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

Year Number of Results
1989 1
1992 5
1993 6
1994 7
1995 6
1996 5
1997 3
1998 7
1999 6
2001 5
2002 5
2003 3
2004 3
2005 3
2006 1
2007 1
2009 2
2010 1
2011 3
2012 4
2013 14
2014 5
2015 4
2016 2
2017 5
2018 3
2019 5
2020 3
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2022 5
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2024 4
2025 2
2026 2

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127 results

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Page 1
Comparison of variant callers using 60 532 multi-ancestry whole genome sequences.
Zhou H, Li Z, Shyr D, Li X, Yang H, Dey R, Tang Y, Maier R, Boerwinkle E, Buyske S, Daly M, Felsenfeld A, Gibbs RA, Gupta N, Hall IM, Matise T, Metcalf GA, Smith A, Reeves C, Sofia HJ, Stitziel NO, Zody MC; NHGRI Genome Sequencing Program (GSP) Consortium; Neale B, Lin X. Zhou H, et al. Among authors: matise t. Brief Bioinform. 2026 Mar 1;27(2):bbag130. doi: 10.1093/bib/bbag130. Brief Bioinform. 2026. PMID: 41894165 Free PMC article.
Epigenetic mechanisms underlying variation of IL-6, a well-established inflammation biomarker and risk factor for cardiovascular disease.
Lundin JI, Peters U, Hu Y, Ammous F, Benjamin EJ, Bis JC, Brody JA, Cushman M, Fuller H, Gignoux C, Guo X, Haessler J, Haiman C, Joehanes R, Kasela S, Kenny E, Lappalainen T, Levy D, Liu C, Liu Y, Loos RJF, Matise T, North KE, Park SL, Ratliff SM, Reiner A, Rich SS, Rotter JI, Smith JA, Sotoodehnia N, Tracy R, Van den Berg D, Ye T, Zhao W, Raffield LM, Kooperberg C; PAGE Study. Lundin JI, et al. Among authors: matise t. Atherosclerosis. 2025 Aug;407:120219. doi: 10.1016/j.atherosclerosis.2025.120219. Epub 2025 May 20. Atherosclerosis. 2025. PMID: 40480020 Free PMC article.
Alterations in DNA Methylation, Proteomic, and Metabolomic Profiles in African Ancestry Populations with APOL1 Risk Alleles.
Zhang X, Scadden AW, Marthi A, Buchanan VL, Qu Y, Ferrier KR, Chen BD, Graff M, Avila J, Boerwinkle E, Buyske S, Clish CB, Cruz D, Fornage M, Gerzsten RE, Gignoux CR, Glover L, Hou L, Justice AE, Kooperberg C, Kramer H, Lange L, Loos RJF, Matise T, Mychaleckyj JC, Olabisi OA, Peters U, Raffield LM, Reiner AP, Rich SS, Rotter JI, Taylor KD, Yu B, Zheng Y, North KE, Mottl AK, Highland HM, Stanislawski MA. Zhang X, et al. Among authors: matise t. J Am Soc Nephrol. 2025 Apr 7;36(8):1490-1504. doi: 10.1681/ASN.0000000688. J Am Soc Nephrol. 2025. PMID: 40193202
Identification of proteins associated with type 2 diabetes risk in diverse racial and ethnic populations.
Liu S, Zhu J, Zhong H, Wu C, Xue H, Darst BF, Guo X, Durda P, Tracy RP, Liu Y, Johnson WC, Taylor KD, Manichaikul AW, Goodarzi MO, Gerszten RE, Clish CB, Chen YI, Highland H, Haiman CA, Gignoux CR, Lange L, Conti DV, Raffield LM, Wilkens L, Marchand LL, North KE, Young KL, Loos RJ, Buyske S, Matise T, Peters U, Kooperberg C, Reiner AP, Yu B, Boerwinkle E, Sun Q, Rooney MR, Echouffo-Tcheugui JB, Daviglus ML, Qi Q, Mancuso N, Li C, Deng Y, Manning A, Meigs JB, Rich SS, Rotter JI, Wu L. Liu S, et al. Among authors: matise t. Diabetologia. 2024 Dec;67(12):2754-2770. doi: 10.1007/s00125-024-06277-3. Epub 2024 Sep 30. Diabetologia. 2024. PMID: 39349773 Free PMC article.
Semi-supervised machine learning method for predicting homogeneous ancestry groups to assess Hardy-Weinberg equilibrium in diverse whole-genome sequencing studies.
Shyr D, Dey R, Li X, Zhou H, Boerwinkle E, Buyske S, Daly M, Gibbs RA, Hall I, Matise T, Reeves C, Stitziel NO, Zody M, Neale BM, Lin X. Shyr D, et al. Among authors: matise t. Am J Hum Genet. 2024 Oct 3;111(10):2129-2138. doi: 10.1016/j.ajhg.2024.08.018. Epub 2024 Sep 12. Am J Hum Genet. 2024. PMID: 39270648 Free PMC article.
Methylation patterns associated with C-reactive protein in racially and ethnically diverse populations.
Lundin JI, Peters U, Hu Y, Ammous F, Avery CL, Benjamin EJ, Bis JC, Brody JA, Carlson C, Cushman M, Gignoux C, Guo X, Haessler J, Haiman C, Joehanes R, Kasela S, Kenny E, Lapalainien T, Levy D, Liu C, Liu Y, Loos RJF, Lu A, Matise T, North KE, Park SL, Ratliff SM, Reiner A, Rich SS, Rotter JI, Smith JA, Sotoodehnia N, Tracy R, Van den Berg D, Xu H, Ye T, Zhao W, Raffield LM, Kooperberg C; PAGE Study. Lundin JI, et al. Among authors: matise t. Epigenetics. 2024 Dec;19(1):2333668. doi: 10.1080/15592294.2024.2333668. Epub 2024 Apr 3. Epigenetics. 2024. PMID: 38571307 Free PMC article.
FAVOR: functional annotation of variants online resource and annotator for variation across the human genome.
Zhou H, Arapoglou T, Li X, Li Z, Zheng X, Moore J, Asok A, Kumar S, Blue EE, Buyske S, Cox N, Felsenfeld A, Gerstein M, Kenny E, Li B, Matise T, Philippakis A, Rehm HL, Sofia HJ, Snyder G; NHGRI Genome Sequencing Program Variant Functional Annotation Working Group; Weng Z, Neale B, Sunyaev SR, Lin X. Zhou H, et al. Among authors: matise t. Nucleic Acids Res. 2023 Jan 6;51(D1):D1300-D1311. doi: 10.1093/nar/gkac966. Nucleic Acids Res. 2023. PMID: 36350676 Free PMC article.
Genome-Wide Epistatic Interaction between DEF1B and APOL1 High-Risk Genotypes for Chronic Kidney Disease.
Vy HMT, Lin BM, Gulamali FF, Kooperberg C, Graff M, Wong J, Campbell KN, Matise TC, Coresh J, Thomas F, Reiner AP, Nassir R, Schnatz PF, Johns T, Buyske S, Haiman C, Cooper R, Loos RJF, Horowitz CR, Gutierrez OM, Do R, Franceschini N, Nadkarni GN. Vy HMT, et al. Among authors: matise tc. Clin J Am Soc Nephrol. 2022 Oct;17(10):1522-1525. doi: 10.2215/CJN.03610322. Epub 2022 Aug 10. Clin J Am Soc Nephrol. 2022. PMID: 35948364 Free PMC article. No abstract available.
127 results