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Agata M. Smogorzewska, Ph.D. - Publications

Affiliations: 
2009- Rockefeller University, New York, NY, United States 
Area:
Genome Maintenance
Website:
https://www.rockefeller.edu/our-scientists/heads-of-laboratories/976-agata-smogorzewska/
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69/86 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Conti BA, Ruiz PD, Broton C, Blobel NJ, Kottemann MC, Sridhar S, Lach FP, Wiley TF, Sasi NK, Carroll T, Smogorzewska A. RTF2 controls replication repriming and ribonucleotide excision at the replisome. Nature Communications. 15: 1943. PMID 38431617 DOI: 10.1038/s41467-024-45947-z  0.363
2023 Ruiz PD, Smogorzewska A. Temporary HMCES-DNA cross-link prevents permanent DNA damage. Cell Reports. 43: 113594. PMID 38141170 DOI: 10.1016/j.celrep.2023.113594  0.39
2023 Conti BA, Ruiz PD, Broton C, Blobel NJ, Kottemann MC, Sridhar S, Lach FP, Wiley T, Sasi NK, Carroll T, Smogorzewska A. RTF2 controls replication repriming and ribonucleotide excision at the replisome. Biorxiv : the Preprint Server For Biology. PMID 36993543 DOI: 10.1101/2023.03.13.532415  0.374
2022 Webster ALH, Sanders MA, Patel K, Dietrich R, Noonan RJ, Lach FP, White RR, Goldfarb A, Hadi K, Edwards MM, Donovan FX, Hoogenboezem RM, Jung M, Sridhar S, Wiley TF, ... ... Smogorzewska A, et al. Genomic signature of Fanconi anaemia DNA repair pathway deficiency in cancer. Nature. PMID 36450981 DOI: 10.1038/s41586-022-05253-4  0.344
2022 Elango R, Panday A, Lach FP, Willis NA, Nicholson K, Duffey EE, Smogorzewska A, Scully R. The structure-specific endonuclease complex SLX4-XPF regulates Tus-Ter-induced homologous recombination. Nature Structural & Molecular Biology. PMID 35941380 DOI: 10.1038/s41594-022-00812-9  0.406
2022 Caballero M, Ge T, Rebelo AR, Seo S, Kim S, Brooks K, Zuccaro M, Kanagaraj R, Vershkov D, Kim D, Smogorzewska A, Smolka M, Benvenisty N, West SC, Egli D, et al. Comprehensive analysis of DNA replication timing across 184 cell lines suggests a role for MCM10 in replication timing regulation. Human Molecular Genetics. PMID 35394024 DOI: 10.1093/hmg/ddac082  0.362
2021 Yang Z, Wu XS, Wei Y, Polyanskaya SA, Iyer SV, Jung M, Lach FP, Adelman ER, Klingbeil O, Milazzo JP, Kramer M, Demerdash OE, Chang K, Goodwin S, Hodges E, ... ... Smogorzewska A, et al. Transcriptional silencing of ALDH2 confers a dependency on Fanconi anemia proteins in acute myeloid leukemia. Cancer Discovery. PMID 33893150 DOI: 10.1158/2159-8290.CD-20-1542  0.343
2021 Giunta S, Hervé S, White RR, Wilhelm T, Dumont M, Scelfo A, Gamba R, Wong CK, Rancati G, Smogorzewska A, Funabiki H, Fachinetti D. CENP-A chromatin prevents replication stress at centromeres to avoid structural aneuploidy. Proceedings of the National Academy of Sciences of the United States of America. 118. PMID 33653953 DOI: 10.1073/pnas.2015634118  0.333
2020 Lach FP, Singh S, Rickman KA, Ruiz PD, Noonan RJ, Hymes KB, DeLacure MD, Kennedy JA, Chandrasekharappa SC, Smogorzewska A. Esophageal Cancer as initial presentation of Fanconi anemia in patients with a hypomorphic FANCA variant. Cold Spring Harbor Molecular Case Studies. PMID 33172906 DOI: 10.1101/mcs.a005595  0.308
