The DOI matches its Crossref record; 204 of the 204 references it cites were found in a registry or an index.
DNA repair deficiency and neurological disease
Open accessAbstract
The ability to respond to genotoxic stress is a prerequisite for the successful development of the nervous system. Mutations in various DNA repair factors can lead to human diseases that are characterized by pronounced neuropathology. In many of these syndromes the neurological component is among the most deleterious aspects of the disease. The nervous system poses a particular challenge in terms of clinical intervention, as the neuropathology associated with these diseases often arises during nervous system development and can be fully penetrant by childhood. Understanding how DNA repair deficiency affects the nervous system will provide a rational basis for therapies targeted at ameliorating the neurological problems in these syndromes.
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
“Deficiencies in DNA repair are known to underlie several neurological conditions in both humans and animal models [103, 147].”
From DNA repair deficiency and senescence in concussed professional athletes involved in contact sports (2019) · cites this paper as [103]
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
Instability and decay of the primary structure of DNA
Lindahl, T. (1993) · Nature · doi:10.1038/362709a0 · Cited by 5,679
ATM and ATR Substrate Analysis Reveals Extensive Protein Networks Responsive to DNA Damage
Matsuoka, S., Ballif, B. A., Smogorzewska, A., McDonald, E. R., Hurov, K. E., Luo, J., Bakalarski, C. E., Zhao, Z., Solimini, N., Lerenthal, Y., et al. (2007) · Science · doi:10.1126/science.1140321 · Cited by 3,075
Mechanisms and Functional Implications of Adult Neurogenesis
Zhao, C., Deng, W., & Gage, F. H. (2008) · Cell · doi:10.1016/j.cell.2008.01.033 · Cited by 3,007
Cell-cycle checkpoints and cancer
Kastan, M. B., & Bartek, J. (2004) · Nature · doi:10.1038/nature03097 · Cited by 2,836
A Single Ataxia Telangiectasia Gene with a Product Similar to PI-3 Kinase
Savitsky, K., Bar-Shira, A., Gilad, S., Rotman, G., Ziv, Y., Vanagaite, L., Tagle, D. A., Smith, S., Uziel, T., Sfez, S., et al. (1995) · Science · doi:10.1126/science.7792600 · Cited by 2,785
ATM and related protein kinases: safeguarding genome integrity
Shiloh, Y. (2003) · Nature Reviews Cancer · doi:10.1038/nrc1011 · Cited by 2,577
Cellular roles of DNA topoisomerases: a molecular perspective
Wang, J. C. (2002) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm831 · Cited by 2,364
ATR: an essential regulator of genome integrity
Cimprich, K. A., & Cortez, D. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2450 · Cited by 1,798
The DNA Damage Response: Ten Years After
Harper, J. W., & Elledge, S. J. (2007) · Molecular Cell · doi:10.1016/j.molcel.2007.11.015 · Cited by 1,705
Bender, A., Krishnan, K. J., Morris, C. M., Taylor, G. A., Reeve, A. K., Perry, R. H., Jaros, E., Hersheson, J. S., Betts, J., Klopstock, T., et al. (2006) · Nature Genetics · doi:10.1038/ng1769 · Cited by 1,570
Flagged first, then by citations
Cited by
Sorted by citations
Playing the End Game: DNA Double-Strand Break Repair Pathway Choice
Chapman, J. R., Taylor, M. R. G., & Boulton, S. J. (2012) · Molecular Cell · doi:10.1016/j.molcel.2012.07.029 · Cited by 1,728
Balancing repair and tolerance of DNA damage caused by alkylating agents
