The Genotype-Tissue Expression (GTEx) project

Cited by (488)

Items 101–200 of 488

1. Sharing and Specificity of Co-expression Networks across 35 Human Tissues
   Pierson, Emma, the GTEx Consortium, Koller, Daphne, Battle, Alexis, Mostafavi, Sara · 2015 · PLOS Computational Biology
2. Genetics of suicide attempts in individuals with and without mental disorders: a population-based genome-wide association study
   Erlangsen, Annette, Appadurai, Vivek, Wang, Yunpeng, Turecki, Gustavo, Mors, Ole, Werge, Thomas, Mortensen, Preben B., Starnawska, Anna, Børglum, Anders D., Schork, Andrew et al. · 2020 · Molecular Psychiatry
3. The RNA-Binding Protein PUM2 Impairs Mitochondrial Dynamics and Mitophagy During Aging
   D’Amico, Davide, Mottis, Adrienne, Potenza, Francesca, Sorrentino, Vincenzo, Li, Hao, Romani, Mario, Lemos, Vera, Schoonjans, Kristina, Zamboni, Nicola, Knott, Graham et al. · 2019 · Molecular Cell
4. Receptor-Mediated Delivery of CRISPR-Cas9 Endonuclease for Cell-Type-Specific Gene Editing
   Rouet, Romain, Thuma, Benjamin A., Roy, Marc D., Lintner, Nathanael G., Rubitski, David M., Finley, James E., Wisniewska, Hanna M., Mendonsa, Rima, Hirsh, Ariana, de Oñate, Lorena et al. · 2018 · Journal of the American Chemical Society
5. Harnessing big ‘omics’ data and AI for drug discovery in hepatocellular carcinoma
   Chen, Bin, Garmire, Lana, Calvisi, Diego F., Chua, Mei-Sze, Kelley, Robin K., Chen, Xin · 2020 · Nature Reviews Gastroenterology & Hepatology
6. Genetics of primary sclerosing cholangitis and pathophysiological implications
   Jiang, Xiaojun, Karlsen, Tom H. · 2017 · Nature Reviews Gastroenterology & Hepatology
7. Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170
   EMBRACE, Dunning, Alison M, GEMO Study Collaborators, HEBON, kConFab Investigators, Michailidou, Kyriaki, Kuchenbaecker, Karoline B, Thompson, Deborah, French, Juliet D, Beesley, Jonathan et al. · 2016 · Nature Genetics
8. World Endometriosis Research Foundation Endometriosis Phenome and Biobanking Harmonisation Project: IV. Tissue collection, processing, and storage in endometriosis research
   Fassbender, Amelie, Rahmioglu, Nilufer, Vitonis, Allison F., Viganò, Paola, Giudice, Linda C., D’Hooghe, Thomas M., Hummelshoj, Lone, Adamson, G. David, Becker, Christian M., Missmer, Stacey A. et al. · 2014 · Fertility and Sterility
9. T cells genetically engineered to overcome death signaling enhance adoptive cancer immunotherapy
   Yamamoto, Tori N., Lee, Ping-Hsien, Vodnala, Suman K., Gurusamy, Devikala, Kishton, Rigel J., Yu, Zhiya, Eidizadeh, Arash, Eil, Robert, Fioravanti, Jessica, Gattinoni, Luca et al. · 2019 · Journal of Clinical Investigation
10. Origins of De Novo Genes in Human and Chimpanzee
    Ruiz-Orera, Jorge, Hernandez-Rodriguez, Jessica, Chiva, Cristina, Sabidó, Eduard, Kondova, Ivanela, Bontrop, Ronald, Marqués-Bonet, Tomàs, Albà, M.Mar · 2015 · PLOS Genetics
11. GWAS for executive function and processing speed suggests involvement of the CADM2 gene
    Ibrahim-Verbaas, C A, Bressler, J, Debette, S, Schuur, M, Smith, A V, Bis, J C, Davies, G, Trompet, S, Smith, J A, Wolf, C et al. · 2016 · Molecular Psychiatry
12. 3DSNP: a database for linking human noncoding SNPs to their three-dimensional interacting genes
    Lu, Yiming, Quan, Cheng, Chen, Hebing, Bo, Xiaochen, Zhang, Chenggang · 2017 · Nucleic Acids Research
13. Sex-Specific Role for the Long Non-coding RNA LINC00473 in Depression
    Issler, Orna, van der Zee, Yentl Y., Ramakrishnan, Aarthi, Wang, Junshi, Tan, Chunfeng, Loh, Yong-Hwee E., Purushothaman, Immanuel, Walker, Deena M., Lorsch, Zachary S., Hamilton, Peter J. et al. · 2020 · Neuron
