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

Year Number of Results
1962 1
1964 1
1965 1
1966 1
1967 1
1972 3
1973 1
1975 1
1976 1
1977 2
1978 5
1981 1
1983 3
1985 2
1988 1
1993 1
1997 1
1998 1
1999 1
2000 2
2001 2
2008 1
2010 2
2011 2
2012 5
2013 6
2014 4
2015 5
2016 9
2017 5
2018 2
2019 4
2020 2
2021 6
2022 9
2023 15
2024 13
2025 12

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121 results

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Page 1
Panel-Based Exome Sequencing for Neuromuscular Disorders as a Diagnostic Service.
Westra D, Schouten MI, Stunnenberg BC, Kusters B, Saris CGJ, Erasmus CE, van Engelen BG, Bulk S, Verschuuren-Bemelmans CC, Gerkes EH, de Geus C, van der Zwaag PA, Chan S, Chung B, Barge-Schaapveld DQCM, Kriek M, Sznajer Y, van Spaendonck-Zwarts K, van der Kooi AJ, Krause A, Schönewolf-Greulich B, de Die-Smulders C, Sallevelt SCEH, Krapels IPC, Rasmussen M, Maystadt I, Kievit AJA, Witting N, Pennings M, Meijer R, Gillissen C, Kamsteeg EJ, Voermans NC. Westra D, et al. J Neuromuscul Dis. 2019;6(2):241-258. doi: 10.3233/JND-180376. J Neuromuscul Dis. 2019. PMID: 31127727 Free article.
Autosomal recessive limb-girdle and Miyoshi muscular dystrophies in the Netherlands: The clinical and molecular spectrum of 244 patients.
Ten Dam L, Frankhuizen WS, Linssen WHJP, Straathof CS, Niks EH, Faber K, Fock A, Kuks JB, Brusse E, de Coo R, Voermans N, Verrips A, Hoogendijk JE, van der Pol L, Westra D, de Visser M, van der Kooi AJ, Ginjaar I. Ten Dam L, et al. Among authors: westra d. Clin Genet. 2019 Aug;96(2):126-133. doi: 10.1111/cge.13544. Epub 2019 May 6. Clin Genet. 2019. PMID: 30919934
Escaping our echo chambers.
Westra D, Hearld LR, Rathert C. Westra D, et al. Health Care Manage Rev. 2024 Jan-Mar 01;49(1):1. doi: 10.1097/HMR.0000000000000393. Health Care Manage Rev. 2024. PMID: 38019458 No abstract available.
Clinical syndromes linked to biallelic germline variants in MCM8 and MCM9.
Helderman NC, Yang T, Palles C, Terlouw D, Mei H, Vorderman RHP, Cats D, Díaz-Gay M, Jongmans MCJ, Ramdien A, van de Beek I, Eleveld TF, Green A, Hes FJ, van den Heuvel-Eibrink MM, Van Der Kelen A, Kliesch S, Kuiper RP, Lakeman IMM, Lashley LEELO, Looijenga LHJ, Oud MS, Steingröver J, Tenenbaum-Rakover Y, Tops CM, Tüttelmann F, de Voer RM, Westra D, Wyrwoll MJ, Golubicki M, Antelo M, Bonjoch L, Terradas M, Valle L, Alexandrov LB, Morreau H, van Wezel T, Castellví-Bel S, Goldberg Y, Nielsen M. Helderman NC, et al. Among authors: westra d. HGG Adv. 2025 Oct 9;6(4):100480. doi: 10.1016/j.xhgg.2025.100480. Epub 2025 Jul 18. HGG Adv. 2025. PMID: 40684266 Free PMC article.
Prenatal cell-free DNA testing of women with pregnancy-associated cancer: a retrospective cross-sectional study.
Heesterbeek CJ, Tjan-Heijnen VCG, Heimovaara JH, Lenaerts L, Lok C, Vriens IJH, Van Opstal D, Boon EMJ, Sie D, de Die-Smulders CEM, Amant F, Macville MVE; Dutch NIPT Consortium. Heesterbeek CJ, et al. Lancet Reg Health Eur. 2024 Aug 7;45:101024. doi: 10.1016/j.lanepe.2024.101024. eCollection 2024 Oct. Lancet Reg Health Eur. 2024. PMID: 39220433 Free PMC article.
Newborn Screening by DNA-First: Systematic Evaluation of the Eligibility of Inherited Metabolic Disorders Based on Treatability.
Veldman A, Sikkema-Raddatz B, Derks TGJ, van Karnebeek CDM, Kiewiet MBG, Mulder MF, Nelen MR, Rubio-Gozalbo ME, Sinke RJ, de Sain-van der Velden MG, Visser G, de Vries MC, Westra D, Williams M, Wevers RA, Heiner-Fokkema MR, van Spronsen FJ. Veldman A, et al. Among authors: westra d. Int J Neonatal Screen. 2024 Dec 28;11(1):1. doi: 10.3390/ijns11010001. Int J Neonatal Screen. 2024. PMID: 39846587 Free PMC article.
Clinical Outcome and Risk Factors for Progression of Prenatally Diagnosed Fetal Ventriculomegaly: A Retrospective Multicenter Study.
Moens A, Albersnagel Z, Veenhof MB, Adama van Scheltema PN, Sikkel E, Hoffer MJV, Faas BHW, Westra D, Feenstra I, Bijlsma EK, Santen GWE, Erasmus CE, Peeters-Scholte CMPCD. Moens A, et al. Among authors: westra d. Prenat Diagn. 2025 Aug;45(9):1089-1099. doi: 10.1002/pd.6816. Epub 2025 May 19. Prenat Diagn. 2025. PMID: 40389808 Free PMC article.
121 results