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

Year Number of Results
1898 1
1899 1
1903 1
1908 1
1914 1
1915 1
1920 1
1945 1
1946 1
1969 1
1972 1
1973 2
1974 2
1975 3
1976 1
1977 2
1978 1
1979 2
1981 4
1982 1
1983 5
1984 4
1985 9
1986 4
1987 4
1988 3
1989 4
1990 1
1991 3
1992 1
1993 6
1994 6
1995 1
1996 3
1997 3
1998 6
1999 3
2000 7
2001 5
2002 5
2003 2
2004 4
2005 12
2006 6
2007 6
2008 8
2009 6
2010 9
2011 6
2012 9
2013 4
2014 4
2015 6
2016 3
2017 9
2018 8
2019 8
2020 18
2021 13
2022 6
2023 20
2024 12
2025 11

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282 results

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Page 1
Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome.
Cousin MA, Creighton BA, Breau KA, Spillmann RC, Torti E, Dontu S, Tripathi S, Ajit D, Edwards RJ, Afriyie S, Bay JC, Harper KM, Beltran AA, Munoz LJ, Falcon Rodriguez L, Stankewich MC, Person RE, Si Y, Normand EA, Blevins A, May AS, Bier L, Aggarwal V, Mancini GMS, van Slegtenhorst MA, Cremer K, Becker J, Engels H, Aretz S, MacKenzie JJ, Brilstra E, van Gassen KLI, van Jaarsveld RH, Oegema R, Parsons GM, Mark P, Helbig I, McKeown SE, Stratton R, Cogne B, Isidor B, Cacheiro P, Smedley D, Firth HV, Bierhals T, Kloth K, Weiss D, Fairley C, Shieh JT, Kritzer A, Jayakar P, Kurtz-Nelson E, Bernier RA, Wang T, Eichler EE, van de Laar IMBH, McConkie-Rosell A, McDonald MT, Kemppainen J, Lanpher BC, Schultz-Rogers LE, Gunderson LB, Pichurin PN, Yoon G, Zech M, Jech R, Winkelmann J; Undiagnosed Diseases Network; Genomics England Research Consortium; Beltran AS, Zimmermann MT, Temple B, Moy SS, Klee EW, Tan QK, Lorenzo DN. Cousin MA, et al. Among authors: stratton r. Nat Genet. 2021 Jul;53(7):1006-1021. doi: 10.1038/s41588-021-00886-z. Epub 2021 Jul 1. Nat Genet. 2021. PMID: 34211179 Free PMC article.
Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders.
Gillentine MA, Wang T, Hoekzema K, Rosenfeld J, Liu P, Guo H, Kim CN, De Vries BBA, Vissers LELM, Nordenskjold M, Kvarnung M, Lindstrand A, Nordgren A, Gecz J, Iascone M, Cereda A, Scatigno A, Maitz S, Zanni G, Bertini E, Zweier C, Schuhmann S, Wiesener A, Pepper M, Panjwani H, Torti E, Abid F, Anselm I, Srivastava S, Atwal P, Bacino CA, Bhat G, Cobian K, Bird LM, Friedman J, Wright MS, Callewaert B, Petit F, Mathieu S, Afenjar A, Christensen CK, White KM, Elpeleg O, Berger I, Espineli EJ, Fagerberg C, Brasch-Andersen C, Hansen LK, Feyma T, Hughes S, Thiffault I, Sullivan B, Yan S, Keller K, Keren B, Mignot C, Kooy F, Meuwissen M, Basinger A, Kukolich M, Philips M, Ortega L, Drummond-Borg M, Lauridsen M, Sorensen K, Lehman A; CAUSES Study; Lopez-Rangel E, Levy P, Lessel D, Lotze T, Madan-Khetarpal S, Sebastian J, Vento J, Vats D, Benman LM, Mckee S, Mirzaa GM, Muss C, Pappas J, Peeters H, Romano C, Elia M, Galesi O, Simon MEH, van Gassen KLI, Simpson K, Stratton R, Syed S, Thevenon J, Palafoll IV, Vitobello A, Bournez M, Faivre L, Xia K; SPARK Consortium; Earl RK, Nowakowski T, Bernier RA, Eichler EE. Gillentine MA, et al. Among authors: stratton r. Genome Med. 2021 Apr 19;13(1):63. doi: 10.1186/s13073-021-00870-6. Genome Med. 2021. PMID: 33874999 Free PMC article.
Isotretinoin-induced myositis.
Hague O, Thanopoulou V, Mangat P, Singh A, Stratton R, Malley T. Hague O, et al. Among authors: stratton r. Oxf Med Case Reports. 2024 Mar 25;2024(3):omae017. doi: 10.1093/omcr/omae017. eCollection 2024 Mar. Oxf Med Case Reports. 2024. PMID: 38532764 Free PMC article.
George R. Martin: Pioneering matrix biologist.
Leask A, Stratton RJ. Leask A, et al. Among authors: stratton rj. Matrix Biol. 2025 Apr;136:69-70. doi: 10.1016/j.matbio.2025.01.007. Epub 2025 Jan 28. Matrix Biol. 2025. PMID: 39884396 No abstract available.
Deletion (2)(q37).
Stratton RF, Tolworthy JA, Young RS. Stratton RF, et al. Am J Med Genet. 1994 Jun 1;51(2):153-5. doi: 10.1002/ajmg.1320510215. Am J Med Genet. 1994. PMID: 8092193 Review.
Chemokines in systemic sclerosis.
King J, Abraham D, Stratton R. King J, et al. Among authors: stratton r. Immunol Lett. 2018 Mar;195:68-75. doi: 10.1016/j.imlet.2017.12.001. Epub 2017 Dec 13. Immunol Lett. 2018. PMID: 29247681 Review. No abstract available.
Stratification of biological therapies by pathobiology in biologic-naive patients with rheumatoid arthritis (STRAP and STRAP-EU): two parallel, open-label, biopsy-driven, randomised trials.
Rivellese F, Nerviani A, Giorli G, Warren L, Jaworska E, Bombardieri M, Lewis MJ, Humby F, Pratt AG, Filer A, Gendi N, Cauli A, Choy E, McInnes I, Durez P, Edwards CJ, Buch MH, Gremese E, Taylor PC, Ng N, Cañete JD, Raizada S, McKay ND, Jadon D, Sainaghi PP, Stratton R, Ehrenstein MR, Ho P, Pereira JP, Dasgupta B, Gorman C, Galloway J, Chinoy H, van der Heijde D, Sasieni P, Barton A, Pitzalis C; STRAP collaborative group. Rivellese F, et al. Among authors: stratton r. Lancet Rheumatol. 2023 Nov;5(11):e648-e659. doi: 10.1016/S2665-9913(23)00241-2. Lancet Rheumatol. 2023. PMID: 38251532 Free article. Clinical Trial.
282 results