Jaenisch, Rudolf
Whitehead Institute for Biomedical Research · Massachusetts Institute of Technology
58 papers on CoChatORCID 0000-0002-2540-7099
Most cited papers
- Verified
Generation of Isogenic Pluripotent Stem Cells Differing Exclusively at Two Early Onset Parkinson Point Mutations
Soldner, F., Laganière, J., Cheng, A. W., Hockemeyer, D., Gao, Q., Alagappan, R., Khurana, V., Golbe, L. I., Myers, R. H., Lindquist, S., et al. (2011) · Cell
Pluripotent Stem Cells ResearchCRISPR and Genetic Engineering
Cited by 728
- Verified
Loss of genomic methylation causes p53-dependent apoptosis and epigenetic deregulation
Jackson-Grusby, L., Beard, C., Possemato, R., Tudor, M., Fambrough, D., Csankovszki, G., Dausman, J., Lee, P., Wilson, C., Lander, E., et al. (2001) · Nature Genetics
Epigenetics and DNA MethylationGenetic Syndromes and Imprinting
Cited by 694
- Verified
Efficient derivation of microglia-like cells from human pluripotent stem cells
Muffat, J., Li, Y., Yuan, B., Mitalipova, M., Omer, A., Corcoran, S., Bakiasi, G., Tsai, L.-H., Aubourg, P., Ransohoff, R. M., et al. (2016) · Nature Medicine
Pluripotent Stem Cells ResearchNeuroinflammation and Neurodegeneration Mechanisms
Cited by 651
- Verified
Reduced cortical activity due to a shift in the balance between excitation and inhibition in a mouse model of Rett Syndrome
Dani, V. S., Chang, Q., Maffei, A., Turrigiano, G. G., Jaenisch, R., & Nelson, S. B. (2005) · Proceedings of the National Academy of Sciences
Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research
Cited by 639
- Verified
Type III collagen is crucial for collagen I fibrillogenesis and for normal cardiovascular development
Liu, X., Wu, H., Byrne, M., Krane, S., & Jaenisch, R. (1997) · Proceedings of the National Academy of Sciences
Connective tissue disorders researchCollagen: Extraction and Characterization
Cited by 614
- Verified
Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice
Tropea, D., Giacometti, E., Wilson, N. R., Beard, C., McCurry, C., Fu, D. D., Flannery, R., Jaenisch, R., & Sur, M. (2009) · Proceedings of the National Academy of Sciences
Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research
Cited by 593
- Verified
Analysis of histone 2B-GFP retention reveals slowly cycling hematopoietic stem cells
Foudi, A., Hochedlinger, K., Van Buren, D., Schindler, J. W., Jaenisch, R., Carey, V., & Hock, H. (2009) · Nature Biotechnology
Hematopoietic Stem Cell TransplantationMesenchymal stem cell research
Cited by 586
- Verified
The disease progression of Mecp2 mutant mice is affected by the level of BDNF expression
Chang, Q., Khare, G., Dani, V., Nelson, S., & Jaenisch, R. (2006) · Neuron
Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research
Cited by 578
- Verified
Functional analysis of activins during mammalian development
Matzuk, M. M., Kumar, T. R., Vassalli, A., Bickenbach, J. R., Roop, D. R., Jaenisch, R., & Bradley, A. (1995) · Nature
Developmental Biology and Gene RegulationCleft Lip and Palate Research
Cited by 578
- Verified
Tet1 is dispensable for maintaining pluripotency and its loss is compatible with embryonic and postnatal development
Dawlaty, M. M., Ganz, K., Powell, B. E., Hu, Y.-C., Markoulaki, S., Cheng, A. W., Gao, Q., Kim, J., Choi, S.-W., Page, D. C., et al. (2011) · Cell stem cell
Pluripotent Stem Cells ResearchEpigenetics and DNA Methylation
Cited by 508
- Verified
Induced Pluripotent Stem Cells Meet Genome Editing
Hockemeyer, D., & Jaenisch, R. (2016) · Cell Stem Cell
Pluripotent Stem Cells ResearchCRISPR and Genetic Engineering
Cited by 499
- Verified
DNA methylation protects hematopoietic stem cell multipotency from myeloerythroid restriction
Bröske, A.-M., Vockentanz, L., Kharazi, S., Huska, M. R., Mancini, E., Scheller, M., Kuhl, C., Enns, A., Prinz, M., Jaenisch, R., et al. (2009) · Nature Genetics
Hematopoietic Stem Cell TransplantationEpigenetics and DNA Methylation
Cited by 478
- Verified
Chromatin structure and gene expression programs of human embryonic and induced pluripotent stem cells
