · doi:10.6084/m9.figshare.14524482
Self-citationAdolphe, C., Xue, A., Fard, A. T., Genovesi, L. A., Yang, J., & Wainwright, B. J. (2021) · Figshare · doi:10.6084/m9.figshare.13727593
Miguel Pérez-enciso, A., Zingaretti, L. M., Ramayo‐Caldas, Y., & de los Campos, G. (2021) · Figshare · doi:10.6084/m9.figshare.15128421
Aygün, N., Liang, D., Crouse, W. L., Keele, G. R., Love, M. I., & Stein, J. L. (2024) · Figshare · doi:10.6084/m9.figshare.26592962
Additional file 6 of MARS: leveraging allelic heterogeneity to increase power of association testing
Hormozdiari, F., Jung, J., Eskin, E., & J. Joo, J. W. (2021) · Figshare · doi:10.6084/m9.figshare.14524497
Self-citationZhang, Y., Quick, C., Yu, K., Barbeira, A., Luca, F., Piqué-Regi, R., Kyung Im, H., & Wen, X. (2020) · Figshare · doi:10.6084/m9.figshare.12940558
Aygün, N., Liang, D., Crouse, W. L., Keele, G. R., Love, M. I., & Stein, J. L. (2024) · Figshare · doi:10.6084/m9.figshare.26592968
Aygün, N., Liang, D., Crouse, W. L., Keele, G. R., Love, M. I., & Stein, J. L. (2024) · Figshare · doi:10.6084/m9.figshare.26592965
Liu, Y., Liu, X., Zheng, Z., Ma, T., Liu, Y., Long, H., Cheng, H., Fang, M., Gong, J., Li, X., et al. (2020) · Figshare · doi:10.6084/m9.figshare.13076481
Self-citationHsiao, Y. J., Li, H., Xue, C. C., Chong, C. C. Y., Zhu, E., Yuan, Q., Yu, M., Cheung, C. M. G., Fan, Q., Sabanayagam, C., et al. (2025) · Ophthalmology Science · doi:10.1016/j.xops.2025.101036 · Cited by 1
Functional characterization of a multi-cancer risk locus on chromosome band 2q33.1 near CASP8Preprint
Kong, H., Choi, J., Zhang, T., Gräwe, C., Xu, M., Thakur, R., Sowards, H., Hennessey, R. C., Vu, A. H., Shi, J., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.01.06.697866
Chen, H., Kaneko, N., Ohyama, Y., & Moriyama, M. (2026) · Journal of Autoimmunity · doi:10.1016/j.jaut.2025.103521
Farm animal evolution demonstrates hidden molecular basis of human traitsPreprint
Connally, N. J., & Sunyaev, S. R. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.02.703413
eQTL in diseased colon tissue identifies potential target genes associated with IBD
Nishiyama, N. C., Silverstein, S., Darlington, K., Ng, M. M. K., Clough, K., Bauer, M. J., Beasley, C., Bharadwaj, A., Ganesan, R., Kapadia, M. R., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-69364-6 · Cited by 1
Qiu, Z., Li, Z., Wu, Y., Chong, J., Chen, C., Li, J., Yang, Y., Lu, Z., Yuan, X., Zhu, Y., et al. (2026) · Research Square · doi:10.21203/rs.3.rs-8960093/v1
Genome wide association and integrative analysis of backfat thickness in a Yorkshire pig population
Wang, J., Cai, X., Zhong, Z., Lin, Q., Gao, Y., Wei, F., Si, J., Li, J., Qiu, X., & Zhang, Z. (2026) · Journal of Animal Science · doi:10.1093/jas/skag074
Zhai, M., Bai, F., Yan, R., & Liu, M. (2026) · Circulation Journal · doi:10.1253/circj.cj-25-1057
Shen, Q., Ding, R., Wen, Z., Feng, D., Zhang, J., Liu, J., Han, Q., Sun, L., Chen, H., Fei, S., et al. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1783844
Xu, S., Guo, G., Gao, J., Fang, Z., Chai, L., Gao, Y., Liu, J., Wang, J., Siqinbateer, & Zhang, L. (2026) · Current Drug Targets · doi:10.2174/0113894501444884260130225445
Dissecting human population variation in single-cell responses to SARS-CoV-2
Aquino, Y. (2023) · theses.fr (ABES) · doi:10.70675/061da45czf5e5z482dzb71dz92b95c997a05
Huang, P., Li, G.-W., Cheng, J., Chen, J., Ho, L., Lin, T., Chiu, F., Wu, C., Chang, S., Chuang, E. Y.-Y., et al. (2026) · EP Europace · doi:10.1093/europace/euag055
Coral, R.-P., Khandaker, G. M., Sanderson, E. C. M., Lau, J. Y. F., & Carvalho, L. A. (2026) · medRxiv · doi:10.64898/2026.04.08.26350416
Kinzy, T. G., Asowata, O. J., Cruz, L. A., Waksmunski, A. R., Cai, J., Mehta, P. A., Mitchell, S. L., Svaren, L. M., Aboobakar, I. F., Alimi, A. A., et al. (2026) · Ophthalmology Science · doi:10.1016/j.xops.2026.101196
Self-citationWang, L., Xu, Z., Luo, G., Wei, W., Guo, M., Yuan, Y., Shi, B., Guan, H., Liu, S., & Li, X. (2026) · Neuropsychiatric Disease and Treatment · doi:10.2147/ndt.s593689
Self-citationGong, T., Xu, Z., Wu, M., & Chen, Z. (2026) · Burns · doi:10.1016/j.burns.2026.108036
Xu, L., Zhou, B., Zhang, D., Shi, Q., Xiong, X., Huang, H., & Yang, Y. (2026) · Research Square · doi:10.21203/rs.3.rs-9412948/v1
Ancestry-specific and multi-ancestry genome-wide association studies of restless legs syndrome
