Fast and accurate long-read alignment with Burrows-Wheeler transform.

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Items 101–200 of 1,225

1. Specification of CNS macrophage subsets occurs postnatally in defined niches
   Masuda, Takahiro, Amann, Lukas, Monaco, Gianni, Sankowski, Roman, Staszewski, Ori, Krueger, Martin, Del Gaudio, Francesca, He, Liqun, Paterson, Neil, Nent, Elisa et al. · 2022 · Nature
2. Repression of Stress-Induced LINE-1 Expression Protects Cancer Cell Subpopulations from Lethal Drug Exposure
   Guler, Gulfem Dilek, Tindell, Charles Albert, Pitti, Robert, Wilson, Catherine, Nichols, Katrina, KaiWai Cheung, Tommy, Kim, Hyo-Jin, Wongchenko, Matthew, Yan, Yibing, Haley, Benjamin et al. · 2017 · Cancer Cell
3. Adaptive evolution of multiple traits through multiple mutations at a single gene
   Linnen, Catherine R., Poh, Yu-Ping, Peterson, Brant K., Barrett, Rowan D. H., Larson, Joanna G., Jensen, Jeffrey D., Hoekstra, Hopi E. · 2013 · Science
4. Genomic insights into the evolutionary origin of Myxozoa within Cnidaria
   Chang, E. Sally, Neuhof, Moran, Rubinstein, Nimrod D., Diamant, Arik, Philippe, Hervé, Huchon, Dorothée, Cartwright, Paulyn · 2015 · Proceedings of the National Academy of Sciences
5. Reciprocal Signaling between Glioblastoma Stem Cells and Differentiated Tumor Cells Promotes Malignant Progression
   Wang, Xiuxing, Prager, Briana C., Wu, Qiulian, Kim, Leo J.Y., Gimple, Ryan C., Shi, Yu, Yang, Kailin, Morton, Andrew R., Zhou, Wenchao, Zhu, Zhe et al. · 2018 · Cell Stem Cell
6. Choice of bacterial DNA extraction method from fecal material influences community structure as evaluated by metagenomic analysis
   Wesolowska-Andersen, Agata, Bahl, Martin Iain, Carvalho, Vera, Kristiansen, Karsten, Sicheritz-Pontén, Thomas, Gupta, Ramneek, Licht, Tine Rask · 2014 · Microbiome
7. Pangenome-based genome inference allows efficient and accurate genotyping across a wide spectrum of variant classes
   Ebler, Jana, Ebert, Peter, Clarke, Wayne E., Rausch, Tobias, Audano, Peter A., Houwaart, Torsten, Mao, Yafei, Korbel, Jan O., Eichler, Evan E., Zody, Michael C. et al. · 2022 · Nature Genetics
8. Mutational signatures of ionizing radiation in second malignancies
   Behjati, Sam, Gundem, Gunes, Wedge, David C., Roberts, Nicola D., Tarpey, Patrick S., Cooke, Susanna L., Van Loo, Peter, Alexandrov, Ludmil B., Ramakrishna, Manasa, Davies, Helen et al. · 2016 · Nature Communications
9. H3.3K27M Cooperates with Trp53 Loss and PDGFRA Gain in Mouse Embryonic Neural Progenitor Cells to Induce Invasive High-Grade Gliomas
   Pathania, Manav, De Jay, Nicolas, Maestro, Nicola, Harutyunyan, Ashot S., Nitarska, Justyna, Pahlavan, Pirasteh, Henderson, Stephen, Mikael, Leonie G., Richard-Londt, Angela, Zhang, Ying et al. · 2017 · Cancer Cell
10. HMGB2 Loss upon Senescence Entry Disrupts Genomic Organization and Induces CTCF Clustering across Cell Types
    Zirkel, Anne, Nikolic, Milos, Sofiadis, Konstantinos, Mallm, Jan-Philipp, Brackley, Chris A., Gothe, Henrike, Drechsel, Oliver, Becker, Christian, Altmüller, Janine, Josipovic, Natasa et al. · 2018 · Molecular Cell