14. Improving the diagnostic yield of exome- sequencing by predicting gene–phenotype associations using large-scale gene expression analysis
    Deelen, Patrick, van Dam, Sipko, Herkert, Johanna C., Karjalainen, Juha M., Brugge, Harm, Abbott, Kristin M., van Diemen, Cleo C., van der Zwaag, Paul A., Gerkes, Erica H., Zonneveld-Huijssoon, Evelien et al. · 2019 · Nature Communications
15. An epigenome-wide association study of sex-specific chronological ageing
    McCartney, Daniel L., Zhang, Futao, Hillary, Robert F., Zhang, Qian, Stevenson, Anna J., Walker, Rosie M., Bermingham, Mairead L., Boutin, Thibaud, Morris, Stewart W., Campbell, Archie et al. · 2020 · Genome Medicine
16. Proteomics analysis of plasma from middle-aged adults identifies protein markers of dementia risk in later life
    Walker, Keenan A., Chen, Jingsha, Shi, Liu, Yang, Yunju, Fornage, Myriam, Zhou, Linda, Schlosser, Pascal, Surapaneni, Aditya, Grams, Morgan E., Duggan, Michael R. et al. · 2023 · Science Translational Medicine
17. Evidence of CNIH3 involvement in opioid dependence
    Nelson, E C, Agrawal, A, Heath, A C, Bogdan, R, Sherva, R, Zhang, B, Al-Hasani, R, Bruchas, M R, Chou, Y-L, Demers, C H et al. · 2016 · Molecular Psychiatry
18. A multimodal whole-slide foundation model for pathology
    Ding, Tong, Wagner, Sophia J., Song, Andrew H., Chen, Richard J., Lu, Ming Y., Zhang, Andrew, Vaidya, Anurag J., Jaume, Guillaume, Shaban, Muhammad, Kim, Ahrong et al. · 2025 · Nature Medicine
19. Predicting drug-target interaction network using deep learning model
    You, Jiaying, McLeod, Robert D., Hu, Pingzhao · 2019 · Computational Biology and Chemistry
20. Exome-wide association study on alanine aminotransferase identifies sequence variants in the GPAM and APOE associated with fatty liver disease
    Jamialahmadi, Oveis, Mancina, Rosellina Margherita, Ciociola, Ester, Tavaglione, Federica, Luukkonen, Panu K., Baselli, Guido, Malvestiti, Francesco, Thuillier, Dorothée, Raverdy, Violeta, Männistö, Ville et al. · 2021 · Gastroenterology
21. KnockTF: a comprehensive human gene expression profile database with knockdown/knockout of transcription factors
    Feng, Chenchen, Song, Chao, Liu, Yuejuan, Qian, Fengcui, Gao, Yu, Ning, Ziyu, Wang, Qiuyu, Jiang, Yong, Li, Yanyu, Li, Meng et al. · 2020 · Nucleic Acids Research
22. Inferring relevant cell types for complex traits by using single-cell gene expression
    Calderon, Diego, Bhaskar, Anand, Knowles, David A., Golan, David, Raj, Towfique, Fu, Audrey Q., Pritchard, Jonathan K. · 2017 · The American Journal of Human Genetics
23. miRNATissueAtlas2: an update to the human miRNA tissue atlas
    Keller, Andreas, Gröger, Laura, Tschernig, Thomas, Solomon, Jeffrey, Laham, Omar, Schaum, Nicholas, Wagner, Viktoria, Kern, Fabian, Schmartz, Georges Pierre, Li, Yongping et al. · 2022 · Nucleic Acids Research
24. Precise reconstruction of the TME using bulk RNA-seq and a machine learning algorithm trained on artificial transcriptomes
    Zaitsev, Aleksandr, Chelushkin, Maksim, Dyikanov, Daniiar, Cheremushkin, Ilya, Shpak, Boris, Nomie, Krystle, Zyrin, Vladimir, Nuzhdina, Ekaterina, Lozinsky, Yaroslav, Zotova, Anastasia et al. · 2022 · Cancer Cell
25. Gene expression links functional networks across cortex and striatum
    Anderson, Kevin M., Krienen, Fenna M., Choi, Eun Young, Reinen, Jenna M., Yeo, B. T. Thomas, Holmes, Avram J. · 2018 · Nature Communications
26. Muscarinic receptor subtype distribution in the central nervous system and relevance to aging and Alzheimer's disease
    Evan P. Lebois, Catherine A. Thorn, Jeremy R. Edgerton, Michael Popiolek, S. Xi · 2017 · Neuropharmacology
