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
Human CtIP promotes DNA end resection
Sartori, A. A., Lukas, C., Coates, J., Mistrik, M., Fu, S., Bartek, J., Baer, R., Lukas, J., & Jackson, S. P. (2007) · Nature · doi:10.1038/nature06337 · Cited by 1,362
Conserved modes of recruitment of ATM, ATR and DNA-PKcs to sites of DNA damage
Falck, J., Coates, J., & Jackson, S. P. (2005) · Nature · doi:10.1038/nature03442 · Cited by 1,304
Base-excision repair of oxidative DNA damage
David, S. S., O'Shea, V. L., & Kundu, S. (2007) · Nature · doi:10.1038/nature05978 · Cited by 1,238
Carney, J. P., Maser, R. S., Olivares, H., Davis, E. M., Le Beau, M., Yates, J. R., Hays, L., Morgan, W. F., & Petrini, J. H. J. (1998) · Cell · doi:10.1016/s0092-8674(00)81175-7 · Cited by 1,226
Stucki, M., Clapperton, J. A., Mohammad, D. H., Yaffe, M. B., Smerdon, S. J., & Jackson, S. P. (2005) · Cell · doi:10.1016/j.cell.2005.09.038 · Cited by 1,164
Deficiencies in DNA damage repair limit the function of haematopoietic stem cells with age
Rossi, D. J., Bryder, D., Seita, J., Nussenzweig, A., Hoeijmakers, J., & Weissman, I. L. (2007) · Nature · doi:10.1038/nature05862 · Cited by 1,115
Single-strand break repair and genetic disease
Caldecott, K. W. (2008) · Nature Reviews Genetics · doi:10.1038/nrg2380 · Cited by 1,097
Requirement of the MRN complex for ATM activation by DNA damage
Uziel, T., Lerenthal, Y., Moyal, L., Andegeko, Y., Mittelman, L., & Shiloh, Y. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg541 · Cited by 1,075
ATM- and cell cycle-dependent regulation of ATR in response to DNA double-strand breaks
Jazayeri, A., Falck, J., Lukas, C., Bartek, J., Smith, G. C. M., Lukas, J., & Jackson, S. P. (2006) · Nature Cell Biology · doi:10.1038/ncb1337 · Cited by 1,064
Stewart, G. S., Maser, R. S., Stankovic, T., Bressan, D. A., Kaplan, M. I., Jaspers, N. G. J., Raams, A., Byrd, P. J., Petrini, J. H. J., & Taylor, A. M. R. (1999) · Cell · doi:10.1016/s0092-8674(00)81547-0 · Cited by 1,060
PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene
Rahman, N., Seal, S., Thompson, D. J., Kelly, P. F., Renwick, A., Elliott, A., Reid, S., Spanova, K., Barfoot, R., Chagtai, T., et al. (2006) · Nature Genetics · doi:10.1038/ng1959 · Cited by 1,026
Ataxia telangiectasia: a human mutation with abnormal radiation sensitivity
Taylor, A. M. R., Harnden, D. G., Arlett, C. F., Harcourt, S. A., Lehmann, A. R., Stevens, S., & Bridges, B. A. (1975) · Nature · doi:10.1038/258427a0 · Cited by 991
Histone H2AX phosphorylation is dispensable for the initial recognition of DNA breaks
Celeste, A., Fernandez-Capetillo, O., Kruhlak, M. J., Pilch, D. R., Staudt, D. W., Lee, A., Bonner, R. F., Bonner, W. M., & Nussenzweig, A. (2003) · Nature Cell Biology · doi:10.1038/ncb1004 · Cited by 989
Molecular views of recombination proteins and their control
West, S. C. (2003) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1127 · Cited by 977
Mechanism and regulation of human non-homologous DNA end-joining
Lieber, M. R., Ma, Y., Pannicke, U., & Schwarz, K. (2003) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1202 · Cited by 973
ATR disruption leads to chromosomal fragmentation and early embryonic lethality
Brown, E. J., & Baltimore, D. (2000) · Genes & Development · doi:10.1101/gad.14.4.397 · Cited by 951
Kraytsberg, Y., Kudryavtseva, E., McKee, A. C., Geula, C., Kowall, N. W., & Khrapko, K. (2006) · Nature Genetics · doi:10.1038/ng1778 · Cited by 896
Puma is an essential mediator of p53-dependent and -independent apoptotic pathways
Jeffers, J. R., Parganas, E., Lee, Y., Yang, C., Wang, J., Brennan, J. A., Maclean, K. H., Han, J., Chittenden, T., Ihle, J. N., et al. (2003) · Cancer Cell · doi:10.1016/s1535-6108(03)00244-7 · Cited by 880
Self-citationThe Fanconi anaemia/BRCA pathway
D'Andrea, A. D., & Grompe, M. (2003) · Nature Reviews Cancer · doi:10.1038/nrc970 · Cited by 822
Cockayne syndrome: Review of 140 cases
Nance, M. A., & Berry, S. A. (1992) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320420115 · Cited by 806
Ruzankina, Y., Pinzon‐Guzman, C., Asare, A., Ong, T., Pontano, L. L., Cotsarelis, G., Zediak, V. P., Velez, M., Bhandoola, A., & Brown, E. J. (2007) · Cell stem cell · doi:10.1016/j.stem.2007.03.002 · Cited by 803
XLF Interacts with the XRCC4-DNA Ligase IV Complex to Promote DNA Nonhomologous End-Joining
Ahnesorg, P., Smith, P., & Jackson, S. P. (2006) · Cell · doi:10.1016/j.cell.2005.12.031 · Cited by 794