11. A Pliable Mediator Acts as a Functional Rather Than an Architectural Bridge between Promoters and Enhancers
    El Khattabi, Laila, Zhao, Haiyan, Kalchschmidt, Jens, Young, Natalie, Jung, Seolkyoung, Van Blerkom, Peter, Kieffer-Kwon, Philippe, Kieffer-Kwon, Kyong-Rim, Park, Solji, Wang, Xiang et al. · 2019 · Cell
12. Semi-automated assembly of high-quality diploid human reference genomes
    Jarvis, Erich D., Formenti, Giulio, Rhie, Arang, Guarracino, Andrea, Yang, Chentao, Wood, Jonathan, Tracey, Alan, Thibaud-Nissen, Francoise, Vollger, Mitchell R., Porubsky, David et al. · 2022 · Nature
13. An organoid‐derived bronchioalveolar model for SARS‐CoV‐2 infection of human alveolar type II‐like cells
    Lamers, Mart M, van der Vaart, Jelte, Knoops, Kèvin, Riesebosch, Samra, Breugem, Tim I, Mykytyn, Anna Z, Beumer, Joep, Schipper, Debby, Bezstarosti, Karel, Koopman, Charlotte D et al. · 2021 · The EMBO Journal
14. Frequent loss of heterozygosity in CRISPR-Cas9–edited early human embryos
    Alanis-Lobato, Gregorio, Zohren, Jasmin, McCarthy, Afshan, Fogarty, Norah M. E., Kubikova, Nada, Hardman, Emily, Greco, Maria, Wells, Dagan, Turner, James M. A., Niakan, Kathy K. · 2021 · Proceedings of the National Academy of Sciences
15. A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndrome
    Buchovecky, Christie M, Turley, Stephen D, Brown, Hannah M, Kyle, Stephanie M, McDonald, Jeffrey G, Liu, Benny, Pieper, Andrew A, Huang, Wenhui, Katz, David M, Russell, David W et al. · 2013 · Nature Genetics
16. Dnmt3a loss predisposes murine hematopoietic stem cells to malignant transformation
    Mayle, Allison, Yang, Liubin, Rodriguez, Benjamin, Zhou, Ting, Chang, Edmund, Curry, Choladda V., Challen, Grant A., Li, Wei, Wheeler, David, Rebel, Vivienne I. et al. · 2015 · Blood
17. De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome
    Suls, Arvid, Jaehn, Johanna A., Kecskés, Angela, Weber, Yvonne, Weckhuysen, Sarah, Craiu, Dana C., Siekierska, Aleksandra, Djémié, Tania, Afrikanova, Tatiana, Gormley, Padhraig et al. · 2013 · The American Journal of Human Genetics
18. CRISPR-Based Adenine Editors Correct Nonsense Mutations in a Cystic Fibrosis Organoid Biobank
    Geurts, Maarten H., de Poel, Eyleen, Amatngalim, Gimano D., Oka, Rurika, Meijers, Fleur M., Kruisselbrink, Evelien, van Mourik, Peter, Berkers, Gitte, de Winter-de Groot, Karin M., Michel, Sabine et al. · 2020 · Cell Stem Cell
19. CRISPR-Cas9-based mutagenesis frequently provokes on-target mRNA misregulation
    Tuladhar, Rubina, Yeu, Yunku, Tyler Piazza, John, Tan, Zhen, Rene Clemenceau, Jean, Wu, Xiaofeng, Barrett, Quinn, Herbert, Jeremiah, Mathews, David H., Kim, James et al. · 2019 · Nature Communications
20. A general approach for detecting expressed mutations in AML cells using single cell RNA-sequencing
    Petti, Allegra A., Williams, Stephen R., Miller, Christopher A., Fiddes, Ian T., Srivatsan, Sridhar N., Chen, David Y., Fronick, Catrina C., Fulton, Robert S., Church, Deanna M., Ley, Timothy J. · 2019 · Nature Communications
