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Results by year

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

Year Number of Results
1944 1
1960 3
1961 5
1962 2
1963 4
1964 2
1965 6
1966 3
1967 3
1968 3
1969 3
1970 6
1971 8
1972 5
1973 4
1974 5
1975 9
1976 5
1977 3
1978 4
1979 4
1980 5
1981 7
1982 9
1983 10
1984 6
1985 6
1986 5
1987 5
1988 6
1989 9
1990 7
1991 10
1992 11
1993 5
1994 4
1995 3
1996 11
1997 13
1998 12
1999 16
2000 16
2001 12
2002 23
2003 21
2004 24
2005 16
2006 17
2007 13
2008 15
2009 23
2010 23
2011 33
2012 21
2013 24
2014 25
2015 19
2016 28
2017 26
2018 17
2019 23
2020 17
2021 23
2022 21
2023 16

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703 results

Results by year

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Page 1
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies.
Hamdan FF, Myers CT, Cossette P, Lemay P, Spiegelman D, Laporte AD, Nassif C, Diallo O, Monlong J, Cadieux-Dion M, Dobrzeniecka S, Meloche C, Retterer K, Cho MT, Rosenfeld JA, Bi W, Massicotte C, Miguet M, Brunga L, Regan BM, Mo K, Tam C, Schneider A, Hollingsworth G; Deciphering Developmental Disorders Study; FitzPatrick DR, Donaldson A, Canham N, Blair E, Kerr B, Fry AE, Thomas RH, Shelagh J, Hurst JA, Brittain H, Blyth M, Lebel RR, Gerkes EH, Davis-Keppen L, Stein Q, Chung WK, Dorison SJ, Benke PJ, Fassi E, Corsten-Janssen N, Kamsteeg EJ, Mau-Them FT, Bruel AL, Verloes A, Õunap K, Wojcik MH, Albert DVF, Venkateswaran S, Ware T, Jones D, Liu YC, Mohammad SS, Bizargity P, Bacino CA, Leuzzi V, Martinelli S, Dallapiccola B, Tartaglia M, Blumkin L, Wierenga KJ, Purcarin G, O'Byrne JJ, Stockler S, Lehman A, Keren B, Nougues MC, Mignot C, Auvin S, Nava C, Hiatt SM, Bebin M, Shao Y, Scaglia F, Lalani SR, Frye RE, Jarjour IT, Jacques S, Boucher RM, Riou E, Srour M, Carmant L, Lortie A, Major P, Diadori P, Dubeau F, D'Anjou G, Bourque G, Berkovic SF, Sadleir LG, Campeau PM, Kibar Z, Lafrenière RG, Girard SL, Mercimek-Mahmutoglu S, Boelman C, Rouleau GA, Scheffer IE, Mefford HC, An… See abstract for full author list ➔ Hamdan FF, et al. Among authors: frye re. Am J Hum Genet. 2017 Nov 2;101(5):664-685. doi: 10.1016/j.ajhg.2017.09.008. Am J Hum Genet. 2017. PMID: 29100083 Free PMC article.
Metabolomic Signatures of Autism Spectrum Disorder.
Brister D, Rose S, Delhey L, Tippett M, Jin Y, Gu H, Frye RE. Brister D, et al. Among authors: frye re. J Pers Med. 2022 Oct 17;12(10):1727. doi: 10.3390/jpm12101727. J Pers Med. 2022. PMID: 36294866 Free PMC article.
Introduction.
Frye RE, Slattery J. Frye RE, et al. Microb Ecol Health Dis. 2015 May 7;26:28168. doi: 10.3402/mehd.v26.28168. eCollection 2015. Microb Ecol Health Dis. 2015. PMID: 25956239 Free PMC article. No abstract available.
The impact of glutathione metabolism in autism spectrum disorder.
Bjørklund G, Doşa MD, Maes M, Dadar M, Frye RE, Peana M, Chirumbolo S. Bjørklund G, et al. Among authors: frye re. Pharmacol Res. 2021 Apr;166:105437. doi: 10.1016/j.phrs.2021.105437. Epub 2021 Jan 22. Pharmacol Res. 2021. PMID: 33493659 Review.
Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society.
Parikh S, Goldstein A, Karaa A, Koenig MK, Anselm I, Brunel-Guitton C, Christodoulou J, Cohen BH, Dimmock D, Enns GM, Falk MJ, Feigenbaum A, Frye RE, Ganesh J, Griesemer D, Haas R, Horvath R, Korson M, Kruer MC, Mancuso M, McCormack S, Raboisson MJ, Reimschisel T, Salvarinova R, Saneto RP, Scaglia F, Shoffner J, Stacpoole PW, Sue CM, Tarnopolsky M, Van Karnebeek C, Wolfe LA, Cunningham ZZ, Rahman S, Chinnery PF. Parikh S, et al. Among authors: frye re. Genet Med. 2017 Dec;19(12):10.1038/gim.2017.107. doi: 10.1038/gim.2017.107. Epub 2017 Jul 27. Genet Med. 2017. PMID: 28749475 Free PMC article. Review.
Editorial: Secondary vs. Idiopathic Autism.
Casanova MF, Casanova EL, Frye RE, Baeza-Velasco C, LaSalle JM, Hagerman RJ, Scherer SW, Natowicz MR. Casanova MF, et al. Among authors: frye re. Front Psychiatry. 2020 Apr 14;11:297. doi: 10.3389/fpsyt.2020.00297. eCollection 2020. Front Psychiatry. 2020. PMID: 32346372 Free PMC article. No abstract available.
703 results