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Year Number of Results
1995 1
1996 1
1998 2
2000 1
2001 1
2002 1
2003 1
2004 4
2005 1
2006 4
2007 1
2008 4
2009 3
2010 1
2011 2
2012 3
2013 4
2015 2
2016 6
2017 3
2018 3
2019 4
2020 1
2021 3
2022 10
2023 4
2024 3
2025 0

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66 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.
Endemic parkinsonism: clusters, biology and clinical features.
Menšíková K, Steele JC, Rosales R, Colosimo C, Spencer P, Lannuzel A, Ugawa Y, Sasaki R, Giménez-Roldán S, Matej R, Tuckova L, Hrabos D, Kolarikova K, Vodicka R, Vrtel R, Strnad M, Hlustik P, Otruba P, Prochazka M, Bares M, Boluda S, Buee L, Ransmayr G, Kaňovský P. Menšíková K, et al. Among authors: vrtel r. Nat Rev Neurol. 2023 Oct;19(10):599-616. doi: 10.1038/s41582-023-00866-3. Epub 2023 Sep 8. Nat Rev Neurol. 2023. PMID: 37684518 Review.
Lewy body disease or diseases with Lewy bodies?
Menšíková K, Matěj R, Colosimo C, Rosales R, Tučková L, Ehrmann J, Hraboš D, Kolaříková K, Vodička R, Vrtěl R, Procházka M, Nevrlý M, Kaiserová M, Kurčová S, Otruba P, Kaňovský P. Menšíková K, et al. Among authors: vrtel r. NPJ Parkinsons Dis. 2022 Jan 10;8(1):3. doi: 10.1038/s41531-021-00273-9. NPJ Parkinsons Dis. 2022. PMID: 35013341 Free PMC article. Review.
Ovarian tumors and genetic predisposition.
Štellmachová Júlia, Vrtěl Petr, Vrtěl Radek, Janíková Mária, Kolaříková Kristýna, Procházka Martin, Vodička Radek. Štellmachová Júlia, et al. Among authors: vrtel radek. Ceska Gynekol. 2022;87(3):211-216. doi: 10.48095/cccg2022211. Ceska Gynekol. 2022. PMID: 35896402 English.
Fetal heart rhabdomyomatosis: a single-center experience.
Pavlicek J, Klaskova E, Kapralova S, Prochazka M, Vrtel R, Gruszka T, Kacerovsky M. Pavlicek J, et al. Among authors: vrtel r. J Matern Fetal Neonatal Med. 2021 Mar;34(5):701-707. doi: 10.1080/14767058.2019.1613365. Epub 2019 May 15. J Matern Fetal Neonatal Med. 2021. PMID: 31032681 Free article.
STAT6 - polymorphisms, haplotypes and epistasis in relation to atopy and asthma.
Godava M, Vrtel R, Vodicka R. Godava M, et al. Among authors: vrtel r. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2013 Jun;157(2):172-80. doi: 10.5507/bp.2013.043. Epub 2013 Jun 6. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2013. PMID: 23752766 Free article. Review.
Reply to: Questioning the cycad theory of Kii ALS-PDC causation.
Menšíková K, Rosales R, Colosimo C, Spencer P, Lannuzel A, Ugawa Y, Sasaki R, Giménez-Roldán S, Matej R, Tuckova L, Hrabos D, Kolarikova K, Vodicka R, Vrtel R, Strnad M, Hlustik P, Otruba P, Prochazka M, Bares M, Boluda S, Buee L, Ransmayr G, Kaňovský P. Menšíková K, et al. Among authors: vrtel r. Nat Rev Neurol. 2024 Mar;20(3):195-196. doi: 10.1038/s41582-024-00938-y. Nat Rev Neurol. 2024. PMID: 38336911 No abstract available.
Clinical-genetic analysis of selected genes involved in the development of the human skeleton in 128 Czech patients with suspected congenital skeletal abnormalities.
Spurná Z, Čapková P, Punová L, DuchoslavovÁ J, Aleksijevic D, Venháčová P, Srovnal J, Štellmachová J, Curtisová V, Bitnerová V, Petřková J, Kolaříková K, Janíková M, Kratochvílová R, Vrtěl P, Vodička R, Vrtěl R, Zapletalová J. Spurná Z, et al. Among authors: vrtel r. Gene. 2024 Jan 20;892:147881. doi: 10.1016/j.gene.2023.147881. Epub 2023 Oct 6. Gene. 2024. PMID: 37806643 Free article.
66 results