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

Year Number of Results
1946 1
1953 1
1957 1
1962 1
1965 4
1967 2
1973 2
1974 1
1975 1
1976 4
1977 1
1979 2
1980 2
1981 4
1982 4
1983 7
1984 3
1985 3
1986 4
1987 5
1988 1
1989 7
1990 8
1991 6
1992 3
1993 4
1994 2
1995 4
1996 6
1997 4
1998 2
1999 6
2000 8
2001 4
2002 6
2003 11
2004 10
2005 6
2006 7
2007 9
2008 17
2009 8
2010 3
2011 6
2012 7
2013 2
2014 6
2015 4
2016 3
2017 1
2018 5
2019 7
2020 9
2021 7
2022 5
2023 8
2024 9
2025 7

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265 results

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Page 1
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes.
Zhou X, Feliciano P, Shu C, Wang T, Astrovskaya I, Hall JB, Obiajulu JU, Wright JR, Murali SC, Xu SX, Brueggeman L, Thomas TR, Marchenko O, Fleisch C, Barns SD, Snyder LG, Han B, Chang TS, Turner TN, Harvey WT, Nishida A, O'Roak BJ, Geschwind DH; SPARK Consortium; Michaelson JJ, Volfovsky N, Eichler EE, Shen Y, Chung WK. Zhou X, et al. Nat Genet. 2022 Sep;54(9):1305-1319. doi: 10.1038/s41588-022-01148-2. Epub 2022 Aug 18. Nat Genet. 2022. PMID: 35982159 Free PMC article.
Glucocorticoid receptor antagonists.
Clark RD. Clark RD. Curr Top Med Chem. 2008;8(9):813-38. doi: 10.2174/156802608784535011. Curr Top Med Chem. 2008. PMID: 18537690 Review.
A novel syndrome associated with prenatal fentanyl exposure.
Wadman E, Fernandes E, Muss C, Powell-Hamilton N, Wojcik MH, Madden JA, Carreon CK, Clark RD, Stenftenagel A, Chikalard K, Kimonis V, Brucker W, Alves C, Gripp KW. Wadman E, et al. Among authors: clark rd. Genet Med Open. 2023 Sep 28;1(1):100834. doi: 10.1016/j.gimo.2023.100834. eCollection 2023. Genet Med Open. 2023. PMID: 39669238 Free PMC article.
Long-read sequencing is required for precision diagnosis of incontinentia pigmenti.
Wojcik MH, Clark RD, Elias AF, Genetti CA, Madden JA, Simpson D, Golkar L, Zalusky MPG, Miller AL, Rodriguez A, Goffena J, Dash CA, Damaraju N, Gibson SB, Storz SHR, Anderson ZB, Gustafson JA, Thiffault I, Farrow EG, Pastinen T, Lin J, Huang JT, Beggs AH, Agrawal PB; Genomics Research to Elucidate the Genetics of Rare Diseases (GREGoR) Consortium; Miller DT, Miller DE. Wojcik MH, et al. Among authors: clark rd. HGG Adv. 2025 Jul 10;6(3):100468. doi: 10.1016/j.xhgg.2025.100468. Epub 2025 Jun 12. HGG Adv. 2025. PMID: 40515401 Free PMC article.
Biallelic variation in the choline and ethanolamine transporter FLVCR1 underlies a severe developmental disorder spectrum.