27. NIH SenNet Consortium to map senescent cells throughout the human lifespan to understand physiological health.
    SenNet Consortium, Writing Group, Lee, Patty J., Benz, Christopher C., Blood, Philip, Börner, Katy, Campisi, Judith, Chen, Feng, Daldrup-Link, Heike, De Jager, Phil et al. · 2022 · Nature Aging
28. Single-cell analysis of somatic mutations in human bronchial epithelial cells in relation to aging and smoking
    Huang, Zhenqiu, Sun, Shixiang, Lee, Moonsook, Maslov, Alexander Y., Shi, Miao, Waldman, Spencer, Marsh, Ava, Siddiqui, Taha, Dong, Xiao, Peter, Yakov et al. · 2022 · Nature Genetics
29. Osteocyte transcriptome mapping identifies a molecular landscape controlling skeletal homeostasis and susceptibility to skeletal disease
    Youlten, Scott E., Kemp, John P., Logan, John G., Ghirardello, Elena J., Sergio, Claudio M., Dack, Michael R. G., Guilfoyle, Siobhan E., Leitch, Victoria D., Butterfield, Natalie C., Komla-Ebri, Davide et al. · 2021 · Nature Communications
30. Identification of novel genome-wide associations for suicidality in UK Biobank, genetic correlation with psychiatric disorders and polygenic association with completed suicide
    Strawbridge, Rona J., Ward, Joey, Ferguson, Amy, Graham, Nicholas, Shaw, Richard J., Cullen, Breda, Pearsall, Robert, Lyall, Laura M., Johnston, Keira J.A., Niedzwiedz, Claire L. et al. · 2019 · EBioMedicine
31. Casein kinase 1α: biological mechanisms and theranostic potential
    Jiang, Shaojie, Zhang, Miaofeng, Sun, Jihong, Yang, Xiaoming · 2018 · Cell Communication and Signaling
32. Systematic analysis of gene expression patterns associated with postmortem interval in human tissues
    Zhu, Yizhang, Wang, Likun, Yin, Yuxin, Yang, Ence · 2017 · Scientific Reports
33. Gene Regulatory Network Analysis Identifies Sex-Linked Differences in Colon Cancer Drug Metabolism
    Camila M. Lopes‐Ramos, Marieke L. Kuijjer, Shuji Ogino, Charles S. Fuchs, Dawn Lisa DeMeo, Kimberly Glass, John F Quackenbush · 2018 · Cancer Research
34. A quantitative framework for characterizing the evolutionary history of mammalian gene expression
    Chen, Jenny, Swofford, Ross, Johnson, Jeremy, Cummings, Beryl B., Rogel, Noga, Lindblad-Toh, Kerstin, Haerty, Wilfried, Palma, Federica di, Regev, Aviv · 2019 · Genome Research
35. GWAS and ExWAS of blood mitochondrial DNA copy number identifies 71 loci and highlights a potential causal role in dementia
    Michael Chong, Pedrum Mohammadi‐Shemirani, Nicolas Perrot, Walter Nelson, Robert W. Morton, Sukrit Narula, Ricky Lali, Irfan I. Khan, Mohammad Daud Khan, Conor S. Judge et al. · 2022 · eLife
36. Efficient Generation of Transcriptomic Profiles by Random Composite Measurements
    Cleary, Brian, Cong, Le, Cheung, Anthea, Lander, Eric S., Regev, Aviv · 2017 · Cell
37. Single-cell analysis reveals different age-related somatic mutation profiles between stem and differentiated cells in human liver
    Brazhnik, K., Sun, S., Alani, O., Kinkhabwala, M., Wolkoff, A. W., Maslov, A. Y., Dong, X., Vijg, J. · 2020 · Science Advances
38. Harnessing big data to characterize immune-related adverse events
