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

Year Number of Results
1946 3
1947 3
1948 3
1949 1
1950 1
1951 2
1952 1
1953 3
1954 4
1955 3
1956 4
1957 4
1958 4
1959 2
1960 3
1961 1
1962 2
1963 7
1964 16
1965 27
1966 44
1967 67
1968 81
1969 149
1970 197
1971 195
1972 283
1973 297
1974 439
1975 368
1976 481
1977 476
1978 570
1979 553
1980 533
1981 581
1982 606
1983 626
1984 784
1985 771
1986 876
1987 922
1988 1050
1989 1127
1990 1218
1991 1437
1992 1627
1993 2125
1994 2183
1995 2093
1996 2152
1997 2123
1998 2087
1999 2239
2000 2388
2001 2557
2002 2382
2003 2578
2004 2530
2005 2876
2006 2930
2007 3163
2008 3315
2009 3327
2010 3753
2011 3819
2012 3977
2013 4210
2014 4422
2015 4724
2016 4382
2017 3536
2018 3858
2019 4364
2020 4564
2021 4694
2022 4717
2023 3267
2024 1574

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109,391 results

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Page 1
Showing results for genes genet
Search for Ginés Benet instead (3 results)
Naming human genes.
[No authors listed] [No authors listed] Nat Genet. 2020 Aug;52(8):751. doi: 10.1038/s41588-020-0679-1. Nat Genet. 2020. PMID: 32747823 No abstract available.
Tumor suppressor genes.
Hinds PW, Weinberg RA. Hinds PW, et al. Curr Opin Genet Dev. 1994 Feb;4(1):135-41. doi: 10.1016/0959-437x(94)90102-3. Curr Opin Genet Dev. 1994. PMID: 8193533 Review.
The mutation of tumor suppressor genes is thought to contribute to tumor growth by inactivating proteins that normally act to limit cell proliferation. ...
The mutation of tumor suppressor genes is thought to contribute to tumor growth by inactivating proteins that normally act to limit c …
Human tumor suppressor genes.
Stanbridge EJ. Stanbridge EJ. Annu Rev Genet. 1990;24:615-57. doi: 10.1146/annurev.ge.24.120190.003151. Annu Rev Genet. 1990. PMID: 2088179 Review. No abstract available.
Digenic inheritance and genetic modifiers.
Deltas C. Deltas C. Clin Genet. 2018 Mar;93(3):429-438. doi: 10.1111/cge.13150. Epub 2018 Jan 25. Clin Genet. 2018. PMID: 28977688 Review.
True DI is when biallelic or even triallelic mutations in 2 distinct genes, in cis or in trans, are necessary and sufficient to cause pathology with a defined diagnosis. In true DI, a heterozygous mutation in each of 2 genes alone is not associated with a recognizab …
True DI is when biallelic or even triallelic mutations in 2 distinct genes, in cis or in trans, are necessary and sufficient to cause …
The origin of new genes: glimpses from the young and old.
Long M, Betrán E, Thornton K, Wang W. Long M, et al. Nat Rev Genet. 2003 Nov;4(11):865-75. doi: 10.1038/nrg1204. Nat Rev Genet. 2003. PMID: 14634634 Review.
Genome data have revealed great variation in the numbers of genes in different organisms, which indicates that there is a fundamental process of genome evolution: the origin of new genes. However, there has been little opportunity to explore how genes with ne …
Genome data have revealed great variation in the numbers of genes in different organisms, which indicates that there is a fundamental …
Evolution of the intron-exon structure of eukaryotic genes.
Long M, de Souza SJ, Gilbert W. Long M, et al. Curr Opin Genet Dev. 1995 Dec;5(6):774-8. doi: 10.1016/0959-437x(95)80010-3. Curr Opin Genet Dev. 1995. PMID: 8745076 Review.
The origin and evolution of intron-exon structures continue to be controversial topics. Two alternative theories, the 'exon theory of genes' and the 'insertional theory of introns', debate the presence or absence of introns in primordial genes. ...This analysis dete …
The origin and evolution of intron-exon structures continue to be controversial topics. Two alternative theories, the 'exon theory of gen …
Evolution and expression of vitellogenin genes.
Wahli W. Wahli W. Trends Genet. 1988 Aug;4(8):227-32. doi: 10.1016/0168-9525(88)90155-2. Trends Genet. 1988. PMID: 3072724 Review. No abstract available.
Monogenic disorders.
Carter CO. Carter CO. J Med Genet. 1977 Oct;14(5):316-20. doi: 10.1136/jmg.14.5.316. J Med Genet. 1977. PMID: 563465 Free PMC article. No abstract available.
ARNSHL gene identification: past, present and future.
Imtiaz A. Imtiaz A. Mol Genet Genomics. 2022 Sep;297(5):1185-1193. doi: 10.1007/s00438-022-01926-x. Epub 2022 Jul 23. Mol Genet Genomics. 2022. PMID: 35869994 Review.
It is genetically highly heterogeneous and about 89 gene loci and 76 gene's mutations have been implicated in the etiology of ARNSHL. ...A thorough study of the strategies used in the identification of reported ARNSHL genes and of their relative success can h …
It is genetically highly heterogeneous and about 89 gene loci and 76 gene's mutations have been implicated in the etiology of …
Genes, environment and the value of prospective cohort studies.
Manolio TA, Bailey-Wilson JE, Collins FS. Manolio TA, et al. Nat Rev Genet. 2006 Oct;7(10):812-20. doi: 10.1038/nrg1919. Nat Rev Genet. 2006. PMID: 16983377 Review.
Case-control studies have many advantages for identifying disease-related genes, but are limited in their ability to detect gene-environment interactions. ...
Case-control studies have many advantages for identifying disease-related genes, but are limited in their ability to detect gene-envi …
109,391 results
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