Calame DG, Wong JH, Panda P, Nguyen DT, Leong NCP, Sangermano R, Patankar SG, Abdel-Hamid MS, AlAbdi L, Safwat S, Flannery KP, Dardas Z, Fatih JM, Murali C, Kannan V, Lotze TE, Herman I, Ammouri F, Rezich B, Efthymiou S, Alavi S, Murphy D, Firoozfar Z, Nasab ME, Bahreini A, Ghasemi M, Haridy NA, Goldouzi HR, Eghbal F, Karimiani EG, Begtrup A, Elloumi H, Srinivasan VM, Gowda VK, Du H, Jhangiani SN, Coban-Akdemir Z, Marafi D, Rodan L, Isikay S, Rosenfeld JA, Ramanathan S, Staton M, Oberg KC, Clark RD, Wenman C, Loughlin S, Saad R, Ashraf T, Male A, Tadros S, Boostani R, Abdel-Salam GMH, Zaki M, Mardi A, Hashemi-Gorji F, Abdalla E, Manzini MC, Pehlivan D, Posey JE, Gibbs RA, Houlden H, Alkuraya FS, Bujakowska K, Maroofian R, Lupski JR, Nguyen LN. Calame DG, et al. Among authors: clark rd. Genet Med. 2025 Jan;27(1):101273. doi: 10.1016/j.gim.2024.101273. Epub 2024 Sep 19. Genet Med. 2025. PMID: 39306721
Genotype-phenotype correlations in RHOBTB2-associated neurodevelopmental disorders.
Langhammer F, Maroofian R, Badar R, Gregor A, Rochman M, Ratliff JB, Koopmans M, Herget T, Hempel M, Kortüm F, Heron D, Mignot C, Keren B, Brooks S, Botti C, Ben-Zeev B, Argilli E, Sherr EH, Gowda VK, Srinivasan VM, Bakhtiari S, Kruer MC, Salih MA, Kuechler A, Muller EA, Blocker K, Kuismin O, Park KL, Kochhar A, Brown K, Ramanathan S, Clark RD, Elgizouli M, Melikishvili G, Tabatadze N, Stark Z, Mirzaa GM, Ong J, Grasshoff U, Bevot A, von Wintzingerode L, Jamra RA, Hennig Y, Goldenberg P, Al Alam C, Charif M, Boulouiz R, Bellaoui M, Amrani R, Al Mutairi F, Tamim AM, Abdulwahab F, Alkuraya FS, Khouj EM, Alvi JR, Sultan T, Hashemi N, Karimiani EG, Ashrafzadeh F, Imannezhad S, Efthymiou S, Houlden H, Sticht H, Zweier C. Langhammer F, et al. Among authors: clark rd. Genet Med. 2023 Aug;25(8):100885. doi: 10.1016/j.gim.2023.100885. Epub 2023 May 8. Genet Med. 2023. PMID: 37165955 Free article.
Response to Hamosh et al.
Biesecker LG, Adam MP, Alkuraya FS, Amemiya AR, Bamshad MJ, Beck AE, Bennett JT, Bird LM, Carey JC, Chung B, Clark RD, Cox TC, Curry C, Dinulos MBP, Dobyns WB, Giampietro PF, Girisha KM, Glass IA, Graham JM Jr, Gripp KW, Haldeman-Englert CR, Hall BD, Innes AM, Kalish JM, Keppler-Noreuil KM, Kosaki K, Kozel BA, Mirzaa GM, Mulvihill JJ, Nowaczyk MJM, Pagon RA, Retterer K, Rope AF, Sanchez-Lara PA, Seaver LH, Shieh JT, Slavotinek AM, Sobering AK, Stevens CA, Stevenson DA, Tan TY, Tan WH, Tsai AC, Weaver DD, Williams MS, Zackai E, Zarate YA. Biesecker LG, et al. Among authors: clark rd. Am J Hum Genet. 2021 Sep 2;108(9):1809-1810. doi: 10.1016/j.ajhg.2021.07.006. Am J Hum Genet. 2021. PMID: 34478656 Free PMC article. No abstract available.
Coral Reef Population Genomics in an Age of Global Change.
Pinsky ML, Clark RD, Bos JT. Pinsky ML, et al. Among authors: clark rd. Annu Rev Genet. 2023 Nov 27;57:87-115. doi: 10.1146/annurev-genet-022123-102748. Epub 2023 Jun 29. Annu Rev Genet. 2023. PMID: 37384733 Free article. Review.
265 results