Fu, D., Calvo, J. A., & Samson, L. D. (2012) · Nature reviews. Cancer · doi:10.1038/nrc3185 · Cited by 977
DNA repair mechanisms in dividing and non-dividing cells
Iyama, T., & Wilson, D. M. (2013) · DNA Repair · doi:10.1016/j.dnarep.2013.04.015 · Cited by 697
Ataxia telangiectasia: a review
Rothblum‐Oviatt, C., Wright, J., Lefton‐Greif, M. A., McGrath‐Morrow, S. A., Crawford, T. O., & Lederman, H. M. (2016) · Orphanet Journal of Rare Diseases · doi:10.1186/s13023-016-0543-7 · Cited by 692
Chapman, J. R., Barral, P., Vannier, J., Borel, V., Steger, M., Tomás‐Loba, A., Sartori, A. A., Adams, I. R., Batista, F. D., & Boulton, S. J. (2013) · Molecular Cell · doi:10.1016/j.molcel.2013.01.002 · Cited by 663
Skourti-Stathaki, K., & Proudfoot, N. J. (2014) · Genes & Development · doi:10.1101/gad.242990.114 · Cited by 552
DNA Damage, DNA Repair, Aging, and NeurodegenerationPreprint
Maynard, S., Fang, E. F., Scheibye‐Knudsen, M., Croteau, D. L., & Bohr, V. A. (2015) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a025130 · Cited by 454
Interaction of FUS and HDAC1 regulates DNA damage response and repair in neurons
Wang, W., Pan, L., Su, S. C., Quinn, E. J., Sasaki, M., Jimenez, J., Mackenzie, I. R., Huang, E. J., & Tsai, L. (2013) · Nature Neuroscience · doi:10.1038/nn.3514 · Cited by 467
DNA Damage/Repair Management in Cancers
Alhmoud, J. F., Woolley, J. F., Moustafa, A. A., & Malki, M. I. (2020) · Cancers · doi:10.3390/cancers12041050 · Cited by 410
Mutations in PNKP cause microcephaly, seizures and defects in DNA repair
Shen, J., Gilmore, E. C., Marshall-Walker, C. A., Haddadin, M. H., Reynolds, J. J., Eyaid, W., Bodell, A., Barry, B. J., Gleason, D., Allen, K., et al. (2010) · Nature Genetics · doi:10.1038/ng.526 · Cited by 294
Cockayne syndrome: Clinical features, model systems and pathways
Karikkineth, A. C., Scheibye-Knudsen, M., Fivenson, E., Croteau, D. L., & Bohr, V. A. (2017) · Ageing Research Reviews · doi:10.1016/j.arr.2016.08.002 · Cited by 262
Mitoxantrone, More than Just Another Topoisomerase II Poison
Evison, B. J., Sleebs, B. E., Watson, K. G., Phillips, D. R., & Cutts, S. M. (2015) · Medicinal Research Reviews · doi:10.1002/med.21364 · Cited by 265
Genetic causes of microcephaly and lessons for neuronal development
Gilmore, E. C., & Walsh, C. A. (2012) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.89 · Cited by 254
Coordination of DNA single strand break repair
Abbotts, R., & Wilson, D. M. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.11.039 · Cited by 240
ATM and the Molecular Pathogenesis of Ataxia Telangiectasia
McKinnon, P. J. (2011) · Annual Review of Pathology Mechanisms of Disease · doi:10.1146/annurev-pathol-011811-132509 · Cited by 245
Self-citationFunctional interrogation of DNA damage response variants with base editing screens
Cuella-Martin, R., Hayward, S. B., Fan, X., Chen, X., Huang, J., Taglialatela, A., Leuzzi, G., Zhao, J., Rabadán, R., Lü, C., et al. (2021) · Cell · doi:10.1016/j.cell.2021.01.041 · Cited by 236
Gruber, R., Zhou, Z., Sukchev, M., Jörß, T., Frappart, P., & Wang, Z. (2011) · Nature Cell Biology · doi:10.1038/ncb2342 · Cited by 242
Maintaining genome stability in the nervous system
McKinnon, P. J. (2013) · Nature Neuroscience · doi:10.1038/nn.3537 · Cited by 229
Self-citationEarly neuronal accumulation of DNA double strand breaks in Alzheimer’s disease
