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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2019 | 2 |
2021 | 2 |
2023 | 2 |
2024 | 0 |
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6 results
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Page 1
Further delineation of the NTHL1 associated syndrome: A report from the French Oncogenetic Consortium.
Clin Genet. 2021 May;99(5):662-672. doi: 10.1111/cge.13925. Epub 2021 Feb 12.
Clin Genet. 2021.
PMID: 33454955
Evaluation of the association of heterozygous germline variants in NTHL1 with breast cancer predisposition: an international multi-center study of 47,180 subjects.
Li N, Zethoven M, McInerny S, Devereux L, Huang YK, Thio N, Cheasley D, Gutiérrez-Enríquez S, Moles-Fernández A, Diez O, Nguyen-Dumont T, Southey MC, Hopper JL, Simard J, Dumont M, Soucy P, Meindl A, Schmutzler R, Schmidt MK, Adank MA, Andrulis IL, Hahnen E, Engel C, Lesueur F, Girard E, Neuhausen SL, Ziv E, Allen J, Easton DF, Scott RJ, Gorringe KL, James PA, Campbell IG.
Li N, et al.
NPJ Breast Cancer. 2021 May 12;7(1):52. doi: 10.1038/s41523-021-00255-3.
NPJ Breast Cancer. 2021.
PMID: 33980861
Free PMC article.
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Lynch syndrome: influence of additional susceptibility variants on cancer risk.
Vibert R, Hasnaoui J, Perrier A, Lefebvre A, Colas C, Dhooge M, Basset N, Chansavang A, Desseignes C, Duval A, Farelly S, Hamzaoui N, Laurent-Puig P, Metras J, Moliere D, Muleris M, Netter J, Touat M, Bielle F, Labreche K, Nicolle R, Perkins G, Warcoin M, Coulet F, Benusiglio PR.
Vibert R, et al.
Eur J Hum Genet. 2023 Sep;31(9):1078-1082. doi: 10.1038/s41431-023-01367-z. Epub 2023 Apr 24.
Eur J Hum Genet. 2023.
PMID: 37088804
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Genomic analyses of germline and somatic variation in high-grade serous ovarian cancer.
Adamson AW, Ding YC, Steele L, Leong LA, Morgan R, Wakabayashi MT, Han ES, Dellinger TH, Lin PS, Hakim AA, Wilczynski S, Warden CD, Tao S, Bedell V, Cristea MC, Neuhausen SL.
Adamson AW, et al.
J Ovarian Res. 2023 Jul 17;16(1):141. doi: 10.1186/s13048-023-01234-x.
J Ovarian Res. 2023.
PMID: 37460928
Free PMC article.
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Contribution of New Adenomatous Polyposis Predisposition Genes in an Unexplained Attenuated Spanish Cohort by Multigene Panel Testing.
Lorca V, Rueda D, Martín-Morales L, Fernández-Aceñero MJ, Grolleman J, Poves C, Llovet P, Tapial S, García-Barberán V, Sanz J, Pérez-Segura P, de Voer RM, Díaz-Rubio E, de la Hoya M, Caldés T, Garre P.
Lorca V, et al.
Sci Rep. 2019 Jul 8;9(1):9814. doi: 10.1038/s41598-019-46403-5.
Sci Rep. 2019.
PMID: 31285513
Free PMC article.
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NTHL1 biallelic mutations seldom cause colorectal cancer, serrated polyposis or a multi-tumor phenotype, in absence of colorectal adenomas.
Belhadj S, Quintana I, Mur P, Munoz-Torres PM, Alonso MH, Navarro M, Terradas M, Piñol V, Brunet J, Moreno V, Lázaro C, Capellá G, Valle L.
Belhadj S, et al.
Sci Rep. 2019 Jun 21;9(1):9020. doi: 10.1038/s41598-019-45281-1.
Sci Rep. 2019.
PMID: 31227763
Free PMC article.
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