2020 Thongthip S, Conti BA, Lach FP, Smogorzewska A. Suppression of non-homologous end joining does not rescue DNA repair defects in Fanconi anemia patient cells. Cell Cycle (Georgetown, Tex.). 1-9. PMID 32865112 DOI: 10.1080/15384101.2020.1810394  0.791
2020 Rickman KA, Noonan RJ, Lach FP, Sridhar S, Wang AT, Abhyankar A, Huang A, Kelly M, Auerbach AD, Smogorzewska A. Distinct roles of BRCA2 in replication fork protection in response to hydroxyurea and DNA interstrand cross-links. Genes & Development. PMID 32354836 DOI: 10.1101/Gad.336446.120  0.547
2020 Jung M, Ramanagoudr-Bhojappa R, van Twest S, Rosti RO, Murphy V, Tan W, Donovan FX, Lach FP, Kimble DC, Jiang C, Vaughan R, Mehta PA, Pierri F, Doufour C, Auerbach AD, ... ... Smogorzewska A, et al. Association of clinical severity with FANCB variant type in Fanconi anemia. Blood. PMID 32106311 DOI: 10.1182/Blood.2019003249  0.363
2020 Ardeljan D, Steranka JP, Liu C, Li Z, Taylor MS, Payer LM, Gorbounov M, Sarnecki JS, Deshpande V, Hruban RH, Boeke JD, Fenyö D, Wu PH, Smogorzewska A, Holland AJ, et al. Cell fitness screens reveal a conflict between LINE-1 retrotransposition and DNA replication. Nature Structural & Molecular Biology. 27: 168-178. PMID 32042151 DOI: 10.1038/S41594-020-0372-1  0.412
2019 Taylor AMR, Rothblum-Oviatt C, Ellis NA, Hickson ID, Meyer S, Crawford TO, Smogorzewska A, Pietrucha B, Weemaes C, Stewart GS. Chromosome instability syndromes. Nature Reviews. Disease Primers. 5: 64. PMID 31537806 DOI: 10.1038/s41572-019-0113-0  0.378
2019 Donovan FX, Solanki A, Mori M, Chavan N, George M, Kumar C S, Okuno Y, Muramastsu H, Yoshida K, Shimamoto A, Takaori-Kondo A, Yabe H, Ogawa S, Kojima S, Yabe M, ... ... Smogorzewska A, et al. A founder variant in the South Asian population leads to a high prevalence of FANCL Fanconi anemia cases in India. Human Mutation. PMID 31513304 DOI: 10.1002/Humu.23914  0.367
2019 Rickman K, Smogorzewska A. Advances in understanding DNA processing and protection at stalled replication forks. The Journal of Cell Biology. 218: 1096-1107. PMID 30670471 DOI: 10.1083/Jcb.201809012  0.493
2019 Jung M, Sridhar S, Goldfarb A, White R, Keahi D, Noonan R, Wiley T, Lach FP, Smogorzewska A. A Novel Source of Endogenous DNA Damage That Requires Repair By the Fanconi Anemia Pathway Blood. 134: 106-106. DOI: 10.1182/Blood-2019-127686  0.477
2019 Smogorzewska A. Fanconi Anemia: A Paradigm for Understanding DNA Repair During Replication. Blood. 134: SCI-32-SCI-32. DOI: 10.1182/Blood-2019-121229  0.532
2018 Kottemann MC, Conti BA, Lach FP, Smogorzewska A. Removal of RTF2 from Stalled Replisomes Promotes Maintenance of Genome Integrity. Molecular Cell. 69: 24-35.e5. PMID 29290612 DOI: 10.1016/J.Molcel.2017.11.035  0.472
2018 Jung M, Ramanagoudr Bhojappa R, Rosti O, Lach FP, Donovan FX, Auerbach AD, Chandrasekharappa SC, Smogorzewska A. Clinical Severity Correlates with in Vitro Residual Function of FANCB Missense Variants Blood. 132: 2588-2588. DOI: 10.1182/Blood-2018-99-111320  0.346
