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

Year Number of Results
1992 3
1993 2
1994 1
1995 5
1996 5
1997 5
1998 6
1999 5
2000 3
2001 1
2002 5
2003 2
2004 4
2005 4
2006 5
2007 3
2008 3
2009 4
2010 4
2011 5
2012 4
2013 2
2014 5
2015 3
2016 4
2017 4
2018 3
2019 3
2020 7
2021 7
2022 5
2023 5
2024 4

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125 results

Results by year

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Page 1
Creation of bladder assembloids mimicking tissue regeneration and cancer.
Kim E, Choi S, Kang B, Kong J, Kim Y, Yoon WH, Lee HR, Kim S, Kim HM, Lee H, Yang C, Lee YJ, Kang M, Roh TY, Jung S, Kim S, Ku JH, Shin K. Kim E, et al. Among authors: yoon wh. Nature. 2020 Dec;588(7839):664-669. doi: 10.1038/s41586-020-3034-x. Epub 2020 Dec 16. Nature. 2020. PMID: 33328632
Autistic Perspectives on the Future of Clinical Autism Research.
Pukki H, Bettin J, Outlaw AG, Hennessy J, Brook K, Dekker M, Doherty M, Shaw SCK, Bervoets J, Rudolph S, Corneloup T, Derwent K, Lee O, Rojas YG, Lawson W, Gutierrez MV, Petek K, Tsiakkirou M, Suoninen A, Minchin J, Döhle R, Lipinski S, Natri H, Reardon E, Estrada GV, Platon O, Chown N, Satsuki A, Milton D, Walker N, Roldan O, Herrán B, Cañedo CL, McCowan S, Johnson M, Turner EJ, Lammers J, Yoon WH. Pukki H, et al. Among authors: yoon wh. Autism Adulthood. 2022 Jun 1;4(2):93-101. doi: 10.1089/aut.2022.0017. Epub 2022 Jun 9. Autism Adulthood. 2022. PMID: 36601072 Free PMC article. No abstract available.
A mitocentric view of Parkinson's disease.
Haelterman NA, Yoon WH, Sandoval H, Jaiswal M, Shulman JM, Bellen HJ. Haelterman NA, et al. Among authors: yoon wh. Annu Rev Neurosci. 2014;37:137-59. doi: 10.1146/annurev-neuro-071013-014317. Epub 2014 May 5. Annu Rev Neurosci. 2014. PMID: 24821430 Free PMC article. Review.
Bi-allelic variants in OGDHL cause a neurodevelopmental spectrum disease featuring epilepsy, hearing loss, visual impairment, and ataxia.
Yap ZY, Efthymiou S, Seiffert S, Vargas Parra K, Lee S, Nasca A, Maroofian R, Schrauwen I, Pendziwiat M, Jung S, Bhoj E, Striano P, Mankad K, Vona B, Cuddapah S, Wagner A, Alvi JR, Davoudi-Dehaghani E, Fallah MS, Gannavarapu S, Lamperti C, Legati A, Murtaza BN, Nadeem MS, Rehman MU, Saeidi K, Salpietro V, von Spiczak S, Sandoval A, Zeinali S, Zeviani M, Reich A; SYNaPS Study Group; University of Washington Center for Mendelian Genomics; Jang C, Helbig I, Barakat TS, Ghezzi D, Leal SM, Weber Y, Houlden H, Yoon WH. Yap ZY, et al. Among authors: yoon wh. Am J Hum Genet. 2021 Dec 2;108(12):2368-2384. doi: 10.1016/j.ajhg.2021.11.003. Epub 2021 Nov 19. Am J Hum Genet. 2021. PMID: 34800363 Free PMC article.
Elevated cholesterol in ATAD3 mutants is a compensatory mechanism that leads to membrane cholesterol aggregation.
Muñoz-Oreja M, Sandoval A, Bruland O, Perez-Rodriguez D, Fernandez-Pelayo U, de Arbina AL, Villar-Fernandez M, Hernández-Eguiazu H, Hernández I, Park Y, Goicoechea L, Pascual-Frías N, Garcia-Ruiz C, Fernandez-Checa J, Martí-Carrera I, Gil-Bea FJ, Hasan MT, Gegg ME, Bredrup C, Knappskog PM, Gereñu-Lopetegui G, Varhaug KN, Bindoff LA, Spinazzola A, Yoon WH, Holt IJ. Muñoz-Oreja M, et al. Among authors: yoon wh. Brain. 2024 Jan 18:awae018. doi: 10.1093/brain/awae018. Online ahead of print. Brain. 2024. PMID: 38242545
Biallelic variants in OGDH encoding oxoglutarate dehydrogenase lead to a neurodevelopmental disorder characterized by global developmental delay, movement disorder, and metabolic abnormalities.
Whittle EF, Chilian M, Karimiani EG, Progri H, Buhas D, Kose M, Ganetzky RD, Toosi MB, Torbati PN, Badv RS, Shelihan I, Yang H, Elloumi HZ, Lee S, Jamshidi Y, Pittman AM, Houlden H, Ignatius E, Rahman S, Maroofian R, Yoon WH, Carroll CJ. Whittle EF, et al. Among authors: yoon wh. Genet Med. 2023 Feb;25(2):100332. doi: 10.1016/j.gim.2022.11.001. Epub 2022 Dec 15. Genet Med. 2023. PMID: 36520152 Free PMC article.
Clonally Selected Lines After CRISPR-Cas Editing Are Not Isogenic.
Panda A, Suvakov M, Mariani J, Drucker KL, Park Y, Jang Y, Kollmeyer TM, Sarkar G, Bae T, Kim JJ, Yoon WH, Jenkins RB, Vaccarino FM, Abyzov A. Panda A, et al. Among authors: yoon wh. CRISPR J. 2023 Apr;6(2):176-182. doi: 10.1089/crispr.2022.0050. CRISPR J. 2023. PMID: 37071670 Free PMC article.
125 results