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Results 11-20 of 33 (Search time: 0.007 seconds).
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PreviewIssue DateTitleAuthor(s)
2014The sheep genome illuminates biology of the rumen and lipid metabolismJiang, Y.; Xie, M.; Chen, W.; Talbot, R.; Maddox, J.; Faraut, T.; Wu, C.; Muzny, D.; Li, Y.; Zhang, W.; Stanton, J.; Brauning, R.; Barris, W.; Hourlier, T.; Aken, B.; Searle, S.; Adelson, D.; Bian, C.; Cam, G.; Chen, Y.; et al.
2018Genome-wide gene-environment interaction in depression: a systematic evaluation of candidate genes: the childhood trauma working-group of PGC-MDDVan der Auwera, S.; Peyrot, W.; Milaneschi, Y.; Hertel, J.; Baune, B.; Breen, G.; Byrne, E.; Dunn, E.; Fisher, H.; Homuth, G.; Levinson, D.; Lewis, C.; Mills, N.; Mullins, N.; Nauck, M.; Pistis, G.; Preisig, M.; Rietschel, M.; Ripke, S.; Sullivan, P.; et al.
2018A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiencyJansen, S.; Hoischen, A.; Coe, B.; Carvill, G.; van Esch, H.; Bosch, D.; Andersen, U.; Baker, C.; Bauters, M.; Bernier, R.; van Bon, B.; Claahsen-van der Grinten, H.; Gecz, J.; Gilissen, C.; Grillo, L.; Hackett, A.; Kleefstra, T.; Koolen, D.; Kvarnung, M.; Larsen, M.; et al.
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.
2016Clinical and molecular analyses of Beckwith–Wiedemann syndrome: comparison between spontaneous conception and assisted reproduction techniquesTenorio, J.; Romanelli, V.; Martin-Trujillo, A.; Fernández, G.; Segovia, M.; Perandones, C.; Pérez Jurado, L.; Esteller, M.; Fraga, M.; Arias, P.; Gordo, G.; Dapía, I.; Mena, R.; Palomares, M.; Pérez de Nanclares, G.; Nevado, J.; García-Miñaur, S.; Santos-Simarro, F.; Martinez-Glez, V.; Vallespín, E.; 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.