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

Year Number of Results
1957 2
1959 1
1961 2
1964 1
1965 1
1967 1
1975 1
1976 1
1978 1
1981 1
1982 1
1984 1
1988 1
1989 2
1990 4
1991 2
1992 6
1993 6
1994 4
1995 5
1996 7
1997 8
1998 7
1999 3
2000 6
2001 2
2002 4
2003 5
2004 3
2005 3
2006 4
2007 4
2008 6
2009 7
2010 7
2011 5
2012 9
2013 15
2014 26
2015 25
2016 27
2017 33
2018 20
2019 29
2020 39
2021 29
2022 31
2023 27
2024 44
2025 35
2026 9

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466 results

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Page 1
Multi-ethnic genome-wide association study for atrial fibrillation.
Roselli C, Chaffin MD, Weng LC, Aeschbacher S, Ahlberg G, Albert CM, Almgren P, Alonso A, Anderson CD, Aragam KG, Arking DE, Barnard J, Bartz TM, Benjamin EJ, Bihlmeyer NA, Bis JC, Bloom HL, Boerwinkle E, Bottinger EB, Brody JA, Calkins H, Campbell A, Cappola TP, Carlquist J, Chasman DI, Chen LY, Chen YI, Choi EK, Choi SH, Christophersen IE, Chung MK, Cole JW, Conen D, Cook J, Crijns HJ, Cutler MJ, Damrauer SM, Daniels BR, Darbar D, Delgado G, Denny JC, Dichgans M, Dörr M, Dudink EA, Dudley SC, Esa N, Esko T, Eskola M, Fatkin D, Felix SB, Ford I, Franco OH, Geelhoed B, Grewal RP, Gudnason V, Guo X, Gupta N, Gustafsson S, Gutmann R, Hamsten A, Harris TB, Hayward C, Heckbert SR, Hernesniemi J, Hocking LJ, Hofman A, Horimoto ARVR, Huang J, Huang PL, Huffman J, Ingelsson E, Ipek EG, Ito K, Jimenez-Conde J, Johnson R, Jukema JW, Kääb S, Kähönen M, Kamatani Y, Kane JP, Kastrati A, Kathiresan S, Katschnig-Winter P, Kavousi M, Kessler T, Kietselaer BL, Kirchhof P, Kleber ME, Knight S, Krieger JE, Kubo M, Launer LJ, Laurikka J, Lehtimäki T, Leineweber K, Lemaitre RN, Li M, Lim HE, Lin HJ, Lin H, Lind L, Lindgren CM, Lokki ML, London B, Loos RJF, Low SK, Lu Y, Lyytikäinen LP, Macfarl… See abstract for full author list ➔ Roselli C, et al. Among authors: daniels br. Nat Genet. 2018 Jun 11;50(9):1225-1233. doi: 10.1038/s41588-018-0133-9. Nat Genet. 2018. PMID: 29892015 Free PMC article.
Detecting structural heart disease from electrocardiograms using AI.
Poterucha TJ, Jing L, Ricart RP, Adjei-Mosi M, Finer J, Hartzel D, Kelsey C, Long A, Rocha D, Ruhl JA, vanMaanen D, Probst MA, Daniels B, Joshi SD, Tastet O, Corbin D, Avram R, Barrios JP, Tison GH, Chiu IM, Ouyang D, Volodarskiy A, Castillo M, Roedan Oliver FA, Malta PP, Ye S, Rosner GF, Dizon JM, Ali SR, Liu Q, Bradley CK, Vaishnava P, Waksmonski CA, DeFilippis EM, Agarwal V, Lebehn M, Kampaktsis PN, Shames S, Beecy AN, Kumaraiah D, Homma S, Schwartz A, Hahn RT, Leon M, Einstein AJ, Maurer MS, Hartman HS, Hughes JW, Haggerty CM, Elias P. Poterucha TJ, et al. Among authors: daniels b. Nature. 2025 Aug;644(8075):221-230. doi: 10.1038/s41586-025-09227-0. Epub 2025 Jul 16. Nature. 2025. PMID: 40670798 Free PMC article.
