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Results by year

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

Year Number of Results
1914 1
1916 1
1919 2
1921 1
1922 1
1928 1
1946 1
1948 1
1952 1
1953 2
1954 2
1955 1
1956 3
1957 1
1958 1
1961 1
1962 2
1963 1
1964 1
1965 2
1966 2
1967 1
1968 3
1969 2
1970 4
1971 2
1972 7
1974 8
1975 3
1976 1
1977 3
1978 1
1979 7
1980 8
1981 4
1982 11
1983 6
1984 9
1985 6
1986 1
1987 9
1988 9
1989 8
1990 8
1991 5
1992 11
1993 7
1994 3
1995 4
1996 11
1997 8
1998 4
1999 6
2000 9
2001 9
2002 13
2003 17
2004 14
2005 27
2006 10
2007 15
2008 13
2009 10
2010 15
2011 16
2012 21
2013 19
2014 24
2015 27
2016 25
2017 19
2018 20
2019 18
2020 32
2021 43
2022 34
2023 33
2024 10

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Publication date

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642 results

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Page 1
Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and mice.
Sheppard SE, Bryant L, Wickramasekara RN, Vaccaro C, Robertson B, Hallgren J, Hulen J, Watson CJ, Faundes V, Duffourd Y, Lee P, Simon MC, de la Cruz X, Padilla N, Flores-Mendez M, Akizu N, Smiler J, Pellegrino Da Silva R, Li D, March M, Diaz-Rosado A, Peixoto de Barcelos I, Choa ZX, Lim CY, Dubourg C, Journel H, Demurger F, Mulhern M, Akman C, Lippa N, Andrews M, Baldridge D, Constantino J, van Haeringen A, Snoeck-Streef I, Chow P, Hing A, Graham JM Jr, Au M, Faivre L, Shen W, Mao R, Palumbos J, Viskochil D, Gahl W, Tifft C, Macnamara E, Hauser N, Miller R, Maffeo J, Afenjar A, Doummar D, Keren B, Arn P, Macklin-Mantia S, Meerschaut I, Callewaert B, Reis A, Zweier C, Brewer C, Saggar A, Smeland MF, Kumar A, Elmslie F, Deshpande C, Nizon M, Cogne B, van Ierland Y, Wilke M, van Slegtenhorst M, Koudijs S, Chen JY, Dredge D, Pier D, Wortmann S, Kamsteeg EJ, Koch J, Haynes D, Pollack L, Titheradge H, Ranguin K, Denommé-Pichon AS, Weber S, Pérez de la Fuente R, Sánchez Del Pozo J, Lezana Rosales JM, Joset P, Steindl K, Rauch A, Mei D, Mari F, Guerrini R, Lespinasse J, Tran Mau-Them F, Philippe C, Dauriat B, Raymond L, Moutton S, Cueto-González AM, Tan TY, Mignot C, Grotto S, Rena… See abstract for full author list ➔ Sheppard SE, et al. Among authors: haynes d. Sci Adv. 2023 Mar 10;9(10):eade1463. doi: 10.1126/sciadv.ade1463. Epub 2023 Mar 10. Sci Adv. 2023. PMID: 36897941 Free PMC article.
Phenotypic expansion of the BPTF-related neurodevelopmental disorder with dysmorphic facies and distal limb anomalies.
Glinton KE, Hurst ACE, Bowling KM, Cristian I, Haynes D, Adstamongkonkul D, Schnappauf O, Beck DB, Brewer C, Parikh AS, Shinde DN, Donaldson A, Brautbar A, Koene S, van Haeringen A, Piton A, Capri Y, Furlan M, Gardella E, Møller RS, van de Beek I, Zuurbier L, Lakeman P, Bayat A, Martinez J, Signer R, Torring PM, Engelund MB, Gripp KW, Amlie-Wolf L, Henderson LB, Midro AT, Tarasów E, Stasiewicz-Jarocka B, Moskal-Jasinska D, Vos P, Boschann F, Stoltenburg C, Puk O, Mero IL, Lossius K, Mignot C, Keren B, Acosta Guio JC, Briceño I, Gomez A, Yang Y, Stankiewicz P. Glinton KE, et al. Among authors: haynes d. Am J Med Genet A. 2021 May;185(5):1366-1378. doi: 10.1002/ajmg.a.62102. Epub 2021 Jan 31. Am J Med Genet A. 2021. PMID: 33522091 Free PMC article.