Akçimen, F., Medeiros, M., Cederberg, K. L. J., Khani, M., Roth, A., Nalls, M. A., Bandrés‐Ciga, S., Dion, P. A., Rouleau, G. A., & Mignot, E. J.-M. (2026) · Nature Communications · doi:10.64898/2026.04.28.26351960
Functional characterization of a multi-cancer risk locus on chromosome band 2q33.1 near CASP8Preprint
Kong, H., Choi, J., Zhang, T., Gräwe, C., Xu, M., Thakur, R., Sowards, H., Hennessey, R. C., Vu, A. H., Shi, J., et al. (2026) · eLife · doi:10.7554/elife.110071
Functional characterization of a multi-cancer risk locus on chromosome band 2q33.1 near CASP8Preprint
Kong, H., Choi, J., Zhang, T., Gräwe, C., Xu, M., Thakur, R., Sowards, H., Hennessey, R. C., Vu, A. H., Shi, J., et al. (2026) · eLife · doi:10.7554/elife.110071.1
Lou, W., Dang, X., & Luo, X. (2026) · Molecular Psychiatry · doi:10.1038/s41380-026-03652-x
Zhu, F., Yao, X., Liu, D., Wang, S., Huang, X., Zhou, J., Wang, S., Tang, S., Lai, D., Yang, S., et al. (2026) · Inflammation Research · doi:10.1007/s00011-026-02268-9
Lin, Y., Li, W., Yang, X., Li, S., Liu, J., Lin, L., & Zhang, B. (2026) · Mammalian Genome · doi:10.1007/s00335-026-10232-5
Genome-Wide Association Study for Glucocorticoid-Induced Ocular Hypertension
Lama, J., Liu, R., Huerta‐Chagoya, A., Li, A., Huynh, K., Stanwyck, L. K., Han, S., Zhao, Y., Chan, W., Chen, L., et al. (2026) · Ophthalmology Science · doi:10.1016/j.xops.2026.101248
Self-citationUltra-fast genetic colocalisation across millions of association signals
Jesse, M., Riet, A.-E., & Alasoo, K. (2026) · PLoS Genetics · doi:10.1371/journal.pgen.1012209 · Cited by 1
Post–genome-wide association study variant-to-function challenges in asthma research
Zhong, X., Salamone, I. M., Nóbrega, M. A., He, X., & Ober, C. (2026) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2026.06.017
Tian, B., Meng, F., Wang, J., Zhang, H., Luo, T., Fu, J., Liu, K., Zhang, W., Zhao, C., Jiao, Y., et al. (2026) · Heart & Lung · doi:10.1016/j.hrtlng.2026.102892
Wang, L., Connelly, G. G., Dalapati, T., Jones, A. G., Schott, B. H., Trimarco, J. D., Heaton, N. S., & Ko, D. C. (2026) · Genome biology · doi:10.1186/s13059-026-04205-9
Multi-ancestry colocalization approaches
Shen, C., Dupuis, J., & Zhang, Q. (2026) · PLoS Genetics · doi:10.1371/journal.pgen.1012221
LocusBlend: Flexible multi-index regional visualization of genomic association signalsPreprint
Yang, C., Cook, N., Zeng, Y., Fu, T., Budde, J., Cruchaga, C., & Belloy, M. E. (2026) · medRxiv · doi:10.64898/2026.07.15.26358129
Metadata
- Authors
- Hormozdiari, F., van de Bunt, M., Segrè, A. V., Li, X., Joo, J. W. J., Bilow, M., Sul, J. H., Sankararaman, S., Pasaniuc, B., & Eskin, E.
- Affiliations
- University of California, Los Angeles (US)
- Broad Institute (US)
- Corresponding author
- Eskin, Eleazar
- ORCID
- Venue
- The American Journal of Human Genetics
- Publisher
- Elsevier BV
- Published
- 2016-12
- Volume
- 99
- Issue
- 6
- Pages
- 1245-1260
- ISSN
- 0002-9297 (ISSN-L)
- PMC
- PMC5142122
- OpenAlex
- W2555614465
- Cited by
- 697
- References
- 50
- Citations by year
- 2026: 69 · 2025: 76 · 2024: 75 · 2023: 90 · 2022: 81 · 2021: 100 · 2020: 78 · 2019: 59 · 2018: 46 · 2017: 22 · 2016: 1
- FWCI
- 34.43
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- The American Journal of Human Genetics (publishedVersion)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- National Institutes of Health (K25-HL080079, P01-HL28481, P01-HL30568, R01 -ES022282, R01-ES021801, R01-GM083198, R01-MH101782, U01-DA024417, U54EB020403)
- Broad Institute (R00-GM 111744-03)
- Novo Nordisk (HHSN268201000029C)
- National Science Foundation (0513612, 0729049, 0731455, 0916676, 1065276, 1302448, 1320589, 1331176)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Mapping and Diversity in Plants and Animals
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bioinformatics and Genomic Networks
- Keywords
- expression quantitative trait loci, GWAS risk loci, colocalization, causal variants, linkage disequilibrium, tissue-specific gene expression, target gene identification, summary statistics, non-coding variants
- MeSH terms
- Gene Expression Regulation, Genotype, Glucose, Humans, Insulin, Models, Genetic, Organ Specificity, Probability, Models, Statistical, Linkage Disequilibrium, Sample Size, Genetic Predisposition to Disease, Quantitative Trait Loci, Genome-Wide Association Study, Datasets as Topic
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review