BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

317 related articles for article (PubMed ID: 36732629)

  • 21. Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of Disease.
    Jolly A; Bayram Y; Turan S; Aycan Z; Tos T; Abali ZY; Hacihamdioglu B; Coban Akdemir ZH; Hijazi H; Bas S; Atay Z; Guran T; Abali S; Bas F; Darendeliler F; Colombo R; Barakat TS; Rinne T; White JJ; Yesil G; Gezdirici A; Gulec EY; Karaca E; Pehlivan D; Jhangiani SN; Muzny DM; Poyrazoglu S; Bereket A; Gibbs RA; Posey JE; Lupski JR
    J Clin Endocrinol Metab; 2019 Aug; 104(8):3049-3067. PubMed ID: 31042289
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Causal and Candidate Gene Variants in a Large Cohort of Women With Primary Ovarian Insufficiency.
    Gorsi B; Hernandez E; Moore MB; Moriwaki M; Chow CY; Coelho E; Taylor E; Lu C; Walker A; Touraine P; Nelson LM; Cooper AR; Mardis ER; Rajkovic A; Yandell M; Welt CK
    J Clin Endocrinol Metab; 2022 Feb; 107(3):685-714. PubMed ID: 34718612
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Selected Genetic Factors Associated with Primary Ovarian Insufficiency.
    Chen M; Jiang H; Zhang C
    Int J Mol Sci; 2023 Feb; 24(5):. PubMed ID: 36901862
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Improving diagnostic precision in primary ovarian insufficiency using comprehensive genetic and autoantibody testing.
    Vogt EC; Bratland E; Berland S; Berentsen R; Lund A; Björnsdottir S; Husebye E; Øksnes M
    Hum Reprod; 2024 Jan; 39(1):177-189. PubMed ID: 37953503
    [TBL] [Abstract][Full Text] [Related]  

  • 25. TP63-truncating variants cause isolated premature ovarian insufficiency.
    Tucker EJ; Jaillard S; Grover SR; van den Bergen J; Robevska G; Bell KM; Sadedin S; Hanna C; Dulon J; Touraine P; Sinclair AH
    Hum Mutat; 2019 Jul; 40(7):886-892. PubMed ID: 30924587
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Identification of novel biallelic variants in BMP15 in two siblings with premature ovarian insufficiency.
    Zhang T; Ma Q; Shen Q; Jiang C; Zou F; Shen Y; Wang Y
    J Assist Reprod Genet; 2022 Sep; 39(9):2125-2134. PubMed ID: 35861920
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Deleterious variants in RNF111 impair female fertility and induce premature ovarian insufficiency in humans and mice.
    Song C; Qin Y; Li Y; Yang B; Guo T; Ma W; Xu D; Xu K; Fu F; Jin L; Wu Y; Tang S; Chen X; Zhang F
    Sci China Life Sci; 2024 Jul; 67(7):1325-1337. PubMed ID: 38874713
    [TBL] [Abstract][Full Text] [Related]  

  • 28. New insights into the genetic basis of premature ovarian insufficiency: Novel causative variants and candidate genes revealed by genomic sequencing.
    Jaillard S; Bell K; Akloul L; Walton K; McElreavy K; Stocker WA; Beaumont M; Harrisson C; Jääskeläinen T; Palvimo JJ; Robevska G; Launay E; Satié AP; Listyasari N; Bendavid C; Sreenivasan R; Duros S; van den Bergen J; Henry C; Domin-Bernhard M; Cornevin L; Dejucq-Rainsford N; Belaud-Rotureau MA; Odent S; Ayers KL; Ravel C; Tucker EJ; Sinclair AH
    Maturitas; 2020 Nov; 141():9-19. PubMed ID: 33036707
    [TBL] [Abstract][Full Text] [Related]  

