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Page 1
Loophole-free Bell inequality violation with superconducting circuits.
Storz S, Schär J, Kulikov A, Magnard P, Kurpiers P, Lütolf J, Walter T, Copetudo A, Reuer K, Akin A, Besse JC, Gabureac M, Norris GJ, Rosario A, Martin F, Martinez J, Amaya W, Mitchell MW, Abellan C, Bancal JD, Sangouard N, Royer B, Blais A, Wallraff A. Storz S, et al. Nature. 2023 May;617(7960):265-270. doi: 10.1038/s41586-023-05885-0. Epub 2023 May 10. Nature. 2023. PMID: 37165240 Free PMC article.
Fast and Unconditional All-Microwave Reset of a Superconducting Qubit.
Magnard P, Kurpiers P, Royer B, Walter T, Besse JC, Gasparinetti S, Pechal M, Heinsoo J, Storz S, Blais A, Wallraff A. Magnard P, et al. Among authors: storz s. Phys Rev Lett. 2018 Aug 10;121(6):060502. doi: 10.1103/PhysRevLett.121.060502. Phys Rev Lett. 2018. PMID: 30141638
CFAP47 is Implicated in X-Linked Polycystic Kidney Disease.
Mori T, Fujimaru T, Liu C, Patterson K, Yamamoto K, Suzuki T, Chiga M, Sekine A, Ubara Y, Miller DE, Zalusky MPG, Mandai S, Ando F, Mori Y, Kikuchi H, Susa K; University of Washington Center for Rare Disease Research; Chong JX, Bamshad MJ, Tan YQ, Zhang F, Uchida S, Sohara E. Mori T, et al. Kidney Int Rep. 2024 Sep 24;9(12):3580-3591. doi: 10.1016/j.ekir.2024.09.013. eCollection 2024 Dec. Kidney Int Rep. 2024. PMID: 39698362 Free PMC article.
High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variation.
Gustafson JA, Gibson SB, Damaraju N, Zalusky MPG, Hoekzema K, Twesigomwe D, Yang L, Snead AA, Richmond PA, De Coster W, Olson ND, Guarracino A, Li Q, Miller AL, Goffena J, Anderson ZB, Storz SHR, Ward SA, Sinha M, Gonzaga-Jauregui C, Clarke WE, Basile AO, Corvelo A, Reeves C, Helland A, Musunuri RL, Revsine M, Patterson KE, Paschal CR, Zakarian C, Goodwin S, Jensen TD, Robb E; 1000 Genomes ONT Sequencing Consortium; University of Washington Center for Rare Disease Research (UW-CRDR); Genomics Research to Elucidate the Genetics of Rare Diseases (GREGoR) Consortium; McCombie WR, Sedlazeck FJ, Zook JM, Montgomery SB, Garrison E, Kolmogorov M, Schatz MC, McLaughlin RN Jr, Dashnow H, Zody MC, Loose M, Jain M, Eichler EE, Miller DE. Gustafson JA, et al. Among authors: storz shr. Genome Res. 2024 Nov 20;34(11):2061-2073. doi: 10.1101/gr.279273.124. Genome Res. 2024. PMID: 39358015 Free PMC article.
Nanopore sequencing of 1000 Genomes Project samples to build a comprehensive catalog of human genetic variation.
Gustafson JA, Gibson SB, Damaraju N, Zalusky MP, Hoekzema K, Twesigomwe D, Yang L, Snead AA, Richmond PA, De Coster W, Olson ND, Guarracino A, Li Q, Miller AL, Goffena J, Anderson Z, Storz SH, Ward SA, Sinha M, Gonzaga-Jauregui C, Clarke WE, Basile AO, Corvelo A, Reeves C, Helland A, Musunuri RL, Revsine M, Patterson KE, Paschal CR, Zakarian C, Goodwin S, Jensen TD, Robb E; 1000 Genomes ONT Sequencing Consortium; University of Washington Center for Rare Disease Research (UW-CRDR); Genomics Research to Elucidate the Genetics of Rare Diseases (GREGoR) Consortium; McCombie WR, Sedlazeck FJ, Zook JM, Montgomery SB, Garrison E, Kolmogorov M, Schatz MC, McLaughlin RN Jr, Dashnow H, Zody MC, Loose M, Jain M, Eichler EE, Miller DE. Gustafson JA, et al. Among authors: storz sh. medRxiv [Preprint]. 2024 Mar 7:2024.03.05.24303792. doi: 10.1101/2024.03.05.24303792. medRxiv. 2024. Update in: Genome Res. 2024 Nov 20;34(11):2061-2073. doi: 10.1101/gr.279273.124 PMID: 38496498 Free PMC article. Updated. Preprint.
Genome Sequences of Subcluster M2 Mycobacteriophages Estes and Aziz.
Fitzgerald SK, Johnson EH, Storz SHR, Ballard C, Battaglia S, Boice M, Bramwell-Butcher J, Dedinsky M, DeKlotz J, Diaz I, Engley A, Ernst L, Gonzales E, Groscost A, Grosser P, Haider A, Harrison M, Husler K, Lau J, Monlux M, Paratore J, Ruesch T, Schlesinger M, Scholes A, Poxleitner MK, Anders KR. Fitzgerald SK, et al. Among authors: storz shr. Microbiol Resour Announc. 2021 Mar 11;10(10):e00104-21. doi: 10.1128/MRA.00104-21. Microbiol Resour Announc. 2021. PMID: 33707327 Free PMC article.
22 results