2017 Mazzucco AE, Smogorzewska A, Kang C, Luo J, Schlabach MR, Xu Q, Patel R, Elledge SJ. Corrigendum: Genetic interrogation of replicative senescence uncovers a dual role for USP28 in coordinating the p53 and GATA4 branches of the senescence program. Genes & Development. 31: 2310. PMID 29284711 DOI: 10.1101/gad.309864.117  0.422
2017 Asur RS, Kimble DC, Lach FP, Jung M, Donovan FX, Kamat A, Noonan RJ, Thomas JW, Park M, Chines P, Vlachos A, Auerbach AD, Smogorzewska A, Chandrasekharappa SC. Somatic mosaicism of an intragenic FANCB duplication in both fibroblast and peripheral blood cells observed in a Fanconi anemia patient leads to milder phenotype. Molecular Genetics & Genomic Medicine. PMID 29193904 DOI: 10.1002/Mgg3.350  0.308
2017 Kimble DC, Lach FP, Gregg SQ, Donovan FX, Flynn EK, Kamat A, Young A, Vemulapalli M, Thomas JW, Mullikin JC, Auerbach AD, Smogorzewska A, Chandrasekharappa SC. A comprehensive approach to identification of pathogenic FANCA variants in Fanconi anemia patients and their families. Human Mutation. PMID 29098742 DOI: 10.1002/Humu.23366  0.365
2017 Mazzucco AE, Smogorzewska A, Kang C, Luo J, Schlabach MR, Xu Q, Patel R, Elledge SJ. Genetic interrogation of replicative senescence uncovers a dual role for USP28 in coordinating the p53 and GATA4 branches of the senescence program. Genes & Development. 31: 1933-1938. PMID 29089421 DOI: 10.1101/Gad.304857.117  0.552
2017 Cottineau J, Kottemann MC, Lach FP, Kang YH, Vély F, Deenick EK, Lazarov T, Gineau L, Wang Y, Farina A, Chansel M, Lorenzo L, Piperoglou C, Ma CS, Nitschke P, ... ... Smogorzewska A, et al. Inherited GINS1 deficiency underlies growth retardation along with neutropenia and NK cell deficiency. The Journal of Clinical Investigation. PMID 28414293 DOI: 10.1172/Jci90727  0.446
2017 Lim PX, Sutherland J, Noonan R, Dananberg A, Holloman W, Smogorzewska A, Jasin M. Abstract A27: Assessing somatic tumor-associated RAD51 mutations and screening for novel dominant-interfering RAD51 proteins Molecular Cancer Research. 15. DOI: 10.1158/1557-3125.Dnarepair16-A27  0.481
2016 Thongthip S, Bellani M, Gregg SQ, Sridhar S, Conti BA, Chen Y, Seidman MM, Smogorzewska A. Fan1 deficiency results in DNA interstrand cross-link repair defects, enhanced tissue karyomegaly, and organ dysfunction. Genes & Development. 30: 645-59. PMID 26980189 DOI: 10.1101/Gad.276261.115  0.773
2016 Donovan FX, Kimble DC, Kim Y, Lach FP, Harper U, Kamat A, Jones M, Sanborn EM, Tryon R, Wagner JE, MacMillan ML, Ostrander EA, Auerbach AD, Smogorzewska A, Chandrasekharappa SC. Paternal or Maternal Uniparental Disomy of Chromosome 16 Resulting in Homozygosity of a Mutant Allele Causes Fanconi Anemia. Human Mutation. PMID 26841305 DOI: 10.1002/Humu.22962  0.342
2015 Wang AT, Kim T, Wagner JE, Conti BA, Lach FP, Huang AL, Molina H, Sanborn EM, Zierhut H, Cornes BK, Abhyankar A, Sougnez C, Gabriel SB, Auerbach AD, Kowalczykowski SC, ... Smogorzewska A, et al. A Dominant Mutation in Human RAD51 Reveals Its Function in DNA Interstrand Crosslink Repair Independent of Homologous Recombination. Molecular Cell. 59: 478-90. PMID 26253028 DOI: 10.1016/J.Molcel.2015.07.009  0.547