Physics in Africa.
Sa'id RS, Fuwape I, Dikandé AM, Mimouni J, Hasford F, Haynes D, Gledhill I, Amolo G, Akin-Ojo O, Eassa N. Sa'id RS, et al. Among authors: haynes d. Nat Rev Phys. 2020;2(10):520-523. doi: 10.1038/s42254-020-0239-8. Epub 2020 Sep 18. Nat Rev Phys. 2020. PMID: 33728404 Free PMC article. Review.
Bilateral cochlear implantation.
Wanna GB, Gifford RH, McRackan TR, Rivas A, Haynes DS. Wanna GB, et al. Among authors: haynes ds. Otolaryngol Clin North Am. 2012 Feb;45(1):81-9. doi: 10.1016/j.otc.2011.08.018. Otolaryngol Clin North Am. 2012. PMID: 22115683 Review.
Loss of Grem1-lineage chondrogenic progenitor cells causes osteoarthritis.
Ng JQ, Jafarov TH, Little CB, Wang T, Ali AM, Ma Y, Radford GA, Vrbanac L, Ichinose M, Whittle S, Hunter DJ, Lannagan TRM, Suzuki N, Goyne JM, Kobayashi H, Wang TC, Haynes DR, Menicanin D, Gronthos S, Worthley DL, Woods SL, Mukherjee S. Ng JQ, et al. Among authors: haynes dr. Nat Commun. 2023 Oct 31;14(1):6909. doi: 10.1038/s41467-023-42199-1. Nat Commun. 2023. PMID: 37907525 Free PMC article.
Management of pneumothorax.
Haynes D, Baumann MH. Haynes D, et al. Semin Respir Crit Care Med. 2010 Dec;31(6):769-80. doi: 10.1055/s-0030-1269837. Epub 2011 Jan 6. Semin Respir Crit Care Med. 2010. PMID: 21213209 Review.
Adverse cutaneous reactions to chemotherapeutic drugs.
Haynes D, Ortega-Loayza AG. Haynes D, et al. Clin Dermatol. 2020 Nov-Dec;38(6):712-728. doi: 10.1016/j.clindermatol.2020.06.007. Epub 2020 Jun 26. Clin Dermatol. 2020. PMID: 33341204 Review.
Sudden hearing loss.
O'Malley MR, Haynes DS. O'Malley MR, et al. Among authors: haynes ds. Otolaryngol Clin North Am. 2008 Jun;41(3):633-49, x-xi. doi: 10.1016/j.otc.2008.01.009. Otolaryngol Clin North Am. 2008. PMID: 18436003 Review.
Contemporary management of jugular paragangliomas.
Wanna GB, Sweeney AD, Haynes DS, Carlson ML. Wanna GB, et al. Among authors: haynes ds. Otolaryngol Clin North Am. 2015 Apr;48(2):331-41. doi: 10.1016/j.otc.2014.12.007. Otolaryngol Clin North Am. 2015. PMID: 25769354 Review.
Rare de novo gain-of-function missense variants in DOT1L are associated with developmental delay and congenital anomalies.
Nil Z, Deshwar AR, Huang Y, Barish S, Zhang X, Choufani S, Le Quesne Stabej P, Hayes I, Yap P, Haldeman-Englert C, Wilson C, Prescott T, Tveten K, Vøllo A, Haynes D, Wheeler PG, Zon J, Cytrynbaum C, Jobling R, Blyth M, Banka S, Afenjar A, Mignot C, Robin-Renaldo F, Keren B, Kanca O, Mao X, Wegner DJ, Sisco K, Shinawi M; Undiagnosed Disease Network; Wangler MF, Weksberg R, Yamamoto S, Costain G, Bellen HJ. Nil Z, et al. Among authors: haynes d. Am J Hum Genet. 2023 Nov 2;110(11):1919-1937. doi: 10.1016/j.ajhg.2023.09.009. Epub 2023 Oct 11. Am J Hum Genet. 2023. PMID: 37827158
642 results