Shanbhag, N. M., Evans, M. D., Mao, W., Nana, A. L., Seeley, W. W., Adame, A., Rissman, R. A., Masliah, E., & Mucke, L. (2019) · Acta Neuropathologica Communications · doi:10.1186/s40478-019-0723-5 · Cited by 214
Absence of RNase H2 triggers generation of immunogenic micronuclei removed by autophagy
Bartsch, K., Knittler, K., Borowski, C., Rudnik, S., Damme, M., Aden, K., Spehlmann, M. E., Frey, N., Saftig, P., Chalaris, A., et al. (2017) · Human Molecular Genetics · doi:10.1093/hmg/ddx283 · Cited by 196
Effects of Atmospheric Pressure Plasmas on Isolated and Cellular DNA—A Review
Arjunan, K. P., Sharma, V. K., & Ptasińska, S. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms16022971 · Cited by 198
Tidying up loose ends: the role of polynucleotide kinase/phosphatase in DNA strand break repair
Weinfeld, M., Mani, R. S., Abdou, I., Aceytuno, R. D., & Glover, J. N. M. (2011) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2011.01.006 · Cited by 204
Yüce, Ö., & West, S. C. (2012) · Molecular and Cellular Biology · doi:10.1128/mcb.01195-12 · Cited by 202
Genomic integrity and the ageing brain
Chow, H.-M., & Herrup, K. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn4020 · Cited by 174
Role of 53BP1 in the Regulation of DNA Double-Strand Break Repair Pathway Choice
Gupta, A. K. D., Hunt, C. R., Chakraborty, S., PANDITA, R. K., Yordy, J. S., Ramnarain, D. B., Horikoshi, N., & Pandita, T. K. (2013) · Radiation Research · doi:10.1667/rr13572.1 · Cited by 162
A Critical Balance: dNTPs and the Maintenance of Genome Stability
Pai, C., & Kearsey, S. E. (2017) · Genes · doi:10.3390/genes8020057 · Cited by 169
Genome integrity and disease prevention in the nervous systemPreprint
McKinnon, P. J. (2017) · Genes & Development · doi:10.1101/gad.301325.117 · Cited by 161
Self-citationMechanisms of FUS mutations in familial amyotrophic lateral sclerosis
Shang, Y., & Huang, E. J. (2016) · Brain Research · doi:10.1016/j.brainres.2016.03.036 · Cited by 164
Katyal, S., Lee, Y., Nitiss, K. C., Downing, S. M., Li, Y., Shimada, M., Zhao, J., Russell, H. R., Petrini, J. H. J., Nitiss, J. L., et al. (2014) · Nature Neuroscience · doi:10.1038/nn.3715 · Cited by 152
Self-citationDNA end resection and its role in DNA replication and DSB repair choice in mammalian cells
Zhao, F., Kim, W., Kloeber, J. A., & Lou, Z. (2020) · Experimental & Molecular Medicine · doi:10.1038/s12276-020-00519-1 · Cited by 163
Genome instability in Alzheimer disease
Hou, Y., Song, H., Croteau, D. L., Akbari, M., & Bohr, V. A. (2017) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2016.04.005 · Cited by 120
CDK5RAP2 functions in centrosome to spindle pole attachment and DNA damage response
Barr, A. R., Kilmartin, J. V., & Gergely, F. (2010) · Journal of Cell Biology · doi:10.1083/jcb.200912163 · Cited by 120
Baiji genomes reveal low genetic variability and new insights into secondary aquatic adaptations
Zhou, X., Sun, F., Xu, S., Fan, G., Zhu, K., Liu, X., Chen, Y., Shi, C., Yang, Y., Huang, Z., et al. (2013) · Nature Communications · doi:10.1038/ncomms3708 · Cited by 123
Richard, P., Feng, S., & Manley, J. L. (2013) · Genes & Development · doi:10.1101/gad.224923.113 · Cited by 118
Proximal tubule ATR regulates DNA repair to prevent maladaptive renal injury responses
Kishi, S., Brooks, C. R., Taguchi, K., Ichimura, T., Mori, Y., Akinfolarin, A., Gupta, N., Galichon, P., Elias, B. C., Suzuki, T., et al. (2019) · Journal of Clinical Investigation · doi:10.1172/jci122313 · Cited by 117
