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

Year Number of Results
1988 1
2002 10
2003 11
2004 8
2005 3
2006 11
2007 14
2008 11
2009 14
2010 14
2011 7
2012 10
2013 18
2014 21
2015 18
2016 11
2017 13
2018 15
2019 15
2020 12
2021 14
2022 12
2023 9
2024 0

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245 results

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Page 1
National population-based estimates for major birth defects, 2010-2014.
Mai CT, Isenburg JL, Canfield MA, Meyer RE, Correa A, Alverson CJ, Lupo PJ, Riehle-Colarusso T, Cho SJ, Aggarwal D, Kirby RS; National Birth Defects Prevention Network. Mai CT, et al. Among authors: meyer re. Birth Defects Res. 2019 Nov 1;111(18):1420-1435. doi: 10.1002/bdr2.1589. Epub 2019 Oct 3. Birth Defects Res. 2019. PMID: 31580536 Free PMC article.
ADGRL1 haploinsufficiency causes a variable spectrum of neurodevelopmental disorders in humans and alters synaptic activity and behavior in a mouse model.
Vitobello A, Mazel B, Lelianova VG, Zangrandi A, Petitto E, Suckling J, Salpietro V, Meyer R, Elbracht M, Kurth I, Eggermann T, Benlaouer O, Lall G, Tonevitsky AG, Scott DA, Chan KM, Rosenfeld JA, Nambot S, Safraou H, Bruel AL, Denommé-Pichon AS, Tran Mau-Them F, Philippe C, Duffourd Y, Guo H, Petersen AK, Granger L, Crunk A, Bayat A, Striano P, Zara F, Scala M, Thomas Q, Delahaye A, de Sainte Agathe JM, Buratti J, Kozlov SV, Faivre L, Thauvin-Robinet C, Ushkaryov Y. Vitobello A, et al. Among authors: meyer r. Am J Hum Genet. 2022 Aug 4;109(8):1436-1457. doi: 10.1016/j.ajhg.2022.06.011. Epub 2022 Jul 30. Am J Hum Genet. 2022. PMID: 35907405 Free PMC article.
Germline C1GALT1C1 mutation causes a multisystem chaperonopathy.
Erger F, Aryal RP, Reusch B, Matsumoto Y, Meyer R, Zeng J, Knopp C, Noel M, Muerner L, Wenzel A, Kohl S, Tschernoster N, Rappl G, Rouvet I, Schröder-Braunstein J, Seibert FS, Thiele H, Häusler MG, Weber LT, Büttner-Herold M, Elbracht M, Cummings SF, Altmüller J, Habbig S, Cummings RD, Beck BB. Erger F, et al. Among authors: meyer r. Proc Natl Acad Sci U S A. 2023 May 30;120(22):e2211087120. doi: 10.1073/pnas.2211087120. Epub 2023 May 22. Proc Natl Acad Sci U S A. 2023. PMID: 37216524 Free PMC article.
Evolocumab in hyperlipidemia.
Meyer RJ. Meyer RJ. N Engl J Med. 2014 Aug 28;371(9):876. doi: 10.1056/NEJMc1408237. N Engl J Med. 2014. PMID: 25162897 No abstract available.
Response to Harcombe.
Desrosiers T, Siega-Riz AM, Mosley B, Meyer R. Desrosiers T, et al. Among authors: meyer r. Birth Defects Res. 2018 Jul 3;110(11):911-912. doi: 10.1002/bdr2.1333. Epub 2018 May 24. Birth Defects Res. 2018. PMID: 29797553 No abstract available.
Response to Camacho.
Desrosiers T, Siega-Riz AM, Mosley B, Meyer R. Desrosiers T, et al. Among authors: meyer r. Birth Defects Res. 2018 Jul 3;110(11):914-915. doi: 10.1002/bdr2.1338. Epub 2018 May 24. Birth Defects Res. 2018. PMID: 29797552 No abstract available.
Surveys and objectifying the subjective.
Meyer RE, Robertson SA. Meyer RE, et al. Vet Anaesth Analg. 2016 Jul;43(4):358-60. doi: 10.1111/vaa.12374. Epub 2016 Apr 1. Vet Anaesth Analg. 2016. PMID: 27038063 No abstract available.
Konstituierende Versammlung der Jungen Humangenetik.
Krey I, Meyer R. Krey I, et al. Among authors: meyer r. Med Genet. 2022 Aug 12;34(2):183. doi: 10.1515/medgen-2022-2129. eCollection 2022 Jun. Med Genet. 2022. PMID: 38835906 Free PMC article. German. No abstract available.
Die GfH-Juniorakademie 2022 – #GfHJAK22 @schlossbuchenau.
Ahting S, Forstner A, Korte M, Krey I, Maier F, Meyer R, Rey-Thol L, Schnabel F. Ahting S, et al. Among authors: meyer r. Med Genet. 2022 Nov 29;34(4):309-312. doi: 10.1515/medgen-2022-2163. eCollection 2022 Dec. Med Genet. 2022. PMID: 38836092 Free PMC article. German. No abstract available.
245 results