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Results by year

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

Year Number of Results
1988 2
1989 7
1990 3
1991 4
1992 1
1993 10
1994 2
1995 3
1996 9
1997 10
1998 6
1999 5
2000 3
2001 2
2002 3
2003 2
2004 1
2005 4
2006 4
2007 1
2008 2
2009 5
2010 4
2011 3
2012 3
2013 2
2014 1
2015 8
2016 4
2017 2
2018 1
2019 2
2020 2
2021 3
2022 3
2024 0

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119 results

Results by year

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Page 1
Defining the disease liability of variants in the cystic fibrosis transmembrane conductance regulator gene.
Sosnay PR, Siklosi KR, Van Goor F, Kaniecki K, Yu H, Sharma N, Ramalho AS, Amaral MD, Dorfman R, Zielenski J, Masica DL, Karchin R, Millen L, Thomas PJ, Patrinos GP, Corey M, Lewis MH, Rommens JM, Castellani C, Penland CM, Cutting GR. Sosnay PR, et al. Among authors: rommens jm. Nat Genet. 2013 Oct;45(10):1160-7. doi: 10.1038/ng.2745. Epub 2013 Aug 25. Nat Genet. 2013. PMID: 23974870 Free PMC article.
Identification of the cystic fibrosis gene: genetic analysis.
Kerem B, Rommens JM, Buchanan JA, Markiewicz D, Cox TK, Chakravarti A, Buchwald M, Tsui LC. Kerem B, et al. Among authors: rommens jm. Science. 1989 Sep 8;245(4922):1073-80. doi: 10.1126/science.2570460. Science. 1989. PMID: 2570460
Progress towards cloning the cystic fibrosis gene.
Tsui LC, Rommens JM, Burns J, Zengerling S, Riordan JR, Carlock LR, Grzeschik KH, Buchwald M. Tsui LC, et al. Among authors: rommens jm. Philos Trans R Soc Lond B Biol Sci. 1988 Jun 15;319(1194):263-73. doi: 10.1098/rstb.1988.0048. Philos Trans R Soc Lond B Biol Sci. 1988. PMID: 2900520 Review.
Bias in CFTR screening panels.
Sosnay PR, Castellani C, Penland CM, Rommens JM, Lewis M, Raraigh KS, Corey M, Cutting GR. Sosnay PR, et al. Among authors: rommens jm. Genet Med. 2016 Feb;18(2):209. doi: 10.1038/gim.2015.105. Epub 2015 Oct 29. Genet Med. 2016. PMID: 26513347 Free PMC article. No abstract available.
Mammographic density: a heritable risk factor for breast cancer.
Boyd NF, Martin LJ, Rommens JM, Paterson AD, Minkin S, Yaffe MJ, Stone J, Hopper JL. Boyd NF, et al. Among authors: rommens jm. Methods Mol Biol. 2009;472:343-60. doi: 10.1007/978-1-60327-492-0_15. Methods Mol Biol. 2009. PMID: 19107441 Review.
Biallelic mutations in DNAJC21 cause Shwachman-Diamond syndrome.
Dhanraj S, Matveev A, Li H, Lauhasurayotin S, Jardine L, Cada M, Zlateska B, Tailor CS, Zhou J, Mendoza-Londono R, Vincent A, Durie PR, Scherer SW, Rommens JM, Heon E, Dror Y. Dhanraj S, et al. Among authors: rommens jm. Blood. 2017 Mar 16;129(11):1557-1562. doi: 10.1182/blood-2016-08-735431. Epub 2017 Jan 6. Blood. 2017. PMID: 28062395 Free article. Clinical Trial. No abstract available.
119 results