DNA Repair Pathways and Mechanisms
Dexheimer, T. S. (2012) · Springer eBooks · doi:10.1007/978-94-007-4590-2_2 · Cited by 133
Passemard, S., Kaindl, A. M., & Verloès, A. (2013) · Handbook of clinical neurology · doi:10.1016/b978-0-444-52891-9.00013-0 · Cited by 115
The genesis of cerebellar interneurons and the prevention of neural DNA damage require XRCC1
Lee, Y., Katyal, S., Li, Y., El‐Khamisy, S. F., Russell, H. R., Caldecott, K. W., & McKinnon, P. J. (2009) · Nature Neuroscience · doi:10.1038/nn.2375 · Cited by 115
Self-citationAge-related motor neuron degeneration in DNA repair-deficient Ercc1 mice
de Waard, M. C., van der Pluijm, I., Borgesius, N. Z., Comley, L. H., Haasdijk, E. D., Rijksen, Y., Ridwan, Y. R., Zondag, G. C. M., Hoeijmakers, J. H. J., Elgersma, Y., et al. (2010) · Acta Neuropathologica · doi:10.1007/s00401-010-0715-9 · Cited by 113
Kass, E. M., Helgadottir, H. R., Chen, C.-C., Barbera, M. A., Wang, R., Westermark, U., Ludwig, T., Moynahan, M. E., & Jasin, M. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1216824110 · Cited by 110
DNA repair in the trinucleotide repeat disorders
Jones, L., Houlden, H., & Tabrizi, S. J. (2016) · The Lancet Neurology · doi:10.1016/s1474-4422(16)30350-7 · Cited by 101
Eitan, E., Tichon, A., Gazit, A., Gitler, D., Slavin, S., & Priel, E. (2012) · EMBO Molecular Medicine · doi:10.1002/emmm.201200212 · Cited by 82
Proteins from the DNA Damage Response: Regulation, Dysfunction, and Anticancer Strategies
Molinaro, C., Martoriati, A., & Cailliau, K. (2021) · Cancers · doi:10.3390/cancers13153819 · Cited by 99
Keeping ribosomal DNA intact: a repeating challenge
Warmerdam, D. O., & Wolthuis, R. M. F. (2018) · Chromosome Research · doi:10.1007/s10577-018-9594-z · Cited by 97
Review: Somatic mutations in neurodegeneration
Leija‐Salazar, M., Piette, C. E., & Proukakis, C. (2018) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12465 · Cited by 86
The origins of glioma: E Pluribus Unum?
Siebzehnrübl, F. A., Reynolds, B. A., Vescovi, A. L., Steindler, D. A., & Deleyrolle, L. P. (2011) · Glia · doi:10.1002/glia.21143 · Cited by 91
Jaarsma, D., van der Pluijm, I., de Waard, M. C., Haasdijk, E. D., Brandt, R. M. C., Vermeij, M., Rijksen, Y., Maas, A., STEEG, H. V., Hoeijmakers, J. H. J., et al. (2011) · PLoS Genetics · doi:10.1371/journal.pgen.1002405 · Cited by 80
ATR maintains select progenitors during nervous system development
Lee, Y., Shull, E. R. P., Frappart, P., Katyal, S., Enriquez-Rios, V. D., Zhao, J., Russell, H. R., Brown, E. J., & McKinnon, P. J. (2012) · The EMBO Journal · doi:10.1038/emboj.2011.493 · Cited by 78
Self-citationSomatic alpha‐synuclein mutations in Parkinson's disease: Hypothesis and preliminary data
Proukakis, C., Houlden, H., & Schapira, A. H. V. (2013) · Movement Disorders · doi:10.1002/mds.25502 · Cited by 74
Living with xeroderma pigmentosum: comprehensive photoprotection for highly photosensitive patients
Tamura, D., DiGiovanna, J. J., Khan, S. G., & Kraemer, K. H. (2014) · Photodermatology Photoimmunology & Photomedicine · doi:10.1111/phpp.12108 · Cited by 73
Progressive cerebellar atrophy and polyneuropathy: expanding the spectrum of PNKP mutations
Poulton, C. J., Oegema, R., Heijsman, D., Hoogeboom, J. A. M., Schot, R., Stroink, H., Willemsen, M. A. A. P., Verheijen, F. W., van der Spek, P. J., Kremer, A., et al. (2012) · Neurogenetics · doi:10.1007/s10048-012-0351-8 · Cited by 73
