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

Year Number of Results
1946 3
1947 3
1948 7
1949 6
1951 2
1952 3
1953 2
1954 3
1955 3
1956 3
1957 3
1958 9
1959 3
1960 1
1961 3
1962 8
1963 16
1964 14
1965 10
1966 21
1967 156
1968 365
1969 398
1970 419
1971 599
1972 659
1973 759
1974 1036
1975 912
1976 739
1977 663
1978 511
1979 512
1980 493
1981 466
1982 617
1983 533
1984 543
1985 541
1986 527
1987 575
1988 609
1989 607
1990 648
1991 741
1992 732
1993 794
1994 846
1995 837
1996 765
1997 882
1998 1254
1999 1206
2000 1526
2001 1751
2002 1563
2003 1637
2004 1665
2005 1687
2006 1719
2007 1826
2008 1971
2009 1749
2010 1943
2011 2046
2012 2228
2013 2340
2014 2280
2015 2497
2016 2680
2017 2263
2018 2175
2019 2353
2020 2175
2021 1911
2022 1131
2023 755
2024 1386
2025 1362
2026 7

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64,954 results

Results by year

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Page 1
Machine learning-based penetrance of genetic variants.
Forrest IS, Vy HMT, Rocheleau G, Jordan DM, Petrazzini BO, Nadkarni GN, Cho JH, Ganapathi M, Huang KL, Chung WK, Do R. Forrest IS, et al. Science. 2025 Aug 28;389(6763):eadm7066. doi: 10.1126/science.adm7066. Epub 2025 Aug 28. Science. 2025. PMID: 40875860
The Psychiatric Genomics Consortium: discoveries and directions.
Agrawal A, Bulik CM, Abebe DS, Andreassen OA, Atkinson EG, Choi KW, Corvin A, Davies HL, Davis LK, Docherty AR, Edenberg HJ, Franke B, Gelernter J, Giusti-Rodríguez P, Hettema JM, Hjerling-Leffler J, Huang H, Johnson EC, Lewis CM, Lu Y, Lynall ME, Martin J, McIntosh AM, Montalvo-Ortiz JL, Mullins N, Nievergelt CM, O'Connell KS, O'Donovan MC, Okewole A, Peterson RE, Posthuma D, Sebat J, Smoller JW, Sud R, Viswanath B, Walters JTR, Won H, Wray NR, Sullivan PF; Coordinating Committee of the Psychiatric Genomics Consortium. Agrawal A, et al. Lancet Psychiatry. 2025 Aug;12(8):600-610. doi: 10.1016/S2215-0366(25)00124-5. Epub 2025 Jun 26. Lancet Psychiatry. 2025. PMID: 40582370 Review.
Fine-mapping genomic loci refines bipolar disorder risk genes.
Koromina M, Ravi A, Panagiotaropoulou G, Schilder BM, Humphrey J, Braun A, Bigdeli T, Chatzinakos C, Coombes BJ, Kim J, Liu X, Terao C, O'Connell KS, Adams MJ, Adolfsson R, Alda M, Alfredsson L, Andlauer TFM, Andreassen OA, Antoniou A, Baune BT, Bengesser S, Biernacka J, Boehnke M, Bosch R, Cairns MJ, Carr VJ, Casas M, Catts S, Cichon S, Corvin A, Craddock N, Dafnas K, Dalkner N, Dannlowski U, Degenhardt F, Di Florio A, Dikeos D, Fellendorf FT, Ferentinos P, Forstner AJ, Forty L, Frye M, Fullerton JM, Gawlik M, Gizer IR, Gordon-Smith K, Green MJ, Grigoroiu-Serbanescu M, Guzman-Parra J, Hahn T, Henskens F, Hillert J, Jablensky AV, Jones L, Jones I, Jonsson L, Kelsoe JR, Kircher T, Kirov G, Kittel-Schneider S, Kogevinas M, Landén M, Leboyer M, Lenger M, Lissowska J, Lochner C, Loughland C, MacIntyre DJ, Martin NG, Maratou E, Mathews CA, Mayoral F, McElroy SL, McGregor NW, McIntosh A, McQuillin A, Michie P, Mitchell PB, Moutsatsou P, Mowry B, Müller-Myhsok B, Myers RM, Nenadić I, Nievergelt CM, Nöthen MM, Nurnberger J, 'Donovan MO, 'Donovan CO, Ophoff RA, Owen MJ, Pantelis C, Pato C, Pato MT, Patrinos GP, Pawlak JM, Perlis RH, Porichi E, Posthuma D, Ramos-Quiroga JA, Reif A, Reiningh… See abstract for full author list ➔ Koromina M, et al. Nat Neurosci. 2025 Jul;28(7):1393-1403. doi: 10.1038/s41593-025-01998-z. Epub 2025 Jun 25. Nat Neurosci. 2025. PMID: 40562893 Free PMC article.
