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

Year Number of Results
2007 3
2008 1
2009 1
2011 1
2015 1
2017 1
2018 1
2019 5
2021 2
2022 2
2023 3
2024 2

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19 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.
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.
[Tuberous sclerosis].
Vrtel R, Fillipová H, Vodicka R, Santavá A, Curtisová V, Foretová L. Vrtel R, et al. Among authors: curtisova v. Klin Onkol. 2009;22 Suppl:S50-3. Klin Onkol. 2009. PMID: 19764397 Review. Czech. No abstract available.
Implementing genetic education in primary care: the Gen-Equip programme.
Paneque M, Cornel MC, Curtisova V, Houwink E, Jackson L, Kent A, Lunt P, Macek M, Stefansdottir V, Turchetti D, Skirton H. Paneque M, et al. Among authors: curtisova v. J Community Genet. 2017 Apr;8(2):147-150. doi: 10.1007/s12687-017-0296-6. Epub 2017 Mar 13. J Community Genet. 2017. PMID: 28289980 Free PMC article.
Screening for congenital defects and genetic diseases of the fetus at University Hospital in Olomouc and sending/ reporting to the National register of reproductive health in the Czech Republic.
Maděrková Tozzi Michaela, Dvořák Jr. Vladimír, Klásková Eva, Šuláková Soňa, Wita Martin, Hálek Jan, Vrtěl Radek, Curtisová Václava, Pilka Radovan, Dušek Ladislav, Ľubušký Marek. Maděrková Tozzi Michaela, et al. Among authors: curtisova vaclava. Ceska Gynekol. 2022;87(3):162-172. doi: 10.48095/cccg2022162. Ceska Gynekol. 2022. PMID: 35896393 English.
MLPA analysis of 32 foetuses with a congenital heart defect and 1 foetus with renal defects - pilot study. The significant frequency rate of presented pathological CNV.
Stefekova A, Capkova P, Capkova Z, Curtisova V, Srovnal J, Mracka E, Klaskova E, Prochazka M. Stefekova A, et al. Among authors: curtisova v. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2022 May;166(2):187-194. doi: 10.5507/bp.2021.019. Epub 2021 Mar 31. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2022. PMID: 33824538 Free article.
Prenatal detection of copy number variants in fetuses with detected congenital devolpmental disordes, from 2015 to 2020 by Multiplex Ligation-Dependent Probe Amplification and microarray analysis.
Štefeková Andrea, Čapková Pavlína, Curtisová Václava, Mracká Enghjargalan, Filipová Hana, Spurná Zuzana, Procházka Martin, Ľubušký Marek, Pilka Radovan, Vrtěl Radek. Štefeková Andrea, et al. Among authors: curtisova vaclava. Ceska Gynekol. 2023;88(3):162-171. doi: 10.48095/cccg2023162. Ceska Gynekol. 2023. PMID: 37344181 English.
A deep intronic recurrent CHEK2 variant c.1009-118_1009-87delinsC affects pre-mRNA splicing and contributes to hereditary breast cancer predisposition.
Zemankova P, Cerna M, Horackova K, Ernst C, Soukupova J, Borecka M, Blümcke B, Cerna L, Cerna M, Curtisova V, Dolezalova T, Duskova P, Dvorakova L, Foretova L, Havranek O, Hauke J, Hahnen E, Hodulova M, Hovhannisyan M, Hruskova L, Janatova M, Janikova M, Jelinkova S, Just P, Kosarova M, Koudova M, Krutilkova V, Machackova E, Matejkova K, Michalovska R, Misove A, Nehasil P, Nemcova B, Novotny J, Panczak A, Pesek P, Scheinost O, Springer D, Stastna B, Stranecky V, Subrt I, Tavandzis S, Tureckova E, Vesela K, Vlckova Z, Vocka M, Wappenschmidt B, Zima T, Kleibl Z, Kleiblova P. Zemankova P, et al. Among authors: curtisova v. Breast. 2024 Mar 25;75:103721. doi: 10.1016/j.breast.2024.103721. Online ahead of print. Breast. 2024. PMID: 38554551 Free PMC article.
The Gen-Equip Project: evaluation and impact of genetics e-learning resources for primary care in six European languages.
Jackson L, O'Connor A, Paneque M, Curtisova V, Lunt PW, Pourova RK, Macek M Jr, Stefansdottir V, Turchetti D, Campos M, Henneman L, Godino L, Skirton H, Cornel MC. Jackson L, et al. Among authors: curtisova v. Genet Med. 2019 Mar;21(3):718-726. doi: 10.1038/s41436-018-0132-3. Epub 2018 Jul 27. Genet Med. 2019. PMID: 30050101 Free PMC article.
19 results