Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
2002 12
2003 16
2004 9
2005 10
2006 7
2007 10
2008 17
2009 9
2010 14
2011 10
2012 8
2013 9
2014 5
2015 12
2016 4
2017 3
2018 4
2019 7
2020 8
2021 5
2022 5
2023 2
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

168 results

Results by year

Filters applied: . Clear all
Page 1
Complement factor H polymorphism in age-related macular degeneration.
Klein RJ, Zeiss C, Chew EY, Tsai JY, Sackler RS, Haynes C, Henning AK, SanGiovanni JP, Mane SM, Mayne ST, Bracken MB, Ferris FL, Ott J, Barnstable C, Hoh J. Klein RJ, et al. Among authors: ott j. Science. 2005 Apr 15;308(5720):385-9. doi: 10.1126/science.1109557. Epub 2005 Mar 10. Science. 2005. PMID: 15761122 Free PMC article.
Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations.
Liu D, Meyer D, Fennessy B, Feng C, Cheng E, Johnson JS, Park YJ, Rieder MK, Ascolillo S, de Pins A, Dobbyn A, Lebovitch D, Moya E, Nguyen TH, Wilkins L, Hassan A; Psychiatric Genomics Consortium Phase 3 Targeted Sequencing of Schizophrenia Study Team; Burdick KE, Buxbaum JD, Domenici E, Frangou S, Hartmann AM, Laurent-Levinson C, Malhotra D, Pato CN, Pato MT, Ressler K, Roussos P, Rujescu D, Arango C, Bertolino A, Blasi G, Bocchio-Chiavetto L, Campion D, Carr V, Fullerton JM, Gennarelli M, González-Peñas J, Levinson DF, Mowry B, Nimgaokar VL, Pergola G, Rampino A, Cervilla JA, Rivera M, Schwab SG, Wildenauer DB, Daly M, Neale B, Singh T, O'Donovan MC, Owen MJ, Walters JT, Ayub M, Malhotra AK, Lencz T, Sullivan PF, Sklar P, Stahl EA, Huckins LM, Charney AW. Liu D, et al. Nat Genet. 2023 Mar;55(3):369-376. doi: 10.1038/s41588-023-01305-1. Epub 2023 Mar 13. Nat Genet. 2023. PMID: 36914870 Free PMC article.
Population genetics: past, present, and future.
Okazaki A, Yamazaki S, Inoue I, Ott J. Okazaki A, et al. Among authors: ott j. Hum Genet. 2021 Feb;140(2):231-240. doi: 10.1007/s00439-020-02208-5. Epub 2020 Jul 18. Hum Genet. 2021. PMID: 32683493 Free PMC article. Review.
Machine learning approaches to explore digenic inheritance.
Okazaki A, Ott J. Okazaki A, et al. Among authors: ott j. Trends Genet. 2022 Oct;38(10):1013-1018. doi: 10.1016/j.tig.2022.04.009. Epub 2022 May 14. Trends Genet. 2022. PMID: 35581032 Free article. Review.
Overview of frequent pattern mining.
Ott J, Park T. Ott J, et al. Genomics Inform. 2022 Dec;20(4):e39. doi: 10.5808/gi.22074. Epub 2022 Dec 30. Genomics Inform. 2022. PMID: 36617647 Free PMC article.
Genetic linkage studies in alopecia areata.
Martinez-Mir A, Zlotogorski A, Ott J, Gordon D, Christiano AM. Martinez-Mir A, et al. Among authors: ott j. J Investig Dermatol Symp Proc. 2003 Oct;8(2):199-203. doi: 10.1046/j.1087-0024.2003.00809.x. J Investig Dermatol Symp Proc. 2003. PMID: 14582673 Free article. Review.
Heterozygosity mapping for human dominant trait variants.
Imai-Okazaki A, Li Y, Horpaopan S, Riazalhosseini Y, Garshasbi M, Mosse YP, Zhang D, Schrauwen I, Sharma A, Fann CSJ, Leal SM, Lathrop M, Ott J. Imai-Okazaki A, et al. Among authors: ott j. Hum Mutat. 2019 Jul;40(7):996-1004. doi: 10.1002/humu.23765. Epub 2019 Apr 24. Hum Mutat. 2019. PMID: 31018026 Free PMC article.
168 results