BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

904 related articles for article (PubMed ID: 26826164)

  • 1. Whole exome sequencing in recurrent early pregnancy loss.
    Qiao Y; Wen J; Tang F; Martell S; Shomer N; Leung PC; Stephenson MD; Rajcan-Separovic E
    Mol Hum Reprod; 2016 May; 22(5):364-72. PubMed ID: 26826164
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Whole exome sequencing in unexplained recurrent miscarriage families identified novel pathogenic genetic causes of euploid miscarriage.
    Wang X; Shi W; Zhao S; Gong D; Li S; Hu C; Chen ZJ; Li Y; Yan J
    Hum Reprod; 2023 May; 38(5):1003-1018. PubMed ID: 36864708
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Next generation sequencing in recurrent pregnancy loss-approaches and outcomes.
    Rajcan-Separovic E
    Eur J Med Genet; 2020 Feb; 63(2):103644. PubMed ID: 30991114
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identifying the causes of recurrent pregnancy loss in consanguineous couples using whole exome sequencing on the products of miscarriage with no chromosomal abnormalities.
    Najafi K; Mehrjoo Z; Ardalani F; Ghaderi-Sohi S; Kariminejad A; Kariminejad R; Najmabadi H
    Sci Rep; 2021 Mar; 11(1):6952. PubMed ID: 33772059
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Potential genetic causes of miscarriage in euploid pregnancies: a systematic review.
    Colley E; Hamilton S; Smith P; Morgan NV; Coomarasamy A; Allen S
    Hum Reprod Update; 2019 Jul; 25(4):452-472. PubMed ID: 31150545
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic diagnosis in first or second trimester pregnancy loss using exome sequencing: a systematic review of human essential genes.
    Robbins SM; Thimm MA; Valle D; Jelin AC
    J Assist Reprod Genet; 2019 Aug; 36(8):1539-1548. PubMed ID: 31273585
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Recurrent pregnancy loss evaluation combined with 24-chromosome microarray of miscarriage tissue provides a probable or definite cause of pregnancy loss in over 90% of patients.
    Popescu F; Jaslow CR; Kutteh WH
    Hum Reprod; 2018 Apr; 33(4):579-587. PubMed ID: 29538673
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Discovery of Pathogenic Variants Associated with Idiopathic Recurrent Pregnancy Loss Using Whole-Exome Sequencing.
    Lee JY; Moon J; Hu HJ; Ryu CS; Ko EJ; Ahn EH; Kim YR; Kim JH; Kim NK
    Int J Mol Sci; 2024 May; 25(10):. PubMed ID: 38791485
    [TBL] [Abstract][Full Text] [Related]  