Ramkumar, H. L., Brooks, B. P., Cao, X., Tamura, D., DiGiovanna, J. J., Kraemer, K. H., & Chan, C.-C. (2011) · Survey of Ophthalmology · doi:10.1016/j.survophthal.2011.03.001 · Cited by 72
Abnormal Eye Movements in Parkinsonism and Movement Disorders
Jung, I., & Kim, J. (2019) · Journal of Movement Disorders · doi:10.14802/jmd.18034 · Cited by 77
Trichothiodystrophy view from the molecular basis of DNA repair/transcription factor TFIIH
Hashimoto, S., & Egly, J. (2009) · Human Molecular Genetics · doi:10.1093/hmg/ddp390 · Cited by 79
Topoisomerases and the regulation of neural function
McKinnon, P. J. (2016) · Nature reviews. Neuroscience · doi:10.1038/nrn.2016.101 · Cited by 71
Self-citationWu, Q., Allouch, A., Martins, I., Brenner, C., Modjtahedi, N., Deutsch, É., & Perfettini, J. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00613 · Cited by 76
Sakai, D., Dixon, J., Dixon, M. J., & Trainor, P. A. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002566 · Cited by 75
Nucleo–cytoplasmic transport defects and protein aggregates in neurodegeneration
Bitetto, G., & Fonzo, A. D. (2020) · Translational Neurodegeneration · doi:10.1186/s40035-020-00205-2 · Cited by 68
De novo mutations, genetic mosaicism and human disease
Mohiuddin, M., Kooy, R. F., & Pearson, C. E. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.983668 · Cited by 69
Shimada, M., Dumitrache, L. C., Russell, H. R., & McKinnon, P. J. (2015) · The EMBO Journal · doi:10.15252/embj.201591363 · Cited by 66
Self-citationWood, L. M., Surendran, S., Reed, R. E., Haas, A. L., Liu, L. F., McKinnon, P. J., & Desai, S. D. (2011) · PLoS ONE · doi:10.1371/journal.pone.0016422 · Cited by 66
Self-citationDNA damage response in microcephaly development of MCPH1 mouse model
Zhou, Z., Tapias, A., Bruhn, C., Gruber, R., Sukchev, M., & Wang, Z. (2013) · DNA repair · doi:10.1016/j.dnarep.2013.04.017 · Cited by 65
Polynucleotide kinase-phosphatase (PNKP) mutations and neurologic disease
Dumitrache, L. C., & McKinnon, P. J. (2017) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2016.04.009 · Cited by 67
Self-citationAnesthetic Isoflurane Induces DNA Damage Through Oxidative Stress and p53 Pathway
Ni, C., Li, C., Dong, Y., Guo, X., Zhang, Y., & Xie, Z. (2016) · Molecular Neurobiology · doi:10.1007/s12035-016-9937-8 · Cited by 61
Mechanistic insights into transcription coupled DNA repair
Pani, B., & Nudler, E. (2017) · DNA repair · doi:10.1016/j.dnarep.2017.06.006 · Cited by 63
Neurogenesis requires TopBP1 to prevent catastrophic replicative DNA damage in early progenitors
Lee, Y., Katyal, S., Downing, S. M., Zhao, J., Russell, H. R., & McKinnon, P. J. (2012) · Nature Neuroscience · doi:10.1038/nn.3097 · Cited by 59
Self-citationSomatic mutations in neurons during aging and neurodegeneration
Verheijen, B. M., Vermulst, M., & van Leeuwen, F. W. (2018) · Acta Neuropathologica · doi:10.1007/s00401-018-1850-y · Cited by 60
Lou, M.-M., Tang, X., Wang, G., He, J., Luo, F., Guan, M., Wang, F., Zou, H., Wang, J., Zhang, Q., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-24236-z · Cited by 58
Sublethal Doses of β-Amyloid Peptide Abrogate DNA-dependent Protein Kinase Activity
Cardinale, A., Racaniello, M., Saladini, S., Chiara, G. D., Mollinari, C., de Stefano, M. C., Pocchiari, M., Garaci, E., & Merlo, D. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.276550 · Cited by 54
