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

Year Number of Results
2012 1
2013 1
2016 2
2017 1
2018 1
2020 1
2021 2
2022 6
2023 2
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13 results
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Page 1
Extra-cardiac diagnoses and postnatal outcomes of fetal tetralogy of fallot.
Sharma R, Niederhoffer KY, Caluseriu O, Cooke CL, Hornberger LK, He R, Eckersley L, Lin L, Rushfeldt M, McBrien A. Sharma R, et al. Among authors: niederhoffer ky. Prenat Diagn. 2022 Feb;42(2):260-266. doi: 10.1002/pd.6102. Epub 2022 Jan 27. Prenat Diagn. 2022. PMID: 35060156
ANKRD26-related thrombocytopenia and myeloid malignancies.
Noris P, Favier R, Alessi MC, Geddis AE, Kunishima S, Heller PG, Giordano P, Niederhoffer KY, Bussel JB, Podda GM, Vianelli N, Kersseboom R, Pecci A, Gnan C, Marconi C, Auvrignon A, Cohen W, Yu JC, Iguchi A, Miller Imahiyerobo A, Boehlen F, Ghalloussi D, De Rocco D, Magini P, Civaschi E, Biino G, Seri M, Savoia A, Balduini CL. Noris P, et al. Among authors: niederhoffer ky. Blood. 2013 Sep 12;122(11):1987-9. doi: 10.1182/blood-2013-04-499319. Blood. 2013. PMID: 24030261 Free article. No abstract available.
Detailed Clinical and Psychological Phenotype of the X-linked HNRNPH2-Related Neurodevelopmental Disorder.
Bain JM, Thornburg O, Pan C, Rome-Martin D, Boyle L, Fan X, Devinsky O, Frye R, Hamp S, Keator CG, LaMarca NM, Maddocks ABR, Madruga-Garrido M, Niederhoffer KY, Novara F, Peron A, Poole-Di Salvo E, Salazar R, Skinner SA, Soares G, Goldman S, Chung WK. Bain JM, et al. Among authors: niederhoffer ky. Neurol Genet. 2021 Jan 29;7(1):e551. doi: 10.1212/NXG.0000000000000551. eCollection 2021 Feb. Neurol Genet. 2021. PMID: 33728377 Free PMC article.
Diagnostic yield of clinical exome sequencing in adulthood in medical genetics clinics.
Mainali A, Athey T, Bahl S, Hung C, Caluseriu O, Chan A, Eaton A, Ghai SJ, Kannu P, MacPherson M, Niederhoffer KY, Siriwardena K, Mercimek-Andrews S. Mainali A, et al. Among authors: niederhoffer ky. Am J Med Genet A. 2023 Feb;191(2):510-517. doi: 10.1002/ajmg.a.63053. Epub 2022 Nov 19. Am J Med Genet A. 2023. PMID: 36401557 Review.
Beckwith-Wiedemann syndrome in sibs discordant for IC2 methylation.
Niederhoffer KY, Peñaherrera M, Pugash D, Rupps R, Arbour L, Tessier F, Choufani S, Zhao C, Manokhina I, Shuman C, Robinson WP, Weksberg R, Boerkoel CF. Niederhoffer KY, et al. Am J Med Genet A. 2012 Jul;158A(7):1662-9. doi: 10.1002/ajmg.a.35377. Epub 2012 May 21. Am J Med Genet A. 2012. PMID: 22615066
13 results