21. Acquired RAS or EGFR mutations and duration of response to EGFR blockade in colorectal cancer
    Van Emburgh, Beth O., Arena, Sabrina, Siravegna, Giulia, Lazzari, Luca, Crisafulli, Giovanni, Corti, Giorgio, Mussolin, Benedetta, Baldi, Federica, Buscarino, Michela, Bartolini, Alice et al. · 2016 · Nature Communications
22. Genetic determinants of co-accessible chromatin regions in activated T cells across humans
    Gate, Rachel E., Cheng, Christine S., Aiden, Aviva P., Siba, Atsede, Tabaka, Marcin, Lituiev, Dmytro, Machol, Ido, Gordon, M. Grace, Subramaniam, Meena, Shamim, Muhammad et al. · 2018 · Nature Genetics
23. The gut microbiome regulates the increases in depressive-type behaviors and in inflammatory processes in the ventral hippocampus of stress vulnerable rats
    Pearson-Leary, Jiah, Zhao, Chunyu, Bittinger, Kyle, Eacret, Darrell, Luz, Sandra, Vigderman, Abigail S., Dayanim, Gabriel, Bhatnagar, Seema · 2020 · Molecular Psychiatry
24. Atlas of breast cancer infiltrated B-lymphocytes revealed by paired single-cell RNA-sequencing and antigen receptor profiling
    Hu, Qingtao, Hong, Yu, Qi, Pan, Lu, Guangqing, Mai, Xueying, Xu, Sheng, He, Xiaoying, Guo, Yu, Gao, Linlin, Jing, Zhiyi et al. · 2021 · Nature Communications
25. Application of single-cell RNA sequencing in optimizing a combinatorial therapeutic strategy in metastatic renal cell carcinoma
    Kim, Kyu-Tae, Lee, Hye Won, Lee, Hae-Ock, Song, Hye Jin, Jeong, Da Eun, Shin, Sang, Kim, Hyunho, Shin, Yoojin, Nam, Do-Hyun, Jeong, Byong Chang et al. · 2016 · Genome Biology
26. Autophagy Regulation of Metabolism Is Required for CD8+ T Cell Anti-tumor Immunity
    DeVorkin, Lindsay, Pavey, Nils, Carleton, Gillian, Comber, Alexandra, Ho, Cally, Lim, Junghyun, McNamara, Erin, Huang, Haochu, Kim, Paul, Zacharias, Lauren G. et al. · 2019 · Cell Reports
27. Tissue-resident memory CD8+ T cells shape local and systemic secondary T cell responses
    Behr, Felix M., Parga-Vidal, Loreto, Kragten, Natasja A. M., van Dam, Teunis J. P., Wesselink, Thomas H., Sheridan, Brian S., Arens, Ramon, van Lier, Rene A. W., Stark, Regina, van Gisbergen, Klaas P. J. M. · 2020 · Nature Immunology
28. Depletion of RUNX1/ETO in t(8;21) AML cells leads to genome-wide changes in chromatin structure and transcription factor binding
    Ptasinska, A, Assi, S A, Mannari, D, James, S R, Williamson, D, Dunne, J, Hoogenkamp, M, Wu, M, Care, M, McNeill, H et al. · 2012 · Leukemia
29. SHANK2 mutations associated with autism spectrum disorder cause hyperconnectivity of human neurons
    Zaslavsky, Kirill, Zhang, Wen-Bo, McCready, Fraser P., Rodrigues, Deivid C., Deneault, Eric, Loo, Caitlin, Zhao, Melody, Ross, P. Joel, El Hajjar, Joelle, Romm, Asli et al. · 2019 · Nature Neuroscience
30. A YAP/FOXM1 axis mediates EMT-associated EGFR inhibitor resistance and increased expression of spindle assembly checkpoint components
    Nilsson, Monique B., Sun, Huiying, Robichaux, Jacqulyne, Pfeifer, Matthias, McDermott, Ultan, Travers, Jon, Diao, Lixia, Xi, Yuanxin, Tong, Pan, Shen, Li et al. · 2020 · Science Translational Medicine
