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Results by year

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

Year Number of Results
1950 1
1951 1
1952 1
1953 2
1955 2
1957 1
1958 1
1960 2
1968 3
1969 10
1970 8
1974 1
1975 4
1976 2
1977 1
1978 5
1979 2
1980 4
1981 2
1982 2
1983 3
1984 3
1985 2
1986 3
1987 2
1988 3
1989 2
1990 4
1992 1
1993 3
1994 3
1995 4
1996 4
1997 5
1998 1
1999 5
2000 6
2001 4
2002 9
2003 13
2004 9
2005 10
2006 16
2007 9
2008 15
2009 16
2010 10
2011 12
2012 20
2013 11
2014 18
2015 14
2016 18
2017 15
2018 11
2019 26
2020 25
2021 29
2022 34
2023 37
2024 9

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Search Results

459 results

Results by year

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Page 1
New Candidates for Autism/Intellectual Disability Identified by Whole-Exome Sequencing.
Bruno LP, Doddato G, Valentino F, Baldassarri M, Tita R, Fallerini C, Bruttini M, Lo Rizzo C, Mencarelli MA, Mari F, Pinto AM, Fava F, Fabbiani A, Lamacchia V, Carrer A, Caputo V, Granata S, Benetti E, Zguro K, Furini S, Renieri A, Ariani F. Bruno LP, et al. Int J Mol Sci. 2021 Dec 14;22(24):13439. doi: 10.3390/ijms222413439. Int J Mol Sci. 2021. PMID: 34948243 Free PMC article. Clinical Trial.
The neurodevelopmental and facial phenotype in individuals with a TRIP12 variant.
Aerden M, Denommé-Pichon AS, Bonneau D, Bruel AL, Delanne J, Gérard B, Mazel B, Philippe C, Pinson L, Prouteau C, Putoux A, Tran Mau-Them F, Viora-Dupont É, Vitobello A, Ziegler A, Piton A, Isidor B, Francannet C, Maillard PY, Julia S, Philippe A, Schaefer E, Koene S, Ruivenkamp C, Hoffer M, Legius E, Theunis M, Keren B, Buratti J, Charles P, Courtin T, Misra-Isrie M, van Haelst M, Waisfisz Q, Wieczorek D, Schmetz A, Herget T, Kortüm F, Lisfeld J, Debray FG, Bramswig NC, Atallah I, Fodstad H, Jouret G, Almoguera B, Tahsin-Swafiri S, Santos-Simarro F, Palomares-Bralo M, López-González V, Kibaek M, Tørring PM, Renieri A, Bruno LP, Õunap K, Wojcik M, Hsieh TC, Krawitz P, Van Esch H. Aerden M, et al. Among authors: bruno lp. Eur J Hum Genet. 2023 Apr;31(4):461-468. doi: 10.1038/s41431-023-01307-x. Epub 2023 Feb 7. Eur J Hum Genet. 2023. PMID: 36747006 Free PMC article.
CAPRIN1 haploinsufficiency causes a neurodevelopmental disorder with language impairment, ADHD and ASD.
Pavinato L, Delle Vedove A, Carli D, Ferrero M, Carestiato S, Howe JL, Agolini E, Coviello DA, van de Laar I, Au PYB, Di Gregorio E, Fabbiani A, Croci S, Mencarelli MA, Bruno LP, Renieri A, Veltra D, Sofocleous C, Faivre L, Mazel B, Safraou H, Denommé-Pichon AS, van Slegtenhorst MA, Giesbertz N, van Jaarsveld RH, Childers A, Rogers RC, Novelli A, De Rubeis S, Buxbaum JD, Scherer SW, Ferrero GB, Wirth B, Brusco A. Pavinato L, et al. Among authors: bruno lp. Brain. 2023 Feb 13;146(2):534-548. doi: 10.1093/brain/awac278. Brain. 2023. PMID: 35979925 Free PMC article.
Microbiota and arthritis: cause or consequence?
Cafaro G, Cruciani G, Bruno L, Dal Pozzolo R, Colangelo A, Tromby F, Nicchi M, Pianese B, Perricone C, Gerli R, Bartoloni E. Cafaro G, et al. Among authors: bruno l. Clin Exp Rheumatol. 2024 May;42(5):1097-1103. doi: 10.55563/clinexprheumatol/f6q4dc. Epub 2024 May 6. Clin Exp Rheumatol. 2024. PMID: 38743445 Free article. Review.
Hereditary ovarian cancer.
Russo A, Calò V, Bruno L, Rizzo S, Bazan V, Di Fede G. Russo A, et al. Among authors: bruno l. Crit Rev Oncol Hematol. 2009 Jan;69(1):28-44. doi: 10.1016/j.critrevonc.2008.06.003. Epub 2008 Jul 24. Crit Rev Oncol Hematol. 2009. PMID: 18656380 Free article. Review.
Idiopathic inflammatory myopathies: one year in review 2023.
Conticini E, Dourado E, Bottazzi F, Cardelli C, Bruno L, Schmidt J, Carli L, Cavagna L, Barsotti S. Conticini E, et al. Among authors: bruno l. Clin Exp Rheumatol. 2024 Feb;42(2):213-224. doi: 10.55563/clinexprheumatol/dh5o6c. Epub 2024 Mar 14. Clin Exp Rheumatol. 2024. PMID: 38488099 Free article. Review.
Defining prognosis in sarcoidosis.
Lopes MC, Amadeu TP, Ribeiro-Alves M, Costa CHD, Silva BRA, Rodrigues LS, Bessa EJC, Bruno LP, Lopes AJ, Rufino R. Lopes MC, et al. Among authors: bruno lp. Medicine (Baltimore). 2020 Nov 25;99(48):e23100. doi: 10.1097/MD.0000000000023100. Medicine (Baltimore). 2020. PMID: 33235069 Free PMC article.
SPTBN5, Encoding the βV-Spectrin Protein, Leads to a Syndrome of Intellectual Disability, Developmental Delay, and Seizures.
Khan A, Bruno LP, Alomar F, Umair M, Pinto AM, Khan AA, Khan A, Saima, Fabbiani A, Zguro K, Furini S, Mencarelli MA, Renieri A, Resciniti S, Peña-Guerra KA, Guzmán-Vega FJ, Arold ST, Ariani F, Khan SN. Khan A, et al. Among authors: bruno lp. Front Mol Neurosci. 2022 Jun 17;15:877258. doi: 10.3389/fnmol.2022.877258. eCollection 2022. Front Mol Neurosci. 2022. PMID: 35782384 Free PMC article.
459 results