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31 results

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Page 1
Common genetic variants contribute to risk of rare severe neurodevelopmental disorders.
Niemi MEK, Martin HC, Rice DL, Gallone G, Gordon S, Kelemen M, McAloney K, McRae J, Radford EJ, Yu S, Gecz J, Martin NG, Wright CF, Fitzpatrick DR, Firth HV, Hurles ME, Barrett JC. Niemi MEK, et al. Among authors: mcaloney k. Nature. 2018 Oct;562(7726):268-271. doi: 10.1038/s41586-018-0566-4. Epub 2018 Sep 26. Nature. 2018. PMID: 30258228 Free PMC article.
Multicohort analysis of the maternal age effect on recombination.
Martin HC, Christ R, Hussin JG, O'Connell J, Gordon S, Mbarek H, Hottenga JJ, McAloney K, Willemsen G, Gasparini P, Pirastu N, Montgomery GW, Navarro P, Soranzo N, Toniolo D, Vitart V, Wilson JF, Marchini J, Boomsma DI, Martin NG, Donnelly P. Martin HC, et al. Among authors: mcaloney k. Nat Commun. 2015 Aug 5;6:7846. doi: 10.1038/ncomms8846. Nat Commun. 2015. PMID: 26242864 Free PMC article.
Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility.
Mbarek H, Steinberg S, Nyholt DR, Gordon SD, Miller MB, McRae AF, Hottenga JJ, Day FR, Willemsen G, de Geus EJ, Davies GE, Martin HC, Penninx BW, Jansen R, McAloney K, Vink JM, Kaprio J, Plomin R, Spector TD, Magnusson PK, Reversade B, Harris RA, Aagaard K, Kristjansson RP, Olafsson I, Eyjolfsson GI, Sigurdardottir O, Iacono WG, Lambalk CB, Montgomery GW, McGue M, Ong KK, Perry JRB, Martin NG, Stefánsson H, Stefánsson K, Boomsma DI. Mbarek H, et al. Among authors: mcaloney k. Am J Hum Genet. 2016 May 5;98(5):898-908. doi: 10.1016/j.ajhg.2016.03.008. Epub 2016 Apr 28. Am J Hum Genet. 2016. PMID: 27132594 Free PMC article.
The Anorexia Nervosa Genetics Initiative: Study description and sample characteristics of the Australian and New Zealand arm.
Kirk KM, Martin FC, Mao A, Parker R, Maguire S, Thornton LM, Zhu G, McAloney K, Freeman JL, Hay P, Madden S, Morgan C, Russell J, Sawyer SM, Hughes EK, Fairweather-Schmidt AK, Fursland A, McCormack J, Wagg F, Jordan J, Kennedy MA, Ward W, Wade TD, Bulik CM, Martin NG. Kirk KM, et al. Among authors: mcaloney k. Aust N Z J Psychiatry. 2017 Jun;51(6):583-594. doi: 10.1177/0004867417700731. Epub 2017 Apr 5. Aust N Z J Psychiatry. 2017. PMID: 28378620 Free article.
Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes.
Rietschel L, Streit F, Zhu G, McAloney K, Frank J, Couvy-Duchesne B, Witt SH, Binz TM; CORtisolNETwork (CORNET) Consortium; Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium (PGC); McGrath J, Hickie IB, Hansell NK, Wright MJ, Gillespie NA, Forstner AJ, Schulze TG, Wüst S, Nöthen MM, Baumgartner MR, Walker BR, Crawford AA, Colodro-Conde L, Medland SE, Martin NG, Rietschel M. Rietschel L, et al. Among authors: mcaloney k. Sci Rep. 2017 Nov 10;7(1):15351. doi: 10.1038/s41598-017-11852-3. Sci Rep. 2017. PMID: 29127340 Free PMC article. Clinical Trial.
Social Competence in Parents Increases Children's Educational Attainment: Replicable Genetically-Mediated Effects of Parenting Revealed by Non-Transmitted DNA.
Bates TC, Maher BS, Colodro-Conde L, Medland SE, McAloney K, Wright MJ, Hansell NK, Okbay A, Kendler KS, Martin NG, Gillespie NA. Bates TC, et al. Among authors: mcaloney k. Twin Res Hum Genet. 2019 Feb;22(1):1-3. doi: 10.1017/thg.2018.75. Epub 2019 Jan 21. Twin Res Hum Genet. 2019. PMID: 30661510
Twenty-Five and Up (25Up) Study: A New Wave of the Brisbane Longitudinal Twin Study.
Mitchell BL, Campos AI, Rentería ME, Parker R, Sullivan L, McAloney K, Couvy-Duchesne B, Medland SE, Gillespie NA, Scott J, Zietsch BP, Lind PA, Martin NG, Hickie IB. Mitchell BL, et al. Among authors: mcaloney k. Twin Res Hum Genet. 2019 Jun;22(3):154-163. doi: 10.1017/thg.2019.27. Epub 2019 Jun 14. Twin Res Hum Genet. 2019. PMID: 31198126
Novel genetic loci affecting facial shape variation in humans.
Xiong Z, Dankova G, Howe LJ, Lee MK, Hysi PG, de Jong MA, Zhu G, Adhikari K, Li D, Li Y, Pan B, Feingold E, Marazita ML, Shaffer JR, McAloney K, Xu SH, Jin L, Wang S, de Vrij FM, Lendemeijer B, Richmond S, Zhurov A, Lewis S, Sharp GC, Paternoster L, Thompson H, Gonzalez-Jose R, Bortolini MC, Canizales-Quinteros S, Gallo C, Poletti G, Bedoya G, Rothhammer F, Uitterlinden AG, Ikram MA, Wolvius E, Kushner SA, Nijsten TE, Palstra RT, Boehringer S, Medland SE, Tang K, Ruiz-Linares A, Martin NG, Spector TD, Stergiakouli E, Weinberg SM, Liu F, Kayser M; International Visible Trait Genetics (VisiGen) Consortium. Xiong Z, et al. Among authors: mcaloney k. Elife. 2019 Nov 26;8:e49898. doi: 10.7554/eLife.49898. Elife. 2019. PMID: 31763980 Free PMC article.
31 results