31. Genome Sequences Reveal Cryptic Speciation in the Human Pathogen Histoplasma capsulatum
    Sepúlveda, Victoria E., Márquez, Roberto, Turissini, David A., Goldman, William E., Matute, Daniel R. · 2017 · mBio
32. Rationally designed APOBEC3B cytosine base editors with improved specificity
    Jin, Shuai, Fei, Hongyuan, Zhu, Zixu, Luo, Yingfeng, Liu, Jinxing, Gao, Shenghan, Zhang, Feng, Chen, Yu-Hang, Wang, Yanpeng, Gao, Caixia · 2020 · Molecular Cell
33. Confirmation of fifth Candida auris clade by whole genome sequencing
    Spruijtenburg, Bram, Badali, Hamid, Abastabar, Mahdi, Mirhendi, Hossein, Khodavaisy, Sadegh, Sharifisooraki, Joobin, Taghizadeh Armaki, Mojtaba, de Groot, Theun, Meis, Jacques F. · 2022 · Emerging Microbes & Infections
34. The Landscape of L1 Retrotransposons in the Human Genome Is Shaped by Pre-insertion Sequence Biases and Post-insertion Selection
    Sultana, Tania, van Essen, Dominic, Siol, Oliver, Bailly-Bechet, Marc, Philippe, Claude, Zine El Aabidine, Amal, Pioger, Léo, Nigumann, Pilvi, Saccani, Simona, Andrau, Jean-Christophe et al. · 2019 · Molecular Cell
35. Quantum computing at the frontiers of biological sciences
    Emani, Prashant S., Warrell, Jonathan, Anticevic, Alan, Bekiranov, Stefan, Gandal, Michael, McConnell, Michael J., Sapiro, Guillermo, Aspuru-Guzik, Alán, Baker, Justin T., Bastiani, Matteo et al. · 2021 · Nature Methods
36. SNPsplit: Allele-specific splitting of alignments between genomes with known SNP genotypes
    Krueger, Felix, Andrews, Simon R. · 2016 · F1000Research
37. Evolutionary insight from whole‐genome sequencing of experimentally evolved microbes
    DETTMAN, JEREMY R., RODRIGUE, NICOLAS, MELNYK, ANITA H., WONG, ALEX, BAILEY, SUSAN F., KASSEN, REES · 2012 · Molecular Ecology
38. Modeling Clinical Responses to Targeted Therapies by Patient-Derived Organoids of Advanced Lung Adenocarcinoma
    Kim, Seok-Young, Kim, Sang-Min, Lim, Sumin, Lee, Ji Yeon, Choi, Su-Jin, Yang, San-Duk, Yun, Mi Ran, Kim, Chang Gon, Gu, Seo Rin, Park, Chaewon et al. · 2021 · Clinical Cancer Research
39. Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes
    Flannick, Jason, Beer, Nicola L, Bick, Alexander G, Agarwala, Vineeta, Molnes, Janne, Gupta, Namrata, Burtt, Noël P, Florez, Jose C, Meigs, James B, Taylor, Herman et al. · 2013 · Nature Genetics
40. Sources of bias in measures of allele-specific expression derived from RNA-seq data aligned to a single reference genome
    Stevenson, Kraig R, Coolon, Joseph D, Wittkopp, Patricia J · 2013 · BMC Genomics
41. Deriving genomic diagnoses without revealing patient genomes
    Jagadeesh, Karthik A., Wu, David J., Birgmeier, Johannes A., Boneh, Dan, Bejerano, Gill · 2017 · Science
42. A survey of k-mer methods and applications in bioinformatics
    Moeckel, Camille, Mareboina, Manvita, Konnaris, Maxwell A., Chan, Candace S.Y., Mouratidis, Ioannis, Montgomery, Austin, Chantzi, Nikol, Pavlopoulos, Georgios A., Georgakopoulos-Soares, Ilias · 2024 · Computational and Structural Biotechnology Journal