    Jing, Ying, Yang, Jingwen, Johnson, Douglas B., Moslehi, Javid J., Han, Leng · 2022 · Nature Reviews Clinical Oncology
39. Interpretable deep learning translation of GWAS and multi-omics findings to identify pathobiology and drug repurposing in Alzheimer’s disease
    Xu, Jielin, Mao, Chengsheng, Hou, Yuan, Luo, Yuan, Binder, Jessica L., Zhou, Yadi, Bekris, Lynn M., Shin, Jiyoung, Hu, Ming, Wang, Fei et al. · 2022 · Cell Reports
40. The landscape of human tissue and cell type specific expression and co-regulation of senescence genes
    Xu, Peng, Wang, Minghui, Song, Won-min, Wang, Qian, Yuan, Guo-Cheng, Sudmant, Peter H., Zare, Habil, Tu, Zhidong, Orr, Miranda E., Zhang, Bin · 2022 · Molecular Neurodegeneration
41. From tissues to cell types and back: single-cell gene expression analysis of tissue architecture
    Chen, Xi, Teichmann, Sarah A., Meyer, Kerstin B. · 2018 · Annual Review of Biomedical Data Science
42. Sex-specific genetic predictors of Alzheimer’s disease biomarkers
    Alzheimer’s Disease Neuroimaging Initiative (ADNI), Deming, Yuetiva, The Alzheimer Disease Genetics Consortium (ADGC), Dumitrescu, Logan, Barnes, Lisa L., Thambisetty, Madhav, Kunkle, Brian, Gifford, Katherine A., Bush, William S., Chibnik, Lori B. et al. · 2018 · Acta Neuropathologica
43. scPower accelerates and optimizes the design of multi-sample single cell transcriptomic studies
    Schmid, Katharina T., Höllbacher, Barbara, Cruceanu, Cristiana, Böttcher, Anika, Lickert, Heiko, Binder, Elisabeth B., Theis, Fabian J., Heinig, Matthias · 2021 · Nature Communications
44. Functional implications of Neandertal introgression in modern humans
    Dannemann, Michael, Prüfer, Kay, Kelso, Janet · 2017 · Genome biology
45. Network medicine framework for identifying drug-repurposing opportunities for COVID-19
    Morselli Gysi, Deisy, do Valle, Ítalo, Zitnik, Marinka, Ameli, Asher, Gan, Xiao, Varol, Onur, Ghiassian, Susan Dina, Patten, J. J., Davey, Robert A., Loscalzo, Joseph et al. · 2021 · Proceedings of the National Academy of Sciences
46. On the origin of proteins in human drusen: The meet, greet and stick hypothesis
    Bergen, Arthur A., Arya, Swati, Koster, Céline, Pilgrim, Matthew G., Wiatrek-Moumoulidis, Dagmara, van der Spek, Peter J., Hauck, Stefanie M., Boon, Camiel J.F., Emri, Eszter, Stewart, Alan J. et al. · 2019 · Progress in Retinal and Eye Research
47. Stress and bronchodilator response in children with asthma
    Brehm, John M., Ramratnam, Sima K., Tse, Sze Man, Croteau-Chonka, Damien C., Pino-Yanes, Maria, Rosas-Salazar, Christian, Litonjua, Augusto A., Raby, Benjamin A., Boutaoui, Nadia, Han, Yueh-Ying et al. · 2015 · American Journal of Respiratory and Critical Care Medicine
48. The TMEM106B FTLD-protective variant, rs1990621, is also associated with increased neuronal proportion
    Li, Zeran, Farias, Fabiana H. G., Dube, Umber, Del-Aguila, Jorge L., Mihindukulasuriya, Kathie A., Fernandez, Maria Victoria, Ibanez, Laura, Budde, John P., Wang, Fengxian, Lake, Allison M. et al. · 2020 · Acta Neuropathologica
49. Whole-genome sequence-based analysis of thyroid function