Handbook of clinical neuropsychology
Filskov, S. B., & Boll, T. J. (1981) · Wiley eBooks · Cited by 777
Neurons born in the adult dentate gyrus form functional synapses with target cells
Toni, N., Laplagne, D. A., Zhao, C., Lombardi, G., Ribak, C. E., Gage, F. H., & Schinder, A. F. (2008) · Nature Neuroscience · doi:10.1038/nn.2156 · Cited by 741
Buck, D., Malivert, L., de Chasseval, R., Barraud, A., Fondanèche, M.-C., Sanal, O., Plebani, A., Stéphan, J.-L., Hufnagel, M., le Deist, F., et al. (2006) · Cell · doi:10.1016/j.cell.2005.12.030 · Cited by 722
A critical role for DNA end-joining proteins in both lymphogenesis and neurogenesis
Gao, Y., Sun, Y., Frank, K. M., Dikkes, P., Fujiwara, Y., Seidl, K. J., Sekiguchi, J. M., Rathbun, G. A., Swat, W., Wang, J., et al. (1998) · Cell · doi:10.1016/s0092-8674(00)81714-6 · Cited by 688
RecQ helicases: caretakers of the genome
Hickson, I. D. (2003) · Nature reviews. Cancer · doi:10.1038/nrc1012 · Cited by 680
Lou, Z., Minter‐Dykhouse, K., Franco, S., Gostissa, M., Rivera, M. A., Celeste, A., Manis, J. P., van Deursen, J., Nussenzweig, A., Paull, T. T., et al. (2006) · Molecular Cell · doi:10.1016/j.molcel.2005.11.025 · Cited by 668
Cell-cycle control and cortical development
Dehay, C., & Kennedy, H. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2097 · Cited by 655
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer
Reid, S., Schindler, D., Hanenberg, H., Barker, K., Hanks, S., Kalb, R., Neveling, K., Kelly, P., Seal, S., Freund, M., et al. (2007) · Nature Genetics · doi:10.1038/ng1947 · Cited by 642
DNA double-strand break repair: From mechanistic understanding to cancer treatment
HELLEDAY, T., LO, J., VANGENT, D., & ENGELWARD, B. (2007) · DNA Repair · doi:10.1016/j.dnarep.2007.02.006 · Cited by 640
The Rad50 zinc-hook is a structure joining Mre11 complexes in DNA recombination and repair
Hopfner, K., Craig, L., Moncalián, G., Zinkel, R. A., Usui, T., Owen, B. A. L., Kärcher, A., Henderson, B., Bodmer, J.-L., McMurray, C. T., et al. (2002) · Nature · doi:10.1038/nature00922 · Cited by 571
DNA Ligase IV Mutations Identified in Patients Exhibiting Developmental Delay and Immunodeficiency
O’Driscoll, M., Cerosaletti, K. M., Girard, P.-M., Dai, Y., Stümm, M., Kysela, B. P., Hirsch, B. A., Gennery, A. R., Palmer, S. E., Seidel, J., et al. (2001) · Molecular Cell · doi:10.1016/s1097-2765(01)00408-7 · Cited by 565
The ATM-mediated DNA-damage response: taking shape
Shiloh, Y. (2006) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2006.05.004 · Cited by 556
Xeroderma Pigmentosum Group F Caused by a Defect in a Structure-Specific DNA Repair Endonuclease
Sijbers, A. M., de Laat, W. L., Ariza, R. R., Biggerstaff, M., Wei, Y.-F., Moggs, J. G., Carter, K. C., Shell, B. K., Evans, E. L., de Jong, M. C., et al. (1996) · Cell · doi:10.1016/s0092-8674(00)80155-5 · Cited by 546
Mitochondrial Disorders in the Nervous System
DiMauro, S., & Schon, E. A. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.30.051606.094302 · Cited by 541
Phosphorylation of SMC1 is a critical downstream event in the ATM–NBS1–BRCA1 pathwayPreprint
Kitagawa, R., Bakkenist, C. J., McKinnon, P. J., & Kastan, M. B. (2004) · Genes & Development · doi:10.1101/gad.1200304 · Cited by 535
Self-citationSenataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2
Moreira, M.-C., Klur, S., Watanabe, M., Nemeth, A. H., Ber, I. L., Moniz, J.-C., Tranchant, C., Aubourg, P. R., Tazir, M., Schöls, L. J., et al. (2004) · Nature Genetics · doi:10.1038/ng1303 · Cited by 534
A role for adult TLX-positive neural stem cells in learning and behaviour
Zhang, C., Zou, Y., He, W., Gage, F. H., & Evans, R. M. (2008) · Nature · doi:10.1038/nature06562 · Cited by 523
Takashima, H., Boerkoel, C. F., John, J., Saifi, G. M., Salih, M. A. M., Armstrong, D., Mao, Y., Quiocho, F. A., Roa, B. B., Nakagawa, M., et al. (2002) · Nature Genetics · doi:10.1038/ng987 · Cited by 522
DNA repair is limiting for haematopoietic stem cells during ageing
Nijnik, A., Woodbine, L., Marchetti, C., Dawson, S., Lambe, T., Liu, C., Rodrigues, N. P., Crockford, T. L., Cabuy, E., Vindigni, A., et al. (2007) · Nature · doi:10.1038/nature05875 · Cited by 518
Henning, K. A., Li, L., Iyer, N., McDaniel, L. D., Reagan, M. S., Legerski, R., Schultz, R. A., Stefanini, M., Lehmann, A. R., Mayne, L. V., et al. (1995) · Cell · doi:10.1016/0092-8674(95)90028-4 · Cited by 507
