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

Year Number of Results
1985 5
1986 2
1987 6
1989 7
1990 2
1991 2
1992 4
1993 15
1994 6
1995 3
1996 7
1997 9
1998 9
1999 16
2000 6
2001 5
2002 1
2003 3
2004 4
2005 6
2006 3
2007 2
2008 1
2010 1
2011 1
2012 2
2013 1
2015 1
2016 1
2019 1
2020 3
2021 1
2023 1
2024 0

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137 results

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Page 1
Imprinting in Prader-Willi and Angelman syndromes.
Nicholls RD, Saitoh S, Horsthemke B. Nicholls RD, et al. Trends Genet. 1998 May;14(5):194-200. doi: 10.1016/s0168-9525(98)01432-2. Trends Genet. 1998. PMID: 9613204 Review.
Insulin secretion deficits in a Prader-Willi syndrome β-cell model are associated with a concerted downregulation of multiple endoplasmic reticulum chaperones.
Koppes EA, Johnson MA, Moresco JJ, Luppi P, Lewis DW, Stolz DB, Diedrich JK, Yates JR 3rd, Wek RC, Watkins SC, Gollin SM, Park HJ, Drain P, Nicholls RD. Koppes EA, et al. Among authors: nicholls rd. PLoS Genet. 2023 Apr 17;19(4):e1010710. doi: 10.1371/journal.pgen.1010710. eCollection 2023 Apr. PLoS Genet. 2023. PMID: 37068109 Free PMC article.
Mosaicism in Prader-Willi syndrome.
Nicholls RD. Nicholls RD. Am J Med Genet. 2000 Jan 17;90(2):175-6. doi: 10.1002/(sici)1096-8628(20000117)90:2<175::aid-ajmg18>3.0.co;2-e. Am J Med Genet. 2000. PMID: 10607961 No abstract available.
137 results