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Heteroplasmy levels of a mitochondrial gene mutation associated with diabetes mellitus decrease in leucocyte DNA upon aging.
't Hart LM, Jansen JJ, Lemkes HH, de Knijff P, Maassen JA. 't Hart LM, et al. Among authors: de knijff p. Hum Mutat. 1996;7(3):193-7. doi: 10.1002/(SICI)1098-1004(1996)7:3<193::AID-HUMU2>3.0.CO;2-C. Hum Mutat. 1996. PMID: 8829651
It was found that 17 out of 18 carriers showed a decrease upon aging (P = 0.001), the average change being -0.69 +/- 0.61% per year. ...
It was found that 17 out of 18 carriers showed a decrease upon aging (P = 0.001), the average change being -0.69 +/- 0.61% per year. …
A new phylogeny of swiftlets (Aves: Apodidae) based on cytochrome-b DNA.
Thomassen HA, Wiersema AT, de Bakker MA, de Knijff P, Hetebrij E, Povel GD. Thomassen HA, et al. Among authors: de bakker ma, de knijff p. Mol Phylogenet Evol. 2003 Oct;29(1):86-93. doi: 10.1016/s1055-7903(03)00066-6. Mol Phylogenet Evol. 2003. PMID: 12967609
The role of selection in the evolution of human mitochondrial genomes.
Kivisild T, Shen P, Wall DP, Do B, Sung R, Davis K, Passarino G, Underhill PA, Scharfe C, Torroni A, Scozzari R, Modiano D, Coppa A, de Knijff P, Feldman M, Cavalli-Sforza LL, Oefner PJ. Kivisild T, et al. Among authors: de knijff p. Genetics. 2006 Jan;172(1):373-87. doi: 10.1534/genetics.105.043901. Epub 2005 Sep 19. Genetics. 2006. PMID: 16172508 Free PMC article.

Phylogenetic analysis of 277 human mitochondrial genomes revealed a significant (P < 0.01) excess of rRNA and nonsynonymous base substitutions among hotspots of recurrent mutation. ...The ratio of nonsynonymous changes from and to threonine and valine differed significa

Phylogenetic analysis of 277 human mitochondrial genomes revealed a significant (P < 0.01) excess of rRNA and nonsynonymous base s

Worldwide population analysis of the 4q and 10q subtelomeres identifies only four discrete interchromosomal sequence transfers in human evolution.
Lemmers RJ, van der Vliet PJ, van der Gaag KJ, Zuniga S, Frants RR, de Knijff P, van der Maarel SM. Lemmers RJ, et al. Among authors: de knijff p. Am J Hum Genet. 2010 Mar 12;86(3):364-77. doi: 10.1016/j.ajhg.2010.01.035. Epub 2010 Mar 4. Am J Hum Genet. 2010. PMID: 20206332 Free PMC article.
Evaluating self-declared ancestry of U.S. Americans with autosomal, Y-chromosomal and mitochondrial DNA.
Lao O, Vallone PM, Coble MD, Diegoli TM, van Oven M, van der Gaag KJ, Pijpe J, de Knijff P, Kayser M. Lao O, et al. Among authors: de knijff p. Hum Mutat. 2010 Dec;31(12):E1875-93. doi: 10.1002/humu.21366. Hum Mutat. 2010. PMID: 20886636 Free PMC article.
IVS10-6T>G, an ancient ATM germline mutation linked with breast cancer.
Broeks A, Urbanus JH, de Knijff P, Devilee P, Nicke M, Klöpper K, Dörk T, Floore AN, van't Veer LJ. Broeks A, et al. Among authors: de knijff p. Hum Mutat. 2003 May;21(5):521-8. doi: 10.1002/humu.10204. Hum Mutat. 2003. PMID: 12673794
., whether it is frequently arising de novo in a population, or whether it can be traced back to a single ancient mutational event. ...
., whether it is frequently arising de novo in a population, or whether it can be traced back to a single ancient mutational event. . …
High-quality mtDNA control region sequences from 680 individuals sampled across the Netherlands to establish a national forensic mtDNA reference database.
Chaitanya L, van Oven M, Brauer S, Zimmermann B, Huber G, Xavier C, Parson W, de Knijff P, Kayser M. Chaitanya L, et al. Among authors: de knijff p. Forensic Sci Int Genet. 2016 Mar;21:158-67. doi: 10.1016/j.fsigen.2015.12.002. Epub 2015 Dec 10. Forensic Sci Int Genet. 2016. PMID: 26774101
Transmission of human mtDNA heteroplasmy in the Genome of the Netherlands families: support for a variable-size bottleneck.
Li M, Rothwell R, Vermaat M, Wachsmuth M, Schröder R, Laros JF, van Oven M, de Bakker PI, Bovenberg JA, van Duijn CM, van Ommen GJ, Slagboom PE, Swertz MA, Wijmenga C; Genome of Netherlands Consortium, Kayser M, Boomsma DI, Zöllner S, de Knijff P, Stoneking M. Li M, et al. Among authors: de bakker pi, de knijff p. Genome Res. 2016 Apr;26(4):417-26. doi: 10.1101/gr.203216.115. Epub 2016 Feb 25. Genome Res. 2016. PMID: 26916109 Free PMC article.
A genome-wide association study identifies a region at chromosome 12 as a potential susceptibility locus for restenosis after percutaneous coronary intervention.
Sampietro ML, Trompet S, Verschuren JJ, Talens RP, Deelen J, Heijmans BT, de Winter RJ, Tio RA, Doevendans PA, Ganesh SK, Nabel EG, Westra HJ, Franke L, van den Akker EB, Westendorp RG, Zwinderman AH, Kastrati A, Koch W, Slagboom PE, de Knijff P, Jukema JW. Sampietro ML, et al. Among authors: de winter rj, de knijff p. Hum Mol Genet. 2011 Dec 1;20(23):4748-57. doi: 10.1093/hmg/ddr389. Epub 2011 Aug 30. Hum Mol Genet. 2011. PMID: 21878436 Free PMC article.
A potential susceptibility locus for restenosis at chromosome 12, including rs10861032 (P(combined) = 1.11 × 10(-7)) and rs9804922 (P(combined) = 1.45 × 10(-6)), was identified in the GWAS and replication phase. In addition, both SNPs were also associated with coron …
A potential susceptibility locus for restenosis at chromosome 12, including rs10861032 (P(combined) = 1.11 × 10(-7)) and rs9804922 ( …
Specific sequence variations within the 4q35 region are associated with facioscapulohumeral muscular dystrophy.
Lemmers RJ, Wohlgemuth M, van der Gaag KJ, van der Vliet PJ, van Teijlingen CM, de Knijff P, Padberg GW, Frants RR, van der Maarel SM. Lemmers RJ, et al. Among authors: de knijff p. Am J Hum Genet. 2007 Nov;81(5):884-94. doi: 10.1086/521986. Epub 2007 Sep 7. Am J Hum Genet. 2007. PMID: 17924332 Free PMC article.
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