43. SORL1 rare variants: a major risk factor for familial early-onset Alzheimer’s disease
    Nicolas, G, Charbonnier, C, Wallon, D, Quenez, O, Bellenguez, C, Grenier-Boley, B, Rousseau, S, Richard, A-C, Rovelet-Lecrux, A, Le Guennec, K et al. · 2016 · Molecular Psychiatry
44. Intraductal papillary mucinous neoplasms arise from multiple independent clones, each with distinct mutations
    Fischer, Catherine G., Beleva Guthrie, Violeta, Braxton, Alicia M., Zheng, Lily, Wang, Pei, Song, Qianqian, Griffin, James F., Chianchiano, Peter E., Hosoda, Waki, Niknafs, Noushin et al. · 2019 · Gastroenterology
45. Genome-wide de novo L1 Retrotransposition Connects Endonuclease Activity with Replication
    Flasch, Diane A., Macia, Ángela, Sánchez, Laura, Ljungman, Mats, Heras, Sara R., García-Pérez, José L., Wilson, Thomas E., Moran, John V. · 2019 · Cell
46. Rare pathogenic variants predispose to hepatocellular carcinoma in nonalcoholic fatty liver disease
    Pelusi, Serena, Baselli, Guido, Pietrelli, Alessandro, Dongiovanni, Paola, Donati, Benedetta, McCain, Misti Vanette, Meroni, Marica, Fracanzani, Anna Ludovica, Romagnoli, Renato, Petta, Salvatore et al. · 2019 · Scientific Reports
47. Accuracy and efficiency of germline variant calling pipelines for human genome data
    Zhao, Sen, Agafonov, Oleg, Azab, Abdulrahman, Stokowy, Tomasz, Hovig, Eivind · 2020 · Scientific Reports
48. Patterns of Genomic Variation in the Opportunistic Pathogen Candida glabrata Suggest the Existence of Mating and a Secondary Association with Humans
    Carreté, Laia, Ksiezopolska, Ewa, Pegueroles, Cinta, Gómez-Molero, Emilia, Saus, Ester, Iraola-Guzmán, Susana, Loska, Damian, Bader, Oliver, Fairhead, Cecile, Gabaldón, Toni · 2018 · Current Biology
49. RNA methylation influences TDP43 binding and disease pathogenesis in models of amyotrophic lateral sclerosis and frontotemporal dementia
    McMillan, Michael, Gomez, Nicolas, Hsieh, Caroline, Bekier, Michael, Li, Xingli, Miguez, Roberto, Tank, Elizabeth M.H., Barmada, Sami J. · 2023 · Molecular Cell
50. Reference genome of wild goat (Capra aegagrus) and sequencing of goat breeds provide insight into genic basis of goat domestication
    Dong, Yang, Zhang, Xiaolei, Xie, Min, Arefnezhad, Babak, Wang, Zongji, Wang, Wenliang, Feng, Shaohong, Huang, Guodong, Guan, Rui, Shen, Wenjing et al. · 2015 · BMC Genomics
51. Single-cell mutational profiling and clonal phylogeny in cancer
    Potter, Nicola E., Ermini, Luca, Papaemmanuil, Elli, Cazzaniga, Giovanni, Vijayaraghavan, Gowri, Titley, Ian, Ford, Anthony, Campbell, Peter, Kearney, Lyndal, Greaves, Mel · 2013 · Genome Research
52. Complete regression of advanced pancreatic ductal adenocarcinomas upon combined inhibition of EGFR and C-RAF
    Blasco, María Teresa, Navas, Carolina, Martín-Serrano, Guillermo, Graña-Castro, Osvaldo, Lechuga, Carmen G., Martín-Díaz, Laura, Djurec, Magdolna, Li, Jing, Morales-Cacho, Lucia, Esteban-Burgos, Laura et al. · 2019 · Cancer Cell
53. Evolutionary analysis of the most polymorphic gene family in falciparum malaria
