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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1952 1
1966 1
1967 2
1972 4
1973 2
1974 6
1975 3
1976 8
1977 2
1978 3
1979 3
1980 5
1981 3
1982 9
1983 9
1984 12
1985 13
1986 16
1987 6
1988 8
1989 8
1990 12
1991 7
1992 16
1993 14
1994 11
1995 12
1996 13
1997 22
1998 19
1999 22
2000 12
2001 23
2002 28
2003 33
2004 27
2005 33
2006 24
2007 26
2008 39
2009 33
2010 31
2011 39
2012 29
2013 53
2014 51
2015 57
2016 32
2017 32
2018 32
2019 33
2020 45
2021 49
2022 32
2023 33
2024 34
2025 16

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1,049 results

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Page 1
De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome.
Chen Y, Dawes R, Kim HC, Ljungdahl A, Stenton SL, Walker S, Lord J, Lemire G, Martin-Geary AC, Ganesh VS, Ma J, Ellingford JM, Delage E, D'Souza EN, Dong S, Adams DR, Allan K, Bakshi M, Baldwin EE, Berger SI, Bernstein JA, Bhatnagar I, Blair E, Brown NJ, Burrage LC, Chapman K, Coman DJ, Compton AG, Cunningham CA, D'Souza P, Danecek P, Délot EC, Dias KR, Elias ER, Elmslie F, Evans CA, Ewans L, Ezell K, Fraser JL, Gallacher L, Genetti CA, Goriely A, Grant CL, Haack T, Higgs JE, Hinch AG, Hurles ME, Kuechler A, Lachlan KL, Lalani SR, Lecoquierre F, Leitão E, Fevre AL, Leventer RJ, Liebelt JE, Lindsay S, Lockhart PJ, Ma AS, Macnamara EF, Mansour S, Maurer TM, Mendez HR, Metcalfe K, Montgomery SB, Moosajee M, Nassogne MC, Neumann S, O'Donoghue M, O'Leary M, Palmer EE, Pattani N, Phillips J, Pitsava G, Pysar R, Rehm HL, Reuter CM, Revencu N, Riess A, Rius R, Rodan L, Roscioli T, Rosenfeld JA, Sachdev R, Shaw-Smith CJ, Simons C, Sisodiya SM, Snell P, St Clair L, Stark Z, Stewart HS, Tan TY, Tan NB, Temple SEL, Thorburn DR, Tifft CJ, Uebergang E, VanNoy GE, Vasudevan P, Vilain E, Viskochil DH, Wedd L, Wheeler MT, White SM, Wojcik M, Wolfe LA, Wolfenson Z, Wright CF, Xiao C, Zocche D, R… See abstract for full author list ➔ Chen Y, et al. Among authors: rubenstein jl. Nature. 2024 Aug;632(8026):832-840. doi: 10.1038/s41586-024-07773-7. Epub 2024 Jul 11. Nature. 2024. PMID: 38991538 Free PMC article.
Editorial Commentary.
Rubenstein JN. Rubenstein JN. Urol Pract. 2024 Jul;11(4):768. doi: 10.1097/UPJ.0000000000000604. Epub 2024 May 9. Urol Pract. 2024. PMID: 38899644 No abstract available.
Human pallial MGE-type GABAergic interneuron cell therapy for chronic focal epilepsy.
Bershteyn M, Bröer S, Parekh M, Maury Y, Havlicek S, Kriks S, Fuentealba L, Lee S, Zhou R, Subramanyam G, Sezan M, Sevilla ES, Blankenberger W, Spatazza J, Zhou L, Nethercott H, Traver D, Hampel P, Kim H, Watson M, Salter N, Nesterova A, Au W, Kriegstein A, Alvarez-Buylla A, Rubenstein J, Banik G, Bulfone A, Priest C, Nicholas CR. Bershteyn M, et al. Among authors: rubenstein j. Cell Stem Cell. 2023 Oct 5;30(10):1331-1350.e11. doi: 10.1016/j.stem.2023.08.013. Cell Stem Cell. 2023. PMID: 37802038 Free PMC article.
Generation of pure GABAergic neurons by transcription factor programming.
Yang N, Chanda S, Marro S, Ng YH, Janas JA, Haag D, Ang CE, Tang Y, Flores Q, Mall M, Wapinski O, Li M, Ahlenius H, Rubenstein JL, Chang HY, Buylla AA, Südhof TC, Wernig M. Yang N, et al. Among authors: rubenstein jl. Nat Methods. 2017 Jun;14(6):621-628. doi: 10.1038/nmeth.4291. Epub 2017 May 15. Nat Methods. 2017. PMID: 28504679 Free PMC article.
Optimizing Nervous System-Specific Gene Targeting with Cre Driver Lines: Prevalence of Germline Recombination and Influencing Factors.
Luo L, Ambrozkiewicz MC, Benseler F, Chen C, Dumontier E, Falkner S, Furlanis E, Gomez AM, Hoshina N, Huang WH, Hutchison MA, Itoh-Maruoka Y, Lavery LA, Li W, Maruo T, Motohashi J, Pai EL, Pelkey KA, Pereira A, Philips T, Sinclair JL, Stogsdill JA, Traunmüller L, Wang J, Wortel J, You W, Abumaria N, Beier KT, Brose N, Burgess HA, Cepko CL, Cloutier JF, Eroglu C, Goebbels S, Kaeser PS, Kay JN, Lu W, Luo L, Mandai K, McBain CJ, Nave KA, Prado MAM, Prado VF, Rothstein J, Rubenstein JLR, Saher G, Sakimura K, Sanes JR, Scheiffele P, Takai Y, Umemori H, Verhage M, Yuzaki M, Zoghbi HY, Kawabe H, Craig AM. Luo L, et al. Among authors: rubenstein jlr. Neuron. 2020 Apr 8;106(1):37-65.e5. doi: 10.1016/j.neuron.2020.01.008. Epub 2020 Feb 5. Neuron. 2020. PMID: 32027825 Free PMC article.
Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism.
Miraoui H, Dwyer AA, Sykiotis GP, Plummer L, Chung W, Feng B, Beenken A, Clarke J, Pers TH, Dworzynski P, Keefe K, Niedziela M, Raivio T, Crowley WF Jr, Seminara SB, Quinton R, Hughes VA, Kumanov P, Young J, Yialamas MA, Hall JE, Van Vliet G, Chanoine JP, Rubenstein J, Mohammadi M, Tsai PS, Sidis Y, Lage K, Pitteloud N. Miraoui H, et al. Among authors: rubenstein j. Am J Hum Genet. 2013 May 2;92(5):725-43. doi: 10.1016/j.ajhg.2013.04.008. Am J Hum Genet. 2013. PMID: 23643382 Free PMC article.
Retroviral vectors.
Nicolas JF, Rubenstein JL. Nicolas JF, et al. Among authors: rubenstein jl. Biotechnology. 1988;10:493-513. doi: 10.1016/b978-0-409-90042-2.50031-3. Biotechnology. 1988. PMID: 3061522 Review. No abstract available.
Reply.
Omidvari AH, Lansdorp-Vogelaar I, Rubenstein JH. Omidvari AH, et al. Among authors: rubenstein jh. Gastroenterology. 2022 Jan;162(1):351-352. doi: 10.1053/j.gastro.2021.09.056. Epub 2021 Sep 28. Gastroenterology. 2022. PMID: 34597673 No abstract available.
1,049 results