The Mre11 complex is required for ATM activation and the G2/M checkpoint
Carson, C. T., Schwartz, R. A., Stracker, T. H., Lilley, C. E., Lee, D. V., & Weitzman, M. D. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg630 · Cited by 502
The cells and molecules that make a cerebellum
Goldowitz, D. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01313-7 · Cited by 497
Genetic regulation of cerebellar development
Wang, V. Y., & Zoghbi, H. Y. (2001) · Nature reviews. Neuroscience · doi:10.1038/35081558 · Cited by 490
Fousteri, M., & Mullenders, L. H. (2008) · Cell Research · doi:10.1038/cr.2008.6 · Cited by 487
A recurrent mutation in PALB2 in Finnish cancer families
Erkko, H., Xia, B., Nikkilä, J., Schleutker, J., Syrjäkoski, K., Mannermaa, A., Kallioniemi, A. H., Pylkäs, K., Karppinen, S., Rapakko, K., et al. (2007) · Nature · doi:10.1038/nature05609 · Cited by 471
Selective Neuronal Vulnerability: Morphological and Molecular Characteristics
Pulsinelli, W. A. (1985) · Progress in brain research · doi:10.1016/s0079-6123(08)61973-1 · Cited by 451
ATM Activation and Its Recruitment to Damaged DNA Require Binding to the C Terminus of Nbs1
You, Z., Chahwan, C., Bailis, J. M., Hunter, T. R., & Russell, P. R. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.13.5363-5379.2005 · Cited by 449
Targeted disruption of the cell-cycle checkpoint gene ATR leads to early embryonic lethality in mice
de Klein, A., Muijtjens, M., van Os, R. P., Verhoeven, Y., Smit, B., Carr, A. M., Lehmann, A. R., & Hoeijmakers, J. H. J. (2000) · Current Biology · doi:10.1016/s0960-9822(00)00447-4 · Cited by 443
Kraemer, K. H., Patronas, N. J., Schiffmann, R., Brooks, B. P., Tamura, D., & DiGiovanna, J. J. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2006.12.020 · Cited by 443
Chk2‐deficient mice exhibit radioresistance and defective p53‐mediated transcription
Takai, H., Naka, K., Okada, Y., Watanabe, M., Harada, N., Saito, S., Anderson, C. W., Appella, E., Nakanishi, M., Suzuki, H., et al. (2002) · The EMBO Journal · doi:10.1093/emboj/cdf506 · Cited by 441
Targeted disruption of the gene encoding DNA ligase IV leads to lethality in embryonic mice
Barnes, D. E., Stamp, G., Rosewell, I. R., Denzel, A., & Lindahl, T. L. (1998) · Current Biology · doi:10.1016/s0960-9822(98)00021-9 · Cited by 438
Almeida, K. H., & Sobol, R. W. (2007) · DNA Repair · doi:10.1016/j.dnarep.2007.01.009 · Cited by 437
ATM stabilizes DNA double-strand-break complexes during V(D)J recombination
Bredemeyer, A. L., Sharma, G. G., Huang, C., Helmink, B. A., Walker, L. M., Khor, K. C., Nuskey, B., Sullivan, K. E., Pandita, T. K., Bassing, C. H., et al. (2006) · Nature · doi:10.1038/nature04866 · Cited by 435
A multistep damage recognition mechanism for global genomic nucleotide excision repair
Sugasawa, K., Okamoto, T., Shimizu, Y., Masutani, C., Iwai, S., & Hanaoka, F. (2001) · Genes & Development · doi:10.1101/gad.866301 · Cited by 435
The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin
Moreira, M.-C., Barbot, C., Tachi, N., Kozuka, N., Uchida, E., Gibson, T. J., Mendonça, P., Costa, M. M. R., Barros, J., Yanagisawa, T., et al. (2001) · Nature Genetics · doi:10.1038/ng1001-189 · Cited by 434
OGG1 initiates age-dependent CAG trinucleotide expansion in somatic cells
Kovtun, I. V., Liu, Y., Bjoras, M., Klungland, A., Wilson, S. H., & McMurray, C. T. (2007) · Nature · doi:10.1038/nature05778 · Cited by 433
Recognition of DNA damage by the Rad4 nucleotide excision repair protein
Min, J., & Pavletich, N. P. (2007) · Nature · doi:10.1038/nature06155 · Cited by 431
Defective DNA single-strand break repair in spinocerebellar ataxia with axonal neuropathy-1
El‐Khamisy, S. F., Saifi, G. M., Weinfeld, M., Johansson, F., Helleday, T., Lupski, J. R., & Caldecott, K. W. (2005) · Nature · doi:10.1038/nature03314 · Cited by 428
Cancer in xeroderma pigmentosum and related disorders of DNA repair
Cleaver, J. E. (2005) · Nature Reviews Cancer · doi:10.1038/nrc1652 · Cited by 427
Herzog, K., Chong, M. J., Kapsetaki, M., Morgan, J. I., & McKinnon, P. J. (1998) · Science · doi:10.1126/science.280.5366.1089 · Cited by 417
Self-citationγH2AX and MDC1: Anchoring the DNA-damage-response machinery to broken chromosomes
Stucki, M., & Jackson, S. P. (2006) · DNA Repair · doi:10.1016/j.dnarep.2006.01.012 · Cited by 412
Date, H., Onodera, O., Tanaka, H., Iwabuchi, K., Uekawa, K., Igarashi, S., Koike, R., Hiroi, T., Yuasa, T., Awaya, Y., et al. (2001) · Nature Genetics · doi:10.1038/ng1001-184 · Cited by 386