    Otto, Thomas D., Assefa, Sammy A., Böhme, Ulrike, Sanders, Mandy J., Kwiatkowski, Dominic P., Pf3k consortium, Berriman, Matt, Newbold, Chris · 2019 · Wellcome Open Research
54. Quantifying Molecular Bias in DNA Data Storage
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55. Substantial somatic genomic variation and selection for BCOR mutations in human induced pluripotent stem cells
    Rouhani, Foad J., Zou, Xueqing, Danecek, Petr, Badja, Cherif, Amarante, Tauanne Dias, Koh, Gene, Wu, Qianxin, Memari, Yasin, Durbin, Richard, Martincorena, Inigo et al. · 2022 · Nature Genetics
56. TET2 mutations are associated with hypermethylation at key regulatory enhancers in normal and malignant hematopoiesis
    Tulstrup, Morten, Soerensen, Mette, Hansen, Jakob Werner, Gillberg, Linn, Needhamsen, Maria, Kaastrup, Katja, Helin, Kristian, Christensen, Kaare, Weischenfeldt, Joachim, Grønbæk, Kirsten · 2021 · Nature Communications
57. Narrow mutational signatures drive acquisition of multidrug resistance in the fungal pathogen Candida glabrata
    Ksiezopolska, Ewa, Schikora-Tamarit, Miquel Àngel, Beyer, Reinhard, Nunez-Rodriguez, Juan Carlos, Schüller, Christoph, Gabaldón, Toni · 2021 · Current Biology
58. Ten new cases further delineate the syndromic intellectual disability phenotype caused by mutations in DYRK1A
    Bronicki, Lucas M, Redin, Claire, Drunat, Severine, Piton, Amélie, Lyons, Michael, Passemard, Sandrine, Baumann, Clarisse, Faivre, Laurence, Thevenon, Julien, Rivière, Jean-Baptiste et al. · 2015 · European Journal of Human Genetics
59. Novel FOXA2 mutation causes Hyperinsulinism, Hypopituitarism with Craniofacial and Endoderm-derived organ abnormalities
    Giri, Dinesh, Vignola, Maria Lillina, Gualtieri, Angelica, Scagliotti, Valeria, McNamara, Paul, Peak, Matthew, Didi, Mohammed, Gaston-Massuet, Carles, Senniappan, Senthil · 2017 · Human Molecular Genetics
60. RNA‐seq Data: Challenges in and Recommendations for Experimental Design and Analysis
    Williams, Alexander G., Thomas, Sean, Wyman, Stacia K., Holloway, Alisha K. · 2014 · Current Protocols in Human Genetics
61. Evolutionary history and adaptation of a human pygmy population of Flores Island, Indonesia
    Tucci, Serena, Vohr, Samuel H., McCoy, Rajiv C., Vernot, Benjamin, Robinson, Matthew R., Barbieri, Chiara, Nelson, Brad J., Fu, Wenqing, Purnomo, Gludhug A., Sudoyo, Herawati et al. · 2018 · Science
62. Patient-Derived Xenografts for Prognostication and Personalized Treatment for Head and Neck Squamous Cell Carcinoma
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63. Philippine Ayta possess the highest level of Denisovan ancestry in the world
    Larena, Maximilian, McKenna, James, Sanchez-Quinto, Federico, Bernhardsson, Carolina, Ebeo, Carlo, Reyes, Rebecca, Casel, Ophelia, Huang, Jin-Yuan, Hagada, Kim Pullupul, Guilay, Dennis et al. · 2021 · Current Biology
64. Coordinated host-pathogen transcriptional dynamics revealed using sorted subpopulations and single macrophages infected with Candida albicans
