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2010 1
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23 results

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Page 1
Regulatory de novo mutations underlying intellectual disability.
De Vas MG, Boulet F, Joshi SS, Garstang MG, Khan TN, Atla G, Parry D, Moore D, Cebola I, Zhang S, Cui W, Lampe AK, Lam WW; Genomics England Research Consortium; Ferrer J, Pradeepa MM, Atanur SS. De Vas MG, et al. Among authors: atanur ss. Life Sci Alliance. 2023 Feb 28;6(5):e202201843. doi: 10.26508/lsa.202201843. Print 2023 May. Life Sci Alliance. 2023. PMID: 36854624 Free PMC article.
De novo mutations in autosomal recessive congenital malformations.
Black HA, Parry D, Atanur SS, Ross D, Rose E, Russell H, Stock S, Warner J, Porteous M, Aitman TJ, Evans MJ. Black HA, et al. Among authors: atanur ss. Genet Med. 2016 Dec;18(12):1325-1326. doi: 10.1038/gim.2016.62. Epub 2016 Jun 9. Genet Med. 2016. PMID: 27280866 Free PMC article. No abstract available.
Combined sequence-based and genetic mapping analysis of complex traits in outbred rats.
Rat Genome Sequencing and Mapping Consortium; Baud A, Hermsen R, Guryev V, Stridh P, Graham D, McBride MW, Foroud T, Calderari S, Diez M, Ockinger J, Beyeen AD, Gillett A, Abdelmagid N, Guerreiro-Cacais AO, Jagodic M, Tuncel J, Norin U, Beattie E, Huynh N, Miller WH, Koller DL, Alam I, Falak S, Osborne-Pellegrin M, Martinez-Membrives E, Canete T, Blazquez G, Vicens-Costa E, Mont-Cardona C, Diaz-Moran S, Tobena A, Hummel O, Zelenika D, Saar K, Patone G, Bauerfeind A, Bihoreau MT, Heinig M, Lee YA, Rintisch C, Schulz H, Wheeler DA, Worley KC, Muzny DM, Gibbs RA, Lathrop M, Lansu N, Toonen P, Ruzius FP, de Bruijn E, Hauser H, Adams DJ, Keane T, Atanur SS, Aitman TJ, Flicek P, Malinauskas T, Jones EY, Ekman D, Lopez-Aumatell R, Dominiczak AF, Johannesson M, Holmdahl R, Olsson T, Gauguier D, Hubner N, Fernandez-Teruel A, Cuppen E, Mott R, Flint J. Rat Genome Sequencing and Mapping Consortium, et al. Among authors: atanur ss. Nat Genet. 2013 Jul;45(7):767-75. doi: 10.1038/ng.2644. Epub 2013 May 26. Nat Genet. 2013. PMID: 23708188 Free PMC article.
A Palindrome-Like Structure on 16p13.3 Is Associated with the Formation of Complex Structural Variations and SRRM2 Haploinsufficiency.
Pagnamenta AT, Yu J, Willis TA, Hashim M, Seaby EG, Walker S, Xian J, Cheng EWY, Tavares ALT, Forzano F, Cox H, Dabir T, Brady AF, Ghali N, Atanur SS, Ennis S, Baralle D, Taylor JC. Pagnamenta AT, et al. Among authors: atanur ss. Hum Mutat. 2023 Apr 11;2023:6633248. doi: 10.1155/2023/6633248. eCollection 2023. Hum Mutat. 2023. PMID: 40225164 Free PMC article.
Impulsivity is a heritable trait in rodents and associated with a novel quantitative trait locus on chromosome 1.
Jupp B, Pitzoi S, Petretto E, Mar AC, Oliver YP, Jordan ER, Taylor S, Atanur SS, Srivastava PK, Saar K, Hubner N, Sommer WH, Staehlin O, Spanagel R, Robinson ES, Schumann G, Moreno M, Everitt BJ, Robbins TW, Aitman TJ, Dalley JW. Jupp B, et al. Among authors: atanur ss. Sci Rep. 2020 Apr 21;10(1):6684. doi: 10.1038/s41598-020-63646-9. Sci Rep. 2020. PMID: 32317713 Free PMC article.
23 results