DNA excision repair at telomeres
Jia, P., Her, C., & Chai, W. (2015) · DNA repair · doi:10.1016/j.dnarep.2015.09.017 · Cited by 54
Microglia-derived extracellular vesicles trigger age-related neurodegeneration upon DNA damage
Arvanitaki, E. S., Goulielmaki, E., Gkirtzimanaki, K., Niotis, G., Tsakani, E., Nenedaki, E., Rouska, I., Kefalogianni, M., Xydias, D., Kalafatakis, I., et al. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2317402121 · Cited by 50
E2F1 and E2F2 induction in response to DNA damage preserves genomic stability in neuronal cells
Castillo, D., Campalans, A., Belluscio, L. M., Carcagno, A. L., Radicella, J. P., Cánepa, E. T., & Pregi, N. (2015) · Cell Cycle · doi:10.4161/15384101.2014.985031 · Cited by 49
Houlihan, S. L., & Feng, Y. (2014) · eLife · doi:10.7554/elife.03297 · Cited by 49
Structural Basis of SOSS1 Complex Assembly and Recognition of ssDNA
Ren, W., Chen, H., Sun, Q., Tang, X., Lim, S. C., Huang, J., & Song, H. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.02.020 · Cited by 48
Chromatin Regulation of DNA Damage Repair and Genome Integrity in the Central Nervous System
Pan, L., Penney, J., & Tsai, L. (2014) · Journal of Molecular Biology · doi:10.1016/j.jmb.2014.08.001 · Cited by 50
Abugable, A. A., Morris, J. L. M., Palminha, N. M., Zaksauskaite, R., Ray, S., & El‐Khamisy, S. F. (2019) · DNA repair · doi:10.1016/j.dnarep.2019.102669 · Cited by 53
DNA double-strand breaks: a potential therapeutic target for neurodegenerative diseases
Thadathil, N., Hori, R. T., Xiao, J., & Khan, M. M. (2019) · Chromosome Research · doi:10.1007/s10577-019-09617-x · Cited by 51
DNA repair deficiency and senescence in concussed professional athletes involved in contact sports
Schwab, N., Grenier, K., & Hazrati, L.-N. (2019) · Acta Neuropathologica Communications · doi:10.1186/s40478-019-0822-3 · Cited by 47
TET proteins: on the frenetic hunt for new cytosine modifications
Delatte, B., & Fuks, F. (2013) · Briefings in Functional Genomics · doi:10.1093/bfgp/elt010 · Cited by 51
Lee, K. Y., Im, J., Shibata, E., & Dutta, A. (2017) · Molecular Cell · doi:10.1016/j.molcel.2017.08.021 · Cited by 46
Should I stay or should I go: VCP/p97-mediated chromatin extraction in the DNA damage response
Dantuma, N. P., Ács, K., & Luijsterburg, M. S. (2014) · Experimental Cell Research · doi:10.1016/j.yexcr.2014.08.025 · Cited by 47
Wang, H., Dharmalingam, P., Vasquez, V., Mitra, J., Boldogh, I. R., Rao, K. S. J., Kent, T. A., MITRA, S. P., & Hegde, M. L. (2016) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2016.09.005 · Cited by 46
ASTE1 promotes shieldin-complex-mediated DNA repair by attenuating end resection
Zhao, F., Kim, W., Gao, H., Liu, C., Zhang, Y., Chen, Y., Deng, M., Zhou, Q., Huang, J., Hu, Q., et al. (2021) · Nature Cell Biology · doi:10.1038/s41556-021-00723-9 · Cited by 47
Tau and DNA Damage in Neurodegeneration
Colnaghi, L., Rondelli, D., Muzi-Falconi, M., & Sertic, S. (2020) · Brain Sciences · doi:10.3390/brainsci10120946 · Cited by 42
Casafont, Í., Palanca, A., Lafarga, V., Berciano, M. T., & Lafarga, M. (2011) · Acta Neuropathologica · doi:10.1007/s00401-011-0869-0 · Cited by 44
Wong, G. C., & Chow, H. (2022) · Journal of Alzheimer s Disease · doi:10.3233/jad-220203 · Cited by 41
Genome instability and loss of protein homeostasis: converging paths to neurodegeneration?
