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Page 1
Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish families.
Mahtani MM, Widén E, Lehto M, Thomas J, McCarthy M, Brayer J, Bryant B, Chan G, Daly M, Forsblom C, Kanninen T, Kirby A, Kruglyak L, Munnelly K, Parkkonen M, Reeve-Daly MP, Weaver A, Brettin T, Duyk G, Lander ES, Groop LC. Mahtani MM, et al. Among authors: kirby a. Nat Genet. 1996 Sep;14(1):90-4. doi: 10.1038/ng0996-90. Nat Genet. 1996. PMID: 8782826
Characterization of the MODY3 phenotype. Early-onset diabetes caused by an insulin secretion defect.
Lehto M, Tuomi T, Mahtani MM, Widén E, Forsblom C, Sarelin L, Gullström M, Isomaa B, Lehtovirta M, Hyrkkö A, Kanninen T, Orho M, Manley S, Turner RC, Brettin T, Kirby A, Thomas J, Duyk G, Lander E, Taskinen MR, Groop L. Lehto M, et al. Among authors: kirby a. J Clin Invest. 1997 Feb 15;99(4):582-91. doi: 10.1172/JCI119199. J Clin Invest. 1997. PMID: 9045858 Free PMC article.
Genomewide linkage analysis of stature in multiple populations reveals several regions with evidence of linkage to adult height.
Hirschhorn JN, Lindgren CM, Daly MJ, Kirby A, Schaffner SF, Burtt NP, Altshuler D, Parker A, Rioux JD, Platko J, Gaudet D, Hudson TJ, Groop LC, Lander ES. Hirschhorn JN, et al. Among authors: kirby a. Am J Hum Genet. 2001 Jul;69(1):106-16. doi: 10.1086/321287. Epub 2001 Jun 15. Am J Hum Genet. 2001. PMID: 11410839 Free PMC article.
Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: a comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22.
Middleton FA, Pato MT, Gentile KL, Morley CP, Zhao X, Eisener AF, Brown A, Petryshen TL, Kirby AN, Medeiros H, Carvalho C, Macedo A, Dourado A, Coelho I, Valente J, Soares MJ, Ferreira CP, Lei M, Azevedo MH, Kennedy JL, Daly MJ, Sklar P, Pato CN. Middleton FA, et al. Among authors: kirby an. Am J Hum Genet. 2004 May;74(5):886-97. doi: 10.1086/420775. Epub 2004 Apr 1. Am J Hum Genet. 2004. PMID: 15060841 Free PMC article.
A high-density screen for linkage in multiple sclerosis.
Sawcer S, Ban M, Maranian M, Yeo TW, Compston A, Kirby A, Daly MJ, De Jager PL, Walsh E, Lander ES, Rioux JD, Hafler DA, Ivinson A, Rimmler J, Gregory SG, Schmidt S, Pericak-Vance MA, Akesson E, Hillert J, Datta P, Oturai A, Ryder LP, Harbo HF, Spurkland A, Myhr KM, Laaksonen M, Booth D, Heard R, Stewart G, Lincoln R, Barcellos LF, Hauser SL, Oksenberg JR, Kenealy SJ, Haines JL; International Multiple Sclerosis Genetics Consortium. Sawcer S, et al. Among authors: kirby a. Am J Hum Genet. 2005 Sep;77(3):454-67. doi: 10.1086/444547. Epub 2005 Jul 29. Am J Hum Genet. 2005. PMID: 16080120 Free PMC article.
Genome scan of schizophrenia.
Levinson DF, Mahtani MM, Nancarrow DJ, Brown DM, Kruglyak L, Kirby A, Hayward NK, Crowe RR, Andreasen NC, Black DW, Silverman JM, Endicott J, Sharpe L, Mohs RC, Siever LJ, Walters MK, Lennon DP, Jones HL, Nertney DA, Daly MJ, Gladis M, Mowry BJ. Levinson DF, et al. Among authors: kirby a. Am J Psychiatry. 1998 Jun;155(6):741-50. doi: 10.1176/ajp.155.6.741. Am J Psychiatry. 1998. PMID: 9619145
No support for linkage to the bipolar regions on chromosomes 4p, 18p, or 18q in 43 schizophrenia pedigrees.
Nancarrow DJ, Levinson DF, Taylor JM, Hayward NK, Walters MK, Lennon DP, Nertney DA, Jones HL, Mahtani MM, Kirby A, Kruglyak L, Brown DM, Crowe RR, Andreasen NC, Black DW, Silverman JM, Mohs RC, Siever LJ, Endicott J, Sharpe L, Mowry BJ. Nancarrow DJ, et al. Among authors: kirby a. Am J Med Genet. 2000 Apr 3;96(2):224-7. Am J Med Genet. 2000. PMID: 10893501 No abstract available.
1,072 results