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

Year Number of Results
1999 1
2000 1
2001 1
2002 3
2003 3
2004 1
2005 2
2006 1
2008 1
2009 3
2010 5
2011 8
2012 5
2013 3
2014 10
2015 26
2016 27
2017 9
2018 10
2019 16
2020 16
2021 13
2022 14
2023 17
2024 7

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179 results

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Page 1
TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands.
van der Meij KRM, Sistermans EA, Macville MVE, Stevens SJC, Bax CJ, Bekker MN, Bilardo CM, Boon EMJ, Boter M, Diderich KEM, de Die-Smulders CEM, Duin LK, Faas BHW, Feenstra I, Haak MC, Hoffer MJV, den Hollander NS, Hollink IHIM, Jehee FS, Knapen MFCM, Kooper AJA, van Langen IM, Lichtenbelt KD, Linskens IH, van Maarle MC, Oepkes D, Pieters MJ, Schuring-Blom GH, Sikkel E, Sikkema-Raddatz B, Smeets DFCM, Srebniak MI, Suijkerbuijk RF, Tan-Sindhunata GM, van der Ven AJEM, van Zelderen-Bhola SL, Henneman L, Galjaard RH, Van Opstal D, Weiss MM; Dutch NIPT Consortium. van der Meij KRM, et al. Among authors: haak mc. Am J Hum Genet. 2019 Dec 5;105(6):1091-1101. doi: 10.1016/j.ajhg.2019.10.005. Epub 2019 Nov 7. Am J Hum Genet. 2019. PMID: 31708118 Free PMC article.
Response to Thibodeau and Langlois.
van Nisselrooij AEL, Aten E, Santen GWE, Haak MC. van Nisselrooij AEL, et al. Among authors: haak mc. Genet Med. 2021 Jan;23(1):244-245. doi: 10.1038/s41436-020-00965-2. Epub 2020 Sep 27. Genet Med. 2021. PMID: 32980862 Free article. No abstract available.
Hematological disorders at birth in complicated monochorionic twins.
Verbeek L, Slaghekke F, Sueters M, Middeldorp JM, Klumper FJ, Haak MC, Oepkes D, Lopriore E. Verbeek L, et al. Among authors: haak mc. Expert Rev Hematol. 2017 Jun;10(6):525-532. doi: 10.1080/17474086.2017.1324290. Epub 2017 May 10. Expert Rev Hematol. 2017. PMID: 28460542 Review.
Discovering a new part of the phenotypic spectrum of Coffin-Siris syndrome in a fetal cohort.
van der Sluijs PJ, Joosten M, Alby C, Attié-Bitach T, Gilmore K, Dubourg C, Fradin M, Wang T, Kurtz-Nelson EC, Ahlers KP, Arts P, Barnett CP, Ashfaq M, Baban A, van den Born M, Borrie S, Busa T, Byrne A, Carriero M, Cesario C, Chong K, Cueto-González AM, Dempsey JC, Diderich KEM, Doherty D, Farholt S, Gerkes EH, Gorokhova S, Govaerts LCP, Gregersen PA, Hickey SE, Lefebvre M, Mari F, Martinovic J, Northrup H, O'Leary M, Parbhoo K, Patrier S, Popp B, Santos-Simarro F, Stoltenburg C, Thauvin-Robinet C, Thompson E, Vulto-van Silfhout AT, Zahir FR, Scott HS, Earl RK, Eichler EE, Vora NL, Wilnai Y, Giordano JL, Wapner RJ, Rosenfeld JA, Haak MC, Santen GWE. van der Sluijs PJ, et al. Among authors: haak mc. Genet Med. 2022 Aug;24(8):1753-1760. doi: 10.1016/j.gim.2022.04.010. Epub 2022 May 18. Genet Med. 2022. PMID: 35579625 Free PMC article.
Atrioventricular septal defect: From embryonic development to long-term follow-up.
Calkoen EE, Hazekamp MG, Blom NA, Elders BB, Gittenberger-de Groot AC, Haak MC, Bartelings MM, Roest AA, Jongbloed MR. Calkoen EE, et al. Among authors: haak mc. Int J Cardiol. 2016 Jan 1;202:784-95. doi: 10.1016/j.ijcard.2015.09.081. Epub 2015 Sep 26. Int J Cardiol. 2016. PMID: 26476030 Review.
TwinLIFE: The Twin Longitudinal Investigation of FEtal Discordance.
Groene SG, Todtenhaupt P, van Zwet EW, van Pel M, Berkhout RJM, Haak MC, Roest AAW, Lopriore E, van Klink JMM, Heijmans BT. Groene SG, et al. Among authors: haak mc. Twin Res Hum Genet. 2019 Dec;22(6):617-622. doi: 10.1017/thg.2019.38. Epub 2019 Jul 25. Twin Res Hum Genet. 2019. PMID: 31342890
179 results