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

Year Number of Results
1993 1
1994 3
1995 1
1996 1
1997 1
1998 1
1999 3
2000 2
2001 2
2002 3
2003 2
2004 3
2005 3
2006 5
2007 4
2008 8
2009 3
2010 6
2011 10
2012 5
2013 9
2014 6
2015 7
2016 5
2017 5
2018 8
2019 13
2020 17
2021 20
2022 16
2023 22
2024 7

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182 results

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Page 1
Long-read sequencing unravels the complexity of structural variants in PRKN in two individuals with early-onset Parkinson's disease.
Cogan G, Daida K, Billingsley KJ, Tesson C, Forlani S, Jornea L, Arnaud L, Tissier L, LeGuern E, Singleton AB, Ferrien M, Gervais Bernard H, Lesage S, Blauwendraat C, Brice A. Cogan G, et al. Among authors: billingsley kj. medRxiv [Preprint]. 2024 May 3:2024.05.02.24306523. doi: 10.1101/2024.05.02.24306523. medRxiv. 2024. PMID: 38746197 Free PMC article. Preprint.
Reasonable expansion of surgical candidates for HCC treatment.
Butensky SD, Billingsley KG, Khan SA. Butensky SD, et al. Among authors: billingsley kg. Clin Liver Dis (Hoboken). 2024 May 8;23(1):e0153. doi: 10.1097/CLD.0000000000000153. eCollection 2024 Jan-Jun. Clin Liver Dis (Hoboken). 2024. PMID: 38720794 Free PMC article.
Assessing methylation detection for primary human tissue using Nanopore sequencing.
Genner R, Akeson S, Meredith M, Jerez PA, Malik L, Baker B, Miano-Burkhardt A; CARD-long-read Team; Paten B, Billingsley KJ, Blauwendraat C, Jain M. Genner R, et al. Among authors: billingsley kj. bioRxiv [Preprint]. 2024 Mar 1:2024.02.29.581569. doi: 10.1101/2024.02.29.581569. bioRxiv. 2024. PMID: 38464144 Free PMC article. Preprint.
Insights into the mechanisms and structure of breakage-fusion-bridge cycles in cervical cancer using long-read sequencing.
Rodriguez I, Rossi NM, Keskus AG, Xie Y, Ahmad T, Bryant A, Lou H, Paredes JG, Milano R, Rao N, Tulsyan S, Boland JF, Luo W, Liu J, O'Hanlon T, Bess J, Mukhina V, Gaykalova D, Yuki Y, Malik L, Billingsley KJ, Blauwendraat C, Carrington M, Yeager M, Mirabello L, Kolmogorov M, Dean M. Rodriguez I, et al. Among authors: billingsley kj. Am J Hum Genet. 2024 Mar 7;111(3):544-561. doi: 10.1016/j.ajhg.2024.01.002. Epub 2024 Feb 1. Am J Hum Genet. 2024. PMID: 38307027
NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations.
Bandres-Ciga S, Faghri F, Majounie E, Koretsky MJ, Kim J, Levine KS, Leonard H, Makarious MB, Iwaki H, Crea PW, Hernandez DG, Arepalli S, Billingsley K, Lohmann K, Klein C, Lubbe SJ, Jabbari E, Saffie-Awad P, Narendra D, Reyes-Palomares A, Quinn JP, Schulte C, Morris HR, Traynor BJ, Scholz SW, Houlden H, Hardy J, Dumanis S, Riley E, Blauwendraat C, Singleton A, Nalls M, Jeff J, Vitale D. Bandres-Ciga S, et al. Among authors: billingsley k. medRxiv [Preprint]. 2023 Nov 14:2023.11.06.23298176. doi: 10.1101/2023.11.06.23298176. medRxiv. 2023. PMID: 37986980 Free PMC article. Preprint.
Long-Read Sequencing Resolves a Complex Structural Variant in PRKN Parkinson's Disease.
Daida K, Funayama M, Billingsley KJ, Malik L, Miano-Burkhardt A, Leonard HL, Makarious MB, Iwaki H, Ding J, Gibbs JR, Ishiguro M, Yoshino H, Ogaki K, Oyama G, Nishioka K, Nonaka R, Akamatsu W, Blauwendraat C, Hattori N. Daida K, et al. Among authors: billingsley kj. Mov Disord. 2023 Dec;38(12):2249-2257. doi: 10.1002/mds.29610. Epub 2023 Nov 5. Mov Disord. 2023. PMID: 37926948
Long-read sequencing resolves a complex structural variant in PRKN Parkinson's disease.
Daida K, Funayama M, Billingsley KJ, Malik L, Miano-Burkhardt A, Leonard HL, Makarious MB, Iwaki H, Ding J, Gibbs JR, Ishiguro M, Yoshino H, Ogaki K, Oyama G, Nishioka K, Nonaka R, Akamatsu W, Blauwendraat C, Hattori N. Daida K, et al. Among authors: billingsley kj. medRxiv [Preprint]. 2023 Aug 21:2023.08.14.23293948. doi: 10.1101/2023.08.14.23293948. medRxiv. 2023. PMID: 37790330 Free PMC article. Updated. Preprint.
182 results