Missense Variants in the Histone Acetyltransferase Complex Component Gene TRRAP Cause Autism and Syndromic Intellectual Disability.
Cogné B, Ehresmann S, Beauregard-Lacroix E, Rousseau J, Besnard T, Garcia T, Petrovski S, Avni S, McWalter K, Blackburn PR, Sanders SJ, Uguen K, Harris J, Cohen JS, Blyth M, Lehman A, Berg J, Li MH, Kini U, Joss S, von der Lippe C, Gordon CT, Humberson JB, Robak L, Scott DA, Sutton VR, Skraban CM, Johnston JJ, Poduri A, Nordenskjöld M, Shashi V, Gerkes EH, Bongers EMHF, Gilissen C, Zarate YA, Kvarnung M, Lally KP, Kulch PA, Daniels B, Hernandez-Garcia A, Stong N, McGaughran J, Retterer K, Tveten K, Sullivan J, Geisheker MR, Stray-Pedersen A, Tarpinian JM, Klee EW, Sapp JC, Zyskind J, Holla ØL, Bedoukian E, Filippini F, Guimier A, Picard A, Busk ØL, Punetha J, Pfundt R, Lindstrand A, Nordgren A, Kalb F, Desai M, Ebanks AH, Jhangiani SN, Dewan T, Coban Akdemir ZH, Telegrafi A, Zackai EH, Begtrup A, Song X, Toutain A, Wentzensen IM, Odent S, Bonneau D, Latypova X, Deb W; CAUSES Study; Redon S, Bilan F, Legendre M, Troyer C, Whitlock K, Caluseriu O, Murphree MI, Pichurin PN, Agre K, Gavrilova R, Rinne T, Park M, Shain C, Heinzen EL, Xiao R, Amiel J, Lyonnet S, Isidor B, Biesecker LG, Lowenstein D, Posey JE, Denommé-Pichon AS; Deciphering Developmental Disorders study; Férec C, … See abstract for full author list ➔ Cogné B, et al. Among authors: daniels b. Am J Hum Genet. 2019 Mar 7;104(3):530-541. doi: 10.1016/j.ajhg.2019.01.010. Epub 2019 Feb 28. Am J Hum Genet. 2019. PMID: 30827496 Free PMC article.
Drug induced pseudolymphoma.
Magro CM, Daniels BH, Crowson AN. Magro CM, et al. Among authors: daniels bh. Semin Diagn Pathol. 2018 Jul;35(4):247-259. doi: 10.1053/j.semdp.2017.11.003. Epub 2018 Feb 1. Semin Diagn Pathol. 2018. PMID: 29361381 Review.
Systems neuroimmunology: current bottlenecks, research priorities and future directions.
Iyer H, Benoist C, Bilbo SD, Boulanger LM, Burton MD, Daniels BP, Deczkowska A, Flajnik MF, Gareau MG, Grace PM, Irazoqui JE, Rosi S, Salinas I, Schaefer A, Sokol CL, Williams DW, Klein RS. Iyer H, et al. Among authors: daniels bp. Nat Immunol. 2025 Mar;26(3):325-329. doi: 10.1038/s41590-025-02092-z. Nat Immunol. 2025. PMID: 39939753 Free PMC article.
Quantifying collectivity.
Daniels BC, Ellison CJ, Krakauer DC, Flack JC. Daniels BC, et al. Curr Opin Neurobiol. 2016 Apr;37:106-113. doi: 10.1016/j.conb.2016.01.012. Epub 2016 Feb 12. Curr Opin Neurobiol. 2016. PMID: 26874472 Free article. Review.
Naturally Occurring Lumazines.
Daniels BJ, Li FF, Furkert DP, Brimble MA. Daniels BJ, et al. J Nat Prod. 2019 Jul 26;82(7):2054-2065. doi: 10.1021/acs.jnatprod.9b00351. Epub 2019 Jul 18. J Nat Prod. 2019. PMID: 31317731 Review.
466 results