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Results 3061-3070 of 3084 (Search time: 0.005 seconds).
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PreviewIssue DateTitleAuthor(s)
2013Somatic point mutation calling in low cellularity tumorsKassahn, K.; Holmes, O.; Nones, K.; Patch, A.; Miller, D.; Christ, A.; Harliwong, I.; Bruxner, T.; Xu, Q.; Anderson, M.; Wood, S.; Leonard, C.; Taylor, D.; Newell, F.; Song, S.; Idrisoglu, S.; Nourse, C.; Nourbakhsh, E.; Manning, S.; Wani, S.; et al.; Jordan, I.
2013Computational approaches to identify functional genetic variants in cancer genomesGonzalez-Perez, A.; Mustonen, V.; Reva, B.; Ritchie, G.; Creixell, P.; Karchin, R.; Vazquez, M.; Fink, J.; Kassahn, K.; Pearson, J.; Bader, G.; Boutros, P.; Muthuswamy, L.; Ouellette, B.; Reimand, J.; Linding, R.; Shibata, T.; Valencia, A.; Butler, A.; Dronov, S.; et al.
2019Searches for continuous gravitational waves from 15 supernova remnants and Fomalhaut b with Advanced LIGOAbbott, B.P.; Abbott, R.; Abbott, T.D.; Abraham, S.; Acernese, F.; Ackley, K.; Adams, C.; Adhikari, R.X.; Adya, V.B.; Affeldt, C.; Agathos, M.; Agatsuma, K.; Aggarwal, N.; Aguiar, O.D.; Aiello, L.; Ain, A.; Ajith, P.; Allen, G.; Allocca, A.; Aloy, M.A.; et al.
2023AugerPrime surface detector electronicsAbdul Halim, A.; Abreu, P.; Aglietta, M.; Allison, P.; Allekotte, I.; Cheminant, K.A.; Almela, A.; Aloisio, R.; Alvarez-Muñiz, J.; Yebra, J.A.; Anastasi, G.A.; Anchordoqui, L.; Andrada, B.; Andringa, S.; Anukriti,; Aramo, C.; Ferreira, P.R.A.; Arnone, E.; Velázquez, J.C.A.; Assiro, R.; et al.
2024High-Dose Docosahexaenoic Acid in Newborns Born at Less Than 29 Weeks' Gestation and Behavior at Age 5 Years: Follow-Up of a Randomized Clinical TrialGould, J.F.; Roberts, R.M.; Anderson, P.J.; Makrides, M.; Sullivan, T.R.; Gibson, R.A.; McPhee, A.J.; Doyle, L.W.; Bednarz, J.M.; Best, K.P.; Opie, G.; Travadi, J.; Cheong, J.L.Y.; Davis, P.G.; Sharp, M.; Simmer, K.; Tan, K.; Morris, S.; Lui, K.; Bolisetty, S.; et al.
2022Potent Stimulation of the Androgen Receptor Instigates a Viral Mimicry Response in Prostate CancerAlizadeh-Ghodsi, M.; Owen, K.L.; Townley, S.L.; Zanker, D.; Rollin, S.P.G.; Hanson, A.R.; Shrestha, R.; Toubia, J.; Gargett, T.; Chernukhin, I.; Luu, J.; Cowley, K.J.; Clark, A.; Carroll, J.S.; Simpson, K.J.; Winter, J.M.; Lawrence, M.G.; Butler, L.M.; Risbridger, G.P.; Thierry, B.; et al.
2024Narrowing the diagnostic gap: Genomes, episignatures, long-read sequencing, and health economic analyses in an exome-negative intellectual disability cohortDias, K.-R.; Shrestha, R.; Schofield, D.; Evans, C.-A.; O'Heir, E.; Zhu, Y.; Zhang, F.; Standen, K.; Weisburd, B.; Stenton, S.L.; Sanchis-Juan, A.; Brand, H.; Talkowski, M.E.; Ma, A.; Ghedia, S.; Wilson, M.; Sandaradura, S.A.; Smith, J.; Kamien, B.; Turner, A.; et al.
2020Mutations disrupting neuritogenesis genes confer risk for cerebral palsyJin, S.C.; Lewis, S.A.; Bakhtiari, S.; Zeng, X.; Sierant, M.C.; Shetty, S.; Nordlie, S.M.; Elie, A.; Corbett, M.A.; Norton, B.Y.; van Eyk, C.L.; Haider, S.; Guida, B.S.; Magee, H.; Liu, J.; Pastore, S.; Vincent, J.B.; Brunstrom-Hernandez, J.; Papavasileiou, A.; Fahey, M.C.; et al.
2023Transient naive reprogramming corrects hiPS cells functionally and epigeneticallyBuckberry, S.; Liu, X.; Poppe, D.; Tan, J.P.; Sun, G.; Chen, J.; Nguyen, T.V.; de Mendoza, A.; Pflueger, J.; Frazer, T.; Vargas-Landín, D.B.; Paynter, J.M.; Smits, N.; Liu, N.; Ouyang, J.F.; Rossello, F.J.; Chy, H.S.; Rackham, O.J.L.; Laslett, A.L.; Breen, J.; et al.
2023Search for Correlations of High-energy Neutrinos Detected in IceCube with Radio-bright AGN and Gamma-Ray Emission from BlazarsAbbasi, R.; Ackermann, M.; Adams, J.; Agarwalla, S.K.; Aguilar, J.A.; Ahlers, M.; Alameddine, J.M.; Amin, N.M.; Andeen, K.; Anton, G.; Argüelles, C.; Ashida, Y.; Athanasiadou, S.; Axani, S.N.; Bai, X.; Balagopal, A.V.; Baricevic, M.; Barwick, S.W.; Basu, V.; Bay, R.; et al.

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