    Taylor, Peter N., Porcu, Eleonora, Chew, Shelby, Campbell, Purdey J., Traglia, Michela, Brown, Suzanne J., Mullin, Benjamin H., Shihab, Hashem A., Min, Josine, Walter, Klaudia et al. · 2015 · Nature Communications
50. Integrated functional genomic analyses of Klinefelter and Turner syndromes reveal global network effects of altered X chromosome dosage
    Zhang, Xianglong, Hong, David, Ma, Shining, Ward, Thomas, Ho, Marcus, Pattni, Reenal, Duren, Zhana, Stankov, Atanas, Bade Shrestha, Sharon, Hallmayer, Joachim et al. · 2020 · Proceedings of the National Academy of Sciences
51. Analytical tools and current challenges in the modern era of neuroepigenomics
    Maze, Ian, Shen, Li, Zhang, Bin, Garcia, Benjamin A, Shao, Ningyi, Mitchell, Amanda, Sun, HaoSheng, Akbarian, Schahram, Allis, C David, Nestler, Eric J · 2014 · Nature Neuroscience
52. Know your target, know your molecule
    Mark E. Bunnage, Adam M. Gilbert, Lyn H. Jones, Erik C. Hett · 2015 · Nature Chemical Biology
53. Novel genetic loci affecting facial shape variation in humans
    Xiong, Ziyi, Dankova, Gabriela, Howe, Laurence J, Lee, Myoung Keun, Hysi, Pirro G, de Jong, Markus A, Zhu, Gu, Adhikari, Kaustubh, Li, Dan, Li, Yi et al. · 2019 · eLife
54. Identification of a regulatory variant that binds FOXA1 and FOXA2 at the CDC123/CAMK1D type 2 diabetes GWAS locus
    Fogarty, Marie P., Cannon, Maren E., Vadlamudi, Swarooparani, Gaulton, Kyle J., Mohlke, Karen L. · 2014 · PLoS Genetics
55. Mapping RNA splicing variations in clinically accessible and nonaccessible tissues to facilitate Mendelian disease diagnosis using RNA-seq
    Joseph K. Aicher, Paul D. Jewell, Jorge Vaquero-Garcia, Yoseph Barash, Elizabeth J. K. Bhoj · 2020 · Genetics in Medicine
56. NAD+ boosting reduces age-associated amyloidosis and restores mitochondrial homeostasis in muscle
    Romani, Mario, Sorrentino, Vincenzo, Oh, Chang-Myung, Li, Hao, de Lima, Tanes Imamura, Zhang, Hongbo, Shong, Minho, Auwerx, Johan · 2021 · Cell Reports
57. A core transcriptional signature of human microglia: derivation and utility in describing region-dependent alterations associated with Alzheimer’s disease
    Patir, Anirudh, Shih, Barbara, McColl, Barry W., Freeman, Tom C. · 2019 · Glia
58. Genome-wide meta-analysis reveals common splice site acceptor variant in CHRNA4 associated with nicotine dependence
    Hancock, D B, Reginsson, G W, Gaddis, N C, Chen, X, Saccone, N L, Lutz, S M, Qaiser, B, Sherva, R, Steinberg, S, Zink, F et al. · 2015 · Translational Psychiatry
59. Novel genome-wide associations for anhedonia, genetic correlation with psychiatric disorders, and polygenic association with brain structure
    Ward, Joey, Lyall, Laura M., Bethlehem, Richard A. I., Ferguson, Amy, Strawbridge, Rona J., Lyall, Donald M., Cullen, Breda, Graham, Nicholas, Johnston, Keira J. A., Bailey, Mark E. S. et al. · 2019 · Translational Psychiatry
60. DDR1 role in fibrosis and its pharmacological targeting
    Solange Moll, Alexis Desmoulière, Marcus Johannes Moeller, Jean‐Claude Pache, Laura Badi, Filippo Arcadu, Hans Georg Richter, Alexander Lee Satz, Sabine Uhles, Andrea Cavalli et al. · 2019 · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research
61. Regulatory SNPs: Altered Transcription Factor Binding Sites Implicated in Complex Traits and Diseases