2015 Rickman KA, Lach FP, Abhyankar A, Donovan FX, Sanborn EM, Kennedy JA, Sougnez C, Gabriel SB, Elemento O, Chandrasekharappa SC, Schindler D, Auerbach AD, Smogorzewska A. Deficiency of UBE2T, the E2 Ubiquitin Ligase Necessary for FANCD2 and FANCI Ubiquitination, Causes FA-T Subtype of Fanconi Anemia. Cell Reports. PMID 26119737 DOI: 10.1016/J.Celrep.2015.06.014  0.404
2015 Wang AT, Smogorzewska A. SnapShot: Fanconi anemia and associated proteins. Cell. 160: 354-354.e1. PMID 25594185 DOI: 10.1016/J.Cell.2014.12.031  0.462
2015 Ouyang J, Garner E, Hallet A, Nguyen HD, Rickman KA, Gill G, Smogorzewska A, Zou L. Noncovalent interactions with SUMO and ubiquitin orchestrate distinct functions of the SLX4 complex in genome maintenance. Molecular Cell. 57: 108-22. PMID 25533185 DOI: 10.1016/J.Molcel.2014.11.015  0.685
2015 Wang AT, Kim T, Wagner JE, Conti BA, Lach FP, Huang AL, Molina H, Sanborn EM, Zierhut H, Cornes BK, Abhyankar A, Sougnez C, Gabriel SB, Auerbach AD, Kowalczykowski SC, ... Smogorzewska A, et al. A Dominant Mutation in Human RAD51 Reveals Its Function in DNA Interstrand Crosslink Repair Independent of Homologous Recombination Molecular Cell. 59: 478-490. DOI: 10.1016/j.molcel.2015.07.009  0.384
2014 Wang R, Persky NS, Yoo B, Ouerfelli O, Smogorzewska A, Elledge SJ, Pavletich NP. DNA repair. Mechanism of DNA interstrand cross-link processing by repair nuclease FAN1. Science (New York, N.Y.). 346: 1127-30. PMID 25430771 DOI: 10.1126/Science.1258973  0.627
2014 Flynn EK, Kamat A, Lach FP, Donovan FX, Kimble DC, Narisu N, Sanborn E, Boulad F, Davies SM, Gillio AP, Harris RE, MacMillan ML, Wagner JE, Smogorzewska A, Auerbach AD, et al. Comprehensive analysis of pathogenic deletion variants in Fanconi anemia genes. Human Mutation. 35: 1342-53. PMID 25168418 DOI: 10.1002/Humu.22680  0.376
2014 Smogorzewska A. Abstract SY33-01: Mechanism of tumor suppression by the Fanconi anemia proteins Cancer Research. 74. DOI: 10.1158/1538-7445.Am2014-Sy33-01  0.552
2014 Wang R, Persky NS, Yoo B, Ouerfelli O, Smogorzewska A, Elledge SJ, Pavletich NP. Mechanism of DNA interstrand cross-link processing by repair nuclease FAN1 Science. 346: 1127-1130. DOI: 10.1126/science.1258973  0.543
2013 Garner E, Kim Y, Lach FP, Kottemann MC, Smogorzewska A. Human GEN1 and the SLX4-associated nucleases MUS81 and SLX1 are essential for the resolution of replication-induced Holliday junctions. Cell Reports. 5: 207-15. PMID 24080495 DOI: 10.1016/J.Celrep.2013.08.041  0.486
2013 Shah S, Kim Y, Ostrovnaya I, Murali R, Schrader KA, Lach FP, Sarrel K, Rau-Murthy R, Hansen N, Zhang L, Kirchhoff T, Stadler Z, Robson M, Vijai J, Offit K, ... Smogorzewska A, et al. Assessment of SLX4 Mutations in Hereditary Breast Cancers. Plos One. 8: e66961. PMID 23840564 DOI: 10.1371/Journal.Pone.0066961  0.434
2013 Chandrasekharappa SC, Lach FP, Kimble DC, Kamat A, Teer JK, Donovan FX, Flynn E, Sen SK, Thongthip S, Sanborn E, Smogorzewska A, Auerbach AD, Ostrander EA. Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia. Blood. 121: e138-48. PMID 23613520 DOI: 10.1182/Blood-2012-12-474585  0.745
