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

Year Number of Results
1971 54
1972 65
1973 85
1974 123
1975 114
1976 148
1977 122
1978 124
1979 148
1980 147
1981 150
1982 127
1983 139
1984 174
1985 177
1986 186
1987 156
1988 147
1989 147
1990 151
1991 136
1992 149
1993 156
1994 157
1995 152
1996 199
1997 179
1998 203
1999 174
2000 158
2001 161
2002 161
2003 160
2004 160
2005 159
2006 163
2007 219
2008 186
2009 232
2010 246
2011 316
2012 330
2013 387
2014 380
2015 304
2016 293
2017 305
2018 316
2019 230
2020 252
2021 242
2022 211
2023 240
2024 109

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8,767 results

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Page 1
A standard of care for individuals with PIK3CA-related disorders: An international expert consensus statement.
Douzgou S, Rawson M, Baselga E, Danielpour M, Faivre L, Kashanian A, Keppler-Noreuil KM, Kuentz P, Mancini GMS, Maniere MC, Martinez-Glez V, Parker VE, Semple RK, Srivastava S, Vabres P, De Wit MY, Graham JM Jr, Clayton-Smith J, Mirzaa GM, Biesecker LG. Douzgou S, et al. Clin Genet. 2022 Jan;101(1):32-47. doi: 10.1111/cge.14027. Epub 2021 Jul 16. Clin Genet. 2022. PMID: 34240408 Free PMC article. Review.
The genetics of incontinence: A scoping review.
Breinbjerg A, Jørgensen CS, Borg B, Rittig S, Kamperis K, Christensen JH. Breinbjerg A, et al. Clin Genet. 2023 Jul;104(1):22-62. doi: 10.1111/cge.14331. Epub 2023 Mar 27. Clin Genet. 2023. PMID: 36973883 Review.
Imagawa-Matsumoto syndrome: SUZ12-related overgrowth disorder.
Imagawa E, Seyama R, Aoi H, Uchiyama Y, Marcarini BG, Furquim I, Honjo RS, Bertola DR, Kim CA, Matsumoto N. Imagawa E, et al. Clin Genet. 2023 Apr;103(4):383-391. doi: 10.1111/cge.14296. Epub 2023 Jan 25. Clin Genet. 2023. PMID: 36645289 Review.
Corrigendum.
[No authors listed] [No authors listed] Clin Genet. 2022 Feb;101(2):272. doi: 10.1111/cge.14092. Clin Genet. 2022. PMID: 34984666 No abstract available.
POU3F3-related disorder: Defining the phenotype and expanding the molecular spectrum.
Rossi A, Blok LS, Neuser S, Klöckner C, Platzer K, Faivre LO, Weigand H, Dentici ML, Tartaglia M, Niceta M, Alfieri P, Srivastava S, Coulter D, Smith L, Vinorum K, Cappuccio G, Brunetti-Pierri N, Torun D, Arslan M, Lauridsen MF, Murch O, Irving R, Lynch SA, Mehta SG, Carmichael J, Zonneveld-Huijssoon E, de Vries B, Kleefstra T, Johannesen KM, Westphall IT, Hughes SS, Smithson S, Evans J, Dudding-Byth T, Simon M, van Binsbergen E, Herkert JC, Beunders G, Oppermann H, Bakal M, Møller RS, Rubboli G, Bayat A. Rossi A, et al. Clin Genet. 2023 Aug;104(2):186-197. doi: 10.1111/cge.14353. Epub 2023 May 10. Clin Genet. 2023. PMID: 37165752
ROSAH syndrome mimicking chronic uveitis.
Fardeau C, Alafaleq M, Dhaenens CM, Dollfus H, Koné-Paut I, Grunewald O, Morel JB, Titah C, Saadoun D, Lazeran PO, Meunier I. Fardeau C, et al. Clin Genet. 2023 Apr;103(4):453-458. doi: 10.1111/cge.14286. Epub 2022 Dec 30. Clin Genet. 2023. PMID: 36543582
8,767 results