    Arina O. Degtyareva, Elena V. Antontseva, Tatiana I. Merkulova · 2021 · International Journal of Molecular Sciences
62. Reduced mitochondrial calcium uptake in macrophages is a major driver of inflammaging
    Seegren, Philip V., Harper, Logan R., Downs, Taylor K., Zhao, Xiao-Yu, Viswanathan, Shivapriya B., Stremska, Marta E., Olson, Rachel J., Kennedy, Joel, Ewald, Sarah E., Kumar, Pankaj et al. · 2023 · Nature Aging
63. GWAS of smoking behaviour in 165,436 Japanese people reveals seven new loci and shared genetic architecture
    Matoba, Nana, Akiyama, Masato, Ishigaki, Kazuyoshi, Kanai, Masahiro, Takahashi, Atsushi, Momozawa, Yukihide, Ikegawa, Shiro, Ikeda, Masashi, Iwata, Nakao, Hirata, Makoto et al. · 2019 · Nature Human Behaviour
64. Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia
    Vijayakrishnan, Jayaram, Studd, James, Broderick, Peter, Kinnersley, Ben, Holroyd, Amy, Law, Philip J., Kumar, Rajiv, Allan, James M., Harrison, Christine J., Moorman, Anthony V. et al. · 2018 · Nature Communications
65. Molecular and phenotypic analysis of rodent models reveals conserved and species-specific modulators of human sarcopenia
    Börsch, Anastasiya, Ham, Daniel J., Mittal, Nitish, Tintignac, Lionel A., Migliavacca, Eugenia, Feige, Jérôme N., Rüegg, Markus A., Zavolan, Mihaela · 2021 · Communications Biology
66. Genomics implicates adaptive and innate immunity in Alzheimer’s and Parkinson’s diseases
    Gagliano, Sarah A., Pouget, Jennie G., Hardy, John, Knight, Jo, Barnes, Michael R., Ryten, Mina, Weale, Michael E. · 2016 · Annals of Clinical and Translational Neurology
67. Identification of key genes associated with polycystic ovary syndrome (PCOS) and ovarian cancer using an integrated bioinformatics analysis
    Juan Zou, Yukun Li, Nianchun Liao, Jue Liu, Qunfeng Zhang, Min Luo, Jiao Xiao, Yanhua Chen, Mengjie Wang, Kexin Chen et al. · 2022 · Journal of Ovarian Research
68. Determinants of transcription factor regulatory range
    Chen, Chen-Hao, Zheng, Rongbin, Tokheim, Collin, Dong, Xin, Fan, Jingyu, Wan, Changxin, Tang, Qin, Brown, Myles, Liu, Jun S., Meyer, Clifford A. et al. · 2020 · Nature Communications
69. Beyond Endometriosis Genome-Wide Association Study: From Genomics to Phenomics to the Patient
    Rahmioglu, Nilufer, Morris, Andrew, Nyholt, Dale, Montgomery, Grant, Becker, Christian, Missmer, Stacey, Zondervan, Krina · 2016 · Seminars in Reproductive Medicine
70. Genetic, epigenetic, and environmental factors controlling oxytocin receptor gene expression
    Danoff, Joshua S., Wroblewski, Kelly L., Graves, Andrew J., Quinn, Graham C., Perkeybile, Allison M., Kenkel, William M., Lillard, Travis S., Parikh, Hardik I., Golino, Hudson F., Gregory, Simon G. et al. · 2021 · Clinical Epigenetics
71. A Strategy for Discovery of Endocrine Interactions with Application to Whole-Body Metabolism
    Seldin, Marcus M., Koplev, Simon, Rajbhandari, Prashant, Vergnes, Laurent, Rosenberg, Gregory M., Meng, Yonghong, Pan, Calvin, Phuong, Thuy M.N., Gharakhanian, Raffi, Che, Nam et al. · 2018 · Cell Metabolism
72. Quantifying the contribution of Neanderthal introgression to the heritability of complex traits
