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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1962 1
1965 1
1966 5
1967 4
1968 7
1969 6
1970 8
1971 1
1972 3
1973 2
1974 5
1975 1
1976 2
1977 1
1978 2
1980 1
1981 2
1982 1
1984 2
1985 4
1986 2
1987 2
1988 3
1989 2
1991 1
1992 1
1996 1
2002 1
2003 1
2006 1
2008 2
2009 4
2010 1
2012 2
2013 4
2014 2
2015 1
2016 3
2017 2
2018 2
2019 3
2021 3
2022 2
2023 4
2024 3

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103 results

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Page 1
ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk.
Stolarova L, Kleiblova P, Zemankova P, Stastna B, Janatova M, Soukupova J, Achatz MI, Ambrosone C, Apostolou P, Arun BK, Auer P, Barnard M, Bertelsen B; Biobank Japan; Blok MJ, Boddicker N, Brunet J, Burnside ES, Calvello M, Campbell I, Chan SH, Chen F, Chiang JB, Coppa A, Cortesi L, Crujeiras-González A; Consortium CZECANCA; De Leeneer K, De Putter R, DePersia A, Devereux L, Domchek S, Efremidis A, Engel C, Ernst C, Evans DGR, Feliubadaló L, Fostira F, Fuentes-Ríos O, Gómez-García EB, González S, Haiman C, Hansen TVO, Hauke J, Hodge J, Hu C, Huang H, Ishak NDB, Iwasaki Y, Konstantopoulou I, Kraft P, Lacey J, Lázaro C, Li N, Lim WK, Lindstrom S, Lori A, Martinez E, Martins A, Matsuda K, Matullo G, McInerny S, Michailidou K, Montagna M, Monteiro ANA, Mori L, Nathanson K, Neuhausen SL, Nevanlinna H, Olson JE, Palmer J, Pasini B, Patel A, Piane M, Poppe B, Radice P, Renieri A, Resta N, Richardson ME, Rosseel T, Ruddy KJ, Santamariña M, Dos Santos ES, Teras L, Toland AE, Trentham-Dietz A, Vachon CM, Volk AE, Weber-Lassalle N, Weitzel JN, Wiesmuller L, Winham S, Yadav S, Yannoukakos D, Yao S, Zampiga V, Zethoven M, Zhang ZW, Zima T, Spurdle AB, Vega A, Rossing M, Del Valle J, De Nicolo… See abstract for full author list ➔ Stolarova L, et al. Clin Cancer Res. 2023 Aug 15;29(16):3037-3050. doi: 10.1158/1078-0432.CCR-23-0212. Clin Cancer Res. 2023. PMID: 37449874 Free PMC article.
Germline multigene panel testing of patients with endometrial cancer.
Kral J, Jelinkova S, Zemankova P, Vocka M, Borecka M, Cerna L, Cerna M, Dostalek L, Duskova P, Foretova L, Havranek O, Horackova K, Hovhannisyan M, Chvojka S, Kalousova M, Kosarova M, Koudova M, Krutilkova V, Machackova E, Nehasil P, Novotny J, Otahalova B, Puchmajerova A, Safarikova M, Slama J, Stranecky V, Subrt I, Tavandzis S, Zikan M, Zima T, Soukupova J, Kleiblova P, Kleibl Z, Janatova M. Kral J, et al. Among authors: subrt i. Oncol Lett. 2023 Apr 12;25(6):216. doi: 10.3892/ol.2023.13802. eCollection 2023 Jun. Oncol Lett. 2023. PMID: 37153042 Free PMC article.
Re: ERCC3, a new ovarian cancer susceptibility gene?
Soukupova J, Zemankova P, Nehasil P, Kleibl Z; CZECANCA consortium. Soukupova J, et al. Eur J Cancer. 2021 Jun;150:278-280. doi: 10.1016/j.ejca.2021.03.014. Epub 2021 Apr 21. Eur J Cancer. 2021. PMID: 33895055 No abstract available.
Cystic ovarian teratoma as a novel tumor and growth hormone deficiency as a new condition presenting in Multiple Endocrine Neoplasia type 2B: Case reports and review of the literature.
Pomahacova R, Paterova P, Nykodymova E, Vaclavikova E, Sykorova P, Personova K, Katra R, Subrt I, Sykora J. Pomahacova R, et al. Among authors: subrt i. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2022 Mar;166(1):105-111. doi: 10.5507/bp.2021.051. Epub 2021 Aug 24. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2022. PMID: 34446941 Free article. Review.
[Syndrome 4p-].
Subrt I, Blehová B. Subrt I, et al. Cesk Pediatr. 1973 Feb;28(2):75-7. Cesk Pediatr. 1973. PMID: 4686581 Czech. No abstract available.
Familial occurrence of 18q.
Subrt I, Pokorný J. Subrt I, et al. Humangenetik. 1970 Sep 17;10(2):181-7. doi: 10.1007/BF00295518. Humangenetik. 1970. PMID: 5507053 No abstract available.
Dicentric chromosome due to an unusual fusion.
Subrt I, Blehová B, Táborský O. Subrt I, et al. Humangenetik. 1971;12(2):136-41. doi: 10.1007/BF00291469. Humangenetik. 1971. PMID: 5568732 No abstract available.
103 results