These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

121 related articles for article (PubMed ID: 35820085)

  • 1. Germline
    Rashed WM; Marcotte EL; Spector LG
    JCO Precis Oncol; 2022 Jul; 6():e2100505. PubMed ID: 35820085
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Parent-of-origin-specific signatures of de novo mutations.
    Goldmann JM; Wong WS; Pinelli M; Farrah T; Bodian D; Stittrich AB; Glusman G; Vissers LE; Hoischen A; Roach JC; Vockley JG; Veltman JA; Solomon BD; Gilissen C; Niederhuber JE
    Nat Genet; 2016 Aug; 48(8):935-9. PubMed ID: 27322544
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Variation in genome-wide mutation rates within and between human families.
    Conrad DF; Keebler JE; DePristo MA; Lindsay SJ; Zhang Y; Casals F; Idaghdour Y; Hartl CL; Torroja C; Garimella KV; Zilversmit M; Cartwright R; Rouleau GA; Daly M; Stone EA; Hurles ME; Awadalla P;
    Nat Genet; 2011 Jun; 43(7):712-4. PubMed ID: 21666693
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair.
    Sherwood K; Ward JC; Soriano I; Martin L; Campbell A; Rahbari R; Kafetzopoulos I; Sproul D; Green A; Sampson JR; Donaldson A; Ong KR; Heinimann K; Nielsen M; Thomas H; Latchford A; Palles C; Tomlinson I
    Nat Commun; 2023 Jun; 14(1):3636. PubMed ID: 37336879
    [TBL] [Abstract][Full Text] [Related]  

  • 5. De Novo Mutations Reflect Development and Aging of the Human Germline.
    Goldmann JM; Veltman JA; Gilissen C
    Trends Genet; 2019 Nov; 35(11):828-839. PubMed ID: 31610893
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Family-based germline sequencing in children with cancer.
    Kuhlen M; Taeubner J; Brozou T; Wieczorek D; Siebert R; Borkhardt A
    Oncogene; 2019 Feb; 38(9):1367-1380. PubMed ID: 30305723
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Meta-analysis of 46,000 germline de novo mutations linked to human inherited disease.
    Lopes-Marques M; Mort M; Carneiro J; Azevedo A; Amaro AP; Cooper DN; Azevedo L
    Hum Genomics; 2024 Feb; 18(1):20. PubMed ID: 38395944
    [TBL] [Abstract][Full Text] [Related]  

  • 8. mirTrios: an integrated pipeline for detection of de novo and rare inherited mutations from trios-based next-generation sequencing.
    Li J; Jiang Y; Wang T; Chen H; Xie Q; Shao Q; Ran X; Xia K; Sun ZS; Wu J
    J Med Genet; 2015 Apr; 52(4):275-81. PubMed ID: 25596308
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Spontaneous de novo germline mutations in humans and mice: rates, spectra, causes and consequences.
    Ohno M
    Genes Genet Syst; 2019 Apr; 94(1):13-22. PubMed ID: 30381610
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Decoding germline de novo point mutations.
    Goriely A
    Nat Genet; 2016 Jul; 48(8):823-4. PubMed ID: 27463396
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification and characterisation of de novo germline structural variants in two commercial pig lines using trio-based whole genome sequencing.
    Steensma MJ; Lee YL; Bouwman AC; Pita Barros C; Derks MFL; Bink MCAM; Harlizius B; Huisman AE; Crooijmans RPMA; Groenen MAM; Mulder HA; Rochus CM
    BMC Genomics; 2023 Apr; 24(1):208. PubMed ID: 37072725
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Point mutations as a source of de novo genetic disease.
    de Ligt J; Veltman JA; Vissers LE
    Curr Opin Genet Dev; 2013 Jun; 23(3):257-63. PubMed ID: 23453690
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Confirming the contribution and genetic spectrum of de novo mutation in infantile spasms: Evidence from a Chinese cohort.
    Liu L; Liu F; Wang Q; Xie H; Li Z; Lu Q; Wang Y; Zhang M; Zhang Y; Picker J; Cui X; Zou L; Chen X
    Mol Genet Genomic Med; 2021 Jun; 9(6):e1689. PubMed ID: 33951346
    [TBL] [Abstract][Full Text] [Related]  

  • 14. New observations on maternal age effect on germline de novo mutations.
    Wong WS; Solomon BD; Bodian DL; Kothiyal P; Eley G; Huddleston KC; Baker R; Thach DC; Iyer RK; Vockley JG; Niederhuber JE
    Nat Commun; 2016 Jan; 7():10486. PubMed ID: 26781218
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Extensive variation in germline de novo mutations in
    Lin Y; Darolti I; van der Bijl W; Morris J; Mank JE
    Genome Res; 2023 Aug; 33(8):1317-1324. PubMed ID: 37442578
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Large, three-generation human families reveal post-zygotic mosaicism and variability in germline mutation accumulation.
    Sasani TA; Pedersen BS; Gao Z; Baird L; Przeworski M; Jorde LB; Quinlan AR
    Elife; 2019 Sep; 8():. PubMed ID: 31549960
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Transgenerational effects of paternal exposures: the role of germline de novo mutations.
    Dehghanbanadaki H; Jimbo M; Fendereski K; Kunisaki J; Horns JJ; Ramsay JM; Gross KX; Pastuszak AW; Hotaling JM
    Andrology; 2024 Feb; ():. PubMed ID: 38396220
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of de novo germline mutations and causal genes for sporadic diseases using trio-based whole-exome/genome sequencing.
    Jin ZB; Li Z; Liu Z; Jiang Y; Cai XB; Wu J
    Biol Rev Camb Philos Soc; 2018 May; 93(2):1014-1031. PubMed ID: 29154454
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A framework for the detection of de novo mutations in family-based sequencing data.
    Francioli LC; Cretu-Stancu M; Garimella KV; Fromer M; Kloosterman WP; ; Samocha KE; Neale BM; Daly MJ; Banks E; DePristo MA; de Bakker PI
    Eur J Hum Genet; 2017 Feb; 25(2):227-233. PubMed ID: 27876817
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genome-wide characteristics of
    Yuen RK; Merico D; Cao H; Pellecchia G; Alipanahi B; Thiruvahindrapuram B; Tong X; Sun Y; Cao D; Zhang T; Wu X; Jin X; Zhou Z; Liu X; Nalpathamkalam T; Walker S; Howe JL; Wang Z; MacDonald JR; Chan A; D'Abate L; Deneault E; Siu MT; Tammimies K; Uddin M; Zarrei M; Wang M; Li Y; Wang J; Wang J; Yang H; Bookman M; Bingham J; Gross SS; Loy D; Pletcher M; Marshall CR; Anagnostou E; Zwaigenbaum L; Weksberg R; Fernandez BA; Roberts W; Szatmari P; Glazer D; Frey BJ; Ring RH; Xu X; Scherer SW
    NPJ Genom Med; 2016 Aug; 1():160271-1602710. PubMed ID: 27525107
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.