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Year Number of Results
1967 2
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1976 3
1977 2
1978 1
1979 1
1981 1
1983 4
1984 2
1985 4
1986 4
1987 3
1988 2
1989 1
1990 4
1991 2
1993 1
1995 2
1996 1
1997 1
1999 4
2000 7
2001 27
2002 30
2003 25
2004 23
2005 24
2006 22
2007 23
2008 21
2009 20
2010 23
2011 28
2012 33
2013 22
2014 17
2015 23
2016 16
2017 13
2018 16
2019 21
2020 26
2021 13
2022 13
2023 11
2024 15
2025 9

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549 results

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Page 1
Genomic architecture of autism from comprehensive whole-genome sequence annotation.
Trost B, Thiruvahindrapuram B, Chan AJS, Engchuan W, Higginbotham EJ, Howe JL, Loureiro LO, Reuter MS, Roshandel D, Whitney J, Zarrei M, Bookman M, Somerville C, Shaath R, Abdi M, Aliyev E, Patel RV, Nalpathamkalam T, Pellecchia G, Hamdan O, Kaur G, Wang Z, MacDonald JR, Wei J, Sung WWL, Lamoureux S, Hoang N, Selvanayagam T, Deflaux N, Geng M, Ghaffari S, Bates J, Young EJ, Ding Q, Shum C, D'Abate L, Bradley CA, Rutherford A, Aguda V, Apresto B, Chen N, Desai S, Du X, Fong MLY, Pullenayegum S, Samler K, Wang T, Ho K, Paton T, Pereira SL, Herbrick JA, Wintle RF, Fuerth J, Noppornpitak J, Ward H, Magee P, Al Baz A, Kajendirarajah U, Kapadia S, Vlasblom J, Valluri M, Green J, Seifer V, Quirbach M, Rennie O, Kelley E, Masjedi N, Lord C, Szego MJ, Zawati MH, Lang M, Strug LJ, Marshall CR, Costain G, Calli K, Iaboni A, Yusuf A, Ambrozewicz P, Gallagher L, Amaral DG, Brian J, Elsabbagh M, Georgiades S, Messinger DS, Ozonoff S, Sebat J, Sjaarda C, Smith IM, Szatmari P, Zwaigenbaum L, Kushki A, Frazier TW, Vorstman JAS, Fakhro KA, Fernandez BA, Lewis MES, Weksberg R, Fiume M, Yuen RKC, Anagnostou E, Sondheimer N, Glazer D, Hartley DM, Scherer SW. Trost B, et al. Cell. 2022 Nov 10;185(23):4409-4427.e18. doi: 10.1016/j.cell.2022.10.009. Cell. 2022. PMID: 36368308 Free PMC article.
Neuron-specific protein network mapping of autism risk genes identifies shared biological mechanisms and disease-relevant pathologies.
Murtaza N, Cheng AA, Brown CO, Meka DP, Hong S, Uy JA, El-Hajjar J, Pipko N, Unda BK, Schwanke B, Xing S, Thiruvahindrapuram B, Engchuan W, Trost B, Deneault E, Calderon de Anda F, Doble BW, Ellis J, Anagnostou E, Bader GD, Scherer SW, Lu Y, Singh KK. Murtaza N, et al. Among authors: trost b. Cell Rep. 2022 Nov 22;41(8):111678. doi: 10.1016/j.celrep.2022.111678. Cell Rep. 2022. PMID: 36417873 Free article.
Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsy.
Fehlings DL, Zarrei M, Engchuan W, Sondheimer N, Thiruvahindrapuram B, MacDonald JR, Higginbotham EJ, Thapa R, Behlim T, Aimola S, Switzer L, Ng P, Wei J, Danthi PS, Pellecchia G, Lamoureux S, Ho K, Pereira SL, de Rijke J, Sung WWL, Mowjoodi A, Howe JL, Nalpathamkalam T, Manshaei R, Ghaffari S, Whitney J, Patel RV, Hamdan O, Shaath R, Trost B, Knights S, Samdup D, McCormick A, Hunt C, Kirton A, Kawamura A, Mesterman R, Gorter JW, Dlamini N, Merico D, Hilali M, Hirschfeld K, Grover K, Bautista NX, Han K, Marshall CR, Yuen RKC, Subbarao P, Azad MB, Turvey SE, Mandhane P, Moraes TJ, Simons E, Maxwell G, Shevell M, Costain G, Michaud JL, Hamdan FF, Gauthier J, Uguen K, Stavropoulos DJ, Wintle RF, Oskoui M, Scherer SW. Fehlings DL, et al. Among authors: trost b. Nat Genet. 2024 Apr;56(4):585-594. doi: 10.1038/s41588-024-01686-x. Epub 2024 Mar 29. Nat Genet. 2024. PMID: 38553553
Asymmetric Catalysis.
Halpern J, Trost BM. Halpern J, et al. Among authors: trost bm. Proc Natl Acad Sci U S A. 2004 Apr 13;101(15):5347. doi: 10.1073/pnas.0401811101. Proc Natl Acad Sci U S A. 2004. PMID: 15082833 Free PMC article. No abstract available.