Ainslie, A. P., Huiting, W., Barazzuol, L., & Bergink, S. (2021) · Open Biology · doi:10.1098/rsob.200296 · Cited by 42
Franzin, R., Stasi, A., Ranieri, E., Netti, G. S., Cantaluppi, V., Gesualdo, L., Stallone, G., & Castellano, G. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.630419 · Cited by 41
Toonen, L. J. A., Schmidt, I., Luijsterburg, M. S., van Attikum, H., & van Roon‐Mom, W. (2016) · Scientific Reports · doi:10.1038/srep35200 · Cited by 42
DNA Damage/Repair Management in Cancers
Alhmoud, J. F., Woolley, J. F., Moustafa, A. A., & Mallei, M. I. (2021) · doi:10.1201/9781003180449-12 · Cited by 40
Dong, Z., Zhang, L., Qiao, M., Ge, J., Liu, A., & Li, Z. (2015) · Talanta · doi:10.1016/j.talanta.2015.08.055 · Cited by 38
Interstrand cross-links arising from strand breaks at true abasic sites in duplex DNA
Yang, Z., Price, N. E., Johnson, K. M., Wang, Y., & Gates, K. S. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx394 · Cited by 40
DNA damage response in neurodevelopment and neuromaintenance
Qing, X., Zhang, G., & Wang, Z. (2022) · FEBS Journal · doi:10.1111/febs.16535 · Cited by 42
R-loop Mediated DNA Damage and Impaired DNA Repair in Spinal Muscular Atrophy
Cuartas, J., & Gangwani, L. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.826608 · Cited by 39
Histone H2AX deficiency causes neurobehavioral deficits and impaired redox homeostasis
Weyemi, U., Paul, B. D., Snowman, A. M., Jailwala, P., Nussenzweig, A., Bonner, W. M., & Snyder, S. H. (2018) · Nature Communications · doi:10.1038/s41467-018-03948-9 · Cited by 37
Quintens, R., Verreet, T., Janssen, A., Neefs, M., Leysen, L., Michaux, A., Verslegers, M., Samari, N., Pani, G., Verheyde, J., et al. (2015) · Biology Open · doi:10.1242/bio.20149969 · Cited by 40
Histone H2AX promotes neuronal health by controlling mitochondrial homeostasis
Weyemi, U., Paul, B. D., Bhattacharya, D., Malla, A. P., Boufraqech, M., Harraz, M. M., Bonner, W. M., & Snyder, S. H. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1820245116 · Cited by 37
Chien, T., Weng, Y., Chang, S., Lai, H., Chiu, F., Kuo, H., Chuang, D., & Chern, Y. (2018) · Molecular Psychiatry · doi:10.1038/s41380-017-0007-z · Cited by 36
Reduced Cancer Incidence in Huntington’s Disease: Analysis in the Registry Study
McNulty, P., Pilcher, R., Ramesh, R., Necuiniate, R., Hughes, A., REGISTRY Investigators of the European Huntington's Disease Network2, Farewell, D. M., Holmans, P., Jones, L., Bonelli, R. M., et al. (2018) · Journal of Huntington s Disease · doi:10.3233/jhd-170263 · Cited by 35
Microcephaly, an etiopathogenic vision
Becerra-Solano, L. E., Mateos-Sánchez, L., & López-Muñoz, E. (2021) · Pediatrics & Neonatology · doi:10.1016/j.pedneo.2021.05.008 · Cited by 35
Metadata
- Authors
- McKinnon, P. J.
- Affiliations
- St. Jude Children's Research Hospital (US)
- Corresponding author
- McKinnon, Peter J.
- ORCID
- McKinnon, Peter J.
- Venue
- Nature Reviews Neuroscience
- Published
- 2009-01-15
- Volume
- 10
- Issue
- 2
- Pages
- 100-112
- ISSN
- 1471-003X (ISSN-L)
- 1471-0048
- PMC
- PMC3064843
- OpenAlex
- W2026709018
- Cited by
- 323
- References
- 204
- Citations by year
- 2026: 15 · 2025: 12 · 2024: 15 · 2023: 15 · 2022: 30 · 2021: 24 · 2020: 23 · 2019: 14 · 2018: 16 · 2017: 22 · 2016: 19 · 2015: 21 · 2014: 18 · 2013: 28 · 2012: 18
- FWCI
- 1.32
- Type
- journal article
- Language
- en
- Update notices
- erratum (2009-01-27)
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature reviews. Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- U.S. Bureau of Land Management
- National Cancer Institute (P01CA096832)
- National Institute of Neurological Disorders and Stroke (R01NS037956)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Health Sciences › Medicine › Pathology and Forensic Medicine › Genetic factors in colorectal cancer
- Keywords
- DNA repair deficiency, DNA damage, brain development, neurological disorders, genotoxic stress, DNA repair mutations, neuropathology, neurodevelopmental disorders
- MeSH terms
- Animals, Humans, Nervous System Diseases, DNA Repair-Deficiency Disorders
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