2013 Kottemann MC, Smogorzewska A. Fanconi anaemia and the repair of Watson and Crick DNA crosslinks. Nature. 493: 356-63. PMID 23325218 DOI: 10.1038/Nature11863  0.532
2013 Kim Y, Spitz GS, Veturi U, Lach FP, Auerbach AD, Smogorzewska A. Regulation of multiple DNA repair pathways by the Fanconi anemia protein SLX4. Blood. 121: 54-63. PMID 23093618 DOI: 10.1182/Blood-2012-07-441212  0.51
2012 Chaki M, Airik R, Ghosh AK, Giles RH, Chen R, Slaats GG, Wang H, Hurd TW, Zhou W, Cluckey A, Gee HY, Ramaswami G, Hong CJ, Hamilton BA, Cervenka I, ... ... Smogorzewska A, et al. Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling. Cell. 150: 533-48. PMID 22863007 DOI: 10.1016/J.Cell.2012.06.028  0.505
2012 Zhou W, Otto EA, Cluckey A, Airik R, Hurd TW, Chaki M, Diaz K, Lach FP, Bennett GR, Gee HY, Ghosh AK, Natarajan S, Thongthip S, Veturi U, Allen SJ, ... ... Smogorzewska A, et al. FAN1 mutations cause karyomegalic interstitial nephritis, linking chronic kidney failure to defective DNA damage repair. Nature Genetics. 44: 910-5. PMID 22772369 DOI: 10.1038/Ng.2347  0.773
2012 Gineau L, Cognet C, Kara N, Lach FP, Dunne J, Veturi U, Picard C, Trouillet C, Eidenschenk C, Aoufouchi S, Alcaïs A, Smith O, Geissmann F, Feighery C, Abel L, ... Smogorzewska A, et al. Partial MCM4 deficiency in patients with growth retardation, adrenal insufficiency, and natural killer cell deficiency. The Journal of Clinical Investigation. 122: 821-32. PMID 22354167 DOI: 10.1172/Jci61014  0.345
2012 Adamson B, Smogorzewska A, Sigoillot FD, King RW, Elledge SJ. A genome-wide homologous recombination screen identifies the RNA-binding protein RBMX as a component of the DNA-damage response. Nature Cell Biology. 14: 318-28. PMID 22344029 DOI: 10.1038/Ncb2426  0.645
2012 Shah S, Lach F, Kim Y, Sarrel K, Rau-Murthy R, Hansen N, Rendleman J, Kirchhoff T, Joseph V, Offit K, Smogorzewska A. Abstract 2600:SLX4mutation in hereditary breast cancer Cancer Research. 72: 2600-2600. DOI: 10.1158/1538-7445.Am2012-2600  0.334
2011 Joo W, Xu G, Persky NS, Smogorzewska A, Rudge DG, Buzovetsky O, Elledge SJ, Pavletich NP. Structure of the FANCI-FANCD2 complex: Insights into the Fanconi anemia DNA repair pathway Science. 333: 312-316. PMID 21764741 DOI: 10.1126/Science.1205805  0.609
2011 Garner E, Smogorzewska A. Ubiquitylation and the Fanconi anemia pathway Febs Letters. 585: 2853-2860. PMID 21605559 DOI: 10.1016/J.Febslet.2011.04.078  0.462
2011 Kim Y, Lach FP, Desetty R, Hanenberg H, Auerbach AD, Smogorzewska A. Mutations of the SLX4 gene in Fanconi anemia. Nature Genetics. 43: 142-6. PMID 21240275 DOI: 10.1038/Ng.750  0.494
2011 Burrows AE, Smogorzewska A, Elledge SJ. Abstract A33: A whole genome RNAi screen identifies BRD7 and BAF180 as p53 regulators required for senescence Cancer Research. 71. DOI: 10.1158/1538-7445.Fbcr11-A33  0.735
2010 Burrows AE, Smogorzewska A, Elledge SJ. Polybromo-associated BRG1-associated factor components BRD7 and BAF180 are critical regulators of p53 required for induction of replicative senescence Proceedings of the National Academy of Sciences of the United States of America. 107: 14280-14285. PMID 20660729 DOI: 10.1073/Pnas.1009559107  0.784