ATM Activation and DNA Damage Response
Lavin, M. F., & Kozlov, S. (2007) · Cell Cycle · doi:10.4161/cc.6.8.4180 · Cited by 386
The neurodegenerative disease protein aprataxin resolves abortive DNA ligation intermediates
Ahel, I., Rass, U., El‐Khamisy, S. F., Katyal, S., Clements, P. M., McKinnon, P. J., Caldecott, K. W., & West, S. C. (2006) · Nature · doi:10.1038/nature05164 · Cited by 383
Self-citationRepair of DNA double strand breaks by non-homologous end joining
Lees‐Miller, S. P. (2003) · Biochimie · doi:10.1016/j.biochi.2003.10.011 · Cited by 378
McKinnon, P. J. (2004) · EMBO Reports · doi:10.1038/sj.embor.7400210 · Cited by 376
Self-citationReaction Mechanism of Human DNA Repair Excision Nuclease
Mu, D., Hsu, D. S., & Sancar, A. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.14.8285 · Cited by 374
Cell Cycle Activation Linked to Neuronal Cell Death Initiated by DNA Damage
Kruman, I. I., Wersto, R. P., Cardozo‐Pelaez, F., Smilenov, L. B., Chan, S. L., Chrest, F. J., Emokpae, R., Gorospe, M., & Mattson, M. P. (2004) · Neuron · doi:10.1016/s0896-6273(04)00017-0 · Cited by 371
Fan, L., Fuss, J. O., Cheng, Q. J., Arvai, A. S., Hammel, M., Roberts, V. A., Cooper, P. K., & Tainer, J. A. (2008) · Cell · doi:10.1016/j.cell.2008.04.030 · Cited by 369
The mechanics of base excision repair, and its relationship to aging and disease
WILSONIII, D., & Bohr, V. A. (2006) · DNA repair · doi:10.1016/j.dnarep.2006.10.017 · Cited by 364
Defective DNA Repair and Neurodegenerative Disease
Rass, U., Ahel, I., & West, S. C. (2007) · Cell · doi:10.1016/j.cell.2007.08.043 · Cited by 358
A NEW CHROMOSOMAL INSTABILITY DISORDER: THE NIJMEGEN BREAKAGE SYNDROME
Weemaes, C. M. R., Hustinx, T. W. J., Scheres, J. M. J. C., Munster, P. J. J. V., Bakkeren, J. A. J. M., & Taalman, R. D. F. M. (1981) · Acta Paediatrica · doi:10.1111/j.1651-2227.1981.tb05740.x · Cited by 353
van der Horst, G. T. J., STEEG, H. V., Berg, R. J. W., van Gool, A. J., de Wit, J., Weeda, G., Morreau, H., Beems, R. B., van Kreijl, C. F., de Gruijl, F. R., et al. (1997) · Cell · doi:10.1016/s0092-8674(00)80223-8 · Cited by 339
Limbo, O., Chahwan, C., Yamada, Y., de Bruin, R. A. M., Wittenberg, C., & Russell, P. R. (2007) · Molecular Cell · doi:10.1016/j.molcel.2007.09.009 · Cited by 322
DNA Strand Break Repair and Human Genetic Disease
McKinnon, P. J., & Caldecott, K. W. (2007) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev.genom.7.080505.115648 · Cited by 321
Self-citationInvolvement of H2AX in the DNA Damage and Repair Response
Martin, O. A., Pilch, D. R., Redon, C. E., & Bonner, W. M. (2003) · Cancer Biology & Therapy · doi:10.4161/cbt.2.3.373 · Cited by 311
The cellular response to general and programmed DNA double strand breaks
Bassing, C. H., & Alt, F. W. (2004) · DNA repair · doi:10.1016/j.dnarep.2004.06.001 · Cited by 309
Coin, F., Oksenych, V., & Egly, J. (2007) · Molecular Cell · doi:10.1016/j.molcel.2007.03.009 · Cited by 294
Mesoscale conformational changes in the DNA-repair complex Rad50/Mre11/Nbs1 upon binding DNA
Moreno‐Herrero, F., de Jager, M., Dekker, N. H., Kanaar, R., Wyman, C., & Dekker, C. (2005) · Nature · doi:10.1038/nature03927 · Cited by 278
Ataxia-telangiectasia-like disorder (ATLD)?its clinical presentation and molecular basis
Taylor, A. M. R., Groom, A., & Byrd, P. J. (2004) · DNA repair · doi:10.1016/j.dnarep.2004.04.009 · Cited by 277
Structure of the DNA Repair Helicase XPD
Liu, H., Rudolf, J., Johnson, K. A., McMahon, S. A., Oke, M., Carter, L. G., McRobbie, A.-M., Brown, S. E., Naismith, J. H., & White, M. F. (2008) · Cell · doi:10.1016/j.cell.2008.04.029 · Cited by 268
Age to survive: DNA damage and aging
Schumacher, B., Garinis, G. A., & Hoeijmakers, J. H. J. (2008) · Trends in Genetics · doi:10.1016/j.tig.2007.11.004 · Cited by 266
Faghri, S., Tamura, D., Kraemer, K. H., & DiGiovanna, J. J. (2008) · Journal of Medical Genetics · doi:10.1136/jmg.2008.058743 · Cited by 264
DNA Helicases, Genomic Instability, and Human Genetic Disease
van Brabant, A. J., Stan, R., & Ellis, N. A. (2000) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev.genom.1.1.409 · Cited by 258
Nijmegen breakage syndrome: clinical manifestation of defective response to DNA double-strand breaks
Digweed, M., & Sperling, K. (2004) · DNA repair · doi:10.1016/j.dnarep.2004.03.004 · Cited by 255
Selective vulnerability in brain hypoxia.