    McArthur, Evonne, Rinker, David C., Capra, John A. · 2021 · Nature Communications
73. ID1 Mediates Escape from TGFβ Tumor Suppression in Pancreatic Cancer
    Huang, Yun-Han, Hu, Jing, Chen, Fei, Lecomte, Nicolas, Basnet, Harihar, David, Charles J., Witkin, Matthew D., Allen, Peter J., Leach, Steven D., Hollmann, Travis J. et al. · 2020 · Cancer Discovery
74. Molecular programs of fibrotic change in aging human lung
    Lee, Seoyeon, Islam, Mohammad Naimul, Boostanpour, Kaveh, Aran, Dvir, Jin, Guangchun, Christenson, Stephanie, Matthay, Michael A., Eckalbar, Walter L., DePianto, Daryle J., Arron, Joseph R. et al. · 2021 · Nature Communications
75. Comprehensive exploration of the genetic contribution of the dopaminergic and serotonergic pathways to psychiatric disorders
    Judit Cabana‐Domínguez, Bàrbara Torrico, Andreas Reif, Noèlia Fernàndez‐Castillo, Bru Cormand · 2022 · Translational Psychiatry
76. Enhancer variants associated with Alzheimer’s disease affect gene expression via chromatin looping
    Kikuchi, Masataka, Hara, Norikazu, Hasegawa, Mai, Miyashita, Akinori, Kuwano, Ryozo, Ikeuchi, Takeshi, Nakaya, Akihiro · 2019 · BMC Medical Genomics
77. Machine learning methods for histopathological image analysis: updates in 2024
    Komura, Daisuke, Ochi, Mieko, Ishikawa, Shumpei · 2025 · Computational and Structural Biotechnology Journal
78. A unified statistical framework for single cell and bulk RNA sequencing data
    Lingxue Zhu, Jing Lei, Bernie Devlin, Kathryn Roeder · 2018 · The Annals of Applied Statistics
79. Glucagon-like peptide-1 receptor agonists and diabetic retinopathy: nationwide cohort and Mendelian randomization studies
    Zheng, Deqiang, Li, Ning, Hou, Rui, Zhang, Xiaoyu, Wu, Lijuan, Sundquist, Jan, Sundquist, Kristina, Ji, Jianguang · 2023 · BMC Medicine
80. A meta-analysis of gene expression quantitative trait loci in brain
    Kim, Y, Xia, K, Tao, R, Giusti-Rodriguez, P, Vladimirov, V, van den Oord, E, Sullivan, P F · 2014 · Translational Psychiatry
81. Genome-Wide Association Study of Circadian Rhythmicity in 71,500 UK Biobank Participants and Polygenic Association with Mood Instability
    Ferguson, Amy, Lyall, Laura M., Ward, Joey, Strawbridge, Rona J., Cullen, Breda, Graham, Nicholas, Niedzwiedz, Claire L., Johnston, Keira J.A., MacKay, Daniel, Biello, Stephany M. et al. · 2018 · EBioMedicine
82. Truncating mutations in RBM12 are associated with psychosis
    Steinberg, Stacy, Gudmundsdottir, Steinunn, Sveinbjornsson, Gardar, Suvisaari, Jaana, Paunio, Tiina, Torniainen-Holm, Minna, Frigge, Michael L, Jonsdottir, Gudrun A, Huttenlocher, Johanna, Arnarsdottir, Sunna et al. · 2017 · Nature Genetics
83. Abdominal aortic aneurysm and cardiometabolic traits share strong genetic susceptibility to lipid metabolism and inflammation
    Shufen Zheng, Philip S. Tsao, Cuiping Pan · 2024 · Nature Communications
84. Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns
    Sliz, Eeva, Kalaoja, Marita, Ahola-Olli, Ari, Raitakari, Olli, Perola, Markus, Salomaa, Veikko, Lehtimäki, Terho, Karhu, Toni, Viinamäki, Heimo, Salmi, Marko et al. · 2019 · Journal of Medical Genetics
