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

Year Number of Results
1952 2
1953 1
1954 1
1956 1
1957 1
1966 1
1981 1
1982 2
1983 2
1985 1
1986 1
1987 2
1988 1
1989 2
1990 3
1991 2
1992 1
1993 3
1994 1
1995 1
1997 1
1998 1
2000 2
2001 1
2002 3
2003 4
2004 3
2005 5
2006 7
2007 2
2008 4
2009 6
2010 3
2011 4
2012 6
2013 5
2014 7
2015 3
2016 7
2017 5
2018 5
2019 3
2020 2
2021 5
2022 9
2023 3
2024 1

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127 results

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Page 1
Heterogeneity of human WT1 gene.
Bielińska E, Matiakowska K, Haus O. Bielińska E, et al. Among authors: haus o. Postepy Hig Med Dosw (Online). 2017 Jul 11;71(0):595-601. doi: 10.5604/01.3001.0010.3840. Postepy Hig Med Dosw (Online). 2017. PMID: 28791954 Review.
Genetical background of intelligence.
Junkiert-Czarnecka A, Haus O. Junkiert-Czarnecka A, et al. Among authors: haus o. Postepy Hig Med Dosw (Online). 2016 Jun 13;70(0):590-8. doi: 10.5604/17322693.1204943. Postepy Hig Med Dosw (Online). 2016. PMID: 27333929 Free article. Review.
[Hereditary prostate cancer].
Heise M, Haus O. Heise M, et al. Among authors: haus o. Postepy Hig Med Dosw (Online). 2014 May 27;68:653-65. doi: 10.5604/17322693.1104682. Postepy Hig Med Dosw (Online). 2014. PMID: 24864115 Free article. Review. Polish.
Gitelman syndrome with normocalciuria - a case report.
Flisiński M, Skalska E, Mączyńska B, Butt-Hussaim N, Sobczyńska-Tomaszewska A, Haus O, Manitius J. Flisiński M, et al. Among authors: haus o. BMC Nephrol. 2022 May 4;23(1):170. doi: 10.1186/s12882-022-02782-y. BMC Nephrol. 2022. PMID: 35509038 Free PMC article.
Association of unbalanced translocation der(1;7) with germline GATA2 mutations.
Kozyra EJ, Göhring G, Hickstein DD, Calvo KR, DiNardo CD, Dworzak M, de Haas V, Starý J, Hasle H, Shimamura A, Fleming MD, Inaba H, Lewis S, Hsu AP, Holland SM, Arnold DE, Mecucci C, Keel SB, Bertuch AA, Tawana K, Barzilai S, Hirabayashi S, Onozawa M, Lei S, Alaiz H, Andrikovics H, Betts D, Beverloo BH, Buechner J, Čermák M, Cervera J, Haus O, Jahnukainen K, Manola KN, Nebral K, Pasquali F, Tchinda J, Turkiewicz D, Van Roy N, Zemanova Z, Pastor VB, Strahm B, Noellke P, Niemeyer CM, Schlegelberger B, Yoshimi A, Wlodarski MW. Kozyra EJ, et al. Among authors: haus o. Blood. 2021 Dec 9;138(23):2441-2445. doi: 10.1182/blood.2021012781. Blood. 2021. PMID: 34469508 Free PMC article. No abstract available.
The impact of oophorectomy on survival from breast cancer in patients with CHEK2 mutations.
Tomiczek-Szwiec J, Szwiec M, Falco M, Cybulski C, Wokolorczyk D, Jakubowska A, Gronwald J, Stawicka M, Godlewski D, Kilar E, Marczyk E, Siołek M, Wiśniowski R, Haus O, Sibilski R, Bodnar L, Sun P, Narod SA, Lubinski J, Huzarski T; Polish Breast Cancer Consortium. Tomiczek-Szwiec J, et al. Among authors: haus o. Br J Cancer. 2022 Jul;127(1):84-91. doi: 10.1038/s41416-022-01770-1. Epub 2022 Mar 7. Br J Cancer. 2022. PMID: 35256754 Free PMC article.
Prenatal identification of partial 3q duplication syndrome.
Pasińska M, Adamczak R, Repczyńska A, Łazarczyk E, Iskra B, Runge AK, Haus O. Pasińska M, et al. Among authors: haus o. BMC Med Genomics. 2019 Jun 13;12(1):85. doi: 10.1186/s12920-019-0547-y. BMC Med Genomics. 2019. PMID: 31196198 Free PMC article.
MicroRNA gene methylation landscape in pediatric B-cell precursor acute lymphoblastic leukemia.
Chaber R, Gurgul A, Tabarkiewicz J, Wróbel G, Szmatoła T, Jasielczuk I, Haus O, Lejman M, Rybka B, Ryczan-Krawczyk R, Jaśkowiec A, Paszek S, Potocka N, Arthur CJ, Bal W, Łach K, Kowal A, Zawlik I, Latos-Grażyńska E. Chaber R, et al. Among authors: haus o. Adv Clin Exp Med. 2022 Mar;31(3):293-305. doi: 10.17219/acem/144170. Adv Clin Exp Med. 2022. PMID: 35092653 Free article.
127 results