2010 Smogorzewska A, Desetty R, Saito TT, Schlabach M, Lach FP, Sowa ME, Clark AB, Kunkel TA, Harper JW, Colaiácovo MP, Elledge SJ. A Genetic Screen Identifies FAN1, a Fanconi Anemia-Associated Nuclease Necessary for DNA Interstrand Crosslink Repair Molecular Cell. 39: 36-47. PMID 20603073 DOI: 10.1016/J.Molcel.2010.06.023  0.605
2009 Knipscheer P, Räschle M, Smogorzewska A, Enoiu M, Ho TV, Schärer OD, Elledge SJ, Walter JC. The Fanconi anemia pathway promotes replication-dependent DNA interstrand cross-link repair. Science (New York, N.Y.). 326: 1698-701. PMID 19965384 DOI: 10.1126/Science.1182372  0.645
2009 Svendsen JM, Smogorzewska A, Sowa ME, O'Connell BC, Gygi SP, Elledge SJ, Harper JW. Mammalian BTBD12/SLX4 Assembles A Holliday Junction Resolvase and Is Required for DNA Repair Cell. 138: 63-77. PMID 19596235 DOI: 10.1016/J.Cell.2009.06.030  0.641
2008 Ishiai M, Kitao H, Smogorzewska A, Tomida J, Kinomura A, Uchida E, Saberi A, Kinoshita E, Kinoshita-Kikuta E, Koike T, Tashiro S, Elledge SJ, Takata M. FANCI phosphorylation functions as a molecular switch to turn on the Fanconi anemia pathway Nature Structural and Molecular Biology. 15: 1138-1146. PMID 18931676 DOI: 10.1038/Nsmb.1504  0.633
2008 Schlabach MR, Luo J, Solimini NL, Hu G, Xu Q, Li MZ, Zhao Z, Smogorzewska A, Sowa ME, Ang XL, Westbrook TF, Liang AC, Chang K, Hackett JA, Harper JW, et al. Cancer proliferation gene discovery through functional genomics Science. 319: 620-624. PMID 18239126 DOI: 10.1126/Science.1149200  0.76
2007 Wang B, Matsuoka S, Ballif BA, Zhang D, Smogorzewska A, Gygi SP, Elledge SJ. Abraxas and RAP80 form a BRCA1 protein complex required for the DNA damage response Science. 316: 1194-1198. PMID 17525340 DOI: 10.1126/Science.1139476  0.649
2007 Matsuoka S, Ballif BA, Smogorzewska A, McDonald ER, Hurov KE, Luo J, Bakalarski CE, Zhao Z, Solimini N, Lerenthal Y, Shiloh Y, Gygi SP, Elledge SJ. ATM and ATR substrate analysis reveals extensive protein networks responsive to DNA damage Science. 316: 1160-1166. PMID 17525332 DOI: 10.1126/Science.1140321  0.605
2007 Smogorzewska A, Matsuoka S, Vinciguerra P, McDonald ER, Hurov KE, Luo J, Ballif BA, Gygi SP, Hofmann K, D'Andrea AD, Elledge SJ. Identification of the FANCI protein, a monoubiquitinated FANCD2 paralog required for DNA repair. Cell. 129: 289-301. PMID 17412408 DOI: 10.1016/J.Cell.2007.03.009  0.626
2004 Wang RC, Smogorzewska A, de Lange T. Homologous recombination generates T-loop-sized deletions at human telomeres. Cell. 119: 355-68. PMID 15507207 DOI: 10.1016/J.Cell.2004.10.011  0.621
2004 Smogorzewska A, de Lange T. Regulation of telomerase by telomeric proteins. Annual Review of Biochemistry. 73: 177-208. PMID 15189140 DOI: 10.1146/Annurev.Biochem.73.071403.160049  0.637
2003 Takai H, Smogorzewska A, de Lange T. DNA damage foci at dysfunctional telomeres. Current Biology : Cb. 13: 1549-56. PMID 12956959 DOI: 10.1016/S0960-9822(03)00542-6  0.677
