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

Year Number of Results
1985 1
1986 1
1988 1
1989 1
1990 1
1991 2
1992 2
1993 2
1994 2
1996 1
1999 1
2003 1
2005 1
2006 2
2008 2
2009 3
2011 4
2012 3
2013 7
2014 4
2015 4
2016 1
2017 1
2018 1
2019 1
2021 3
2022 2
2023 3

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55 results

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Page 1
The contribution of de novo coding mutations to autism spectrum disorder.
Iossifov I, O'Roak BJ, Sanders SJ, Ronemus M, Krumm N, Levy D, Stessman HA, Witherspoon KT, Vives L, Patterson KE, Smith JD, Paeper B, Nickerson DA, Dea J, Dong S, Gonzalez LE, Mandell JD, Mane SM, Murtha MT, Sullivan CA, Walker MF, Waqar Z, Wei L, Willsey AJ, Yamrom B, Lee YH, Grabowska E, Dalkic E, Wang Z, Marks S, Andrews P, Leotta A, Kendall J, Hakker I, Rosenbaum J, Ma B, Rodgers L, Troge J, Narzisi G, Yoon S, Schatz MC, Ye K, McCombie WR, Shendure J, Eichler EE, State MW, Wigler M. Iossifov I, et al. Among authors: murtha mt. Nature. 2014 Nov 13;515(7526):216-21. doi: 10.1038/nature13908. Epub 2014 Oct 29. Nature. 2014. PMID: 25363768 Free PMC article.
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.
Sanders SJ, He X, Willsey AJ, Ercan-Sencicek AG, Samocha KE, Cicek AE, Murtha MT, Bal VH, Bishop SL, Dong S, Goldberg AP, Jinlu C, Keaney JF 3rd, Klei L, Mandell JD, Moreno-De-Luca D, Poultney CS, Robinson EB, Smith L, Solli-Nowlan T, Su MY, Teran NA, Walker MF, Werling DM, Beaudet AL, Cantor RM, Fombonne E, Geschwind DH, Grice DE, Lord C, Lowe JK, Mane SM, Martin DM, Morrow EM, Talkowski ME, Sutcliffe JS, Walsh CA, Yu TW; Autism Sequencing Consortium; Ledbetter DH, Martin CL, Cook EH, Buxbaum JD, Daly MJ, Devlin B, Roeder K, State MW. Sanders SJ, et al. Among authors: murtha mt. Neuron. 2015 Sep 23;87(6):1215-1233. doi: 10.1016/j.neuron.2015.09.016. Neuron. 2015. PMID: 26402605 Free PMC article.
De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
Sanders SJ, Murtha MT, Gupta AR, Murdoch JD, Raubeson MJ, Willsey AJ, Ercan-Sencicek AG, DiLullo NM, Parikshak NN, Stein JL, Walker MF, Ober GT, Teran NA, Song Y, El-Fishawy P, Murtha RC, Choi M, Overton JD, Bjornson RD, Carriero NJ, Meyer KA, Bilguvar K, Mane SM, Sestan N, Lifton RP, Günel M, Roeder K, Geschwind DH, Devlin B, State MW. Sanders SJ, et al. Among authors: murtha mt. Nature. 2012 Apr 4;485(7397):237-41. doi: 10.1038/nature10945. Nature. 2012. PMID: 22495306 Free PMC article.
Evolution of Hox genes.
Ruddle FH, Bartels JL, Bentley KL, Kappen C, Murtha MT, Pendleton JW. Ruddle FH, et al. Among authors: murtha mt. Annu Rev Genet. 1994;28:423-42. doi: 10.1146/ Annu Rev Genet. 1994. PMID: 7893134 Review. No abstract available.
North Asian population relationships in a global context.
Kidd KK, Evsanaa B, Togtokh A, Brissenden JE, Roscoe JM, Dogan M, Neophytou PI, Gurkan C, Bulbul O, Cherni L, Speed WC, Murtha M, Kidd JR, Pakstis AJ. Kidd KK, et al. Among authors: murtha m. Sci Rep. 2022 May 4;12(1):7214. doi: 10.1038/s41598-022-10706-x. Sci Rep. 2022. PMID: 35508562 Free PMC article.
Genetic relationships of Southwest Asian and Mediterranean populations.
Kidd KK, Bulbul O, Gurkan C, Dogan M, Dogan S, Neophytou PI, Cherni L, Gurwitz D, Speed WC, Murtha M, Kidd JR, Pakstis AJ. Kidd KK, et al. Among authors: murtha m. Forensic Sci Int Genet. 2021 Jul;53:102528. doi: 10.1016/j.fsigen.2021.102528. Epub 2021 May 14. Forensic Sci Int Genet. 2021. PMID: 34020230
Expression and function of human ribonuclease 4 in the kidney and urinary tract.
Bender K, Schwartz LL, Cohen A, Vasquez CM, Murtha MJ, Eichler T, Thomas JP, Jackson A, Spencer JD. Bender K, et al. Among authors: murtha mj. Am J Physiol Renal Physiol. 2021 May 1;320(5):F972-F983. doi: 10.1152/ajprenal.00592.2020. Epub 2021 Apr 5. Am J Physiol Renal Physiol. 2021. PMID: 33818125 Free PMC article.
55 results