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

Year Number of Results
2003 1
2004 1
2008 2
2009 1
2010 1
2011 2
2012 7
2013 6
2014 7
2015 6
2016 7
2017 9
2018 12
2019 14
2020 8
2021 2
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76 results
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Page 1
Inherited genetic susceptibility to acute lymphoblastic leukemia in Down syndrome.
Brown AL, de Smith AJ, Gant VU, Yang W, Scheurer ME, Walsh KM, Chernus JM, Kallsen NA, Peyton SA, Davies GE, Ehli EA, Winick N, Heerema NA, Carroll AJ, Borowitz MJ, Wood BL, Carroll WL, Raetz EA, Feingold E, Devidas M, Barcellos LF, Hansen HM, Morimoto L, Kang AY, Smirnov I, Healy J, Laverdière C, Sinnett D, Taub JW, Birch JM, Thompson P, Spector LG, Pombo-de-Oliveira MS, DeWan AT, Mullighan CG, Hunger SP, Pui CH, Loh ML, Zwick ME, Metayer C, Ma X, Mueller BA, Sherman SL, Wiemels JL, Relling MV, Yang JJ, Lupo PJ, Rabin KR. Brown AL, et al. Among authors: ehli ea. Blood. 2019 Oct 10;134(15):1227-1237. doi: 10.1182/blood.2018890764. Blood. 2019. PMID: 31350265 Free PMC article.
APOBEC mutation drives early-onset squamous cell carcinomas in recessive dystrophic epidermolysis bullosa.
Cho RJ, Alexandrov LB, den Breems NY, Atanasova VS, Farshchian M, Purdom E, Nguyen TN, Coarfa C, Rajapakshe K, Prisco M, Sahu J, Tassone P, Greenawalt EJ, Collisson EA, Wu W, Yao H, Su X, Guttmann-Gruber C, Hofbauer JP, Hashmi R, Fuentes I, Benz SC, Golovato J, Ehli EA, Davis CM, Davies GE, Covington KR, Murrell DF, Salas-Alanis JC, Palisson F, Bruckner AL, Robinson W, Has C, Bruckner-Tuderman L, Titeux M, Jonkman MF, Rashidghamat E, Lwin SM, Mellerio JE, McGrath JA, Bauer JW, Hovnanian A, Tsai KY, South AP. Cho RJ, et al. Among authors: ehli ea. Sci Transl Med. 2018 Aug 22;10(455):eaas9668. doi: 10.1126/scitranslmed.aas9668. Sci Transl Med. 2018. PMID: 30135250
Avera Twin Register Growing Through Online Consenting and Survey Collection.
Kittelsrud JM, Ehli EA, Petersen V, Jung T, Beck JJ, Kallsen N, Huizenga P, Holm B, Davies GE. Kittelsrud JM, et al. Among authors: ehli ea. Twin Res Hum Genet. 2019 Dec;22(6):686-690. doi: 10.1017/thg.2019.73. Epub 2019 Oct 14. Twin Res Hum Genet. 2019. PMID: 31608846 Review.
The Nigerian Twin and Sibling Registry: An Update.
Hur YM, Jeong HU, Kang MC, Ajose F, Kim JW, Beck JJ, Hottenga JJ, Mbarek H, Finnicum CT, Ehli EA, Martin NG, de Geus EJ, Boomsma DI, Davies GE, Bates T. Hur YM, et al. Among authors: ehli ea. Twin Res Hum Genet. 2019 Dec;22(6):637-640. doi: 10.1017/thg.2019.110. Epub 2019 Dec 3. Twin Res Hum Genet. 2019. PMID: 31796140
Biological insights into multiple birth: genetic findings from UK Biobank.
Mbarek H, van de Weijer MP, van der Zee MD, Ip HF, Beck JJ, Abdellaoui A, Ehli EA, Davies GE, Baselmans BML, Nivard MG, Bartels M, de Geus EJ, Boomsma DI. Mbarek H, et al. Among authors: ehli ea. Eur J Hum Genet. 2019 Jun;27(6):970-979. doi: 10.1038/s41431-019-0355-z. Epub 2019 Feb 13. Eur J Hum Genet. 2019. PMID: 30760885 Free PMC article.
The role of genetic variation in DGKK on moderate and severe hypospadias.
Richard MA, Sok P, Canon S, Brown AL, Peckham-Gregory EC, Nembhard WN, Carmichael SL, Ehli EA, Kallsen NA, Peyton SA, Davies GE, Patel A, Zamilpa I, Wyatt RA, Hobbs CA, Scheurer ME, Lupo PJ. Richard MA, et al. Among authors: ehli ea. Birth Defects Res. 2019 Aug 1;111(13):932-937. doi: 10.1002/bdr2.1522. Epub 2019 May 18. Birth Defects Res. 2019. PMID: 31102501 Free PMC article.
76 results
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