2002 Smogorzewska A, Karlseder J, Holtgreve-Grez H, Jauch A, de Lange T. DNA ligase IV-dependent NHEJ of deprotected mammalian telomeres in G1 and G2. Current Biology : Cb. 12: 1635-44. PMID 12361565 DOI: 10.1016/S0960-9822(02)01179-X  0.771
2002 Smogorzewska A, de Lange T. Different telomere damage signaling pathways in human and mouse cells. The Embo Journal. 21: 4338-48. PMID 12169636 DOI: 10.1093/Emboj/Cdf433  0.619
2002 Karlseder J, Smogorzewska A, de Lange T. Senescence induced by altered telomere state, not telomere loss. Science (New York, N.Y.). 295: 2446-9. PMID 11923537 DOI: 10.1126/Science.1069523  0.76
2000 Smogorzewska A, Van Steensel B, Bianchi A, Oelmann S, Schaefer MR, Schnapp G, De Lange T. Control of human telomere length by TRF1 and TRF2 Molecular and Cellular Biology. 20: 1659-1668. PMID 10669743 DOI: 10.1128/Mcb.20.5.1659-1668.2000  0.617
1998 Van Steensel B, Smogorzewska A, De Lange T. TRF2 protects human telomeres from end-to-end fusions Cell. 92: 401-413. PMID 9476899 DOI: 10.1016/S0092-8674(00)80932-0  0.637
1997 Broccoli D, Smogorzewska A, Chong L, de Lange T. Human telomeres contain two distinct Myb-related proteins, TRF1 and TRF2. Nature Genetics. 17: 231-5. PMID 9326950 DOI: 10.1038/ng1097-231  0.738
Low-probability matches (unlikely to be authored by this person)
2015 Beltran H, Eng K, Mosquera JM, Sigaras A, Romanel A, Rennert H, Kossai M, Pauli C, Faltas B, Fontugne J, Park K, Banfelder J, Prandi D, Madhukar N, Zhang T, ... ... Smogorzewska A, et al. Whole-Exome Sequencing of Metastatic Cancer and Biomarkers of Treatment Response. Jama Oncology. 1: 466-74. PMID 26181256 DOI: 10.1001/Jamaoncol.2015.1313  0.287
2020 Jung M, Mehta PA, Jiang CS, Rosti RO, Usleaman G, Correa da Rosa JM, Lach FP, Goodridge E, Auerbach AD, Davies SM, Smogorzewska A, Boulad F. Comparison of the clinical phenotype and haematological course of siblings with Fanconi anaemia. British Journal of Haematology. PMID 32866285 DOI: 10.1111/Bjh.17061  0.284
2020 Schultz-Rogers L, Lach FP, Rickman KA, Ferrer A, Mangaonkar AA, Schwab TL, Schmitz CT, Clark KJ, Dsouza NR, Zimmermann MT, Litzow M, Jacobi N, Klee EW, Smogorzewska A, Patnaik MM. Homozygous missense variant in UBE2T is associated with mild Fanconi anemia phenotype. Haematologica. PMID 32646888 DOI: 10.3324/Haematol.2020.259275  0.265
2020 Conti BA, Smogorzewska A. Mechanisms of direct replication restart at stressed replisomes. Dna Repair. 95: 102947. PMID 32853827 DOI: 10.1016/J.Dnarep.2020.102947  0.252
2024 Chandrasekharappa SC, Ramangoudr-Bhojappa R, Lach FP, Donovan FX, Maxwell R, Rosenberg A, MacMillan ML, Wagner JE, Auerbach AD, Smogorzewska A, Tryon RK. FANCA c.3624C>T (p.Ser1208=) is a hypomorphic splice variant associated with delayed onset of Fanconi anemia. Blood Advances. PMID 38191666 DOI: 10.1182/bloodadvances.2023011888  0.25
2023 Nguyen HT, Tang W, Webster ALH, Whiteaker JR, Chandler CM, Errazquin R, Roohollahi K, Fritzke M, Hoskins EE, Jonlin E, Wakefield L, Sullivan LB, Chen EY, Dorsman J, Brakenhoff R, ... ... Smogorzewska A, et al. Fanconi anemia-isogenic head and neck cancer cell line pairs - a basic and translational science resource. International Journal of Cancer. PMID 36912284 DOI: 10.1002/ijc.34506  0.236