Guenther, M. G., Frampton, G. M., Soldner, F., Hockemeyer, D., Mitalipova, M., Jaenisch, R., & Young, R. A. (2010) · Cell Stem Cell
Pluripotent Stem Cells ResearchGenomics and Chromatin Dynamics
Cited by 456
- Verified
Induction of Expansion and Folding in Human Cerebral Organoids
Li, Y., Muffat, J., Omer, A., Bosch, I., Lancaster, M. A., Sur, M., Gehrke, L., Knoblich, J. A., & Jaenisch, R. (2017) · Cell Stem Cell
Neurogenesis and neuroplasticity mechanismsFetal and Pediatric Neurological Disorders
Cited by 436
- Verified
Technical Challenges in Using Human Induced Pluripotent Stem Cells to Model Disease
Saha, K., & Jaenisch, R. (2009) · Cell Stem Cell
Pluripotent Stem Cells ResearchCRISPR and Genetic Engineering
Cited by 411
- Verified
3D Chromosome Regulatory Landscape of Human Pluripotent Cells
Ji, X., Dadon, D. B., Powell, B. E., Fan, Z. P., Borges-Rivera, D., Shachar, S., Weintraub, A. S., Hnisz, D., Pegoraro, G., Lee, T. I., et al. (2016) · Cell Stem Cell
Genomics and Chromatin DynamicsPluripotent Stem Cells Research
Cited by 400
- Verified
Loss of Tet Enzymes Compromises Proper Differentiation of Embryonic Stem Cells
Dawlaty, M. M., Breiling, A., Le, T., Barrasa, M. I., Raddatz, G., Gao, Q., Powell, B. E., Cheng, A. W., Faull, K. F., Lyko, F., et al. (2014) · Developmental Cell
Epigenetics and DNA MethylationPluripotent Stem Cells Research
Cited by 338
- Verified
Parkinson-causing α-synuclein missense mutations shift native tetramers to monomers as a mechanism for disease initiation
Dettmer, U., Newman, A. J., Soldner, F., Luth, E. S., Kim, N. C., von Saucken, V. E., Sanderson, J. B., Jaenisch, R., Bartels, T., & Selkoe, D. (2015) · Nature Communications
Parkinson's Disease Mechanisms and TreatmentsAlzheimer's disease research and treatments
Cited by 317
- Verified
Lipidomic Analysis of α-Synuclein Neurotoxicity Identifies Stearoyl CoA Desaturase as a Target for Parkinson Treatment
Fanning, S., Haque, A., Imberdis, T., Baru, V., Barrasa, M. I., Nuber, S., Termine, D., Ramalingam, N., Ho, G. P. H., Noble, T., et al. (2019) · Molecular Cell
Parkinson's Disease Mechanisms and TreatmentsAlzheimer's disease research and treatments
Cited by 285
- Verified
Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2
Giacometti, E., Luikenhuis, S., Beard, C., & Jaenisch, R. (2007) · Proceedings of the National Academy of Sciences
Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research
Cited by 271
- Verified
Genetic and Chemical Correction of Cholesterol Accumulation and Impaired Autophagy in Hepatic and Neural Cells Derived from Niemann-Pick Type C Patient-Specific iPS Cells
Maetzel, D., Sarkar, S., Wang, H., Abi-Mosleh, L., Xu, P., Cheng, A. W., Gao, Q., Mitalipova, M., & Jaenisch, R. (2014) · Stem Cell Reports
Lysosomal Storage Disorders ResearchGlycogen Storage Diseases and Myoclonus
Cited by 195
- Verified
X-linked H3K27me3 demethylase Utx is required for embryonic development in a sex-specific manner
Welstead, G. G., Creyghton, M. P., Bilodeau, S., Cheng, A. W., Markoulaki, S., Young, R. A., & Jaenisch, R. (2012) · Proceedings of the National Academy of Sciences
Epigenetics and DNA MethylationPluripotent Stem Cells Research
Cited by 194
- Verified
Mutations in the WRN Gene in Mice Accelerate Mortality in a p53-Null Background
Lombard, D. B., Beard, C., Johnson, B., Marciniak, R. A., Dausman, J., Bronson, R., Buhlmann, J. E., Lipman, R., Curry, R., Sharpe, A., et al. (2000) · Molecular and Cellular Biology
Telomeres, Telomerase, and SenescenceGenetics, Aging, and Longevity in Model Organisms
Cited by 187
- Verified
Human physiomimetic model integrating microphysiological systems of the gut, liver, and brain for studies of neurodegenerative diseases
Trapecar, M., Wogram, E., Svoboda, D., Communal, C., Omer, A., Lungjangwa, T., Sphabmixay, P., Velazquez, J., Schneider, K., Wright, C. W., et al. (2021) · Science Advances
3D Printing in Biomedical ResearchPluripotent Stem Cells Research
Cited by 176
Go further with a free account
Verify every reference, keep papers in a library, and ask questions across them.
Sign up - it is free