Cervós‐Navarro, J., & Diemer, N. H. (1991) · PubMed · Cited by 252
Transcription — guarding the genome by sensing DNA damage
Ljungman, M. E., & Lane, D. P. (2004) · Nature reviews. Cancer · doi:10.1038/nrc1435 · Cited by 238
Mitochondrial DNA repair in aging and disease
Druzhyna, N., Wilson, G. L., & LeDoux, S. P. (2008) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2008.03.002 · Cited by 225
Crystal Structure of the FeS Cluster–Containing Nucleotide Excision Repair Helicase XPD
Wolski, S. C., Kuper, J., Hänzelmann, P., Truglio, J. J., Croteau, D. L., Houten, B. V., & Kisker, C. (2008) · PLoS Biology · doi:10.1371/journal.pbio.0060149 · Cited by 224
Role of DNA–PK in the cellular response to DNA double-strand breaks
Burma, S., & Chen, D. J. (2004) · DNA repair · doi:10.1016/j.dnarep.2004.03.021 · Cited by 223
Maser, R. S., Zinkel, R. A., & Petrini, J. H. J. (2001) · Nature Genetics · doi:10.1038/86920 · Cited by 219
Handbook of Clinical Neurology
Greer, M. (1972) · Neurology · doi:10.1212/wnl.22.7.769 · Cited by 215
TDP1 facilitates chromosomal single‐strand break repair in neurons and is neuroprotective in vivo
Katyal, S., El‐Khamisy, S. F., Russell, H. R., Li, Y., Ju, L., Caldecott, K. W., & McKinnon, P. J. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601869 · Cited by 209
Self-citationBer, I. L. (2004) · Brain · doi:10.1093/brain/awh080 · Cited by 208
O’Driscoll, M., Gennery, A. R., Seidel, J., CONCANNON, P. J., & Jeggo, P. A. (2004) · DNA repair · doi:10.1016/j.dnarep.2004.03.025 · Cited by 208
SCAN1 mutant Tdp1 accumulates the enzyme–DNA intermediate and causes camptothecin hypersensitivity
Interthal, H., Chen, H. J., Kehl‐Fie, T. E., Zotzmann, J., Leppard, J. B., & Champoux, J. J. (2005) · The EMBO Journal · doi:10.1038/sj.emboj.7600694 · Cited by 203
Clements, P. M., Breslin, C., Deeks, E. D., Byrd, P. J., Ju, L., Bieganowski, P., Brenner, C., Moreira, M.-C., Taylor, A. M. R., & Caldecott, K. W. (2004) · DNA repair · doi:10.1016/j.dnarep.2004.06.017 · Cited by 203
Suraweera, A., Bécherel, O. J., Chen, P., Rundle, N. T., Woods, R. G., Nakamura, J., Gatei, M. H., Criscuolo, C., Filla, A., Chessa, L., et al. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200701042 · Cited by 200
Shared Genetic Susceptibility to Breast Cancer, Brain Tumors, and Fanconi Anemia
Offit, K., Levran, O., Mullaney, B., Mah, K., Nafa, K., Batish, S. D., Diotti, R. A., Schneider, H., Deffenbaugh, A. M., Scholl, T., et al. (2003) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/djg072 · Cited by 200
Homologous recombination-mediated double-strand break repair
Wyman, C., Ristić, D., & Kanaar, R. (2004) · DNA repair · doi:10.1016/j.dnarep.2004.03.037 · Cited by 195
Ito, S., Kuraoka, I., Chymkowitch, P., Compe, E., Takedachi, A., Ishigami, C., Coin, F., Egly, J., & Tanaka, K. (2007) · Molecular Cell · doi:10.1016/j.molcel.2007.03.013 · Cited by 194
Nouspikel, T., & Hanawalt, P. C. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.5.1562-1570.2000 · Cited by 194
Mitochondrial DNA damage and repair in neurodegenerative disorders
Yang, J., Weissman, L., Bohr, V. A., & Mattson, M. P. (2008) · DNA repair · doi:10.1016/j.dnarep.2008.03.012 · Cited by 187
Taylor, A. M. R. (1987) · Journal of Medical Genetics · doi:10.1136/jmg.24.5.317-a · Cited by 186
Karanjawala, Z. E., Murphy, N., Hinton, D. R., Hsieh, C., & Lieber, M. R. (2002) · Current Biology · doi:10.1016/s0960-9822(02)00684-x · Cited by 184
Ataxia-telangiectasia: diagnosis and treatment
Perlman, S., Becker-Catania, S. G., & Gatti, R. A. (2003) · Seminars in Pediatric Neurology · doi:10.1016/s1071-9091(03)00026-3 · Cited by 181
Central nervous system manifestations of mitochondrial disorders
Finsterer, J. (2006) · Acta Neurologica Scandinavica · doi:10.1111/j.1600-0404.2006.00671.x · Cited by 180
Saxowsky, T. T., & Doetsch, P. W. (2006) · Chemical Reviews · doi:10.1021/cr040466q · Cited by 179
DNA repair, mitochondria, and neurodegeneration
Weissman, L., de Souza-Pinto, N. C., Stevnsner, T., & Bohr, V. A. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.08.061 · Cited by 175
An essential function for NBS1 in the prevention of ataxia and cerebellar defects
Frappart, P., Tong, W., Demuth, I., Radovanovic, I., Herceg, Z., Aguzzi, A., Digweed, M., & Wang, Z. (2005) · Nature Medicine · doi:10.1038/nm1228 · Cited by 165
Reardon, J. T., Mu, D., & Sancar, A. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.32.19451 · Cited by 161
Friedberg, E. C., & Meira, L. B. (2005) · DNA repair · doi:10.1016/j.dnarep.2005.09.009 · Cited by 160
Cell division in the CNS: Protective response or lethal event in post-mitotic neurons?