2013 Shah S, Kim Y, Ostrovnaya I, Murali R, Schrader KA, Lach FP, Sarrel K, Rau-Murthy R, Hansen N, Zhang L, Kirchhoff T, Stadler Z, Robson M, Vijai J, Offit K, ... Smogorzewska A, et al. Identification of the nonsense SLX4 variant and evaluation of pathogenicity of the SLX4 variants by complementation assay. Plos One. DOI: 10.1371/Journal.Pone.0066961.G001  0.231
2011 Birkeland AC, Auerbach AD, Sanborn E, Parashar B, Kuhel WI, Chandrasekharappa SC, Smogorzewska A, Kutler DI. Postoperative clinical radiosensitivity in patients with fanconi anemia and head and neck squamous cell carcinoma. Archives of Otolaryngology--Head & Neck Surgery. 137: 930-4. PMID 21930984 DOI: 10.1001/Archoto.2011.154  0.228
2004 Smogorzewska A, Flood JG, Long WH, Dighe AS. Paraprotein interference in automated chemistry analyzers. Clinical Chemistry. 50: 1691-3. PMID 15331512 DOI: 10.1373/Clinchem.2004.037499  0.228
2015 Kutler DI, Patel KR, Auerbach AD, Kennedy J, Lach FP, Sanborn E, Cohen MA, Kuhel WI, Smogorzewska A. Natural history and management of Fanconi anemia patients with head and neck cancer: A 10 year follow-up. The Laryngoscope. PMID 26484938 DOI: 10.1002/Lary.25726  0.223
2017 Lv Z, Rickman KA, Yuan L, Williams K, Selvam SP, Woosley AN, Howe PH, Ogretmen B, Smogorzewska A, Olsen SK. S. pombe Uba1-Ubc15 Structure Reveals a Novel Regulatory Mechanism of Ubiquitin E2 Activity. Molecular Cell. PMID 28162934 DOI: 10.1016/J.Molcel.2017.01.008  0.215
2006 Smogorzewska A, Brandt JT, Chandler WL, Cunningham MT, Hayes TE, Olson JD, Kottke-Marchant K, Van Cott EM. Effect of fondaparinux on coagulation assays: results of College of American Pathologists proficiency testing. Archives of Pathology & Laboratory Medicine. 130: 1605-11. PMID 17076521 DOI: 10.1043/1543-2165(2006)130[1605:Eofoca]2.0.Co;2  0.204
2006 Hull MJ, Griggs D, Knoepp SM, Smogorzewska A, Nixon A, Flood JG. Postmortem urine immunoassay showing false-positive phencyclidine reactivity in a case of fatal tramadol overdose. The American Journal of Forensic Medicine and Pathology. 27: 359-62. PMID 17133040 DOI: 10.1097/01.Paf.0000233534.59330.C2  0.196
2018 Balla T, Baccarini M, Barr M, Castellani V, Cimini D, Ephrussi A, Etienne-Manneville S, Haigis M, Kapoor T, Leschziner A, Manning BD, Meyer T, Miller L, Nachury M, Prinz W, ... Smogorzewska A, et al. New editorial board members Journal of Cell Biology. 217: 1-3. DOI: 10.1083/Jcb.201712071  0.173
2005 Smogorzewska A, Dzik W. Transfusion medicine illustrated. Volume-reduced apheresis platelets. Transfusion. 45: 651. PMID 15847649 DOI: 10.1111/J.1537-2995.2005.04486.X  0.163
2021 Lee RH, Kang H, Yom SS, Smogorzewska A, Johnson DE, Grandis JR. Treatment of Fanconi Anemia-Associated Head and Neck Cancer: Opportunities to Improve Outcomes. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. PMID 34045293 DOI: 10.1158/1078-0432.CCR-21-1259  0.157
2021 Jung M, Smogorzewska A. Endogenous formaldehyde destroys blood stem cells. Blood. 137: 1988-1990. PMID 33856442 DOI: 10.1182/blood.2020010541  0.079
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