  • 29. No mutations in the PSMC3IP gene identified in a Swedish cohort of women with primary ovarian insufficiency.
    Norling A; Hirschberg AL; Karlsson L; Rodriguez-Wallberg KA; Iwarsson E; Wedell A; Barbaro M
    Sex Dev; 2014; 8(4):146-50. PubMed ID: 24481226
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Genetics of primary ovarian insufficiency: new developments and opportunities.
    Qin Y; Jiao X; Simpson JL; Chen ZJ
    Hum Reprod Update; 2015; 21(6):787-808. PubMed ID: 26243799
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mutations in the mitochondrial ribosomal protein MRPS22 lead to primary ovarian insufficiency.
    Chen A; Tiosano D; Guran T; Baris HN; Bayram Y; Mory A; Shapiro-Kulnane L; Hodges CA; Akdemir ZC; Turan S; Jhangiani SN; van den Akker F; Hoppel CL; Salz HK; Lupski JR; Buchner DA
    Hum Mol Genet; 2018 Jun; 27(11):1913-1926. PubMed ID: 29566152
    [TBL] [Abstract][Full Text] [Related]  

  • 32. ZSWIM7 Is Associated With Human Female Meiosis and Familial Primary Ovarian Insufficiency.
    McGlacken-Byrne SM; Le Quesne Stabej P; Del Valle I; Ocaka L; Gagunashvili A; Crespo B; Moreno N; James C; Bacchelli C; Dattani MT; Williams HJ; Kelberman D; Achermann JC; Conway GS
    J Clin Endocrinol Metab; 2022 Jan; 107(1):e254-e263. PubMed ID: 34402903
    [TBL] [Abstract][Full Text] [Related]  

  • 33. STAG3 truncating variant as the cause of primary ovarian insufficiency.
    Le Quesne Stabej P; Williams HJ; James C; Tekman M; Stanescu HC; Kleta R; Ocaka L; Lescai F; Storr HL; Bitner-Glindzicz M; Bacchelli C; Conway GS;
    Eur J Hum Genet; 2016 Jan; 24(1):135-8. PubMed ID: 26059840
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Premature ovarian insufficiency: clinical orientations for genetic testing and genetic counseling.
    Barros F; Carvalho F; Barros A; Dória S
    Porto Biomed J; 2020; 5(3):e62. PubMed ID: 33299945
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Novel variants in women with premature ovarian function decline identified via whole-exome sequencing.
    Tang R; Yu Q
    J Assist Reprod Genet; 2020 Oct; 37(10):2487-2502. PubMed ID: 32789750
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A novel heterozygous splice-altering mutation in HFM1 may be a cause of premature ovarian insufficiency.
    Zhe J; Chen S; Chen X; Liu Y; Li Y; Zhou X; Zhang J
    J Ovarian Res; 2019 Jul; 12(1):61. PubMed ID: 31279343
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency.
    Turkyilmaz A; Alavanda C; Ates EA; Geckinli BB; Polat H; Gokcu M; Karakaya T; Cebi AH; Soylemez MA; Guney Aİ; Ata P; Arman A
    J Assist Reprod Genet; 2022 Mar; 39(3):695-710. PubMed ID: 35066699
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Two rare loss-of-function variants in the STAG3 gene leading to primary ovarian insufficiency.
    França MM; Nishi MY; Funari MFA; Lerario AM; Baracat EC; Hayashida SAY; Maciel GAR; Jorge AAL; Mendonca BB
    Eur J Med Genet; 2019 Mar; 62(3):186-189. PubMed ID: 30006057
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A homozygous NOBOX truncating variant causes defective transcriptional activation and leads to primary ovarian insufficiency.
    Li L; Wang B; Zhang W; Chen B; Luo M; Wang J; Wang X; Cao Y; Kee K
    Hum Reprod; 2017 Jan; 32(1):248-255. PubMed ID: 27836978
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Pathogenic variants of meiotic double strand break (DSB) formation genes PRDM9 and ANKRD31 in premature ovarian insufficiency.
    Wang Y; Guo T; Ke H; Zhang Q; Li S; Luo W; Qin Y
    Genet Med; 2021 Dec; 23(12):2309-2315. PubMed ID: 34257419
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.