Yang, Y., & Herrup, K. (2006) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2006.10.002 · Cited by 157
Zhou, T. (2005) · Nucleic Acids Research · doi:10.1093/nar/gki170 · Cited by 153
The Rad50 hook domain is a critical determinant of Mre11 complex functions
Wiltzius, J. J. W., Hohl, M., Fleming, J. C., & Petrini, J. H. J. (2005) · Nature Structural & Molecular Biology · doi:10.1038/nsmb928 · Cited by 152
When transcription and repair meet: a complex system
Lainé, J., & Egly, J. (2006) · Trends in Genetics · doi:10.1016/j.tig.2006.06.006 · Cited by 152
Fan, L., Arvai, A. S., Cooper, P. K., Iwai, S., Hanaoka, F., & Tainer, J. A. (2006) · Molecular Cell · doi:10.1016/j.molcel.2006.02.017 · Cited by 151
Spinocerebellar ataxia with axonal neuropathy: consequence of a Tdp1 recessive neomorphic mutation?
Hirano, R., Interthal, H., Huang, C., Nakamura, T., Deguchi, K., Choi, K., Bhattacharjee, M. B., Arimura, K., Umehara, F., Izumo, S., et al. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601885 · Cited by 146
Effects of abasic sites and DNA single-strand breaks on prokaryotic RNA polymerases.
Zhou, W., & Doetsch, P. W. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.14.6601 · Cited by 145
Schwartz, S. (1987) · Europe PMC (PubMed Central) · Cited by 142
Synthetic lethality between mutation in Atm and DNA-PK cs during murine embryogenesis
Gurley, K. E., & Kemp, C. J. (2001) · Current Biology · doi:10.1016/s0960-9822(01)00048-3 · Cited by 142
Ctp1/CtIP and the MRN Complex Collaborate in the Initial Steps of Homologous Recombination
Takeda, S., Nakamura, K. M., Taniguchi, Y., & Paull, T. T. (2007) · Molecular Cell · doi:10.1016/j.molcel.2007.10.016 · Cited by 139
Chen, P., Peng, C., Luff, J., Spring, K. J., Watters, D. J., Bottle, S. E., Furuya, S., & Lavin, M. F. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-36-11453.2003 · Cited by 134
Lee, Y., Chong, M. J., & McKinnon, P. J. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-17-06687.2001 · Cited by 132
Self-citationNeurological symptoms and natural course of xeroderma pigmentosum
Anttinen, A., Koulu, L., Nikoskelainen, E., Portin, R., Kurki, T., Erkinjuntti, M., Jaspers, N. G. J., Raams, A., Green, M. H. L., Lehmann, A. R., et al. (2008) · Brain · doi:10.1093/brain/awn126 · Cited by 132
Ataxia—ocular motor aprilaxia: A syndrome mimicking ataxia‐telangiectasia
Aicardi, J. F., Barbosa, C., Andermann, E., Andermann, F., Morcos, R., Ghanem, Q., Fukuyama, Y., Awaya, Y., & Moe, P. G. (1988) · Annals of Neurology · doi:10.1002/ana.410240404 · Cited by 131
Loss of Neuronal Cell Cycle Control in Ataxia-Telangiectasia: A Unified Disease Mechanism
Yang, Y. F., & Herrup, K. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.4946-04.2005 · Cited by 129
Girard, P.-M., Kysela, B. P., Härer, C. J., Doherty, A. J., & Jeggo, P. A. (2004) · Human Molecular Genetics · doi:10.1093/hmg/ddh274 · Cited by 126
Mechanisms of Disease: DNA repair defects and neurological disease
Subba Rao, K. (2007) · Nature Clinical Practice Neurology · doi:10.1038/ncpneuro0448 · Cited by 121
BRCA2 is required for neurogenesis and suppression of medulloblastoma
Frappart, P., Lee, Y., Lamont, J. M., & McKinnon, P. J. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601703 · Cited by 114
Self-citationChen, Y.-Z., Hashemi, S. H., Anderson, S. K., Huang, Y., Moreira, M.-C., Lynch, D. R., Glass, I. A., Chance, P. F., & Bennett, C. L. (2006) · Neurobiology of Disease · doi:10.1016/j.nbd.2006.02.007 · Cited by 111
Proliferation and apoptosis in the developing human neocortex
Chan, W. Y., Lorke, D. E., Tiu, S. C., & Yew, D. T. W. (2002) · The Anatomical Record · doi:10.1002/ar.10100 · Cited by 111
Murai, M., Enokido, Y., Inamura, N., Yoshino, M., Nakatsu, Y., van der Horst, G. T. J., Hoeijmakers, J. H. J., Tanaka, K., & Hatanaka, H. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.231329598 · Cited by 109
Mutations in senataxin responsible for Quebec cluster of ataxia with neuropathy
Duquette, A., Roddier, K., McNabb-Baltar, J. Y., Gosselin, I., St‐Denis, A., Dicaire, M., Loisel, L., Labuda, D., Marchand, L., Mathieu, J., et al. (2005) · Annals of Neurology · doi:10.1002/ana.20408 · Cited by 108
Saar, K., Chrzańowska, K., Stümm, M., Jung, M., Nürnberg, G., Wienker, T. F., Seemanová, E., Wegner, R. ‐., Reis, A., & Sperling, K. (1997) · Europe PMC (PubMed Central) · Cited by 106
Responding to DNA double strand breaks in the nervous system
Lee, Y., & McKinnon, P. J. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.07.026 · Cited by 105
Self-citationActions of Aprataxin in Multiple DNA Repair Pathways
Rass, U., Ahel, I., & West, S. C. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m611489200 · Cited by 104