  • 9. No evidence for mutations in NLRP7, NLRP2 or KHDC3L in women with unexplained recurrent pregnancy loss or infertility.
    Aghajanova L; Mahadevan S; Altmäe S; Stavreus-Evers A; Regan L; Sebire N; Dixon P; Fisher RA; Van den Veyver IB
    Hum Reprod; 2015 Jan; 30(1):232-8. PubMed ID: 25376457
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
    Lord J; McMullan DJ; Eberhardt RY; Rinck G; Hamilton SJ; Quinlan-Jones E; Prigmore E; Keelagher R; Best SK; Carey GK; Mellis R; Robart S; Berry IR; Chandler KE; Cilliers D; Cresswell L; Edwards SL; Gardiner C; Henderson A; Holden ST; Homfray T; Lester T; Lewis RA; Newbury-Ecob R; Prescott K; Quarrell OW; Ramsden SC; Roberts E; Tapon D; Tooley MJ; Vasudevan PC; Weber AP; Wellesley DG; Westwood P; White H; Parker M; Williams D; Jenkins L; Scott RH; Kilby MD; Chitty LS; Hurles ME; Maher ER;
    Lancet; 2019 Feb; 393(10173):747-757. PubMed ID: 30712880
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Targeted whole exome sequencing and Drosophila modelling to unveil the molecular basis of primary ovarian insufficiency.
    Bestetti I; Barbieri C; Sironi A; Specchia V; Yatsenko SA; De Donno MD; Caslini C; Gentilini D; Crippa M; Larizza L; Marozzi A; Rajkovic A; Toniolo D; Bozzetti MP; Finelli P
    Hum Reprod; 2021 Oct; 36(11):2975-2991. PubMed ID: 34480478
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Simultaneous Detection of CNVs and SNVs Improves the Diagnostic Yield of Fetuses with Ultrasound Anomalies and Normal Karyotypes.
    Qi Q; Jiang Y; Zhou X; Meng H; Hao N; Chang J; Bai J; Wang C; Wang M; Guo J; Ouyang Y; Xu Z; Xiao M; Zhang VW; Liu J
    Genes (Basel); 2020 Nov; 11(12):. PubMed ID: 33255631
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic Variants Contributing to Early Recurrent Pregnancy Loss Etiology Identified by Sequencing Approaches.
    Quintero-Ronderos P; Laissue P
    Reprod Sci; 2020 Aug; 27(8):1541-1552. PubMed ID: 32430708
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of genetic alterations in couples and their products of conceptions from recurrent pregnancy loss in North Indian population.
    Srivastava P; Bamba C; Chopra S; Rohilla M; Chaudhry C; Kaur A; Panigrahi I; Mandal K
    Front Genet; 2023; 14():1155211. PubMed ID: 37260775
    [No Abstract]   [Full Text] [Related]  

  • 15. Systematic molecular analyses for 115 karyotypically normal men with isolated non-obstructive azoospermia.
    Muranishi Y; Kobori Y; Katoh-Fukui Y; Tamaoka S; Hattori A; Osaka A; Okada H; Nakabayashi K; Hata K; Kawai T; Ogata-Kawata H; Iwahata T; Saito K; Kon M; Shinohara N; Fukami M
    Hum Reprod; 2024 May; 39(5):1131-1140. PubMed ID: 38511217
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Exome sequencing reveals novel causes as well as new candidate genes for human globozoospermia.
    Oud MS; Okutman Ö; Hendricks LAJ; de Vries PF; Houston BJ; Vissers LELM; O'Bryan MK; Ramos L; Chemes HE; Viville S; Veltman JA
    Hum Reprod; 2020 Jan; 35(1):240-252. PubMed ID: 31985809
    [TBL] [Abstract][Full Text] [Related]  

  • 17. IL-10 gene promoter and intron polymorphisms and changes in IL-10 secretion in women with idiopathic recurrent miscarriage.
    Qaddourah RH; Magdoud K; Saldanha FL; Mahmood N; Mustafa FE; Mahjoub T; Almawi WY
    Hum Reprod; 2014 May; 29(5):1025-34. PubMed ID: 24626804
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study.
    Petrovski S; Aggarwal V; Giordano JL; Stosic M; Wou K; Bier L; Spiegel E; Brennan K; Stong N; Jobanputra V; Ren Z; Zhu X; Mebane C; Nahum O; Wang Q; Kamalakaran S; Malone C; Anyane-Yeboa K; Miller R; Levy B; Goldstein DB; Wapner RJ
    Lancet; 2019 Feb; 393(10173):758-767. PubMed ID: 30712878
    [TBL] [Abstract][Full Text] [Related]  

  • 19. NLRP7 variants in spontaneous abortions with multilocus imprinting disturbances from women with recurrent pregnancy loss.
    Sazhenova EA; Nikitina TV; Vasilyev SA; Tolmacheva EN; Vasilyeva OY; Markov AV; Yuryev SY; Skryabin NA; Zarubin AA; Kolesnikov NA; Stepanov VA; Lebedev IN
    J Assist Reprod Genet; 2021 Nov; 38(11):2893-2908. PubMed ID: 34554362
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome.
    Chen MJ; Wei SY; Yang WS; Wu TT; Li HY; Ho HN; Yang YS; Chen PL
    Hum Reprod; 2015 Jul; 30(7):1732-42. PubMed ID: 25924657
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 46.