Assigning Targetable Molecular Pathways to Transdiagnostic Subgroups Across Autism and Related Neurodevelopmental Disorders.
Ellegood J, Beauchamp A, Yee Y, Devenyi G, Ziolkowski J, Qiu L, Askalan R, Ayub M, Suetterlin P, Donovan A, Basson MA, Quesnel KM, Berube NG, Woo T, Beversdorf D, Bjornsson H, Blakely R, Crawley J, Crosbie J, Orr BO, Davis GW, Genestine M, DiCicco-Bloom E, Egan S, Fink KD, Asbury S, Lai J, Rilett K, Foster JA, Vincent JB, Frankland P, Georgiades S, Penagarikano O, Geschwind D, Giger RJ, Markx S, Gogos J, Golzio C, Pagani M, Gozzi A, Pacey LK, Hampson D, Huang TN, Yen TL, Hsueh YP, Iaboni A, Amar M, Iakoucheva LM, Jones JK, Kelly E, Kieffer B, Bae M, Jung H, Kim H, Park H, Roh JD, Kim E, Konopka G, Laliberte C, Lefebvre JL, Eagleson K, Levitt P, Bach AM, Cunningham TJ, Fisher E, Miller K, Mills A, Muotri A, Nicolson R, Noakes LS, Nieman BJ, Canales CP, Nord AS, Nutter LM, Tam E, Osborne LR, Clipperton-Allen A, Page D, Babineau B, Palmer TD, Yan K, Picketts D, Xia Q, Powell CM, Raznahan A, Robins DM, Rumbaugh G, Sengar AS, Salter MW, Schachar RJ, D'Abate L, Bradley CA, Scherer SW, Copping NW, Petkova SP, Silverman JL, Singh KK, Kim NS, Yoon KK, Ming GL, Song H, Spring S, Nakatani J, Nakai N, Nomura J, Takumi T, Taylor M, Tsai P, Bruce M, Jones KL, Van de Water J, Van Eede MC, Kerr T… See abstract for full author list ➔ Ellegood J, et al. Among authors: trost b. bioRxiv [Preprint]. 2025 Mar 8:2025.03.04.641443. doi: 10.1101/2025.03.04.641443. bioRxiv. 2025. PMID: 40568076 Free PMC article. Preprint.
Chromosome X-Wide Common Variant Association Study (XWAS) in Autism Spectrum Disorder.
Mendes M, Chen DZ, Engchuan W, Leal TP, Thiruvahindrapuram B, Trost B, Howe JL, Pellecchia G, Nalpathamkalam T, Alexandrova R, Salazar NB, McKee EA, Alfaro NR, Lai MC, Bandres-Ciga S, Roshandel D, Bradley CA, Anagnostou E, Sun L, Scherer SW. Mendes M, et al. Among authors: trost b. medRxiv [Preprint]. 2024 Jul 18:2024.07.18.24310640. doi: 10.1101/2024.07.18.24310640. medRxiv. 2024. Update in: Am J Hum Genet. 2025 Jan 2;112(1):135-153. doi: 10.1016/j.ajhg.2024.11.008. PMID: 39108515 Free PMC article. Updated. Preprint.
Genetic variants in DDX53 contribute to autism spectrum disorder associated with the Xp22.11 locus.
Scala M, Bradley CA, Howe JL, Trost B, Salazar NB, Shum C, Mendes M, Reuter MS, Anagnostou E, MacDonald JR, Ko SY, Frankland PW, Charlebois J, Elsabbagh M, Granger L, Anadiotis G, Pullano V, Brusco A, Keller R, Parisotto S, Pedro HF, Lusk L, McDonnell PP, Helbig I, Mullegama SV; Undiagnosed Diseases Network; Douine ED, Corona RI, Russell BE, Nelson SF, Graziano C, Schwab M, Simone L, Zara F, Scherer SW. Scala M, et al. Among authors: trost b. Am J Hum Genet. 2025 Jan 2;112(1):154-167. doi: 10.1016/j.ajhg.2024.11.003. Epub 2024 Dec 19. Am J Hum Genet. 2025. PMID: 39706195 Free PMC article.
Total synthesis of bryostatin 3.
Trost BM, Wang Y, Buckl AK, Huang Z, Nguyen MH, Kuzmina O. Trost BM, et al. Science. 2020 May 29;368(6494):1007-1011. doi: 10.1126/science.abb7271. Science. 2020. PMID: 32467391
Chromosome X-wide common variant association study in autism spectrum disorder.
Mendes M, Chen DZ, Engchuan W, Leal TP, Thiruvahindrapuram B, Trost B, Howe JL, Pellecchia G, Nalpathamkalam T, Alexandrova R, Salazar NB, McKee EA, Rivera-Alfaro N, Lai MC, Bandres-Ciga S, Roshandel D, Bradley CA, Anagnostou E, Sun L, Scherer SW. Mendes M, et al. Among authors: trost b. Am J Hum Genet. 2025 Jan 2;112(1):135-153. doi: 10.1016/j.ajhg.2024.11.008. Epub 2024 Dec 19. Am J Hum Genet. 2025. PMID: 39706197 Free PMC article.
549 results