Miao, Z., Agama, K., Sordet, O., Povirk, L. F., Kohn, K. W., & Pommier, Y. G. (2006) · DNA repair · doi:10.1016/j.dnarep.2006.07.004 · Cited by 102
Mitochondrial DNA, base excision repair and neurodegeneration
de Souza-Pinto, N. C., Wilson, D. M., Stevnsner, T., & Bohr, V. A. (2008) · DNA repair · doi:10.1016/j.dnarep.2008.03.011 · Cited by 102
The Pathogenesis of Ataxia-Telangiectasia
Gatti, R. A., Becker-Catania, S., Chun, H. H., Sun, X., Mitui, M., Lai, C.-H., Khanlou, N., Babaei, M., Cheng, R., Clark, C., et al. (2001) · Clinical Reviews in Allergy & Immunology · doi:10.1385/criai:20:1:87 · Cited by 101
Ataxia-telangiectasia: the pattern of cerebellar atrophy on MRI
Tavani, F., Zimmerman, R. A., Berry, G. T., Sullivan, K. E., Gatti, R. A., & Bingham, P. (2003) · Neuroradiology · doi:10.1007/s00234-003-0945-9 · Cited by 101
Neurological defects in trichothiodystrophy reveal a coactivator function of TFIIH
Compe, E., Malerba, M., Soler, L., Marescaux, J., Borrelli, E., & Egly, J. (2007) · Nature Neuroscience · doi:10.1038/nn1990 · Cited by 95
Mitochondrial DNA ligase III function is independent of Xrcc1
Lakshmipathy, U. (2000) · Nucleic Acids Research · doi:10.1093/nar/28.20.3880 · Cited by 95
The Involvement of DNA-Damage and -Repair Defects in Neurological Dysfunction
Kulkarni, A., & Wilson, D. M. (2008) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2008.01.009 · Cited by 89
DNA strand breaks, neurodegeneration and aging in the brain
Katyal, S., & McKinnon, P. J. (2008) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2008.03.008 · Cited by 87
Self-citationRapid phosphorylation of histone H2A.X following ionotropic glutamate receptor activation
Crowe, S. L., Movsesyan, V. A., Jorgensen, T. J., & Kondratyev, A. D. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04768.x · Cited by 87
Distel, L. V., Neubauer, S., Varon, R., Holter, W., & Grabenbauer, G. G. (2003) · Medical and Pediatric Oncology · doi:10.1002/mpo.10275 · Cited by 86
Xeroderma pigmentosum genes: Functions inside and outside DNA repair
Sugasawa, K. (2007) · Carcinogenesis · doi:10.1093/carcin/bgm282 · Cited by 83
Repair of DNA Covalently Linked to Protein
Connelly, J. C., & Leach, D. R. F. (2004) · Molecular Cell · doi:10.1016/s1097-2765(04)00056-5 · Cited by 82
The Fanconi anemia/BRCA pathway: A coordinator of cross-link repair
Mirchandani, K. D., & D’Andrea, A. D. (2006) · Experimental Cell Research · doi:10.1016/j.yexcr.2006.06.014 · Cited by 82
Ataxia-Telangiectasia and Related Diseases
Frappart, P., & McKinnon, P. J. (2006) · NeuroMolecular Medicine · doi:10.1385/nmm:8:4:495 · Cited by 81
Self-citationMcMurray, C. T. (2008) · DNA repair · doi:10.1016/j.dnarep.2008.03.013 · Cited by 78
Brooks, P. J., Cheng, T., & Cooper, L. D. (2008) · DNA repair · doi:10.1016/j.dnarep.2008.01.017 · Cited by 78
Neurodegeneration in hereditary nucleotide repair disorders
Itoh, M., Hayashi, M., Shioda, K., Minagawa, M., Isa, F., Tamagawa, K., Morimatsu, Y., & Oda, M. (1999) · Brain and Development · doi:10.1016/s0387-7604(99)00033-9 · Cited by 75
Fernandes, N. D., Sun, Y., Chen, S., Paul, P., Shaw, R. J., Cantley, L. C., & Price, B. D. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m412065200 · Cited by 74
Nucleotide excision repair and neurological diseases
Nouspikel, T. (2008) · DNA repair · doi:10.1016/j.dnarep.2008.03.015 · Cited by 73
Neurological manifestations in xeroderma pigmentosum
Mimaki, T., Itoh, N., Abe, J., Tagawa, T., Sato, K., Yabuuchi, H., & Takebe, H. (1986) · Annals of Neurology · doi:10.1002/ana.410200112 · Cited by 73
Medulloblastoma With Adverse Reaction to Radiation Therapy in Nijmegen Breakage Syndrome
Bakhshi, S., Cerosaletti, K. M., CONCANNON, P. J., Bawle, E. V., Fontanesi, J., Gatti, R. A., & Bhambhani, K. J. (2003) · Journal of Pediatric Hematology/Oncology · doi:10.1097/00043426-200303000-00013 · Cited by 69
When parsimony backfires: Neglecting DNA repair may doom neurons in Alzheimer's disease
Nouspikel, T., & Hanawalt, P. C. (2003) · BioEssays · doi:10.1002/bies.10227 · Cited by 69
A subgroup of spinocerebellar ataxias defective in DNA damage responses
Gueven, N., Chen, P., Nakamura, J., Bécherel, O. J., Kijas, A. W., Grattan‐Smith, P. J., & Lavin, M. F. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2006.12.010 · Cited by 60
Disease-associated Mutations Inactivate AMP-Lysine Hydrolase Activity of Aprataxin
Seidle, H. F., Bieganowski, P., & Brenner, C. H. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m502889200 · Cited by 60
The Contribution of the DNA Damage Response to Neuronal Viability
Barzilai, A. (2006) · Antioxidants and Redox Signaling · doi:10.1089/ars.2007.9.211 · Cited by 59
Fanconi DNA repair pathway is required for survival and long‐term maintenance of neural progenitors