    Muñoz, José F., Delorey, Toni, Ford, Christopher B., Li, Bi Yu, Thompson, Dawn A., Rao, Reeta P., Cuomo, Christina A. · 2019 · Nature Communications
65. Analysis of deletion breakpoints from 1,092 humans reveals details of mutation mechanisms
    Abyzov, Alexej, Li, Shantao, Kim, Daniel Rhee, Mohiyuddin, Marghoob, Stütz, Adrian M., Parrish, Nicholas F., Mu, Xinmeng Jasmine, Clark, Wyatt, Chen, Ken, Hurles, Matthew et al. · 2015 · Nature Communications
66. Atezolizumab plus anthracycline-based chemotherapy in metastatic triple-negative breast cancer: the randomized, double-blind phase 2b ALICE trial
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67. Transient expression of Bcl6 is sufficient for oncogenic function and induction of mature B-cell lymphoma
    Green, Michael R., Vicente-Dueñas, Carolina, Romero-Camarero, Isabel, Long Liu, Chih, Dai, Bo, González-Herrero, Inés, García-Ramírez, Idoia, Alonso-Escudero, Esther, Iqbal, Javeed, Chan, Wing C. et al. · 2014 · Nature Communications
68. Biology and medicine in the landscape of quantum advantages
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69. The Genomic History of the Bronze Age Southern Levant
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70. Heterogeneity in the inter-tumor transcriptome of high risk prostate cancer
    Wyatt, Alexander W, Mo, Fan, Wang, Kendric, McConeghy, Brian, Brahmbhatt, Sonal, Jong, Lina, Mitchell, Devon M, Johnston, Rebecca L, Haegert, Anne, Li, Estelle et al. · 2014 · Genome Biology
71. Nuclear DNA from two early Neandertals reveals 80,000 years of genetic continuity in Europe
    Peyrégne, Stéphane, Slon, Viviane, Mafessoni, Fabrizio, de Filippo, Cesare, Hajdinjak, Mateja, Nagel, Sarah, Nickel, Birgit, Essel, Elena, Le Cabec, Adeline, Wehrberger, Kurt et al. · 2019 · Science Advances
72. Gene duplicates cause hybrid lethality between sympatric species of Mimulus
    Zuellig, Matthew P., Sweigart, Andrea L. · 2018 · PLOS Genetics
73. DNA damage contributes to neurotoxic inflammation in Aicardi-Goutières syndrome astrocytes
    Giordano, Anna Maria Sole, Luciani, Marco, Gatto, Francesca, Abou Alezz, Monah, Beghè, Chiara, Della Volpe, Lucrezia, Migliara, Alessandro, Valsoni, Sara, Genua, Marco, Dzieciatkowska, Monika et al. · 2022 · Journal of Experimental Medicine
74. Lethal Disorder of Mitochondrial Fission Caused by Mutations in DNM1L
    Yoon, Grace, Malam, Zeenat, Paton, Tara, Marshall, Christian R., Hyatt, Ella, Ivakine, Zhenya, Scherer, Stephen W., Lee, Kyong-Soon, Hawkins, Cynthia, Cohn, Ronald D. et al. · 2016 · The Journal of Pediatrics
75. Unusual metabolic diversity of hyperalkaliphilic microbial communities associated with subterranean serpentinization at the cedars
    Suzuki, Shino, Ishii, Shun’ichi, Hoshino, Tatsuhiko, Rietze, Amanda, Tenney, Aaron, Morrill, Penny L, Inagaki, Fumio, Kuenen, J Gijs, Nealson, Kenneth H · 2017 · The ISME Journal
76. Activating ERBB2/HER2 mutations indicate susceptibility to pan-HER inhibitors in Lynch and Lynch-like colorectal cancer