85. METTL14 downregulation drives S100A4+ monocyte-derived macrophages via MyD88/NF-κB pathway to promote MAFLD progression
    Wang, Yue-fan, Zhang, Wen-li, Li, Zhi-xuan, Liu, Yue, Tan, Jian, Yin, Hao-zan, Zhang, Zhi-chao, Piao, Xian-jie, Ruan, Min-hao, Dai, Zhi-hui et al. · 2024 · Signal Transduction and Targeted Therapy
86. Genome-wide association identifies the first risk loci for psychosis in Alzheimer disease
    DeMichele-Sweet, Mary Ann A., Klei, Lambertus, Creese, Byron, Harwood, Janet C., Weamer, Elise A., McClain, Lora, Sims, Rebecca, Hernandez, Isabel, Moreno-Grau, Sonia, Tárraga, Lluís et al. · 2021 · Molecular Psychiatry
87. Sensitive detection of chromatin-altering polymorphisms reveals autoimmune disease mechanisms
    del Rosario, Ricardo Cruz-Herrera, Poschmann, Jeremie, Rouam, Sigrid Laure, Png, Eileen, Khor, Chiea Chuen, Hibberd, Martin Lloyd, Prabhakar, Shyam · 2015 · Nature Methods
88. Admixture mapping identifies novel loci for obstructive sleep apnea in Hispanic/Latino Americans
    Wang, Heming, Cade, Brian E, Sofer, Tamar, Sands, Scott A, Chen, Han, Browning, Sharon R, Stilp, Adrienne M, Louie, Tin L, Thornton, Timothy A, Johnson, W Craig et al. · 2019 · Human Molecular Genetics
89. Genome-wide DNA methylation meta-analysis in the brains of suicide completers
    Policicchio, Stefania, Washer, Sam, Viana, Joana, Iatrou, Artemis, Burrage, Joe, Hannon, Eilis, Turecki, Gustavo, Kaminsky, Zachary, Mill, Jonathan, Dempster, Emma L. et al. · 2020 · Translational Psychiatry
90. SNCA Is a Functionally Low-Expressed Gene in Lung Adenocarcinoma
    Yuanliang Yan, Zhijie Xu, Xiaofang Hu · 2018 · Genes
91. Advances in Non-Coding RNA Sequencing
    Julia Micheel, Aram Safrastyan, Damian Wollny · 2021 · Non-Coding RNA
92. PharmVar GeneFocus : SLCO1B1
    Laura B. Ramsey, Li Gong, Seung‐been Lee, Jonathan B. Wagner, Xujia Zhou, Katrin Sangkuhl, Solomon M. Adams, Robert J. Straka, Philip E. Empey, Erin C. Boone et al. · 2022 · Clinical Pharmacology & Therapeutics
93. Impact and Evolutionary Determinants of Neanderthal Introgression on Transcriptional and Post-Transcriptional Regulation
    Silvert, Martin, Quintana-Murci, Lluis, Rotival, Maxime · 2019 · The American Journal of Human Genetics
94. The lncRNA Toolkit: Databases and In Silico Tools for lncRNA Analysis
    Pinkney, Holly R., Wright, Brandon M., Diermeier, Sarah D. · 2020 · Non-Coding RNA
95. Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics
    Barbeira, Alvaro N., Dickinson, Scott P., Bonazzola, Rodrigo, Zheng, Jiamao, Wheeler, Heather E., Torres, Jason M., Torstenson, Eric S., Shah, Kaanan P., Garcia, Tzintzuni, Edwards, Todd L. et al. · 2018 · Nature Communications
96. Variants encoding a restricted carboxy-terminal domain of SLC12A2 cause hereditary hearing loss in humans
    Hideki Mutai, Koichiro Wasano, Yukihide Momozawa, Yoichiro Kamatani, Fuyuki Miya, Sawako Masuda, Noriko Morimoto, Kiyomitsu Nara, Satoe Takahashi, Tatsuhiko Tsunoda et al. · 2020 · PLoS Genetics
97. Epigenome-Wide Association Study of Cognitive Functioning in Middle-Aged Monozygotic Twins
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