AAV gene therapy for autosomal recessive deafness 9: a single-arm trial.
Qi J, Zhang L, Lu L, Tan F, Cheng C, Lu Y, Dong W, Zhou Y, Fu X, Jiang L, Tan C, Zhang S, Sun S, Song H, Duan M, Zha D, Sun Y, Gao X, Xu L, Zeng FG, Chai R. Qi J, et al. Nat Med. 2025 Sep;31(9):2917-2926. doi: 10.1038/s41591-025-03773-w. Epub 2025 Jul 2. Nat Med. 2025. PMID: 40603731 Clinical Trial.
Transferability of European-derived Alzheimer's disease polygenic risk scores across multiancestry populations.
Nicolas A, Sherva R, Grenier-Boley B, Kim Y, Kikuchi M, Timsina J, de Rojas I, Dalmasso MC, Zhou X, Le Guen Y, Arboleda-Bustos CE, Camargos Bicalho MA, Guerchet M, van der Lee S, Goss M, Castillo A, Bellenguez C, Küçükali F, Satizabal CL, Fongang B, Yang Q, Peters O, Schneider A, Dichgans M, Rujescu D, Scherbaum N, Deckert J, Riedel-Heller S, Hausner L, Molina-Porcel L, Düzel E, Grimmer T, Wiltfang J, Heilmann-Heimbach S, Moebus S, Tegos T, Scarmeas N, Dols-Icardo O, Moreno F, Pérez-Tur J, Bullido MJ, Pastor P, Sánchez-Valle R, Álvarez V, Cao H, Ip NY, Fu AKY, Ip FCF, Olivar N, Muchnik C, Cuesta C, Campanelli L, Solis P, Politis DG, Kochen S, Brusco LI, Boada M, García-González P, Puerta R, Mir P, Real LM, Piñol-Ripoll G, García-Alberca JM, Royo JL, Rodriguez-Rodriguez E, Soininen H, Heikkinen S, de Mendonça A, Mehrabian S, Traykov L, Hort J, Vyhnalek M, Rasmussen KL, Thomassen JQ, Pijnenburg YAL, Holstege H, van Swieten JC, Seelaar H, Claassen JAHR, Jansen WJ, Ramakers I, Verhey F, van der Lugt A, Scheltens P, Ortega-Rojas J, Concha Mera AG, Mahecha MF, Pardo R, Arboleda G, Bahrami S, Fominykh V, Selbæk G, Graff C, Papenberg G, Giedraitis V, Boland A, Deleuze JF, de Marco LA, de … See abstract for full author list ➔ Nicolas A, et al. Nat Genet. 2025 Jul;57(7):1598-1610. doi: 10.1038/s41588-025-02227-w. Epub 2025 Jun 18. Nat Genet. 2025. PMID: 40533518 Free PMC article.
Monoallelic mutations in MMD2 cause autosomal dominant aggressive periodontitis.
Iwata T, Mizoguchi Y, Yoshimoto T, Tsumura M, Sakura F, Johnson JR, Matsuda S, Ouhara K, Nagatani Y, Asano T, Ohnishi H, Kato Z, Mihara K, Kanegane H, Ueda T, Sasaki S, Taniguchi Y, Ninomiya Y, Ohno Y, Suzuki-Takedachi K, Sotomaru Y, Sakuma T, Yamamoto T, Matsuda Y, Kume K, Sanui T, Nishimura F, Kajiya M, Ueki Y, Kurihara H, Morino H, Okada S, Kawakami H, Mizuno N. Iwata T, et al. J Exp Med. 2025 Sep 1;222(9):e20231911. doi: 10.1084/jem.20231911. Epub 2025 Jul 15. J Exp Med. 2025. PMID: 40663042 Free PMC article.
Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers.
Wouters M, Ehlers L, Van Eynde W, Kars ME, Delafontaine S, Kienapfel V, Dzhus M, Schrijvers R, De Haes P, Struyf S, Bucciol G, Itan Y, Bolze A, Voet A, Hombrouck A, Moens L, Ogunjimi B, Meyts I. Wouters M, et al. J Exp Med. 2025 Nov 3;222(11):e20250499. doi: 10.1084/jem.20250499. Epub 2025 Aug 27. J Exp Med. 2025. PMID: 40864493 Free PMC article.
Pleiotropic and sex-specific genetic mechanisms of circulating metabolic markers.
van der Meer D, Rahman Z, Ottas A, Parekh P, Kutrolli G, Stinson SE, Koromina M, Rokicki J, Sønderby IE, Parker N, Tesfaye M, Hindley G, Rødevand LN, Koch E; Estonian Biobank Research Team; Steen NE, Berg JP, O'Connell KS, Smeland OB, Frei O, Dale AM, Djurovic S, Lehto K, Alver M, Milani L, Shadrin AA, Andreassen OA. van der Meer D, et al. Nat Commun. 2025 May 28;16(1):4961. doi: 10.1038/s41467-025-60058-z. Nat Commun. 2025. PMID: 40436851 Free PMC article.
64,954 results
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