    Kloth, Michael, Ruesseler, Vanessa, Engel, Christoph, Koenig, Katharina, Peifer, Martin, Mariotti, Erika, Kuenstlinger, Helen, Florin, Alexandra, Rommerscheidt-Fuss, Ursula, Koitzsch, Ulrike et al. · 2016 · Gut
77. Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer’s disease
    On behalf of the European Early-Onset Dementia (EU EOD) consortium, De Roeck, Arne, Van den Bossche, Tobi, van der Zee, Julie, Verheijen, Jan, De Coster, Wouter, Van Dongen, Jasper, Dillen, Lubina, Baradaran-Heravi, Yalda, Heeman, Bavo et al. · 2017 · Acta Neuropathologica
78. Metabolic mechanism of colistin resistance and its reverting in Vibrio alginolyticus
    Li, Lu, Su, Yu‐bin, Peng, Bo, Peng, Xuan‐xian, Li, Hui · 2020 · Environmental Microbiology
79. Bifidobacterium bifidum and the infant gut microbiota: an intriguing case of microbe‐host co‐evolution
    Duranti, Sabrina, Lugli, Gabriele Andrea, Milani, Christian, James, Kieran, Mancabelli, Leonardo, Turroni, Francesca, Alessandri, Giulia, Mangifesta, Marta, Mancino, Walter, Ossiprandi, Maria Cristina et al. · 2019 · Environmental Microbiology
80. Genetic variants of phospholipase C-γ2 alter the phenotype and function of microglia and confer differential risk for Alzheimer’s disease
    Tsai, Andy P., Dong, Chuanpeng, Lin, Peter Bor-Chian, Oblak, Adrian L., Viana Di Prisco, Gonzalo, Wang, Nian, Hajicek, Nicole, Carr, Adam J., Lendy, Emma K., Hahn, Oliver et al. · 2023 · Immunity
81. ABCA7 rare variants and Alzheimer disease risk
    Le Guennec, Kilan, Nicolas, Gaël, Quenez, Olivier, Charbonnier, Camille, Wallon, David, Bellenguez, Céline, Grenier-Boley, Benjamin, Rousseau, Stéphane, Richard, Anne-Claire, Rovelet-Lecrux, Anne et al. · 2016 · Neurology
82. The genomic landscape of 8-oxodG reveals enrichment at specific inherently fragile promoters
    Gorini, Francesca, Scala, Giovanni, Di Palo, Giacomo, Dellino, Gaetano Ivan, Cocozza, Sergio, Pelicci, Pier Giuseppe, Lania, Luigi, Majello, Barbara, Amente, Stefano · 2020 · Nucleic Acids Research
83. Deconstructing Stepwise Fate Conversion of Human Fibroblasts to Neurons by MicroRNAs
    Cates, Kitra, McCoy, Matthew J., Kwon, Ji-Sun, Liu, Yangjian, Abernathy, Daniel G., Zhang, Bo, Liu, Shaopeng, Gontarz, Paul, Kim, Woo Kyung, Chen, Shawei et al. · 2021 · Cell Stem Cell
84. All-Food-Seq (AFS): a quantifiable screen for species in biological samples by deep DNA sequencing
    Ripp, Fabian, Krombholz, Christopher Felix, Liu, Yongchao, Weber, Mathias, Schäfer, Anne, Schmidt, Bertil, Köppel, Rene, Hankeln, Thomas · 2014 · BMC Genomics
85. Hallstatt miners consumed blue cheese and beer during the Iron Age and retained a non-Westernized gut microbiome until the Baroque period
    Maixner, Frank, Sarhan, Mohamed S., Huang, Kun D., Tett, Adrian, Schoenafinger, Alexander, Zingale, Stefania, Blanco-Míguez, Aitor, Manghi, Paolo, Cemper-Kiesslich, Jan, Rosendahl, Wilfried et al. · 2021 · Current Biology
86. Whole genome sequencing analysis demonstrates therapy‐induced echinocandin resistance in Candida auris isolates
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