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

Year Number of Results
1951 1
1952 3
1984 1
1986 1
1989 1
1991 3
1993 2
1994 3
1995 6
1996 3
1997 3
1998 5
1999 5
2000 5
2001 8
2002 4
2003 8
2004 8
2005 8
2006 8
2007 14
2008 22
2009 21
2010 18
2011 17
2012 18
2013 22
2014 18
2015 20
2016 17
2017 26
2018 19
2019 31
2020 37
2021 33
2022 35
2023 20
2024 13

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428 results

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Page 1
Defining and conceptualising the commercial determinants of health.
Gilmore AB, Fabbri A, Baum F, Bertscher A, Bondy K, Chang HJ, Demaio S, Erzse A, Freudenberg N, Friel S, Hofman KJ, Johns P, Abdool Karim S, Lacy-Nichols J, de Carvalho CMP, Marten R, McKee M, Petticrew M, Robertson L, Tangcharoensathien V, Thow AM. Gilmore AB, et al. Among authors: de carvalho cmp. Lancet. 2023 Apr 8;401(10383):1194-1213. doi: 10.1016/S0140-6736(23)00013-2. Epub 2023 Mar 23. Lancet. 2023. PMID: 36966782 Review.
High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population.
Mitani T, Isikay S, Gezdirici A, Gulec EY, Punetha J, Fatih JM, Herman I, Akay G, Du H, Calame DG, Ayaz A, Tos T, Yesil G, Aydin H, Geckinli B, Elcioglu N, Candan S, Sezer O, Erdem HB, Gul D, Demiral E, Elmas M, Yesilbas O, Kilic B, Gungor S, Ceylan AC, Bozdogan S, Ozalp O, Cicek S, Aslan H, Yalcintepe S, Topcu V, Bayram Y, Grochowski CM, Jolly A, Dawood M, Duan R, Jhangiani SN, Doddapaneni H, Hu J, Muzny DM; Baylor-Hopkins Center for Mendelian Genomics; Marafi D, Akdemir ZC, Karaca E, Carvalho CMB, Gibbs RA, Posey JE, Lupski JR, Pehlivan D. Mitani T, et al. Among authors: carvalho cmb. Am J Hum Genet. 2021 Oct 7;108(10):1981-2005. doi: 10.1016/j.ajhg.2021.08.009. Epub 2021 Sep 28. Am J Hum Genet. 2021. PMID: 34582790 Free PMC article.
Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes.
Scala M, Nishikawa M, Ito H, Tabata H, Khan T, Accogli A, Davids L, Ruiz A, Chiurazzi P, Cericola G, Schulte B, Monaghan KG, Begtrup A, Torella A, Pinelli M, Denommé-Pichon AS, Vitobello A, Racine C, Mancardi MM, Kiss C, Guerin A, Wu W, Gabau Vila E, Mak BC, Martinez-Agosto JA, Gorin MB, Duz B, Bayram Y, Carvalho CMB, Vengoechea JE, Chitayat D, Tan TY, Callewaert B, Kruse B, Bird LM, Faivre L, Zollino M, Biskup S; Undiagnosed Diseases Network; Telethon Undiagnosed Diseases Program; Striano P, Nigro V, Severino M, Capra V, Costain G, Nagata KI. Scala M, et al. Among authors: carvalho cmb. Brain. 2022 Sep 14;145(9):3308-3327. doi: 10.1093/brain/awac106. Brain. 2022. PMID: 35851598 Free PMC article.
The impact of neighborhood context on telomere length: A systematic review.
Coimbra BM, Carvalho CM, van Zuiden M, Williamson RE, Ota VK, Mello AF, Belangero SI, Olff M, Mello MF. Coimbra BM, et al. Among authors: carvalho cm. Health Place. 2022 Mar;74:102746. doi: 10.1016/j.healthplace.2022.102746. Epub 2022 Feb 2. Health Place. 2022. PMID: 35123384 Review.
Craniofacial phenotypes associated with Robinow syndrome.
Conlon CJ, Abu-Ghname A, Raghuram AC, Davis MJ, Guillen DE, Sutton VR, Carvalho CMB, Maricevich RS. Conlon CJ, et al. Among authors: carvalho cmb. Am J Med Genet A. 2021 Dec;185(12):3606-3612. doi: 10.1002/ajmg.a.61986. Epub 2020 Nov 25. Am J Med Genet A. 2021. PMID: 33237614
Extremity anomalies associated with Robinow syndrome.
Abu-Ghname A, Trost J, Davis MJ, Sutton VR, Zhang C, Guillen DE, Carvalho CMB, Maricevich RS. Abu-Ghname A, et al. Among authors: carvalho cmb. Am J Med Genet A. 2021 Dec;185(12):3584-3592. doi: 10.1002/ajmg.a.61884. Epub 2020 Sep 25. Am J Med Genet A. 2021. PMID: 32974972
428 results