Sii-Felice, K., Etienne, O., Hoffschir, F., Mathieu, C., Riou, L., Barroca, V., Haton, C., Arwert, F., Fouchet, P., Boussin, F. D., et al. (2008) · The EMBO Journal · doi:10.1038/emboj.2008.14 · Cited by 59
Farina, L., Uggetti, C., Ottolini, A., Martelli, A., Bergamaschi, R., Sibilla, L., Zappoli, F., Egitto, M. G., & Lanzi, G. (1994) · Journal of Computer Assisted Tomography · doi:10.1097/00004728-199409000-00008 · Cited by 56
Mouse models of DNA double-strand break repair and neurological disease
Frappart, P., & McKinnon, P. J. (2008) · DNA repair · doi:10.1016/j.dnarep.2008.03.007 · Cited by 53
Self-citationCranial MRI in ataxia-telangiectasia
Sardanelli, F., Parodi, R. C., Ottonello, C., Renzetti, E., Saitta, S., Lignana, E., & Mancardi, G. (1995) · Neuroradiology · doi:10.1007/bf00588526 · Cited by 52
Early Events in the DNA Damage Response
Ward, I. M., & Chen, J. (2004) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(04)63001-8 · Cited by 50
In cis autosomal dominant mutation of Senataxin associated with tremor/ataxia syndrome
Bassuk, A. G., Chen, Y. Z., Batish, S. D., Nagan, N., Opal, P., Chance, P. F., & Bennett, C. L. (2006) · Neurogenetics · doi:10.1007/s10048-006-0067-8 · Cited by 49
DNA single-strand break repair and spinocerebellar ataxia with axonal neuropathy-1
El‐Khamisy, S. F., & Caldecott, K. W. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.08.048 · Cited by 49
Novel mutations in the senataxin DNA/RNA helicase domain in ataxia with oculomotor apraxia 2
Fogel, B. L., & Perlman, S. (2006) · Neurology · doi:10.1212/01.wnl.0000247661.19601.28 · Cited by 49
Sidwell, R. U., Sandison, A., Wing, J., Fawcett, H. D., Seet, J., Fisher, C., Nardò, T., Stefanini, M., Lehmann, A. R., & Cream, J. J. (2006) · British Journal of Dermatology · doi:10.1111/j.1365-2133.2006.07272.x · Cited by 42
Human diseases deficient in RecQ helicases
Harrigan, J. A. (2003) · Biochimie · doi:10.1016/j.biochi.2003.10.006 · Cited by 40
Cerebellar cortex ultrastructure in ataxia‐telangiectasia
Paula‐Barbosa, M. M., Ruela, C., Tavares, M. A., Pontes, C., Saraiva, A., & Cruz, C. (1983) · Annals of Neurology · doi:10.1002/ana.410130312 · Cited by 38
Spinocerebellar ataxia with ocular motor apraxia and DNA repair
Onodera, O. (2006) · Neuropathology · doi:10.1111/j.1440-1789.2006.00741.x · Cited by 33
Purkinje cell degeneration in mice lacking the xeroderma pigmentosum group G gene
Sun, X., Harada, Y., Takahashi, S., Shiomi, N., & Shiomi, T. (2001) · Journal of Neuroscience Research · doi:10.1002/jnr.1085 · Cited by 30
Premature aging in Werner's syndrome spares the central nervous system
Postiglione, A., Soricelli, A., Covelli, E. M., Iazzetta, N., Ruocco, A., Milan, G., Santoro, L., Alfano, B., & Brunetti, A. (1996) · Neurobiology of Aging · doi:10.1016/0197-4580(96)00033-4 · Cited by 29
Adult-onset xeroderma pigmentosum neurological disease--observations in an autopsy case.
Robbins, J. H., Kraemer, K. H., Merchant, S. N., & Brumback, R. A. (2002) · PubMed · Cited by 29
Cranial MRI in the Nijmegen breakage syndrome
Bekiesińska‐Figatowska, M., Chrzańowska, K., Sikorska, J., Walecki, J. M., Krajewska‐Walasek, M., wiak, S. J., & Kleijer, W. J. (2000) · Neuroradiology · doi:10.1007/s002340050011 · Cited by 28
Nicolaou, P., Georghiou, A., Votsi, C., Middleton, L. T., Zamba‐Papanicolaou, E., & Christodoulou, K. (2008) · BMC Medical Genetics · doi:10.1186/1471-2350-9-28 · Cited by 27
Arning, L., Schöls, L. J., Cin, H., Souquet, M., Epplen, J. T., & Timmann, D. (2008) · Neurogenetics · doi:10.1007/s10048-008-0139-z · Cited by 23
Is the sensory neuropathy in ataxia-telangiectasia distinguishable from that in Friedreich's ataxia?
Barbieri, F., Santoro, L., Crisci, C., Massini, R., Russo, E., & Campanella, G. (1986) · Acta Neuropathologica · doi:10.1007/bf00688296 · Cited by 21
DNA-damage checkpoints: location, location, location
Wood, J. L., & Chen, J. (2008) · Trends in Cell Biology · doi:10.1016/j.tcb.2008.07.006 · Cited by 20
Accelerated aging of the brain in Werner's syndrome
Kakigi, R., Endo, C., Neshige, R., Kohno, H., & Kuroda, Y. (1992) · Neurology · doi:10.1212/wnl.42.4.922 · Cited by 19
Sugawara, M., Wada, C., Okawa, S., Kobayashi, M., Sageshima, M., Imota, T., & Toyoshima, I. (2007) · European Neurology · doi:10.1159/000109256 · Cited by 18
Xeroderma Pigmentosum and Medulloblastoma: Chromosomal Damage to Lymphocytes during Radiotherapy
Giannelli, F., Avery, J., Polani, P. E., Terrell, C., & Giammusso, V. (1981) · Radiation Research · doi:10.2307/3575764 · Cited by 16
Hassin‐Baer, S., Bar‐Shira, A., Gilad, S., Galanty, Y., Khosravi, R., Lossos, A., Giladi, N., Weitz, R., Zeev, B. B., Goldhammer, Y., et al. (1999) · Journal of Neurology · doi:10.1007/s004150050438 · Cited by 15
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
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