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Results 11-20 of 32 (Search time: 0.011 seconds).
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PreviewIssue DateTitleAuthor(s)
2016The genetic history of Peruvian Quechua-Lamistas and Chankas: uniparental DNA Patterns among autochthonous Amazonian and Andean populationsSandoval, J.; Lacerda, D.; Acosta, O.; Jota, M.; Robles-Ruiz, P.; Salazar-Granara, A.; Vieira, P.; Paz-y-Miño, C.; Fujita, R.; Santos, F.; Jin, L.; Li, H.; Li, S.; Swamikrishnan, P.; Javed, A.; Parida, L.; Royyuru, A.; Mitchell, R.; Zalloua, P.; Adhikarla, S.; et al.
2013MLL2 mutation detection in 86 patients with Kabuki syndrome: a genotype-phenotype studyMakrythanasis, P.; van Bon, B.; Steehouwer, M.; Rodríguez-Santiago, B.; Simpson, M.; Dias, P.; Anderlid, B.; Arts, P.; Bhat, M.; Augello, B.; Biamino, E.; Bongers, E.; del Campo, M.; Cordeiro, I.; Cueto-González, A.; Cuscó, I.; Deshpande, C.; Frysira, E.; Izatt, L.; Flores, R.; et al.
2016A generic method of engagement to elicit regional coastal management optionsDichmont, C.; Dutra, L.; Owens, R.; Jebreen, E.; Thompson, C.; Deng, R.; van Putten, E.; Pascual, R.; Dambacher, J.; Warne, M.; Quinn, R.; Thébaud, O.; Bennett, J.; Read, M.; Wachenfeld, D.; Davies, J.; Garland, A.; Dunning, M.; Collier, C.; Waycott, M.; et al.
2018The genomic history of southeastern EuropeMathieson, I.; Alpaslan-Roodenberg, S.; Posth, C.; Szécsényi-Nagy, A.; Rohland, N.; Mallick, S.; Olalde, I.; Broomandkhoshbacht, N.; Candilio, F.; Cheronet, O.; Fernandes, D.; Ferry, M.; Gamarra, B.; Fortes, G.; Haak, W.; Harney, E.; Jones, E.; Keating, D.; Krause-Kyora, B.; Kucukkalipci, I.; et al.
2015A meta-analysis of gene expression signatures of blood pressure and hypertensionHuan, T.; Esko, T.; Peters, M.; Pilling, L.; Schramm, K.; Schurmann, C.; Chen, B.; Liu, C.; Joehanes, R.; Johnson, A.; Yao, C.; Ying, S.; Courchesne, P.; Milani, L.; Raghavachari, N.; Wang, R.; Liu, P.; Reinmaa, E.; Dehghan, A.; Hofman, A.; et al.
2017A recurrent de novo nonsense variant in ZSWIM6 results in severe intellectual disability without frontonasal or limb malformationsPalmer, E.; Kumar, R.; Gordon, C.; Shaw, M.; Hubert, L.; Carroll, R.; Rio, M.; Murray, L.; Leffler, M.; Dudding-Byth, T.; Oufadem, M.; Lalani, S.; Lewis, A.; Xia, F.; Tam, A.; Webster, R.; Brammah, S.; Filippini, F.; Pollard, J.; Spies, J.; et al.
2018Developing reproducible bioinformatics analysis workflows for heterogeneous computing environments to support African genomicsBaichoo, S.; Souilmi, Y.; Panji, S.; Botha, G.; Meintjes, A.; Hazelhurst, S.; Bendou, H.; de Beste, E.; Mpangase, P.; Souiai, O.; Alghali, M.; Yi, L.; O'Connor, B.; Crusoe, M.; Armstrong, D.; Aron, S.; Joubert, F.; Ahmed, A.; Mbiyavanga, M.; van Heusden, P.; et al.
2017YY1 haploinsufficiency causes an intellectual disability syndrome featuring transcriptional and chromatin dysfunctionGabriele, M.; Vulto-van Silfhout, A.; Germain, P.; Vitriolo, A.; Kumar, R.; Douglas, E.; Haan, E.; Kosaki, K.; Takenouchi, T.; Rauch, A.; Steindl, K.; Frengen, E.; Misceo, D.; Pedurupillay, C.; Stromme, P.; Rosenfeld, J.; Shao, Y.; Craigen, W.; Schaaf, C.; Rodriguez-Buritica, D.; et al.
2017Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domainsGeisheker, M.; Heymann, G.; Wang, T.; Coe, B.; Turner, T.; Stessman, H.; Hoekzema, K.; Kvarnung, M.; Shaw, M.; Friend, K.; Liebelt, J.; Barnett, C.; Thompson, E.; Haan, E.; Guo, H.; Anderlid, B.; Nordgren, A.; Lindstrand, A.; Vandeweyer, G.; Alberti, A.; et al.
2012Prognostically significant fusion oncogenes in Pakistani patients with adult acute lymphoblastic leukemia and their association with disease biology and outcomeSabir, N.; Iqbal, Z.; Aleem, A.; Awan, T.; Naeem, T.; Asad, S.; Tahir, A.; Absar, M.; Hasanato, R.; Basit, S.; Chishti, M.; Ul-Haque, M.; Khalid, A.; Sabar, M.; Rasool, M.; Karim, S.; Khan, M.; Samreen, B.; Akram, A.; Siddiqi, M.; et al.